Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Man-Yu Wu"'
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Dissertation/ Thesis
A Study of Frédéric Chopin's Pedal Technique of 'Nocturnes'
Autor: Man-yu Wu, 吳曼羽
101
This research aims to investigate the pedal technique of F. Chopin’s “Nocturnes.” The author realizes the importance of pedal technique in F. Chopin’s piano works based on the meaning behind pedal writing. The author expects that pia
Externí odkaz: http://ndltd.ncl.edu.tw/handle/79497611117903759908
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4
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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5
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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6
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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7
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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10
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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