PubMed (GeneRIF) for id: 10166

Year	Number of Results
2001	1
2003	1
2004	1
2005	1
2006	1
2007	1
2008	2
2009	1
2010	1
2012	4
2013	1
2018	2
2023	1
2024	1

1

Deficiency in SLC25A15, a hypoxia-responsive gene, promotes hepatocellular carcinoma by reprogramming glutamine metabolism.

Zhang Q, Wei T, Jin W, Yan L, Shi L, Zhu S, Bai Y, Zeng Y, Yin Z, Yang J, Zhang W, Wu M, Zhang Y, Peng G, Roessler S, Liu L. Zhang Q, et al. J Hepatol. 2024 Feb;80(2):293-308. doi: 10.1016/j.jhep.2023.10.024. Epub 2023 Oct 30. J Hepatol. 2024. PMID: 38450598

2

Overexpression of SLC25A15 is involved in the proliferation of cutaneous melanoma and leads to poor prognosis.

Ji SM. Ji SM. Med Sci (Paris). 2018 Oct;34 Focus issue F1:74-80. doi: 10.1051/medsci/201834f113. Epub 2018 Nov 7. Med Sci (Paris). 2018. PMID: 30403179 Free article.

3

Structure/function relationships of the human mitochondrial ornithine/citrulline carrier by Cys site-directed mutagenesis. Relevance to mercury toxicity.

Giangregorio N, Tonazzi A, Console L, Galluccio M, Porcelli V, Indiveri C. Giangregorio N, et al. Int J Biol Macromol. 2018 Dec;120(Pt A):93-99. doi: 10.1016/j.ijbiomac.2018.08.069. Epub 2018 Aug 16. Int J Biol Macromol. 2018. PMID: 30121301

4

The mitochondrial transporter family SLC25: identification, properties and physiopathology.

Palmieri F. Palmieri F. Mol Aspects Med. 2013 Apr-Jun;34(2-3):465-84. doi: 10.1016/j.mam.2012.05.005. Epub 2012 Dec 23. Mol Aspects Med. 2013. PMID: 23266187 Review.

5

Long-term follow-up of four patients affected by HHH syndrome.

Kim SZ, Song WJ, Nyhan WL, Ficicioglu C, Mandell R, Shih VE. Kim SZ, et al. Clin Chim Acta. 2012 Jul 11;413(13-14):1151-5. doi: 10.1016/j.cca.2012.03.015. Epub 2012 Mar 23. Clin Chim Acta. 2012. PMID: 22465082

6

Insights into the mutation-induced HHH syndrome from modeling human mitochondrial ornithine transporter-1.

Wang JF, Chou KC. Wang JF, et al. PLoS One. 2012;7(1):e31048. doi: 10.1371/journal.pone.0031048. Epub 2012 Jan 26. PLoS One. 2012. PMID: 22292090 Free PMC article.

7

Substrate specificity of the two mitochondrial ornithine carriers can be swapped by single mutation in substrate binding site.

Monné M, Miniero DV, Daddabbo L, Robinson AJ, Kunji ER, Palmieri F. Monné M, et al. J Biol Chem. 2012 Mar 9;287(11):7925-34. doi: 10.1074/jbc.M111.324855. Epub 2012 Jan 19. J Biol Chem. 2012. PMID: 22262851 Free PMC article.

8

Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.

Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ. Hendrickson SL, et al. PLoS One. 2010 Sep 21;5(9):e12862. doi: 10.1371/journal.pone.0012862. PLoS One. 2010. PMID: 20877624 Free PMC article.

9

Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study.

Tessa A, Fiermonte G, Dionisi-Vici C, Paradies E, Baumgartner MR, Chien YH, Loguercio C, de Baulny HO, Nassogne MC, Schiff M, Deodato F, Parenti G, Rutledge SL, Vilaseca MA, Melone MA, Scarano G, Aldamiz-Echevarría L, Besley G, Walter J, Martinez-Hernandez E, Hernandez JM, Pierri CL, Palmieri F, Santorelli FM. Tessa A, et al. Hum Mutat. 2009 May;30(5):741-8. doi: 10.1002/humu.20930. Hum Mutat. 2009. PMID: 19242930

10

Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15.

Debray FG, Lambert M, Lemieux B, Soucy JF, Drouin R, Fenyves D, Dubé J, Maranda B, Laframboise R, Mitchell GA. Debray FG, et al. J Med Genet. 2008 Nov;45(11):759-64. doi: 10.1136/jmg.2008.059097. J Med Genet. 2008. PMID: 18978333 Free article.

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16 results

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