Hertzano R - Search Results

1

Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development.

Fiolka K, Hertzano R, Vassen L, Zeng H, Hermesh O, Avraham KB, Dührsen U, Möröy T. Fiolka K, et al. Among authors: hertzano r. EMBO Rep. 2006 Mar;7(3):326-33. doi: 10.1038/sj.embor.7400618. Epub 2006 Jan 6. EMBO Rep. 2006. PMID: 16397623 Free PMC article.

2

Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene.

Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW, Avraham KB. Hertzano R, et al. Hum Mol Genet. 2004 Sep 15;13(18):2143-53. doi: 10.1093/hmg/ddh218. Epub 2004 Jul 14. Hum Mol Genet. 2004. PMID: 15254021

3

Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity.

Clough RL, Sud R, Davis-Silberman N, Hertzano R, Avraham KB, Holley M, Dawson SJ. Clough RL, et al. Among authors: hertzano r. Biochem Biophys Res Commun. 2004 Nov 5;324(1):372-81. doi: 10.1016/j.bbrc.2004.09.074. Biochem Biophys Res Commun. 2004. PMID: 15465029

4

Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system.

Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. Hertzano R, et al. Eur J Neurosci. 2007 Feb;25(4):999-1005. doi: 10.1111/j.1460-9568.2007.05332.x. Eur J Neurosci. 2007. PMID: 17331196 Free article.

5

A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells.

Hertzano R, Shalit E, Rzadzinska AK, Dror AA, Song L, Ron U, Tan JT, Shitrit AS, Fuchs H, Hasson T, Ben-Tal N, Sweeney HL, de Angelis MH, Steel KP, Avraham KB. Hertzano R, et al. PLoS Genet. 2008 Oct 3;4(10):e1000207. doi: 10.1371/journal.pgen.1000207. PLoS Genet. 2008. PMID: 18833301 Free PMC article.

6

Integration of transcriptomics, proteomics, and microRNA analyses reveals novel microRNA regulation of targets in the mammalian inner ear.

Elkan-Miller T, Ulitsky I, Hertzano R, Rudnicki A, Dror AA, Lenz DR, Elkon R, Irmler M, Beckers J, Shamir R, Avraham KB. Elkan-Miller T, et al. Among authors: hertzano r. PLoS One. 2011 Apr 5;6(4):e18195. doi: 10.1371/journal.pone.0018195. PLoS One. 2011. PMID: 21483685 Free PMC article.

7

The Genomics of Auditory Function and Disease.

Taiber S, Gwilliam K, Hertzano R, Avraham KB. Taiber S, et al. Among authors: hertzano r. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:275-299. doi: 10.1146/annurev-genom-121321-094136. Epub 2022 Jun 6. Annu Rev Genomics Hum Genet. 2022. PMID: 35667089 Free PMC article. Review.

8

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.

Rhodes CR, Hertzano R, Fuchs H, Bell RE, de Angelis MH, Steel KP, Avraham KB. Rhodes CR, et al. Among authors: hertzano r. Mamm Genome. 2004 Sep;15(9):686-97. doi: 10.1007/s00335-004-2344-x. Mamm Genome. 2004. PMID: 15389316

9

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.

Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB. Walsh T, et al. Among authors: hertzano r. Proc Natl Acad Sci U S A. 2002 May 28;99(11):7518-23. doi: 10.1073/pnas.102091699. Proc Natl Acad Sci U S A. 2002. PMID: 12032315 Free PMC article.

10

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss.

Donaudy F, Ferrara A, Esposito L, Hertzano R, Ben-David O, Bell RE, Melchionda S, Zelante L, Avraham KB, Gasparini P. Donaudy F, et al. Among authors: hertzano r. Am J Hum Genet. 2003 Jun;72(6):1571-7. doi: 10.1086/375654. Epub 2003 May 6. Am J Hum Genet. 2003. PMID: 12736868 Free PMC article.

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