Belyantseva IA - Search Results

1

Gamma-actin is required for cytoskeletal maintenance but not development.

Belyantseva IA, Perrin BJ, Sonnemann KJ, Zhu M, Stepanyan R, McGee J, Frolenkov GI, Walsh EJ, Friderici KH, Friedman TB, Ervasti JM. Belyantseva IA, et al. Proc Natl Acad Sci U S A. 2009 Jun 16;106(24):9703-8. doi: 10.1073/pnas.0900221106. Epub 2009 Jun 3. Proc Natl Acad Sci U S A. 2009. PMID: 19497859 Free PMC article.

2

Cochlear outer hair cell electromotility can provide force for both low and high intensity distortion product otoacoustic emissions.

Frolenkov GI, Belyantseva IA, Kurc M, Mastroianni MA, Kachar B. Frolenkov GI, et al. Among authors: belyantseva ia. Hear Res. 1998 Dec;126(1-2):67-74. doi: 10.1016/s0378-5955(98)00150-6. Hear Res. 1998. PMID: 9872135

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

Two distinct Ca(2+)-dependent signaling pathways regulate the motor output of cochlear outer hair cells.

Frolenkov GI, Mammano F, Belyantseva IA, Coling D, Kachar B. Frolenkov GI, et al. Among authors: belyantseva ia. J Neurosci. 2000 Aug 15;20(16):5940-8. doi: 10.1523/JNEUROSCI.20-16-05940.2000. J Neurosci. 2000. PMID: 10934241 Free PMC article.

6

Water permeability of cochlear outer hair cells: characterization and relationship to electromotility.

Belyantseva IA, Frolenkov GI, Wade JB, Mammano F, Kachar B. Belyantseva IA, et al. J Neurosci. 2000 Dec 15;20(24):8996-9003. doi: 10.1523/JNEUROSCI.20-24-08996.2000. J Neurosci. 2000. PMID: 11124975 Free PMC article.

7

Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells.

Belyantseva IA, Adler HJ, Curi R, Frolenkov GI, Kachar B. Belyantseva IA, et al. J Neurosci. 2000 Dec 15;20(24):RC116. doi: 10.1523/JNEUROSCI.20-24-j0002.2000. J Neurosci. 2000. PMID: 11125015 Free PMC article.

8

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.

9

Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice.

Di Palma F, Belyantseva IA, Kim HJ, Vogt TF, Kachar B, Noben-Trauth K. Di Palma F, et al. Among authors: belyantseva ia. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14994-9. doi: 10.1073/pnas.222425399. Epub 2002 Oct 25. Proc Natl Acad Sci U S A. 2002. PMID: 12403827 Free PMC article.

10

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

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