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Items: 1 to 20 of 89


Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.

Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, Sahel JA, El-Amraoui A, Petit C.

J Cell Biol. 2012 Oct 15;199(2):381-99. doi: 10.1083/jcb.201202012. Epub 2012 Oct 8.


Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells.

Reiners J, Reidel B, El-Amraoui A, Boëda B, Huber I, Petit C, Wolfrum U.

Invest Ophthalmol Vis Sci. 2003 Nov;44(11):5006-15.


Interactions in the network of Usher syndrome type 1 proteins.

Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C.

Hum Mol Genet. 2005 Feb 1;14(3):347-56. Epub 2004 Dec 8.


Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.

Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U.

Exp Eye Res. 2006 Jul;83(1):97-119. Epub 2006 Mar 20. Review.


A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.

Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C.

Development. 2008 Apr;135(8):1427-37. doi: 10.1242/dev.012922. Epub 2008 Mar 13.


The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.

Papal S, Cortese M, Legendre K, Sorusch N, Dragavon J, Sahly I, Shorte S, Wolfrum U, Petit C, El-Amraoui A.

Hum Mol Genet. 2013 Sep 15;22(18):3773-88. doi: 10.1093/hmg/ddt228. Epub 2013 May 23.


Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.

Yan D, Kamiya K, Ouyang XM, Liu XZ.

Int J Exp Pathol. 2011 Feb;92(1):66-71. doi: 10.1111/j.1365-2613.2010.00751.x. Epub 2010 Dec 13.


A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells.

Maerker T, van Wijk E, Overlack N, Kersten FF, McGee J, Goldmann T, Sehn E, Roepman R, Walsh EJ, Kremer H, Wolfrum U.

Hum Mol Genet. 2008 Jan 1;17(1):71-86. Epub 2007 Sep 28.


The retinal phenotype of Usher syndrome: pathophysiological insights from animal models.

El-Amraoui A, Petit C.

C R Biol. 2014 Mar;337(3):167-77. doi: 10.1016/j.crvi.2013.12.004. Epub 2014 Mar 20. Review.


SANS (USH1G) expression in developing and mature mammalian retina.

Overlack N, Maerker T, Latz M, Nagel-Wolfrum K, Wolfrum U.

Vision Res. 2008 Feb;48(3):400-12. Epub 2007 Oct 17.


Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.

Bauß K, Knapp B, Jores P, Roepman R, Kremer H, Wijk EV, Märker T, Wolfrum U.

Hum Mol Genet. 2014 Aug 1;23(15):3923-42. doi: 10.1093/hmg/ddu104. Epub 2014 Mar 8.


Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids.

Bahloul A, Michel V, Hardelin JP, Nouaille S, Hoos S, Houdusse A, England P, Petit C.

Hum Mol Genet. 2010 Sep 15;19(18):3557-65. doi: 10.1093/hmg/ddq271. Epub 2010 Jul 16.


The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins.

Yan J, Pan L, Chen X, Wu L, Zhang M.

Proc Natl Acad Sci U S A. 2010 Mar 2;107(9):4040-5. doi: 10.1073/pnas.0911385107. Epub 2010 Feb 8.


Roles and interactions of usher 1 proteins in the outer retina.

Lillo C, Kitamoto J, Williams DS.

Adv Exp Med Biol. 2006;572:341-8.


Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.

Reiners J, van Wijk E, Märker T, Zimmermann U, Jürgens K, te Brinke H, Overlack N, Roepman R, Knipper M, Kremer H, Wolfrum U.

Hum Mol Genet. 2005 Dec 15;14(24):3933-43. Epub 2005 Nov 21.


Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina.

Overlack N, Kilic D, Bauss K, Märker T, Kremer H, van Wijk E, Wolfrum U.

Biochim Biophys Acta. 2011 Oct;1813(10):1883-92. doi: 10.1016/j.bbamcr.2011.05.015. Epub 2011 Jul 13.


Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D.

Lagziel A, Overlack N, Bernstein SL, Morell RJ, Wolfrum U, Friedman TB.

Mol Vis. 2009 Sep 12;15:1843-57.

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