questionsmedicales.fr
Phénomènes génétiques
Variation génétique
Variation génétique : Questions médicales fréquentes
Diagnostic
5
Tests génétiques
Séquençage de l'ADN
Anomalies génétiques
Tests de dépistage
Hérédité
Transmission génétique
Génome
Maladies génétiques
Imagerie médicale
Maladies héréditaires
Symptômes
5
Symptômes
Troubles génétiques
Maladies héréditaires
Variations génétiques
Développement
Retards de développement
Âge d'apparition
Maladies génétiques
Asymptomatique
Variations génétiques
Prévention
5
Prévention
Tests génétiques
Dépistage
Prévention des maladies
Conseils génétiques
Risques héréditaires
Alimentation
Facteurs de risque
Vaccinations
Prévention des maladies infectieuses
Traitements
5
Thérapie génique
Traitements médicaux
Thérapie génique
Efficacité des traitements
Prévention
Traitements préventifs
Médecine personnalisée
Traitements ciblés
Médicaments
Traitements symptomatiques
Complications
5
Complications
Troubles organiques
Cancer
Variations génétiques
Complications
Gestion des symptômes
Qualité de vie
Limitations fonctionnelles
Soins spécialisés
Suivi médical
Facteurs de risque
5
Facteurs de risque
Antécédents familiaux
Environnement
Interactions génétiques
Facteurs socio-économiques
Accès aux soins
Populations
Variations génétiques
{
"@context": "https://schema.org",
"@graph": [
{
"@type": "MedicalWebPage",
"name": "Variation génétique : Questions médicales les plus fréquentes",
"headline": "Variation génétique : Comprendre les symptômes, diagnostics et traitements",
"description": "Guide complet et accessible sur les Variation génétique : explications, diagnostics, traitements et prévention. Information médicale validée destinée aux patients.",
"datePublished": "2024-05-13",
"dateModified": "2026-08-01",
"inLanguage": "fr",
"medicalAudience": [
{
"@type": "MedicalAudience",
"name": "Grand public",
"audienceType": "Patient",
"healthCondition": {
"@type": "MedicalCondition",
"name": "Variation génétique"
},
"suggestedMinAge": 18,
"suggestedGender": "unisex"
},
{
"@type": "MedicalAudience",
"name": "Médecins",
"audienceType": "Physician",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "France"
}
},
{
"@type": "MedicalAudience",
"name": "Chercheurs",
"audienceType": "Researcher",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "International"
}
}
],
"reviewedBy": {
"@type": "Person",
"name": "Dr Olivier Menir",
"jobTitle": "Expert en Médecine",
"description": "Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale",
"url": "/static/pages/docteur-olivier-menir.html",
"alumniOf": {
"@type": "EducationalOrganization",
"name": "Université Paris Descartes"
}
},
"isPartOf": {
"@type": "MedicalWebPage",
"name": "Phénomènes génétiques",
"url": "https://questionsmedicales.fr/mesh/D055614",
"about": {
"@type": "MedicalCondition",
"name": "Phénomènes génétiques",
"code": {
"@type": "MedicalCode",
"code": "D055614",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05"
}
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Hétérogénéité génétique",
"alternateName": "Genetic Heterogeneity",
"url": "https://questionsmedicales.fr/mesh/D018740",
"about": {
"@type": "MedicalCondition",
"name": "Hétérogénéité génétique",
"code": {
"@type": "MedicalCode",
"code": "D018740",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.331"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Hétéroplasmie",
"alternateName": "Heteroplasmy",
"url": "https://questionsmedicales.fr/mesh/D000081942",
"about": {
"@type": "MedicalCondition",
"name": "Hétéroplasmie",
"code": {
"@type": "MedicalCode",
"code": "D000081942",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.461"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation",
"alternateName": "Mutation",
"url": "https://questionsmedicales.fr/mesh/D009154",
"about": {
"@type": "MedicalCondition",
"name": "Mutation",
"code": {
"@type": "MedicalCode",
"code": "D009154",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Déséquilibre allélique",
"alternateName": "Allelic Imbalance",
"url": "https://questionsmedicales.fr/mesh/D022981",
"about": {
"@type": "MedicalCondition",
"name": "Déséquilibre allélique",
"code": {
"@type": "MedicalCode",
"code": "D022981",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.029"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Perte d'hétérozygotie",
"alternateName": "Loss of Heterozygosity",
"url": "https://questionsmedicales.fr/mesh/D019656",
"about": {
"@type": "MedicalCondition",
"name": "Perte d'hétérozygotie",
"code": {
"@type": "MedicalCode",
"code": "D019656",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.029.530"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Perte d'hétérozygotie",
"alternateName": "Loss of Heterozygosity",
"url": "https://questionsmedicales.fr/mesh/D019656",
"about": {
"@type": "MedicalCondition",
"name": "Perte d'hétérozygotie",
"code": {
"@type": "MedicalCode",
"code": "D019656",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.029.530"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mésappariement de bases",
"alternateName": "Base Pair Mismatch",
"url": "https://questionsmedicales.fr/mesh/D020137",
"about": {
"@type": "MedicalCondition",
"name": "Mésappariement de bases",
"code": {
"@type": "MedicalCode",
"code": "D020137",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.060"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Aberrations des chromosomes",
"alternateName": "Chromosome Aberrations",
"url": "https://questionsmedicales.fr/mesh/D002869",
"about": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes",
"code": {
"@type": "MedicalCode",
"code": "D002869",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Caryotype anormal",
"alternateName": "Abnormal Karyotype",
"url": "https://questionsmedicales.fr/mesh/D059786",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype anormal",
"code": {
"@type": "MedicalCode",
"code": "D059786",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.024"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chimérisme",
"alternateName": "Chimerism",
"url": "https://questionsmedicales.fr/mesh/D046528",
"about": {
"@type": "MedicalCondition",
"name": "Chimérisme",
"code": {
"@type": "MedicalCode",
"code": "D046528",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.125"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Cassure de chromosome",
"alternateName": "Chromosome Breakage",
"url": "https://questionsmedicales.fr/mesh/D019457",
"about": {
"@type": "MedicalCondition",
"name": "Cassure de chromosome",
"code": {
"@type": "MedicalCode",
"code": "D019457",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.175"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromothripsis",
"alternateName": "Chromothripsis",
"url": "https://questionsmedicales.fr/mesh/D000072837",
"about": {
"@type": "MedicalCondition",
"name": "Chromothripsis",
"code": {
"@type": "MedicalCode",
"code": "D000072837",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.310"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Isochromosomes",
"alternateName": "Isochromosomes",
"url": "https://questionsmedicales.fr/mesh/D018404",
"about": {
"@type": "MedicalCondition",
"name": "Isochromosomes",
"code": {
"@type": "MedicalCode",
"code": "D018404",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.430"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Micronoyaux à chromosomes défectueux",
"alternateName": "Micronuclei, Chromosome-Defective",
"url": "https://questionsmedicales.fr/mesh/D048629",
"about": {
"@type": "MedicalCondition",
"name": "Micronoyaux à chromosomes défectueux",
"code": {
"@type": "MedicalCode",
"code": "D048629",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.570"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mosaïcisme",
"alternateName": "Mosaicism",
"url": "https://questionsmedicales.fr/mesh/D009030",
"about": {
"@type": "MedicalCondition",
"name": "Mosaïcisme",
"code": {
"@type": "MedicalCode",
"code": "D009030",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.595"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromosomes en anneau",
"alternateName": "Ring Chromosomes",
"url": "https://questionsmedicales.fr/mesh/D012303",
"about": {
"@type": "MedicalCondition",
"name": "Chromosomes en anneau",
"code": {
"@type": "MedicalCode",
"code": "D012303",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.760"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Aberrations des chromosomes sexuels",
"alternateName": "Sex Chromosome Aberrations",
"url": "https://questionsmedicales.fr/mesh/D012729",
"about": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes sexuels",
"code": {
"@type": "MedicalCode",
"code": "D012729",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Caryotype XYY",
"alternateName": "XYY Karyotype",
"url": "https://questionsmedicales.fr/mesh/D014997",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype XYY",
"code": {
"@type": "MedicalCode",
"code": "D014997",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815.970"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Caryotype XYY",
"alternateName": "XYY Karyotype",
"url": "https://questionsmedicales.fr/mesh/D014997",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype XYY",
"code": {
"@type": "MedicalCode",
"code": "D014997",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815.970"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromosome Philadelphie",
"alternateName": "Philadelphia Chromosome",
"url": "https://questionsmedicales.fr/mesh/D010677",
"about": {
"@type": "MedicalCondition",
"name": "Chromosome Philadelphie",
"code": {
"@type": "MedicalCode",
"code": "D010677",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.870.680"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Disomie uniparentale",
"alternateName": "Uniparental Disomy",
"url": "https://questionsmedicales.fr/mesh/D024182",
"about": {
"@type": "MedicalCondition",
"name": "Disomie uniparentale",
"code": {
"@type": "MedicalCode",
"code": "D024182",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.935"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Caryotype anormal",
"alternateName": "Abnormal Karyotype",
"url": "https://questionsmedicales.fr/mesh/D059786",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype anormal",
"code": {
"@type": "MedicalCode",
"code": "D059786",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.024"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chimérisme",
"alternateName": "Chimerism",
"url": "https://questionsmedicales.fr/mesh/D046528",
"about": {
"@type": "MedicalCondition",
"name": "Chimérisme",
"code": {
"@type": "MedicalCode",
"code": "D046528",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.125"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Cassure de chromosome",
"alternateName": "Chromosome Breakage",
"url": "https://questionsmedicales.fr/mesh/D019457",
"about": {
"@type": "MedicalCondition",
"name": "Cassure de chromosome",
"code": {
"@type": "MedicalCode",
"code": "D019457",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.175"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromothripsis",
"alternateName": "Chromothripsis",
"url": "https://questionsmedicales.fr/mesh/D000072837",
"about": {
"@type": "MedicalCondition",
"name": "Chromothripsis",
"code": {
"@type": "MedicalCode",
"code": "D000072837",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.310"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Isochromosomes",
"alternateName": "Isochromosomes",
"url": "https://questionsmedicales.fr/mesh/D018404",
"about": {
"@type": "MedicalCondition",
"name": "Isochromosomes",
"code": {
"@type": "MedicalCode",
"code": "D018404",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.430"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Micronoyaux à chromosomes défectueux",
"alternateName": "Micronuclei, Chromosome-Defective",
"url": "https://questionsmedicales.fr/mesh/D048629",
"about": {
"@type": "MedicalCondition",
"name": "Micronoyaux à chromosomes défectueux",
"code": {
"@type": "MedicalCode",
"code": "D048629",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.570"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mosaïcisme",
"alternateName": "Mosaicism",
"url": "https://questionsmedicales.fr/mesh/D009030",
"about": {
"@type": "MedicalCondition",
"name": "Mosaïcisme",
"code": {
"@type": "MedicalCode",
"code": "D009030",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.595"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromosomes en anneau",
"alternateName": "Ring Chromosomes",
"url": "https://questionsmedicales.fr/mesh/D012303",
"about": {
"@type": "MedicalCondition",
"name": "Chromosomes en anneau",
"code": {
"@type": "MedicalCode",
"code": "D012303",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.760"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Aberrations des chromosomes sexuels",
"alternateName": "Sex Chromosome Aberrations",
"url": "https://questionsmedicales.fr/mesh/D012729",
"about": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes sexuels",
"code": {
"@type": "MedicalCode",
"code": "D012729",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Caryotype XYY",
"alternateName": "XYY Karyotype",
"url": "https://questionsmedicales.fr/mesh/D014997",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype XYY",
"code": {
"@type": "MedicalCode",
"code": "D014997",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815.970"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Caryotype XYY",
"alternateName": "XYY Karyotype",
"url": "https://questionsmedicales.fr/mesh/D014997",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype XYY",
"code": {
"@type": "MedicalCode",
"code": "D014997",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815.970"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromosome Philadelphie",
"alternateName": "Philadelphia Chromosome",
"url": "https://questionsmedicales.fr/mesh/D010677",
"about": {
"@type": "MedicalCondition",
"name": "Chromosome Philadelphie",
"code": {
"@type": "MedicalCode",
"code": "D010677",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.870.680"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Disomie uniparentale",
"alternateName": "Uniparental Disomy",
"url": "https://questionsmedicales.fr/mesh/D024182",
"about": {
"@type": "MedicalCondition",
"name": "Disomie uniparentale",
"code": {
"@type": "MedicalCode",
"code": "D024182",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.935"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Codon non-sens",
"alternateName": "Codon, Nonsense",
"url": "https://questionsmedicales.fr/mesh/D018389",
"about": {
"@type": "MedicalCondition",
"name": "Codon non-sens",
"code": {
"@type": "MedicalCode",
"code": "D018389",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.195"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation avec décalage du cadre de lecture",
"alternateName": "Frameshift Mutation",
"url": "https://questionsmedicales.fr/mesh/D016368",
"about": {
"@type": "MedicalCondition",
"name": "Mutation avec décalage du cadre de lecture",
"code": {
"@type": "MedicalCode",
"code": "D016368",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.265"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation gain de fonction",
"alternateName": "Gain of Function Mutation",
"url": "https://questionsmedicales.fr/mesh/D000073659",
"about": {
"@type": "MedicalCondition",
"name": "Mutation gain de fonction",
"code": {
"@type": "MedicalCode",
"code": "D000073659",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.288"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation germinale",
"alternateName": "Germ-Line Mutation",
"url": "https://questionsmedicales.fr/mesh/D018095",
"about": {
"@type": "MedicalCondition",
"name": "Mutation germinale",
"code": {
"@type": "MedicalCode",
"code": "D018095",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.350"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation perte de fonction",
"alternateName": "Loss of Function Mutation",
"url": "https://questionsmedicales.fr/mesh/D000073658",
"about": {
"@type": "MedicalCondition",
"name": "Mutation perte de fonction",
"code": {
"@type": "MedicalCode",
"code": "D000073658",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.538"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Accumulation de mutations",
"alternateName": "Mutation Accumulation",
"url": "https://questionsmedicales.fr/mesh/D000067552",
"about": {
"@type": "MedicalCondition",
"name": "Accumulation de mutations",
"code": {
"@type": "MedicalCode",
"code": "D000067552",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.594"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation faux-sens",
"alternateName": "Mutation, Missense",
"url": "https://questionsmedicales.fr/mesh/D020125",
"about": {
"@type": "MedicalCondition",
"name": "Mutation faux-sens",
"code": {
"@type": "MedicalCode",
"code": "D020125",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.650"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation ponctuelle",
"alternateName": "Point Mutation",
"url": "https://questionsmedicales.fr/mesh/D017354",
"about": {
"@type": "MedicalCondition",
"name": "Mutation ponctuelle",
"code": {
"@type": "MedicalCode",
"code": "D017354",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.675"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutation inapparente",
"alternateName": "Silent Mutation",
"url": "https://questionsmedicales.fr/mesh/D000069456",
"about": {
"@type": "MedicalCondition",
"name": "Mutation inapparente",
"code": {
"@type": "MedicalCode",
"code": "D000069456",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.803"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mutations synthétiques létales",
"alternateName": "Synthetic Lethal Mutations",
"url": "https://questionsmedicales.fr/mesh/D000072020",
"about": {
"@type": "MedicalCondition",
"name": "Mutations synthétiques létales",
"code": {
"@type": "MedicalCode",
"code": "D000072020",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.917"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Variation de phase",
"alternateName": "Phase Variation",
"url": "https://questionsmedicales.fr/mesh/D000090502",
"about": {
"@type": "MedicalCondition",
"name": "Variation de phase",
"code": {
"@type": "MedicalCode",
"code": "D000090502",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.693"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Polymorphisme génétique",
"alternateName": "Polymorphism, Genetic",
"url": "https://questionsmedicales.fr/mesh/D011110",
"about": {
"@type": "MedicalCondition",
"name": "Polymorphisme génétique",
"code": {
"@type": "MedicalCode",
"code": "D011110",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Variation structurale du génome",
"alternateName": "Genomic Structural Variation",
"url": "https://questionsmedicales.fr/mesh/D056914",
"about": {
"@type": "MedicalCondition",
"name": "Variation structurale du génome",
"code": {
"@type": "MedicalCode",
"code": "D056914",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.297"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Variations de nombre de copies de segment d'ADN",
"alternateName": "DNA Copy Number Variations",
"url": "https://questionsmedicales.fr/mesh/D056915",
"about": {
"@type": "MedicalCondition",
"name": "Variations de nombre de copies de segment d'ADN",
"code": {
"@type": "MedicalCode",
"code": "D056915",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.297.500"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Variations de nombre de copies de segment d'ADN",
"alternateName": "DNA Copy Number Variations",
"url": "https://questionsmedicales.fr/mesh/D056915",
"about": {
"@type": "MedicalCondition",
"name": "Variations de nombre de copies de segment d'ADN",
"code": {
"@type": "MedicalCode",
"code": "D056915",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.297.500"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Variants pharmacogénomiques",
"alternateName": "Pharmacogenomic Variants",
"url": "https://questionsmedicales.fr/mesh/D000071184",
"about": {
"@type": "MedicalCondition",
"name": "Variants pharmacogénomiques",
"code": {
"@type": "MedicalCode",
"code": "D000071184",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.446"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Polymorphisme de restriction",
"alternateName": "Polymorphism, Restriction Fragment Length",
"url": "https://questionsmedicales.fr/mesh/D012150",
"about": {
"@type": "MedicalCondition",
"name": "Polymorphisme de restriction",
"code": {
"@type": "MedicalCode",
"code": "D012150",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.595"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Polymorphisme de nucléotide simple",
"alternateName": "Polymorphism, Single Nucleotide",
"url": "https://questionsmedicales.fr/mesh/D020641",
"about": {
"@type": "MedicalCondition",
"name": "Polymorphisme de nucléotide simple",
"code": {
"@type": "MedicalCode",
"code": "D020641",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.598"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Polymorphisme de conformation simple brin",
"alternateName": "Polymorphism, Single-Stranded Conformational",
"url": "https://questionsmedicales.fr/mesh/D018807",
"about": {
"@type": "MedicalCondition",
"name": "Polymorphisme de conformation simple brin",
"code": {
"@type": "MedicalCode",
"code": "D018807",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.795.600"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Quasi-espèce",
"alternateName": "Quasispecies",
"url": "https://questionsmedicales.fr/mesh/D000074704",
"about": {
"@type": "MedicalCondition",
"name": "Quasi-espèce",
"code": {
"@type": "MedicalCode",
"code": "D000074704",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.897"
}
}
}
],
"about": {
"@type": "MedicalCondition",
"name": "Variation génétique",
"alternateName": "Genetic Variation",
"code": {
"@type": "MedicalCode",
"code": "D014644",
"codingSystem": "MeSH"
}
},
"author": [
{
"@type": "Person",
"name": "Yoshimichi Fukuta",
"url": "https://questionsmedicales.fr/author/Yoshimichi%20Fukuta",
"affiliation": {
"@type": "Organization",
"name": "Japan International Research Center for Agricultural Sciences, Tsukuba 305-8686, Japan."
}
},
{
"@type": "Person",
"name": "Jeong-Hwa Choi",
"url": "https://questionsmedicales.fr/author/Jeong-Hwa%20Choi",
"affiliation": {
"@type": "Organization",
"name": "Department of Food Science and Nutrition, Keimyung University, Daegu42601, Republic of Korea."
}
},
{
"@type": "Person",
"name": "Angelos Koutras",
"url": "https://questionsmedicales.fr/author/Angelos%20Koutras",
"affiliation": {
"@type": "Organization",
"name": "Division of Oncology, Department of Medicine, University of Patras, Patras, Greece."
}
},
{
"@type": "Person",
"name": "Paula Soria-Chacartegui",
"url": "https://questionsmedicales.fr/author/Paula%20Soria-Chacartegui",
"affiliation": {
"@type": "Organization",
"name": "Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain."
}
},
{
"@type": "Person",
"name": "Dolores Ochoa",
"url": "https://questionsmedicales.fr/author/Dolores%20Ochoa",
"affiliation": {
"@type": "Organization",
"name": "Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain."
}
}
],
"citation": [
{
"@type": "ScholarlyArticle",
"name": "Revisiting the Role of Genetic Variation in Adaptation.",
"datePublished": "2023-09-07",
"url": "https://questionsmedicales.fr/article/37792924",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1086/726012"
}
},
{
"@type": "ScholarlyArticle",
"name": "Genetic variations of CYP3A4 on the metabolism of itraconazole in vitro.",
"datePublished": "2023-10-18",
"url": "https://questionsmedicales.fr/article/37863381",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1016/j.fct.2023.114101"
}
},
{
"@type": "ScholarlyArticle",
"name": "The influence of HLA genetic variation on plasma protein expression.",
"datePublished": "2024-07-31",
"url": "https://questionsmedicales.fr/article/39085222",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1038/s41467-024-50583-8"
}
},
{
"@type": "ScholarlyArticle",
"name": "Genetic variation for tolerance to pre-harvest sprouting in mungbean (",
"datePublished": "2024-07-23",
"url": "https://questionsmedicales.fr/article/39071133",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.7717/peerj.17609"
}
},
{
"@type": "ScholarlyArticle",
"name": "Genetic Variation, Polyploidy, Hybridization Influencing the Aroma Profiles of",
"datePublished": "2024-10-18",
"url": "https://questionsmedicales.fr/article/39457463",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.3390/genes15101339"
}
}
],
"breadcrumb": {
"@type": "BreadcrumbList",
"itemListElement": [
{
"@type": "ListItem",
"position": 1,
"name": "questionsmedicales.fr",
"item": "https://questionsmedicales.fr"
},
{
"@type": "ListItem",
"position": 2,
"name": "Phénomènes génétiques",
"item": "https://questionsmedicales.fr/mesh/D055614"
},
{
"@type": "ListItem",
"position": 3,
"name": "Variation génétique",
"item": "https://questionsmedicales.fr/mesh/D014644"
}
]
}
},
{
"@type": "MedicalWebPage",
"name": "Article complet : Variation génétique - Questions et réponses",
"headline": "Questions et réponses médicales fréquentes sur Variation génétique",
"description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.",
"datePublished": "2026-08-31",
"inLanguage": "fr",
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Diagnostic",
"headline": "Diagnostic sur Variation génétique",
"description": "Comment détecte-t-on une variation génétique ?\nQuels signes indiquent une variation génétique ?\nLes variations génétiques sont-elles héréditaires ?\nQuel rôle joue le génome dans le diagnostic ?\nPeut-on identifier des variations par imagerie médicale ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-diagnostic"
},
{
"@type": "MedicalWebPage",
"name": "Symptômes",
"headline": "Symptômes sur Variation génétique",
"description": "Quels symptômes sont liés aux variations génétiques ?\nLes variations génétiques causent-elles des maladies ?\nComment les variations affectent-elles le développement ?\nLes symptômes apparaissent-ils à tout âge ?\nLes variations génétiques sont-elles asymptomatiques ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-symptômes"
},
{
"@type": "MedicalWebPage",
"name": "Prévention",
"headline": "Prévention sur Variation génétique",
"description": "Peut-on prévenir les variations génétiques ?\nQuel rôle joue le dépistage dans la prévention ?\nLes conseils génétiques aident-ils à prévenir ?\nL'alimentation influence-t-elle les variations ?\nLes vaccinations préviennent-elles des maladies génétiques ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-prévention"
},
{
"@type": "MedicalWebPage",
"name": "Traitements",
"headline": "Traitements sur Variation génétique",
"description": "Quels traitements existent pour les maladies génétiques ?\nLa thérapie génique est-elle efficace ?\nPeut-on prévenir les maladies par des traitements ?\nLes traitements sont-ils personnalisés ?\nQuels médicaments sont utilisés pour les variations génétiques ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-traitements"
},
{
"@type": "MedicalWebPage",
"name": "Complications",
"headline": "Complications sur Variation génétique",
"description": "Quelles complications peuvent survenir ?\nLes variations génétiques augmentent-elles le risque de cancer ?\nLes complications sont-elles réversibles ?\nComment les variations affectent-elles la qualité de vie ?\nLes complications nécessitent-elles des soins spécialisés ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-complications"
},
{
"@type": "MedicalWebPage",
"name": "Facteurs de risque",
"headline": "Facteurs de risque sur Variation génétique",
"description": "Quels sont les facteurs de risque des variations génétiques ?\nL'environnement joue-t-il un rôle ?\nLe mode de vie influence-t-il les variations ?\nLes facteurs socio-économiques affectent-ils les variations ?\nLes variations génétiques sont-elles plus fréquentes chez certaines populations ?",
"url": "https://questionsmedicales.fr/mesh/D014644#section-facteurs de risque"
}
]
},
{
"@type": "FAQPage",
"mainEntity": [
{
"@type": "Question",
"name": "Comment détecte-t-on une variation génétique ?",
"position": 1,
"acceptedAnswer": {
"@type": "Answer",
"text": "On utilise des tests génétiques comme le séquençage de l'ADN pour identifier les variations."
}
},
{
"@type": "Question",
"name": "Quels signes indiquent une variation génétique ?",
"position": 2,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des anomalies dans les résultats de tests génétiques peuvent signaler une variation."
}
},
{
"@type": "Question",
"name": "Les variations génétiques sont-elles héréditaires ?",
"position": 3,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines variations peuvent être transmises de génération en génération."
}
},
{
"@type": "Question",
"name": "Quel rôle joue le génome dans le diagnostic ?",
"position": 4,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le génome fournit des informations sur les variations pouvant causer des maladies."
}
},
{
"@type": "Question",
"name": "Peut-on identifier des variations par imagerie médicale ?",
"position": 5,
"acceptedAnswer": {
"@type": "Answer",
"text": "Non, l'imagerie ne détecte pas les variations génétiques, mais les effets des maladies."
}
},
{
"@type": "Question",
"name": "Quels symptômes sont liés aux variations génétiques ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes varient selon la maladie, incluant des troubles métaboliques ou neurologiques."
}
},
{
"@type": "Question",
"name": "Les variations génétiques causent-elles des maladies ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines variations peuvent être responsables de maladies héréditaires."
}
},
{
"@type": "Question",
"name": "Comment les variations affectent-elles le développement ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elles peuvent influencer le développement physique et cognitif, entraînant des retards."
}
},
{
"@type": "Question",
"name": "Les symptômes apparaissent-ils à tout âge ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Pas toujours, certains symptômes peuvent se manifester à l'enfance ou à l'âge adulte."
}
},
{
"@type": "Question",
"name": "Les variations génétiques sont-elles asymptomatiques ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines variations peuvent ne pas provoquer de symptômes visibles."
}
},
{
"@type": "Question",
"name": "Peut-on prévenir les variations génétiques ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les variations génétiques sont naturelles, mais certaines maladies peuvent être évitées par des tests."
}
},
{
"@type": "Question",
"name": "Quel rôle joue le dépistage dans la prévention ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le dépistage permet d'identifier les risques et de prendre des mesures préventives."
}
},
{
"@type": "Question",
"name": "Les conseils génétiques aident-ils à prévenir ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, ils informent sur les risques et les options pour les familles à risque."
}
},
{
"@type": "Question",
"name": "L'alimentation influence-t-elle les variations ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une alimentation saine peut réduire le risque de maladies liées à certaines variations."
}
},
{
"@type": "Question",
"name": "Les vaccinations préviennent-elles des maladies génétiques ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "Non, les vaccinations ne préviennent pas les variations génétiques, mais les maladies infectieuses."
}
},
{
"@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": "Peut-on prévenir les maladies par des traitements ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certains traitements peuvent réduire le risque de développer des maladies génétiques."
}
},
{
"@type": "Question",
"name": "Les traitements sont-ils personnalisés ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les traitements peuvent être adaptés en fonction des variations génétiques spécifiques."
}
},
{
"@type": "Question",
"name": "Quels médicaments sont utilisés pour les variations génétiques ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des médicaments spécifiques peuvent traiter les symptômes ou les causes des maladies génétiques."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications varient selon la maladie, incluant des troubles organiques ou fonctionnels."
}
},
{
"@type": "Question",
"name": "Les variations génétiques augmentent-elles le risque de cancer ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines variations génétiques sont associées à un risque accru de cancer."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles réversibles ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines complications peuvent être gérées, mais d'autres peuvent être permanentes."
}
},
{
"@type": "Question",
"name": "Comment les variations affectent-elles la qualité de vie ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elles peuvent entraîner des limitations physiques et psychologiques, affectant la qualité de vie."
}
},
{
"@type": "Question",
"name": "Les complications nécessitent-elles des soins spécialisés ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines complications peuvent nécessiter des soins médicaux spécialisés et un suivi."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque des variations génétiques ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les antécédents familiaux, l'âge et l'environnement peuvent influencer les variations."
}
},
{
"@type": "Question",
"name": "L'environnement joue-t-il un rôle ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des facteurs environnementaux peuvent interagir avec les variations génétiques."
}
},
{
"@type": "Question",
"name": "Le mode de vie influence-t-il les variations ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines habitudes de vie, comme le tabagisme, peuvent exacerber les effets des variations."
}
},
{
"@type": "Question",
"name": "Les facteurs socio-économiques affectent-ils les variations ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, l'accès aux soins et l'éducation peuvent influencer la gestion des variations."
}
},
{
"@type": "Question",
"name": "Les variations génétiques sont-elles plus fréquentes chez certaines populations ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines variations peuvent être plus courantes dans des groupes ethniques spécifiques."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 01/08/2026
Contenu vérifié selon les dernières recommandations médicales
4 publications dans cette catégorie
Affiliations :
Japan International Research Center for Agricultural Sciences, Tsukuba 305-8686, Japan.
Publications dans "Variation génétique" :
3 publications dans cette catégorie
Affiliations :
Department of Food Science and Nutrition, Keimyung University, Daegu42601, Republic of Korea.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Division of Oncology, Department of Medicine, University of Patras, Patras, Greece.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Section of Biostatistics, Hellenic Cooperative Oncology Group, Data Office, Athens, Greece.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Division of Oncology, Department of Medicine, University Hospital, Medical School, University of Patras, Patras, Greece.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Molecular Oncology, Hellenic Foundation for Cancer Research/Aristotle University of Thessaloniki, Thessaloniki, Greece.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Third Department of Medical Oncology, Agii Anargiri Cancer Hospital, Athens, Greece.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Molecular Oncology, Hellenic Foundation for Cancer Research/Aristotle University of Thessaloniki, Thessaloniki, Greece.
Aristotle University of Thessaloniki, Thessaloniki, Greece.
German Oncology Center, Limassol, Cyprus.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia. MT628@medschl.cam.ac.uk.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Animal and Poultry Production Division, Desert Research Center, 11753, Mataryia, Egypt.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Publications dans "Variation génétique" :
2 publications dans cette catégorie
Affiliations :
Institute of Clinical Molecular Biology, Kiel University, 24118 Kiel, Germany.
Publications dans "Variation génétique" :
AbstractEvolutionary biologists have thought about the role of genetic variation during adaptation for a very long time-before we understood the organization of the genetic code, the provenance of gen...
Itraconazole is a triazole anti-infective drug that has been proven to prevent and treat a variety of fungal and viral infections and has been considered to be a potential therapeutic remedy for COVID...
Genetic variation in the human leukocyte antigen (HLA) loci is associated with risk of immune-mediated diseases, but the molecular effects of HLA polymorphism are unclear. Here we examined the effects...
Pre-harvest sprouting (PHS) is one of the important abiotic stresses in mungbean which significantly reduces yield and quality of the produce. This study was conducted to evaluate the genetic variabil...
The fragrance and aroma of...
This review focuses on the...
These findings provide valuable insights for breeding strategies aimed at improving fruit quality and aligning with consumer preferences. Present review not only elucidates the complex interplay betwe...
Large-scale genomic studies have significantly increased our knowledge of genetic variability across populations. Regional genetic profiling is essential for distinguishing common benign variants from...
Breast cancer is the most frequent cancer among women. Genetics are the main risk factor for breast cancer. Statistics show that 15-25% of breast cancers are inherited among those with cancer-prone re...
A search of the PubMed database was carried out spanning from 2005 to July 2024, yielding a total of 768 articles that delve into the realm of familial breast cancer, concerning genes and genetic synd...
We report on a set of 20 familial breast cancer -associated genes into high, moderate, and low penetrance levels. Additionally, 10 genetic disorders were found to be linked with familial breast cancer...
Familial breast cancer has been linked to several genetic diseases and mutations, according to studies. Screening for genetic disorders is recommended by National Comprehensive Cancer Network recommen...
Symbiotic nitrogen fixation differs among Bradyrhizobium japonicum strains. Soybean inoculated with USDA123 has a lower yield than strains known to have high nitrogen fixation efficiency, such as USDA...
Seventy-three G. max accessions with significantly different nodule number of USDA110 and USDA123 were identified. After double inoculating 35 of the 73 accessions, it was observed that PI189939, PI31...
High-throughput phenotyping systems to characterize nodule number and occupancy were developed, and soybean germplasm restricting rhizobium strain USDA123 but preferring USDA110 was identified. The la...
The progression of many solid tumors is accompanied by temporal and spatial changes in the stiffness of the extracellular matrix (ECM). Cancer cells adapt to soft and stiff ECM through mechanisms that...
The elevation of atmospheric CO...