Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Tien Chun Yang"'
Autor:
Shin-Yun Chen, Wei-Ta Chen, Tsorng-Harn Fong, Jiun-Lin Horng, Cheng-Ying Chu, Haojan Yang, Tien-Chun Yang
Publikováno v:
Heliyon, Vol 10, Iss 22, Pp e40106- (2024)
This report presents a novel anatomical variant of the second dorsal metacarpal artery (SDMA). In this unique case, the SDMA abnormally penetrates the second dorsal interosseous muscle (SDIM), dividing into two major branches. A deep dorsal branch of
Externí odkaz:
https://doaj.org/article/259ebd3aed96477d88460866e2bcaa1f
Autor:
Kang-Chieh Huang, Mong-Lien Wang, Shih-Jen Chen, Jean-Cheng Kuo, Won-Jing Wang, Phan Nguyen Nhi Nguyen, Karl J. Wahlin, Jyh-Feng Lu, Audrey A. Tran, Michael Shi, Yueh Chien, Aliaksandr A. Yarmishyn, Ping-Hsing Tsai, Tien-Chun Yang, Wann-Neng Jane, Chia-Ching Chang, Chi-Hsien Peng, Thorsten M. Schlaeger, Shih-Hwa Chiou
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 906-923 (2019)
Summary: X-linked juvenile retinoschisis (XLRS), linked to mutations in the RS1 gene, is a degenerative retinopathy with a retinal splitting phenotype. We generated human induced pluripotent stem cells (hiPSCs) from patients to study XLRS in a 3D ret
Externí odkaz:
https://doaj.org/article/b9f017c6d6624217abb79abd14c148e3
Autor:
Elham Rastegari, Yu-Jer Hsiao, Wei-Yi Lai, Yun-Hsien Lai, Tien-Chun Yang, Shih-Jen Chen, Pin-I Huang, Shih-Hwa Chiou, Chung-Yuan Mou, Yueh Chien
Publikováno v:
Pharmaceutics, Vol 13, Iss 7, p 1067 (2021)
The efficient and safe delivery of therapeutic drugs, proteins, and nucleic acids are essential for meaningful therapeutic benefits. The field of nanomedicine shows promising implications in the development of therapeutics by delivering diagnostic an
Externí odkaz:
https://doaj.org/article/a9122d1a8afe41f889140fdd5fe915f1
Publikováno v:
Journal of Molecular Endocrinology. 71
The pathogenesis of hypertension is not fully understood; endothelin 1 (EDN1) is involved in developing essential hypertension. EDN1 can promote vascular smooth muscle cell (VSMC) proliferation or hypertrophy through autocrine and paracrine effects.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385b3f6afd04aaef106bc9f8713c4bd4
https://doi.org/10.1530/jme-22-0178
https://doi.org/10.1530/jme-22-0178
Autor:
Aliaksandr A. Yarmishyn, Yu Bai Chou, Shih Jie Chou, Tai Chi Lin, Tien Chun Yang, Shih Hwa Chiou, An Guor Wang, Mong Lien Wang, Shih-Jen Chen, De Kuang Hwang, Wei Kuang Yu, Chih Chien Hsu, Pin Chen Lu, Yi Ping Yang
Publikováno v:
Human Molecular Genetics. 29:1454-1464
The mutations in the genes encoding the subunits of complex I of the mitochondrial electron transport chain are the most common cause of Leber’s hereditary optic neuropathy (LHON), a maternal hereditary disease characterized by retinal ganglion cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cbc9915e986151d7f65e256e34d7477
https://doi.org/10.1093/hmg/ddaa063
https://doi.org/10.1093/hmg/ddaa063
Autor:
Chia-Yu Chang, Aliaksandr A. Yarmishyn, Shih Jen Chen, Ming Long Tsai, De Kuang Hwang, Yun Hsien Lai, Tien Chun Yang, Hsin Yu Yang, Mong Lien Wang, Chih Chien Hsu, Yonhua Tzeng, Chia-Ching Chang, Yi Ping Yang, Shih Hwa Chiou, Yen Shiang Mao
Publikováno v:
Acta Biomaterialia. 101:484-494
Nanodiamonds (NDs) are considered to be relatively safe carbon nanomaterials used for the transmission of DNA, proteins and drugs. The feasibility of utilizing the NDs to deliver CRISPR-Cas9 system for gene editing has not been clearly studied. There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2674dd823be959b5ac210a1c7db4f87
https://doi.org/10.1016/j.actbio.2019.10.037
https://doi.org/10.1016/j.actbio.2019.10.037
Autor:
Yu Jer Hsiao, Shih Hwa Chiou, Pin I. Huang, Yun Hsien Lai, Tien Chun Yang, Shih-Jen Chen, Chung-Yuan Mou, Yueh Chien, Wei Yi Lai, Elham Rastegari
Publikováno v:
Pharmaceutics
Pharmaceutics, Vol 13, Iss 1067, p 1067 (2021)
Pharmaceutics, Vol 13, Iss 1067, p 1067 (2021)
The efficient and safe delivery of therapeutic drugs, proteins, and nucleic acids are essential for meaningful therapeutic benefits. The field of nanomedicine shows promising implications in the development of therapeutics by delivering diagnostic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::820964b42752c098eec820a4ee217b52
http://europepmc.org/articles/PMC8309088
http://europepmc.org/articles/PMC8309088
Autor:
Ping Hsing Tsai, Audrey A. Tran, Wann-Neng Jane, Aliaksandr A. Yarmishyn, Yueh Chien, Shih Hwa Chiou, Chi Hsien Peng, Tien Chun Yang, Kang Chieh Huang, Chia-Ching Chang, Thorsten M. Schlaeger, Shih Jen Chen, Won Jing Wang, Jean Cheng Kuo, Karl J. Wahlin, Phan Nguyen Nhi Nguyen, Jyh Feng Lu, Michael Shi, Mong Lien Wang
Publikováno v:
Stem Cell Reports
Stem Cell Reports, Vol 13, Iss 5, Pp 906-923 (2019)
Stem Cell Reports, Vol 13, Iss 5, Pp 906-923 (2019)
Summary X-linked juvenile retinoschisis (XLRS), linked to mutations in the RS1 gene, is a degenerative retinopathy with a retinal splitting phenotype. We generated human induced pluripotent stem cells (hiPSCs) from patients to study XLRS in a 3D reti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dafe748d9678f5e05e5f56e13c96ea89
http://europepmc.org/articles/PMC6895767
http://europepmc.org/articles/PMC6895767
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