COG8 deficiency causes new congenital disorder of glycosylation type IIh-Reference-Cited by-同舟云学术

COG8 deficiency causes new congenital disorder of glycosylation type IIh

Published:2007-03-01 Issue:7 Volume:16 Page:731-741
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Kranz Christian,Ng Bobby G.,Sun Liangwu,Sharma Vandana,Eklund Erik A.,Miura Yoshiaki,Ungar Daniel,Lupashin Vladimir,Winkel R. Dennis,Cipollo John F.,Costello Catherine E.,Loh Eva,Hong Wanjin,Freeze Hudson H.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/7/731/1853310/ddm028.pdf

Reference37 articles.

1. Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function;Ungar;J. Cell. Biol.,2002

2. The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic;Whyte;Dev. Cell.,2001

3. Subunit architecture of the conserved oligomeric Golgi complex;Ungar;J. Biol. Chem.,2005

4. Genetic analysis of the subunit organization and function of the conserved oligomeric Golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells;Oka;J. Biol. Chem.,2005

5. Retrograde transport on the COG railway;Ungar;Trends Cell. Biol.,2006

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