Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Zaohua Huang"'
Autor:
Nicholas C. Gosstola, Zaohua Huang, Xiaoying Tong, Aida Nourbakhsh, Zheng-Yi Chen, Derek M. Dykxhoorn, Xue Zhong Liu
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102017- (2020)
UMi028-A-1 hiPSC line contains a CRISPR/Cas9-induced heterozygous, hearing loss-associated variant (V60L (GTA > TTA)) in the Purinergic Receptor P2X2 (P2RX2) gene. This line, derived from an unaffected male iPSC line, has been successfully characteri
Externí odkaz:
https://doaj.org/article/40d0ee6b88e94a7dad955dcb5db7417a
Autor:
Arti Vashist, Venkata Atluri, Andrea Raymond, Ajeet Kaushik, Tiyash Parira, Zaohua Huang, Andriy Durygin, Asahi Tomitaka, Roozbeh Nikkhah-Moshaie, Atul Vashist, Marisela Agudelo, Hitendra S. Chand, Ilyas Saytashev, Jessica C. Ramella-Roman, Madhavan Nair
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 8 (2020)
The emerging field of theranostics for advanced healthcare has raised the demand for effective and safe delivery systems consisting of therapeutics and diagnostics agents in a single monarchy. This requires the development of multi-functional bio-pol
Externí odkaz:
https://doaj.org/article/99ca5a7845784548abc3468690b47923
Autor:
Zaohua Huang, Madahavan Nair
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract HIV/AIDS remains a major health threat despite significant advances in the prevention and treatment of HIV infection. The major reason is the inability of existing treatments to eradicate the multiple HIV reservoirs in the human body, includ
Externí odkaz:
https://doaj.org/article/580f767fb9304939ba1dc095b42df5a7
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e71213 (2013)
NOTCH1 is a member of the NOTCH receptor family, a group of single-pass trans-membrane receptors. NOTCH signaling is highly conserved in evolution and mediates communication between adjacent cells. NOTCH receptors have been implicated in cell fate de
Externí odkaz:
https://doaj.org/article/c722dd7a843e4332a18d8406fe9749bf
Autor:
Wan Du, Volkan Ergin, Corena Loeb, Mingqian Huang, Stewart Silver, Ariel Miura Armstrong, Zaohua Huang, Channabasavaiah B. Gurumurthy, Hinrich Staecker, Xuezhong Liu, Zheng-Yi Chen
Publikováno v:
Molecular Therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdf780a87b04fde4b314d9005a0f5ef8
https://doi.org/10.1016/j.ymthe.2023.05.005
https://doi.org/10.1016/j.ymthe.2023.05.005
Publikováno v:
Critical Reviews in Biomedical Engineering. 47:495-505
Liposomes, one of the most promising drug delivery carriers, have been extensively studied for the treatment of various diseases and have made their way to the market. Magnetic nanoparticles have been attracting great interest for diagnostic and ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69492b2212599ab691bc6d13cd87beba
https://doi.org/10.1615/critrevbiomedeng.2020033002
https://doi.org/10.1615/critrevbiomedeng.2020033002
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:
Zaohua Huang, Aida Nourbakhsh, Xiaoying Tong, Nicholas C. Gosstola, Derek M. Dykxhoorn, Xue Zhong Liu, Zheng-Yi Chen
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102017-(2020)
UMi028-A-1 hiPSC line contains a CRISPR/Cas9-induced heterozygous, hearing loss-associated variant (V60L (GTA > TTA)) in the Purinergic Receptor P2X2 (P2RX2) gene. This line, derived from an unaffected male iPSC line, has been successfully characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97945027a345f41787dcc1cefe1fc1b4
http://www.sciencedirect.com/science/article/pii/S1873506120303184
http://www.sciencedirect.com/science/article/pii/S1873506120303184
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
