Fuu Jen Tsai
China Medical University (Taiwan)
1017 Papers
7.8K Citations
Fuu Jen Tsai is an academic researcher from China Medical University (Taiwan). The author has contributed to research in topics: Genotype & Medicine. The author has an hindex of 63, co-authored 1012 publications. Previous affiliations of Fuu Jen Tsai include Tatung University & Taipei Physical Education College.
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Papers
An increase in phosphorylation and truncation of crystallin with the progression of cataracts.
TL;DR: Crystallin αB and βA4 and phosphorylation and truncation of crystallin in the lens might contribute to the formation of cataracts.
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The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese
Yun-Ping Lim,Yu An Hsu,Kun Hsi Tsai,Fuu Jen Tsai,Cheng Yuan Peng,Wen Ling Liao,Dong-Zong Hung,Ni Tien,Ni Tien,Chien Yih Lin,Lei Wan,Lei Wan +11 more
TL;DR: The presence of STAT6 SNPs and the association with SVR demonstrated that STAT6 polymorphisms might influence the therapeutic outcomes of patients infected with HCV-1 under standard-of-care (SOC) treatment.
Association of genetic variations in GNB1 with response to peginterferon plus ribavirin therapy for chronic hepatitis C in a Chinese population in Taiwan
Yun-Ping Lim,Fuu Jen Tsai,Wen Ling Liao,Ni Tien,Ni Tien,Dong-Zong Hung,Cheng Yuan Peng,Lei Wan,Lei Wan +8 more
TL;DR: The data for GNB 1 SNPs and the association of RVR showed that GNB1 polymorphisms might be associated with the therapeutic outcomes of HCV-1 andHCV-2 infected patients under standard of care (SOC) treatment.
Association of the PLEKHO2 and PLEKHH1 gene polymorphisms with type 2 diabetic retinopathy in a Taiwanese population
Eric C. Han,Yu Chuen Huang,Jane-Ming Lin,Hui Ju Lin,Jer-Yuarn Wu,Cheng-Chun Lee,Fuu Jen Tsai +6 more
TL;DR: The current findings suggest that the rs832882 and rs3742872 polymorphisms may be harbouring retinopathy susceptibility in a Taiwanese population, and implicate the pathological role of PH domain-containing proteins in DR development.
Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency
TL;DR: It is recommended that more methods, including microsatellite linkage analysis and direct sequencing, should be performed with direct amplification of known mutations in prenatal diagnosis of CAH to avoid misdiagnosis.
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