Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 226


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.


MicroRNA gene expression in the mouse inner ear.

Weston MD, Pierce ML, Rocha-Sanchez S, Beisel KW, Soukup GA.

Brain Res. 2006 Sep 21;1111(1):95-104. Epub 2006 Aug 10.


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.


[Epigenetics--a new perspective for the study of deafness].

Xu F, Wang HJ, Ma D.

Yi Chuan. 2012 Mar;34(3):253-9. Review. Chinese.


Deafness genes for nonsyndromic hearing loss and current studies in China.

Xiao Z, Xie D.

Chin Med J (Engl). 2002 Jul;115(7):1078-81. Review.


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.


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.


The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival.

Wallis D, Hamblen M, Zhou Y, Venken KJ, Schumacher A, Grimes HL, Zoghbi HY, Orkin SH, Bellen HJ.

Development. 2003 Jan;130(1):221-32.


Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene.

Li S, Price SM, Cahill H, Ryugo DK, Shen MM, Xiang M.

Development. 2002 Jul;129(14):3523-32.


Connexins in hearing loss: a comprehensive overview.

Sabag AD, Dagan O, Avraham KB.

J Basic Clin Physiol Pharmacol. 2005;16(2-3):101-16. Review.


Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene.

Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW, Avraham KB.

Hum Mol Genet. 2004 Sep 15;13(18):2143-53. Epub 2004 Jul 14.


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.


MicroRNA-183 family members regulate sensorineural fates in the inner ear.

Li H, Kloosterman W, Fekete DM.

J Neurosci. 2010 Mar 3;30(9):3254-63. doi: 10.1523/JNEUROSCI.4948-09.2010.


A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss.

Modamio-Hoybjor S, Mencia A, Goodyear R, del Castillo I, Richardson G, Moreno F, Moreno-Pelayo MA.

Am J Hum Genet. 2007 Jun;80(6):1076-89. Epub 2007 Apr 24.


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.


Gene expression differences in quiescent versus regenerating hair cells of avian sensory epithelia: implications for human hearing and balance disorders.

Hawkins RD, Bashiardes S, Helms CA, Hu L, Saccone NL, Warchol ME, Lovett M.

Hum Mol Genet. 2003 Jun 1;12(11):1261-72.


Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.

Naranjo S, Voesenek K, de la Calle-Mustienes E, Robert-Moreno A, Kokotas H, Grigoriadou M, Economides J, Van Camp G, Hilgert N, Moreno F, Alsina B, Petersen MB, Kremer H, Gómez-Skarmeta JL.

Hum Genet. 2010 Oct;128(4):411-9. doi: 10.1007/s00439-010-0864-x. Epub 2010 Jul 29.


The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear.

Kiernan AE, Xu J, Gridley T.

PLoS Genet. 2006 Jan;2(1):e4. Epub 2006 Jan 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.


Characterisation of DRASIC in the mouse inner ear.

Hildebrand MS, de Silva MG, Klockars T, Rose E, Price M, Smith RJ, McGuirt WT, Christopoulos H, Petit C, Dahl HH.

Hear Res. 2004 Apr;190(1-2):149-60.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk