Titre : Phénomènes génétiques

Phénomènes génétiques : Questions médicales fréquentes

Questions fréquentes et termes MeSH associés

Diagnostic 5

#1

Comment diagnostiquer une maladie génétique ?

Un diagnostic repose sur des tests génétiques, l'examen clinique et l'historique familial.
Maladies génétiques Tests génétiques
#2

Quels tests sont utilisés pour les anomalies chromosomiques ?

Les caryotypes et les analyses de microdélétions sont couramment utilisés.
Anomalies chromosomiques Caryotype
#3

Qu'est-ce qu'un test de porteur ?

C'est un test pour déterminer si une personne est porteuse d'une mutation génétique.
Tests de porteur Mutations génétiques
#4

Quels symptômes indiquent une maladie génétique ?

Des symptômes variés comme des malformations, des troubles du développement ou des maladies chroniques.
Symptômes Maladies héréditaires
#5

Comment l'historique familial aide-t-il au diagnostic ?

Il permet d'identifier des patterns héréditaires et des risques accrus de maladies.
Antécédents familiaux Épidémiologie génétique

Symptômes 5

#1

Quels sont les symptômes des maladies génétiques ?

Les symptômes varient, incluant des anomalies physiques, des troubles mentaux ou des maladies métaboliques.
Symptômes Maladies métaboliques
#2

Les maladies génétiques peuvent-elles être asymptomatiques ?

Oui, certaines personnes peuvent être porteuses sans présenter de symptômes visibles.
Maladies héréditaires Porteurs
#3

Comment les symptômes évoluent-ils avec l'âge ?

Certains symptômes peuvent s'aggraver avec l'âge, tandis que d'autres peuvent apparaître tardivement.
Âge Évolution des maladies
#4

Quels symptômes sont associés à la fibrose kystique ?

Toux persistante, infections pulmonaires fréquentes et problèmes digestifs.
Fibrose kystique Symptômes respiratoires
#5

Les maladies génétiques affectent-elles le développement ?

Oui, elles peuvent entraîner des retards de développement physique et cognitif.
Développement Retards de développement

Prévention 5

#1

Peut-on prévenir les maladies génétiques ?

Certaines maladies peuvent être prévenues par des tests de porteur et des conseils génétiques.
Prévention Conseils génétiques
#2

Quel rôle joue le dépistage prénatal ?

Le dépistage prénatal permet d'identifier des anomalies génétiques chez le fœtus.
Dépistage prénatal Anomalies génétiques
#3

Comment les conseils génétiques aident-ils ?

Ils fournissent des informations sur les risques héréditaires et les options de reproduction.
Conseils génétiques Risques héréditaires
#4

Les vaccinations peuvent-elles prévenir des maladies génétiques ?

Non, les vaccinations ne préviennent pas les maladies génétiques, mais elles préviennent des infections.
Vaccinations Prévention des infections
#5

Quelles sont les recommandations pour les familles à risque ?

Les familles à risque devraient consulter un généticien pour évaluer les options de dépistage.
Familles à risque Généticiens

Traitements 5

#1

Quels traitements existent pour les maladies génétiques ?

Les traitements incluent la thérapie génique, les médicaments et la gestion des symptômes.
Thérapie génique Traitements médicaux
#2

La thérapie génique est-elle efficace ?

Elle peut être efficace pour certaines maladies, mais les résultats varient selon les cas.
Thérapie génique Efficacité des traitements
#3

Comment gérer les symptômes d'une maladie génétique ?

La gestion peut inclure des médicaments, des thérapies physiques et un suivi régulier.
Gestion des symptômes Thérapies
#4

Les traitements sont-ils personnalisés ?

Oui, les traitements peuvent être adaptés en fonction des mutations spécifiques et des symptômes.
Médecine personnalisée Mutations génétiques
#5

Quelles sont les avancées en recherche génétique ?

Des avancées incluent la thérapie génique, CRISPR et des traitements ciblés pour certaines maladies.
Recherche génétique CRISPR

Complications 5

#1

Quelles complications peuvent survenir avec les maladies génétiques ?

Les complications incluent des troubles de santé chroniques, des handicaps et des risques accrus de cancers.
Complications Troubles de santé
#2

Les maladies génétiques augmentent-elles le risque de cancer ?

Oui, certaines mutations génétiques sont associées à un risque accru de cancers spécifiques.
Cancer Mutations génétiques
#3

Comment les maladies génétiques affectent-elles la qualité de vie ?

Elles peuvent entraîner des limitations physiques, des problèmes psychologiques et des besoins médicaux accrus.
Qualité de vie Limitations physiques
#4

Les complications sont-elles prévisibles ?

Certaines complications peuvent être anticipées, mais d'autres peuvent survenir de manière imprévisible.
Complications Prévisibilité
#5

Quelles sont les implications psychologiques des maladies génétiques ?

Elles peuvent entraîner de l'anxiété, de la dépression et des défis émotionnels pour les patients et les familles.
Implications psychologiques Anxiété

Facteurs de risque 5

#1

Quels sont les facteurs de risque pour les maladies génétiques ?

Les facteurs incluent l'hérédité, l'âge parental avancé et certaines expositions environnementales.
Facteurs de risque Hérédité
#2

L'âge des parents influence-t-il les maladies génétiques ?

Oui, un âge parental avancé est associé à un risque accru de certaines anomalies chromosomiques.
Âge parental Anomalies chromosomiques
#3

Les antécédents familiaux augmentent-ils le risque ?

Oui, des antécédents familiaux de maladies génétiques augmentent le risque pour les descendants.
Antécédents familiaux Risque génétique
#4

Les facteurs environnementaux jouent-ils un rôle ?

Oui, certaines expositions environnementales peuvent interagir avec des prédispositions génétiques.
Facteurs environnementaux Interactions génétiques
#5

Comment le mode de vie influence-t-il les maladies génétiques ?

Un mode de vie sain peut atténuer certains risques, mais ne peut pas prévenir les maladies génétiques.
Mode de vie Prévention
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"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." } } ] } ] }
Dr Olivier Menir

Contenu validé par Dr Olivier Menir

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

Sous-catégories

521 au total
└─

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

Auteurs principaux

Thomas W Baumgarte

2 publications dans cette catégorie

Affiliations :
  • Department of Physics and Astronomy, Bowdoin College, Brunswick, Maine 04011, USA.
Publications dans "Phénomènes génétiques" :

Carsten Gundlach

2 publications dans cette catégorie

Affiliations :
  • School of Mathematical Sciences, University of Southampton, Southampton SO17 1BJ, United Kingdom.
Publications dans "Phénomènes génétiques" :

David Hilditch

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" :

Stefania E Kapsetaki

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" :

Luis H Cisneros

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" :

Carlo C Maley

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" :

Tim T Morris

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" :

Neil M Davies

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" :

Gibran Hemani

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" :

George Davey Smith

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" :

Albert K Engstfeld

1 publication dans cette catégorie

Affiliations :
  • Institute of Electrochemistry, Ulm University, 89081, Ulm, Germany.
Publications dans "Phénomènes génétiques" :
  • Interface Phenomena.
    Chemphyschem : a European journal of chemical physics and physical chemistry 2021-11-08

Harry Hoster

1 publication dans cette catégorie

Affiliations :
  • Department of Chemistry, Lancaster University, Bailrigg, Lancaster, United Kingdom.
Publications dans "Phénomènes génétiques" :
  • Interface Phenomena.
    Chemphyschem : a European journal of chemical physics and physical chemistry 2021-11-08

Olaf M Magnussen

1 publication dans cette catégorie

Affiliations :
  • Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel, 24118, Kiel, Germany.
Publications dans "Phénomènes génétiques" :
  • Interface Phenomena.
    Chemphyschem : a European journal of chemical physics and physical chemistry 2021-11-08

Susanne Berchtold

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" :

Julia Beil

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" :

Christian Raff

1 publication dans cette catégorie

Affiliations :
  • Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :

Irina Smirnow

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" :

Martina Schell

1 publication dans cette catégorie

Affiliations :
  • Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :

Janina D'Alvise

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" :

Silvia Gross

1 publication dans cette catégorie

Affiliations :
  • Department of Internal Medicine VIII, University Hospital Tübingen, D-72076 Tübingen, Germany.
Publications dans "Phénomènes génétiques" :

Sources (10000 au total)

Beat phenomena of oscillating readouts.

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...