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CYP4F2 is a human-specific determinant of circulating N-acyl amino acid levels.
Tanzo, Julia T; Li, Veronica L; Wiggenhorn, Amanda L; Moya-Garzon, Maria Dolores; Wei, Wei; Lyu, Xuchao; Dong, Wentao; Tahir, Usman A; Chen, Zsu-Zsu; Cruz, Daniel E; Deng, Shuliang; Shi, Xu; Zheng, Shuning; Guo, Yan; Sims, Mario; Abu-Remaileh, Monther; Wilson, James G; Gerszten, Robert E; Long, Jonathan Z; Benson, Mark D.
Afiliação
  • Tanzo JT; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Stanford Diabetes Research Center, Stanford University, Stanford, California, USA.
  • Li VL; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Department of Chemistry, Stanford University, Stanford, California, USA; Wu Tsai Human Performance Alliance, Stanford University, California, U
  • Wiggenhorn AL; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Department of Chemistry, Stanford University, Stanford, California, USA.
  • Moya-Garzon MD; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA.
  • Wei W; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Department of Biology, Stanford University, Stanford, California, USA.
  • Lyu X; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Wu Tsai Human Performance Alliance, Stanford University, California, USA.
  • Dong W; Stanford ChEM-H, Stanford University, Stanford, California, USA; Department of Chemical Engineering, Stanford University, Stanford, California, USA.
  • Tahir UA; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Chen ZZ; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Cruz DE; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Deng S; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Shi X; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Zheng S; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Guo Y; Univ of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Sims M; Univ of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Abu-Remaileh M; Stanford ChEM-H, Stanford University, Stanford, California, USA; Department of Chemical Engineering, Stanford University, Stanford, California, USA.
  • Wilson JG; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Gerszten RE; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA; Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA.
  • Long JZ; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA; Stanford ChEM-H, Stanford University, Stanford, California, USA; Stanford Diabetes Research Center, Stanford University, Stanford, California, USA; Wu Tsai Human Performance Alliance, Stanford University, Cal
  • Benson MD; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: mbenson@bidmc.harvard.edu.
J Biol Chem ; 299(6): 104764, 2023 06.
Article em En | MEDLINE | ID: mdl-37121548
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Oleicos / Família 4 do Citocromo P450 / Aminoácidos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2023 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: Ácidos Oleicos / Família 4 do Citocromo P450 / Aminoácidos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos