Citations for
1DLST
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.
Remacha L, Pirman D, Mahoney CE, Coloma J, Calsina B, Currás-Freixes M, Letón R, Torres-Pérez R, Richter S, Pita G, Herráez B, Cianchetta G, Honrado E, Maestre L, Urioste M, Aller J, García-Uriarte Ó, Gálvez MÁ, Luque RM, Lahera M, Moreno-Rengel C, Eisenhofer G, Montero-Conde C, Rodríguez-Antona C, Llorca Ó, Smolen GA, Robledo M, Cascón A.
Am J Hum Genet 104(4):651-664. doi: 10.1016/j.ajhg.2019.02.017. Epub 2019 Mar 28. Erratum in: Am J Hum Genet. 2019 May 2;104(5):1008-1010. 2019
2DLST
Inhibition of MicroRNA-146a and Overexpression of Its Target Dihydrolipoyl Succinyltransferase Protect Against Pressure Overload-Induced Cardiac Hypertrophy and Dysfunction.
Heggermont WA, Papageorgiou AP, Quaegebeur A, Deckx S, Carai P, Verhesen W, Eelen G, Schoors S, van Leeuwen R, Alekseev S, Elzenaar I, Vinckier S, Pokreisz P, Walravens AS, Gijsbers R, Van Den Haute C, Nickel A, Schroen B, van Bilsen M, Janssens S, Maack C, Pinto Y, Carmeliet P, Heymans S.
Circulation 136(8):747-761. doi: 10.1161/CIRCULATIONAHA.116.024171. Epub 2017 Jun 13. 2017
3DLST
The TCA cycle transferase DLST is important for MYC-mediated leukemogenesis.
Anderson NM, Li D, Peng HL, Laroche FJ, Mansour MR, Gjini E, Aioub M, Helman DJ, Roderick JE, Cheng T, Harrold I, Samaha Y, Meng L, Amsterdam A, Neuberg DS, Denton TT, Sanda T, Kelliher MA, Singh A, Look AT, Feng H.
Leukemia 30(6):1365-74. doi: 10.1038/leu.2016.26. Epub 2016 Feb 15. 2016
4DLST
A novel protein found in the I bands of myofibrils is produced by alternative splicing of the DLST gene.
Matuda S, Arimura T, Kimura A, Takekura H, Ohta S, Nakano K.
Biochim Biophys Acta 1800(1):31-9. doi: 10.1016/j.bbagen.2009.10.003. Epub 2009 Oct 9. 2010
5DLST
Mice deficient in dihydrolipoyl succinyl transferase show increased vulnerability to mitochondrial toxins.
Yang L, Shi Q, Ho DJ, Starkov AA, Wille EJ, Xu H, Chen HL, Zhang S, Stack CM, Calingasan NY, Gibson GE, Beal MF.
Neurobiol Dis 36(2):320-30. doi: 10.1016/j.nbd.2009.07.023. Epub 2009 Aug 4. 2009
6DLST
Substantial linkage disequilibrium across the dihydrolipoyl succinyltransferase gene region without Alzheimer's disease association.
Brown AM, Gordon D, Lee H, Caudy M, Haroutunian V, Blass JP.
Neurochem Res 29(3):629-35. 2004
7DLST
Truncated product of the bifunctional DLST gene involved in biogenesis of the respiratory chain.
Kanamori T, Nishimaki K, Asoh S, Ishibashi Y, Takata I, Kuwabara T, Taira K, Yamaguchi H, Sugihara S, Yamazaki T, Ihara Y, Nakano K, Matuda S, Ohta S.
EMBO J 22(12):2913-23. 2003
8DLST
Isolation and sequence analysis of the rat dihydrolipoamide succinyltransferase gene.
Nakano K, Tanabe M, Nakagawa S, Ohta S, Suzuki S, Shimura M, Matuda S.
DNA Seq 13(6):363-7. 2002
9DLST
Alzheimer's disease and DLST genotype.
Nakano K, Ohta S, Nishimaki K, Miki T, Matuda S.
Lancet 350(9088):1367-8. No abstract available. 1997
10AD3, DLST
Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease.
Cruts M, et al.
Neurosci Lett 199 : 73-77. 1995
11DLST
Isolation, characterization, and mapping of gene encoding dihydrolipoyl succinyltransferase (E2k) of human alpha-ketoglutarate dehydrogenase complex.
Ali G, et al.
Somat Cell Mol Genet 20 : 99-105. 1994
12DLST, DLSTP
Isolation, characterization and structural organization of the gene and pseudogene for the dihydrolipoamide succinyltransferase component of the human 2-oxoglutarate dehydrogenase complex.
Nakano K, et al.
Eur J Biochem 224 : 179-189. 1994
13DLST
An unspliced cDNA for human dihydrolipoamide succinyltransferase : characterization and mapping of the gene to chromosome 14q24.2-q24.3.
Nakano K, et al.
Biochem Biophys Res Commun 196 : 527-533. 1993
14DLST, DLSTP
Human dihydrolipoamide succinyltransferase : cDNA cloning and localization on chromosome 14q24.2-q24.3.
Nakano K, et al.
Biochim Biophys Acta 1216 : 360-368. 1993
15DLST, DLSTP
Isolation and characterization of the human E2k gene : a candidate for the FAD gene defect on chromosome 14q24.3.
Ali G, et al.
Am J Hum Genet 53 : 659. 1993