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Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
Gorvin, Caroline M; Loh, Nellie Y; Stechman, Michael J; Falcone, Sara; Hannan, Fadil M; Ahmad, Bushra N; Piret, Sian E; Reed, Anita Ac; Jeyabalan, Jeshmi; Leo, Paul; Marshall, Mhairi; Sethi, Siddharth; Bass, Paul; Roberts, Ian; Sanderson, Jeremy; Wells, Sara; Hough, Tertius A; Bentley, Liz; Christie, Paul T; Simon, Michelle M; Mallon, Ann-Marie; Schulz, Herbert; Cox, Roger D; Brown, Matthew A; Huebner, Norbert; Brown, Steve D; Thakker, Rajesh V.
Afiliação
  • Gorvin CM; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Loh NY; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Stechman MJ; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Falcone S; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Hannan FM; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Ahmad BN; Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, UK.
  • Piret SE; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Reed AA; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Jeyabalan J; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Leo P; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Marshall M; Translational Genomics Group, Institute of Health and Biomedical Innovation, School of Biomedical Sciences, Queensland University of Technology (QUT) at Translational Research Institute, Brisbane, Australia.
  • Sethi S; Translational Genomics Group, Institute of Health and Biomedical Innovation, School of Biomedical Sciences, Queensland University of Technology (QUT) at Translational Research Institute, Brisbane, Australia.
  • Bass P; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Roberts I; Department of Cellular Pathology, Royal Free Hospital, London, UK.
  • Sanderson J; Department of Cellular Pathology, John Radcliffe Hospital, Oxford, UK.
  • Wells S; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Hough TA; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Bentley L; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Christie PT; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Simon MM; Academic Endocrine Unit, Oxford Centre for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Mallon AM; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Schulz H; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Cox RD; Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
  • Brown MA; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
  • Huebner N; Translational Genomics Group, Institute of Health and Biomedical Innovation, School of Biomedical Sciences, Queensland University of Technology (QUT) at Translational Research Institute, Brisbane, Australia.
  • Brown SD; Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
  • Thakker RV; Mary Lyon Centre and Mammalian Genetics Unit, Medical Research Council Harwell Institute, Harwell, UK.
J Bone Miner Res ; 34(7): 1324-1335, 2019 07.
Article em En | MEDLINE | ID: mdl-30830987
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas Nucleares / Mutação de Sentido Incorreto / Nefrocalcinose Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Bone Miner Res Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas Nucleares / Mutação de Sentido Incorreto / Nefrocalcinose Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Bone Miner Res Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido