Degenerative phenotypes caused by the combined deficiency of murine HIP1 and HIP1r are rescued by human HIP1-Reference-Cited by-同舟云学术

Degenerative phenotypes caused by the combined deficiency of murine HIP1 and HIP1r are rescued by human HIP1

Published:2007-04-23 Issue:11 Volume:16 Page:1279-1292
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bradley Sarah V.,Hyun Teresa S.,Oravecz-Wilson Katherine I.,Li Lina,Waldorff Erik I.,Ermilov Alexander N.,Goldstein Steven A.,Zhang Claire X.,Drubin David G.,Varela Kate,Parlow Al,Dlugosz Andrzej A.,Ross Theodora S.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/16/11/1279/17243530/ddm076.pdf

Reference51 articles.

1. HIP1 and HIP1r stabilize receptor tyrosine kinases and bind 3-phosphoinositides via epsin N-terminal homology domains;Hyun;J. Biol. Chem.,2004

2. The actin-binding protein Hip1R associates with clathrin during early stages of endocytosis and promotes clathrin assembly in vitro;Engqvist-Goldstein;J. Cell Biol.,2001

3. HIP1 functions in clathrin-mediated endocytosis through binding to clathrin and adaptor protein 2;Metzler;J. Biol. Chem.,2001

4. Clathrin- and AP-2-binding sites in HIP1 uncover a general assembly role for endocytic accessory proteins;Mishra;J. Biol. Chem.,2001

5. Huntingtin interacting protein 1 Is a clathrin coat binding protein required for differentiation of late spermatogenic progenitors;Rao;Mol. Cell. Biol.,2001

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