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Links from PubMed

Items: 7

1.

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

Bradley SV, Hyun TS, Oravecz-Wilson KI, Li L, Waldorff EI, Ermilov AN, Goldstein SA, Zhang CX, Drubin DG, Varela K, Parlow A, Dlugosz AA, Ross TS.

Hum Mol Genet. 2007 Jun 1;16(11):1279-92. Epub 2007 Apr 23.

2.

The Sla2p/HIP1/HIP1R family: similar structure, similar function in endocytosis?

Gottfried I, Ehrlich M, Ashery U.

Biochem Soc Trans. 2010 Feb;38(Pt 1):187-91. doi: 10.1042/BST0380187. Review.

PMID:
20074057
3.

HIP1: trafficking roles and regulation of tumorigenesis.

Hyun TS, Ross TS.

Trends Mol Med. 2004 Apr;10(4):194-9. Review.

PMID:
15059611
4.

The multiple roles of CUX1: insights from mouse models and cell-based assays.

Sansregret L, Nepveu A.

Gene. 2008 Apr 15;412(1-2):84-94. doi: 10.1016/j.gene.2008.01.017. Epub 2008 Feb 2. Review.

PMID:
18313863
5.

Animal models for genetic neuromuscular diseases.

Vainzof M, Ayub-Guerrieri D, Onofre PC, Martins PC, Lopes VF, Zilberztajn D, Maia LS, Sell K, Yamamoto LU.

J Mol Neurosci. 2008 Mar;34(3):241-8. doi: 10.1007/s12031-007-9023-9. Epub 2008 Jan 18. Review.

PMID:
18202836
7.

Phenotype of the taurine transporter knockout mouse.

Warskulat U, Heller-Stilb B, Oermann E, Zilles K, Haas H, Lang F, Häussinger D.

Methods Enzymol. 2007;428:439-58. Review.

PMID:
17875433
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