Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Chun-Lian JIN"'
Autor:
Dong Hua Cao, Xiao Li Liu, Kai Mu, Xiang Wei Ma, Jing Li Sun, Xiao Zhong Bai, Chang Kun Lin, Chun Lian Jin
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 3, Pp 226-230 (2014)
OBJECTIVE: Hemophilia B is caused by coagulation defects in the factor IX gene located in Xq27.1 on the X chromosome. A wide range of mutations, showing extensive molecular heterogeneity, have been described in hemophilia B patients. Our study was ai
Externí odkaz:
https://doaj.org/article/22cf7a9e3f3949109374dbbd69ea790c
Autor:
Jing Li Sun, Xiao Zhong Bai, Xiang Wei Ma, Xiao Li Liu, Chun Lian Jin, Dong Hua Cao, Kai Mu, Chang Kun Lin
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 31, Iss 3, Pp 226-230 (2014)
Turkish Journal of Hematology, Vol 31, Iss 3, Pp 226-230 (2014)
Hemophilia B is caused by coagulation defects in the factor IX gene located in Xq27.1 on the X chromosome. A wide range of mutations, showing extensive molecular heterogeneity, have been described in hemophilia B patients. Our study was aimed at gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::952d7394ea1401ebea282baa699ab1cd
http://europepmc.org/articles/PMC4287022
http://europepmc.org/articles/PMC4287022
Autor:
Xiao-Ming Li, Chun-Yi Li, Yan-Yan Zhao, Cai-Xia Liu, Hong Liu, Gui-Yuan Sun, Kai-Lai Sun, Chun-lian Jin, Guang-rong Qiu, Fangjie Chen, Fu-Cai Li
Publikováno v:
Hereditas (Beijing). 32:397-403
Establishment of integrated course system in human development and genetics is an important part of course reformation, and the improvement of this system is achieved by integrating the content of course, stabilizing teaching force, building teaching
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9f362648831a182199127995a765245
https://doi.org/10.3724/sp.j.1005.2010.00397
https://doi.org/10.3724/sp.j.1005.2010.00397
Publikováno v:
Hereditas (Beijing). 31:1214-1220
To investigate the role of gene Gli3 in idiopathic congenital talipes equinovarus (ICTEV), we constructed the Gli3 luciferase reporter gene expression vectors to analyze the promoter activity of the rat gene Gli3. The regulatory element in the promot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::840a925a1f7da2a8f2338776db3dbe4e
https://doi.org/10.3724/sp.j.1005.2009.01214
https://doi.org/10.3724/sp.j.1005.2009.01214
Publikováno v:
Hereditas (Beijing). 31:600-604
For the past two decades, the dominant methods to identify susceptibility genes of complex disease were linkage analysis and association study. Linkage analysis usually identifies broad intervals, which can encompass dozens to hundreds of candidate g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d63846b8c3585bc2557aa6557ffe93f
https://doi.org/10.3724/sp.j.1005.2009.00600
https://doi.org/10.3724/sp.j.1005.2009.00600
Publikováno v:
Hereditas (Beijing). 30:723-727
RT-PCR was used to detect the expressions of COL1A1 mRNA in 20 patients with idiopathic congenital talipes equinovarus (ICTEV). The primers were designed by Primer 5 according to sequences of -1 031 bp～ +30 bp and the first intron of COL1A1. PCR-DG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49799db3f012c96338a39f61d4e7ad63
https://doi.org/10.3724/sp.j.1005.2008.00723
https://doi.org/10.3724/sp.j.1005.2008.00723
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(5)
To investigate the mechanism of transcription regulation of GLI3 gene in idiopathic congenital talipes equinovarus.pGL3-Gli3 luciferase report vectors were constructed, and the activity of Gli3 promoter was explored. A P-Match software was used to an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ba8282d6164d40c39b74948d23421e7
https://pubmed.ncbi.nlm.nih.gov/23042389
https://pubmed.ncbi.nlm.nih.gov/23042389
Publikováno v:
Molecular medicine reports. 7(3)
The collagen, type IX, alpha 1 (COL9A1) gene was previously identified as a candidate gene for idiopathic congenital talipes equinovarus (ICTEV), a congenital lower limb deformity in humans. In the present study, increased expression levels of COL9A1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aecc4958949c4e2c812f5412e41621da
https://pubmed.ncbi.nlm.nih.gov/23254326
https://pubmed.ncbi.nlm.nih.gov/23254326
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(3)
To investigate the relationship between GLI3 gene and pathogenesis of idiopathic congenital talipes equinovarus (ICTEV).Potential mutations in the coding region of GLI3 were detected among 84 patients with ICTEV by denaturing gradient electrophoresis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4bcf20040ca7a4073e20228bc64e18f9
https://pubmed.ncbi.nlm.nih.gov/22678783
https://pubmed.ncbi.nlm.nih.gov/22678783
Publikováno v:
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 13(6)
COL9A1 gene is located in the susceptibility region of idiopathic congenital talipes equinovarus (ICTEV) (6q12-13). This study aimed to investigate the expression of the COL9A1 gene and the distribution of single nucleotide polymorphism (SNP) of COL9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e3a01bb0e4a7ed7a0bd1d13d3c851a7
https://pubmed.ncbi.nlm.nih.gov/21672422
https://pubmed.ncbi.nlm.nih.gov/21672422