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5. Mutations in SLC13A5 cause autosomal-recessive epileptic encephalopathy with seizure onset in the first days of life. Thevenon J; Milh M; Feillet F; St-Onge J; Duffourd Y; Jugé C; Roubertie A; Héron D; Mignot C; Raffo E; Isidor B; Wahlen S; Sanlaville D; Villeneuve N; Darmency-Stamboul V; Toutain A; Lefebvre M; Chouchane M; Huet F; Lafon A; de Saint Martin A; Lesca G; El Chehadeh S; Thauvin-Robinet C; Masurel-Paulet A; Odent S; Villard L; Philippe C; Faivre L; Rivière JB Am J Hum Genet; 2014 Jul; 95(1):113-20. PubMed ID: 24995870 [TBL] [Abstract][Full Text] [Related]
6. Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy. Alsemari A; Guzmán-Vega FJ; Meyer BF; Arold ST Pediatr Neurol; 2024 Feb; 151():68-72. PubMed ID: 38113697 [TBL] [Abstract][Full Text] [Related]
7. SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome. Schossig A; Bloch-Zupan A; Lussi A; Wolf NI; Raskin S; Cohen M; Giuliano F; Jurgens J; Krabichler B; Koolen DA; de Macena Sobreira NL; Maurer E; Muller-Bolla M; Penzien J; Zschocke J; Kapferer-Seebacher I J Med Genet; 2017 Jan; 54(1):54-62. PubMed ID: 27600704 [TBL] [Abstract][Full Text] [Related]
8. Disruption of the sodium-dependent citrate transporter SLC13A5 in mice causes alterations in brain citrate levels and neuronal network excitability in the hippocampus. Henke C; Töllner K; van Dijk RM; Miljanovic N; Cordes T; Twele F; Bröer S; Ziesak V; Rohde M; Hauck SM; Vogel C; Welzel L; Schumann T; Willmes DM; Kurzbach A; El-Agroudy NN; Bornstein SR; Schneider SA; Jordan J; Potschka H; Metallo CM; Köhling R; Birkenfeld AL; Löscher W Neurobiol Dis; 2020 Sep; 143():105018. PubMed ID: 32682952 [TBL] [Abstract][Full Text] [Related]
9. Consequences of NaCT/SLC13A5/mINDY deficiency: good versus evil, separated only by the blood-brain barrier. Kopel JJ; Bhutia YD; Sivaprakasam S; Ganapathy V Biochem J; 2021 Feb; 478(3):463-486. PubMed ID: 33544126 [TBL] [Abstract][Full Text] [Related]
10. Analysis of naturally occurring mutations in the human uptake transporter NaCT important for bone and brain development and energy metabolism. Selch S; Chafai A; Sticht H; Birkenfeld AL; Fromm MF; König J Sci Rep; 2018 Jul; 8(1):11330. PubMed ID: 30054523 [TBL] [Abstract][Full Text] [Related]
11. Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity. Kopel J; Grooms A; Ganapathy V; Clothier J Psychiatr Genet; 2021 Feb; 31(1):32-35. PubMed ID: 33290383 [TBL] [Abstract][Full Text] [Related]
12. Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycle. Bainbridge MN; Cooney E; Miller M; Kennedy AD; Wulff JE; Donti T; Jhangiani SN; Gibbs RA; Elsea SH; Porter BE; Graham BH Mol Genet Metab; 2017 Aug; 121(4):314-319. PubMed ID: 28673551 [TBL] [Abstract][Full Text] [Related]
13. Discovery and characterization of novel inhibitors of the sodium-coupled citrate transporter (NaCT or SLC13A5). Huard K; Brown J; Jones JC; Cabral S; Futatsugi K; Gorgoglione M; Lanba A; Vera NB; Zhu Y; Yan Q; Zhou Y; Vernochet C; Riccardi K; Wolford A; Pirman D; Niosi M; Aspnes G; Herr M; Genung NE; Magee TV; Uccello DP; Loria P; Di L; Gosset JR; Hepworth D; Rolph T; Pfefferkorn JA; Erion DM Sci Rep; 2015 Dec; 5():17391. PubMed ID: 26620127 [TBL] [Abstract][Full Text] [Related]
14. A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangement in an Iraqi family with epileptic encephalopathy. Duan R; Saadi NW; Grochowski CM; Bhadila G; Faridoun A; Mitani T; Du H; Fatih JM; Jhangiani SN; Akdemir ZC; Gibbs RA; Pehlivan D; Posey JE; Marafi D; Lupski JR Am J Med Genet A; 2021 Jul; 185(7):1972-1980. PubMed ID: 33797191 [TBL] [Abstract][Full Text] [Related]
15. Carbamazepine efficacy in a severe electro-clinical presentation of SLC13A5-epilepsy. Santalucia R; Vilain C; Soblet J; De Laet C; Vuckovic A; König J; Aeby A Ann Clin Transl Neurol; 2022 Jul; 9(7):1095-1099. PubMed ID: 35633140 [TBL] [Abstract][Full Text] [Related]
16. Structure and inhibition mechanism of the human citrate transporter NaCT. Sauer DB; Song J; Wang B; Hilton JK; Karpowich NK; Mindell JA; Rice WJ; Wang DN Nature; 2021 Mar; 591(7848):157-161. PubMed ID: 33597751 [TBL] [Abstract][Full Text] [Related]
17. SLC13A5 Deficiency Disorder: From Genetics to Gene Therapy. Goodspeed K; Liu JS; Nye KL; Prasad S; Sadhu C; Tavakkoli F; Bilder DA; Minassian BA; Bailey RM Genes (Basel); 2022 Sep; 13(9):. PubMed ID: 36140822 [TBL] [Abstract][Full Text] [Related]
18. Defective enamel and bone development in sodium-dependent citrate transporter (NaCT) Slc13a5 deficient mice. Irizarry AR; Yan G; Zeng Q; Lucchesi J; Hamang MJ; Ma YL; Rong JX PLoS One; 2017; 12(4):e0175465. PubMed ID: 28406943 [TBL] [Abstract][Full Text] [Related]
19. GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders. Ohba C; Shiina M; Tohyama J; Haginoya K; Lerman-Sagie T; Okamoto N; Blumkin L; Lev D; Mukaida S; Nozaki F; Uematsu M; Onuma A; Kodera H; Nakashima M; Tsurusaki Y; Miyake N; Tanaka F; Kato M; Ogata K; Saitsu H; Matsumoto N Epilepsia; 2015 Jun; 56(6):841-8. PubMed ID: 25864721 [TBL] [Abstract][Full Text] [Related]
20. A specialized metabolic pathway partitions citrate in hydroxyapatite to impact mineralization of bones and teeth. Dirckx N; Zhang Q; Chu EY; Tower RJ; Li Z; Guo S; Yuan S; Khare PA; Zhang C; Verardo A; Alejandro LO; Park A; Faugere MC; Helfand SL; Somerman MJ; Riddle RC; de Cabo R; Le A; Schmidt-Rohr K; Clemens TL Proc Natl Acad Sci U S A; 2022 Nov; 119(45):e2212178119. PubMed ID: 36322718 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]