"Isoleucine" 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.
An essential branched-chain aliphatic amino acid found in many proteins. It is an isomer of LEUCINE. It is important in hemoglobin synthesis and regulation of blood sugar and energy levels.
| Descriptor ID |
D007532
|
| MeSH Number(s) |
D12.125.070.577 D12.125.142.383
|
| Concept/Terms |
Isoleucine- Isoleucine
- L-Isoleucine
- Isoleucine, L-Isomer
- Isoleucine, L Isomer
- L-Isomer Isoleucine
|
Below are MeSH descriptors whose meaning is more general than "Isoleucine".
Below are MeSH descriptors whose meaning is more specific than "Isoleucine".
This graph shows the total number of publications written about "Isoleucine" by people in this website by year, and whether "Isoleucine" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2006 | 0 | 4 | 4 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Isoleucine" by people in Profiles.
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Trefely S, Huber K, Liu J, Noji M, Stransky S, Singh J, Doan MT, Lovell CD, von Krusenstiern E, Jiang H, Bostwick A, Pepper HL, Izzo L, Zhao S, Xu JP, Bedi KC, Rame JE, Bogner-Strauss JG, Mesaros C, Sidoli S, Wellen KE, Snyder NW. Quantitative subcellular acyl-CoA analysis reveals distinct nuclear metabolism and isoleucine-dependent histone propionylation. Mol Cell. 2022 01 20; 82(2):447-462.e6.
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Cordeiro JM, Barajas-Martinez H, Hong K, Burashnikov E, Pfeiffer R, Orsino AM, Wu YS, Hu D, Brugada J, Brugada P, Antzelevitch C, Dumaine R, Brugada R. Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome. Circulation. 2006 Nov 07; 114(19):2026-33.
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Ingram-Smith C, Woods BI, Smith KS. Characterization of the acyl substrate binding pocket of acetyl-CoA synthetase. Biochemistry. 2006 Sep 26; 45(38):11482-90.
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Akbas N, Hochstrasser H, Deplazes J, Tomiuk J, Bauer P, Walter U, Behnke S, Riess O, Berg D. Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra. Neurosci Lett. 2006 Oct 16; 407(1):16-9.
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Liang TW, Truax AC, Trojanowski JQ, Lee VM, Stern MB, Kotzbauer PT. Partial deficit of pantothenate kinase 2 catalytic activity in a case of tremor-predominant neurodegeneration with brain iron accumulation. Mov Disord. 2006 May; 21(5):718-22.
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Tang W, Halling DB, Black DJ, Pate P, Zhang JZ, Pedersen S, Altschuld RA, Hamilton SL. Apocalmodulin and Ca2+ calmodulin-binding sites on the CaV1.2 channel. Biophys J. 2003 Sep; 85(3):1538-47.
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Ercikan-Abali EA, Waltham MC, Dicker AP, Schweitzer BI, Gritsman H, Banerjee D, Bertino JR. Variants of human dihydrofolate reductase with substitutions at leucine-22: effect on catalytic and inhibitor binding properties. Mol Pharmacol. 1996 Mar; 49(3):430-7.
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Cohen M, Rabinowitz M. Analysis of grande and petite yeast mitochondrial DNA by tRNA hybridization. Biochim Biophys Acta. 1972 Oct 11; 281(2):192-201.
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Gabuzda TG, Silver RK, Chui LC, Lewis HB. The formation of foetal and adult haemoglobin in cell cultures of neonatal calf marrow. Br J Haematol. 1970 Nov; 19(5):621-33.