Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 18

1.

Trans-implant treatment of chronic recurrent maxillary sinusitis via dynamic implants with an internal port: Experience with 31 cases.

Nahlieli O, Dar RA, Dror AA, Abba M, Sela E, Srouji S.

Int J Oral Maxillofac Surg. 2020 Feb 13. pii: S0901-5027(20)30047-3. doi: 10.1016/j.ijom.2020.01.025. [Epub ahead of print]

PMID:
32061430
2.

A mouse model for benign paroxysmal positional vertigo with genetic predisposition for displaced otoconia.

Dror AA, Taiber S, Sela E, Handzel O, Avraham KB.

Genes Brain Behav. 2020 Jan 2:e12635. doi: 10.1111/gbb.12635. [Epub ahead of print]

PMID:
31898392
3.

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.

4.

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;123(2):740-50. doi: 10.1172/JCI66911. Epub 2013 Jan 25.

5.

Integration of human and mouse genetics reveals pendrin function in hearing and deafness.

Dror AA, Brownstein Z, Avraham KB.

Cell Physiol Biochem. 2011;28(3):535-44. doi: 10.1159/000335163. Epub 2011 Nov 18. Review.

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.

PLoS One. 2011 Apr 5;6(4):e18195. doi: 10.1371/journal.pone.0018195.

7.

Hearing loss: a common disorder caused by many rare alleles.

Raviv D, Dror AA, Avraham KB.

Ann N Y Acad Sci. 2010 Dec;1214:168-79. doi: 10.1111/j.1749-6632.2010.05868.x. Review.

8.

A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA.

Walsh VL, Raviv D, Dror AA, Shahin H, Walsh T, Kanaan MN, Avraham KB, King MC.

Mamm Genome. 2011 Apr;22(3-4):170-7. doi: 10.1007/s00335-010-9310-6. Epub 2010 Dec 17.

PMID:
21165622
9.

Hearing impairment: a panoply of genes and functions.

Dror AA, Avraham KB.

Neuron. 2010 Oct 21;68(2):293-308. doi: 10.1016/j.neuron.2010.10.011. Review.

10.

Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutation.

Dror AA, Politi Y, Shahin H, Lenz DR, Dossena S, Nofziger C, Fuchs H, Hrabé de Angelis M, Paulmichl M, Weiner S, Avraham KB.

J Biol Chem. 2010 Jul 9;285(28):21724-35. doi: 10.1074/jbc.M110.120188. Epub 2010 May 4.

11.

Hearing loss: mechanisms revealed by genetics and cell biology.

Dror AA, Avraham KB.

Annu Rev Genet. 2009;43:411-37. doi: 10.1146/annurev-genet-102108-134135. Review.

PMID:
19694516
12.

CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development.

Geller SF, Guerin KI, Visel M, Pham A, Lee ES, Dror AA, Avraham KB, Hayashi T, Ray CA, Reh TA, Bermingham-McDonogh O, Triffo WJ, Bao S, Isosomppi J, Västinsalo H, Sankila EM, Flannery JG.

PLoS Genet. 2009 Aug;5(8):e1000607. doi: 10.1371/journal.pgen.1000607. Epub 2009 Aug 14.

13.

Mice with vestibular deficiency display hyperactivity, disorientation, and signs of anxiety.

Avni R, Elkan T, Dror AA, Shefer S, Eilam D, Avraham KB, Mintz M.

Behav Brain Res. 2009 Sep 14;202(2):210-7. doi: 10.1016/j.bbr.2009.03.033. Epub 2009 Apr 1.

PMID:
19463703
14.

MicroRNAs are essential for development and function of inner ear hair cells in vertebrates.

Friedman LM, Dror AA, Mor E, Tenne T, Toren G, Satoh T, Biesemeier DJ, Shomron N, Fekete DM, Hornstein E, Avraham KB.

Proc Natl Acad Sci U S A. 2009 May 12;106(19):7915-20. doi: 10.1073/pnas.0812446106. Epub 2009 Apr 28.

15.

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.

PLoS Genet. 2008 Oct 3;4(10):e1000207. doi: 10.1371/journal.pgen.1000207.

16.

A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum.

Brownstein ZN, Dror AA, Gilony D, Migirov L, Hirschberg K, Avraham KB.

Arch Otolaryngol Head Neck Surg. 2008 Apr;134(4):403-7. doi: 10.1001/archotol.134.4.403.

PMID:
18427006
17.

Mouse models to study inner ear development and hereditary hearing loss.

Friedman LM, Dror AA, Avraham KB.

Int J Dev Biol. 2007;51(6-7):609-31. Review.

18.

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.

Eur J Neurosci. 2007 Feb;25(4):999-1005.

Supplemental Content

Support Center