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Journal Abstract Search

347 related items for PubMed ID: 12139397

  • 1. Molecular basis for glucose-galactose malabsorption.
    Wright EM, Turk E, Martin MG.
    Cell Biochem Biophys; 2002; 36(2-3):115-21. PubMed ID: 12139397
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  • 2. Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.
    Turk E, Zabel B, Mundlos S, Dyer J, Wright EM.
    Nature; 1991 Mar 28; 350(6316):354-6. PubMed ID: 2008213
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  • 6. Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.
    Turk E, Klisak I, Bacallao R, Sparkes RS, Wright EM.
    Genomics; 1993 Sep 28; 17(3):752-4. PubMed ID: 8244393
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  • 7. A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.
    Kasahara M, Maeda M, Hayashi S, Mori Y, Abe T.
    Biochim Biophys Acta; 2001 May 31; 1536(2-3):141-7. PubMed ID: 11406349
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  • 10. Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.
    Xin B, Wang H.
    Clin Genet; 2011 Jan 31; 79(1):86-91. PubMed ID: 20486940
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  • 11. Compound missense mutations in the sodium/D-glucose cotransporter result in trafficking defects.
    Martín MG, Lostao MP, Turk E, Lam J, Kreman M, Wright EM.
    Gastroenterology; 1997 Apr 31; 112(4):1206-12. PubMed ID: 9098004
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  • 16. Structural insights into genetic variants of Na(+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure.
    Raja M, Kinne RK.
    Cell Biochem Biophys; 2012 Jun 31; 63(2):151-8. PubMed ID: 22383112
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  • 17. [30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype].
    Desjeux JF, Wright EM.
    Ann Gastroenterol Hepatol (Paris); 1993 Oct 31; 29(5):263-6; discussion 266-8. PubMed ID: 8250522
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