Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hai-xiao Xie"'
Autor:
Le-Yao Xing, Guan-Han Meng, Ji-Xian Yang, Ming-Han Xu, Yi-Ming Xu, Hai-Xiao Xie, Ai-Jie Wang, Yi-Lu Sun
Publikováno v:
Environmental Science and Ecotechnology, Vol 21, Iss , Pp 100422- (2024)
Remediating soil contaminated with polycyclic aromatic hydrocarbons (PAHs) presents a significant environmental challenge due to their toxic and carcinogenic properties. Traditional PAHs remediation methods—chemical, thermal, and bioremediation—a
Externí odkaz:
https://doaj.org/article/078442fae6b74aa0840d78994c30387e
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 28(6)
To analyze the molecular pathogenesis by analysis of phenotype and gene mutation in families with hereditary coagulation factor V (FⅤ) defect caused by complex heterozygous mutation.Plasma pro-thrombin time (PT), activated partial thromboplastin ti
Autor:
Xiao-li Yang, Yong-Ping Chen, Yanhui Jin, Mingshan Wang, Hai-xiao Xie, Bi-cheng Chen, Lihong Yang, Fang-xiu Zheng, Jinchen Li
Publikováno v:
Genetics and molecular research : GMR. 13(2)
We investigated the alteration of coagulation state in a protein C (PC) deficiency pedigree and the impact of the PC gene mutations. The pedigree of a proband with cerebral hemorrhagic infarction had sixteen members with four generations. The plasma
Autor:
Li-hong, Yang, Li-qing, Zhu, Ying-yu, Wang, Hai-xiao, Xie, Yao-sheng, Xie, Yan-hui, Jin, Ming-shan, Wang, Bi-cheng, Chen, Xiao-li, Yang
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 34(9)
To analyze genetic mutation and explore its molecular pathogenesis for an hereditary protein C (PC) deficient consanguineous pedigree.The pedigree included three generations and contained eight members. PC activity (PC:A), PC antigen (PC:Ag) and othe
Autor:
Hai-xiao, Xie, Mei-yan, Lv, Xiao-li, Yang, Ming-shan, Wang, Yang, Zhang, Li-qing, Zhu, Yan-hui, Jin, Li-hong, Yang
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 34(3)
To identify the genotype and pathogenesis in four Chinese pedigrees with Factor Ⅻ deficiency.Activated partial thromboplastin time (APTT), FⅫ procoagulant activity (FⅫ∶C), FⅫ antigen(FⅫ∶Ag)and other coagulant parameters were detecte
Autor:
Yao-sheng, Xie, Yang, Zhang, Li-qing, Zhu, Yan-hui, Jin, Li-hong, Yang, Hai-xiao, Xie, Ming-shan, Wang, Xiao-li, Yang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(2)
To screen potential mutation and explore the underlying mechanism for a consanguineous pedigree featuring hereditary coagulation factor Ⅴ (FⅤ) deficiency.Clinical diagnosis was validated by coagulant parameter assays of prothrombin time (PT), act
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(4)
To investigate potential mutations and clinical features of 9 unrelated patients with inherited coagulation factor VII (FVII) deficiency.Clinical diagnosis was validated by assaying of coagulation parameters including prothrombin time, activated part
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 32(12)
To perform gene analysis and family survey of a patient with combined inherited FVII and FX deficiency, and to identify the gene mutation of this patient.The phenotype diagnosis was validated by coagulant parameter assay on prothrombin time (PT), act
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 28(6)
To analyze genetic mutation and explore its molecular pathogenesis for an hereditary coagulation factor XII(F XII) deficiency in a pedigree featuring consanguineous marriage.Activated partial thromboplastin time (APTT), F XII procoagulant activity (F
[An inherited coagulation factor VII deficiency pedigree caused by homozygous mutation of His348Gln]
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 28(1)
To investigate the gene mutation and the molecular pathogenesis of an inherited coagulation factor VII (F VII) deficiency pedigree with consanguineous marriage.The diagnosis was validated by coagulant parameter assay on the prothrombin time (PT), act