188 related articles for article (PubMed ID: 24687295)
21. A key role of the mitochondrial citrate carrier (SLC25A1) in TNFα- and IFNγ-triggered inflammation.
Infantino V; Iacobazzi V; Menga A; Avantaggiati ML; Palmieri F
Biochim Biophys Acta; 2014 Nov; 1839(11):1217-1225. PubMed ID: 25072865
[TBL] [Abstract][Full Text] [Related]
22. The Mitochondrial Citrate Carrier SLC25A1/CIC and the Fundamental Role of Citrate in Cancer, Inflammation and Beyond.
Mosaoa R; Kasprzyk-Pawelec A; Fernandez HR; Avantaggiati ML
Biomolecules; 2021 Jan; 11(2):. PubMed ID: 33499062
[TBL] [Abstract][Full Text] [Related]
23. A mouse model of L-2-hydroxyglutaric aciduria, a disorder of metabolite repair.
Rzem R; Achouri Y; Marbaix E; Schakman O; Wiame E; Marie S; Gailly P; Vincent MF; Veiga-da-Cunha M; Van Schaftingen E
PLoS One; 2015; 10(3):e0119540. PubMed ID: 25763823
[TBL] [Abstract][Full Text] [Related]
24. D-2-hydroxyglutaric aciduria: hypotonia, cortical blindness, seizures, cardiomyopathy, and cylindrical spirals in skeletal muscle.
Baker NS; Sarnat HB; Jack RM; Patterson K; Shaw DW; Herndon SP
J Child Neurol; 1997 Jan; 12(1):31-6. PubMed ID: 9010793
[TBL] [Abstract][Full Text] [Related]
25. Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant.
Balaraju S; Töpf A; McMacken G; Kumar VP; Pechmann A; Roper H; Vengalil S; Polavarapu K; Nashi S; Mahajan NP; Barbosa IA; Deshpande C; Taylor RW; Cossins J; Beeson D; Laurie S; Kirschner J; Horvath R; McFarland R; Nalini A; Lochmüller H
Eur J Hum Genet; 2020 Mar; 28(3):373-377. PubMed ID: 31527857
[TBL] [Abstract][Full Text] [Related]
26.
Wang L; Zhang H; Zhang Y; Song Y
Microb Cell Fact; 2019 Sep; 18(1):154. PubMed ID: 31506101
[TBL] [Abstract][Full Text] [Related]
27. Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cells.
Lamp J; Keyser B; Koeller DM; Ullrich K; Braulke T; Mühlhausen C
J Biol Chem; 2011 May; 286(20):17777-84. PubMed ID: 21454630
[TBL] [Abstract][Full Text] [Related]
28. Expanding the Clinical Spectrum of Mitochondrial Citrate Carrier (SLC25A1) Deficiency: Facial Dysmorphism in Siblings with Epileptic Encephalopathy and Combined D,L-2-Hydroxyglutaric Aciduria.
Prasun P; Young S; Salomons G; Werneke A; Jiang YH; Struys E; Paige M; Avantaggiati ML; McDonald M
JIMD Rep; 2015; 19():111-5. PubMed ID: 25614306
[TBL] [Abstract][Full Text] [Related]
29. Progress in understanding 2-hydroxyglutaric acidurias.
Kranendijk M; Struys EA; Salomons GS; Van der Knaap MS; Jakobs C
J Inherit Metab Dis; 2012 Jul; 35(4):571-87. PubMed ID: 22391998
[TBL] [Abstract][Full Text] [Related]
30. 3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.
Wortmann SB; Kremer BH; Graham A; Willemsen MA; Loupatty FJ; Hogg SL; Engelke UF; Kluijtmans LA; Wanders RJ; Illsinger S; Wilcken B; Cruysberg JR; Das AM; Morava E; Wevers RA
Neurology; 2010 Sep; 75(12):1079-83. PubMed ID: 20855850
[TBL] [Abstract][Full Text] [Related]
31. Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.
Napoli E; Tassone F; Wong S; Angkustsiri K; Simon TJ; Song G; Giulivi C
J Biol Chem; 2015 Sep; 290(38):23240-53. PubMed ID: 26221035
[TBL] [Abstract][Full Text] [Related]
32. A conserved role for the mitochondrial citrate transporter Sea/SLC25A1 in the maintenance of chromosome integrity.
Morciano P; Carrisi C; Capobianco L; Mannini L; Burgio G; Cestra G; De Benedetto GE; Corona DF; Musio A; Cenci G
Hum Mol Genet; 2009 Nov; 18(21):4180-8. PubMed ID: 19654186
[TBL] [Abstract][Full Text] [Related]
33. [Congenital myasthenic syndrome related to SLC25A1 gene variant: two cases report and literature review].
Li WH; Wu BB; Zhou SZ
Zhonghua Er Ke Za Zhi; 2021 Jan; 59(1):42-46. PubMed ID: 33397003
[No Abstract] [Full Text] [Related]
34. Acetylation of human mitochondrial citrate carrier modulates mitochondrial citrate/malate exchange activity to sustain NADPH production during macrophage activation.
Palmieri EM; Spera I; Menga A; Infantino V; Porcelli V; Iacobazzi V; Pierri CL; Hooper DC; Palmieri F; Castegna A
Biochim Biophys Acta; 2015 Aug; 1847(8):729-38. PubMed ID: 25917893
[TBL] [Abstract][Full Text] [Related]
35. SLC25A1 promotes tumor growth and survival by reprogramming energy metabolism in colorectal cancer.
Yang Y; He J; Zhang B; Zhang Z; Jia G; Liu S; Wu T; He X; Wang N
Cell Death Dis; 2021 Nov; 12(12):1108. PubMed ID: 34839347
[TBL] [Abstract][Full Text] [Related]
36. Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
Muntau AC; Röschinger W; Merkenschlager A; van der Knaap MS; Jakobs C; Duran M; Hoffmann GF; Roscher AA
Neuropediatrics; 2000 Jun; 31(3):137-40. PubMed ID: 10963100
[TBL] [Abstract][Full Text] [Related]
37. Eyelid myoclonia with absence seizures in a child with l-2 hydroxyglutaric aciduria: findings of magnetic resonance imaging.
Mete A; Isikay S; Sirikci A; Ozkur A; Bayram M
Pediatr Neurol; 2012 Mar; 46(3):195-7. PubMed ID: 22353300
[TBL] [Abstract][Full Text] [Related]
38. Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria.
Struys EA; Salomons GS; Achouri Y; Van Schaftingen E; Grosso S; Craigen WJ; Verhoeven NM; Jakobs C
Am J Hum Genet; 2005 Feb; 76(2):358-60. PubMed ID: 15609246
[TBL] [Abstract][Full Text] [Related]
39. [L-2-hydroxyglutaric aciduria: report on two cases].
Wagner S; Vianey-Saban C; Salomons GS; Schmitt E; Feillet F
Arch Pediatr; 2014 Jan; 21(1):78-85. PubMed ID: 24321868
[TBL] [Abstract][Full Text] [Related]
40. Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes.
Collado MS; Armstrong AJ; Olson M; Hoang SA; Day N; Summar M; Chapman KA; Reardon J; Figler RA; Wamhoff BR
Mol Genet Metab; 2020 Jul; 130(3):183-196. PubMed ID: 32451238
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
