Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.

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A genome-wide association study of red-blood cell fatty acids and ratios incorporating dietary covariates: Framingham Heart Study Offspring Cohort.

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Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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P1476

Genetic Variants at BCL11A and ...... alassemia Intermedia Patients.

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P2093

Biyan Chen

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Chenguang Zheng

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Guojian Li

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Haiyang Zheng

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Hongwei Wei

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Sheng He

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Sheng Yi

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Yun Chen

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Yunli Lai

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P2860

A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.

Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.

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scholarly article

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10.1080/03630269.2016.1253586

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Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.

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P2860

P2860

Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.

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