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300 related items for PubMed ID: 25417848

  • 1. Feline cystinuria caused by a missense mutation in the SLC3A1 gene.
    Mizukami K, Raj K, Giger U.
    J Vet Intern Med; 2015 Jan; 29(1):120-5. PubMed ID: 25417848
    [Abstract] [Full Text] [Related]

  • 2. Cystinuria Associated with Different SLC7A9 Gene Variants in the Cat.
    Mizukami K, Raj K, Osborne C, Giger U.
    PLoS One; 2016 Jan; 11(7):e0159247. PubMed ID: 27404572
    [Abstract] [Full Text] [Related]

  • 3. [Cystinuria caused by a SLC7A9 missense mutation in Siamese-crossbred littermates in Germany].
    Hilton S, Mizukami K, Giger U.
    Tierarztl Prax Ausg K Kleintiere Heimtiere; 2017 Aug 11; 45(4):265-272. PubMed ID: 28585658
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  • 4. Molecular genetic analysis of SLC3A1 and SLC7A9 genes in Czech and Slovak cystinuric patients.
    Skopková Z, Hrabincová E, Stástná S, Kozák L, Adam T.
    Ann Hum Genet; 2005 Sep 11; 69(Pt 5):501-7. PubMed ID: 16138908
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  • 5. SLC3A1 and SLC7A9 mutations in autosomal recessive or dominant canine cystinuria: a new classification system.
    Brons AK, Henthorn PS, Raj K, Fitzgerald CA, Liu J, Sewell AC, Giger U.
    J Vet Intern Med; 2013 Sep 11; 27(6):1400-8. PubMed ID: 24001348
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  • 7. Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs.
    Henthorn PS, Liu J, Gidalevich T, Fang J, Casal ML, Patterson DF, Giger U.
    Hum Genet; 2000 Oct 11; 107(4):295-303. PubMed ID: 11129328
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  • 8. Analysis of a 1-year-old cystinuric patient with recurrent renal stones.
    Tanzer F, Ozgur A, Bardakci F, Cankorkmaz L, Ayan S.
    Int J Urol; 2006 Oct 11; 13(10):1347-9. PubMed ID: 17010017
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  • 11. Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients.
    Bisceglia L, Fischetti L, Bonis PD, Palumbo O, Augello B, Stanziale P, Carella M, Zelante L.
    Mol Genet Metab; 2010 Jan 11; 99(1):42-52. PubMed ID: 19782624
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  • 12. Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria.
    Yuen YP, Lam CW, Lai CK, Tong SF, Li PS, Tam S, Kwan EY, Chan SY, Tsang WK, Chan KY, Mak WL, Cheng CW, Chan YW.
    Kidney Int; 2006 Jan 11; 69(1):123-8. PubMed ID: 16374432
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  • 14. Digenic Inheritance in Cystinuria Mouse Model.
    Espino M, Font-Llitjós M, Vilches C, Salido E, Prat E, López de Heredia M, Palacín M, Nunes V.
    PLoS One; 2015 Jan 11; 10(9):e0137277. PubMed ID: 26359869
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  • 16. Delineation of cystinuria in Saudi Arabia: A case series.
    Obaid A, Nashabat M, Al Fakeeh K, Al Qahtani AT, Alfadhel M.
    BMC Nephrol; 2017 Feb 06; 18(1):50. PubMed ID: 28166740
    [Abstract] [Full Text] [Related]

  • 17. Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria.
    Koulivand L, Mohammadi M, Ezatpour B, Salehi R, Markazi S, Dashti S, Kheirollahi M.
    Urolithiasis; 2015 Oct 06; 43(5):447-53. PubMed ID: 26123750
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  • 18. Spectrum of mutations in cystinuria patients presenting with prenatal hyperechoic colon.
    Tostivint I, Royer N, Nicolas M, Bourillon A, Czerkiewicz I, Becker PH, Muller F, Benoist JF.
    Clin Genet; 2017 Dec 06; 92(6):632-638. PubMed ID: 28646536
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  • 19. Human gene mutations. Gene symbol: SLC3A1. Disease: cystinuria.
    Bisceglia L, Reznik-Wolf H, Di Perna M, Pras E.
    Hum Genet; 2007 Sep 06; 122(2):215. PubMed ID: 18386386
    [No Abstract] [Full Text] [Related]

  • 20. Human gene mutations. Gene symbol: SLC3A1. Disease: cystinuria.
    Bisceglia L, Stanziale P, Zelante L.
    Hum Genet; 2007 Sep 06; 122(2):209. PubMed ID: 18386352
    [No Abstract] [Full Text] [Related]

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