Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.

Animals Chromosome Mapping Circadian Rhythm Disease Susceptibility Genetic Predisposition to Disease Humans Melatonin / biosynthesis Quantitative Trait Loci Quantitative Trait, Heritable Smith-Magenis Syndrome / diagnosis
CLOCK RAI1 circadian clock circadian cycle melatonin neurogenetics

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
19 Jul 2019
Historique:
received: 09 05 2019
revised: 08 07 2019
accepted: 17 07 2019
entrez: 24 7 2019
pubmed: 25 7 2019
medline: 28 12 2019
Statut: epublish

Résumé

Smith-Magenis syndrome (SMS), linked to

Identifiants

DOI: 10.3390/ijms20143533 PMID: 31330985 PMC: PMC6679101
pubmed: 31330985
pii: ijms20143533
doi: 10.3390/ijms20143533
pmc: PMC6679101
pii:
doi:

Substances chimiques

Melatonin JL5DK93RCL

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Références

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Auteurs

Alice Poisson (A)

GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Q19 Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), 69678 Bron, France. alice.poisson@ch-le-vinatier.fr.

Alain Nicolas (A)

GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Q19 Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), 69678 Bron, France.

Idriss Bousquet (I)

GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Q19 Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), 69678 Bron, France.

Véronique Raverot (V)

Laboratoire d'hormonologie-CBPE, CHU de Lyon, 59, boulevard Pinel, 69677 Bron, France.
ORCID: 0000-0003-4336-1271

Claude Gronfier (C)

Lyon Neuroscience Research Center, Integrative Physiology of the Brain Arousal Systems, Waking Team, Inserm UMRS 1028, CNRS UMR 5292, Université Claude Bernard Lyon 1, Université de Lyon, 69675 Lyon, France.
ORCID: 0000-0002-6549-799X

Caroline Demily (C)

GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Q19 Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), 69678 Bron, France.

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Techniques d'investigation › Techniques génétiques › Cartographie chromosomique › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Phénomènes physiologiques › Phénomènes chronobiologiques › Périodicité › Rythme circadien › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Phénomènes physiologiques › Constitution physique › Prédisposition aux maladies › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Phénomènes génétiques › Génotype › Prédisposition génétique à une maladie › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Primates › Haplorhini › Catarrhini › Hominidae › Humains › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Mélatonine › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Phénomènes génétiques › Structures génétiques › Génome › Composants de génome › Locus génétiques › Locus de caractère quantitatif › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Phénomènes génétiques › Modes de transmission héréditaire › Caractère quantitatif héréditaire › Smith-Magenis Syndrome: Molecular Basis of a...
questionsmedicales.fr › Malformations et maladies congénitales, héréditaires et néonatales › Maladies génétiques congénitales › Maladies chromosomiques › Syndrome de Smith-Magenis › Smith-Magenis Syndrome: Molecular Basis of a...