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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.


This graph shows the total number of publications written about "Hemoglobin, Sickle" by people in Harvard Catalyst Profiles by year, and whether "Hemoglobin, Sickle" was a major or minor topic of these publication.
Bar chart showing 51 publications over 26 distinct years, with a maximum of 4 publications in 2001 and 2007 and 2019
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.