Cystine

solute carrier family 7 member 9 ; Homo sapiens







15 Article(s)
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Pub. Year
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1 32602810 Computational analysis identifies druggable mutations in human rBAT mediated Cystinuria. 2021 Sep 2
2 33262960 Diversity of Phenotype and Genetic Etiology of 23 Cystinuria Saudi Patients: A Retrospective Study. 2020 1
3 30069816 In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. 2018 Oct 1
4 18074125 Evaluation of cystine transport in cultured human kidney cells and establishment of cystinuria type I phenotype by antisense technology. 2008 Feb 2
5 16845473 SLC7A9 cDNA cloning and mutational analysis of SLC3A1 and SLC7A9 in canine cystinuria. 2006 Jul 1
6 14561219 Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b0,+AT. 2004 Feb 1 1
7 14770309 The ancillary proteins of HATs: SLC3 family of amino acid transporters. 2004 Feb 2
8 12621979 [From gene to disease; SLC3A1, SLC7A9 and cystinuria]. 2003 Feb 8 2
9 12036192 Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the disease. 2002 May 1
10 12167606 rBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidney. 2002 Sep 4
11 12234283 Cystinuria in children: distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes. 2002 Oct 3
12 12371955 SLC7A9 mutations in all three cystinuria subtypes. 2002 Nov 1
13 11318953 Human cystinuria-related transporter: localization and functional characterization. 2001 May 2
14 10810228 The molecular basis of cystinuria: an update. 2000 May-Jun 1
15 11042122 Cysteine residues in the C-terminus of the neutral- and basic-amino-acid transporter heavy-chain subunit contribute to functional properties of the system b(0,+)-type amino acid transporter. 2000 Nov 1 1