Zobrazeno 1 - 10
of 17
pro vyhledávání: '"You‐Ren Wu"'
Autor:
Shih‐Jie Chou, Yi‐Ping Yang, Min‐Ren Chiang, Chih‐Ying Chen, Henkie Isahwan Ahmad Mulyadi Lai, Yi‐Ying Lin, You‐Ren Wu, I‐Chieh Wang, Aliaksandr A. Yarmishyn, Guang‐Yuh Chiou, Tai‐Chi Lin, De‐Kuang Hwang, Shih‐Jen Chen, Yueh Chien, Shang‐Hsiu Hu, Shih‐Hwa Chiou
Publikováno v:
Small Science, Vol 4, Iss 8, Pp n/a-n/a (2024)
Eye fundus diseases, such as retinal degenerative diseases, which lead to blindness in ≈12% of individuals aged >65 years, cause permanent damage to retinal cells. The antioxidant quercetin (QC) is promising for the effective treatment of eye fundu
Externí odkaz:
https://doaj.org/article/05be5d5726224b24893f31a9b79382e9
Autor:
En-Tung Tsai, Shih-Yuan Peng, You-Ren Wu, Tai-Chi Lin, Chih-Ying Chen, Yu-Hao Liu, Yu-Hsin Tseng, Yu-Jer Hsiao, Huan-Chin Tseng, Wei-Yi Lai, Yi-Ying Lin, Yi-Ping Yang, Shih-Hwa Chiou, Shih-Pin Chen, Yueh Chien
Publikováno v:
Cells, Vol 12, Iss 22, p 2617 (2023)
Background: Mesenchymal stem cells (MSCs) hold promise for cell-based therapy, yet the sourcing, quality, and invasive methods of MSCs impede their mass production and quality control. Induced pluripotent stem cell (iPSC)-derived MSCs (iMSCs) can be
Externí odkaz:
https://doaj.org/article/de9638d7b9de491d809231a5b6e50331
Autor:
Huai-En Lu, Yi-Ping Yang, Yan-Ting Chen, You-Ren Wu, Chia-Lin Wang, Fu-Ting Tsai, De-Kuang Hwang, Tai-Chi Lin, Shih-Jen Chen, An-Guor Wang, Patrick C.H. Hsieh, Shih-Hwa Chiou
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 56-60 (2018)
Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by homoplasmic point mutations in complex I subunit genes of mitochondrial DNA. In this report, we generated an induced pluripotent stem cell (iPSCs) li
Externí odkaz:
https://doaj.org/article/27f2e3f493304657a38a2d0a004a5c4f
Autor:
You-Ren Wu, 吳祐任
105
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by homoplasmic point mutations in Complex I subunit genes of mitochondrial DNA. LHON is characterized by incomplete penetrance, as only part
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by homoplasmic point mutations in Complex I subunit genes of mitochondrial DNA. LHON is characterized by incomplete penetrance, as only part
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/8z523p
Autor:
You-Ren Wu, 吳友仁
101
This study numerically investigated the convective heat transfer of nanofluid in vertical channels and inclined closed rectangles. A widely used software FLUENT was utilized to perform calculation on the heat transfer of nanofluids. Six nano
This study numerically investigated the convective heat transfer of nanofluid in vertical channels and inclined closed rectangles. A widely used software FLUENT was utilized to perform calculation on the heat transfer of nanofluids. Six nano
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/59605161580401424307
Autor:
Lenore K. Beitel, Evguenia P. Bekman, Xianwei Chen, Shih-Jen Chen, Shih-Hwa Chiou, Sangmi Chung, Michael D. Coleman, Simão T. da Rocha, Dhanjit Kumar Das, Iveta Demirova, Thomas M. Durcan, Allison D. Ebert, Gundars Goldsteins, Philip Gorwood, Alastair I. Grainger, Eric J. Hill, Christine Klein, Jari Koistinaho, Nihay Laham-Karam, Šárka Lehtonen, Zhenqing Liu, Carina Maranga, Gilles Maussion, Peiyan Ni, Rivka Ofir, H. Rheinallt Parri, Luisa Pimentel, Lidiia Plotnikova, Aleksandar Rakovic, Nicolas Ramoz, Cecilia Rocha, Philip Seibler, Bipin Raj Shekhar, Yanhong Shi, Tuuli-Maria Sonninen, Michael Telias, Adriana A. Vieira, An-Guor Wang, Anne Weissbach, Emily Welby, You-Ren Wu, Qingqiu Yang, Tien-Chun Yang, Aliaksandr A. Yarmishyn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::679c1522948ef46595a53d42724d267a
https://doi.org/10.1016/b978-0-323-85764-2.01002-4
https://doi.org/10.1016/b978-0-323-85764-2.01002-4
Autor:
Shih Hwa Chiou, Shih-Jen Chen, Tien Chun Yang, Aliaksandr A. Yarmishyn, An-Guor Wang, You-Ren Wu
Leber’s hereditary optic neuropathy (LHON) is the maternally inherited mitochondrial disease caused by homoplasmic mutations in the mitochondrial electron transport chain. The pathological mechanism of LHON is still unclear. The feature of incomple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ea5b25fddd33955805d11f92c8236b6
https://doi.org/10.1016/b978-0-323-85764-2.00013-2
https://doi.org/10.1016/b978-0-323-85764-2.00013-2
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose Retinal ganglion cell (RGC) transplantation is a therapeutic approach to replace irreversibly degenerated RGCs in diseases such as glaucoma. However, the application of primary RGCs is limited by the availability of tissues. The goal of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28110fdf1c276e50c1da8ce92d252eed
https://doi.org/10.1167/iovs.62.13.26
https://doi.org/10.1167/iovs.62.13.26
Autor:
Patrick C.H. Hsieh, Huai En Lu, Yi Ping Yang, Tai Chi Lin, De Kuang Hwang, Fu Ting Tsai, Shih-Jen Chen, Chia-Lin Wang, Shih Hwa Chiou, Yan Ting Chen, An Guor Wang, You Ren Wu
Publikováno v:
Stem Cell Research, Vol 28, Iss, Pp 56-60 (2018)
Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by homoplasmic point mutations in complex I subunit genes of mitochondrial DNA. In this report, we generated an induced pluripotent stem cell (iPSCs) li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b238fefffcd3b9c15cd485581f0ee9
https://pubmed.ncbi.nlm.nih.gov/29427840
https://pubmed.ncbi.nlm.nih.gov/29427840
Autor:
Aliaksandr A. Yarmishyn, Tien Chun Yang, Yan Ting Chen, Hsin Chen Lee, De Kuang Hwang, An Guor Wang, Chi Hsien Peng, Shih Hwa Chiou, Yi Ping Yang, Waradee Buddhakosai, Shih-Jen Chen, You Ren Wu, Chia-Ning Shen
Publikováno v:
Experimental cell research. 363(2)
Leber’s hereditary optic neuropathy (LHON) is the maternally inherited mitochondrial disease caused by homoplasmic mutations in mitochondrial electron transport chain Complex I subunit genes. The mechanism of its incomplete penetrance is still larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8900f624d50f6af9b151ac7335331bb6
https://pubmed.ncbi.nlm.nih.gov/29366807
https://pubmed.ncbi.nlm.nih.gov/29366807