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Results: 1 to 20 of 133

1.

Ankrd6 is a mammalian functional homolog of drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear.

Jones C, Qian D, Kim SM, Li S, Ren D, Knapp L, Sprinzak D, Avraham KB, Matsuzaki F, Chi F, Chen P.

Dev Biol. 2014 Sep 9. pii: S0012-1606(14)00420-5. doi: 10.1016/j.ydbio.2014.08.029. [Epub ahead of print]

PMID:
25218921
[PubMed - as supplied by publisher]
2.

Israel Society for Auditory Research (ISAR): 2014 Annual Scientific Conference.

Banai K, Avraham KB.

J Basic Clin Physiol Pharmacol. 2014 Sep 1;25(3):267-8. doi: 10.1515/jbcpp-2014-0077. No abstract available.

PMID:
25205708
[PubMed - in process]
3.

Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness.

Sokolov M, Brownstein Z, Frydman M, Avraham KB.

J Basic Clin Physiol Pharmacol. 2014 Sep 1;25(3):289-92. doi: 10.1515/jbcpp-2014-0053.

PMID:
25153233
[PubMed - in process]
4.

Balance deficit enhances anxiety and balance training decreases anxiety in vestibular mutant mice.

Shefer S, Gordon C, Avraham KB, Mintz M.

Behav Brain Res. 2014 Jun 29. pii: S0166-4328(14)00429-X. doi: 10.1016/j.bbr.2014.06.046. [Epub ahead of print]

PMID:
24983660
[PubMed - as supplied by publisher]
5.

Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways.

Rudnicki A, Isakov O, Ushakov K, Shivatzki S, Weiss I, Friedman LM, Shomron N, Avraham KB.

BMC Genomics. 2014 Jun 18;15:484. doi: 10.1186/1471-2164-15-484.

PMID:
24942165
[PubMed - in process]
Free PMC Article
6.

Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness.

Dror AA, Lenz DR, Shivatzki S, Cohen K, Ashur-Fabian O, Avraham KB.

Mamm Genome. 2014 Aug;25(7-8):304-16. doi: 10.1007/s00335-014-9515-1. Epub 2014 Apr 24.

PMID:
24760582
[PubMed - in process]
7.

microRNA-224 regulates Pentraxin 3, a component of the humoral arm of innate immunity, in inner ear inflammation.

Rudnicki A, Shivatzki S, Beyer LA, Takada Y, Raphael Y, Avraham KB.

Hum Mol Genet. 2014 Jun 15;23(12):3138-46. doi: 10.1093/hmg/ddu023. Epub 2014 Jan 26.

PMID:
24470395
[PubMed - in process]
8.

MicroRNAs in sensorineural diseases of the ear.

Ushakov K, Rudnicki A, Avraham KB.

Front Mol Neurosci. 2013 Dec 23;6:52. doi: 10.3389/fnmol.2013.00052. Review.

PMID:
24391537
[PubMed]
Free PMC Article
9.

The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry.

Behar DM, Davidov B, Brownstein Z, Ben-Yosef T, Avraham KB, Shohat M.

Genet Test Mol Biomarkers. 2014 Feb;18(2):123-6. doi: 10.1089/gtmb.2013.0328. Epub 2013 Dec 24.

PMID:
24367894
[PubMed - in process]
10.

Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy.

Takada Y, Beyer LA, Swiderski DL, O'Neal AL, Prieskorn DM, Shivatzki S, Avraham KB, Raphael Y.

Hear Res. 2014 Mar;309:124-35. doi: 10.1016/j.heares.2013.11.009. Epub 2013 Dec 12.

PMID:
24333301
[PubMed - in process]
11.

Rescue from hearing loss in Usher's syndrome.

Avraham KB.

N Engl J Med. 2013 Oct 31;369(18):1758-60. doi: 10.1056/NEJMcibr1311048. No abstract available.

PMID:
24171523
[PubMed - indexed for MEDLINE]
12.

Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing.

Brownstein Z, Abu-Rayyan A, Karfunkel-Doron D, Sirigu S, Davidov B, Shohat M, Frydman M, Houdusse A, Kanaan M, Avraham KB.

Eur J Hum Genet. 2014 Jun;22(6):768-75. doi: 10.1038/ejhg.2013.232. Epub 2013 Oct 9.

PMID:
24105371
[PubMed - in process]
13.

Advances in genetic diagnostics for hereditary hearing loss.

Idan N, Brownstein Z, Shivatzki S, Avraham KB.

J Basic Clin Physiol Pharmacol. 2013;24(3):165-70. doi: 10.1515/jbcpp-2013-0063. Review.

PMID:
24006325
[PubMed - indexed for MEDLINE]
14.

A "Tric" to tighten cell-cell junctions in the cochlea for hearing.

Higashi T, Lenz DR, Furuse M, Avraham KB.

J Clin Invest. 2013 Sep 3;123(9):3712-5. doi: 10.1172/JCI69651. Epub 2013 Aug 27.

PMID:
23979155
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Israel Society for Auditory Research (ISAR): 2013 Annual Scientific Conference.

Avraham KB.

J Basic Clin Physiol Pharmacol. 2013;24(3):163-4. doi: 10.1515/jbcpp-2013-0108. No abstract available.

PMID:
23959661
[PubMed - indexed for MEDLINE]
16.

Time-dependent gene expression analysis of the developing superior olivary complex.

Ehmann H, Hartwich H, Salzig C, Hartmann N, Clément-Ziza M, Ushakov K, Avraham KB, Bininda-Emonds OR, Hartmann AK, Lang P, Friauf E, Nothwang HG.

J Biol Chem. 2013 Sep 6;288(36):25865-79. doi: 10.1074/jbc.M113.490508. Epub 2013 Jul 26.

PMID:
23893414
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.

Parzefall T, Shivatzki S, Lenz DR, Rathkolb B, Ushakov K, Karfunkel D, Shapira Y, Wolf M, Mohr M, Wolf E, Sabrautzki S, de Angelis MH, Frydman M, Brownstein Z, Avraham KB.

Hum Mutat. 2013 Aug;34(8):1102-10. doi: 10.1002/humu.22339. Epub 2013 May 8.

PMID:
23606368
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

The LINC complex is essential for hearing.

Horn HF, Brownstein Z, Lenz DR, Shivatzki S, Dror AA, Dagan-Rosenfeld O, Friedman LM, Roux KJ, Kozlov S, Jeang KT, Frydman M, Burke B, Stewart CL, Avraham KB.

J Clin Invest. 2013 Feb 1;123(2):740-50. doi: 10.1172/JCI66911. Epub 2013 Jan 25.

PMID:
23348741
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Egr2::cre mediated conditional ablation of dicer disrupts histogenesis of mammalian central auditory nuclei.

Rosengauer E, Hartwich H, Hartmann AM, Rudnicki A, Satheesh SV, Avraham KB, Nothwang HG.

PLoS One. 2012;7(11):e49503. doi: 10.1371/journal.pone.0049503. Epub 2012 Nov 12.

PMID:
23152916
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Genomic advances for gene discovery in hereditary hearing loss.

Avraham KB, Kanaan M.

J Basic Clin Physiol Pharmacol. 2012 Sep 7;23(3):93-7. doi: 10.1515/jbcpp-2012-0033. Review.

PMID:
22962211
[PubMed - indexed for MEDLINE]

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