"Hemochromatosis Protein" 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 membrane protein and MHC class I antigen. It contains an IMMUNOGLOBULIN C1-SET DOMAIN and interacts with BETA 2-MICROGLOBULIN. It may also regulate the interaction of TRANSFERRIN with the TRANSFERRIN RECEPTOR. Mutations in the HFE gene are associated with cases of FAMILIAL HEMOCHROMATOSIS.
| Descriptor ID |
D000071020
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| MeSH Number(s) |
D12.776.395.550.489.200 D12.776.543.550.439.200 D23.050.301.500.100.363 D23.050.705.552.100.375
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hemochromatosis Protein".
Below are MeSH descriptors whose meaning is more specific than "Hemochromatosis Protein".
This graph shows the total number of publications written about "Hemochromatosis Protein" by people in this website by year, and whether "Hemochromatosis Protein" 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 |
|---|
| 1997 | 0 | 1 | 1 |
| 2017 | 5 | 4 | 9 |
| 2018 | 0 | 5 | 5 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hemochromatosis Protein" by people in Profiles.
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COVID-19 infections are also affected by human ACE1 D/I polymorphism. Clin Chem Lab Med. 2020 06 25; 58(7):1125-1126.
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Genetic factors influencing hemoglobin levels in 15,567 blood donors: results from the Danish Blood Donor Study. Transfusion. 2019 01; 59(1):226-231.
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Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians. Blood Cells Mol Dis. 2018 11; 73:14-21.
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Urinary biomarkers predict advanced acute kidney injury after cardiovascular surgery. Crit Care. 2018 Apr 26; 22(1):108.
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Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype. Hepatol Int. 2018 Mar; 12(2):83-86.
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Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases. PLoS One. 2018; 13(3):e0193867.
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The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease. Am J Hematol. 2018 03; 93(3):383-393.
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Reduction of body iron in HFE-related haemochromatosis and moderate iron overload (Mi-Iron): a multicentre, participant-blinded, randomised controlled trial. Lancet Haematol. 2017 Dec; 4(12):e607-e614.
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A Novel Approach to Improving Utilization of Laboratory Testing. Arch Pathol Lab Med. 2018 Feb; 142(2):243-247.
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The Effect of Iron Status on Risk of Coronary Artery Disease: A Mendelian Randomization Study-Brief Report. Arterioscler Thromb Vasc Biol. 2017 09; 37(9):1788-1792.