Dylan E Jones
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Explore the profile of Dylan E Jones including associated specialties, affiliations and a list of published articles.
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9
Citations
56
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Recent Articles
1.
Jennings E, Abi-Rached Z, Jones D, Ryan R
Clin Chim Acta
. 2023 Nov;
551:117629.
PMID: 37935273
The acylcarnitines comprise a wide range of acyl groups linked via an ester bond to the hydroxyl group of L-carnitine. Mass spectrometry methods are capable of measuring the relative abundance...
2.
Jones D, Jennings E, Ryan R
Metabolites
. 2022 May;
12(5).
PMID: 35629880
A growing number of inborn errors of metabolism (IEM) have been identified that manifest 3-methylglutaconic (3MGC) aciduria as a phenotypic feature. In primary 3MGC aciduria, IEM-dependent deficiencies in leucine pathway...
3.
Jones D, Romenskaia I, Kosma D, Ryan R
FEBS J
. 2021 Dec;
289(10):2948-2958.
PMID: 34877790
3-Methylglutaconic (3MGC) aciduria occurs in numerous inborn errors associated with compromised mitochondrial energy metabolism. In these disorders, 3MGC CoA is produced de novo from acetyl CoA in three steps with...
4.
Berger K, Pauwels E, Parkinson G, Landberg G, Le T, Demillo V, et al.
J Med Chem
. 2021 Aug;
64(17):12865-12876.
PMID: 34428050
Cyclotriazadisulfonamide (CADA) compounds selectively down-modulate two human proteins of potential therapeutic interest, cluster of differentiation 4 (CD4) and sortilin. Progranulin is secreted from some breast cancer cells, causing dedifferentiation of...
5.
Jones D, Klacking E, Ryan R
Clin Chim Acta
. 2021 Aug;
522:96-104.
PMID: 34411555
A growing number of inborn errors of metabolism (IEM) associated with compromised mitochondrial energy metabolism manifest an unusual phenotypic feature: 3-methylglutaconic (3MGC) aciduria. Two major categories of 3MGC aciduria, primary...
6.
Jones D, Ricker J, Geary L, Kosma D, Ryan R
JIMD Rep
. 2021 Mar;
58(1):61-69.
PMID: 33728248
3-Methylglutaconic (3MGC) aciduria is a common phenotypic feature of a growing number of inborn errors of metabolism. "Primary" 3MGC aciduria is caused by deficiencies in leucine pathway enzymes while "secondary"...
7.
Young R, Jones D, Diacovich L, Witkowski A, Ryan R
Biochem Biophys Res Commun
. 2020 Dec;
534:261-265.
PMID: 33280817
3-methylglutaconic (3MGC) aciduria is associated with a growing number of discrete inborn errors of metabolism. Herein, an antibody-based approach to detection/quantitation of 3MGC acid has been pursued. When trans-3MGC acid...
8.
Jones D, Perez L, Ryan R
Clin Chim Acta
. 2019 Nov;
502:233-239.
PMID: 31730811
3-methylglutaric (3MG) acid is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies. 3MG acid is excreted in urine of individuals harboring deficiencies in...
9.
Ali R, Anugu S, Chawla R, Demillo V, Goulinet-Mateo F, Gyawali S, et al.
ACS Omega
. 2019 Feb;
4(1):1254-1264.
PMID: 30729225
Macrocyclic triamine disulfonamides can be synthesized by double Tsuji-Trost -allylation reaction of open-chain disulfonamides with 2-alkylidene-1,3-propanediyl bis(carbonates). The previously used Atkins-Richman macrocyclization method generally gives lower yields and requires more...