"Hemoglobins, Abnormal" 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.
Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains.
| Descriptor ID |
D006455
|
| MeSH Number(s) |
D12.776.124.400.463 D12.776.422.316.762.426
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobins, Abnormal".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobins, Abnormal".
This graph shows the total number of publications written about "Hemoglobins, Abnormal" by people in this website by year, and whether "Hemoglobins, Abnormal" 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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2005 | 0 | 2 | 2 |
| 2007 | 2 | 0 | 2 |
| 2009 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hemoglobins, Abnormal" by people in Profiles.
-
Hemoglobin fractionation by Sebia Capillarys 2 Flex Piercing System as primary method for evaluation of hemoglobinopathies. Clin Chim Acta. 2021 Aug; 519:193-197.
-
Misidentification of unstable, low oxygen affinity hemoglobin variant. Clin Chim Acta. 2020 Oct; 509:177-179.
-
Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A). Hemoglobin. 2018 Jul; 42(4):269-271.
-
Hemoglobin Kirklareli (a H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding. J Biol Chem. 2017 02 10; 292(6):2542-2555.
-
CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes. Protein Cell. 2015 May; 6(5):363-372.
-
Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin. J Biol Chem. 2014 Aug 08; 289(32):22342-57.
-
The clinical and laboratory spectrum of Hb C [?6(A3)Glu?Lys, GAG>AAG] disease. Hemoglobin. 2013; 37(1):16-25.
-
Familial secondary erythrocytosis due to increased oxygen affinity is caused by destabilization of the T state of hemoglobin Brigham (a2?2(Pro100Leu)). Protein Sci. 2012 Oct; 21(10):1444-55.
-
A hemoglobin variant associated with neonatal cyanosis and anemia. N Engl J Med. 2011 May 12; 364(19):1837-43.
-
The diagnostic dilemma of congenital unstable hemoglobinopathies. Pediatr Blood Cancer. 2010 Dec 15; 55(7):1393-5.