Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Eunyoung, Yi"'
Autor:
Jingjing Sherry Wu, Eunyoung Yi, Marco Manca, Hamad Javaid, Amanda M Lauer, Elisabeth Glowatzki
Publikováno v:
eLife, Vol 9 (2020)
Lateral olivocochlear (LOC) efferent neurons modulate auditory nerve fiber (ANF) activity using a large repertoire of neurotransmitters, including dopamine (DA) and acetylcholine (ACh). Little is known about how individual neurotransmitter systems ar
Externí odkaz:
https://doaj.org/article/d3ef715b83414d75ae0d886e5f6ea2c1
Publikováno v:
Experimental Neurobiology. 31:243-259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd0b2f6bf3b5fcfefaf0b5c5543ec53a
https://doi.org/10.5607/en22013
https://doi.org/10.5607/en22013
Publikováno v:
Experimental Neurobiology. 30:319-328
The TMEM43 has been studied in human diseases such as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5) and auditory neuropathy spectrum disorder (ANSD). In the heart, the p.(Ser358Leu) mutation has been shown to alter intercalated disc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba5cc987dc38917e7dd5ae2bb6fac175
https://doi.org/10.5607/en21028
https://doi.org/10.5607/en21028
Publikováno v:
Experimental Neurobiology
Kv3 family K+ channels, by ensuring speedy repolarization of action potential, enable rapid and high frequency neuronal firing and high precision temporal coding of auditory information in various auditory synapses in the brain. Expression of differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7729a08872eb9a3e4f8060cc118747af
http://europepmc.org/articles/PMC7649084
http://europepmc.org/articles/PMC7649084
Publikováno v:
Journal of Nanoscience and Nanotechnology. 20:5515-5519
Hearing loss is one of the major complications of diabetes mellitus and significantly lowers the quality of life of diabetic patients. In studies using diabetic animal models hearing loss have been frequently associated with damages to cochlear affer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5032e0ab23d32be22437f513f936cb3
https://doi.org/10.1166/jnn.2020.17654
https://doi.org/10.1166/jnn.2020.17654
Publikováno v:
Experimental Neurobiology
The TMEM43 has been studied in human diseases such as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5) and auditory neuropathy spectrum disorder (ANSD). In the heart, the p.(Ser358Leu) mutation has been shown to alter intercalated disc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d756ac8e5a48d08faa4c2a06656265b5
https://pubmed.ncbi.nlm.nih.gov/34737237
https://pubmed.ncbi.nlm.nih.gov/34737237
Publikováno v:
Journal of Nanoscience and Nanotechnology. 19:915-921
Obesity is a metabolic disorder associated with chronic oxidative stress and inflammation. Recruitment of inflammatory cells to adipose tissue and subsequent production of a large amount of reactive oxygen species (ROS) facilitates adipocyte differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::607bfc576b7e0594ac4a806efadb3837
https://doi.org/10.1166/jnn.2019.15915
https://doi.org/10.1166/jnn.2019.15915
Autor:
Minwoo Wendy, Jang, Doo-Yi, Oh, Eunyoung, Yi, Xuezhong, Liu, Jie, Ling, Nayoung, Kim, Kushal, Sharma, Tai Young, Kim, Seungmin, Lee, Ah-Reum, Kim, Min Young, Kim, Min-A, Kim, Mingyu, Lee, Jin-Hee, Han, Jae Joon, Han, Hye-Rim, Park, Bong Jik, Kim, Sang-Yeon, Lee, Dong Ho, Woo, Jayoung, Oh, Soo-Jin, Oh, Tingting, Du, Ja-Won, Koo, Seung-Ha, Oh, Hyun-Woo, Shin, Moon-Woo, Seong, Kyu-Yup, Lee, Un-Kyung, Kim, Jung Bum, Shin, Shushan, Sang, Xinzhang, Cai, Lingyun, Mei, Chufeng, He, Susan H, Blanton, Zheng-Yi, Chen, Hongsheng, Chen, Xianlin, Liu, Aida, Nourbakhsh, Zaohua, Huang, Kwon-Woo, Kang, Woong-Yang, Park, Yong, Feng, C Justin, Lee, Byung Yoon, Choi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Auditory neuropathy spectrum disorder (ANSD) is a confounding auditory disease in which the subjects respond to sound but have difficulties in speech discrimination. Herein, we examined two Asian families with hereditary late-age–onset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1daff5e8939ee1868d76922be5655b04
https://pubmed.ncbi.nlm.nih.gov/34050020
https://pubmed.ncbi.nlm.nih.gov/34050020
Autor:
Minwoo Wendy Jang, C. Justin Lee, Nayoung K.D. Kim, Aida Nourbakhsh, Seungmin Lee, Yong Feng, Jayoung Oh, Dong Ho Woo, Bong Jik Kim, Eunyoung Yi, Sang Yeon Lee, Lingyun Mei, Kyu Yup Lee, Doo Yi Oh, Zaohua Huang, Jie Ling, Shushan Sang, Tai Young Kim, Jae Joon Han, Min Young Kim, Byung Yoon Choi, Mingyu Lee, Hongsheng Chen, Min-A Kim, Kushal Sharma, Tingting Du, Xinzhang Cai, Soo Jin Oh, Hyun Woo Shin, Woong-Yang Park, Jin Hee Han, Susan H. Blanton, Jung-Bum Shin, Kwon Woo Kang, Ja Won Koo, Un Kyung Kim, Zheng-Yi Chen, Xianlin Liu, Ah Reum Kim, Moon Woo Seong, Chufeng He, Hye Rim Park, Seung Ha Oh, Xuezhong Liu
Publikováno v:
Proceedings of the National Academy of Sciences. 118
Genes that are primarily expressed in cochlear glia-like supporting cells (GLSs) have not been clearly associated with progressive deafness. Herein, we present a deafness locus mapped to chromosome 3p25.1 and an auditory neuropathy spectrum disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220ccb1967b752b8146bfe394bd65f84
https://doi.org/10.1073/pnas.2019681118
https://doi.org/10.1073/pnas.2019681118
Autor:
Min Young Kim, Xianlin Liu, Seungmin Lee, Byung Yoon Choi, Yong Feng, Lingyun Mei, Jin Hee Han, Jayoung Oh, Minwoo Wendy Jang, Moon Woo Seong, Kyu Yup Lee, Zaohua Huang, Dong Ho Woo, Bong Jik Kim, Aida Nourbakhsh, Nayoung K.D. Kim, Hongsheng Chen, Min-A Kim, Eunyoung Yi, C. Justin Lee, Jie Ling, Jae Joon Han, Tai Young Kim, Woong-Yang Park, Kushal Sharma, Mingyu Lee, Xinzhang Cai, Doo-Yi Oh, Un-Kyung Kim, Ja Won Koo, Sang-Yeon Lee, Chufeng He, Ting-Ting Du, Hye-Rim Park, Shushan Sang, Seung Ha Oh, Ah Reum Kim, Zheng-Yi Chen, Susan H. Blanton, Jung-Bum Shin, Soo Jin Oh, Hyun Woo Shin, Xuezhong Liu
Genes that are primarily expressed in cochlear glia-like supporting cells (GLSs) have never been clearly associated with progressive deafness. Herein, we present a novel deafness locus mapped to chromosome 3p25.1 and a new auditory neuropathy spectru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaa3ddcf6762b103d7c4b96d4cb858bc
https://doi.org/10.1101/2020.07.27.222323
https://doi.org/10.1101/2020.07.27.222323
