Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Yu-Shu Shih"'
Autor:
Hsiao-Wen Kao, Der-Cherng Liang, Jin-Hou Wu, Ming-Chung Kuo, Po-Nan Wang, Chao-Ping Yang, Yu-Shu Shih, Tung-Huei Lin, Yu-Hui Huang, Lee-Yung Shih
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 16, Iss 6, Pp 481-488 (2014)
Minimally differentiated acute myeloid leukemia (AML-M0) is a rare subtype of AML with poor prognosis. Although genetic alterations are increasingly reported in AML, the gene mutations have not been comprehensively studied in AML-M0. We aimed to exam
Externí odkaz:
https://doaj.org/article/a937f8574a3a4612af6fec7fb555354d
Autor:
Hsiao-Wen Kao, Masashi Sanada, Der-Cherng Liang, Chang-Liang Lai, En-Hui Lee, Ming-Chung Kuo, Tung-Liang Lin, Yu-Shu Shih, Jin-Hou Wu, Chein-Fuang Huang, Seishi Ogawa, Lee-Yung Shih
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 13, Iss 11, Pp 1035-1042 (2011)
The molecular pathogenesis of myelodysplastic syndrome (MDS) and its progression to secondary acute myeloid leukemia (sAML) remain to be explored. Somatic C-CBL mutations were recently described in MDS. Our study aimed to determine the role of C-CBL
Externí odkaz:
https://doaj.org/article/942611ed06c648c58ce9c205bbd2f627
Autor:
Tung-Liang Lin, Yasunobu Nagata, Hsiao-Wen Kao, Masashi Sanada, Yusuke Okuno, Chein-Fuang Huang, Der-Cherng Liang, Ming-Chung Kuo, Chang-Liang Lai, En-Hui Lee, Yu-Shu Shih, Hiroko Tanaka, Yuichi Shiraishi, Kenichi Chiba, Tung-Huei Lin, Jin-Hou Wu, Satoru Miyano, Seishi Ogawa, Lee-Yung Shih
Publikováno v:
Haematologica, Vol 99, Iss 1 (2014)
Somatic mutations of TET2, IDH1, and IDH2 have been described in myelodysplastic syndrome. The impact of these mutations on outcome of myelodysplastic syndrome and their progression to secondary acute myeloid leukemia remains unclear. Mutation status
Externí odkaz:
https://doaj.org/article/d53cabcadf364b7ab452678d42049b06
Autor:
Yu-shu shih, 石昱書
89
The objectives were to investigate the in vivo and in vitro regulation of gonadotropin-releasing hormone (GnRH) and gonadotropin II (GTH II) using sex steroids in the protandrous black porgy, Acanthopagrus schlegeli. Estradiol-17b (E2) signif
The objectives were to investigate the in vivo and in vitro regulation of gonadotropin-releasing hormone (GnRH) and gonadotropin II (GTH II) using sex steroids in the protandrous black porgy, Acanthopagrus schlegeli. Estradiol-17b (E2) signif
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/59843834508625797914
Autor:
Der-Cherng Liang, Ming-Chun Chiu, Tung-Huei Lin, Yu-Shu Shih, Chein-Fuang Huang, Ming-Chung Kuo, Ying-Jung Huang, Sung-Tzu Liang, Lee-Yung Shih, Shu-Chun Tsai
Supplementary Figure S1 and Tables S1-3. Figure S1. Frequencies and distribution of co-operating mutations in RUNX1 mutationpositive patients. Table S1. Comparison of clinicohematological characteristics according to the biological activities of RUNX
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e6ea4418272604a22f5910130ebe7e
https://doi.org/10.1158/1078-0432.22455140.v1
https://doi.org/10.1158/1078-0432.22455140.v1
Autor:
Der-Cherng Liang, Ming-Chun Chiu, Tung-Huei Lin, Yu-Shu Shih, Chein-Fuang Huang, Ming-Chung Kuo, Ying-Jung Huang, Sung-Tzu Liang, Lee-Yung Shih, Shu-Chun Tsai
Purpose: Transcription factor RUNX1 is essential for normal hematopoiesis. High mutation frequencies of RUNX1 gene in chronic myelomonocytic leukemia (CMML) and myelodysplastic syndromes (MDS) have been described, whereas the biologic significances o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fd03bb25b98934bd954dbbef9f9399c
https://doi.org/10.1158/1078-0432.c.6522935.v1
https://doi.org/10.1158/1078-0432.c.6522935.v1
Autor:
Tung-Huei Lin, Hsiao-Wen Kao, Ming-Chung Kuo, Yu-Shu Shih, Po-Nan Wang, Chao-Ping Yang, Yu-Hui Huang, Der-Cherng Liang, Lee-Yung Shih, Jin-Hou Wu
Publikováno v:
Neoplasia (New York, N.Y.)
Neoplasia: An International Journal for Oncology Research, Vol 16, Iss 6, Pp 481-488 (2014)
Neoplasia: An International Journal for Oncology Research, Vol 16, Iss 6, Pp 481-488 (2014)
Minimally differentiated acute myeloid leukemia (AML-M0) is a rare subtype of AML with poor prognosis. Although genetic alterations are increasingly reported in AML, the gene mutations have not been comprehensively studied in AML-M0. We aimed to exam
Autor:
Yasunobu Nagata, Chang-Liang Lai, Masashi Sanada, Kenichi Chiba, Satoru Miyano, Yuichi Shiraishi, Seishi Ogawa, Ming-Chung Kuo, Lee-Yung Shih, Hiroko Tanaka, Chein-Fuang Huang, Jin-Hou Wu, Der-Cherng Liang, Tung-Huei Lin, Tung-Liang Lin, En-Hui Lee, Hsiao-Wen Kao, Yu-Shu Shih, Yusuke Okuno
Publikováno v:
Haematologica. 99:28-36
Somatic mutations of TET2, IDH1, and IDH2 have been described in myelodysplastic syndrome. The impact of these mutations on outcome of myelodysplastic syndrome and their progression to secondary acute myeloid leukemia remains unclear. Mutation status
Autor:
Yu-Shu Shih, Der-Cherng Liang, Ting-Chi Yeh, Yu-Hui Huang, Tang-Her Jaing, Iou-Jih Hung, Ying-Jung Huang, Jen-Yin Hou, Lee-Yung Shih, Tung-Huei Lin, Chao-Ping Yang, Shih-Hsiang Chen, Hsi-Che Liu
Publikováno v:
Blood. 121:2988-2995
Gene mutations involving epigenetic regulators recently have been described in adult acute myeloid leukemia (AML). Similar studies are limited in children. We analyzed gene mutations and cooperation in pediatric AML with special reference on mutated
Autor:
Tung-Liang Lin, Jin-Hou Wu, Tung-Huei Lin, Sung-Tzu Liang, Yu-Shu Shih, Po-Nan Wang, Der-Cherng Liang, Chen-Yu Lai, Lee-Yung Shih, Hsiao-Wen Kao, Chun-Hui Lin, Po Dunn, Ming-Chung Kuo
Publikováno v:
Oncotarget
// Hsiao-Wen Kao 1, 2 , Der-Cherng Liang 3 , Ming-Chung Kuo 1, 4 , Jin-Hou Wu 1 , Po Dunn 1, 4 , Po-Nan Wang 1 , Tung-Liang Lin 1 , Yu-Shu Shih 1 , Sung-Tzu Liang 3 , Tung-Huei Lin 1 , Chen-Yu Lai 4 , Chun-Hui Lin 3 , Lee-Yung Shih 1, 4 1 Division of