"Sickle Cell Trait" 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.
The condition of being heterozygous for hemoglobin S.
Descriptor ID |
D012805
|
MeSH Number(s) |
C15.378.071.141.150.150.670 C15.378.420.155.668 C16.320.070.150.670 C16.320.365.155.668
|
Concept/Terms |
Sickle Cell Trait- Sickle Cell Trait
- Cell Trait, Sickle
- Cell Traits, Sickle
- Sickle Cell Traits
- Trait, Sickle Cell
- Traits, Sickle Cell
|
Below are MeSH descriptors whose meaning is more general than "Sickle Cell Trait".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Anemia, Sickle Cell [C15.378.071.141.150.150]
- Sickle Cell Trait [C15.378.071.141.150.150.670]
- Hemoglobinopathies [C15.378.420]
- Anemia, Sickle Cell [C15.378.420.155]
- Sickle Cell Trait [C15.378.420.155.668]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Anemia, Sickle Cell [C16.320.070.150]
- Sickle Cell Trait [C16.320.070.150.670]
- Hemoglobinopathies [C16.320.365]
- Anemia, Sickle Cell [C16.320.365.155]
- Sickle Cell Trait [C16.320.365.155.668]
Below are MeSH descriptors whose meaning is more specific than "Sickle Cell Trait".
This graph shows the total number of publications written about "Sickle Cell Trait" by people in this website by year, and whether "Sickle Cell Trait" 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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2005 | 1 | 0 | 1 |
2007 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Sickle Cell Trait" by people in Profiles.
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SMARCB1 regulates a TFCP2L1-MYC transcriptional switch promoting renal medullary carcinoma transformation and ferroptosis resistance. Nat Commun. 2023 05 26; 14(1):3034.
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SMARCB1 regulates the hypoxic stress response in sickle cell trait. Proc Natl Acad Sci U S A. 2023 05 23; 120(21):e2209639120.
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Outcomes of kidney donors with sickle cell trait: A preliminary analysis. Clin Transplant. 2022 06; 36(6):e14626.
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Acute care utilization in pediatric sickle cell disease and sickle cell trait in the USA: prevalence, temporal trends, and cost. Eur J Pediatr. 2020 Nov; 179(11):1701-1710.
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Sickle Cell Trait Testing Should Not Be a Player in NCAA Athletics: Examining the Media's Role in Disseminating Awareness and Information. J Pediatr Hematol Oncol. 2018 07; 40(5):414-415.
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Sickle solubility test to screen for sickle cell trait: what's the harm? Hematology Am Soc Hematol Educ Program. 2015; 2015:433-5.
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Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans. JAMA. 2014 Nov 26; 312(20):2115-25.
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Therapeutic plasmapheresis and red blood cell exchange in a sickle cell trait patient with rhabdomyolysis. J Clin Apher. 2012; 27(6):342-5.
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Sickle cell trait and fatal rhabdomyolysis in football training: a case study. Med Sci Sports Exerc. 2010 Jan; 42(1):3-7.
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Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations. BMC Genet. 2007 Aug 10; 8:52.