Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Tsung Sheng Su"'
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 44, Iss 1, Pp 52-56 (2005)
Objective: To share our experience of prenatal classical phenylketonuria (PKU) diagnosis using the polymerase chain reaction (PCR), automatic sequencing, and linkage analysis with short tandem repeats (STRs). Materials and Methods: Eight pregnant wom
Externí odkaz:
https://doaj.org/article/8c3b2a1537c3447180fc4e3c565370a6
Autor:
Hung-Kun Chao, Szu-Hui Chiang, Victor Tramjay Fwu, Miao-Zeng Huang, Tsung-Sheng Su, Cheng-Yi Cheng, Ying Liang, Dau-Ming Niu, Kwang-Jen Hsiao
Publikováno v:
Journal of Human Genetics. 59:145-152
Phenylalanine hydroxylase (PAH) deficiency is responsible for most cases of phenylketonuria (PKU). In this study of the PAH mutation spectrum in the Taiwanese population, 139 alleles were identified including 34 different mutations. The V190G, Q267R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01679501b664250968abab24a557815c
https://doi.org/10.1038/jhg.2013.136
https://doi.org/10.1038/jhg.2013.136
Publikováno v:
Biochemical and Biophysical Research Communications. 377:257-261
Argininosuccinate synthetase (ASS), a key enzyme in the urea cycle, participates in many metabolic processes including arginine biosynthesis and the citrulline-nitric oxide (NO) cycle. Factors like diets, hormones and pro-inflammatory stimuli are kno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5909545da61685b10f23c8fee27a26
https://doi.org/10.1016/j.bbrc.2008.09.118
https://doi.org/10.1016/j.bbrc.2008.09.118
Autor:
Tsung Sheng Su, Alice Chien Chang, Ting Fen Tsai, Shih Chang Shiue, Kong-Bung Choo, Miao Zeng Huang, Chiu Jung Huang
Publikováno v:
Journal of Biomedical Science
Background Argininosuccinate synthetase (ASS) participates in urea and nitric oxide production and is a rate-limiting enzyme in arginine biosynthesis. Regulation of ASS expression appears complex and dynamic. In addition to transcriptional regulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19921c22377531420ac227371c6bfdcf
http://europepmc.org/articles/PMC4308890
http://europepmc.org/articles/PMC4308890
Autor:
Ting-Fen Tsai1, Tsung-Sheng Su1,2,3
Publikováno v:
European Journal of Biochemistry. 4/1/95, Vol. 229 Issue 1, p233-238. 6p.
Publikováno v:
Human Genetics. 110:235-243
The liver-specific phenylalanine hydroxylase catalyzes the conversion of phenylalanine to tyrosine. Genetic defects in the gene result in the autosomal recessive disorder phenylketonuria. We have identified a phenylalanine hydroxylase mutation, desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a06664fc1ea1b25764eade6a3ed4cd
https://doi.org/10.1007/s00439-002-0677-7
https://doi.org/10.1007/s00439-002-0677-7
Publikováno v:
Molecular Carcinogenesis. 26:69-73
Exposure to aflatoxin B(1) (AFB(1)) is one of the risk factors for developing hepatoma. In rats, activation of the ras gene is a prevalent event in AFB(1)-induced hepatocarcinogenesis. It is not clear whether a similar event occurs in humans. By anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e073af2a5827ce5983cfa576fec3a23
https://doi.org/10.1002/(sici)1098-2744(199910)26:2<69::aid-mc1>3.0.co
https://doi.org/10.1002/(sici)1098-2744(199910)26:2<69::aid-mc1>3.0.co
Autor:
Wen-Ling Hwang, Tsung-Sheng Su
Publikováno v:
Journal of General Virology. 79:2181-2189
Hepatitis B virus (HBV) polymerase (P) gene is translated from the bicistronic pregenomic RNA with the core (C) gene in the first cistron. The P ORF is preceded by the C AUG and three AUG codons within the C region, where a minicistron of 7 amino aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec54bb8dd7e4be65151aa754ee91aa0c
https://doi.org/10.1099/0022-1317-79-9-2181
https://doi.org/10.1099/0022-1317-79-9-2181
Publikováno v:
DNA and Cell Biology. 17:717-725
Citrullinemia is a human genetic disease caused by a deficient argininosuccinate synthetase. In fibroblasts established from a citrullinemia patient with a mutation at the 3' splice site of the terminal intron of the gene, three cryptic 3' splice sit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d70b201222d3b3db9c2a7a6118ea7d
https://doi.org/10.1089/dna.1998.17.717
https://doi.org/10.1089/dna.1998.17.717
Publikováno v:
Journal of Virological Methods. 51:61-73
Molecular genetic studies have revealed that the human hepatitis B viral (HBV) Pol protein, a polypeptide of about 94 kDa, contains four domains. These are the 5'-terminal protein, spacer, RNA reverse transcriptase/DNA polymerase, and RNase H, respec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b701c0bfbe1be585a6df1b870a48f7bf
https://doi.org/10.1016/0166-0934(94)00118-z
https://doi.org/10.1016/0166-0934(94)00118-z