Mburu P - Search Results

1

The actin-binding proteins eps8 and gelsolin have complementary roles in regulating the growth and stability of mechanosensory hair bundles of mammalian cochlear outer hair cells.

Olt J, Mburu P, Johnson SL, Parker A, Kuhn S, Bowl M, Marcotti W, Brown SD. Olt J, et al. Among authors: mburu p. PLoS One. 2014 Jan 27;9(1):e87331. doi: 10.1371/journal.pone.0087331. eCollection 2014. PLoS One. 2014. PMID: 24475274 Free PMC article.

2

Unravelling the genetics of deafness.

Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD. Steel KP, et al. Among authors: mburu p. Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Ann Otol Rhinol Laryngol Suppl. 1997. PMID: 9153119 Review.

3

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.

Liu XZ, Walsh J, Mburu P, Kendrick-Jones J, Cope MJ, Steel KP, Brown SD. Liu XZ, et al. Among authors: mburu p. Nat Genet. 1997 Jun;16(2):188-90. doi: 10.1038/ng0697-188. Nat Genet. 1997. PMID: 9171832

4

Mutation analysis of the mouse myosin VIIA deafness gene.

Mburu P, Liu XZ, Walsh J, Saw D Jr, Cope MJ, Gibson F, Kendrick-Jones J, Steel KP, Brown SD. Mburu P, et al. Genes Funct. 1997 Jun;1(3):191-203. doi: 10.1046/j.1365-4624.1997.00020.x. Genes Funct. 1997. PMID: 9680294

5

ENU mutagenesis and the search for deafness genes.

Hardisty RE, Mburu P, Brown SD. Hardisty RE, et al. Among authors: mburu p. Br J Audiol. 1999 Oct;33(5):279-83. doi: 10.3109/03005369909090110. Br J Audiol. 1999. PMID: 10890141

6

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP. Tsai H, et al. Among authors: mburu p. Hum Mol Genet. 2001 Mar 1;10(5):507-12. doi: 10.1093/hmg/10.5.507. Hum Mol Genet. 2001. PMID: 11181574

7

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, Rump A, Hardisty RE, Blanchard S, Coimbra RS, Perfettini I, Parkinson N, Mallon AM, Glenister P, Rogers MJ, Paige AJ, Moir L, Clay J, Rosenthal A, Liu XZ, Blanco G, Steel KP, Petit C, Brown SD. Mburu P, et al. Nat Genet. 2003 Aug;34(4):421-8. doi: 10.1038/ng1208. Nat Genet. 2003. PMID: 12833159

8

Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.

Kikkawa Y, Mburu P, Morse S, Kominami R, Townsend S, Brown SD. Kikkawa Y, et al. Among authors: mburu p. Hum Mol Genet. 2005 Feb 1;14(3):391-400. doi: 10.1093/hmg/ddi035. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590699

9

Whirlin complexes with p55 at the stereocilia tip during hair cell development.

Mburu P, Kikkawa Y, Townsend S, Romero R, Yonekawa H, Brown SD. Mburu P, et al. Proc Natl Acad Sci U S A. 2006 Jul 18;103(29):10973-8. doi: 10.1073/pnas.0600923103. Epub 2006 Jul 7. Proc Natl Acad Sci U S A. 2006. PMID: 16829577 Free PMC article.

10

Quiet as a mouse: dissecting the molecular and genetic basis of hearing.

Brown SD, Hardisty-Hughes RE, Mburu P. Brown SD, et al. Among authors: mburu p. Nat Rev Genet. 2008 Apr;9(4):277-90. doi: 10.1038/nrg2309. Epub 2008 Feb 19. Nat Rev Genet. 2008. PMID: 18283275 Review.

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