Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dan-Qing Qin"'
Publikováno v:
Hemoglobin. 46:245-248
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be0bde91df8c78da7d1ccb632b8e4446
https://doi.org/10.1080/03630269.2022.2118604
https://doi.org/10.1080/03630269.2022.2118604
Publikováno v:
Hemoglobin. 46(4)
β-Thalassemia (β-thal), a highly prevalent disease in tropical and subtropical regions of Southern China, is caused mainly by point mutations in the β-globin gene cluster. However, large deletions have also been found to contribute to some types o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b717cad215ac7b0dd023963134046030
https://pubmed.ncbi.nlm.nih.gov/36210651
https://pubmed.ncbi.nlm.nih.gov/36210651
Autor:
Li, DU, Cui-Ze, Yao, Xiu-Qin, Bao, Jie, Liang, Teng-Long, Yuan, Dan-Qing, Qin, Ji-Cheng, Wang
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 29(4)
To investigate whether β-globin gene 3'UTR+101GC (HBB:c.*233GC) variant has genetic effect and provide basis for gene diagnosis and genetic counseling.Whole blood cell analysis and capillary zone electrophoresis (CZE) were used to analyze the hemato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a502ddc76fee08874f70958594260bf7
https://pubmed.ncbi.nlm.nih.gov/34362515
https://pubmed.ncbi.nlm.nih.gov/34362515
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 29(4)
To analyze the hematological characteristics of ChineseHemoglobin electrophoresis and blood routine test were used to analyze the hematological indexes of all peripheral blood samples，PCR-Flow fluorescent hybridization and Gap-PCR were used to dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2e0361a8331bde8237c9a7fc28303dd2
https://pubmed.ncbi.nlm.nih.gov/34362510
https://pubmed.ncbi.nlm.nih.gov/34362510
Autor:
Li Du, Xiangcheng Zhou, Liang Zhang, Dan-Qing Qin, Jian Ma, Ji-Cheng Wang, Cui-Ze Yao, Xiuqin Bao
Background: α-thalassemia, with carrier rates of 11.31% and 17.55% respectively in Guangdong and Guangxi province, is a highly prevalent disease in Southern China and tropical and subtropical regions and is mainly caused by deletion in α-globin gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0275fb74c98ff027b92545611c356c55
https://doi.org/10.21203/rs.3.rs-765129/v1
https://doi.org/10.21203/rs.3.rs-765129/v1
Autor:
Ji-Cheng, Wang, Hao, Guo, Hua-Jie, Huang, Teng-Long, Yuan, Cui-Ze, Yao, Dan-Qing, Qin, Li, DU
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 28(6)
To analyze the hematological characteristics of Hb Broomhill and Hb Hornchurch, and prenatal diagnosis should be carried out in two families.RBC parameters and hemoglobin electrophoretogram were analyzed on the peripheral blood of all patients, and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c699cfa96ec3606d2015634442a52175
https://pubmed.ncbi.nlm.nih.gov/33283737
https://pubmed.ncbi.nlm.nih.gov/33283737
Autor:
Dan-Qing, Qin, Li, DU, Hong-Ke, Ding, Ji-Cheng, Wang, Teng-Long, Yuan, Cui-Ze, Yao, Fei-Fei, Lan
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 28(2)
To investigate the gene diagnosis and phenotypes analysis for a couple with β-thalassemia suspected from of blood routine test and hemoglobin electrophoresis, as well as the prenatal gene diagnosis of the fetus.The gene mutation of β-globin in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a65e54572157d2f4b6f45185373ce11
https://pubmed.ncbi.nlm.nih.gov/32319399
https://pubmed.ncbi.nlm.nih.gov/32319399
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 27(5)
To perform genetic analysis, prenatal diagnosis and preimplantation genetic diagnosis (PGD) in a family with a rare deletional β- thalassemia.Hematological parameters of the peripheral blood collected from all the family members were analyzed by who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce2f8b7009cc51c27cfaaafc248ab02f
https://pubmed.ncbi.nlm.nih.gov/31607316
https://pubmed.ncbi.nlm.nih.gov/31607316