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46 results for Transcription+Factor+Brn-3C+-+genetics

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ArticlesPeer ReviewedFull Text
In Vivo Generation of Immature Inner Hair Cells in Neonatal Mouse Cochleae by Ectopic Atoh1 Expression
Author / Creator:Liu, Zhiyong ; Fang, Jie ; Dearman, Jennifer ; Zhang, Lingli ; Zuo, Jian
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-02, Vol.9 (2), p.e89377-e89377
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Aldh inhibitor restores auditory function in a mouse model of human deafness
Author / Creator:Zhu, Guang-Jie ; Gong, Sihao ; Ma, Deng-Bin ; Tao, Tao ; He, Wei-Qi ; Zhang, Linqing ; Wang, Fang ; Qian, Xiao-Yun ; Zhou, Han ; Fan, Chi ; Wang, Pei ; Chen, Xin ; Zhao, Wei ; Sun, Jie ; Chen, Huaqun ; Wang, Ye ; Gao, Xiang ; Zuo, Jian ; Zhu, Min-Sheng ; Gao, Xia ; Wan, Guoqiang
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2020-09, Vol.16 (9), p.e1009040
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POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
Author / Creator:Kitano, Tomohiro ; Miyagawa, Maiko ; Nishio, Shin-ya ; Moteki, Hideaki ; Oda, Kiyoshi ; Ohyama, Kenji ; Miyazaki, Hiromitsu ; Hidaka, Hiroshi ; Nakamura, Ken-ichi ; Murata, Takaaki ; Matsuoka, Rina ; Ohta, Yoko ; Nishiyama, Nobuhiro ; Kumakawa, Kozo ; Furutate, Sakiko ; Iwasaki, Satoshi ; Yamada, Takechiyo ; Ohta, Yumi ; Uehara, Natsumi ; Noguchi, Yoshihiro ; Usami, Shin-ichi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-05, Vol.12 (5), p.e0177636-e0177636
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A Novel Atoh1 “Self-Terminating” Mouse Model Reveals the Necessity of Proper Atoh1 Level and Duration for Hair Cell Differentiation and Viability
Author / Creator:Pan, Ning ; Jahan, Israt ; Kersigo, Jennifer ; Duncan, Jeremy S. ; Kopecky, Benjamin ; Fritzsch, Bernd
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-01, Vol.7 (1), p.e30358-e30358
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Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families
Author / Creator:Bai, Xiaohui ; Zhang, Fengguo ; Xiao, Yun ; Jin, Yu ; Zheng, Qingyin ; Wang, Haibo ; Xu, Lei
Publisher:England: John Wiley & Sons, Inc
Journal title:Journal of cellular and molecular medicine, 2020-06, Vol.24 (12), p.6978-6987
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Transcription factor induced conversion of human fibroblasts towards the hair cell lineage
Author / Creator:Duran Alonso, María Beatriz ; Lopez Hernandez, Iris ; de la Fuente, Miguel Angel ; Garcia-Sancho, Javier ; Giraldez, Fernando ; Schimmang, Thomas
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-07, Vol.13 (7), p.e0200210
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Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study
Author / Creator:Mutai, Hideki ; Suzuki, Naohiro ; Shimizu, Atsushi ; Torii, Chiharu ; Namba, Kazunori ; Morimoto, Noriko ; Kudoh, Jun ; Kaga, Kimitaka ; Kosaki, Kenjiro ; Matsunaga, Tatsuo
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2013-10, Vol.8 (1), p.172-172, Article 172
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Functional Correlation of Two Novel Nonsense POU4F3 Mutations Causing Late‐Onset Progressive Nonsyndromic Hearing Loss in DFNA15 Families
Author / Creator:Zhang, Tianyang ; Wang, Wei ; Zhang, Luping ; He, Jingchun
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2025-05, Vol.13 (5), p.e70100-n/a
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A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss
Author / Creator:Lin, Yin-Hung ; Lin, Yi-Hsin ; Lu, Ying-Chang ; Liu, Tien-Chen ; Chen, Chien-Yu ; Hsu, Chuan-Jen ; Chen, Pei-Lung ; Wu, Chen-Chi
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-08, Vol.7 (1), p.7551-6, Article 7551
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Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss
Author / Creator:Cai, Xin Zhang ; Li, Ying ; Xia, Lu ; Peng, Yu ; He, Chu Feng ; Jiang, Lu ; Feng, Yong ; Xia, Kun ; Liu, Xue Zhong ; Mei, Ling Yun ; Hu, Zheng Mao
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2017-02, Vol.62 (2), p.317-320
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ArticlesPeer ReviewedFull Text
The cell adhesion molecule Sdk1 shapes assembly of a retinal circuit that detects localized edges
Author / Creator:Rochon, Pierre-Luc ; Theriault, Catherine ; Rangel Olguin, Aline Giselle ; Krishnaswamy, Arjun
Publisher:England: eLife Sciences Publications Ltd
Journal title:eLife, 2021-09, Vol.10
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ArticlesPeer ReviewedFull Text
A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities
Author / Creator:Bai, Dan ; Zhang, Xudong ; Li, Yu ; Ni, Jing ; Lan, Kai
Publisher:United States: Hindawi
Journal title:BioMed research international, 2021, Vol.2021 (1), p.5574136-5574136
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ArticlesPeer ReviewedFull Text
BDNF gene therapy induces auditory nerve survival and fiber sprouting in deaf Pou4f3 mutant mice
Author / Creator:Fukui, H. ; Wong, H. T. ; Beyer, L. A. ; Case, B. G. ; Swiderski, D. L. ; Di Polo, A. ; Ryan, A. F. ; Raphael, Y.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2012-11, Vol.2 (1), p.838-838, Article 838
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ArticlesPeer ReviewedFull Text
Transcription Factors with Conserved Binding Sites Near ATOH1 on the POU4F3 Gene Enhance the Induction of Cochlear Hair Cells
Author / Creator:Ikeda, Ryoukichi ; Pak, Kwang ; Chavez, Eduardo ; Ryan, Allen F.
Publisher:Boston: Springer US
Journal title:Molecular neurobiology, 2015-04, Vol.51 (2), p.672-684
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ArticlesPeer ReviewedFull Text
Genetic Interactions between Brn3 Transcription Factors in Retinal Ganglion Cell Type Specification
Author / Creator:Shi, Melody ; Kumar, Sumit R. ; Motajo, Oluwaseyi ; Kretschmer, Friedrich ; Mu, Xiuqian ; Badea, Tudor C.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-10, Vol.8 (10), p.e76347-e76347
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ArticlesPeer ReviewedFull Text
SNP Linkage Analysis and Whole Exome Sequencing Identify a Novel POU4F3 Mutation in Autosomal Dominant Late-Onset Nonsyndromic Hearing Loss (DFNA15)
Author / Creator:Kim, Hee-Jin ; Won, Hong-Hee ; Park, Kyoung-Jin ; Hong, Sung Hwa ; Ki, Chang-Seok ; Cho, Sang Sun ; Venselaar, Hanka ; Vriend, Gert ; Kim, Jong-Won
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-11, Vol.8 (11), p.e79063
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ArticlesPeer ReviewedFull Text
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
Author / Creator:Kang, Dong-Yang ; Zhang, Mei-Guang ; Lin, Xi ; Dai, Pu ; Su, Yu ; Wang, Guo-Jian ; Huang, Sha-Sha ; Bai, Dan ; Yuan, Yong-Yi ; Wang, Wei-Qian ; Xu, Jin-Cao ; Gao, Xue ; Li, Jia
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:BioMed research international, 2018-01, Vol.2018 (2018), p.1-7
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Intrinsic Photosensitive Retinal Ganglion Cells in the Diurnal Rodent, Arvicanthis ansorgei
Author / Creator:Karnas, Diana ; Hicks, David ; Mordel, Jérôme ; Pévet, Paul ; Meissl, Hilmar
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-08, Vol.8 (8), p.e73343-e73343
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Aminoglycoside-Induced Hair Cell Death of Inner Ear Organs Causes Functional Deficits in Adult Zebrafish (Danio rerio)
Author / Creator:Uribe, Phillip M. ; Sun, Huifang ; Wang, Kevin ; Asuncion, James D. ; Wang, Qi ; Chen, Chien-Wei ; Steyger, Peter S. ; Smith, Michael E. ; Matsui, Jonathan I.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-03, Vol.8 (3), p.e58755
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Triage of Atypical Glandular Cell by SOX1 and POU4F3 Methylation: A Taiwanese Gynecologic Oncology Group (TGOG) Study
Author / Creator:Chang, Cheng-Chang ; Ou, Yu-Che ; Wang, Kung-Liahng ; Chang, Ting-Chang ; Cheng, Ya-Min ; Chen, Chi-Hau ; Chu, Tang-Yuan ; Hsu, Shih-Tien ; Liou, Wen-Shiung ; Chang, Yin-Yi ; Wu, Hua-Hsi ; Chen, Tze-Ho ; Lai, Hung-Cheng
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-06, Vol.10 (6), p.e0128705-e0128705
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Showing 21 to 40 of 46 results

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In Vivo Generation of Immature Inner Hair Cells in Neonatal Mouse Cochleae by Ectopic Atoh1 Expression

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Aldh inhibitor restores auditory function in a mouse model of human deafness

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POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

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A Novel Atoh1 “Self-Terminating” Mouse Model Reveals the Necessity of Proper Atoh1 Level and Duration for Hair Cell Differentiation and Viability

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Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families

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Transcription factor induced conversion of human fibroblasts towards the hair cell lineage

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Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

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Functional Correlation of Two Novel Nonsense POU4F3 Mutations Causing Late‐Onset Progressive Nonsyndromic Hearing Loss in DFNA15 Families

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A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss

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Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss

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The cell adhesion molecule Sdk1 shapes assembly of a retinal circuit that detects localized edges

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A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities

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BDNF gene therapy induces auditory nerve survival and fiber sprouting in deaf Pou4f3 mutant mice

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Transcription Factors with Conserved Binding Sites Near ATOH1 on the POU4F3 Gene Enhance the Induction of Cochlear Hair Cells

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Genetic Interactions between Brn3 Transcription Factors in Retinal Ganglion Cell Type Specification

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SNP Linkage Analysis and Whole Exome Sequencing Identify a Novel POU4F3 Mutation in Autosomal Dominant Late-Onset Nonsyndromic Hearing Loss (DFNA15)

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A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

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Intrinsic Photosensitive Retinal Ganglion Cells in the Diurnal Rodent, Arvicanthis ansorgei

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Aminoglycoside-Induced Hair Cell Death of Inner Ear Organs Causes Functional Deficits in Adult Zebrafish (Danio rerio)

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Triage of Atypical Glandular Cell by SOX1 and POU4F3 Methylation: A Taiwanese Gynecologic Oncology Group (TGOG) Study

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