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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1987 | 1 |
1991 | 1 |
2009 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli.
Hum Genet. 1991 Apr;86(6):545-51. doi: 10.1007/BF00201539.
Hum Genet. 1991.
PMID: 1902818
Purification and properties of short chain acyl-CoA, medium chain acyl-CoA, and isovaleryl-CoA dehydrogenases from human liver.
Finocchiaro G, Ito M, Tanaka K.
Finocchiaro G, et al.
J Biol Chem. 1987 Jun 15;262(17):7982-9.
J Biol Chem. 1987.
PMID: 3597357
Free article.
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Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screening.
Maier EM, Gersting SW, Kemter KF, Jank JM, Reindl M, Messing DD, Truger MS, Sommerhoff CP, Muntau AC.
Maier EM, et al.
Hum Mol Genet. 2009 May 1;18(9):1612-23. doi: 10.1093/hmg/ddp079. Epub 2009 Feb 18.
Hum Mol Genet. 2009.
PMID: 19224950
Free PMC article.
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Human METTL20 is a mitochondrial lysine methyltransferase that targets the β subunit of electron transfer flavoprotein (ETFβ) and modulates its activity.
Małecki J, Ho AY, Moen A, Dahl HA, Falnes PØ.
Małecki J, et al.
J Biol Chem. 2015 Jan 2;290(1):423-34. doi: 10.1074/jbc.M114.614115. Epub 2014 Nov 21.
J Biol Chem. 2015.
PMID: 25416781
Free PMC article.
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