Friedman TB - Search Results

1

The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness.

Jiang F, Takagi Y, Shams A, Heissler SM, Friedman TB, Sellers JR, Bird JE. Jiang F, et al. Among authors: friedman tb. J Biol Chem. 2021 Jan-Jun;296:100243. doi: 10.1074/jbc.RA120.014903. Epub 2021 Jan 9. J Biol Chem. 2021. PMID: 33372036 Free PMC article.

2

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB. Wang A, et al. Among authors: friedman tb. Science. 1998 May 29;280(5368):1447-51. doi: 10.1126/science.280.5368.1447. Science. 1998. PMID: 9603736

3

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, Fridell RA. Liang Y, et al. Among authors: friedman tb. Genomics. 1999 Nov 1;61(3):243-58. doi: 10.1006/geno.1999.5976. Genomics. 1999. PMID: 10552926

4

Unconventional myosins and the genetics of hearing loss.

Friedman TB, Sellers JR, Avraham KB. Friedman TB, et al. Am J Med Genet. 1999 Sep 24;89(3):147-57. doi: 10.1002/(sici)1096-8628(19990924)89:3<147::aid-ajmg5>3.0.co;2-6. Am J Med Genet. 1999. PMID: 10704189 Review.

5

DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.

Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA. Friedman TB, et al. Adv Otorhinolaryngol. 2000;56:131-44. doi: 10.1159/000059094. Adv Otorhinolaryngol. 2000. PMID: 10868225 Review. No abstract available.

6

Human myosin XVBP is a transcribed pseudogene.

Boger ET, Sellers JR, Friedman TB. Boger ET, et al. Among authors: friedman tb. J Muscle Res Cell Motil. 2001;22(5):477-83. doi: 10.1023/a:1014507705858. J Muscle Res Cell Motil. 2001. PMID: 11964073

7

DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation.

Friedman TB, Hinnant JT, Ghosh M, Boger ET, Riazuddin S, Lupski JR, Potocki L, Wilcox ER. Friedman TB, et al. Adv Otorhinolaryngol. 2002;61:124-30. doi: 10.1159/000066824. Adv Otorhinolaryngol. 2002. PMID: 12408074

8

Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.

Belyantseva IA, Boger ET, Naz S, Frolenkov GI, Sellers JR, Ahmed ZM, Griffith AJ, Friedman TB. Belyantseva IA, et al. Among authors: friedman tb. Nat Cell Biol. 2005 Feb;7(2):148-56. doi: 10.1038/ncb1219. Epub 2005 Jan 16. Nat Cell Biol. 2005. PMID: 15654330

9

Deafness and stria vascularis defects in S1P2 receptor-null mice.

Kono M, Belyantseva IA, Skoura A, Frolenkov GI, Starost MF, Dreier JL, Lidington D, Bolz SS, Friedman TB, Hla T, Proia RL. Kono M, et al. Among authors: friedman tb. J Biol Chem. 2007 Apr 6;282(14):10690-6. doi: 10.1074/jbc.M700370200. Epub 2007 Feb 6. J Biol Chem. 2007. PMID: 17284444 Free article.

10

Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.

Riazuddin S, Nazli S, Ahmed ZM, Yang Y, Zulfiqar F, Shaikh RS, Zafar AU, Khan SN, Sabar F, Javid FT, Wilcox ER, Tsilou E, Boger ET, Sellers JR, Belyantseva IA, Riazuddin S, Friedman TB. Riazuddin S, et al. Among authors: friedman tb. Hum Mutat. 2008 Apr;29(4):502-11. doi: 10.1002/humu.20677. Hum Mutat. 2008. PMID: 18181211

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