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Insulin secretion deficits in a Prader-Willi syndrome ß-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperones.
Koppes, Erik A; Johnson, Marie A; Moresco, James J; Luppi, Patrizia; Lewis, Dale W; Stolz, Donna B; Diedrich, Jolene K; Yates, John R; Wek, Ronald C; Watkins, Simon C; Gollin, Susanne M; Park, Hyun Jung; Drain, Peter; Nicholls, Robert D.
Afiliação
  • Koppes EA; Division of Genetic and Genomic Medicine, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Johnson MA; Division of Genetic and Genomic Medicine, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Moresco JJ; Department of Molecular Medicine and Neurobiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Luppi P; Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
  • Lewis DW; Department of Human Genetics, University of Pittsburgh School of Public Health, Pittsburgh, Pennsylvania, United States of America.
  • Stolz DB; Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
  • Diedrich JK; Department of Molecular Medicine and Neurobiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Yates JR; Department of Molecular Medicine and Neurobiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Wek RC; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.
  • Watkins SC; Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
  • Gollin SM; Department of Human Genetics, University of Pittsburgh School of Public Health, Pittsburgh, Pennsylvania, United States of America.
  • Park HJ; Department of Human Genetics, University of Pittsburgh School of Public Health, Pittsburgh, Pennsylvania, United States of America.
  • Drain P; Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
  • Nicholls RD; Division of Genetic and Genomic Medicine, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
PLoS Genet ; 19(4): e1010710, 2023 04.
Article em En | MEDLINE | ID: mdl-37068109
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos