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Items: 1 to 20 of 44

1.

NF-κB controls four genes encoding core enzymes of tricarboxylic acid cycle.

Zhou F, Xu X, Wu J, Wang D, Wang J.

Gene. 2017 Jul 20;621:12-20. doi: 10.1016/j.gene.2017.04.012. Epub 2017 Apr 8.

PMID:
28400269
2.

Mitochondrial purine and pyrimidine metabolism and beyond.

Wang L.

Nucleosides Nucleotides Nucleic Acids. 2016 Dec;35(10-12):578-594. Review.

PMID:
27906631
3.

Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations.

Kacso G, Ravasz D, Doczi J, Németh B, Madgar O, Saada A, Ilin P, Miller C, Ostergaard E, Iordanov I, Adams D, Vargedo Z, Araki M, Araki K, Nakahara M, Ito H, Gál A, Molnár MJ, Nagy Z, Patocs A, Adam-Vizi V, Chinopoulos C.

Biochem J. 2016 Oct 15;473(20):3463-3485. Epub 2016 Aug 5.

4.

A Balanced Tissue Composition Reveals New Metabolic and Gene Expression Markers in Prostate Cancer.

Tessem MB, Bertilsson H, Angelsen A, Bathen TF, Drabløs F, Rye MB.

PLoS One. 2016 Apr 21;11(4):e0153727. doi: 10.1371/journal.pone.0153727. eCollection 2016.

5.

Novel mutation in SUCLA2 identified on sequencing analysis.

Güngör O, Özkaya AK, Güngör G, Karaer K, Dilber C, Aydin K.

Pediatr Int. 2016 Jul;58(7):659-61. doi: 10.1111/ped.12921. Epub 2016 Mar 8.

PMID:
26952923
6.

Influences of XDH genotype by gene-gene interactions with SUCLA2 for thiopurine-induced leukopenia in Korean patients with Crohn's disease.

Park SK, Hong M, Ye BD, Kim KJ, Park SH, Yang DH, Hwang SW, Kwak MS, Lee HS, Song K, Yang SK.

Scand J Gastroenterol. 2016;51(6):684-91. doi: 10.3109/00365521.2015.1133698. Epub 2016 Jan 14.

PMID:
26863601
7.

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
8.

Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.

Carrozzo R, Verrigni D, Rasmussen M, de Coo R, Amartino H, Bianchi M, Buhas D, Mesli S, Naess K, Born AP, Woldseth B, Prontera P, Batbayli M, Ravn K, Joensen F, Cordelli DM, Santorelli FM, Tulinius M, Darin N, Duno M, Jouvencel P, Burlina A, Stangoni G, Bertini E, Redonnet-Vernhet I, Wibrand F, Dionisi-Vici C, Uusimaa J, Vieira P, Osorio AN, McFarland R, Taylor RW, Holme E, Ostergaard E.

J Inherit Metab Dis. 2016 Mar;39(2):243-52. doi: 10.1007/s10545-015-9894-9. Epub 2015 Oct 16.

PMID:
26475597
9.

Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria.

Liu Y, Li X, Wang Q, Ding Y, Song J, Yang Y.

Brain Dev. 2016 Jan;38(1):61-7. doi: 10.1016/j.braindev.2015.05.002. Epub 2015 May 28.

PMID:
26028457
10.

Genomic and Clinicopathologic Features of Primary Myelofibrosis With Isolated 13q Deletion.

Mehrotra M, Patel KP, Chen T, Miranda RN, Wang Y, Zuo Z, Muddasani R, Mishra BM, Abraham R, Luthra R, Lu G.

Clin Lymphoma Myeloma Leuk. 2015 Aug;15(8):496-505.e1-2. doi: 10.1016/j.clml.2015.03.018. Epub 2015 Apr 3.

PMID:
26027540
11.

Localization of SUCLA2 and SUCLG2 subunits of succinyl CoA ligase within the cerebral cortex suggests the absence of matrix substrate-level phosphorylation in glial cells of the human brain.

Dobolyi A, Bagó AG, Gál A, Molnár MJ, Palkovits M, Adam-Vizi V, Chinopoulos C.

J Bioenerg Biomembr. 2015 Apr;47(1-2):33-41. doi: 10.1007/s10863-014-9586-4. Epub 2014 Nov 5.

PMID:
25370487
13.

Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion.

Matilainen S, Isohanni P, Euro L, Lönnqvist T, Pihko H, Kivelä T, Knuutila S, Suomalainen A.

Eur J Hum Genet. 2015 Mar;23(3):325-30. doi: 10.1038/ejhg.2014.128. Epub 2014 Jul 2. Review.

14.

A novel SUCLA2 mutation in a Portuguese child associated with "mild" methylmalonic aciduria.

Nogueira C, Meschini MC, Nesti C, Garcia P, Diogo L, Valongo C, Costa R, Videira A, Vilarinho L, Santorelli FM.

J Child Neurol. 2015 Feb;30(2):228-32. doi: 10.1177/0883073814527158. Epub 2014 Mar 20.

PMID:
24659738
15.

Measurement of succinyl-carnitine and methylmalonyl-carnitine on dried blood spot by liquid chromatography-tandem mass spectrometry.

Rizzo C, Boenzi S, Inglese R, la Marca G, Muraca M, Martinez TB, Johnson DW, Zelli E, Dionisi-Vici C.

Clin Chim Acta. 2014 Feb 15;429:30-3. doi: 10.1016/j.cca.2013.11.016. Epub 2013 Nov 22.

PMID:
24269713
16.

Exclusive neuronal expression of SUCLA2 in the human brain.

Dobolyi A, Ostergaard E, Bagó AG, Dóczi T, Palkovits M, Gál A, Molnár MJ, Adam-Vizi V, Chinopoulos C.

Brain Struct Funct. 2015 Jan;220(1):135-51. doi: 10.1007/s00429-013-0643-2. Epub 2013 Oct 2.

PMID:
24085565
17.

The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine.

Jaberi E, Chitsazian F, Ali Shahidi G, Rohani M, Sina F, Safari I, Malakouti Nejad M, Houshmand M, Klotzle B, Elahi E.

J Hum Genet. 2013 Aug;58(8):526-30. doi: 10.1038/jhg.2013.45. Epub 2013 Jun 13.

PMID:
23759946
18.

Nuclear factors: roles related to mitochondrial deafness.

Luo LF, Hou CC, Yang WX.

Gene. 2013 May 15;520(2):79-89. doi: 10.1016/j.gene.2013.03.041. Epub 2013 Mar 17. Review.

PMID:
23510774
19.

Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options.

El-Hattab AW, Scaglia F.

Neurotherapeutics. 2013 Apr;10(2):186-98. doi: 10.1007/s13311-013-0177-6. Review.

20.

A novel homozygous mutation in SUCLA2 gene identified by exome sequencing.

Lamperti C, Fang M, Invernizzi F, Liu X, Wang H, Zhang Q, Carrara F, Moroni I, Zeviani M, Zhang J, Ghezzi D.

Mol Genet Metab. 2012 Nov;107(3):403-8. doi: 10.1016/j.ymgme.2012.08.020. Epub 2012 Sep 7.

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