Hemoglobin, Sickle
"Hemoglobin, Sickle" 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 resulting from the substitution of valine for glutamic acid at position 6 of the beta chain of the globin moiety. The heterozygous state results in sickle cell trait, the homozygous in sickle cell anemia.
Descriptor ID |
D006451
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MeSH Number(s) |
D12.776.124.400.463.588 D12.776.422.316.762.426.588
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Concept/Terms |
Deoxyhemoglobin S- Deoxyhemoglobin S
- S, Deoxyhemoglobin
- Deoxygenated Sickle Hemoglobin
- Hemoglobin, Deoxygenated Sickle
- Sickle Hemoglobin, Deoxygenated
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Below are MeSH descriptors whose meaning is more general than "Hemoglobin, Sickle".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin, Sickle".
This graph shows the total number of publications written about "Hemoglobin, Sickle" by people in UAMS Profiles by year, and whether "Hemoglobin, Sickle" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2016 | 0 | 1 | 1 | 2015 | 0 | 1 | 1 | 2004 | 0 | 1 | 1 | 1997 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hemoglobin, Sickle" by people in Profiles over the past ten years.
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Cai C, Nedosekin DA, Menyaev YA, Sarimollaoglu M, Proskurnin MA, Zharov VP. Photoacoustic Flow Cytometry for Single Sickle Cell Detection In Vitro and In Vivo. Anal Cell Pathol (Amst). 2016; 2016:2642361.
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Pandey S, Cottler-Fox M, Drobena G. Hemoglobin Variants Acquired Post-Exchange Transfusion in Pediatric Sickle Cell Disease (SCD) Patients. Ann Clin Lab Sci. 2015; 45(6):627-30.
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