Mass spectrometry-based proteomic analysis reveals the interacting partners of lipin1

Author:

Wang Jian1,Wang Song1,Yan Chongjia1,Deng Yunxia2,Huang Zhiwei2,Shi Ping1ORCID

Affiliation:

1. State Key Laboratory of Bioreactor Engineering; East China University of Science and Technology, 130 Meilong Road; Shanghai 200237 China

2. College of Chemistry, Chemical Engineering and Biotechnology; Donghua University, 2999 Renmin Road; Shanghai 201620 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Genetics,Molecular Biology,Biochemistry

Reference45 articles.

1. The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissuespecific defects in lipoprotein lipase and hepatic lipase activities;Langner;J. Biol. Chem.,1989

2. Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin;P'eterfy;Nat. Genet.,2001

3. Adipose tissue deficiency, glucose intolerance, and increased atherosclerosis result from mutation in the mouse fatty liver dystrophy (fld) gene;Reue;J. Lipid Res.,2000

4. Three mammalian lipins act as phosphatidate phosphatases with distinct tissue expression patterns;Donkor;J. Biol. Chem.,2007

5. Lipin-The bridge between hepatic glycerolipid biosynthesis and lipoprotein metabolism;Bou;BA-Mol. Cell Biol. L.,2010

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