Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Man-Yu Wu"'
2
Frequencies of HKααand anti-HKααAlleles in Chinese Carriers of Silent Deletionalα-Thalassemia
Autor: Jian Li, Dong-Zhi Li, Man-Yu Wu, Yan Li, Shu-Chen Li
Publikováno v: Hemoglobin. 39:407-411
The HKαα (HongKongαα) allele is an unusual rearrangement of the α-globin gene cluster containing both the -α(3.7) (rightward) and ααα(anti 4.2) crossover deletion/duplication. The anti-HKαα (anti-HongKongαα) allele is the reciprocal prod
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c92fe879a9e89fb4d288e6f0f4043e01
https://doi.org/10.3109/03630269.2015.1071268
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3
Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child
Autor: Man-Yu Wu, Sha Liu, Yongling Zhang, Dong-Zhi Li, Hua Jiang
Publikováno v: Pediatric Hematology and Oncology. 32:349-353
Thalassemia intermedia is an inherited hemoglobin disorder characterized by a significant genetic and clinical heterogeneity. A wide spectrum of different genotypes-homozygous, heterozygous, and compound heterozygous-have been found to be responsible
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f043dd792bc789da6ccd7c89100761a4
https://doi.org/10.3109/08880018.2015.1040932
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4
A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia
Autor: Man-Yu Wu, Yi He, Jin-Mei Yan, Dong-Zhi Li
Publikováno v: British Journal of Haematology. 176:984-986
Keywords: human α-globin gene (HBA1/2); regulation; hemoglobin; thalassaemia; hypersensitive site
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::75f462b6a67e30bb9022ca532dcb64bb
https://doi.org/10.1111/bjh.14005
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6
The Codon 35 (A > G) (HBB: c.107A > G) at theα-βChain Interface of theβ-Globin Gene: A Silent Mutation?
Autor: Man-Yu Wu, Dong-Zhi Li
Publikováno v: Hemoglobin. 40:56-58
Tyr35β is located at the convergence of the α1β1, α1β2 and α1α2 interfaces of Hb A. We here report a Chinese family in whom the codon 35 (A > G) (HBB: c.107A > G) mutation of the β-globin gene was not associated with the thalassemic phenotype
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::20d7805721f14b625b15741dcf5d2346
https://doi.org/10.3109/03630269.2015.1099547
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9
The Codon 35 (A G) (HBB: c.107A G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?
Autor: Man-Yu, Wu, Dong-Zhi, Li
Publikováno v: Hemoglobin. 40(1)
Tyr35β is located at the convergence of the α1β1, α1β2 and α1α2 interfaces of Hb A. We here report a Chinese family in whom the codon 35 (A G) (HBB: c.107A G) mutation of the β-globin gene was not associated with the thalassemic phenotype pre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b4b3256afea8c6a496b43e22c836cf4c
https://pubmed.ncbi.nlm.nih.gov/26754300
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10
Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population
Autor: Dong-Zhi Li, Xing-Mei Xie, Man-Yu Wu
Publikováno v: Hemoglobin. 39(6)
α(+)-Thalassemia (α(+)-thal) is common in Southern China. The high frequency could be due to over dominant selection through malaria. Two molecular mechanisms that produce α(+)-thal have been defined; one results in the -α(3.7) (rightward) deleti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6f6eace177b44f9549f244264e49b9d
https://pubmed.ncbi.nlm.nih.gov/26290492
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