About: abnormal hemoglobins

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hemoglobins characterized by structural alterations within the molecule

Attributes	Values
rdf:type	Item
description	hemoglobins characterized by structural alterations within the molecule (en)
rdfs:label	abnormal hemoglobins (en)
skos:prefLabel	abnormal hemoglobins (en)
name	abnormal hemoglobins (en)
subclass of	wds:Q77836916-af9396e3-41b1-394b-135b-4293b4bef79d
subclass of	hemoglobin
skos:altLabel	Hemoglobins, Abnormal (en) abnormal haemoglobin (en) abnormal hemoglobin (en)
UMLS CUI	wds:Q77836916-5E8A3FB1-BDF9-4D66-9923-95B3777CB7B2
MeSH descriptor ID	wds:Q77836916-185EE657-89EC-4EFE-88E9-6A75B7F44651
MeSH tree code	wds:Q77836916-9409c956-425b-3e29-56d9-0db1a61dabf5 wds:Q77836916-a2bd915b-4a27-47c7-e34b-76c486e2ef3d
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D006455
MeSH tree code	http://id.nlm.nih.gov/mesh/D12.776.124.400.463 http://id.nlm.nih.gov/mesh/D12.776.422.316.762.426
UMLS CUI	C0019047
MeSH descriptor ID	D006455
MeSH tree code	D12.776.124.400.463 D12.776.422.316.762.426
suggests the existence of	wds:Q77836916-4a1ad41f-4206-32a7-2c23-5b9d0001d245
suggests the existence of	hemoglobinopathy
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q77836916
is symptoms and signs of	hemoglobinopathy
is symptoms and signs of	wds:Q1642147-83497e76-41bb-d967-b386-252e3619bec0
is subclass of of	sickle hemoglobin Hemoglobin M
is subclass of of	wds:Q76876892-3058aff1-4116-2c7e-51b0-08b56c6d8e2f wds:Q76829973-4ea7d72a-4fdd-cf43-a34b-47e7ec16c2f5
is main subject of	Ligand Kinetics in Hemoglobin Hiroshima Oxygen-equilibrium characteristics of abnormal hemoglobin Hiroshima (α2β2143 Asp) Characterization of hemoglobin Burke [beta 107 (G9) Gly replaced by Arg] Radiation-induced mutations at mouse hemoglobin loci BETA THALASSEMIA-HEMOGLOBIN D ALPHA. A FAMILY REPORT Occurrence of Hæmoglobin H in Leukæmia Hemoglobin J Meerut: alpha120 Ala leads to Glu Kinetics and Mechanism of Deoxyhemoglobin S Gelation: A New Approach to Understanding Sickle Cell Disease Electron Microscope and High Resolution Autoradiographic Studies of the Erythroblasts in Haemoglobin H Disease A new look at the protection of hemoglobin AS and AC genotypes against plasmodium falciparum infection: a census tract approach Abnormal Precipitation of Oxyhemoglobin S by Mechanical Shaking Haemoglobin bucureşti β42 (CD1) Phe → Leu, a cause of unstable haemoglobin haemolytic anaemia Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore Population genetics of haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency, with particular reference to the malaria hypothesis Mechanism of charge compensation and impairment of co-operative functions in haemoglobin Tacoma (Arg B12(30)β → ser) Blood Groups, Abnormal Haemoglobins and Other Genetical Characters in Three Gujarati-Speaking Groups Haemoglobin Titusville: alpha94 Asp replaced by Asn. A new haemoglobin with a lowered affinity for oxygen STUDIES ON SEVERAL GENETIC HEMATOLOGICAL TRAITS OF THE MEXICAN POPULATION. 8. HEMOGLOBIN S, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, AND OTHER CHARACTERISTICS IN A MALARIAL REGION Structure of Hemoglobin S Fibers: Optical Determination of the Molecular Orientation in Sickled Erythrocytes Structure and function of haemoglobin Philly (Tyr C1 (35) beta replaced by Phe) Ultrastructural Features of Erythrocyte and Hemoglobin Sickling Reversible and irreversible sickling: a distinction by electron microscopy Thermodynamic analysis of the chemical inhibition of Sickle-Cell hemoglobin gelation Relations between oxygen saturation and aggregation of sickle-cell hemoglobin Formation of needle-like aggregates in stirred solutions of hemoglobin S1 DEFECTS OF HEMOGLOBIN AND THE METHEMOGLOBIN REDUCTASE SOME ASPECTS OF HAEMOGLOBIN E AND ITS GENETIC INTERACTION WITH THALASSAEMIA Noncovalent Modification of Deoxyhemoglobin S Solubility and Erythrocyte Sickling Acetylation of Sickle Cell Hemoglobin by Aspirin Oxygen Equilibrium and Kinetics of Isolated Subunits from Hemoglobin Kansas Reversible solubility of deoxyhemoglobin S The effect of β73Asn on the interactions of sickling hemoglobins Binding of carbon monoxide to hemoglobin Zürich. Proposal for a kinetic model RATE OF SICKLING OF RED CELLS DURING DEOXYGENATION OF BLOOD FROM PERSONS WITH VARIOUS SICKLING DISORDERS ABNORMAL HEMOGLOBINS IN NORTH-KYUSHU, JAPAN, WITH SPECIAL REFERENCE TO HB-KOKURA AND HB-FUKUOKA THE CHARACTERIZATION OF HEMOGLOBIN SHIMONOSEKI Calorimetric and optical characterization of sickle cell hemoglobin gelation A thermodynamic model for gelation of sickle-cell hemoglobin The Clinical and Haematological Findings in Children Inheriting Two Types of Thalassaemia: High-A2Type β-Thalassaemia, and High-F Type or δβ-Thalassaemia Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition Erythrocyte function and marrow regulation in hemoglobin Bethesda (β145 histidine) Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln) Three-dimensional structure of abnormal human haemoglobins Chesapeake and J Capetown Are human hemoglobin variants distributed randomly among the positions? Hb Strasbourg alpha2beta2 20 (B2) Val leads to Asp: a variant at the same locus as Hb Olympia beta 20 Val leads to Met A comparison between evolutionary substitutions and variants in human hemoglobins Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins Structure of the zeta chain of human embryonic hemoglobin Oxygen dissociation curve of haemoglobin portland Hæmoglobin H Disease in Thailand: a Genetical Study Structure of hemoglobins Zürich [His E7(63)beta replaced by Arg] and Sydney [Val E11(67)beta replaced by Ala] and role of the distal residues in ligand binding Functional Properties of Hemoglobin Zurich Hemoglobin Beth Israel. A mutant causing clinically apparent cyanosis Nuclear magnetic resonance study of heme-heme interaction in hemoglobin M Milwaukee: implications concerning the mechanism of cooperative ligand binding in normal hemoglobin Ethylisocyanide equilibria of hemoglobins M Iwate, M Boston, M Hyde Park, M Saskatoon, and M Milwaukee-I in half-ferric and fully reduced states Nuclear Magnetic Resonance Studies of Haemoglobin M Milwaukee Some observations on the properties of hemoglobin MMilwaukee-1 Oxygen equilibrium of hemoglobin MHyde Park Intermolecular interactions of oxygenated sickle hemoglobin molecules in cells and cell-free solutions Pregelation Aggregation of Sickle Cell Hemoglobin α-Chain contacts in the polymerization of sickle haemoglobin Polymorphism of sickle cell hemoglobin fibers HEMOGLOBIN: A REVIEW Hemoglobin E: Distribution and population dynamics Haemoglobin J Paris in the South of Portugal (Algarve) Proton nuclear magnetic resonance studies of hemoglobins Osler (β145HC2 Tyr → Asp) and McKees Rocks (β145HC2 Tyr →Term): an assignment for an important tertiary structural probe in hemoglobin The binding of 2,3-diphosphoglycerate as a conformational probe of human hemoglobins High resolution EPR studies of the fine structure of heme proteins. Third harmonic detection approach Moessbauer investigations of high-spin ferrous heme proteins. II. Chloroperoxidase, horseradish peroxidase, and hemoglobin

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