Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ming Ching Ho"'
Autor:
Shih-Ping Liu, Yu-Hung Hsu, Ching-Ying Huang, Ming-Ching Ho, Yu-Che Cheng, Cheng-Hao Wen, Huai-En Lu, Chon-Haw Tsai, Woei-Cherng Shyu, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 39-43 (2018)
Sialidosis is a rare autosomal recessive disorder that affects the intralysosomal catabolism of sialylated glycoconjugates and is involved in cellular immune response. Mutations in NEU1, which encodes the sialidase enzyme, result in sialidosis. Siali
Externí odkaz:
https://doaj.org/article/c1bf9b454a24419c8c5994688cc5aa91
Autor:
Yu-Che Cheng, Ching-Ying Huang, Ming-Ching Ho, Yu-Hung Hsu, Shih-Han Syu, Huai-En Lu, Han-I Lin, Chin-Hsien Lin, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 1-5 (2018)
Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK2 p.G2385R is an Asian specific genetic risk factor for sporadic Parkinson's disease. We generated two induced pluripotent stem cells (iPSCs), IBMS-iP
Externí odkaz:
https://doaj.org/article/f1d5cc0ddc224aa8b86c5b0dbe21abff
Autor:
Yu-Ting Wu, Yu-Hung Hsu, Ching-Ying Huang, Ming-Ching Ho, Yu-Che Cheng, Cheng-Hao Wen, Hui-Wen Ko, Huai-En Lu, Yen-Chun Chen, Chia-Ling Tsai, Yi-Chao Hsu, Yau-Huei Wei, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 27, Iss , Pp 10-14 (2018)
Mitochondrial defects are associated with clinical manifestations from common diseases to rare genetic disorders. Myoclonus epilepsy associated with ragged-red fibers (MERRF) syndrome results from an A to G transition at nucleotide position 8344 in t
Externí odkaz:
https://doaj.org/article/1ac8a05a9b114e69884c09e1c5764f87
Autor:
Jia-Jung Lee, Ming-Ching Ho, Ching-Ying Huang, Cheng-Hao Wen, Yu-Che Cheng, Yu-Hung Hsu, Daw-Yang Hwang, Huai-En Lu, Hung-Chun Chen, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 83-87 (2017)
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most prevalent monogenic kidney disorder leading to kidney failure. We generated induced pluripotent stem cells (iPSCs) from a 37-year-old man carrying a PKD1 Q533X mutation who suffered fro
Externí odkaz:
https://doaj.org/article/ea7fa7e2ff9947f89198d0e3caf78711
Autor:
Chin-Hsien Lin, Yu-Che Cheng, Han-I Lin, Ming-Ching Ho, Yu-Hung Hsu, Cheng-Hao Wen, Hui-Wen Ko, Huai-En Lu, Ching-Ying Huang, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 123-127 (2017)
Parkinson's disease (PD) is a progressive neurodegenerative disorder caused by interactions between genetic and environmental factors. Leucine rich repeat kinase (LRRK2) is the most prevalent mutation in autosomal-dominant inheritance of PD. Here, we
Externí odkaz:
https://doaj.org/article/b66f18682c7a433d8fb30e601c600330
Autor:
Ming-Ching Ho, Ching-Ying Huang, Jia-Jung Lee, Shih-Han Hsu, Yu-Che Cheng, Yu-Hung Hsu, Daw-Yang Hwang, Huai-En Lu, Hung-Chun Chen, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 38-41 (2017)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most commonly inherited forms of polycystic kidney disease, and is characterized by the growth of numerous cysts in both kidneys. Here we generated an induced pluripotent stem cell (i
Externí odkaz:
https://doaj.org/article/00e0c51ee16345da8d4d2b6ad197dfcb
Autor:
Yu-Hung Hsu, Yu-Ting Wu, Ching-Ying Huang, Ming-Ching Ho, Yu-Che Cheng, Shih-Han Syu, Huai-En Lu, Yen-Chun Chen, Chia-Ling Tsai, Hung-Ching Lin, Yau-Huei Wei, Yi-Chao Hsu, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 245-249 (2017)
Sensorineural hearing loss (SNHL) is a prevalent form of deafness commonly arising from damage to the cochlear sensory hair cells and degeneration of the spiral ganglion neurons. In this study, Sendai virus was used to generate an induced pluripotent
Externí odkaz:
https://doaj.org/article/32aa0f6da77d4187872ba6dfe65c4340
Autor:
Ching-Ying Huang, Ming-Ching Ho, Jia-Jung Lee, Daw-Yang Hwang, Hui-Wen Ko, Yu-Che Cheng, Yu-Hung Hsu, Huai-En Lu, Hung-Chun Chen, Patrick C.H. Hsieh
Publikováno v:
Stem Cell Research, Vol 24, Iss C, Pp 139-143 (2017)
Autosomal dominant polycystic kidney disease is one of the most prevalent forms of inherited cystic kidney disease, and can be characterized by kidney cyst formation and enlargement. Here we report the generation of a Type 1 ADPKD disease iPS cell li
Externí odkaz:
https://doaj.org/article/95aaa12e2e794cb2bf1830339cf043dc
Autor:
Patrick C.H. Hsieh, Chin-Hsien Lin, Ching-Ying Huang, Ming-Ching Ho, Yu-Che Cheng, Shih-Han Syu, Han-I Lin, Huai-En Lu, Yu-Hung Hsu
Publikováno v:
Stem Cell Research, Vol 28, Iss, Pp 1-5 (2018)
Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK2 p.G2385R is an Asian specific genetic risk factor for sporadic Parkinson's disease. We generated two induced pluripotent stem cells (iPSCs), IBMS-iP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce28788e06385b0fb27c6846acb5caf6
http://www.sciencedirect.com/science/article/pii/S1873506118300400
http://www.sciencedirect.com/science/article/pii/S1873506118300400
Autor:
Patrick C.H. Hsieh, Yu-Hung Hsu, Ming-Ching Ho, Yen-Chun Chen, Yau-Huei Wei, Huai-En Lu, Cheng-Hao Wen, Chia-Ling Tsai, Ching-Ying Huang, Yu-Ting Wu, Yi-Chao Hsu, Hui-Wen Ko, Yu-Che Cheng
Publikováno v:
Stem Cell Research, Vol 27, Iss, Pp 10-14 (2018)
Mitochondrial defects are associated with clinical manifestations from common diseases to rare genetic disorders. Myoclonus epilepsy associated with ragged-red fibers (MERRF) syndrome results from an A to G transition at nucleotide position 8344 in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::010103445119eb1b97bf191f78756e19
http://www.sciencedirect.com/science/article/pii/S1873506117302726
http://www.sciencedirect.com/science/article/pii/S1873506117302726