Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yanlian Liang"'
Publikováno v:
Zhongguo shuxue zazhi, Vol 35, Iss 12, Pp 1266-1269 (2022)
Objective To investigate the family inheritance of α-Thalassemla gene and the risk of severe anemia in neonates caused by cold IgG anti-M. Methods ABO, Rh, MN blood groups and the specificity of unexpected antibody were identified by blood group ser
Externí odkaz:
https://doaj.org/article/f96a4ee5ba664bcaa06e99d6b7fec606
Publikováno v:
Zhongguo shuxue zazhi, Vol 35, Iss 9, Pp 887-891 (2022)
Objective To analyze the polymorphisms of GYPA and GYPB mRNA spliceosomes associated with MNS blood group, and to explore the mechanism of subcellular localization of GPA and GPB protein isomerism encoded by various spliceosomes as well as the expres
Externí odkaz:
https://doaj.org/article/a993c7c2fae44767b67beb9b6e369de1
Publikováno v:
Zhongguo shuxue zazhi, Vol 35, Iss 9, Pp 895-899 (2022)
Objective To study the molecular mechanism of 9 samples with rare RhD variants and their RhD epitopes and protein structure. Methods The 9 blood samples with rare RhD variants were collected from 210 644 blood donors of Shenzhen Blood Center. Regular
Externí odkaz:
https://doaj.org/article/7344c2a0c69f4d71bd0d00645159f493
Autor:
Yanlian Liang, Jianwei Ren, Fuling Zhong, Wenxu Hong, Yuqing Su, Fan Wu, Shuang Liang, Jun Liu, Shuanghua Fang, Yanwen Liang, Xiuchu Fan, Jiansuo Lin, Yi Liu, Bo Feng, Yunping Xu
Publikováno v:
Vox sanguinisREFERENCES. 117(5)
The molecular basis of MNS blood group variants is not fully clear yet. In this study, we have characterized mRNA variants of GYPA and GYPB genes to reveal whether alternative RNA splicing may cause antigenic diversity of the MNS system.Total RNA was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b3f2ba6b19829281e81a74f8f11efd3
https://pubmed.ncbi.nlm.nih.gov/35138639
https://pubmed.ncbi.nlm.nih.gov/35138639
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 22(2)
To study the molecular genetic background of B subtype in Chinese Han population and identify novel allele at the ABO locus.Ten samples from randomly selected blood donors of normal B phenotype used as control, and six samples from individuals diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::758ed7f68917000311b5f23637e165d4
https://pubmed.ncbi.nlm.nih.gov/15793770
https://pubmed.ncbi.nlm.nih.gov/15793770