Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function-Reference-Cited by-同舟云学术

Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function

Published:2010-08-02 Issue:8 Volume:120 Page:2889-2899
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Zeissig Sebastian,Dougan Stephanie K.,Barral Duarte C.,Junker Yvonne,Chen Zhangguo,Kaser Arthur,Ho Madelyn,Mandel Hannah,McIntyre Adam,Kennedy Susan M.,Painter Gavin F.,Veerapen Natacha,Besra Gurdyal S.,Cerundolo Vincenzo,Yue Simon,Beladi Sarah,Behar Samuel M.,Chen Xiuxu,Gumperz Jenny E.,Breckpot Karine,Raper Anna,Baer Amanda,Exley Mark A.,Hegele Robert A.,Cuchel Marina,Rader Daniel J.,Davidson Nicholas O.,Blumberg Richard S.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference67 articles.

1. The Role of the Microsomal Triglygeride Transfer Protein in Abetalipoproteinemia

2. The physiological and molecular regulation of lipoprotein assembly and secretion

3. Analysis of the role of microsomal triglyceride transfer protein in the liver of tissue-specific knockout mice

4. Knockout of the abetalipoproteinemia gene in mice: Reduced lipoprotein secretion in heterozygotes and embryonic lethality in homozygotes

5. CD1 antigen presentation: how it works

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