Belyantseva IA - Search Results

1

Pathophysiology of human hearing loss associated with variants in myosins.

Miyoshi T, Belyantseva IA, Sajeevadathan M, Friedman TB. Miyoshi T, et al. Among authors: belyantseva ia. Front Physiol. 2024 Mar 18;15:1374901. doi: 10.3389/fphys.2024.1374901. eCollection 2024. Front Physiol. 2024. PMID: 38562617 Free PMC article. Review.

2

Tricellulin deficiency affects tight junction architecture and cochlear hair cells.

Nayak G, Lee SI, Yousaf R, Edelmann SE, Trincot C, Van Itallie CM, Sinha GP, Rafeeq M, Jones SM, Belyantseva IA, Anderson JM, Forge A, Frolenkov GI, Riazuddin S. Nayak G, et al. Among authors: belyantseva ia. J Clin Invest. 2013 Sep;123(9):4036-49. doi: 10.1172/JCI69031. Epub 2013 Aug 27. J Clin Invest. 2013. PMID: 23979167 Free PMC article.

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: belyantseva ia. Genomics. 1999 Nov 1;61(3):243-58. doi: 10.1006/geno.1999.5976. Genomics. 1999. PMID: 10552926

4

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: belyantseva ia. Hum Mol Genet. 2000 Jul 22;9(12):1729-38. doi: 10.1093/hmg/9.12.1729. Hum Mol Genet. 2000. PMID: 10915760

5

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. Cell. 2001 Jan 12;104(1):165-72. doi: 10.1016/s0092-8674(01)00200-8. Cell. 2001. PMID: 11163249 Free article.

6

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: belyantseva ia. Hum Mol Genet. 2003 Aug 15;12(16):2049-61. doi: 10.1093/hmg/ddg210. Hum Mol Genet. 2003. PMID: 12913076

7

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. Among authors: belyantseva ia. 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.

8

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: belyantseva ia. 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

9

Stereocilia: the long and the short of it.

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

10

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. 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.

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