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A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency.
Talsness, Dana M; Owings, Katie G; Coelho, Emily; Mercenne, Gaelle; Pleinis, John M; Partha, Raghavendran; Hope, Kevin A; Zuberi, Aamir R; Clark, Nathan L; Lutz, Cathleen M; Rodan, Aylin R; Chow, Clement Y.
Afiliação
  • Talsness DM; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, United States.
  • Owings KG; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, United States.
  • Coelho E; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, United States.
  • Mercenne G; Department of Internal Medicine, Division of Nephrology and Hypertension, and Molecular Medicine Program, University of Utah, Salt Lake City, United States.
  • Pleinis JM; Department of Internal Medicine, Division of Nephrology and Hypertension, and Molecular Medicine Program, University of Utah, Salt Lake City, United States.
  • Partha R; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, United States.
  • Hope KA; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, United States.
  • Zuberi AR; Genetic Resource Science, The Jackson Laboratory, Bar Harbor, United States.
  • Clark NL; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, United States.
  • Lutz CM; Genetic Resource Science, The Jackson Laboratory, Bar Harbor, United States.
  • Rodan AR; Department of Internal Medicine, Division of Nephrology and Hypertension, and Molecular Medicine Program, University of Utah, Salt Lake City, United States.
  • Chow CY; Medical Service, Veterans Affairs Salt Lake City Health Care System, Salt Lake City, United States.
Elife ; 92020 12 14.
Article em En | MEDLINE | ID: mdl-33315011
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Defeitos Congênitos da Glicosilação / Peptídeo-N4-(N-acetil-beta-glucosaminil) Asparagina Amidase / Membro 2 da Família 12 de Carreador de Soluto Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Defeitos Congênitos da Glicosilação / Peptídeo-N4-(N-acetil-beta-glucosaminil) Asparagina Amidase / Membro 2 da Família 12 de Carreador de Soluto Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article