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Ting-Fen Tsai
Ting-Fen Tsai
National Yang Ming Chiao Tung University
在 nycu.edu.tw 的电子邮件经过验证
标题
引用次数
引用次数
年份
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
13148*2021
MicroRNA-122 plays a critical role in liver homeostasis and hepatocarcinogenesis
WC Tsai, SD Hsu, CS Hsu, TC Lai, SJ Chen, R Shen, Y Huang, HC Chen, ...
The Journal of clinical investigation 122 (8), 2884-2897, 2012
9382012
Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice
YF Chen, CH Kao, YT Chen, CH Wang, CY Wu, CY Tsai, FC Liu, ...
Genes & development 23 (10), 1183-1194, 2009
2862009
Genetics of Angelman syndrome
Y Jiang, E Lev-Lehman, J Bressler, TF Tsai, AL Beaudet
The American Journal of Human Genetics 65 (1), 1-6, 1999
2331999
Cul3-KLHL20 ubiquitin ligase governs the turnover of ULK1 and VPS34 complexes to control autophagy termination
CC Liu, YC Lin, YH Chen, CM Chen, LY Pang, HA Chen, PR Wu, MY Lin, ...
Molecular cell 61 (1), 84-97, 2016
2312016
Autophagy suppresses tumorigenesis of hepatitis B virus‐associated hepatocellular carcinoma through degradation of microRNA‐224
SH Lan, SY Wu, R Zuchini, XZ Lin, IJ Su, TF Tsai, YJ Lin, CT Wu, HS Liu
Hepatology 59 (2), 505-517, 2014
2142014
The Spectrum of Mutations in UBE3A Causing Angelman Syndrome
P Fang, E Lev-Lehman, TF Tsai, T Matsuura, CS Benton, JS Sutcliffe, ...
Human molecular genetics 8 (1), 129-135, 1999
2051999
Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing …
TF Tsai, Y Jiang, J Bressler, D Armstrong, AL Beaudet
Human molecular genetics 8 (8), 1357-1364, 1999
1931999
Imprinting in angelman and Prader-Willi syndromes
Y Jiang, TF Tsai, J Bressler, AL Beaudet
Current opinion in genetics & development 8 (3), 334-342, 1998
1511998
Blocking of G1/S transition and cell death in the regenerating liver of Hepatitis B virus X protein transgenic mice
BK Wu, CC Li, HJ Chen, JL Chang, KS Jeng, CK Chou, MT Hsu, TF Tsai
Biochemical and biophysical research communications 340 (3), 916-928, 2006
1402006
Enhanced expression of vascular endothelial growth factor‐A in ground glass hepatocytes and its implication in hepatitis B virus hepatocarcinogenesis
JC Yang, CF Teng, HC Wu, HW Tsai, HC Chuang, TF Tsai, YH Hsu, ...
Hepatology 49 (6), 1962-1971, 2009
1292009
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
J Bressler, TF Tsai, MY Wu, SF Tsai, MA Ramirez, D Armstrong, ...
Nature genetics 28 (3), 232-240, 2001
1292001
HURP permits MTOC sorting for robust meiotic spindle bipolarity, similar to extra centrosome clustering in cancer cells
M Breuer, A Kolano, M Kwon, CC Li, TF Tsai, D Pellman, S Brunet, ...
Journal of Cell Biology 191 (7), 1251-1260, 2010
1272010
Hepatitis B virus X protein enhances the transcriptional activity of the androgen receptor through c‐Src and glycogen synthase kinase‐3β kinase pathways
WJ Yang, CJ Chang, SH Yeh, WH Lin, SH Wang, TF Tsai, DS Chen, ...
Hepatology 49 (5), 1515-1524, 2009
1202009
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
TF Tsai, D Armstrong, AL Beaudet
Nature genetics 22 (1), 15-16, 1999
1141999
CLEC4F is an inducible C-type lectin in F4/80-positive cells and is involved in alpha-galactosylceramide presentation in liver
CY Yang, JB Chen, TF Tsai, YC Tsai, CY Tsai, PH Liang, TL Hsu, CY Wu, ...
PloS one 8 (6), e65070, 2013
1132013
Wolfram Syndrome protein, Miner1, regulates sulphydryl redox status, the unfolded protein response, and Ca2+ homeostasis
SE Wiley, AY Andreyev, AS Divakaruni, R Karisch, G Perkins, EA Wall, ...
EMBO molecular medicine 5 (6), 904-918, 2013
1102013
Glycine N‐methyltransferase−/− mice develop chronic hepatitis and glycogen storage disease in the liver
SP Liu, YS Li, YJ Chen, EP Chiang, AFY Li, YH Lee, TF Tsai, M Hsiao, ...
Hepatology 46 (5), 1413-1425, 2007
1082007
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain
MY Wu, TF Tsai, AL Beaudet
Genes & development 20 (20), 2859-2870, 2006
1062006
Cisd2 modulates the differentiation and functioning of adipocytes by regulating intracellular Ca2+ homeostasis
CH Wang, YF Chen, CY Wu, PC Wu, YL Huang, CH Kao, CH Lin, LS Kao, ...
Human molecular genetics 23 (18), 4770-4785, 2014
972014
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