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Phénomènes génétiques
Phénomènes génétiques : Questions médicales fréquentes
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},
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},
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},
{
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},
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},
{
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},
{
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},
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},
{
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},
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},
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},
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},
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},
{
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},
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},
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},
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},
{
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}
},
{
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}
},
{
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},
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},
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"identifier": {
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}
},
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}
},
{
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}
},
{
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}
},
{
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}
},
{
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}
},
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},
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}
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},
{
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}
},
{
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},
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},
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}
},
{
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}
},
{
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},
{
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},
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},
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{
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},
{
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},
{
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},
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}
},
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}
},
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}
}
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},
{
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},
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},
{
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},
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},
{
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}
},
{
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}
},
{
"@type": "MedicalWebPage",
"name": "Gènes suppresseurs de tumeur",
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"about": {
"@type": "MedicalCondition",
"name": "Gènes suppresseurs de tumeur",
"code": {
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}
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},
{
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},
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},
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},
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},
{
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},
{
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},
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},
{
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]
},
{
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},
{
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},
{
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},
{
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{
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"propertyID": "MeSH Tree",
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}
},
{
"@type": "MedicalWebPage",
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"about": {
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},
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"propertyID": "MeSH Tree",
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}
}
}
]
},
{
"@type": "MedicalWebPage",
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"@type": "MedicalCondition",
"name": "ADN caténé",
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"@type": "MedicalCode",
"code": "D043864",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
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}
}
},
{
"@type": "MedicalWebPage",
"name": "ADN superhélicoïdal",
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"about": {
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"codingSystem": "MeSH"
},
"identifier": {
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"propertyID": "MeSH Tree",
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}
}
},
{
"@type": "MedicalWebPage",
"name": "ADN concaténé",
"alternateName": "DNA, Concatenated",
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"name": "ADN concaténé",
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"codingSystem": "MeSH"
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"propertyID": "MeSH Tree",
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}
}
},
{
"@type": "MedicalWebPage",
"name": "ADN cruciforme",
"alternateName": "DNA, Cruciform",
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"name": "ADN cruciforme",
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"codingSystem": "MeSH"
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"@type": "PropertyValue",
"propertyID": "MeSH Tree",
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}
},
{
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}
},
{
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}
},
{
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}
},
{
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}
},
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},
{
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}
},
{
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}
}
]
},
{
"@type": "MedicalWebPage",
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"name": "Appariement de bases",
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}
},
{
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}
},
{
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}
},
{
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}
},
{
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},
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},
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}
]
},
{
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}
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}
},
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}
},
{
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}
},
{
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}
},
{
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}
},
{
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}
},
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},
{
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},
{
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}
},
{
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}
},
{
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"name": "Plasmides",
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}
},
"hasPart": [
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},
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}
},
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},
{
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},
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}
},
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}
},
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}
}
]
},
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}
},
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"item": "https://recherchemedicale.com/mesh/D055614"
}
]
}
},
{
"@type": "MedicalWebPage",
"name": "Article complet : Phénomènes génétiques - Questions et réponses",
"headline": "Questions et réponses médicales fréquentes sur Phénomènes génétiques",
"description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.",
"datePublished": "2025-01-22",
"inLanguage": "fr",
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Diagnostic",
"headline": "Diagnostic sur Phénomènes génétiques",
"description": "Comment diagnostiquer une maladie génétique ?\nQuels tests sont utilisés pour les anomalies chromosomiques ?\nQu'est-ce qu'un test de porteur ?\nQuels symptômes indiquent une maladie génétique ?\nComment l'historique familial aide-t-il au diagnostic ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-diagnostic"
},
{
"@type": "MedicalWebPage",
"name": "Symptômes",
"headline": "Symptômes sur Phénomènes génétiques",
"description": "Quels sont les symptômes des maladies génétiques ?\nLes maladies génétiques peuvent-elles être asymptomatiques ?\nComment les symptômes évoluent-ils avec l'âge ?\nQuels symptômes sont associés à la fibrose kystique ?\nLes maladies génétiques affectent-elles le développement ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-symptômes"
},
{
"@type": "MedicalWebPage",
"name": "Prévention",
"headline": "Prévention sur Phénomènes génétiques",
"description": "Peut-on prévenir les maladies génétiques ?\nQuel rôle joue le dépistage prénatal ?\nComment les conseils génétiques aident-ils ?\nLes vaccinations peuvent-elles prévenir des maladies génétiques ?\nQuelles sont les recommandations pour les familles à risque ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-prévention"
},
{
"@type": "MedicalWebPage",
"name": "Traitements",
"headline": "Traitements sur Phénomènes génétiques",
"description": "Quels traitements existent pour les maladies génétiques ?\nLa thérapie génique est-elle efficace ?\nComment gérer les symptômes d'une maladie génétique ?\nLes traitements sont-ils personnalisés ?\nQuelles sont les avancées en recherche génétique ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-traitements"
},
{
"@type": "MedicalWebPage",
"name": "Complications",
"headline": "Complications sur Phénomènes génétiques",
"description": "Quelles complications peuvent survenir avec les maladies génétiques ?\nLes maladies génétiques augmentent-elles le risque de cancer ?\nComment les maladies génétiques affectent-elles la qualité de vie ?\nLes complications sont-elles prévisibles ?\nQuelles sont les implications psychologiques des maladies génétiques ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-complications"
},
{
"@type": "MedicalWebPage",
"name": "Facteurs de risque",
"headline": "Facteurs de risque sur Phénomènes génétiques",
"description": "Quels sont les facteurs de risque pour les maladies génétiques ?\nL'âge des parents influence-t-il les maladies génétiques ?\nLes antécédents familiaux augmentent-ils le risque ?\nLes facteurs environnementaux jouent-ils un rôle ?\nComment le mode de vie influence-t-il les maladies génétiques ?",
"url": "https://recherchemedicale.com/mesh/D055614#section-facteurs de risque"
}
]
},
{
"@type": "FAQPage",
"mainEntity": [
{
"@type": "Question",
"name": "Comment diagnostiquer une maladie génétique ?",
"position": 1,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un diagnostic repose sur des tests génétiques, l'examen clinique et l'historique familial."
}
},
{
"@type": "Question",
"name": "Quels tests sont utilisés pour les anomalies chromosomiques ?",
"position": 2,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les caryotypes et les analyses de microdélétions sont couramment utilisés."
}
},
{
"@type": "Question",
"name": "Qu'est-ce qu'un test de porteur ?",
"position": 3,
"acceptedAnswer": {
"@type": "Answer",
"text": "C'est un test pour déterminer si une personne est porteuse d'une mutation génétique."
}
},
{
"@type": "Question",
"name": "Quels symptômes indiquent une maladie génétique ?",
"position": 4,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des symptômes variés comme des malformations, des troubles du développement ou des maladies chroniques."
}
},
{
"@type": "Question",
"name": "Comment l'historique familial aide-t-il au diagnostic ?",
"position": 5,
"acceptedAnswer": {
"@type": "Answer",
"text": "Il permet d'identifier des patterns héréditaires et des risques accrus de maladies."
}
},
{
"@type": "Question",
"name": "Quels sont les symptômes des maladies génétiques ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes varient, incluant des anomalies physiques, des troubles mentaux ou des maladies métaboliques."
}
},
{
"@type": "Question",
"name": "Les maladies génétiques peuvent-elles être asymptomatiques ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines personnes peuvent être porteuses sans présenter de symptômes visibles."
}
},
{
"@type": "Question",
"name": "Comment les symptômes évoluent-ils avec l'âge ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certains symptômes peuvent s'aggraver avec l'âge, tandis que d'autres peuvent apparaître tardivement."
}
},
{
"@type": "Question",
"name": "Quels symptômes sont associés à la fibrose kystique ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Toux persistante, infections pulmonaires fréquentes et problèmes digestifs."
}
},
{
"@type": "Question",
"name": "Les maladies génétiques affectent-elles le développement ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, elles peuvent entraîner des retards de développement physique et cognitif."
}
},
{
"@type": "Question",
"name": "Peut-on prévenir les maladies génétiques ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines maladies peuvent être prévenues par des tests de porteur et des conseils génétiques."
}
},
{
"@type": "Question",
"name": "Quel rôle joue le dépistage prénatal ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le dépistage prénatal permet d'identifier des anomalies génétiques chez le fœtus."
}
},
{
"@type": "Question",
"name": "Comment les conseils génétiques aident-ils ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Ils fournissent des informations sur les risques héréditaires et les options de reproduction."
}
},
{
"@type": "Question",
"name": "Les vaccinations peuvent-elles prévenir des maladies génétiques ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Non, les vaccinations ne préviennent pas les maladies génétiques, mais elles préviennent des infections."
}
},
{
"@type": "Question",
"name": "Quelles sont les recommandations pour les familles à risque ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les familles à risque devraient consulter un généticien pour évaluer les options de dépistage."
}
},
{
"@type": "Question",
"name": "Quels traitements existent pour les maladies génétiques ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les traitements incluent la thérapie génique, les médicaments et la gestion des symptômes."
}
},
{
"@type": "Question",
"name": "La thérapie génique est-elle efficace ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elle peut être efficace pour certaines maladies, mais les résultats varient selon les cas."
}
},
{
"@type": "Question",
"name": "Comment gérer les symptômes d'une maladie génétique ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "La gestion peut inclure des médicaments, des thérapies physiques et un suivi régulier."
}
},
{
"@type": "Question",
"name": "Les traitements sont-ils personnalisés ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les traitements peuvent être adaptés en fonction des mutations spécifiques et des symptômes."
}
},
{
"@type": "Question",
"name": "Quelles sont les avancées en recherche génétique ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des avancées incluent la thérapie génique, CRISPR et des traitements ciblés pour certaines maladies."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec les maladies génétiques ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications incluent des troubles de santé chroniques, des handicaps et des risques accrus de cancers."
}
},
{
"@type": "Question",
"name": "Les maladies génétiques augmentent-elles le risque de cancer ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines mutations génétiques sont associées à un risque accru de cancers spécifiques."
}
},
{
"@type": "Question",
"name": "Comment les maladies génétiques affectent-elles la qualité de vie ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elles peuvent entraîner des limitations physiques, des problèmes psychologiques et des besoins médicaux accrus."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles prévisibles ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines complications peuvent être anticipées, mais d'autres peuvent survenir de manière imprévisible."
}
},
{
"@type": "Question",
"name": "Quelles sont les implications psychologiques des maladies génétiques ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elles peuvent entraîner de l'anxiété, de la dépression et des défis émotionnels pour les patients et les familles."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque pour les maladies génétiques ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs incluent l'hérédité, l'âge parental avancé et certaines expositions environnementales."
}
},
{
"@type": "Question",
"name": "L'âge des parents influence-t-il les maladies génétiques ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un âge parental avancé est associé à un risque accru de certaines anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les antécédents familiaux augmentent-ils le risque ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des antécédents familiaux de maladies génétiques augmentent le risque pour les descendants."
}
},
{
"@type": "Question",
"name": "Les facteurs environnementaux jouent-ils un rôle ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines expositions environnementales peuvent interagir avec des prédispositions génétiques."
}
},
{
"@type": "Question",
"name": "Comment le mode de vie influence-t-il les maladies génétiques ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un mode de vie sain peut atténuer certains risques, mais ne peut pas prévenir les maladies génétiques."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 22/11/2024
Contenu vérifié selon les dernières recommandations médicales
└─
Sélection
Breeding
D001947
-
G05.090
└─
Reprogrammation cellulaire
Cellular Reprogramming
D065150
-
G05.135
└─
Évolution clonale
Clonal Evolution
D060965
-
G05.158
└─
Consanguinité
Consanguinity
D003241
-
G05.180
└─
Clivage de l'ADN
DNA Cleavage
D053837
-
G05.193
└─
Altération de l'ADN
DNA Damage
D004249
-
G05.200
└─
Méthylation de l'ADN
DNA Methylation
D019175
-
G05.206
└─
Empaquetage de l'ADN
DNA Packaging
D042003
-
G05.213
└─
Réparation de l'ADN
DNA Repair
D004260
-
G05.219
└─
Réplication de l'ADN
DNA Replication
D004261
-
G05.226
└─
Effet fondateur
Founder Effect
D018703
-
G05.285
└─
Expression des gènes
Gene Expression
D015870
-
G05.297
└─
Régulation de l'expression des gènes
Gene Expression Regulation
D005786
-
G05.308
└─
Fréquence d'allèle
Gene Frequency
D005787
-
G05.330
└─
Ordre des gènes
Gene Order
D023061
-
G05.340
└─
Pool des gènes
Gene Pool
D005788
-
G05.342
└─
Réarrangement des gènes
Gene Rearrangement
D015321
-
G05.344
└─
Contexte génétique
Genetic Background
D000068617
-
G05.346
└─
Aptitude génétique
Genetic Fitness
D056084
-
G05.347
└─
Liaison génétique
Genetic Linkage
D008040
-
G05.348
└─
Fardeau génétique
Genetic Load
D040741
-
G05.350
└─
Structures génétiques
Genetic Structures
D040342
-
G05.360
└─
Variation génétique
Genetic Variation
D014644
-
G05.365
└─
Instabilité du génome
Genomic Instability
D042822
-
G05.370
└─
Génotype
Genotype
D005838
-
G05.380
└─
Hérédité
Heredity
D040941
-
G05.390
└─
Vigueur hybride
Hybrid Vigor
D006823
-
G05.400
└─
Dépression de consanguinité
Inbreeding Depression
D000071422
-
G05.410
└─
Modes de transmission héréditaire
Inheritance Patterns
D040582
-
G05.420
└─
Mutagenèse
Mutagenesis
D016296
-
G05.558
└─
Dénaturation d'acide nucléique
Nucleic Acid Denaturation
D009691
-
G05.627
└─
Phénotype
Phenotype
D010641
-
G05.695
└─
Ploïdies
Ploidies
D011003
-
G05.700
└─
Recombinaison génétique
Recombination, Genetic
D011995
-
G05.728
└─
Clivage de l'ARN
RNA Cleavage
D059367
-
G05.755
└─
Sélection génétique
Selection, Genetic
D012641
-
G05.783
└─
Similitude de séquences
Sequence Homology
D017385
-
G05.810
└─
Similitude structurale de protéines
Structural Homology, Protein
D040681
-
G05.820
└─
Sympatrie
Sympatry
D061350
-
G05.910
└─└─
Hybridation génétique
Hybridization, Genetic
D006824
-
G05.090.390
└─└─
Croisement consanguin
Inbreeding
D007178
-
G05.090.403
└─└─
Reproduction sélective
Selective Breeding
D000068618
-
G05.090.701
└─└─
Division du noyau cellulaire
Cell Nucleus Division
D048750
-
G05.113.220
└─└─
Adduits à l'ADN
DNA Adducts
D018736
-
G05.200.104
└─└─
Cassures de l'ADN
DNA Breaks
D053960
-
G05.200.210
└─└─
Dégradation nécrotique de l'ADN
DNA Degradation, Necrotic
D053836
-
G05.200.220
└─└─
Fragmentation de l'ADN
DNA Fragmentation
D053938
-
G05.200.230
└─└─
Réparation de l'ADN par jonction d'extrémités
DNA End-Joining Repair
D059766
-
G05.219.200
└─└─
Réparation de mésappariement de l'ADN
DNA Mismatch Repair
D053843
-
G05.219.220
└─└─
Réponse SOS (génétique)
SOS Response, Genetics
D013014
-
G05.219.830
└─└─
Déroulement de la réplication de l'ADN
DNA Replication Timing
D042522
-
G05.226.760
└─└─
Endoréplication
Endoreduplication
D062951
-
G05.226.820
└─└─
Phase S
S Phase
D016196
-
G05.226.880
└─└─
Biosynthèse des protéines
Protein Biosynthesis
D014176
-
G05.297.670
└─└─
Transcription génétique
Transcription, Genetic
D014158
-
G05.297.700
└─└─
Assemblage et désassemblage de la chromatine
Chromatin Assembly and Disassembly
D042002
-
G05.308.095
└─└─
Expression génique ectopique
Ectopic Gene Expression
D000066630
-
G05.308.202
└─└─
Épigenèse génétique
Epigenesis, Genetic
D044127
-
G05.308.203
└─└─
Épistasie
Epistasis, Genetic
D004843
-
G05.308.207
└─└─
Décalage ribosomique
Frameshifting, Ribosomal
D018965
-
G05.308.215
└─└─
Régulation de l'expression des gènes archéens
Gene Expression Regulation, Archaeal
D019848
-
G05.308.290
└─└─
Régulation de l'expression des gènes bactériens
Gene Expression Regulation, Bacterial
D015964
-
G05.308.300
└─└─
Régulation de l'expression des gènes au cours du développement
Gene Expression Regulation, Developmental
D018507
-
G05.308.310
└─└─
Régulation de l'expression des gènes codant pour des enzymes
Gene Expression Regulation, Enzymologic
D015971
-
G05.308.320
└─└─
Régulation de l'expression des gènes fongiques
Gene Expression Regulation, Fungal
D015966
-
G05.308.330
└─└─
Régulation de l'expression des gènes tumoraux
Gene Expression Regulation, Neoplastic
D015972
-
G05.308.370
└─└─
Régulation de l'expression des gènes végétaux
Gene Expression Regulation, Plant
D018506
-
G05.308.375
└─└─
Régulation de l'expression des gènes viraux
Gene Expression Regulation, Viral
D015967
-
G05.308.385
└─└─
Modification traductionnelle des protéines
Protein Modification, Translational
D046188
-
G05.308.670
└─└─
Maturation post-transcriptionnelle des ARN
RNA Processing, Post-Transcriptional
D012323
-
G05.308.700
└─└─
Activation de la transcription
Transcriptional Activation
D015533
-
G05.308.800
└─└─
Flux des gènes
Gene Flow
D051456
-
G05.330.159
└─└─
Profil génétique
Genetic Profile
D000076610
-
G05.346.500
└─└─
Déséquilibre de liaison
Linkage Disequilibrium
D015810
-
G05.348.500
└─└─
Lod score
Lod Score
D008126
-
G05.348.750
└─└─
Structures de chromosome
Chromosome Structures
D022004
-
G05.360.160
└─└─
Chromosomes
Chromosomes
D002875
-
G05.360.162
└─└─
Banque de gènes
Gene Library
D015723
-
G05.360.325
└─└─
Code génétique
Genetic Code
D005815
-
G05.360.335
└─└─
Vecteurs génétiques
Genetic Vectors
D005822
-
G05.360.337
└─└─
Génome
Genome
D016678
-
G05.360.340
└─└─
Code histone
Histone Code
D042421
-
G05.360.360
└─└─
Conformation d'acide nucléique
Nucleic Acid Conformation
D009690
-
G05.360.580
└─└─
Plasmides
Plasmids
D010957
-
G05.360.600
└─└─
Matrices (génétique)
Templates, Genetic
D013698
-
G05.360.840
└─└─
Transcriptome
Transcriptome
D059467
-
G05.360.920
└─└─
Hétérogénéité génétique
Genetic Heterogeneity
D018740
-
G05.365.331
└─└─
Hétéroplasmie
Heteroplasmy
D000081942
-
G05.365.461
└─└─
Mutation
Mutation
D009154
-
G05.365.590
└─└─
Variation de phase
Phase Variation
D000090502
-
G05.365.693
└─└─
Polymorphisme génétique
Polymorphism, Genetic
D011110
-
G05.365.795
└─└─
Quasi-espèce
Quasispecies
D000074704
-
G05.365.897
└─└─
Instabilité des chromosomes
Chromosomal Instability
D043171
-
G05.370.180
└─└─
Instabilité des microsatellites
Microsatellite Instability
D053842
-
G05.370.590
└─└─
Dosage génique
Gene Dosage
D018628
-
G05.380.350
└─└─
Prédisposition génétique à une maladie
Genetic Predisposition to Disease
D020022
-
G05.380.355
└─└─
Haplotypes
Haplotypes
D006239
-
G05.380.360
└─└─
Hémizygote
Hemizygote
D057898
-
G05.380.371
└─└─
Hétérozygote
Heterozygote
D006579
-
G05.380.383
└─└─
Homozygote
Homozygote
D006720
-
G05.380.554
└─└─
Anticipation génétique
Anticipation, Genetic
D020132
-
G05.420.040
└─└─
Hérédité extrachromosomique
Extrachromosomal Inheritance
D005111
-
G05.420.275
└─└─
Gènes dominants
Genes, Dominant
D005799
-
G05.420.320
└─└─
Gènes récessifs
Genes, Recessive
D005808
-
G05.420.325
└─└─
Gènes liés au chromosome X
Genes, X-Linked
D050172
-
G05.420.457
└─└─
Gènes liés au chromosome Y
Genes, Y-Linked
D050173
-
G05.420.523
└─└─
Hérédité multifactorielle
Multifactorial Inheritance
D020412
-
G05.420.590
└─└─
Hérédité paternelle
Paternal Inheritance
D000072740
-
G05.420.623
└─└─
Caractère quantitatif héréditaire
Quantitative Trait, Heritable
D019655
-
G05.420.720
└─└─
Substitution d'acide aminé
Amino Acid Substitution
D019943
-
G05.558.109
└─└─
Duplication chromosomique
Chromosome Duplication
D058674
-
G05.558.164
└─└─
Expansion de séquence répétée de l'ADN
DNA Repeat Expansion
D042622
-
G05.558.220
└─└─
Amplification de gène
Gene Amplification
D005784
-
G05.558.315
└─└─
Duplication de gène
Gene Duplication
D020440
-
G05.558.320
└─└─
Mutation de type INDEL
INDEL Mutation
D054643
-
G05.558.370
└─└─
Mutagenèse par insertion
Mutagenesis, Insertional
D016254
-
G05.558.550
└─└─
Non-disjonction génétique
Nondisjunction, Genetic
D009630
-
G05.558.620
└─└─
Délétion de séquence
Sequence Deletion
D017384
-
G05.558.800
└─└─
Inversion de séquence
Sequence Inversion
D057345
-
G05.558.805
└─└─
Suppression génétique
Suppression, Genetic
D013489
-
G05.558.835
└─└─
Translocation génétique
Translocation, Genetic
D014178
-
G05.558.860
└─└─
Endophénotypes
Endophenotypes
D058068
-
G05.695.224
└─└─
Interaction entre gènes et environnement
Gene-Environment Interaction
D059647
-
G05.695.337
└─└─
Marqueurs génétiques
Genetic Markers
D005819
-
G05.695.450
└─└─
Pléiotropie
Genetic Pleiotropy
D058685
-
G05.695.550
└─└─
Pénétrance
Penetrance
D019683
-
G05.695.650
└─└─
Sérogroupe
Serogroup
D065288
-
G05.695.825
└─└─
Aneuploïdie
Aneuploidy
D000782
-
G05.700.131
└─└─
Diploïdie
Diploidy
D004171
-
G05.700.264
└─└─
Haploïdie
Haploidy
D006238
-
G05.700.456
└─└─
Polyploïdie
Polyploidy
D011123
-
G05.700.740
└─└─
Conjugaison génétique
Conjugation, Genetic
D003227
-
G05.728.200
└─└─
Fusion de gènes
Gene Fusion
D050939
-
G05.728.385
└─└─
Transfert horizontal de gène
Gene Transfer, Horizontal
D022761
-
G05.728.390
└─└─
Recombinaison homologue
Homologous Recombination
D059765
-
G05.728.615
└─└─
Transduction génétique
Transduction, Genetic
D014161
-
G05.728.850
└─└─
Transfection
Transfection
D014162
-
G05.728.860
└─└─
Transformation génétique
Transformation, Genetic
D014170
-
G05.728.865
└─└─
Recombinaison V(D)J
V(D)J Recombination
D060152
-
G05.728.932
└─└─
Sélection sexuelle
Sexual Selection
D000082723
-
G05.783.500
└─└─
Similitude de séquences d'acides aminés
Sequence Homology, Amino Acid
D017386
-
G05.810.200
└─└─
Similitude de séquences d'acides nucléiques
Sequence Homology, Nucleic Acid
D012689
-
G05.810.550
└─└─└─
Introgression génétique
Genetic Introgression
D000079425
-
G05.090.390.500
└─└─└─
Ségrégation des chromosomes
Chromosome Segregation
D020090
-
G05.113.220.625
└─└─└─
Méiose
Meiosis
D008540
-
G05.113.220.687
└─└─└─
Mitose
Mitosis
D008938
-
G05.113.220.781
└─└─└─
Cassures double-brin de l'ADN
DNA Breaks, Double-Stranded
D053903
-
G05.200.210.220
└─└─└─
Cassures simple-brin de l'ADN
DNA Breaks, Single-Stranded
D053904
-
G05.200.210.230
└─└─└─
Transcription inverse
Reverse Transcription
D048348
-
G05.297.700.500
└─└─└─
Élongation de la transcription
Transcription Elongation, Genetic
D061805
-
G05.297.700.562
└─└─└─
Initiation de la transcription
Transcription Initiation, Genetic
D061785
-
G05.297.700.625
└─└─└─
Terminaison de la transcription
Transcription Termination, Genetic
D061806
-
G05.297.700.687
└─└─└─
Effets de position chromosomique
Chromosomal Position Effects
D055012
-
G05.308.203.124
└─└─└─
Compensation de dosage génétique
Dosage Compensation, Genetic
D004303
-
G05.308.203.249
└─└─└─
Mémoire épigénétique
Epigenetic Memory
D000094363
-
G05.308.203.280
└─└─└─
Répression épigénétique
Epigenetic Repression
D063185
-
G05.308.203.311
└─└─└─
Extinction de l'expression des gènes
Gene Silencing
D020868
-
G05.308.203.374
└─└─└─
Empreinte génomique
Genomic Imprinting
D018392
-
G05.308.203.500
└─└─└─
Induction enzymatique
Enzyme Induction
D004790
-
G05.308.320.200
└─└─└─
Répression enzymatique
Enzyme Repression
D004794
-
G05.308.320.300
└─└─└─
Régulation de l'expression des gènes dans la leucémie
Gene Expression Regulation, Leukemic
D015973
-
G05.308.370.500
└─└─└─
Dérivation de ribosome
Ribosome Shunting
D000094409
-
G05.308.385.500
└─└─└─
Maturation post-traductionnelle des protéines
Protein Processing, Post-Translational
D011499
-
G05.308.670.600
└─└─└─
Dégradation des ARNm non-sens
Nonsense Mediated mRNA Decay
D059365
-
G05.308.700.112
└─└─└─
Maturation de l'extrémité 3' des ARN
RNA 3' End Processing
D026721
-
G05.308.700.225
└─└─└─
Édition des ARN
RNA Editing
D017393
-
G05.308.700.250
└─└─└─
Épissage des ARN
RNA Splicing
D012326
-
G05.308.700.700
└─└─└─
Séquence riche en AT
AT Rich Sequence
D020856
-
G05.360.080.040
└─└─└─
Séquence riche en GC
GC Rich Sequence
D020862
-
G05.360.080.380
└─└─└─
Régions d'ancrage à la matrice nucléaire
Matrix Attachment Regions
D045170
-
G05.360.080.534
└─└─└─
Séquences d'acides nucléiques régulatrices
Regulatory Sequences, Nucleic Acid
D012045
-
G05.360.080.689
└─└─└─
Séquences répétées d'acides nucléiques
Repetitive Sequences, Nucleic Acid
D012091
-
G05.360.080.708
└─└─└─
Centromère
Centromere
D002503
-
G05.360.160.165
└─└─└─
Chromatides
Chromatids
D002842
-
G05.360.160.175
└─└─└─
Chromatine
Chromatin
D002843
-
G05.360.160.180
└─└─└─
Complexe synaptonémal
Synaptonemal Complex
D013573
-
G05.360.160.830
└─└─└─
Télomère
Telomere
D016615
-
G05.360.160.845
└─└─└─
Chromosomes d'archéobactérie
Chromosomes, Archaeal
D019847
-
G05.360.162.167
└─└─└─
Chromosomes de bactérie
Chromosomes, Bacterial
D002876
-
G05.360.162.190
└─└─└─
Chromosomes de champignon
Chromosomes, Fungal
D015825
-
G05.360.162.360
└─└─└─
Chromosomes d'insecte
Chromosomes, Insect
D059006
-
G05.360.162.440
└─└─└─
Chromosomes de mammifère
Chromosomes, Mammalian
D033481
-
G05.360.162.520
└─└─└─
Chromosomes de plante
Chromosomes, Plant
D032461
-
G05.360.162.560
└─└─└─
Caryotype
Karyotype
D059785
-
G05.360.162.679
└─└─└─
Chromosomes sexuels
Sex Chromosomes
D012730
-
G05.360.162.865
└─└─└─
Banque de peptides
Peptide Library
D019151
-
G05.360.325.640
└─└─└─
Anticodon
Anticodon
D000926
-
G05.360.335.060
└─└─└─
Cadres de lecture
Reading Frames
D016364
-
G05.360.335.760
└─└─└─
Chromosomes artificiels
Chromosomes, Artificial
D022201
-
G05.360.337.249
└─└─└─
Épigénome
Epigenome
D000081122
-
G05.360.340.006
└─└─└─
Exome
Exome
D059472
-
G05.360.340.011
└─└─└─
Composants de génome
Genome Components
D040481
-
G05.360.340.024
└─└─└─
Taille du génome
Genome Size
D059646
-
G05.360.340.037
└─└─└─
Génome d'helminthe
Genome, Helminth
D049751
-
G05.360.340.337
└─└─└─
Génome humain
Genome, Human
D015894
-
G05.360.340.350
└─└─└─
Génome d'insecte
Genome, Insect
D049750
-
G05.360.340.357
└─└─└─
Génome microbien
Genome, Microbial
D064349
-
G05.360.340.358
└─└─└─
Génome mitochondrial
Genome, Mitochondrial
D054629
-
G05.360.340.360
└─└─└─
Génome végétal
Genome, Plant
D018745
-
G05.360.340.365
└─└─└─
Génome plastidique
Genome, Plastid
D054627
-
G05.360.340.370
└─└─└─
Génome de protozoaire
Genome, Protozoan
D018503
-
G05.360.340.397
└─└─└─
Banque génomique
Genomic Library
D015698
-
G05.360.340.425
└─└─└─
Métagénome
Metagenome
D054892
-
G05.360.340.550
└─└─└─
Appariement de bases
Base Pairing
D020029
-
G05.360.580.100
└─└─└─
Forme A de l'ADN
DNA, A-Form
D044704
-
G05.360.580.114
└─└─└─
Forme B de l'ADN
DNA, B-Form
D059371
-
G05.360.580.121
└─└─└─
Forme C de l'ADN
DNA, C-Form
D044705
-
G05.360.580.128
└─└─└─
ADN circulaire
DNA, Circular
D004270
-
G05.360.580.156
└─└─└─
ADN concaténé
DNA, Concatenated
D044708
-
G05.360.580.212
└─└─└─
ADN cruciforme
DNA, Cruciform
D045566
-
G05.360.580.325
└─└─└─
ADN simple brin
DNA, Single-Stranded
D004277
-
G05.360.580.437
└─└─└─
Forme Z de l'ADN
DNA, Z-Form
D043542
-
G05.360.580.493
└─└─└─
G-quadruplexes
G-Quadruplexes
D054856
-
G05.360.580.550
└─└─└─
Motifs nucléotidiques
Nucleotide Motifs
D059372
-
G05.360.580.662
└─└─└─
Structures en boucle R
R-Loop Structures
D000080870
-
G05.360.580.690
└─└─└─
Pliage de l'ARN
RNA Folding
D059370
-
G05.360.580.718
└─└─└─
ARN double brin
RNA, Double-Stranded
D012330
-
G05.360.580.775
└─└─└─
Plasmides bactériocinogènes
Bacteriocin Plasmids
D003086
-
G05.360.600.080
└─└─└─
Cosmides
Cosmids
D003360
-
G05.360.600.250
└─└─└─
Facteur F
F Factor
D005144
-
G05.360.600.300
└─└─└─
Plasmides de l'hémolysine
Hemolysin Factors
D006459
-
G05.360.600.430
└─└─└─
Plasmides lactose
Lactose Factors
D007786
-
G05.360.600.500
└─└─└─
Plasmides inducteurs de tumeurs de plantes
Plant Tumor-Inducing Plasmids
D036741
-
G05.360.600.550
└─└─└─
Facteurs R
R Factors
D011815
-
G05.360.600.600
└─└─└─
Déséquilibre allélique
Allelic Imbalance
D022981
-
G05.365.590.029
└─└─└─
Mésappariement de bases
Base Pair Mismatch
D020137
-
G05.365.590.060
└─└─└─
Aberrations des chromosomes
Chromosome Aberrations
D002869
-
G05.365.590.175
└─└─└─
Codon non-sens
Codon, Nonsense
D018389
-
G05.365.590.195
└─└─└─
Mutation avec décalage du cadre de lecture
Frameshift Mutation
D016368
-
G05.365.590.265
└─└─└─
Mutation gain de fonction
Gain of Function Mutation
D000073659
-
G05.365.590.288
└─└─└─
Mutation germinale
Germ-Line Mutation
D018095
-
G05.365.590.350
└─└─└─
Mutation perte de fonction
Loss of Function Mutation
D000073658
-
G05.365.590.538
└─└─└─
Accumulation de mutations
Mutation Accumulation
D000067552
-
G05.365.590.594
└─└─└─
Mutation faux-sens
Mutation, Missense
D020125
-
G05.365.590.650
└─└─└─
Mutation ponctuelle
Point Mutation
D017354
-
G05.365.590.675
└─└─└─
Mutation inapparente
Silent Mutation
D000069456
-
G05.365.590.803
└─└─└─
Mutations synthétiques létales
Synthetic Lethal Mutations
D000072020
-
G05.365.590.917
└─└─└─
Variation structurale du génome
Genomic Structural Variation
D056914
-
G05.365.795.297
└─└─└─
Variants pharmacogénomiques
Pharmacogenomic Variants
D000071184
-
G05.365.795.446
└─└─└─
Polymorphisme de restriction
Polymorphism, Restriction Fragment Length
D012150
-
G05.365.795.595
└─└─└─
Polymorphisme de nucléotide simple
Polymorphism, Single Nucleotide
D020641
-
G05.365.795.598
└─└─└─
Polymorphisme de conformation simple brin
Polymorphism, Single-Stranded Conformational
D018807
-
G05.365.795.600
└─└─└─
Fragilité des chromosomes
Chromosome Fragility
D002873
-
G05.370.180.180
└─└─└─
Haploinsuffisance
Haploinsufficiency
D057895
-
G05.380.350.500
└─└─└─
Gènes chloroplastiques
Genes, Chloroplast
D061125
-
G05.420.275.249
└─└─└─
Gènes de mitochondrie
Genes, Mitochondrial
D050259
-
G05.420.275.500
└─└─└─
Hérédité maternelle
Maternal Inheritance
D000072741
-
G05.420.275.750
└─└─└─
Expansion de trinucléotide répété
Trinucleotide Repeat Expansion
D019680
-
G05.558.220.865
└─└─└─
Délétion de gène
Gene Deletion
D017353
-
G05.558.800.320
└─└─└─
Inversion chromosomique
Chromosome Inversion
D007446
-
G05.558.805.500
└─└─└─
Monosomie
Monosomy
D009006
-
G05.700.131.500
└─└─└─
Tétrasomie
Tetrasomy
D058670
-
G05.700.131.625
└─└─└─
Trisomie
Trisomy
D014314
-
G05.700.131.750
└─└─└─
Tétraploïdie
Tetraploidy
D057891
-
G05.700.740.249
└─└─└─
Triploïdie
Triploidy
D057885
-
G05.700.740.500
└─└─└─
Fusion oncogène
Oncogene Fusion
D050596
-
G05.728.385.500
└─└─└─
Crossing-over
Crossing Over, Genetic
D003434
-
G05.728.615.200
└─└─└─
Conversion des gènes
Gene Conversion
D005785
-
G05.728.615.475
└─└─└─
Réparation de l'ADN par recombinaison
Recombinational DNA Repair
D059767
-
G05.728.615.612
└─└─└─
Échange de chromatides soeurs
Sister Chromatid Exchange
D012854
-
G05.728.615.750
└─└─└─
Synténie
Synteny
D026801
-
G05.810.550.830
└─└─└─└─
Prophase I de méiose
Meiotic Prophase I
D049469
-
G05.113.220.687.500
└─└─└─└─
Anaphase
Anaphase
D000705
-
G05.113.220.781.050
└─└─└─└─
Points de contrôle de la phase M du cycle cellulaire
M Phase Cell Cycle Checkpoints
D059566
-
G05.113.220.781.338
└─└─└─└─
Métaphase
Metaphase
D008677
-
G05.113.220.781.625
└─└─└─└─
Prométaphase
Prometaphase
D049468
-
G05.113.220.781.812
└─└─└─└─
Prophase
Prophase
D011418
-
G05.113.220.781.906
└─└─└─└─
Télophase
Telophase
D013692
-
G05.113.220.781.953
└─└─└─└─
Points de cassure de chromosome
Chromosome Breakpoints
D056905
-
G05.200.210.170.500
└─└─└─└─
Inactivation du chromosome X
X Chromosome Inactivation
D049951
-
G05.308.203.249.970
└─└─└─└─
Systèmes CRISPR-Cas
CRISPR-Cas Systems
D064113
-
G05.308.203.374.394
└─└─└─└─
Interférence par ARN
RNA Interference
D034622
-
G05.308.203.374.790
└─└─└─└─
ADP-Ribosylation
ADP-Ribosylation
D000074744
-
G05.308.670.600.200
└─└─└─└─
Citrullination
Citrullination
D000076302
-
G05.308.670.600.300
└─└─└─└─
Prénylation des protéines
Protein Prenylation
D017368
-
G05.308.670.600.400
└─└─└─└─
Épissage des protéines
Protein Splicing
D019154
-
G05.308.670.600.700
└─└─└─└─
Ubiquitination
Ubiquitination
D054875
-
G05.308.670.600.831
└─└─└─└─
Réponse aux protéines mal repliées
Unfolded Protein Response
D056811
-
G05.308.670.600.850
└─└─└─└─
Polyadénylation
Polyadenylation
D026723
-
G05.308.700.225.710
└─└─└─└─
Épissage alternatif
Alternative Splicing
D017398
-
G05.308.700.700.100
└─└─└─└─
Épissage en trans
Trans-Splicing
D020040
-
G05.308.700.700.750
└─└─└─└─
Réseaux de régulation génique
Gene Regulatory Networks
D053263
-
G05.360.080.689.360
└─└─└─└─
Séquences régulatrices de l'acide ribonucléique
Regulatory Sequences, Ribonucleic Acid
D038621
-
G05.360.080.689.687
└─└─└─└─
Séquence d'encapsidation virale
Viral Packaging Sequence
D000086502
-
G05.360.080.689.905
└─└─└─└─
Duplications génomiques segmentaires
Segmental Duplications, Genomic
D056916
-
G05.360.080.708.565
└─└─└─└─
Séquences répétées terminales
Terminal Repeat Sequences
D020079
-
G05.360.080.708.850
└─└─└─└─
Kinétochores
Kinetochores
D018386
-
G05.360.160.165.500
└─└─└─└─
Euchromatine
Euchromatin
D022041
-
G05.360.160.180.270
└─└─└─└─
Hétérochromatine
Heterochromatin
D006570
-
G05.360.160.180.383
└─└─└─└─
Nucléosomes
Nucleosomes
D009707
-
G05.360.160.180.625
└─└─└─└─
Complexe shelterine
Shelterin Complex
D000089804
-
G05.360.160.845.500
└─└─└─└─
Chromosomes polytènes
Polytene Chromosomes
D059007
-
G05.360.162.440.500
└─└─└─└─
Chromosomes humains
Chromosomes, Human
D002877
-
G05.360.162.520.300
└─└─└─└─
Chromatine sexuelle
Sex Chromatin
D012728
-
G05.360.162.865.800
└─└─└─└─
Chromosome X
X Chromosome
D014960
-
G05.360.162.865.982
└─└─└─└─
Chromosome Y
Y Chromosome
D014998
-
G05.360.162.865.983
└─└─└─└─
Usage des codons
Codon Usage
D000081183
-
G05.360.335.355.113
└─└─└─└─
Chromosomes artificiels de bactérie
Chromosomes, Artificial, Bacterial
D022202
-
G05.360.337.249.170
└─└─└─└─
Chromosomes artificiels de mammifère
Chromosomes, Artificial, Mammalian
D022221
-
G05.360.337.249.190
└─└─└─└─
Chromosome artificiel du bactériophage P1
Chromosomes, Artificial, P1 Bacteriophage
D027042
-
G05.360.337.249.195
└─└─└─└─
Chromosomes artificiels de levure
Chromosomes, Artificial, Yeast
D018244
-
G05.360.337.249.200
└─└─└─└─
Sites d'attachement (microbiologie)
Attachment Sites, Microbiological
D001287
-
G05.360.340.024.079
└─└─└─└─
Ilots CpG
CpG Islands
D018899
-
G05.360.340.024.159
└─└─└─└─
Séquence instable d'ADN
DNA Sequence, Unstable
D043243
-
G05.360.340.024.189
└─└─└─└─
ADN intergénique
DNA, Intergenic
D021901
-
G05.360.340.024.220
└─└─└─└─
Gènes
Genes
D005796
-
G05.360.340.024.340
└─└─└─└─
Locus génétiques
Genetic Loci
D056426
-
G05.360.340.024.380
└─└─└─└─
Éléments isolateurs
Insulator Elements
D038101
-
G05.360.340.024.420
└─└─└─└─
Séquences répétées dispersées
Interspersed Repetitive Sequences
D020071
-
G05.360.340.024.425
└─└─└─└─
Isochores
Isochores
D032085
-
G05.360.340.024.430
└─└─└─└─
Régulon
Regulon
D018085
-
G05.360.340.024.742
└─└─└─└─
Réplicon
Replicon
D012093
-
G05.360.340.024.745
└─└─└─└─
Sites étiquetés par des séquences
Sequence Tagged Sites
D016324
-
G05.360.340.024.810
└─└─└─└─
Éléments silenceurs transcriptionnels
Silencer Elements, Transcriptional
D037941
-
G05.360.340.024.815
└─└─└─└─
Séquences répétées en tandem
Tandem Repeat Sequences
D020080
-
G05.360.340.024.850
└─└─└─└─
Gènes d'helminthe
Genes, Helminth
D017238
-
G05.360.340.337.500
└─└─└─└─
Gènes d'insecte
Genes, Insect
D017344
-
G05.360.340.357.500
└─└─└─└─
Gènes microbiens
Genes, Microbial
D064351
-
G05.360.340.358.024
└─└─└─└─
Génome d'archéobactérie
Genome, Archaeal
D020745
-
G05.360.340.358.050
└─└─└─└─
Génome bactérien
Genome, Bacterial
D016680
-
G05.360.340.358.207
└─└─└─└─
Génome fongique
Genome, Fungal
D016681
-
G05.360.340.358.365
└─└─└─└─
Génome viral
Genome, Viral
D016679
-
G05.360.340.358.840
└─└─└─└─
Gènes de plante
Genes, Plant
D017343
-
G05.360.340.365.500
└─└─└─└─
Génome de chloroplaste
Genome, Chloroplast
D054628
-
G05.360.340.370.200
└─└─└─└─
Gènes de protozoaire
Genes, Protozoan
D017125
-
G05.360.340.397.500
└─└─└─└─
ADN caténé
DNA, Catenated
D043864
-
G05.360.580.156.084
└─└─└─└─
ADN superhélicoïdal
DNA, Superhelical
D004278
-
G05.360.580.156.250
└─└─└─└─
Perte d'hétérozygotie
Loss of Heterozygosity
D019656
-
G05.365.590.029.530
└─└─└─└─
Caryotype anormal
Abnormal Karyotype
D059786
-
G05.365.590.175.024
└─└─└─└─
Chimérisme
Chimerism
D046528
-
G05.365.590.175.125
└─└─└─└─
Cassure de chromosome
Chromosome Breakage
D019457
-
G05.365.590.175.175
└─└─└─└─
Chromothripsis
Chromothripsis
D000072837
-
G05.365.590.175.310
└─└─└─└─
Isochromosomes
Isochromosomes
D018404
-
G05.365.590.175.430
└─└─└─└─
Micronoyaux à chromosomes défectueux
Micronuclei, Chromosome-Defective
D048629
-
G05.365.590.175.570
└─└─└─└─
Mosaïcisme
Mosaicism
D009030
-
G05.365.590.175.595
└─└─└─└─
Chromosomes en anneau
Ring Chromosomes
D012303
-
G05.365.590.175.760
└─└─└─└─
Aberrations des chromosomes sexuels
Sex Chromosome Aberrations
D012729
-
G05.365.590.175.815
└─└─└─└─
Disomie uniparentale
Uniparental Disomy
D024182
-
G05.365.590.175.935
└─└─└─└─
Variations de nombre de copies de segment d'ADN
DNA Copy Number Variations
D056915
-
G05.365.795.297.500
└─└─└─└─
Délétion de segment de chromosome
Chromosome Deletion
D002872
-
G05.700.131.500.500
└─└─└─└─└─
Appariement des chromosomes
Chromosome Pairing
D023902
-
G05.113.220.781.906.250
└─└─└─└─└─
Stade pachytène
Pachytene Stage
D049471
-
G05.113.220.781.906.750
└─└─└─└─└─
Poly(ADP-ribosylation)
Poly ADP Ribosylation
D000074747
-
G05.308.670.600.200.500
└─└─└─└─└─
Sumoylation
Sumoylation
D058207
-
G05.308.670.600.831.500
└─└─└─└─└─
Dégradation associée au réticulum endoplasmique
Endoplasmic Reticulum-Associated Degradation
D060746
-
G05.308.670.600.850.500
└─└─└─└─└─
Sites internes d'entrée des ribosomes
Internal Ribosome Entry Sites
D000067556
-
G05.360.080.689.687.093
└─└─└─└─└─
Riborégulateur
Riboswitch
D058928
-
G05.360.080.689.687.124
└─└─└─└─└─
Séquences répétées inversées
Inverted Repeat Sequences
D055029
-
G05.360.080.708.800.325
└─└─└─└─└─
Répétition terminale longue du VIH
HIV Long Terminal Repeat
D016325
-
G05.360.080.708.850.400
└─└─└─└─└─
Protéine-2 de liaison aux répétitions télomériques
Telomeric Repeat Binding Protein 2
D035341
-
G05.360.160.845.500.500
└─└─└─└─└─
Chromosomes humains 1-3
Chromosomes, Human, 1-3
D002900
-
G05.360.162.520.300.235
└─└─└─└─└─
Chromosomes humains 4-5
Chromosomes, Human, 4-5
D002905
-
G05.360.162.520.300.280
└─└─└─└─└─
Chromosomes humains 6-12 et X
Chromosomes, Human, 6-12 and X
D002906
-
G05.360.162.520.300.325
└─└─└─└─└─
Chromosomes humains 13-15
Chromosomes, Human, 13-15
D002901
-
G05.360.162.520.300.370
└─└─└─└─└─
Chromosomes humains 16-18
Chromosomes, Human, 16-18
D002902
-
G05.360.162.520.300.415
└─└─└─└─└─
Chromosomes humains 19-20
Chromosomes, Human, 19-20
D002903
-
G05.360.162.520.300.460
└─└─└─└─└─
Chromosomes humains 21-22 et Y
Chromosomes, Human, 21-22 and Y
D002904
-
G05.360.162.520.300.505
└─└─└─└─└─
Chromosomes X humains
Chromosomes, Human, X
D041321
-
G05.360.162.865.982.500
└─└─└─└─└─
Chromosomes Y humains
Chromosomes, Human, Y
D041322
-
G05.360.162.865.983.500
└─└─└─└─└─
Chromosomes artificiels humains
Chromosomes, Artificial, Human
D022222
-
G05.360.337.249.190.117
└─└─└─└─└─
Sites fragiles de chromosome
Chromosome Fragile Sites
D043283
-
G05.360.340.024.189.610
└─└─└─└─└─
Allèles
Alleles
D000483
-
G05.360.340.024.340.030
└─└─└─└─└─
Composants de gène
Gene Components
D040461
-
G05.360.340.024.340.137
└─└─└─└─└─
Gènes cdc
Genes, cdc
D018816
-
G05.360.340.024.340.220
└─└─└─└─└─
Gènes du développement
Genes, Developmental
D050437
-
G05.360.340.024.340.230
└─└─└─└─└─
Gènes dupliqués
Genes, Duplicate
D020131
-
G05.360.340.024.340.250
└─└─└─└─└─
Gènes essentiels
Genes, Essential
D020043
-
G05.360.340.024.340.270
└─└─└─└─└─
Gènes létaux
Genes, Lethal
D005804
-
G05.360.340.024.340.350
└─└─└─└─└─
Gènes modificateurs
Genes, Modifier
D060045
-
G05.360.340.024.340.370
└─└─└─└─└─
Gènes tumoraux
Genes, Neoplasm
D052138
-
G05.360.340.024.340.375
└─└─└─└─└─
Gènes chevauchants
Genes, Overlapping
D005807
-
G05.360.340.024.340.385
└─└─└─└─└─
Gènes RAG-1
Genes, RAG-1
D016654
-
G05.360.340.024.340.400
└─└─└─└─└─
Gènes régulateurs
Genes, Regulator
D005809
-
G05.360.340.024.340.425
└─└─└─└─└─
Gènes rapporteurs
Genes, Reporter
D017930
-
G05.360.340.024.340.435
└─└─└─└─└─
Gène sry
Genes, sry
D024282
-
G05.360.340.024.340.450
└─└─└─└─└─
Gènes suppresseurs
Genes, Suppressor
D016153
-
G05.360.340.024.340.460
└─└─└─└─└─
Gènes de synthèse
Genes, Synthetic
D005813
-
G05.360.340.024.340.465
└─└─└─└─└─
Gènes du récepteur des cellules T
Genes, T-Cell Receptor
D019672
-
G05.360.340.024.340.475
└─└─└─└─└─
Famille multigénique
Multigene Family
D005810
-
G05.360.340.024.340.645
└─└─└─└─└─
Pseudogènes
Pseudogenes
D011544
-
G05.360.340.024.340.700
└─└─└─└─└─
Transgènes
Transgenes
D019076
-
G05.360.340.024.340.825
└─└─└─└─└─
Région génomique du complexe Achaete-Scute
Achaete-Scute Complex Genome Region
D058145
-
G05.360.340.024.380.124
└─└─└─└─└─
Région de contrôle de locus
Locus Control Region
D019901
-
G05.360.340.024.380.249
└─└─└─└─└─
Organisateur nucléolaire
Nucleolus Organizer Region
D009697
-
G05.360.340.024.380.875
└─└─└─└─└─
Régions pseudo-autosomiques
Pseudoautosomal Regions
D000071439
-
G05.360.340.024.380.906
└─└─└─└─└─
Locus de caractère quantitatif
Quantitative Trait Loci
D040641
-
G05.360.340.024.380.937
└─└─└─└─└─
Région du complexe t
t-Complex Genome Region
D056427
-
G05.360.340.024.380.968
└─└─└─└─└─
Éléments transposables d'ADN
DNA Transposable Elements
D004251
-
G05.360.340.024.425.200
└─└─└─└─└─
Ilots génomiques
Genomic Islands
D044404
-
G05.360.340.024.425.500
└─└─└─└─└─
Rétroéléments
Retroelements
D018626
-
G05.360.340.024.425.800
└─└─└─└─└─
Origine de réplication
Replication Origin
D018741
-
G05.360.340.024.745.725
└─└─└─└─└─
Clustered regularly interspaced short palindromic repeats
Clustered Regularly Interspaced Short Palindromic Repeats
D064112
-
G05.360.340.024.850.069
└─└─└─└─└─
ADN satellite
DNA, Satellite
D004276
-
G05.360.340.024.850.150
└─└─└─└─└─
Répétitions microsatellites
Microsatellite Repeats
D018895
-
G05.360.340.024.850.500
└─└─└─└─└─
Répétitions minisatellites
Minisatellite Repeats
D018598
-
G05.360.340.024.850.550
└─└─└─└─└─
Gènes d'archée
Genes, Archaeal
D019766
-
G05.360.340.358.050.500
└─└─└─└─└─
Gènes bactériens
Genes, Bacterial
D005798
-
G05.360.340.358.207.249
└─└─└─└─└─
Opéron
Operon
D009876
-
G05.360.340.358.207.500
└─└─└─└─└─
Gènes fongiques
Genes, Fungal
D005800
-
G05.360.340.358.365.500
└─└─└─└─└─
Gènes viraux
Genes, Viral
D005814
-
G05.360.340.358.840.500
└─└─└─└─└─
Caryotype XYY
XYY Karyotype
D014997
-
G05.365.590.175.815.970
└─└─└─└─└─
Chromosome Philadelphie
Philadelphia Chromosome
D010677
-
G05.365.590.175.870.680
└─└─└─└─└─└─
Chromosomes humains de la paire 1
Chromosomes, Human, Pair 1
D002878
-
G05.360.162.520.300.235.240
└─└─└─└─└─└─
Chromosomes humains de la paire 2
Chromosomes, Human, Pair 2
D002889
-
G05.360.162.520.300.235.245
└─└─└─└─└─└─
Chromosomes humains de la paire 3
Chromosomes, Human, Pair 3
D002893
-
G05.360.162.520.300.235.250
└─└─└─└─└─└─
Chromosomes humains de la paire 4
Chromosomes, Human, Pair 4
D002894
-
G05.360.162.520.300.280.285
└─└─└─└─└─└─
Chromosomes humains de la paire 5
Chromosomes, Human, Pair 5
D002895
-
G05.360.162.520.300.280.290
└─└─└─└─└─└─
Chromosomes humains de la paire 6
Chromosomes, Human, Pair 6
D002896
-
G05.360.162.520.300.325.330
└─└─└─└─└─└─
Chromosomes humains de la paire 7
Chromosomes, Human, Pair 7
D002897
-
G05.360.162.520.300.325.335
└─└─└─└─└─└─
Chromosomes humains de la paire 8
Chromosomes, Human, Pair 8
D002898
-
G05.360.162.520.300.325.340
└─└─└─└─└─└─
Chromosomes humains de la paire 9
Chromosomes, Human, Pair 9
D002899
-
G05.360.162.520.300.325.345
└─└─└─└─└─└─
Chromosomes humains de la paire 10
Chromosomes, Human, Pair 10
D002879
-
G05.360.162.520.300.325.350
└─└─└─└─└─└─
Chromosomes humains de la paire 11
Chromosomes, Human, Pair 11
D002880
-
G05.360.162.520.300.325.355
└─└─└─└─└─└─
Chromosomes humains de la paire 12
Chromosomes, Human, Pair 12
D002881
-
G05.360.162.520.300.325.360
└─└─└─└─└─└─
Chromosomes humains de la paire 13
Chromosomes, Human, Pair 13
D002882
-
G05.360.162.520.300.370.375
└─└─└─└─└─└─
Chromosomes humains de la paire 14
Chromosomes, Human, Pair 14
D002883
-
G05.360.162.520.300.370.380
└─└─└─└─└─└─
Chromosomes humains de la paire 15
Chromosomes, Human, Pair 15
D002884
-
G05.360.162.520.300.370.385
└─└─└─└─└─└─
Chromosomes humains de la paire 16
Chromosomes, Human, Pair 16
D002885
-
G05.360.162.520.300.415.420
└─└─└─└─└─└─
Chromosomes humains de la paire 17
Chromosomes, Human, Pair 17
D002886
-
G05.360.162.520.300.415.425
└─└─└─└─└─└─
Chromosomes humains de la paire 18
Chromosomes, Human, Pair 18
D002887
-
G05.360.162.520.300.415.430
└─└─└─└─└─└─
Chromosomes humains de la paire 19
Chromosomes, Human, Pair 19
D002888
-
G05.360.162.520.300.460.465
└─└─└─└─└─└─
Chromosomes humains de la paire 20
Chromosomes, Human, Pair 20
D002890
-
G05.360.162.520.300.460.470
└─└─└─└─└─└─
Chromosomes humains de la paire 21
Chromosomes, Human, Pair 21
D002891
-
G05.360.162.520.300.505.510
└─└─└─└─└─└─
Chromosomes humains de la paire 22
Chromosomes, Human, Pair 22
D002892
-
G05.360.162.520.300.505.515
└─└─└─└─└─└─
Codon
Codon
D003062
-
G05.360.340.024.340.137.190
└─└─└─└─└─└─
Exons
Exons
D005091
-
G05.360.340.024.340.137.232
└─└─└─└─└─└─
Étiquettes de séquences exprimées
Expressed Sequence Tags
D020224
-
G05.360.340.024.340.137.275
└─└─└─└─└─└─
Région 3' flanquante
3' Flanking Region
D024509
-
G05.360.340.024.340.137.290
└─└─└─└─└─└─
Région 5' flanquante
5' Flanking Region
D024506
-
G05.360.340.024.340.137.295
└─└─└─└─└─└─
Introns
Introns
D007438
-
G05.360.340.024.340.137.515
└─└─└─└─└─└─
Cadres ouverts de lecture
Open Reading Frames
D016366
-
G05.360.340.024.340.137.650
└─└─└─└─└─└─
Éléments de régulation transcriptionnelle
Regulatory Elements, Transcriptional
D050436
-
G05.360.340.024.340.137.750
└─└─└─└─└─└─
Signaux de polyadénylation
RNA 3' Polyadenylation Signals
D039104
-
G05.360.340.024.340.137.775
└─└─└─└─└─└─
Séquence d'oligopyrimidines en région 5' terminale d'ARN
RNA 5' Terminal Oligopyrimidine Sequence
D038641
-
G05.360.340.024.340.137.785
└─└─└─└─└─└─
Sites d'épissage d'ARN
RNA Splice Sites
D022821
-
G05.360.340.024.340.137.800
└─└─└─└─└─└─
Régions non traduites
Untranslated Regions
D020506
-
G05.360.340.024.340.137.910
└─└─└─└─└─└─
Gènes homéotiques
Genes, Homeobox
D005801
-
G05.360.340.024.340.230.500
└─└─└─└─└─└─
Gènes de chaine lourde d'immunoglobuline
Genes, Immunoglobulin Heavy Chain
D050438
-
G05.360.340.024.340.335.300
└─└─└─└─└─└─
Gènes de chaine légère d'immunoglobuline
Genes, Immunoglobulin Light Chain
D050439
-
G05.360.340.024.340.335.310
└─└─└─└─└─└─
Exons VDJ
VDJ Exons
D050441
-
G05.360.340.024.340.335.655
└─└─└─└─└─└─
Oncogènes
Oncogenes
D009857
-
G05.360.340.024.340.375.500
└─└─└─└─└─└─
Gènes imbriqués
Nested Genes
D032041
-
G05.360.340.024.340.385.600
└─└─└─└─└─└─
Gènes suppresseurs de tumeur
Genes, Tumor Suppressor
D016147
-
G05.360.340.024.340.415.400
└─└─└─└─└─└─
Gènes araC
Genes, araC
D005797
-
G05.360.340.024.340.425.412
└─└─└─└─└─└─
Gènes switch
Genes, Switch
D005812
-
G05.360.340.024.340.425.420
└─└─└─└─└─└─
Gènes de la chaine alpha du récepteur des lymphocytes T
Genes, T-Cell Receptor alpha
D019673
-
G05.360.340.024.340.475.050
└─└─└─└─└─└─
Gènes de la chaine bêta du récepteur des lymphocytes T
Genes, T-Cell Receptor beta
D019674
-
G05.360.340.024.340.475.080
└─└─└─└─└─└─
Gènes de la chaine delta du récepteur des lymphocytes T
Genes, T-Cell Receptor delta
D019676
-
G05.360.340.024.340.475.240
└─└─└─└─└─└─
Gènes de la chaine gamma du récepteur des lymphocytes T
Genes, T-Cell Receptor gamma
D019675
-
G05.360.340.024.340.475.400
└─└─└─└─└─└─
Gènes MDR
Genes, MDR
D019450
-
G05.360.340.024.340.645.500
└─└─└─└─└─└─
Gènes d'ARN ribosomique
Genes, rRNA
D020459
-
G05.360.340.024.340.645.750
└─└─└─└─└─└─
Gènes-suicide transgéniques
Genes, Transgenic, Suicide
D041722
-
G05.360.340.024.340.825.500
└─└─└─└─└─└─
Rétrovirus endogènes
Endogenous Retroviruses
D020077
-
G05.360.340.024.425.800.175
└─└─└─└─└─└─
Éléments LINE
Long Interspersed Nucleotide Elements
D020084
-
G05.360.340.024.425.800.400
└─└─└─└─└─└─
Éléments SINE
Short Interspersed Nucleotide Elements
D020086
-
G05.360.340.024.425.800.800
└─└─└─└─└─└─
Répétitions de dinucléotides
Dinucleotide Repeats
D018900
-
G05.360.340.024.850.500.150
└─└─└─└─└─└─
Répétitions de trinucléotides
Trinucleotide Repeats
D018911
-
G05.360.340.024.850.500.850
└─└─└─└─└─└─
Opéron lac
Lac Operon
D007763
-
G05.360.340.358.207.500.545
└─└─└─└─└─└─
Régions opératrices (génétique)
Operator Regions, Genetic
D009875
-
G05.360.340.358.207.500.645
└─└─└─└─└─└─
Opéron d'ARNr
rRNA Operon
D012407
-
G05.360.340.358.207.500.817
└─└─└─└─└─└─
Gènes fongiques du type conjugant
Genes, Mating Type, Fungal
D049770
-
G05.360.340.358.365.500.089
└─└─└─└─└─└─
Gènes env
Genes, env
D015752
-
G05.360.340.358.840.500.172
└─└─└─└─└─└─
Gènes gag
Genes, gag
D015750
-
G05.360.340.358.840.500.258
└─└─└─└─└─└─
Gènes précoces
Genes, Immediate-Early
D017781
-
G05.360.340.358.840.500.345
└─└─└─└─└─└─
Gènes de particule intracisternale de type A
Genes, Intracisternal A-Particle
D007426
-
G05.360.340.358.840.500.360
└─└─└─└─└─└─
Gènes nef
Genes, nef
D015754
-
G05.360.340.358.840.500.600
└─└─└─└─└─└─
Gènes pol
Genes, pol
D015751
-
G05.360.340.358.840.500.667
└─└─└─└─└─└─
Gènes pX
Genes, pX
D016355
-
G05.360.340.358.840.500.735
└─└─└─└─└─└─
Gènes rev
Genes, rev
D015757
-
G05.360.340.358.840.500.775
└─└─└─└─└─└─
Gènes tat
Genes, tat
D015756
-
G05.360.340.358.840.500.850
└─└─└─└─└─└─
Gènes vif
Genes, vif
D016341
-
G05.360.340.358.840.500.890
└─└─└─└─└─└─
Gènes vpr
Genes, vpr
D016334
-
G05.360.340.358.840.500.897
└─└─└─└─└─└─
Gènes vpu
Genes, vpu
D016338
-
G05.360.340.358.840.500.900
└─└─└─└─└─└─└─
Codon d'initiation
Codon, Initiator
D018387
-
G05.360.340.024.340.137.190.225
└─└─└─└─└─└─└─
Codon stop
Codon, Terminator
D018388
-
G05.360.340.024.340.137.190.250
└─└─└─└─└─└─└─
Éléments activateurs (génétique)
Enhancer Elements, Genetic
D004742
-
G05.360.340.024.340.137.750.249
└─└─└─└─└─└─└─
Régions promotrices (génétique)
Promoter Regions, Genetic
D011401
-
G05.360.340.024.340.137.750.680
└─└─└─└─└─└─└─
Régions terminatrices (génétique)
Terminator Regions, Genetic
D013728
-
G05.360.340.024.340.137.750.830
└─└─└─└─└─└─└─
Site d'initiation de la transcription
Transcription Initiation Site
D024363
-
G05.360.340.024.340.137.750.840
└─└─└─└─└─└─└─
Régions 3' non traduites
3' Untranslated Regions
D020413
-
G05.360.340.024.340.137.910.880
└─└─└─└─└─└─└─
Régions 5' non traduites
5' Untranslated Regions
D020121
-
G05.360.340.024.340.137.910.885
└─└─└─└─└─└─└─
Exons de la région charnière
Hinge Exons
D052058
-
G05.360.340.024.340.335.300.249
└─└─└─└─└─└─└─
Région switch des immunoglobulines
Immunoglobulin Switch Region
D007134
-
G05.360.340.024.340.335.300.500
└─└─└─└─└─└─└─
Proto-oncogènes
Proto-Oncogenes
D011519
-
G05.360.340.024.340.375.500.791
└─└─└─└─└─└─└─
Gènes APC
Genes, APC
D017491
-
G05.360.340.024.340.415.400.050
└─└─└─└─└─└─└─
Gène BRCA1
Genes, BRCA1
D019398
-
G05.360.340.024.340.415.400.100
└─└─└─└─└─└─└─
Gène BRCA2
Genes, BRCA2
D024522
-
G05.360.340.024.340.415.400.105
└─└─└─└─└─└─└─
Gènes DCC
Genes, DCC
D016163
-
G05.360.340.024.340.415.400.200
└─└─└─└─└─└─└─
Gènes MCC
Genes, MCC
D017431
-
G05.360.340.024.340.415.400.320
└─└─└─└─└─└─└─
Gènes nf1
Genes, Neurofibromatosis 1
D016514
-
G05.360.340.024.340.415.400.340
└─└─└─└─└─└─└─
Gènes nf2
Genes, Neurofibromatosis 2
D016515
-
G05.360.340.024.340.415.400.345
└─└─└─└─└─└─└─
Gènes p16
Genes, p16
D019942
-
G05.360.340.024.340.415.400.375
└─└─└─└─└─└─└─
Gènes p53
Genes, p53
D016158
-
G05.360.340.024.340.415.400.385
└─└─└─└─└─└─└─
Gènes du rétinoblastome
Genes, Retinoblastoma
D016161
-
G05.360.340.024.340.415.400.400
└─└─└─└─└─└─└─
Gènes de la tumeur de Wilms
Genes, Wilms Tumor
D016162
-
G05.360.340.024.340.415.400.420
└─└─└─└─└─└─└─
Séquences Alu
Alu Elements
D020087
-
G05.360.340.024.425.800.800.050
└─└─└─└─└─└─└─└─
Éléments E-box
E-Box Elements
D024721
-
G05.360.340.024.340.137.750.249.240
└─└─└─└─└─└─└─└─
Activateur du VIH
HIV Enhancer
D016322
-
G05.360.340.024.340.137.750.249.400
└─└─└─└─└─└─└─└─
Éléments de réponse
Response Elements
D020218
-
G05.360.340.024.340.137.750.680.765
└─└─└─└─└─└─└─└─
Boite TATA
TATA Box
D016385
-
G05.360.340.024.340.137.750.680.850
└─└─└─└─└─└─└─└─
Éléments riches en AU
AU Rich Elements
D063307
-
G05.360.340.024.340.137.910.880.500
└─└─└─└─└─└─└─└─
Gènes abl
Genes, abl
D016313
-
G05.360.340.024.340.375.500.791.100
└─└─└─└─└─└─└─└─
Gènes bcl-1
Genes, bcl-1
D019940
-
G05.360.340.024.340.375.500.791.148
└─└─└─└─└─└─└─└─
Gènes bcl-2
Genes, bcl-2
D019254
-
G05.360.340.024.340.375.500.791.150
└─└─└─└─└─└─└─└─
Gènes erbA
Genes, erbA
D018776
-
G05.360.340.024.340.375.500.791.290
└─└─└─└─└─└─└─└─
Gènes erbB
Genes, erbB
D018815
-
G05.360.340.024.340.375.500.791.295
└─└─└─└─└─└─└─└─
Gènes fms
Genes, fms
D016236
-
G05.360.340.024.340.375.500.791.325
└─└─└─└─└─└─└─└─
Gènes fos
Genes, fos
D016762
-
G05.360.340.024.340.375.500.791.330
└─└─└─└─└─└─└─└─
Gènes jun
Genes, jun
D016758
-
G05.360.340.024.340.375.500.791.365
└─└─└─└─└─└─└─└─
Gènes mos
Genes, mos
D016258
-
G05.360.340.024.340.375.500.791.400
└─└─└─└─└─└─└─└─
Gènes myb
Genes, myb
D020570
-
G05.360.340.024.340.375.500.791.418
└─└─└─└─└─└─└─└─
Gènes myc
Genes, myc
D016259
-
G05.360.340.024.340.375.500.791.420
└─└─└─└─└─└─└─└─
Gènes ras
Genes, ras
D011905
-
G05.360.340.024.340.375.500.791.550
└─└─└─└─└─└─└─└─
Gènes rel
Genes, rel
D020573
-
G05.360.340.024.340.375.500.791.552
└─└─└─└─└─└─└─└─
Gènes sis
Genes, sis
D020571
-
G05.360.340.024.340.375.500.791.560
└─└─└─└─└─└─└─└─
Gènes src
Genes, src
D016391
-
G05.360.340.024.340.375.500.791.570
└─└─└─└─└─└─└─└─└─
Éléments de réponse aux anti-oxydants
Antioxidant Response Elements
D061745
-
G05.360.340.024.340.137.750.680.765.040
└─└─└─└─└─└─└─└─└─
Élément de réponse au sérum
Serum Response Element
D027602
-
G05.360.340.024.340.137.750.680.765.800
└─└─└─└─└─└─└─└─└─
Élément de réponse à la vitamine D
Vitamin D Response Element
D030181
-
G05.360.340.024.340.137.750.680.765.920
└─└─└─└─└─└─└─└─└─
Gènes erbB-1
Genes, erbB-1
D018773
-
G05.360.340.024.340.375.500.791.295.300
└─└─└─└─└─└─└─└─└─
Gènes erbB-2
Genes, erbB-2
D018734
-
G05.360.340.024.340.375.500.791.295.305
2 publications dans cette catégorie
Affiliations :
Department of Physics and Astronomy, Bowdoin College, Brunswick, Maine 04011, USA.
Publications dans "Phénomènes génétiques" :
2 publications dans cette catégorie
Affiliations :
School of Mathematical Sciences, University of Southampton, Southampton SO17 1BJ, United Kingdom.
Publications dans "Phénomènes génétiques" :
2 publications dans cette catégorie
Affiliations :
Centro de Astrofísica e Gravitação-CENTRA, Departamento de Física, Instituto Superior Técnico-IST, Universidade de Lisboa-UL, Avenida Rovisco Pais 1, 1049-001 Lisboa, Portugal.
Publications dans "Phénomènes génétiques" :
2 publications dans cette catégorie
Affiliations :
Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA. stefania.kapsetaki@tufts.edu.
Biodesign Center for Biocomputing, Security and Society, Arizona State University, Tempe, AZ, USA. stefania.kapsetaki@tufts.edu.
Department of Biology, School of Arts and Sciences, Tufts University, Medford, MA, USA. stefania.kapsetaki@tufts.edu.
Publications dans "Phénomènes génétiques" :
2 publications dans cette catégorie
Affiliations :
Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Biodesign Center for Biocomputing, Security and Society, Arizona State University, Tempe, AZ, USA.
School of Life Sciences, Arizona State University, Tempe, AZ, USA.
Publications dans "Phénomènes génétiques" :
2 publications dans cette catégorie
Affiliations :
Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
Biodesign Center for Biocomputing, Security and Society, Arizona State University, Tempe, AZ, USA.
School of Life Sciences, Arizona State University, Tempe, AZ, USA.
Biodesign Center for Mechanisms of Evolution, Arizona State University, Tempe, AZ, USA.
Center for Evolution and Medicine, Arizona State University, Tempe, AZ, USA.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Medical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol BS8 2BN, UK.
Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, UK.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Medical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol BS8 2BN, UK.
Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, UK.
K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Norway.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Medical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol BS8 2BN, UK.
Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, UK.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Medical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol BS8 2BN, UK.
Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, UK.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Institute of Electrochemistry, Ulm University, 89081, Ulm, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Chemistry, Lancaster University, Bailrigg, Lancaster, United Kingdom.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel, 24118, Kiel, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Cluster of Excellence iFIT (EXC 2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Cluster of Excellence iFIT (EXC 2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, D-72076 Tübingen, Germany.
German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Cluster of Excellence iFIT (EXC 2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Core Facility for Medical Bioanalytics, Institute for Ophthalmic Research, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
1 publication dans cette catégorie
Affiliations :
Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :
An astrophysicist and an artist craft evocative portraits of warping spacetime....
This review focuses on experimental work on nonlinear phenomena in microfluidics, which for the most part are phenomena for which the velocity of a fluid flowing through a microfluidic channel does no...
The type, distribution pattern and time course of spontaneous muscular activity are important for the diagnostics of neuromuscular diseases in the clinical practice. In neurogenic lesions with motor a...
Water scarcity raises important concerns with respect to human sustainability and the preservation of important ecosystem functions. To satisfy water requirements, seawater desalination represents one...
This study investigates the oxidation behavior of Cu...
There is no crisis of replication and generalizability in psychological science, only misunderstanding or forgetting the fundamental nature of psychological phenomena and resultant implications for em...
To demonstrate slowly varying, erroneous magnetic field gradients for oscillating readouts due to the mechanically resonant behavior of gradient systems....
Projections of a static phantom were acquired using a one-dimensional (1D) EPI sequence with varying EPI frequencies ranging from 1121 to 1580 Hz on clinical 3T systems (30 mT/m, 200 T/m/s). Phase due...
A beat phenomenon resulting in a slowly varying phase was observed. Its temporal frequency was given by the difference between the EPI frequency and the mechanical resonance frequency of the activated...
Oscillating readouts such as those used in EPI can result in low-frequency, erroneous phase contributions, which are explained by the beat phenomenon. Therefore, EPI phase-correction approaches may ne...
Despite recent advances in the study of complex systems, which were recognized by the Nobel Prize in Physics in 2021, glass transition and the physicochemical phenomena that occur in the supercooled l...
We comment on the limits of relying on prior literature when constructing the design space for an integrative experiment; the adaptive nature of social and behavioral phenomena and the implications fo...
This perspective explores the potential of emergence phenomena in large language models (LLMs) to transform data management and analysis in radiology. We provide a concise explanation of LLMs, define ...