Moleuclar pathology of human haemoglobin: stereochemical interpretation of abnormal oxygen affinities.
about
Nature of O2 and CO binding to metalloporphyrins and heme proteinsHemoglobinopathic erythrocytosis due to a new electrophoretically silent variant, hemoglobin San Diego (beta109 (G11)val--met)Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.Myoglobin in primary muscular disease. I. Duchenne muscular dystrophy. II. Muscular dystrophy of distal typeProtein-heme interaction in hemoglobin: evidence from Raman difference spectroscopy.Carbon monoxide binding to iron porphyrinsStructural and functional studies on hemoglobin Bethesda (alpha2beta2 145His), a varient associated with compensatory erythrocytosis.Erythrocyte function and marrow regulation in hemoglobin Bethesda (beta-145 histidine)Oxygen equilibrium of hemoglobin EHemoglobin San Diego (beta 109 (G11) val--met). Crystal structure of the deoxy formHemoglobin 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 Okaloosa (beta 48 (CD7) leucine leads to arginine). An unstable variant with low oxygen affinity.Allostery and cooperativity revisited.Hemoglobin E: its oxygen affinity in relation with the ionic environment.Allosteric interpretation of haemoglobin properties.Polycythaemia and high affinity haemoglobins.A hypothesis for the increased oxygen affinity in haemoglobin Malmö.Methods for detection of hemoglobin variants and hemoglobinopathies in the routine clinical laboratory.Climbing mountains: a profile of Max Perutz 1914-2002: a life in science.Polar bear hemoglobin and human Hb A0: same 2,3-diphosphoglycerate binding site but asymmetry of the binding?The oxygen affinity of haemoglobin Hammersmith.Application of an automatic oxygenation technique to analysis of oxygen equilibrium curves for hemoglobinopathic red cells and functional screening of clinically important hemoglobinopathies.Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect.Hemoglobin A2 Honai (alpha 2 delta 2(90)(F6)Glu----Val): a new delta chain variant.A silent hemoglobin variant detected by HPLC: hemoglobin City of Hope beta 69 (E13) Gly----Ser.Hb Watts [alpha 74(EF3) or alpha 75(EF4)Asp-->0]: a shortened alpha chain variant due to the deletion of three nucleotides in exon 2 of the alpha 2-globin gene.Hb Agenogi [β90(F6)Glu→Lys (GAG>AAG) HBB: c.271G>A)] in a Pregnant Thai Woman.Comparative structure of myoglobin: primates and tree-shrew.Employing aqueous CdTe quantum dots with diversified surface functionalities to discriminate between heme (Fe(ii)) and hemin (Fe(iii))
P2860
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P2860
Moleuclar pathology of human haemoglobin: stereochemical interpretation of abnormal oxygen affinities.
description
1971 nî lūn-bûn
@nan
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
1971年學術文章
@zh
1971年學術文章
@zh-hant
name
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@en
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@nl
type
label
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@en
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@nl
prefLabel
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@en
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@nl
P2093
P356
P1433
P1476
Moleuclar pathology of human h ...... of abnormal oxygen affinities.
@en
P2093
P2860
P2888
P304
P356
10.1038/232408A0
P407
P577
1971-08-01T00:00:00Z
P6179
1005825097