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Items: 1 to 20 of 74

1.

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.

2.

MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness.

Friedman LM, Avraham KB.

Mamm Genome. 2009 Sep-Oct;20(9-10):581-603. doi: 10.1007/s00335-009-9230-5. Epub 2009 Oct 30. Review.

PMID:
19876605
3.

Therapeutics of hearing loss: expectations vs reality.

Atar O, Avraham KB.

Drug Discov Today. 2005 Oct 1;10(19):1323-30. Review.

PMID:
16214677
4.

Genetic disorders with both hearing loss and cardiovascular abnormalities.

Belmont JW, Craigen W, Martinez H, Jefferies JL.

Adv Otorhinolaryngol. 2011;70:66-74. doi: 10.1159/000322474. Epub 2011 Feb 24. Review.

PMID:
21358187
5.

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.

Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC.

Hum Mol Genet. 2002 Aug 1;11(16):1887-98.

PMID:
12140191
6.

Hearing impairment in mice with the cmd/cmd (cartilage matrix deficiency) mutant gene.

Yoo TJ, Cho H, Yamada Y.

Ann N Y Acad Sci. 1991;630:265-7.

PMID:
1952601
7.

Human hereditary hearing impairment: mouse models can help to solve the puzzle.

Vrijens K, Van Laer L, Van Camp G.

Hum Genet. 2008 Nov;124(4):325-48. doi: 10.1007/s00439-008-0556-y. Epub 2008 Sep 11. Review.

PMID:
18784944
8.

[Update on physiology and pathophysiology of the inner ear: pathomechanisms of sensorineural hearing loss].

Strenzke N, Pauli-Magnus D, Meyer A, Brandt A, Maier H, Moser T.

HNO. 2008 Jan;56(1):27-36. doi: 10.1007/s00106-007-1640-7. Review. German.

PMID:
18210004
9.

An introduction to the genetics of normal and defective hearing.

Martini A, Mazzoli M, Kimberling W.

Ann N Y Acad Sci. 1997 Dec 29;830:361-74. Review.

PMID:
9616696
12.

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.

Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C.

Nat Genet. 2006 Jul;38(7):770-8. Epub 2006 Jun 25.

PMID:
16804542
13.

MicroRNAs in inner ear biology and pathogenesis.

Patel M, Hu BH.

Hear Res. 2012 May;287(1-2):6-14. doi: 10.1016/j.heares.2012.03.008. Epub 2012 Mar 29. Review.

14.

Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.

Parker LL, Gao J, Zuo J.

Brain Res. 2006 May 26;1091(1):235-42. Epub 2006 Apr 21.

PMID:
16630581
15.

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
16.

The molecular and structural basis of hearing impairment in mice with the cpk mutant gene.

Cho H, Buchanan J, Strong D, Yamada Y, Yoo TJ.

Ann N Y Acad Sci. 1991;630:262-4.

PMID:
1952600
17.

An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss.

Guipponi M, Toh MY, Tan J, Park D, Hanson K, Ballana E, Kwong D, Cannon PZ, Wu Q, Gout A, Delorenzi M, Speed TP, Smith RJ, Dahl HH, Petersen M, Teasdale RD, Estivill X, Park WJ, Scott HS.

Hum Mutat. 2008 Jan;29(1):130-41.

PMID:
17918732
18.

[Genetic type of progressive hearing loss].

Martini A.

Acta Otorhinolaryngol Ital. 1998 Aug;18(4 Suppl 59):21-7. Review. Italian.

PMID:
10205929
19.

Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation.

Pau H, Hawker K, Fuchs H, De Angelis MH, Steel KP.

Otol Neurotol. 2004 Sep;25(5):707-13.

PMID:
15353999
20.

Cochlear molecules and hereditary deafness.

Yan D, Liu XZ.

Front Biosci. 2008 May 1;13:4972-83. Review.

PMID:
18508562

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