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Hepatic estrogen transcriptional activity and estrogen receptor a gene expression are negatively correlated with fibrosis stage in patients with nonalcoholic fatty liver disease (NAFLD)

Publication ,  Conference
Suzuki, A; Spencer, HJ; Moylan, CA; Dranoff, JA; Abdelmalek, MF; Guy, CD; Diehl, AM
Published in: HEPATOLOGY
October 1, 2016

Duke Scholars

Published In

HEPATOLOGY

EISSN

1527-3350

ISSN

0270-9139

Publication Date

October 1, 2016

Volume

64

Start / End Page

105A / 105A

Location

Boston, MA

Publisher

WILEY

Conference Name

67th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases (AASLD)

Related Subject Headings

  • Gastroenterology & Hepatology
  • 3204 Immunology
  • 3202 Clinical sciences
  • 1107 Immunology
  • 1103 Clinical Sciences
  • 1101 Medical Biochemistry and Metabolomics
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Suzuki, A., Spencer, H. J., Moylan, C. A., Dranoff, J. A., Abdelmalek, M. F., Guy, C. D., & Diehl, A. M. (2016). Hepatic estrogen transcriptional activity and estrogen receptor a gene expression are negatively correlated with fibrosis stage in patients with nonalcoholic fatty liver disease (NAFLD). In HEPATOLOGY (Vol. 64, pp. 105A-105A). Boston, MA: WILEY.
Suzuki, Ayako, Horace J. Spencer, Cynthia A. Moylan, Jonathan A. Dranoff, Manal F. Abdelmalek, Cynthia D. Guy, and Anna Mae Diehl. “Hepatic estrogen transcriptional activity and estrogen receptor a gene expression are negatively correlated with fibrosis stage in patients with nonalcoholic fatty liver disease (NAFLD).” In HEPATOLOGY, 64:105A-105A. WILEY, 2016.
Journal cover image

Published In

HEPATOLOGY

EISSN

1527-3350

ISSN

0270-9139

Publication Date

October 1, 2016

Volume

64

Start / End Page

105A / 105A

Location

Boston, MA

Publisher

WILEY

Conference Name

67th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases (AASLD)

Related Subject Headings

  • Gastroenterology & Hepatology
  • 3204 Immunology
  • 3202 Clinical sciences
  • 1107 Immunology
  • 1103 Clinical Sciences
  • 1101 Medical Biochemistry and Metabolomics