Avraham KB - Search Results

1

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. Among authors: avraham kb. 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.

2

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Vahava O, et al. Among authors: avraham kb. Science. 1998 Mar 20;279(5358):1950-4. doi: 10.1126/science.279.5358.1950. Science. 1998. PMID: 9506947

3

Unconventional myosins and the genetics of hearing loss.

Friedman TB, Sellers JR, Avraham KB. Friedman TB, et al. Among authors: avraham kb. 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.

4

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.

Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB. Frydman M, et al. Among authors: avraham kb. Arch Otolaryngol Head Neck Surg. 2000 May;126(5):633-7. doi: 10.1001/archotol.126.5.633. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10807331

5

Auditory and vestibular mouse mutants: models for human deafness.

Ahituv N, Avraham KB. Ahituv N, et al. Among authors: avraham kb. J Basic Clin Physiol Pharmacol. 2000;11(3):181-91. doi: 10.1515/jbcpp.2000.11.3.181. J Basic Clin Physiol Pharmacol. 2000. PMID: 11041382 Review.

6

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Vreugde S, et al. Among authors: avraham kb. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623

7

The clinical presentation of DFNA15/POU4F3.

Gottfried I, Huygen PL, Avraham KB. Gottfried I, et al. Among authors: avraham kb. Adv Otorhinolaryngol. 2002;61:92-7. doi: 10.1159/000066819. Adv Otorhinolaryngol. 2002. PMID: 12408069 No abstract available.

8

A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.

Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. Ben-Yosef T, et al. Among authors: avraham kb. N Engl J Med. 2003 Apr 24;348(17):1664-70. doi: 10.1056/NEJMoa021502. N Engl J Med. 2003. PMID: 12711741 Free article. No abstract available.

9

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: avraham kb. 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.

10

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Karolyi IJ, et al. Among authors: avraham kb. Hum Mol Genet. 2003 Nov 1;12(21):2797-805. doi: 10.1093/hmg/ddg308. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966030

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