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Select item 32453651.

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13

Muhammad Ansar, Kwanghyuk Lee, Syed Kamran-ul-Hassan Naqvi, Paula B. Andrade, Sulman Basit, Regie Lyn P. Santos-Cortez, Wasim Ahmad, Suzanne M. Leal

J Hum Genet. Author manuscript; available in PMC 2012 Jun 1.

Published in final edited form as: J Hum Genet. 2011 Dec; 56(12): 866–868. Published online 2011 Sep 22. doi: 10.1038/jhg.2011.110

PMCID:: PMC3245365

Abstract Article PDF–569K

Select item 17358552.

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

S Naz, A Griffith, S Riazuddin, L Hampton, J Battey, S Khan, S Riazuddin, E Wilcox, T Friedman

J Med Genet. 2004 Aug; 41(8): 591–595. doi: 10.1136/jmg.2004.018523

PMCID:: PMC1735855

Summary PDF–662K

Select item 34096963.

Unique Transgenic Animal Model for Hereditary Hearing Loss

Maura Cosetti, David Culang, Sumankrishna Kotla, Peter O’Brien, Daniel F. Eberl, Frances Hannan

Ann Otol Rhinol Laryngol. Author manuscript; available in PMC 2012 Aug 1.

Published in final edited form as: Ann Otol Rhinol Laryngol. 2008 Nov; 117(11): 827–833. doi: 10.1177/000348940811701106

PMCID:: PMC3409696

Abstract Article PDF–722K

Select item 34775104.

Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice

Elizabeth A. Hurd, Joseph A. Micucci, Elyse N. Reamer, Donna M. Martin

Mech Dev. Author manuscript; available in PMC 2013 Sep 1.

Published in final edited form as: Mech Dev. 2012 Sep; 129(9-12): 308–323. Published online 2012 Jun 15. doi: 10.1016/j.mod.2012.06.002

Correction in:: Cells Dev. 2022 Apr 19; 170: 203779.

PMCID:: PMC3477510

Abstract Article PDF–5.2M

Select item 38785085.

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

Feng Xin, Yongyi Yuan, Xiaoming Deng, Mingyu Han, Guojian Wang, Jiandong Zhao, Xue Gao, Jun Liu, Fei Yu, Dongyi Han, Pu Dai

J Transl Med. 2013; 11: 312. Published online 2013 Dec 17. doi: 10.1186/1479-5876-11-312

PMCID:: PMC3878508

Abstract Article PDF–218K

Select item 38738806.

The role of Six1 in mammalian auditory system development

Weiming Zheng, Li Huang, Zhu-Bo Wei, Derek Silvius, Bihui Tang, Pin-Xian Xu

Development. Author manuscript; available in PMC 2013 Dec 27.

Published in final edited form as: Development. 2003 Sep; 130(17): 3989–4000. doi: 10.1242/dev.00628

PMCID:: PMC3873880

Abstract Article PDF–8.1M

Select item 38654977.

Progression of Neurogenesis in the Inner Ear Requires Inhibition of Sox2 Transcription by Neurogenin1 and Neurod1

Lale Evsen, Satoko Sugahara, Masanori Uchikawa, Hisato Kondoh, Doris K. Wu

J Neurosci. 2013 Feb 27; 33(9): 3879–3890. doi: 10.1523/JNEUROSCI.4030-12.2013

PMCID:: PMC3865497

Abstract Article PDF–5.7M

Select item 38353698.

SLC26A4 Variations Among Graves’ Hyper-Functioning Thyroid Gland

Hassen Hadj-Kacem, Rihab Kallel, Salima Belguith-Maalej, Mouna Mnif, Ilhem Charfeddine, Abdelmounem Ghorbel, Mohamed Abid, Hammadi Ayadi, Saber Masmoudi

Dis Markers. 2010; 29(2): 63–69. Published online 2010 Nov 2. doi: 10.3233/DMA-2010-0727

PMCID:: PMC3835369

Summary PDF–1.5M

Select item 38250389.

The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population

S. IOSSA, V. CORVINO, P. GIANNINI, R. SALVATO, M. CAVALIERE, M. PANETTI, G. PANETTI, B. PIANTEDOSI, E. MARCIANO, A. FRANZÈ

Acta Otorhinolaryngol Ital. 2013 Oct; 33(5): 320–323.

PMCID:: PMC3825038

Abstract Article PDF–304K

Select item 380586410.

Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders

Sampathkumar Rangasamy, Santosh R. D’Mello, Vinodh Narayanan

Neurotherapeutics. 2013 Oct; 10(4): 742–756. Published online 2013 Oct 9. doi: 10.1007/s13311-013-0227-0

PMCID:: PMC3805864

Abstract Article PDF–590K

Select item 376485711.

Postsynaptic mechanisms underlying the excitatory action of histamine on medial vestibular nucleus neurons in rats

Xiao-Yang Zhang, Lei Yu, Qian-Xing Zhuang, Shi-Yu Peng, Jing-Ning Zhu, Jian-Jun Wang

Br J Pharmacol. 2013 Sep; 170(1): 156–169. Published online 2013 Aug 15. doi: 10.1111/bph.12256

PMCID:: PMC3764857

Abstract Article PDF–2.7M

Select item 375326812.

Deletion of Sema3a or plexinA1/plexinA3 Causes Defects in Sensory Afferent Projections of Statoacoustic Ganglion Neurons

Kei-ichi Katayama, Fumiyasu Imai, Fumikazu Suto, Yutaka Yoshida

PLoS One. 2013; 8(8): e72512. Published online 2013 Aug 26. doi: 10.1371/journal.pone.0072512

PMCID:: PMC3753268

Abstract Article PDF–11M

Select item 370919113.

Identification of Allelic Variants of Pendrin (SLC26A4) with Loss and Gain of Function

Silvia Dossena, Aigerim Bizhanova, Charity Nofziger, Emanuele Bernardinelli, Josef Ramsauer, Peter Kopp, Markus Paulmichl

Cell Physiol Biochem. 2011 Nov; 28(3): 467–476. doi: 10.1159/000335108

PMCID:: PMC3709191

Abstract Article PDF–481K

Select item 367916314.

Global Profiling in Vestibular Schwannomas Shows Critical Deregulation of MicroRNAs and Upregulation in Those Included in Chromosomal Region 14q32

Miguel Torres-Martin, Luis Lassaletta, Jose M. de Campos, Alberto Isla, Javier Gavilan, Giovanny R. Pinto, Rommel R. Burbano, Farida Latif, Barbara Melendez, Javier S. Castresana, Juan A. Rey

PLoS One. 2013; 8(6): e65868. Published online 2013 Jun 11. doi: 10.1371/journal.pone.0065868

PMCID:: PMC3679163

Abstract Article PDF–865K

Select item 361653815.

siRNA Targeting Hes5 Augments Hair Cell Regeneration in Aminoglycoside-damaged Mouse Utricle

Jae Yun Jung, Matt R. Avenarius, Swetlana Adamsky, Evgenia Alpert, Elena Feinstein, Yehoash Raphael

Mol Ther. 2013 Apr; 21(4): 834–841. Published online 2013 Feb 26. doi: 10.1038/mt.2013.18

PMCID:: PMC3616538

Abstract Article PDF–1.0M

Select item 359745216.

Microarray analysis of gene expression in vestibular schwannomas reveals SPP1/MET signaling pathway and androgen receptor deregulation

MIGUEL TORRES-MARTIN, LUIS LASSALETTA, JESUS SAN-ROMAN-MONTERO, JOSE M. DE CAMPOS, ALBERTO ISLA, JAVIER GAVILAN, BARBARA MELENDEZ, GIOVANNY R. PINTO, ROMMEL R. BURBANO, JAVIER S. CASTRESANA, JUAN A. REY

Int J Oncol. 2013 Mar; 42(3): 848–862. Published online 2013 Jan 24. doi: 10.3892/ijo.2013.1798

PMCID:: PMC3597452

Abstract Article PDF–667K

Select item 387921217.

The Candidate Splicing Factor Sfswap Regulates Growth and Patterning of Inner Ear Sensory Organs

Yalda Moayedi, Martin L. Basch, Natasha L. Pacheco, Simon S. Gao, Rosalie Wang, Wilbur Harrison, Ningna Xiao, John S. Oghalai, Paul A. Overbeek, Graeme Mardon, Andrew K. Groves

PLoS Genet. 2014 Jan; 10(1): e1004055. Published online 2014 Jan 2. doi: 10.1371/journal.pgen.1004055

PMCID:: PMC3879212

Abstract Article PDF–11M

Select item 345798318.

Glutamate Transporters EAAT4 and EAAT5 Are Expressed in Vestibular Hair Cells and Calyx Endings

Antoine Dalet, Jérémie Bonsacquet, Sophie Gaboyard-Niay, Irina Calin-Jageman, Robstein L. Chidavaenzi, Stephanie Venteo, Gilles Desmadryl, Jay M. Goldberg, Anna Lysakowski, Christian Chabbert

PLoS One. 2012; 7(9): e46261. Published online 2012 Sep 25. doi: 10.1371/journal.pone.0046261

PMCID:: PMC3457983

Abstract Article PDF–1.9M

Select item 337673719.

TRPC3 and TRPC6 are essential for normal mechanotransduction in subsets of sensory neurons and cochlear hair cells

Kathryn Quick, Jing Zhao, Niels Eijkelkamp, John E. Linley, Francois Rugiero, James J. Cox, Ramin Raouf, Martine Gringhuis, Jane E. Sexton, Joel Abramowitz, Ruth Taylor, Andy Forge, Jonathan Ashmore, Nerissa Kirkwood, Corné J. Kros, Guy P. Richardson, Marc Freichel, Veit Flockerzi, Lutz Birnbaumer, John N. Wood

Open Biol. 2012 May; 2(5): 120068. doi: 10.1098/rsob.120068

PMCID:: PMC3376737

Abstract Article PDF–1.4M

Select item 337608620.

2E4/Kaptin (KPTN) – a candidate gene for the hearing loss locus, DFNA4

E. L. BEARER, A. F. CHEN, A. H. CHEN, Z. LI, H.-F. MARK, R. J. H. SMITH, C. L. JACKSON

Ann Hum Genet. Author manuscript; available in PMC 2012 Jun 15.

Published in final edited form as: Ann Hum Genet. 2000 May; 64(Pt 3): 189–196. doi: 10.1046/j.1469-1809.2000.6430189.x

PMCID:: PMC3376086

Abstract Article PDF–825K

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