"HLA-DQ alpha-Chains" 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.
Transmembrane proteins that form the alpha subunits of the HLA-DQ antigens.
| Descriptor ID |
D059848
|
| MeSH Number(s) |
D12.776.395.550.509.400.430.500 D12.776.543.550.440.400.430.500 D23.050.301.500.400.400.430.500 D23.050.301.500.450.400.430.500 D23.050.705.552.410.400.430.500 D23.050.705.552.450.400.430.500
|
| Concept/Terms |
HLA-DQ alpha-Chains- HLA-DQ alpha-Chains
- HLA DQ alpha Chains
- alpha-Chains, HLA-DQ
- HLA Class II Histocompatibility Antigen, DQ alpha Chains
|
Below are MeSH descriptors whose meaning is more general than "HLA-DQ alpha-Chains".
Below are MeSH descriptors whose meaning is more specific than "HLA-DQ alpha-Chains".
This graph shows the total number of publications written about "HLA-DQ alpha-Chains" by people in this website by year, and whether "HLA-DQ alpha-Chains" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 1 | 0 | 1 |
| 2017 | 2 | 2 | 4 |
| 2018 | 1 | 1 | 2 |
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Below are the most recent publications written about "HLA-DQ alpha-Chains" by people in Profiles.
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The influence of HLA genotype on the severity of COVID-19 infection. HLA. 2021 07; 98(1):14-22.
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Association between the HLA genotype and the severity of COVID-19 infection among South Asians. J Med Virol. 2021 07; 93(7):4430-4437.
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NCAM protein and SARS-COV-2 surface proteins: In-silico hypothetical evidence for the immunopathogenesis of Guillain-Barré syndrome. Med Hypotheses. 2020 Dec; 145:110342.
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Amino acid signatures in the HLA class II peptide-binding region associated with protection/susceptibility to the severe West Nile Virus disease. PLoS One. 2018; 13(10):e0205557.
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Letter: predicting azathioprine-associated pancreatitis in IBD-phenotype or genotype? Aliment Pharmacol Ther. 2018 04; 47(7):1042-1043.
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Genome-Wide Analysis of Genetic Risk Factors for Rheumatic Heart Disease in Aboriginal Australians Provides Support for Pathogenic Molecular Mimicry. J Infect Dis. 2017 12 12; 216(11):1460-1470.
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Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome. Pediatr Nephrol. 2018 03; 33(3):473-483.
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[Recurrent respiratory papillomatosis in a pediatric patient: case report]. Rev Chil Pediatr. 2017 Jun; 88(3):393-397.
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Absence of autoreactive CD4+ T-cells targeting HLA-DQA1*01:02/DQB1*06:02 restricted hypocretin/orexin epitopes in narcolepsy type 1 when detected by EliSpot. J Neuroimmunol. 2017 08 15; 309:7-11.
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Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci. PLoS One. 2012; 7(5):e36926.