Abnormal Haem Binding and Globin SH Group Blockade in Unstable Haemoglobins

No abstract is available for this paper.

• Publication year

  1968

• Venue

  Nature

• Publication date

  1968-06-29

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/2181214A0PMID 4968903
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Exchange of heme among hemoglobins and between hemoglobin and albumin.

  1968cited by this paper
• Haemoglobin sydney: Beta-67 (E11) valine modified to alanine: an emerging pattern of unstable haemoglobins.

  1967cited by this paper
• On the mechanism of the dissociation of haemoglobin.

  1967cited by this paper
• Haemoglobin Sydney: β67 (EII) Valine→ Alanine : an Emerging Pattern of Unstable Haemoglobins

  1967cited by this paper
• A study of the conformation of human globin in solution by optical methods.

  1967cited by this paper
• Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)

  1967cited by this paper
• Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser).

  1967cited by this paper
• Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body Anaemia

  1966cited by this paper
• Exchange of heme among hemoglobin molecules.

  1966cited by this paper
• ABSORPTION SPECTRA OF INCLUSION BODIES IN BETA-THALASSEMIA.

  1965cited by this paper
• OXIDATIVE HEMOLYSIS AND ERYTHROCYTE METABOLISM IN HEREDITARY ACATALASIA.

  1965cited by this paper
• Brief Report: Absorption Spectra of Inclusion Bodies in β-Thalassemia

  1965cited by this paper
• Structure and function of haemoglobin: I. A tentative atomic model of horse oxyhaemoglobin

  1965cited by this paper
• THE CHARACTERIZATION OF MODIFIED HUMAN HEMOGLOBIN. I. REACTION WITH IODOACETAMIDE AND N-ETHYLMALEIMIDE.

  1964cited by this paper
• Hereditary Heinz‐Body Anaemia

  1964cited by this paper
• Effects of sulfhydryl inhibition on red blood cells. I. Mechanism of hemolysis.

  1962cited by this paper
• Effects of sulfhydryl inhibition on red blood cells. II. Studies in vivo.

  1962cited by this paper
• Oxidative hemolysis and precipitation of hemoglobin. II. Role of thiols in oxidant drug action.

  1961cited by this paper
• Oxidative hemolysis and precipitation of hemoglobin. I. Heinz body anemias as an acceleration of red cell aging.

  1960cited by this paper
• Studies on the structure of hemoglobin. II. Properties of reconstituted protohemoglobin and protoporphyrin-globin.

  1959cited by this paper
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  1959cited by this paper
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  1958cited by this paper
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  1958cited by this paper
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  1954cited by this paper

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  1994cites this paper
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  1980cites this paper
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  1980cites this paper
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  1980cites this paper
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  1978cites this paper
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  1978cites this paper
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  1978cites this paper
• Reconstitution of native human hemoglobin from separated globin chains and alloplex intermediates.

  1977cites this paper
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  1976cites this paper
• Role of pentose-phosphate pathway in haemolytic crisis of chronic copper toxicity of sheep.

  1976cites this paper
• Reactions of phenyldiazene and ring-substituted phenyldiazenes with ferrihemoglobin.

  1976cites this paper
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  1976cites this paper
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  1976cites this paper
• UNSTABLE‐HAEMOGLOBIN HAEMOLYTIC ANAEMIA

  1976cites this paper
• The unstable haemoglobins.

  1976cites this paper
• Reactivity of the beta-93 SH groups in Hb Köln.

  1976cites this paper
• Altered Erythropoiesis and Increased Hemolysis in Hemoglobin M Akita (M Hyde Park 692 His → Tyr) Disease

  1976cites this paper
• Hemoglobin E, an oxidatively unstable mutation.

  1975cites this paper
• Mechanism of induction of haemolytic anaemia by phenylhydrazine

  1975cites this paper
• Chapter 31 – Drugs, Hormones, and the Red Cell

  1975cites this paper
• Chapter 5 – The Morphology of Adult Red Cells

  1974cites this paper
• Cation content and transport characteristics of the sickle-cell erythrocyte and their relationship with structural changes in the membrane.

  1974cites this paper
• Studies of hemoglobin denaturation and Heinz body formation in the unstable hemoglobins.

  1974cites this paper
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  1974cites this paper
• Studies on the mechanism of the effect of hydroxylamine on hemoglobin assembly in rabbit reticulocytes.

  1974cites this paper
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  1974cites this paper
• Hemoglobin Abraham Lincoln, beta32 (B14) leucine leads to proline. An unstable variant producing severe hemolytic disease.

  1973cites this paper
• Hemoglobin Abraham Lincoln, β32 (B14) Leucine → Proline AN UNSTABLE VARIANT PRODUCING SEVERE HEMOLYTIC DISEASE

  1973cites this paper
• AN UNSTABLE VARIANT PRODUCING SEVERE HEMOLYTIC DISEASE

  1973cites this paper
• Comparison of human hemoglobin A carrying glutathione as a mixed disulfide with the naturally occurring human hemoglobin A.

  1973cites this paper
• Haemoglobin Nottingham, Beta FG 5 (98) Valgly: A New Unstable Haemoglobin Producing Severe Haemolysis

  1973cites this paper
• Haemichrome formation during the in vitro oxidation of Hb Köln.

  1973cites this paper
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  1972cites this paper
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  1972cites this paper
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  1972cites this paper
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  1972cites this paper
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  1972cites this paper
• BIBLIOGRAPHY

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  1971cites this paper
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  1971cites this paper
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  1970cites this paper
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  1970cites this paper
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  1970cites this paper
• The role of hemoglobin heme loss in Heinz body formation: studies with a partially heme-deficient hemoglobin and with genetically unstable hemoglobins.

  1970cites this paper
• Membrane alterations associated with hemoglobinopathies.

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• Unstable hemoglobins: the role of heme loss in Heinz body formation.

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• Mechanisms of Heinz body formation and attachment to red cell membrane.

  1970cites this paper
• Drug-associated hemolytic anemia.

  1970cites this paper
• In Vitro Studies of Red Cell Metabolism in Haemoglobin H Disease

  1970cites this paper
• Glutathione metabolism of the erythrocyte. The enzymic cleavage of glutathione-haemoglobin preparations by glutathione reductase.

  1970cites this paper
• Die hämolytischen Anämien

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• The Metabolism and Function of Red Cells with Inherited Defects

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  1969cites this paper
• Drug-induced hemolytic anemia.

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• Variations in the structure of human haemoglobin. With particular reference to the unstable haemoglobins.

  1969cites this paper
• DISEASES OF FUNCTION AND STABILITY OF HAEMOGLOBIN

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• Hemoglobin Hasharon (alpha-2-47 his(CD5)beta-2): a hemoglobin found in low concentration.

  1969cites this paper
• Current concepts: Heinz-body anemias.

  1969cites this paper
• a Hemoglobin Found in Low Concentration

  1969cites this paper
• RECENT STUDIES ON PYRROLE METABOLISM IN THALASSEMIA *

  1969cites this paper
• Hemoglobin Hasharon (α247 his(CD5)β2): a hemoglobin found in low concentration

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• Heinz-Body Anemias

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• Genetic control of hemoglobin synthesis and the thalassemia syndromes.

  1969cites this paper
• Hemoglobin sabine beta 91 (f 7) leu to pro. An unstable variant causing severe anemia with inclusion bodies.

  1969cites this paper
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  1968cites this paper
• Molecular Pathology of Human Haemoglobin

  1968cites this paper
• Altered sulfhydryl reactivity of hemoglobins and red blood cell membranes in congenital Heinz body hemolytic anemia.

  1968cites this paper
• Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.

  1968cites this paper