Carnitine

trimethyllysine hydroxylase, epsilon ; Homo sapiens







13 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 34506728 Controlled lipid β-oxidation and carnitine biosynthesis by a vitamin D metabolite. 2022 Apr 21 3
2 30898847 Investigating the active site of human trimethyllysine hydroxylase. 2019 Apr 10 2
3 28045275 Evidence That Trimethyllysine Hydroxylase Catalyzes the Formation of (2S,3S)-3-Hydroxy-Nε-trimethyllysine. 2017 Jan 20 2
4 28116387 Fluorinated trimethyllysine as a 19F NMR probe for trimethyllysine hydroxylase catalysis. 2017 Feb 7 2
5 28703319 Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis. 2017 Aug 1
6 27730239 Substrate scope for trimethyllysine hydroxylase catalysis. 2016 Oct 25 2
7 27965989 Human carnitine biosynthesis proceeds via (2S,3S)-3-hydroxy-Nε-trimethyllysine. 2016 Dec 22 2
8 25943046 Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation. 2015 Sep 1
9 25220864 Expression and purification of active, stabilized trimethyllysine hydroxylase. 2014 Dec 2
10 23497718 Genes involved in carnitine synthesis and carnitine uptake are up-regulated in the liver of sows during lactation. 2013 Mar 14 1
11 22566635 A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. 2012 May 22 1
12 23092983 Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. 2012 Oct 23 1
13 15754339 Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting. 2005 Sep 2