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Items: 1 to 20 of 123

1.

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
2.

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.

3.

[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.

PMID:
22425943
4.

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.

5.

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.

6.

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.

7.

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.

PMID:
16904081
8.

Insights into inner ear-specific gene regulation: Epigenetics and non-coding RNAs in inner ear development and regeneration.

Doetzlhofer A, Avraham KB.

Semin Cell Dev Biol. 2017 May;65:69-79. doi: 10.1016/j.semcdb.2016.11.002. Epub 2016 Nov 9. Review.

9.

Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness.

Nickel R, Forge A.

Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):452-7. doi: 10.1097/MOO.0b013e32830e20b0. Review.

PMID:
18797288
10.

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.

11.

MicroRNAs: effective elements in ear-related diseases and hearing loss.

Mahmoudian-Sani MR, Mehri-Ghahfarrokhi A, Ahmadinejad F, Hashemzadeh-Chaleshtori M, Saidijam M, Jami MS.

Eur Arch Otorhinolaryngol. 2017 Jun;274(6):2373-2380. doi: 10.1007/s00405-017-4470-6. Epub 2017 Feb 21. Review.

PMID:
28224282
12.

MEKK4 Signaling Regulates Sensory Cell Development and Function in the Mouse Inner Ear.

Haque K, Pandey AK, Zheng HW, Riazuddin S, Sha SH, Puligilla C.

J Neurosci. 2016 Jan 27;36(4):1347-61. doi: 10.1523/JNEUROSCI.1853-15.2016.

13.

Exploring regulatory networks of miR-96 in the developing inner ear.

Lewis MA, Buniello A, Hilton JM, Zhu F, Zhang WI, Evans S, van Dongen S, Enright AJ, Steel KP.

Sci Rep. 2016 Mar 18;6:23363. doi: 10.1038/srep23363.

14.

Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.

Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, Najmabadi H, Friedman TB, Bartles JR, Smith RJ, Kohrman DC.

Am J Hum Genet. 2010 Feb 12;86(2):148-60. doi: 10.1016/j.ajhg.2010.01.016. Epub 2010 Feb 4.

15.

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts.

Tian C, Gagnon LH, Longo-Guess C, Korstanje R, Sheehan SM, Ohlemiller KK, Schrader AD, Lett JM, Johnson KR.

Hum Mol Genet. 2017 Oct 1;26(19):3722-3735. doi: 10.1093/hmg/ddx257.

PMID:
28934385
16.

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.

17.

Progressive Hearing Loss in Mice Carrying a Mutation in Usp53.

Kazmierczak M, Harris SL, Kazmierczak P, Shah P, Starovoytov V, Ohlemiller KK, Schwander M.

J Neurosci. 2015 Nov 25;35(47):15582-98. doi: 10.1523/JNEUROSCI.1965-15.2015.

18.

Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes.

Shu Y, Tao Y, Wang Z, Tang Y, Li H, Dai P, Gao G, Chen ZY.

Hum Gene Ther. 2016 Sep;27(9):687-99. doi: 10.1089/hum.2016.053. Epub 2016 Jun 24.

19.

Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis.

Hertzano R, Elkon R, Kurima K, Morrisson A, Chan SL, Sallin M, Biedlingmaier A, Darling DS, Griffith AJ, Eisenman DJ, Strome SE.

PLoS Genet. 2011 Sep;7(9):e1002309. doi: 10.1371/journal.pgen.1002309. Epub 2011 Sep 29.

20.

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.

Walsh T, Pierce SB, Lenz DR, Brownstein Z, Dagan-Rosenfeld O, Shahin H, Roeb W, McCarthy S, Nord AS, Gordon CR, Ben-Neriah Z, Sebat J, Kanaan M, Lee MK, Frydman M, King MC, Avraham KB.

Am J Hum Genet. 2010 Jul 9;87(1):101-9. doi: 10.1016/j.ajhg.2010.05.011. Epub 2010 Jun 17.

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