"Hemoglobin M" 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.
A group of abnormal hemoglobins in which amino acid substitutions take place in either the alpha or beta chains but near the heme iron. This results in facilitated oxidation of the hemoglobin to yield excess methemoglobin which leads to cyanosis.
| Descriptor ID |
D006449
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| MeSH Number(s) |
D12.776.124.400.463.510 D12.776.422.316.762.426.510
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobin M".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin M".
This graph shows the total number of publications written about "Hemoglobin M" by people in this website by year, and whether "Hemoglobin M" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 2 | 0 | 2 |
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Below are the most recent publications written about "Hemoglobin M" by people in Profiles.
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Heterogeneity between Two a Subunits of a2ß2 Human Hemoglobin and O2 Binding Properties: Raman, 1H Nuclear Magnetic Resonance, and Terahertz Spectra. Biochemistry. 2017 11 21; 56(46):6125-6136.
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Congenital Methemoglobinemia: It is Time for National Level Registry System. J Pediatr Hematol Oncol. 2017 11; 39(8):629.