about
Hemoglobinopathic erythrocytosis due to a new electrophoretically silent variant, hemoglobin San Diego (beta109 (G11)val--met)Hemoglobin Hiroshima (beta-143 histidine--aspartic acid): a newly identified fast moving beta chain variant associated with increased oxygen affinity and compensatory erythremiaThrombocytopenia and erythrocytosis in mice with a mutation in the gene encoding the hemoglobin β minor chain.Hemoglobin Yakina. II. High blood oxygen affinity associated with compensatory erythrocytosis and normal hemodynamicsHemoglobin Syracuse (alpha2beta2-143(H21)His leads to Pro), a new high-affinity variant detected by special electrophoretic methods. Observations on the auto-oxidation of normal and variant hemoglobinsHemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemia.Hemoglobin olympia ( 20 valine leads to methionine): an electrophoretically silent variant associated with high oxygen affinity and erythrocytosisHemoglobin brigham (alpha2Abeta2100 Pro--Leu). Hemoglobin variant associated with familial erythrocytosis.Erythrocytosis associated with hemoglobin Rainier: oxygen equilibria and marrow regulationRestoring allosterism with compensatory mutations in hemoglobinHb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant.Hb Setif: G1 (94) Asp-Tyr. A new chain hemoglobin variant with substitution of the residue involved in hydrogen bond between unlike subunits.Polycythaemia and high affinity haemoglobins.2,3-Diphosphoglycerate: its role in health and disease.Multiple hemoglobin alpha-chain loci in monkeys, apes, and man.Table of abnormal human globins.Diseases of function and stability of haemoglobin.Structure-function relations of human hemoglobins.Hemoglobin Yoshizuka (G10(108)beta asparagine--aspartic acid): a new variant with a reduced oxygen affinity from a Japanese family.Subunit dissociation of certain abnormal human hemoglobins.Hemoglobin variants.Properties of a recombinant human hemoglobin with aspartic acid 99(beta), an important intersubunit contact site, substituted by lysine.A recombinant human hemoglobin with asparagine-102(beta) substituted by alanine has a limiting low oxygen affinity, reduced marginally by chloride.Moleuclar pathology of human haemoglobin: stereochemical interpretation of abnormal oxygen affinities.A proposed mechanism for subunit interaction in hemoglobin.Secondary erythrocytosis due to compound homozygosity, but not compound heterozygosity, for Hb Luton and α-thalassemia: a family study.Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine.Molecular Pathology of Human Haemoglobin
P2860
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P2860
description
1967 nî lūn-bûn
@nan
1967 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1967 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1967年の論文
@ja
1967年論文
@yue
1967年論文
@zh-hant
1967年論文
@zh-hk
1967年論文
@zh-mo
1967年論文
@zh-tw
1967年论文
@wuu
name
Hemoglobin Yakina. I. Clinical and biochemical studies
@ast
Hemoglobin Yakina. I. Clinical and biochemical studies
@en
Hemoglobin Yakina. I. Clinical and biochemical studies
@nl
type
label
Hemoglobin Yakina. I. Clinical and biochemical studies
@ast
Hemoglobin Yakina. I. Clinical and biochemical studies
@en
Hemoglobin Yakina. I. Clinical and biochemical studies
@nl
prefLabel
Hemoglobin Yakina. I. Clinical and biochemical studies
@ast
Hemoglobin Yakina. I. Clinical and biochemical studies
@en
Hemoglobin Yakina. I. Clinical and biochemical studies
@nl
P2093
P2860
P356
P1476
Hemoglobin Yakina. I. Clinical and biochemical studies
@en
P2093
P2860
P304
P356
10.1172/JCI105674
P407
P577
1967-11-01T00:00:00Z