Skip to main content
Journal cover image

PARACRINE HEDGEHOG SIGNALING BETWEEN CHOLANGIOCYTES AND MYOFIBROBLASTS PROMOTES NKT CELL MIGRATION TOWARDS BILIARY EPITHELIAL CELLS: A NOVEL MECHANISM FOR NKT CELL ACCUMULATION IN PRIMARY BILIARY CIRRHOSIS

Publication ,  Conference
Omenetti, A; Syn, W-K; Jung, Y; Witek, RP; Choi, SS; Gershwin, ME; Diehl, AM
Published in: HEPATOLOGY
October 1, 2008

Duke Scholars

Published In

HEPATOLOGY

ISSN

0270-9139

Publication Date

October 1, 2008

Volume

48

Issue

4

Start / End Page

595A / 596A

Location

San Francisco, CA

Publisher

JOHN WILEY & SONS INC

Conference Name

59th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases

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
Omenetti, A., Syn, W.-K., Jung, Y., Witek, R. P., Choi, S. S., Gershwin, M. E., & Diehl, A. M. (2008). PARACRINE HEDGEHOG SIGNALING BETWEEN CHOLANGIOCYTES AND MYOFIBROBLASTS PROMOTES NKT CELL MIGRATION TOWARDS BILIARY EPITHELIAL CELLS: A NOVEL MECHANISM FOR NKT CELL ACCUMULATION IN PRIMARY BILIARY CIRRHOSIS. In HEPATOLOGY (Vol. 48, pp. 595A-596A). San Francisco, CA: JOHN WILEY & SONS INC.
Omenetti, Alessia, Wing-Kin Syn, Youngmi Jung, Rafal P. Witek, Steve S. Choi, M Eric Gershwin, and Anna Mae Diehl. “PARACRINE HEDGEHOG SIGNALING BETWEEN CHOLANGIOCYTES AND MYOFIBROBLASTS PROMOTES NKT CELL MIGRATION TOWARDS BILIARY EPITHELIAL CELLS: A NOVEL MECHANISM FOR NKT CELL ACCUMULATION IN PRIMARY BILIARY CIRRHOSIS.” In HEPATOLOGY, 48:595A-596A. JOHN WILEY & SONS INC, 2008.
Journal cover image

Published In

HEPATOLOGY

ISSN

0270-9139

Publication Date

October 1, 2008

Volume

48

Issue

4

Start / End Page

595A / 596A

Location

San Francisco, CA

Publisher

JOHN WILEY & SONS INC

Conference Name

59th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases

Related Subject Headings

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