Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Xue-Wei Tang"'
Publikováno v:
Hemoglobin. 46:137-139
The 3' untranslated region (3'UTR) is associated with mRNA stability because of its involvement in 3' end processing, polyadenylation, and mRNA capping. Mutations located in this area can cause a phenotype compatible with β
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e12b4ff62fa1add109719a3c65bd812d
https://doi.org/10.1080/03630269.2022.2086135
https://doi.org/10.1080/03630269.2022.2086135
Publikováno v:
Hemoglobin. 44:427-431
Genetic recombination between homologous sequences on the human globin gene clusters can lead to the creation of fusion genes. In this study, we report the detection of an α-globin fusion gene by using real-time polymerase chain reaction (qPCR)-base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ffca8e26805fb3e0a68cdd7be677169
https://doi.org/10.1080/03630269.2020.1838923
https://doi.org/10.1080/03630269.2020.1838923
Autor:
Fan Jiang, Xue-Wei Tang, Can Liao, Hang Lu, Dong-Zhi Li, Lian-Dong Zuo, Jian Li, Jian-Ying Zhou, Gui-Lan Chen
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-12 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Individuals with δβ-thalassemia/HPFH and β-thalassemia usually present with intermedia or thalassemia major. No large-scale survey on HPFH/δβ-thalassemia in southern China has been reported to date. The purpose of this study was to ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::401ab652669f046aca7085f3e6286a07
http://link.springer.com/article/10.1186/s12881-020-0981-x
http://link.springer.com/article/10.1186/s12881-020-0981-x
Publikováno v:
Hemoglobin. 45(4)
We describe a new δ/β fusion gene causing β-thalassemia (β-thal) trait and its formation mechanism. The proband was a 39-year-old woman who presented with persistent microcytic microcytosis without iron deficiency. Molecular diagnoses revealed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60d25e66063b637cfd5f829cc56be9f8
https://pubmed.ncbi.nlm.nih.gov/34309467
https://pubmed.ncbi.nlm.nih.gov/34309467
Autor:
Gui-Lan Chen, Fan Jiang, Ai-Ping Ju, Jian Li, Jian-Ying Zhou, Lian-Dong Zuo, Dong-Zhi Li, Xue-Wei Tang
Publikováno v:
Hemoglobin. 44:153-155
Hb Westmead (α122(H5)His>Gln) (HBA2: c.369C>G) is a common α-globin variant causing α-thalassemia (α-thal) in Mainland China. In this study, we report the hematological characteristics in Hb Westme...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9987b915cb299c8d6875638ee783021
https://doi.org/10.1080/03630269.2020.1768109
https://doi.org/10.1080/03630269.2020.1768109
Autor:
Li-Li Xu, Gui-Lan Chen, Jian Li, Xue-Wei Tang, Fan Jiang, Lian-Dong Zuo, Dong-Zhi Li, Jian-Ying Zhou
Publikováno v:
Hemoglobin. 44:86-88
Hb Constant Spring (Hb CS) (HBA2: c.427T>C) is a common α-globin variant causing α-thalassemia (α-thal) phenotypes in mainland China. In this study, we evaluated the efficiency of erythrocyte param...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0bb16d82c3d566a00dba5946a9d50ce
https://doi.org/10.1080/03630269.2020.1755979
https://doi.org/10.1080/03630269.2020.1755979
Publikováno v:
International Journal of Laboratory Hematology. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c4ae02dbd3b29bc25b553cf69a53ac8
https://doi.org/10.1111/ijlh.13505
https://doi.org/10.1111/ijlh.13505
Publikováno v:
International journal of laboratory hematologyREFERENCES. 43(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::416b651e583a9f86ba6a2d37b483c67a
https://pubmed.ncbi.nlm.nih.gov/33687151
https://pubmed.ncbi.nlm.nih.gov/33687151
Autor:
Fan, Jiang, Ai-Ping, Mao, Yin-Yin, Liu, Feng-Zhi, Liu, Yan-Lin, Li, Jian, Li, Jian-Ying, Zhou, Xue-Wei, Tang, Ai-Ping, Ju, Fa-Tao, Li, Jun-Hui, Wan, Lian-Dong, Zuo, Dong-Zhi, Li
Publikováno v:
Gene. 825:146438
Gap- polymerase chain reaction (PCR), reverse dot-blot assay (RDB), real-time PCR based multicolor melting curve analysis (MMCA assay), multiplex ligation-dependent probe amplification (MLPA) and Sanger sequencing are conventional methods to diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb496d6bf8949c371d36fa1e501e227
https://doi.org/10.1016/j.gene.2022.146438
https://doi.org/10.1016/j.gene.2022.146438
Autor:
Fan, Jiang, Ai-Ping, Ju, Jian, Li, Gui-Lan, Chen, Jian-Ying, Zhou, Xue-Wei, Tang, Lian-Dong, Zuo, Dong-Zhi, Li
Publikováno v:
Hemoglobin. 44(3)
Hb Westmead (α122(H5)HisGln) (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac07f88c68354a579ad178ad1f343e84
https://pubmed.ncbi.nlm.nih.gov/32436451
https://pubmed.ncbi.nlm.nih.gov/32436451