Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xiao-Liu Shi"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract Background Bardet–Biedl syndrome (BBS) is a rare and genetically heterogeneous disease with a broad spectrum of clinical features, including but not limited to rod‐cone dystrophy, postaxial polydactyly, central obesity, intellectual disa
Externí odkaz:
https://doaj.org/article/d7535304d2fb463faf0f5c0e89cefeb6
Autor:
Qing Wang, Zhi-Ping Jiang, Jing Zeng, Yan Zhu, Hua-Lin Cai, Da-Xiong Xiang, Qun He, Xiao-Liu Shi, An-Ni Zhong, Xie-Lan Zhao, Ping Xu
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 23, Iss 1 (2020)
Purpose: We investigated the relationship between imatinib trough concentrations and genetic polymorphisms with efficacy of imatinib in Chinese patients with chronic myeloid leukemia (CML). Methods: There were 171 eligible patients. Peripheral blood
Externí odkaz:
https://doaj.org/article/136b081e766e4cd59a29f9722d206214
Publikováno v:
World Journal of Gastroenterology
Aim To examine the effects of aspirin and enoxaparin on liver function, coagulation index and histopathology in a rat model of liver fibrosis. METHODS Forty-five male Sprague-Dawley rats were randomly divided into the control group (n = 5) and model
Publikováno v:
World Chinese Journal of Digestology. 25:241
Autor:
Hong-Bo, He, Zheng-Mao, Hu, He-Jun, Li, Yong, Zhu, Xiao-Liu, Shi, Guang-Hua, Lei, Jiang-Nan, Zhou, Kang-Hua, Li
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 32(2)
To detect the mutations of EXT2 gene in hereditary multiple exostoses (HME) families and to investigate the sensitivity of denaturant gradient gel electrophoresis (DGGE) in screening the mutations in EXT2 gene.Five HME families and 3 sporadic patient
[Sequence polymorphism of the promoter region of gene STK11 in patients with Peutz-Jeghers syndrome]
Autor:
Xin, Yi, Mao-Jin, Yao, Yong-Jun, Wang, Jian-Guang, Tang, Wen-Feng, Ning, Xiang-Ping, Wang, Shi-Quan, Zhou, Chen-Jie, Li, Fei, Wang, Kun, Xia, Xiao-Liu, Shi
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 32(1)
To explore the relationship between the sequence variation of the promoter region (-1543 approximately -1160) of STK11 gene and the risk of developing Peutz-Jeghers syndrome (PJS).The sequences of the promoter region of 14 PJS patients (7 patients ar
Autor:
Xia, Sun, Xin-Zhen, Yin, Ling-Qian, Wu, Xiao-Liu, Shi, Zheng-Mao, Hu, Xiao-Ping, Liu, Qian, Pan, He-Ping, Dai, Kun, Xia, Jia-Hui, Xia
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 30(5)
To identify the gene causing diffuse palmoplantar keratoderma in a Chinese pedigree.Four normal individuals and 3 patients in a diffuse palmoplantar keratoderma family and 10 unrelated control samples were recruited. The hotspot of the mutations of k
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 29(5)
To make clear the relationship between the X chromosome abnormality and sydromic deafness through genetic analysis of a pedigree with X-linked syndromic deafness.The chromosome number and structure of the family members were analyzed by the standard
Autor:
Zi-An, Xiao, Ding-Hua, Xie, Liang-Qun, Huang, Xiao-Liu, Shi, Kun, Xia, Shu, Yang, Jia-Hui, Xia
Publikováno v:
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 29(4)
To screen and identify the interactive proteins with connexin 26 (Cx26) by the yeast two hybrid technique.The whole coding region of Cx26 (GJB2) gene was amplified from normal human genomic DNA by polymerase chain reaction (PCR). The "bait" Cx26 was
Autor:
Liang-Qun, Huang, Xiao-Liu, Shi, Zhi-Ping, Tan, Hai-Yan, Fang, Duo, Zheng, Jia-Hui, Xia, Kun, Xia
Publikováno v:
Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica. 34(2)
Connexin 31 is a member of connexin family. The carboxy-terminal cytosolic domain of connexin 31 contains several potential phosphorylation sites. In this work, a yeast two-hybrid protein interaction screen have been used to identify proteins that bi