Amino Acid Transport Systems, Basic
"Amino Acid Transport Systems, Basic" 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.
Amino acid transporter systems capable of transporting basic amino acids (AMINO ACIDS, BASIC).
MeSH Number(s)
D12.776.157.530.200.374
D12.776.543.585.200.374
Concept/Terms
Amino Acid Transport Systems, Basic- Amino Acid Transport Systems, Basic
- Cationic Amino Acid Transport Proteins
- Amino Acid Transport Systems, Cationic
- Cationic Amino Acid Transport Systems
- Basic Amino Acid Transport Systems
- Basic Amino Acid Transport Proteins
- Cationic Amino Acid Transporters
Below are MeSH descriptors whose meaning is more general than "Amino Acid Transport Systems, Basic".
Below are MeSH descriptors whose meaning is more specific than "Amino Acid Transport Systems, Basic".
This graph shows the total number of publications written about "Amino Acid Transport Systems, Basic" by people in Harvard Catalyst Profiles by year, and whether "Amino Acid Transport Systems, Basic" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2000 | 1 | 1 | 2 |
| 2001 | 0 | 3 | 3 |
| 2002 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2015 | 0 | 1 | 1 |
| 2016 | 0 | 2 | 2 |
| 2017 | 2 | 0 | 2 |
| 2018 | 0 | 2 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
Below are the most recent publications written about "Amino Acid Transport Systems, Basic" by people in Profiles.
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SLC7A3: In Silico Prediction of a Potential New Cause of Childhood Epilepsy. Neuropediatrics. 2022 02; 53(1):46-51.
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Membrane Lipid Requirements of the Lysine Transporter Lyp1 from Saccharomyces cerevisiae. J Mol Biol. 2020 06 26; 432(14):4023-4031.
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IRE1a-XBP1 controls T cell function in ovarian cancer by regulating mitochondrial activity. Nature. 2018 10; 562(7727):423-428.
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Urea Cycle Dysregulation Generates Clinically Relevant Genomic and Biochemical Signatures. Cell. 2018 09 06; 174(6):1559-1570.e22.
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Genetic variation in SLC7A2 interacts with calcium and magnesium intakes in modulating the risk of colorectal polyps. J Nutr Biochem. 2017 09; 47:35-40.
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Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease. Kidney Int. 2017 06; 91(6):1426-1435.
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Milder Form of Urea Cycle Defect Revisited: Report and Review of Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria (HHH) Syndrome Diagnosed in a Teenage Girl Presenting with Recurrent Encephalopathy. Ann Acad Med Singap. 2016 Dec; 45(12):563-566.
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Orientation-specific RAG activity in chromosomal loop domains contributes to Tcrd V(D)J recombination during T cell development. J Exp Med. 2016 08 22; 213(9):1921-36.
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The mTORC1/4E-BP pathway coordinates hemoglobin production with L-leucine availability. Sci Signal. 2015 Apr 14; 8(372):ra34.
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Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet. 2012 Dec 15; 21(24):5329-43.