Friedman TB - Search Results

1

ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points.

Krey JF, Liu C, Belyantseva IA, Bateschell M, Dumont RA, Goldsmith J, Chatterjee P, Morrill RS, Fedorov LM, Foster S, Kim J, Nuttall AL, Jones SM, Choi D, Friedman TB, Ricci AJ, Zhao B, Barr-Gillespie PG. Krey JF, et al. Among authors: friedman tb. J Cell Biol. 2022 Apr 4;221(4):e202109134. doi: 10.1083/jcb.202109134. Epub 2022 Feb 17. J Cell Biol. 2022. PMID: 35175278 Free PMC article.

2

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

3

The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells.

Anderson DW, Probst FJ, Belyantseva IA, Fridell RA, Beyer L, Martin DM, Wu D, Kachar B, Friedman TB, Raphael Y, Camper SA. Anderson DW, et al. Among authors: friedman tb. Hum Mol Genet. 2000 Jul 22;9(12):1729-38. doi: 10.1093/hmg/9.12.1729. Hum Mol Genet. 2000. PMID: 10915760

4

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

Wilcox ER, Burton QL, Naz S, Riazuddin S, Smith TN, Ploplis B, Belyantseva I, Ben-Yosef T, Liburd NA, Morell RJ, Kachar B, Wu DK, Griffith AJ, Riazuddin S, Friedman TB. Wilcox ER, et al. Among authors: friedman tb. Cell. 2001 Jan 12;104(1):165-72. doi: 10.1016/s0092-8674(01)00200-8. Cell. 2001. PMID: 11163249 Free article.

5

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB. Ben-Yosef T, et al. Among authors: friedman tb. Hum Mol Genet. 2003 Aug 15;12(16):2049-61. doi: 10.1093/hmg/ddg210. Hum Mol Genet. 2003. PMID: 12913076

6

Recent advances in the understanding of syndromic forms of hearing loss.

Friedman TB, Schultz JM, Ben-Yosef T, Pryor SP, Lagziel A, Fisher RA, Wilcox ER, Riazuddin S, Ahmed ZM, Belyantseva IA, Griffith AJ. Friedman TB, et al. Ear Hear. 2003 Aug;24(4):289-302. doi: 10.1097/01.AUD.0000079804.00047.CE. Ear Hear. 2003. PMID: 12923420 Review. No abstract available.

7

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.

Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabar MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER. Ahmed ZM, et al. Among authors: friedman tb. Hum Mol Genet. 2003 Dec 15;12(24):3215-23. doi: 10.1093/hmg/ddg358. Epub 2003 Oct 21. Hum Mol Genet. 2003. PMID: 14570705

8

Stereocilia: the long and the short of it.

Belyantseva IA, Labay V, Boger ET, Griffith AJ, Friedman TB. Belyantseva IA, et al. Among authors: friedman tb. Trends Mol Med. 2003 Nov;9(11):458-61. doi: 10.1016/j.molmed.2003.09.008. Trends Mol Med. 2003. PMID: 14604820

9

Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle.

Belyantseva IA, Boger ET, Friedman TB. Belyantseva IA, et al. Among authors: friedman tb. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):13958-63. doi: 10.1073/pnas.2334417100. Epub 2003 Nov 10. Proc Natl Acad Sci U S A. 2003. PMID: 14610277 Free PMC article.

10

Genetic insights into the morphogenesis of inner ear hair cells.

Frolenkov GI, Belyantseva IA, Friedman TB, Griffith AJ. Frolenkov GI, et al. Among authors: friedman tb. Nat Rev Genet. 2004 Jul;5(7):489-98. doi: 10.1038/nrg1377. Nat Rev Genet. 2004. PMID: 15211351 Review. No abstract available.

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