A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes-Reference-Cited by-同舟云学术

A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes

Published:2019-01-08 Issue:9 Volume:28 Page:1548-1560
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Gershlick David C¹,Ishida Morié¹,Jones Julie R²,Bellomo Allison²,Bonifacino Juan S¹,Everman David B²

Affiliation:

1. Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA

2. Greenwood Genetic Center, Greenwood, SC, USA

Funder

National Institute of Child Health and Human Development

South Carolina Department of Disabilities and Special Needs

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/28/9/1548/28543294/ddy423.pdf

Reference40 articles.

1. Transport according to GARP: receiving retrograde cargo at the trans-Golgi network;Bonifacino;Trends Cell Biol.,2011

2. Membrane tethering complexes in the endosomal system;Spang;Front. Cell Dev. Biol.,2016

3. Vps51p links the VFT complex to the SNARE Tlg1p;Siniossoglou;J. Biol. Chem.,2002

4. Vps51p mediates the association of the GARP (Vps52/53/54) complex with the late Golgi t-SNARE Tlg1p;Conibear;Mol. Biol. Cell,2003

5. Characterization of the human GARP (Golgi associated retrograde protein) complex;Liewen;Exp. Cell Res.,2005

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