"Hemoglobin H" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
| Descriptor ID |
D006447
|
| MeSH Number(s) |
D12.776.124.400.463.463 D12.776.422.316.762.426.463
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobin H".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin H".
This graph shows the total number of publications written about "Hemoglobin H" by people in this website by year, and whether "Hemoglobin H" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemoglobin H" by people in Profiles.
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Griffith WP, Kaltashov IA. Protein conformational heterogeneity as a binding catalyst: ESI-MS study of hemoglobin H formation. Biochemistry. 2007 Feb 20; 46(7):2020-6.
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Kutlar F, Adamkiewicz TV, Markowitz RB, Holley L, Kutlar A. An alpha-2 globin gene initiation codon mutation in a Vietnamese patient with Hb H disease. Ann N Y Acad Sci. 1998 Jun 30; 850:398-400.