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Insights into genetic variants associated with NASH-fibrosis from metabolite profiling.
Mann, Jake P; Pietzner, Maik; Wittemans, Laura B; Rolfe, Emmanuela De Lucia; Kerrison, Nicola D; Imamura, Fumiaki; Forouhi, Nita G; Fauman, Eric; Allison, Michael E; Griffin, Jules L; Koulman, Albert; Wareham, Nicholas J; Langenberg, Claudia.
Afiliação
  • Mann JP; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Pietzner M; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Wittemans LB; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Rolfe EL; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Kerrison ND; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Imamura F; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Forouhi NG; MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0SL, UK.
  • Fauman E; Internal Medicine Research Unit, Pfizer Worldwide Research, Development and Medical, Cambridge, MA 02142, USA.
  • Allison ME; Liver Unit, Department of Medicine, Cambridge Biomedical Research Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, UK.
  • Griffin JL; MRC Human Nutrition Research, University of Cambridge, Cambridge CB1 9NL, UK.
  • Koulman A; Department of Biochemistry, Cambridge Systems Biology Centre, University of Cambridge, Cambridge CB2 1GA, UK.
  • Wareham NJ; MRC Human Nutrition Research, University of Cambridge, Cambridge CB1 9NL, UK.
  • Langenberg C; Department of Biochemistry, Cambridge Systems Biology Centre, University of Cambridge, Cambridge CB2 1GA, UK.
Hum Mol Genet ; 29(20): 3451-3463, 2020 12 18.
Article em En | MEDLINE | ID: mdl-32720691
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Metaboloma / Hepatopatia Gordurosa não Alcoólica / Cirrose Hepática Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Metaboloma / Hepatopatia Gordurosa não Alcoólica / Cirrose Hepática Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido