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Morphological, behavioral and cellular analyses revealed different phenotypes in Wolfram syndrome wfs1a and wfs1b zebrafish mutant lines.
Crouzier, Lucie; Richard, Elodie M; Diez, Camille; Alzaeem, Hala; Denus, Morgane; Cubedo, Nicolas; Delaunay, Thomas; Glendenning, Emily; Baxendale, Sarah; Liévens, Jean-Charles; Whitfield, Tanya T; Maurice, Tangui; Delprat, Benjamin.
Afiliação
  • Crouzier L; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Richard EM; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Diez C; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Alzaeem H; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Denus M; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Cubedo N; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Delaunay T; IES, Université Montpellier, CNRS, Montpellier, France.
  • Glendenning E; Development, Regeneration and Neurophysiology, School of Biosciences, University of Sheffield, Sheffield S10 2TN, UK.
  • Baxendale S; Development, Regeneration and Neurophysiology, School of Biosciences, University of Sheffield, Sheffield S10 2TN, UK.
  • Liévens JC; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Whitfield TT; Development, Regeneration and Neurophysiology, School of Biosciences, University of Sheffield, Sheffield S10 2TN, UK.
  • Maurice T; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
  • Delprat B; MMDN, Université Montpellier, EPHE, INSERM, Montpellier, France.
Hum Mol Genet ; 31(16): 2711-2727, 2022 08 23.
Article em En | MEDLINE | ID: mdl-35325133
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Wolfram / Atrofia Óptica Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Wolfram / Atrofia Óptica Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França