Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
about
Customizing the genome as therapy for the β-hemoglobinopathiesEpistasis and the sensitivity of phenotypic screens for beta thalassaemiaThe potential of gene therapy approaches for the treatment of hemoglobinopathies: achievements and challengesHomozygous beta thalassaemia in LiberiaHaemoglobin Lepore in CyprusThalassaemia types and their incidence in SardiniaBeta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.Synthesis of globin chains in sickle -thalassemia.Beta-thalassemia in the American Negro.Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.Free alpha-globin pool in human bone marrow.beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].α-Globin as a molecular target in the treatment of β-thalassemiaThe emergence and maintenance of sickle cell hotspots in the MediterraneanPathophysiology and Clinical Manifestations of the β-Thalassemias.Modification of hemoglobin H disease by sickle trait.A normal beta-globin allele as a modifier gene ameliorating the severity of alpha-thalassemia in mice.Modifier genes in Mendelian disorders: the example of hemoglobin disorders.Acceptance of the 2003 John Howland Award: a journey in clinical research.Understanding α-globin gene regulation and implications for the treatment of β-thalassemia.Emerging cellular and gene therapies for congenital anemias.Equal synthesis of - and -globin chains in erythroid precursors in heterozygous -thalassemia.A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor.Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia.Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia.Pathophysiology and treatment of patients with beta-thalassemia - an update.Letter: Anaemia in beta-thalassaemic carriers.Erythropoiesis: insights into pathophysiology and treatments in 2017.Haemoglobin's chaperone
P2860
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P2860
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
description
1970 nî lūn-bûn
@nan
1970年の論文
@ja
1970年論文
@yue
1970年論文
@zh-hant
1970年論文
@zh-hk
1970年論文
@zh-mo
1970年論文
@zh-tw
1970年论文
@wuu
1970年论文
@zh
1970年论文
@zh-cn
name
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@ast
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@en
type
label
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@ast
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@en
prefLabel
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@ast
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@en
P2860
P356
P1476
Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
@en
P2093
P2860
P304
P356
10.1172/JCI106274
P407
P577
1970-04-01T00:00:00Z