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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…
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National Institutes of Health
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Related topics
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14 relations
Broader (1)
Hemoglobin
Hemoglobin H inclusion bodies:PrThr:Pt:Bld:Ord
Hemoglobin H:PrThr:Pt:Bld:Ord:Heat denaturation
Process of secretion
Thalassemia
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Narrower (1)
hemoglobin Icaria
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
[Study on RBC Oxygen-Carrying Function with the Incubation Time].
Man Luo
,
Y. Huang
,
Bao-chang Su
,
Yun-Feng Shi
,
Hong Zhang
,
Xun-da Ye
Guang pu xue yu guang pu fen xi = Guang pu
2015
Corpus ID: 13196005
The cycle of Hemoglobin oxygenation and deoxidation plays an important role in driving structure and regulating function of red…
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2014
2014
Metabolic Pathways Related to Oxidative Stress in Patients With Hemoglobin H Disease and Iron Overload
S. Chiou
,
C. Tsao
,
+4 authors
L. Tsai
Journal of clinical laboratory analysis (Print)
2014
Corpus ID: 33993416
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
Parisa Sadighara
2009
Corpus ID: 56262063
Abs tr ac t: Oxidative stress occurs when the balance between oxidants and biochemical antioxidants is disrupted because of the…
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2005
2005
Decreased a Globin mRNA in Nucleated Red Cell Precursors in a Thalassemia
F. Ramirez
,
J. Wolff
,
A. Bank
2005
Corpus ID: 29067765
The a thalassemias are associated with a decrease in a chain synthesis. Hemoglobin H (HbH) disease is a moderately severe form of…
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1991
1991
Alpha-thalassemic traits are common in the Taiwanese population: usefulness of a modified hemoglobin H preparation for prevalence studies.
C. K. Lin
,
S. H. Lee
,
C. C. Wang
,
M. Jiang
,
H. Hsu
Journal of Laboratory and Clinical Medicine
1991
Corpus ID: 45508016
The aim of this study was to determine the crude prevalence of alpha-thalassemia traits in Taiwan. A total of 1435 healthy…
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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
Chung‐King Lin
,
M. Jiang
,
C. Chien
,
Man L. Yang
,
Hsi-Hsu Lin
,
Hong‐Wen Peng
Journal of clinical laboratory analysis (Print)
1991
Corpus ID: 9939462
We evaluated 61 patients with two screening tests for alpha‐thalassemia traits on the basis of endonuclease gene mapping…
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1975
1975
Effect of urea on the kinetics of ligand combination reactions of hemoglobins A and H, alphaSH chains and myoglobin.
V. Sharma
,
J. Everse
,
H. Ranney
Journal of Molecular Biology
1975
Corpus ID: 37408750
1967
1967
Oxidative precipitation of hemoglobin H and its relation to reduced glutathione.
T. Gabuzda
,
M. T. Laforet
,
F. Gardner
Journal of Laboratory and Clinical Medicine
1967
Corpus ID: 34968505
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