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Hemoglobin H

Known as: Hemoglobin H [Chemical/Ingredient], h hemoglobin 
An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA… 
National Institutes of Health

Related topics

Related topics

14 relations

Broader (1)

Hemoglobin
Hemoglobin H inclusion bodies:PrThr:Pt:Bld:OrdHemoglobin H:PrThr:Pt:Bld:Ord:Heat denaturationProcess of secretionThalassemia

Narrower (1)

hemoglobin Icaria

Papers overview

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2015
2015
[Study on RBC Oxygen-Carrying Function with the Incubation Time].
The cycle of Hemoglobin oxygenation and deoxidation plays an important role in driving structure and regulating function of red… 
2014
2014
Metabolic Pathways Related to Oxidative Stress in Patients With Hemoglobin H Disease and Iron Overload
Iron overload is a major complication in patients with hemoglobin H (Hb H) disease and causes damage of tissues. 
2009
2009
RBC: Tool for Oxidant Agents Screening Test
Abs tr ac t: Oxidative stress occurs when the balance between oxidants and biochemical antioxidants is disrupted because of the… 
2008
2008
Successful resuscitation of unexpected neonatal hemorrhagic shock due to massive feto‐maternal hemorrhage
SIR— Massive feto-maternal hemorrhage (MFH) resulting in neonatal shock is an exceptional event. MFH is defined as the loss of… 
2005
2005
Decreased a Globin mRNA in Nucleated Red Cell Precursors in a Thalassemia
The a thalassemias are associated with a decrease in a chain synthesis. Hemoglobin H (HbH) disease is a moderately severe form of… 
2002
2002
Oxidative Stress in Patients with Primary Pulmonary Hypertension
We studied the role of oxidative stress in the pathogenesis of primary pulmonary hypertension. In patients with primary pulmonary… 
1991
1991
Alpha-thalassemic traits are common in the Taiwanese population: usefulness of a modified hemoglobin H preparation for prevalence studies.
The aim of this study was to determine the crude prevalence of alpha-thalassemia traits in Taiwan. A total of 1435 healthy… 
1991
1991
Comparison of two screening methods, modified hb h preparation and the osmotic fragility test, for alpha‐thalassemic traits on the basis of gene mapping
We evaluated 61 patients with two screening tests for alpha‐thalassemia traits on the basis of endonuclease gene mapping… 
1975
1975
Effect of urea on the kinetics of ligand combination reactions of hemoglobins A and H, alphaSH chains and myoglobin.
1967
1967
Oxidative precipitation of hemoglobin H and its relation to reduced glutathione.
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