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Items: 1 to 20 of 40

1.
A Noncoding Point Mutation of Zeb1 Causes Multiple Developmental Malformations and Obesity in Twirler Mice
Kiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, Kelly Monahan, Karl B. Shpargel, Garani Nadaraja, Yoshiyuki Kawashima, Kyu Yup Lee, Taku Ito, Yujiro Higashi, David J. Eisenman, Scott E. Strome, Andrew J. Griffith
PLoS Genet. 2011 Sep; 7(9): e1002307. Published online 2011 Sep 29. doi: 10.1371/journal.pgen.1002307
PMCID:
PMC3183090
AbstractArticlePDF–2.7M
2.
Auditory and vestibular phenotypes associated with GATA3 mutation
Wade Chien, Jennifer W. Leiding, Amy P. Hsu, Chris Zalewski, Kelly King, Steven M. Holland, Carmen Brewer
Otol Neurotol. Author manuscript; available in PMC 2015 Apr 1.
Published in final edited form as: Otol Neurotol. 2014 Apr; 35(4): 577–581. doi: 10.1097/MAO.0000000000000238
PMCID:
PMC4108448
AbstractArticlePDF–263K
3.
Hearing characteristics and otoradiological abnormalities in three patients with novel pathogenic variants of KMT2D‐related Kabuki syndrome
Zhoushu Zheng, Lu Ding, Meihong Wang, Yinghui Zhang, Yihui Yang, Ming Tang, Jun Xu, Liangjiong Wang, Junhua Wu, Haibo Li
Mol Genet Genomic Med. 2024 Jan; 12(1): e2306. Published online 2023 Nov 3. doi: 10.1002/mgg3.2306
PMCID:
PMC10767598
AbstractArticlePDF–1.3M
4.
Gene miles-apart is required for formation of otic vesicle and hair cells in zebrafish
Z-y Hu, Q-y Zhang, W Qin, J-w Tong, Q Zhao, Y Han, J Meng, J-p Zhang
Cell Death Dis. 2013 Oct; 4(10): e900. Published online 2013 Oct 31. doi: 10.1038/cddis.2013.432
PMCID:
PMC3920936
AbstractArticlePDF–2.6M
5.
Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects
Georg Steffes, Beatriz Lorente-Cánovas, Selina Pearson, Rachael H. Brooker, Sarah Spiden, Amy E. Kiernan, Jean-Louis Guénet, Karen P. Steel
PLoS One. 2012; 7(11): e51065. Published online 2012 Nov 30. doi: 10.1371/journal.pone.0051065
PMCID:
PMC3511360
AbstractArticlePDF–8.9M
6.
Mutation analysis of Netrin 1 and HMX3 genes in patients with superior semicircular canal dehiscence syndrome
Nikola Roknic, Alexander Huber, Stefan C. A. Hegemann, Rudolf Häusler, Nicolas Gürtler
Acta Otolaryngol. 2012 Oct; 132(10): 1061–1065. Published online 2012 Jul 10. doi: 10.3109/00016489.2012.681797
PMCID:
PMC3477893
AbstractArticlePDF–167K
7.
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
AbstractArticlePDF–5.2M
8.
Head Bobber: An Insertional Mutation Causes Inner Ear Defects, Hyperactive Circling, and Deafness
Giuseppina Somma, Heather M. Alger, Ryan M. McGuire, Jim D. Kretlow, Fernanda R. Ruiz, Svetlana A. Yatsenko, Pawel Stankiewicz, Wilbur Harrison, Etai Funk, Antonio Bergamaschi, John S. Oghalai, Antonios G. Mikos, Paul A. Overbeek, Fred A. Pereira
J Assoc Res Otolaryngol. 2012 Jun; 13(3): 335–349. Published online 2012 Mar 2. doi: 10.1007/s10162-012-0316-5
PMCID:
PMC3346896
AbstractArticlePDF–1.0M
9.
Mutation of Rubie, a Novel Long Non-Coding RNA Located Upstream of Bmp4, Causes Vestibular Malformation in Mice
Kristina A. Roberts, Victoria E. Abraira, Andrew F. Tucker, Lisa V. Goodrich, Nancy C. Andrews
PLoS One. 2012; 7(1): e29495. Published online 2012 Jan 12. doi: 10.1371/journal.pone.0029495
PMCID:
PMC3257225
AbstractArticlePDF–1.3M
10.
Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene
Fan-Suo Geng, Leila Abbas, Sarah Baxendale, Celia J. Holdsworth, A. George Swanson, Krasimir Slanchev, Matthias Hammerschmidt, Jacek Topczewski, Tanya T. Whitfield
Development. 2013 Nov 1; 140(21): 4362–4374. doi: 10.1242/dev.098061
PMCID:
PMC4007713
AbstractArticle
11.
CHD7 Mutational Analysis and Clinical Considerations for Auditory Rehabilitation in Deaf Patients with CHARGE Syndrome
Mee Hyun Song, Hyun-Ju Cho, Hee Keun Lee, Tae Jun Kwon, Won-Sang Lee, Sanghee Oh, Jinwoong Bok, Jae Young Choi, Un-Kyung Kim
PLoS One. 2011; 6(9): e24511. Published online 2011 Sep 13. doi: 10.1371/journal.pone.0024511
PMCID:
PMC3172230
AbstractArticlePDF–700K
12.
Potential Roles of Arnt2 in Zebrafish Larval Development
Adrian J. Hill, Tisha C. King Heiden, Warren Heideman, Richard E. Peterson
Zebrafish. 2009 Mar; 6(1): 79–91. doi: 10.1089/zeb.2008.0536
PMCID:
PMC3140857
AbstractArticlePDF–627K
13.
TEMPORAL BONE ABNORMALITIES IN CHILDREN WITH GJB2 MUTATIONS
Margaret A. Kenna, Heidi L. Rehm, Anna Frangulov, Henry A. Feldman, Caroline D. Robson
Laryngoscope. Author manuscript; available in PMC 2012 Mar 1.
Published in final edited form as: Laryngoscope. 2011 Mar; 121(3): 630–635. Published online 2011 Feb 4. doi: 10.1002/lary.21414
PMCID:
PMC3061391
AbstractArticlePDF–757K
14.
MicroRNA-183 Family Members Regulate Sensorineural Fates in the Inner Ear
Haiqiong Li, Wigard Kloosterman, Donna M. Fekete
J Neurosci. 2010 Mar 3; 30(9): 3254–3263. doi: 10.1523/JNEUROSCI.4948-09.2010
PMCID:
PMC2848753
AbstractArticlePDF–2.7M
15.
Requirement for Lmo4 in the Vestibular Morphogenesis of Mouse Inner Ear
Min Deng, Ling Pan, Xiaoling Xie, Lin Gan
Dev Biol. Author manuscript; available in PMC 2010 Feb 1.
Published in final edited form as: Dev Biol. 2010 Feb 1; 338(1): 38–49. Published online 2009 Nov 10. doi: 10.1016/j.ydbio.2009.11.003
PMCID:
PMC2812651
AbstractArticlePDF–3.6M
16.
Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear
Yukako Asai, Dylan K. Chan, Catherine J. Starr, James A. Kappler, Richard Kollmar, A. J. Hudspeth
Proc Natl Acad Sci U S A. 2006 Jun 13; 103(24): 9069–9074. Published online 2006 Jun 5. doi: 10.1073/pnas.0603453103
PMCID:
PMC1474007
AbstractArticlePDF–1.6M
17.
Heterozygosity Mapping of Partially Congenic Lines: Mapping of a Semidominant Neurological Mutation, Wheels (Whl), on Mouse Chromosome 4
P. M. Nolan, P. J. Sollars, B. A. Bohne, W. J. Ewens, G. E. Pickard, M. Bucan
Genetics. 1995 May; 140(1): 245–254. doi: 10.1093/genetics/140.1.245
PMCID:
PMC1206551
SummaryPDF–3.4M
18.
The Nuclear Receptor Nor-1 Is Essential for Proliferation of the Semicircular Canals of the Mouse Inner Ear
Tiia Ponnio, Quiana Burton, Fred A. Pereira, Doris K. Wu, Orla M. Conneely
Mol Cell Biol. 2002 Feb; 22(3): 935–945. doi: 10.1128/MCB.22.3.935-945.2002
PMCID:
PMC133552
AbstractArticlePDF–1.3M
19.
MicroRNA-194 Regulates the Development and Differentiation of Sensory Patches and Statoacoustic Ganglion of Inner Ear by Fgf4
Hui Cao, Jianbo Shi, Jintao Du, Kaitian Chen, Chang Dong, Di Jiang, Hongyan Jiang
Med Sci Monit. 2018; 24: 1712–1723. Published online 2018 Mar 23. doi: 10.12659/MSM.906277
PMCID:
PMC5880017
AbstractArticlePDF–7.2M
20.
lmo4a Contributes to Zebrafish Inner Ear and Vestibular Development via Regulation of the Bmp Pathway
Le Sun, Lu Ping, Ruzhen Gao, Bo Zhang, Xiaowei Chen
Genes (Basel) 2023 Jul; 14(7): 1371. Published online 2023 Jun 28. doi: 10.3390/genes14071371
PMCID:
PMC10378989
AbstractArticlePDF–5.8M

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