HIP1 and HIP1r Stabilize Receptor Tyrosine Kinases and Bind 3-Phosphoinositides via Epsin N-terminal Homology Domains-Reference-Cited by-同舟云学术

HIP1 and HIP1r Stabilize Receptor Tyrosine Kinases and Bind 3-Phosphoinositides via Epsin N-terminal Homology Domains

Published:2004-04 Issue:14 Volume:279 Page:14294-14306
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Hyun Teresa S.,Rao Dinesh S.,Saint-Dic Djenann,Michael L. Evan,Kumar Priti D.,Bradley Sarah V.,Mizukami Ikuko F.,Oravecz-Wilson Katherine I.,Ross Theodora S.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference44 articles.

1. Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)

2. Altered receptor trafficking in Huntingtin Interacting Protein 1-transformed cells

3. Fusion of Huntingtin Interacting Protein 1 to Platelet-Derived Growth Factor β Receptor (PDGFβR) in Chronic Myelomonocytic Leukemia With t(5;7)(q33;q11.2)

4. Huntingtin-interacting protein 1 is overexpressed in prostate and colon cancer and is critical for cellular survival

5. HIP1 and HIP12 Display Differential Binding to F-actin, AP2, and Clathrin

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