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Items: 1 to 20 of 23

1.

Socioeconomic status and DNA methylation from birth through mid-childhood: a prospective study in Project Viva.

Laubach ZM, Perng W, Cardenas A, Rifas-Shiman SL, Oken E, DeMeo D, Litonjua AA, Duca RC, Godderis L, Baccarelli A, Hivert MF.

Epigenomics. 2019 Sep;11(12):1413-1427. doi: 10.2217/epi-2019-0040. Epub 2019 Sep 11.

PMID:
31509016
2.

The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism.

Wehbe Z, Behringer S, Alatibi K, Watkins D, Rosenblatt D, Spiekerkoetter U, Tucci S.

Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Nov;1864(11):1629-1643. doi: 10.1016/j.bbalip.2019.07.012. Epub 2019 Jul 31.

PMID:
31376476
3.

Association of rs4784227-CASC16 (LOC643714 locus) and rs4782447-ACSF3 polymorphisms and their association with breast cancer risk among Iranian population.

Tajbakhsh A, Farjami Z, Darroudi S, Ayati SH, Vakili F, Asghari M, Alimardani M, Abedini S, Kushyar MM, Pasdar A.

EXCLI J. 2019 Jun 18;18:429-438. doi: 10.17179/excli2019-1374. eCollection 2019.

4.

Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort.

Levtova A, Waters PJ, Buhas D, Lévesque S, Auray-Blais C, Clarke JTR, Laframboise R, Maranda B, Mitchell GA, Brunel-Guitton C, Braverman NE.

J Inherit Metab Dis. 2019 Jan;42(1):107-116. doi: 10.1002/jimd.12032.

PMID:
30740739
5.

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program.

Navarrete R, Leal F, Vega AI, Morais-López A, Garcia-Silva MT, Martín-Hernández E, Quijada-Fraile P, Bergua A, Vives I, García-Jiménez I, Yahyaoui R, Pedrón-Giner C, Belanger-Quintana A, Stanescu S, Cañedo E, García-Campos O, Bueno-Delgado M, Delgado-Pecellín C, Vitoria I, Rausell MD, Balmaseda E, Couce ML, Desviat LR, Merinero B, Rodríguez-Pombo P, Ugarte M, Pérez-Cerdá C, Pérez B.

Eur J Hum Genet. 2019 Apr;27(4):556-562. doi: 10.1038/s41431-018-0330-0. Epub 2019 Jan 9.

PMID:
30626930
6.

Role of the malonyl-CoA synthetase ACSF3 in mitochondrial metabolism.

Bowman CE, Wolfgang MJ.

Adv Biol Regul. 2019 Jan;71:34-40. doi: 10.1016/j.jbior.2018.09.002. Epub 2018 Sep 5. Review.

PMID:
30201289
7.

Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants.

Brasil S, Leal F, Vega A, Navarrete R, Ecay MJ, Desviat LR, Riera C, Padilla N, de la Cruz X, Couce ML, Martin-Hernández E, Morais A, Pedrón C, Peña-Quintana L, Rigoldi M, Specola N, de Almeida IT, Vives I, Yahyaoui R, Rodríguez-Pombo P, Ugarte M, Pérez-Cerda C, Merinero B, Pérez B.

Orphanet J Rare Dis. 2018 Jul 24;13(1):125. doi: 10.1186/s13023-018-0862-y.

8.

Dynamic Expression Profile, Regulatory Mechanism and Correlation with Egg-laying Performance of ACSF Gene Family in Chicken (Gallus gallus).

Tian W, Zheng H, Yang L, Li H, Tian Y, Wang Y, Lyu S, Brockmann GA, Kang X, Liu X.

Sci Rep. 2018 May 31;8(1):8457. doi: 10.1038/s41598-018-26903-6.

9.

A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3.

Monteuuis G, Suomi F, Kerätär JM, Masud AJ, Kastaniotis AJ.

Biochem J. 2017 Nov 6;474(22):3783-3797. doi: 10.1042/BCJ20170416.

PMID:
28986507
10.

Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles.

Kuster A, Arnoux JB, Barth M, Lamireau D, Houcinat N, Goizet C, Doray B, Gobin S, Schiff M, Cano A, Amsallem D, Barnerias C, Chaumette B, Plaze M, Slama A, Ioos C, Desguerre I, Lebre AS, de Lonlay P, Christa L; Individual contributors who contributed to this work.

J Inherit Metab Dis. 2018 Jan;41(1):129-139. doi: 10.1007/s10545-017-0079-6. Epub 2017 Sep 18.

PMID:
28924877
11.

ACSF3 and Mal(onate)-Adapted Mitochondria.

Lombard DB, Zhao Y.

Cell Chem Biol. 2017 Jun 22;24(6):649-650. doi: 10.1016/j.chembiol.2017.06.004.

12.

The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency.

Bowman CE, Rodriguez S, Selen Alpergin ES, Acoba MG, Zhao L, Hartung T, Claypool SM, Watkins PA, Wolfgang MJ.

Cell Chem Biol. 2017 Jun 22;24(6):673-684.e4. doi: 10.1016/j.chembiol.2017.04.009. Epub 2017 May 4.

13.

Epigenome-wide association study of rheumatoid arthritis identifies differentially methylated loci in B cells.

Julià A, Absher D, López-Lasanta M, Palau N, Pluma A, Waite Jones L, Glossop JR, Farrell WE, Myers RM, Marsal S.

Hum Mol Genet. 2017 Jul 15;26(14):2803-2811. doi: 10.1093/hmg/ddx177.

PMID:
28475762
14.

Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.

Reid ES, Papandreou A, Drury S, Boustred C, Yue WW, Wedatilake Y, Beesley C, Jacques TS, Anderson G, Abulhoul L, Broomfield A, Cleary M, Grunewald S, Varadkar SM, Lench N, Rahman S, Gissen P, Clayton PT, Mills PB.

Brain. 2016 Nov 1;139(11):2844-2854. doi: 10.1093/brain/aww221.

15.

Targeted exome sequencing for the identification of complementation groups in methylmalonic aciduria: A south Indian experience.

Devi AR, Naushad SM.

Clin Biochem. 2017 Jan;50(1-2):68-72. doi: 10.1016/j.clinbiochem.2016.08.016. Epub 2016 Aug 31.

PMID:
27591164
16.

A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin.

Molloy AM, Pangilinan F, Mills JL, Shane B, O'Neill MB, McGaughey DM, Velkova A, Abaan HO, Ueland PM, McNulty H, Ward M, Strain JJ, Cunningham C, Casey M, Cropp CD, Kim Y, Bailey-Wilson JE, Wilson AF, Brody LC.

Am J Hum Genet. 2016 May 5;98(5):869-882. doi: 10.1016/j.ajhg.2016.03.005. Epub 2016 Apr 28.

17.

A New Approach for Fast Metabolic Diagnostics in CMAMMA.

de Sain-van der Velden MG, van der Ham M, Jans JJ, Visser G, Prinsen HC, Verhoeven-Duif NM, van Gassen KL, van Hasselt PM.

JIMD Rep. 2016;30:15-22. Epub 2016 Feb 27.

18.

Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism.

Pupavac M, Tian X, Chu J, Wang G, Feng Y, Chen S, Fenter R, Zhang VW, Wang J, Watkins D, Wong LJ, Rosenblatt DS.

Mol Genet Metab. 2016 Mar;117(3):363-8. doi: 10.1016/j.ymgme.2016.01.008. Epub 2016 Jan 23.

PMID:
26827111
19.

Analysis of differentially expressed genes and microRNAs in alcoholic liver disease.

Liu Y, Chen SH, Jin X, Li YM.

Int J Mol Med. 2013 Mar;31(3):547-54. doi: 10.3892/ijmm.2013.1243. Epub 2013 Jan 15.

PMID:
23337955
20.

The CBFA2T3/ACSF3 locus is recurrently involved in IGH chromosomal translocation t(14;16)(q32;q24) in pediatric B-cell lymphoma with germinal center phenotype.

Salaverria I, Akasaka T, Gesk S, Szczepanowski M, Burkhardt B, Harder L, Damm-Welk C, Oschlies I, Klapper W, Dyer MJ, Siebert R.

Genes Chromosomes Cancer. 2012 Apr;51(4):338-43.

PMID:
22420028

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