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The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder.
Hiebler, Shandi; Masuda, Tomohiro; Hacia, Joseph G; Moser, Ann B; Faust, Phyllis L; Liu, Anita; Chowdhury, Nivedita; Huang, Ning; Lauer, Amanda; Bennett, Jean; Watkins, Paul A; Zack, Donald J; Braverman, Nancy E; Raymond, Gerald V; Steinberg, Steven J.
Afiliação
  • Hiebler S; Department of Neurogenetics, Hugo W. Moser Research Institute at Kennedy Krieger, 707 N. Broadway, Baltimore, MD, USA.
  • Masuda T; Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Hacia JG; Department of Biochemistry and Molecular Biology, Institute for Genetic Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Moser AB; Department of Neurogenetics, Hugo W. Moser Research Institute at Kennedy Krieger, 707 N. Broadway, Baltimore, MD, USA.
  • Faust PL; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Liu A; Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • Chowdhury N; Department of Neurogenetics, Hugo W. Moser Research Institute at Kennedy Krieger, 707 N. Broadway, Baltimore, MD, USA.
  • Huang N; Department of Neurogenetics, Hugo W. Moser Research Institute at Kennedy Krieger, 707 N. Broadway, Baltimore, MD, USA.
  • Lauer A; Department of Biochemistry and Molecular Biology, Institute for Genetic Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Bennett J; Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Watkins PA; F.M. Kirby Center for Molecular Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Zack DJ; Department of Neurogenetics, Hugo W. Moser Research Institute at Kennedy Krieger, 707 N. Broadway, Baltimore, MD, USA.
  • Braverman NE; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Raymond GV; Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Steinberg SJ; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Mol Genet Metab ; 111(4): 522-532, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24503136
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Zellweger / Adenosina Trifosfatases / Mutação de Sentido Incorreto / Modelos Animais de Doenças Limite: Animals / Female / Humans / Male Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Zellweger / Adenosina Trifosfatases / Mutação de Sentido Incorreto / Modelos Animais de Doenças Limite: Animals / Female / Humans / Male Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos