Avraham KB - Search Results

1

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

2

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.

Avraham KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Mooseker MS, Copeland NG, Jenkins NA. Avraham KB, et al. Nat Genet. 1995 Dec;11(4):369-75. doi: 10.1038/ng1295-369. Nat Genet. 1995. PMID: 7493015

3

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice.

Avraham KB, Hasson T, Sobe T, Balsara B, Testa JR, Skvorak AB, Morton CC, Copeland NG, Jenkins NA. Avraham KB, et al. Hum Mol Genet. 1997 Aug;6(8):1225-31. doi: 10.1093/hmg/6.8.1225. Hum Mol Genet. 1997. PMID: 9259267

4

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

5

Role of myosin VI in the differentiation of cochlear hair cells.

Self T, Sobe T, Copeland NG, Jenkins NA, Avraham KB, Steel KP. Self T, et al. Among authors: avraham kb. Dev Biol. 1999 Oct 15;214(2):331-41. doi: 10.1006/dbio.1999.9424. Dev Biol. 1999. PMID: 10525338 Free article.

6

The genetics of hearing loss.

Ben-David O, Avraham KB. Ben-David O, et al. Among authors: avraham kb. J Basic Clin Physiol Pharmacol. 1999;10(3):163-71. doi: 10.1515/jbcpp.1999.10.3.163. J Basic Clin Physiol Pharmacol. 1999. PMID: 10529903 Review. No abstract available.

7

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.

8

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

9

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB. Kiernan AE, et al. Among authors: avraham kb. J Neurocytol. 1999 Oct-Nov;28(10-11):969-85. doi: 10.1023/a:1007090626294. J Neurocytol. 1999. PMID: 10900098

10

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

Hrabé de Angelis MH, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, Heffner S, Pargent W, Wuensch K, Jung M, Reis A, Richter T, Alessandrini F, Jakob T, Fuchs E, Kolb H, Kremmer E, Schaeble K, Rollinski B, Roscher A, Peters C, Meitinger T, Strom T, Steckler T, Holsboer F, Klopstock T, Gekeler F, Schindewolf C, Jung T, Avraham K, Behrendt H, Ring J, Zimmer A, Schughart K, Pfeffer K, Wolf E, Balling R. Hrabé de Angelis MH, et al. Nat Genet. 2000 Aug;25(4):444-7. doi: 10.1038/78146. Nat Genet. 2000. PMID: 10932192

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

187 results

Search Page

Filters