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Hemoglobin H Disease

Known as: HEMOGLOBIN H DISEASE, DELETIONAL, ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE, Hemoglobin H 
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by… 
National Institutes of Health

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Hematopoietic and Lymphoid CellHematopoietic and Lymphoid Tissue

Broader (1)

alpha-Thalassemia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
CFD model of ITER CICC. Part VI: Heat and mass transfer between cable region and central channel
2003
2003
The place of capillary electrophoresis techniques in screening for haemoglobinopathies
Background: Capillary zone electrophoresis (CZE) methods are new laboratory diagnostic tools. The screening of haemoglobin (Hb… 
2000
2000
Molecular characterization and PCR detection of a deletional HPFH: Application to rapid prenatal diagnosis for compound heterozygotes of this defect with β‐thalassemia in a Chinese family
Hereditary persistence of fetal hemoglobin (HPFH) is one of the hemoglobinopathies in which the fetal γ‐globin genes remain… 
1999
1999
Human bleomycin hydrolase binds ribosomal proteins.
Bleomycin hydrolase (BH) is a cysteine proteinase that inactivates the anticancer drug bleomycin. Yeast BH forms a homohexameric… 
1998
1998
Essential binding and functional domains of human bleomycin hydrolase.
Bleomycin hydrolase (BH) is unusual among cysteine proteinases because it appears to form multihomomeric structures, inactivates… 
1998
1998
An evolutionarily conserved cysteine protease, human bleomycin hydrolase, binds to the human homologue of ubiquitin-conjugating enzyme 9.
Bleomycin hydrolase (BH) is a highly conserved cysteine proteinase that deamidates and inactivates the anticancer drug bleomycin… 
1998
1998
Binding of dihydroartemisinin to hemoglobin H: role in drug accumulation and host-induced antimalarial ineffectiveness of alpha-thalassemic erythrocytes.
Dihydroartemisinin and other artemisinin derivatives are relatively ineffective against Plasmodium falciparum infecting alpha… 
1995
1995
Optimizing the Detection of Hemoglobin H Disease
Hemoglobin (Hb) H disease is a mild to severe chronic hemolytic anemia. The disease most commonly results from an absence of… 
Highly Cited
1985
Highly Cited
1985
Plasmodium falciparum in vitro: diminished growth in hemoglobin H disease erythrocytes.
Studies of the ability of Plasmodium falciparum to grow in vitro in the red blood cells of subjects with certain beta-thalassemia… 
1984
1984
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype.
In this study we have correlated the presence/absence of rare red blood cells with HbH inclusions with the alpha-globin genotype… 
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