Single nucleotide polymorphism-mediated translational suppression of endoplasmic reticulum mannosidase I modifies the onset of end-stage liver disease in alpha1-antitrypsin deficiency-Reference-Cited by-同舟云学术

Single nucleotide polymorphism-mediated translational suppression of endoplasmic reticulum mannosidase I modifies the onset of end-stage liver disease in alpha1-antitrypsin deficiency

Published:2009-03-19 Issue:1 Volume:50 Page:275-281
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Pan Shujuan,Huang Lu,McPherson John,Muzny Donna,Rouhani Farshid,Brantly Mark,Gibbs Richard,Sifers Richard N.

Publisher

Wiley

Subject

Hepatology

Reference30 articles.

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3. Structure and variation of human alpha 1-antitrypsin;Carrell;Nature,1982

4. Alpha-1-antitrypsin deficiency: accumulation or degradation of mutant variants within the hepatic endoplasmic reticulum;Sifers;Am J Respir Cell Mol Biol,1989

5. Accumulation of the insoluble PiZ variant of human alpha 1-antitrypsin within the hepatic endoplasmic reticulum does not elevate the steady-state level of grp78/BiP;Graham;J Biol Chem,1990

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