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Items: 1 to 20 of 31

1.

Usher syndrome: molecular links of pathogenesis, proteins and pathways.

Kremer H, van Wijk E, Märker T, Wolfrum U, Roepman R.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R262-70. Review.

PMID:
16987892
2.

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.

PMID:
16545802
3.
4.

Usher protein functions in hair cells and photoreceptors.

Cosgrove D, Zallocchi M.

Int J Biochem Cell Biol. 2014 Jan;46:80-9. doi: 10.1016/j.biocel.2013.11.001. Epub 2013 Nov 12. Review.

5.

Update on Usher syndrome.

Saihan Z, Webster AR, Luxon L, Bitner-Glindzicz M.

Curr Opin Neurol. 2009 Feb;22(1):19-27. Review.

PMID:
19165952
6.

Protein networks and complexes in photoreceptor cilia.

Roepman R, Wolfrum U.

Subcell Biochem. 2007;43:209-35. Review.

PMID:
17953396
7.

Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Mathur P, Yang J.

Biochim Biophys Acta. 2015 Mar;1852(3):406-20. doi: 10.1016/j.bbadis.2014.11.020. Epub 2014 Dec 4. Review.

8.

Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches.

Bonnet C, El-Amraoui A.

Curr Opin Neurol. 2012 Feb;25(1):42-9. doi: 10.1097/WCO.0b013e32834ef8b2. Review.

PMID:
22185901
9.

[Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles].

El-Amraoui A, Lefèvre G, Hardelin JP, Petit C.

Med Sci (Paris). 2005 Aug-Sep;21(8-9):737-40. Review. French.

10.

The molecular genetics of Usher syndrome.

Ahmed ZM, Riazuddin S, Riazuddin S, Wilcox ER.

Clin Genet. 2003 Jun;63(6):431-44. Review.

PMID:
12786748
11.

Structures of usher syndrome 1 proteins and their complexes.

Pan L, Zhang M.

Physiology (Bethesda). 2012 Feb;27(1):25-42. doi: 10.1152/physiol.00037.2011. Review.

12.

Composition and function of the Crumbs protein complex in the mammalian retina.

Gosens I, den Hollander AI, Cremers FP, Roepman R.

Exp Eye Res. 2008 May;86(5):713-26. doi: 10.1016/j.exer.2008.02.005. Epub 2008 Feb 26. Review.

PMID:
18407265
13.

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.

PMID:
24702843
14.

Development of the hair bundle and mechanotransduction.

Nayak GD, Ratnayaka HS, Goodyear RJ, Richardson GP.

Int J Dev Biol. 2007;51(6-7):597-608. Review.

15.

Molecular analysis of the supramolecular usher protein complex in the retina. Harmonin as the key protein of the Usher syndrome.

Reiners J, Wolfrum U.

Adv Exp Med Biol. 2006;572:349-53. Review. No abstract available.

PMID:
17249595
16.

Cadherins and mechanotransduction by hair cells.

Müller U.

Curr Opin Cell Biol. 2008 Oct;20(5):557-66. doi: 10.1016/j.ceb.2008.06.004. Epub 2008 Jul 30. Review.

17.

Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy.

Williams DS.

Vision Res. 2008 Feb;48(3):433-41. Epub 2007 Oct 23. Review.

18.

Genetic heterogeneity in Usher syndrome.

Keats BJ, Savas S.

Am J Med Genet A. 2004 Sep 15;130A(1):13-6. Review.

PMID:
15368488
19.

Genetics and pathological mechanisms of Usher syndrome.

Yan D, Liu XZ.

J Hum Genet. 2010 Jun;55(6):327-35. doi: 10.1038/jhg.2010.29. Epub 2010 Apr 9. Review.

20.

[Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models].

Liang LZ, Zheng BJ, Zheng J, Fang F, Wu Y, Guan MX.

Sheng Li Xue Bao. 2012 Aug 25;64(4):481-8. Review. Chinese.

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