Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jyh-Chwan Wang"'
Autor:
Yi-Hao Yen, Jyh-Chwan Wang, Chao-Hung Hung, Sheng-Nan Lu, Jing-Houng Wang, Tsung-Hui Hu, Kwong-Ming Kee, Chang-Chun Hsiao, Chuan-Mo Lee
Publikováno v:
Journal of the Formosan Medical Association, Vol 114, Iss 7, Pp 652-658 (2015)
Whether serum proteome changes can predict treatment response in chronic hepatitis C remains unclear. We investigated the association between serum proteome changes and virological responses in chronic hepatitis C virus genotype 1b (HCV-1b) patients
Externí odkaz:
https://doaj.org/article/fdb589a0dd7f42d48bb52d23e48948a2
Autor:
Sheng Nan Lu, Chao-Hung Hung, Chuan Mo Lee, Chien-Hung Chen, Jing Houng Wang, Tsung Hui Hu, Chi Sin Changchien, Jyh–Chwan Wang
Publikováno v:
Gastroenterology. 133:1466-1474
Background & Aims: This longitudinal study investigated the interactions and roles of hepatitis B virus (HBV) genotypes, pre-S deletions, and core promoter and precore mutations on the progression of liver disease in hepatitis B e antigen (HBeAg)-neg
Autor:
Jyh-Chwan Wang, Tsung-Hui Hu, Chi-Sin Changchien, Jing-Houng Wang, Chao-Hung Hung, Sheng-Nan Lu, Chien-Hung Chen, Chuan-Mo Lee
Publikováno v:
Journal of Hepatology. 44:76-82
The aim of this study was to compare the serial sequence changes of precore and core promoter regions in hepatitis B e antigen (HBeAg)-positive chronic hepatitis B (CHB) patients with and without HBeAg clearance in lamivudine treatment.Precore and co
Autor:
Cheng-Ho Tsai, Yu-San Chou, Hsin-Fu Liu, Jan-Gowth Chang, Tzu-Yao Yang, Hung-I Yeh, Jyh-Chwan Wang, Nancy M. Wang
Publikováno v:
International Journal of Cardiology. 73:191-195
Recent studies have shown that a C825T polymorphism of the gene encoding the G protein beta3 subunit contributes to the genesis of essential hypertension. However, the link between the gene and blood pressure is not consistently found in different po
Autor:
Chang Hai Tsai, Jan-Gowth Chang, Yuh-Jyh Jong, Shuan-Pei Lin, Chih-Peng Chang, Hung Li, Cheng Chun Lee, Jyh Chwan Wang, Tzu Yao Yang, Hsiu Mei Hsieh-Li
Publikováno v:
Journal of the Neurological Sciences. 173:147-153
Spinal muscular atrophy (SMA) is a disorder characterized by degeneration of the anterior horn cells of the spinal cord. The gene most highly associated with SMA is the survival motor neuron (SMN) gene. In this study, we present an analysis of messen
Autor:
Jyh-Chwan Wang, Mu-Ching Shih, Yi-Jen Chen, Jan-Gowth Chang, Chih-Peng Chang, Liuh-L Perng, Matty Tsai, Shou-Tung Chen, Kun-Tu Yeh, Shi-Yau Yu
Publikováno v:
Cancer Investigation. 18:123-129
Loss of heterozygosity of chromosome 10q has been reported in hepatoma. Areas with a high rate of loss of genetic material could harbor putative tumor suppressor genes. PTEN/MMAC1, a candidate tumor suppressor gene located at chromosome 10q23.3, has
Autor:
Hsi-Huang Tseng, Chih-Peng Chang, Jyh-Chwan Wang, Jan-Gowth Chang, Hsiao-Jui Wei, Tsung-Hsien Su, Ting-An Chang
Publikováno v:
International Journal of Cancer. 76:216-222
Carcinoma of the uterine cervix is a common malignancy, and many affected women, have been found to exhibit loss of heterozygosity (LOH) in the chromosome 3p region. Recent studies have localized the FHIT (fragile histidine triad) gene in this region
Autor:
Chaur Jong Hu, Jan-Gowth Chang, Man Chi Lo, Wen Pin Wang, Jyh Chwan Wang, Chih-Peng Chang, Yuh-Jyh Jong
Publikováno v:
Clinical Chemistry. 44:270-274
A 1.5-Mb duplication on chromosome 17p11.2-p12 (CMT1A duplication) caused by a misalignment of the CMT1A repeat sequences (CMT1A-REPs) is associated with Charcot–Marie–Tooth disease type 1A (CMT1A). A hotspot of crossover breakpoints located in a
Publikováno v:
American Journal of Hematology. 52:243-247
Prenatal diagnosis was carried out on a woman who had previously given birth to a son with a spontaneous mutation of C-->T transition at nt 31133 of the factor IX (F.IX) gene. The diagnosis was performed on chorionic villi sampling by the method of a
Human RhDel Is Caused by a Deletion of 1,013 bp Between Introns 8 and 9 Including Exon 9 of RHD Gene
Autor:
Jan-Gowth Chang, Jyh-Chwan Wang, Tzu-Yao Yang, Kun-Wu Tsan, Mu-Ching Shih, Ching-Tien Peng, Chang-Hai Tsai
Publikováno v:
Blood. 92:2602-2604