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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1993 2
1994 4
1995 5
1996 6
1997 5
1998 8
1999 8
2000 12
2001 9
2002 7
2003 13
2004 8
2005 30
2006 13
2007 14
2008 7
2009 7
2010 11
2011 5
2012 8
2013 8
2014 10
2015 15
2016 12
2017 13
2018 10
2019 11
2020 10
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2022 14
2023 14
2024 3

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283 results

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Page 1
Cysteine transporter SLC3A1 promotes breast cancer tumorigenesis.
Jiang Y, Cao Y, Wang Y, Li W, Liu X, Lv Y, Li X, Mi J. Jiang Y, et al. Theranostics. 2017 Feb 26;7(4):1036-1046. doi: 10.7150/thno.18005. eCollection 2017. Theranostics. 2017. PMID: 28382174 Free PMC article.
Consistently, overexpression of SLC3A1 enhanced tumorigenesis of breast cancer cells, whereas blocking SLC3A1 either with specific siRNA or SLC3A1 specific inhibitor sulfasalazine suppressed tumor growth and also abolished dietary NAC-promoted tumor growth. C …
Consistently, overexpression of SLC3A1 enhanced tumorigenesis of breast cancer cells, whereas blocking SLC3A1 either with spec …
Cystinuria: an update on pathophysiology, genetics, and clinical management.
D'Ambrosio V, Capolongo G, Goldfarb D, Gambaro G, Ferraro PM. D'Ambrosio V, et al. Pediatr Nephrol. 2022 Aug;37(8):1705-1711. doi: 10.1007/s00467-021-05342-y. Epub 2021 Nov 23. Pediatr Nephrol. 2022. PMID: 34812923 Review.
To date, two genes have been identified as disease-causative: SLC3A1 and SLC7A9, encoding for the two subunits of the heterodimeric transporter. ...
To date, two genes have been identified as disease-causative: SLC3A1 and SLC7A9, encoding for the two subunits of the heterodimeric t …
Interpretation of SLC3A1 and SLC7A9 variants in cystinuria patients: The significance of the PM3 criterion and protein stability.
Lee B, Lee SY, Han DH, Park HD. Lee B, et al. Urolithiasis. 2023 Jul 13;51(1):94. doi: 10.1007/s00240-023-01466-y. Urolithiasis. 2023. PMID: 37439839 Free PMC article.
Cystinuria is a genetic disorder caused by defects in the b(0,+) transporter system, which is composed of rBAT and b(0,+)AT coded by SLC3A1 and SLC7A9, respectively. Variants in SLC3A1 and SLC7A9 follow autosomal recessive inheritance and autosomal dominant inherita …
Cystinuria is a genetic disorder caused by defects in the b(0,+) transporter system, which is composed of rBAT and b(0,+)AT coded by SLC3 …
Cystinuria.
Mattoo A, Goldfarb DS. Mattoo A, et al. Semin Nephrol. 2008 Mar;28(2):181-91. doi: 10.1016/j.semnephrol.2008.01.011. Semin Nephrol. 2008. PMID: 18359399 Review.
Although cystinuria is a relatively common disorder, it accounts for no more than 1% of all urinary tract stones. Thus far, mutations in 2 genes, SLC3A1 and SLC7A9, have been identified as being responsible for most cases of cystinuria by encoding defective subunits of the …
Although cystinuria is a relatively common disorder, it accounts for no more than 1% of all urinary tract stones. Thus far, mutations in 2 g …
Cystinuria.
Dello Strologo L, Rizzoni G. Dello Strologo L, et al. Acta Paediatr Suppl. 2006 Jul;95(452):31-3. doi: 10.1080/08035320600649473. Acta Paediatr Suppl. 2006. PMID: 16801163 Review.
A new classification is therefore needed: type A due to two mutations of SLC3A1 on chromosome 2, and type B due to two mutations of SLC7A9 on chromosome 19. ...
A new classification is therefore needed: type A due to two mutations of SLC3A1 on chromosome 2, and type B due to two mutations of S …
A Novel Mutation in SLC3A1 Gene in Patients With Cystinuria.
Markazi S, Kheirollahi M, Doosti A, Mohammadi M, Koulivand L. Markazi S, et al. Iran J Kidney Dis. 2016 Jan;10(1):44-7. Iran J Kidney Dis. 2016. PMID: 26837681 Free article.
In molecular term, cystinuria is classified as type A (mutations on SLC3A1 gene) and type B (mutations on SLC7A9 gene). This report describes 7 patients with early onset of cystine calculus formation. We are report a new mutation in SLC3A1 gene in exon 1. A novel nu …
In molecular term, cystinuria is classified as type A (mutations on SLC3A1 gene) and type B (mutations on SLC7A9 gene). This report d …
Pediatric Cystinuria Patient With Novel Mutation in SLC3A1.
Watanabe Y, Abe Y, Sakamoto S, Morimoto E, Taki Y, Hibino S, Fukagai T, Watanabe S. Watanabe Y, et al. Glob Pediatr Health. 2019 Jul 18;6:2333794X19862441. doi: 10.1177/2333794X19862441. eCollection 2019. Glob Pediatr Health. 2019. PMID: 31367653 Free PMC article. No abstract available.
Declaration: Novel SLC3A1 mutation in a cystinuria patient with xanthine stones: a case report.
Bai P, Zhang W, Lai L, Huang H, Qin J, Duan B, Wang H, Chen Y, Jia Y, Xing J, Wang T, Chen B. Bai P, et al. BMC Urol. 2023 Jul 31;23(1):130. doi: 10.1186/s12894-023-01300-y. BMC Urol. 2023. PMID: 37525149 Free PMC article.
CONCLUSION: Genetic testing by next-generation sequencing technology showed that the patient carried the homozygous nonsense mutation c.1113 C> A (p.Tyr371*) in the SLC3A1 gene, which was judged to be a functionally pathogenic variant. ...
CONCLUSION: Genetic testing by next-generation sequencing technology showed that the patient carried the homozygous nonsense mutation c.1113 …
Tissue distribution, hormonal regulation, ontogeny, diurnal expression, and induction of mouse cystine transporters Slc3a1 and Slc7a9.
Wu KC, Reisman SA, Klaassen CD. Wu KC, et al. Free Radic Res. 2020 Jul;54(7):525-534. doi: 10.1080/10715762.2020.1812597. Epub 2020 Sep 1. Free Radic Res. 2020. PMID: 32873097 Free PMC article.
Duodenal and hepatic Slc3a1 was higher in females than males. Hepatic Slc3a1 was high during darkness and low during daytime. ...High doses of diquat but not acetaminophen induced Slc3a1, suggesting Slc3a1 may respond to oxidative stress but not necess …
Duodenal and hepatic Slc3a1 was higher in females than males. Hepatic Slc3a1 was high during darkness and low during daytime. …
Population genetics analysis of SLC3A1 and SLC7A9 revealed the etiology of cystine stone may be more than what our current genetic knowledge can explain.
Wu CW, Badreddine J, Chang J, Huang YM, Kim FJ, Wild T, Tsai AC, Meeks N, Donalisio Da Silva R, Molina WR, Schumacher FR. Wu CW, et al. Urolithiasis. 2023 Aug 10;51(1):101. doi: 10.1007/s00240-023-01473-z. Urolithiasis. 2023. PMID: 37561200
BACKGROUND: Cystine stone is a Mendelian genetic disease caused by SLC3A1 or SLC7A9. In this study, we aimed to estimate the genetic prevalence of cystine stones and compare it with the clinical prevalence to better understand the disease etiology. METHODS: We analyzed gen …
BACKGROUND: Cystine stone is a Mendelian genetic disease caused by SLC3A1 or SLC7A9. In this study, we aimed to estimate the genetic …
283 results