A disease-associated mutation in thyroid hormone receptor α1 causes hearing loss and sensory hair cell patterning defects in mice.

Animals Deafness Hearing Loss / genetics Mice Mutation Thyroid Hormone Receptors alpha / genetics Thyroid Hormones

Journal

Science signaling
ISSN: 1937-9145
Titre abrégé: Sci Signal
Pays: United States
ID NLM: 101465400

Informations de publication

Date de publication:
14 06 2022
Historique:
entrez: 14 6 2022
pubmed: 15 6 2022
medline: 18 6 2022
Statut: ppublish

Résumé

Resistance to thyroid hormone due to mutations in

Identifiants

DOI: 10.1126/scisignal.abj4583 PMID: 35700264
pubmed: 35700264
doi: 10.1126/scisignal.abj4583
doi:

Substances chimiques

Thyroid Hormone Receptors alpha 0
Thyroid Hormones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

eabj4583

Auteurs

Corentin Affortit (C)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.
ORCID: 0000-0003-3109-4575

Fabian Blanc (F)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.
Department of ENT and Head and Neck Surgery, University Hospital of Montpellier, Montpellier, France.
ORCID: 0000-0001-5843-7086

Jamal Nasr (J)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.

Jean-Charles Ceccato (JC)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.
ORCID: 0000-0003-3342-8727

Suzy Markossian (S)

Institut de Génomique Fonctionnelle de Lyon (IGFL), INRAE USC1370, CNRS (UMR5242), ENS, Lyon, France.
ORCID: 0000-0003-3545-569X

Romain Guyot (R)

Institut de Génomique Fonctionnelle de Lyon (IGFL), INRAE USC1370, CNRS (UMR5242), ENS, Lyon, France.
ORCID: 0000-0002-0029-6222

Jean-Luc Puel (JL)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.
ORCID: 0000-0002-3772-5190

Frédéric Flamant (F)

Institut de Génomique Fonctionnelle de Lyon (IGFL), INRAE USC1370, CNRS (UMR5242), ENS, Lyon, France.
ORCID: 0000-0002-3360-2345

Jing Wang (J)

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, Montpellier, France.
Department of ENT and Head and Neck Surgery, University Hospital of Montpellier, Montpellier, France.
ORCID: 0000-0002-2670-719X

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › A disease-associated mutation in thyroid...
questionsmedicales.fr › États, signes et symptômes pathologiques › Signes et symptômes › Manifestations neurologiques › Troubles sensitifs › Troubles de l'audition › Perte d'audition › Surdité › A disease-associated mutation in thyroid...
questionsmedicales.fr › États, signes et symptômes pathologiques › Signes et symptômes › Manifestations neurologiques › Troubles sensitifs › Troubles de l'audition › Perte d'audition › A disease-associated mutation in thyroid...
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Rodentia › Muridae › Murinae › Souris › A disease-associated mutation in thyroid...
questionsmedicales.fr › Phénomènes génétiques › Variation génétique › Mutation › A disease-associated mutation in thyroid...
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Récepteurs cytoplasmiques et nucléaires › Récepteurs des hormones thyroïdiennes › Récepteurs alpha des hormones thyroïdiennes › A disease-associated mutation in thyroid...
questionsmedicales.fr › Hormones thyroïdiennes › A disease-associated mutation in thyroid...