نتایج جستجو برای: tmc1 gene

تعداد نتایج: 1141439  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Reo Maeda Katie S Kindt Weike Mo Clive P Morgan Timothy Erickson Hongyu Zhao Rachel Clemens-Grisham Peter G Barr-Gillespie Teresa Nicolson

The tip link protein protocadherin 15 (PCDH15) is a central component of the mechanotransduction complex in auditory and vestibular hair cells. PCDH15 is hypothesized to relay external forces to the mechanically gated channel located near its cytoplasmic C terminus. How PCDH15 is coupled to the transduction machinery is not clear. Using a membrane-based two-hybrid screen to identify proteins th...

Journal: :International journal of oncology 2010
Tse-Chou Cheng Shan-Shan Hsieh Wen-Lin Hsu Yu-Fang Chen Hwei-Hon Ho Lai-Fa Sheu

Epstein-Barr nuclear antigen 1 (EBNA-1) is consistently expressed in all EBV-associated gastric carcinomas. We explored its biological effects in gastric carcinoma cells by expressing the protein in two Epstein-Barr virus (EBV)-negative gastric carcinoma cell lines (SCM1 and TMC1). EBNA1-expressing SCM1 and TMC1 cells displayed no significant differences in growth rates, respectively, compared ...

2017
Timothy Erickson Clive P Morgan Jennifer Olt Katherine Hardy Elisabeth Busch-Nentwich Reo Maeda Rachel Clemens Jocelyn F Krey Alex Nechiporuk Peter G Barr-Gillespie Walter Marcotti Teresa Nicolson

Transmembrane O-methyltransferase (TOMT/LRTOMT) is responsible for non-syndromic deafness DFNB63. However, the specific defects that lead to hearing loss have not been described. Using a zebrafish model of DFNB63, we show that the auditory and vestibular phenotypes are due to a lack of mechanotransduction (MET) in Tomt-deficient hair cells. GFP-tagged Tomt is enriched in the Golgi of hair cells...

2014
Aparna Ganapathy Nishtha Pandey C. R. Srikumari Srisailapathy Rajeev Jalvi Vikas Malhotra Mohan Venkatappa Arunima Chatterjee Meenakshi Sharma Rekha Santhanam Shelly Chadha Arabandi Ramesh Arun K. Agarwal Raghunath R. Rangasayee Anuranjan Anand

Mutations in the autosomal genes TMPRSS3, TMC1, USHIC, CDH23 and TMIE are known to cause hereditary hearing loss. To study the contribution of these genes to autosomal recessive, non-syndromic hearing loss (ARNSHL) in India, we examined 374 families with the disorder to identify potential mutations. We found four mutations in TMPRSS3, eight in TMC1, ten in USHIC, eight in CDH23 and three in TMI...

زمینه و هدف: ناشنوایی متداول‌ترین نقص حسی در انسان است. ناشنوایی ممکن است هدایتی، حسی- عصبی یا ترکیبی از هر دو، سندرومی یا غیرسندرومی، پیش از تکلم یا پس از تکلم باشد. به دلیل پیچیدگی مکانیسم شنوایی جای تعجب نیست که چند صد ژن در ایجاد ناشنوایی توارثی نقش داشته باشند. تاکنون 152 لوکوس شناسایی شده که با رایج‌ترین نوع ناشنوایی یعنی ناشنوایی غیرسندرومی مرتبط هستند. هدف از این مطالعه تجزیه و تحلیل پی...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Yanmeng Guo Yuping Wang Wei Zhang Shan Meltzer Damiano Zanini Yue Yu Jiefu Li Tong Cheng Zhenhao Guo Qingxiu Wang Julie S Jacobs Yashoda Sharma Daniel F Eberl Martin C Göpfert Lily Yeh Jan Yuh Nung Jan Zuoren Wang

Drosophila larval locomotion, which entails rhythmic body contractions, is controlled by sensory feedback from proprioceptors. The molecular mechanisms mediating this feedback are little understood. By using genetic knock-in and immunostaining, we found that the Drosophila melanogaster transmembrane channel-like (tmc) gene is expressed in the larval class I and class II dendritic arborization (...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید