about
Blood antioxidant status and urinary levels of catecholamine metabolites in beta-thalassemiaA complex gene superfamily encodes actin in petuniaHemolytic disease of the newborn caused by a new deletion of the entire beta-globin clusterEffect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytesPolymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.Diminished type I collagen synthesis and reduced alpha 1(I) collagen messenger RNA in cultured fibroblasts from patients with dominantly inherited (type I) osteogenesis imperfecta.Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.DNA restriction fragment analysis of the proopiomelanocortin gene in schizophrenia and bipolar disorders.beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin gene.Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.Multiple arrangements of the human embryonic zeta globin genes.A developmentally stable chromatin structure in the human beta-globin gene clusterA beta-thalassemia lesion abolishes the same Mst II site as the sickle mutationRespiratory Burst Enzymes, Pro-Oxidants and Antioxidants Status in Bangladeshi Population with β-Thalassemia Major.Hematological and biochemical status of Beta-thalassemia major patients in Bangladesh: A comparative analysis.Premature translation termination mediates triosephosphate isomerase mRNA degradation.Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.A mutation in the beta-globin gene detected in the progeny of a female mouse treated with ethylnitrosourea."Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.Thalassaemia genes in Peninsular Arabs.A molecular clock based on the expansion of gene families.Thalassemic hemoglobinopathies.Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.Alternate organization of alpha G-Philadelphia globin genes among U.S. black and Italian Caucasian heterozygotes.Generation of a monoclonal antibody specific for Hb G-Philadelphia [alpha 2(68)(E17)Asn----Lys beta 2] and development of an immunoassay.
P2860
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P2860
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年学术文章
@wuu
1982年学术文章
@zh-cn
1982年学术文章
@zh-hans
1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
@yue
1982年學術文章
@zh
1982年學術文章
@zh-hant
name
Thalassemia revisited.
@en
type
label
Thalassemia revisited.
@en
prefLabel
Thalassemia revisited.
@en
P1433
P1476
Thalassemia revisited.
@en
P2093
Weatherall DJ
P356
10.1016/0092-8674(82)90084-8
P407
P577
1982-05-01T00:00:00Z