Alagramam KN - Search Results

1

A new spontaneous mutation in the mouse protocadherin 15 gene.

Zheng QY, Yu H, Washington JL 3rd, Kisley LB, Kikkawa YS, Pawlowski KS, Wright CG, Alagramam KN. Zheng QY, et al. Among authors: alagramam kn. Hear Res. 2006 Sep;219(1-2):110-20. doi: 10.1016/j.heares.2006.06.010. Epub 2006 Aug 2. Hear Res. 2006. PMID: 16887306 Free PMC article.

2

A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.

Alagramam KN, Kwon HY, Cacheiro NL, Stubbs L, Wright CG, Erway LC, Woychik RP. Alagramam KN, et al. Genetics. 1999 Aug;152(4):1691-9. doi: 10.1093/genetics/152.4.1691. Genetics. 1999. PMID: 10430593 Free PMC article.

3

Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer.

Alagramam KN, Zahorsky-Reeves J, Wright CG, Pawlowski KS, Erway LC, Stubbs L, Woychik RP. Alagramam KN, et al. Hear Res. 2000 Oct;148(1-2):181-91. doi: 10.1016/s0378-5955(00)00152-0. Hear Res. 2000. PMID: 10978835

4

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.

Alagramam KN, Murcia CL, Kwon HY, Pawlowski KS, Wright CG, Woychik RP. Alagramam KN, et al. Nat Genet. 2001 Jan;27(1):99-102. doi: 10.1038/83837. Nat Genet. 2001. PMID: 11138007

5

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

Alagramam KN, Yuan H, Kuehn MH, Murcia CL, Wayne S, Srisailpathy CR, Lowry RB, Knaus R, Van Laer L, Bernier FP, Schwartz S, Lee C, Morton CC, Mullins RF, Ramesh A, Van Camp G, Hageman GS, Woychik RP, Smith RJ. Alagramam KN, et al. Hum Mol Genet. 2001 Aug 1;10(16):1709-18. doi: 10.1093/hmg/10.16.1709. Hum Mol Genet. 2001. PMID: 11487575

6

A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.

Hampton LL, Wright CG, Alagramam KN, Battey JF, Noben-Trauth K. Hampton LL, et al. Among authors: alagramam kn. Hear Res. 2003 Jun;180(1-2):67-75. doi: 10.1016/s0378-5955(03)00107-2. Hear Res. 2003. PMID: 12782354

7

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. Adato A, et al. Among authors: alagramam kn. Hum Mol Genet. 2005 Feb 1;14(3):347-56. doi: 10.1093/hmg/ddi031. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590703

8

Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.

Washington JL 3rd, Pitts D, Wright CG, Erway LC, Davis RR, Alagramam K. Washington JL 3rd, et al. Hear Res. 2005 Apr;202(1-2):161-9. doi: 10.1016/j.heares.2004.09.014. Hear Res. 2005. PMID: 15811708

9

Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.

Alagramam KN, Stahl JS, Jones SM, Pawlowski KS, Wright CG. Alagramam KN, et al. J Assoc Res Otolaryngol. 2005 Jun;6(2):106-18. doi: 10.1007/s10162-004-5032-3. Epub 2005 Jun 10. J Assoc Res Otolaryngol. 2005. PMID: 15952048 Free PMC article.

10

A quantitative survey of gravity receptor function in mutant mouse strains.

Jones SM, Johnson KR, Yu H, Erway LC, Alagramam KN, Pollak N, Jones TA. Jones SM, et al. Among authors: alagramam kn. J Assoc Res Otolaryngol. 2005 Dec;6(4):297-310. doi: 10.1007/s10162-005-0009-4. J Assoc Res Otolaryngol. 2005. PMID: 16235133 Free PMC article.

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