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Journal Abstract Search

205 related items for PubMed ID: 2008213

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorption.
    Martín MG, Turk E, Kerner C, Zabel B, Wirth S, Wright EM.
    Prenat Diagn; 1996 May 28; 16(5):458-62. PubMed ID: 8844006
    [Abstract] [Full Text] [Related]

  • 3. Molecular basis for glucose-galactose malabsorption.
    Wright EM, Turk E, Martin MG.
    Cell Biochem Biophys; 2002 May 28; 36(2-3):115-21. PubMed ID: 12139397
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
    Martín MG, Turk E, Lostao MP, Kerner C, Wright EM.
    Nat Genet; 1996 Feb 28; 12(2):216-20. PubMed ID: 8563765
    [Abstract] [Full Text] [Related]

  • 6. [Glucose-galactose malabsorption. The first reported case in Denmark].
    Boisen KA, Hjelt K.
    Ugeskr Laeger; 1999 Jun 28; 161(26):4008-9. PubMed ID: 10402938
    [Abstract] [Full Text] [Related]

  • 7. [Thirty years of research on congenital glucose and galactose malabsorption: from phenotype to genotype].
    Desjeux JF, Wright EM.
    Bull Acad Natl Med; 1993 Jan 28; 177(1):125-31; discussion 132-5. PubMed ID: 8319109
    [Abstract] [Full Text] [Related]

  • 8. [30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype].
    Desjeux JF, Wright EM.
    Ann Gastroenterol Hepatol (Paris); 1993 Oct 28; 29(5):263-6; discussion 266-8. PubMed ID: 8250522
    [Abstract] [Full Text] [Related]

  • 9. 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 28; 63(2):151-8. PubMed ID: 22383112
    [Abstract] [Full Text] [Related]

  • 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 28; 79(1):86-91. PubMed ID: 20486940
    [Abstract] [Full Text] [Related]

  • 11. The Na+/glucose cotransporter (SGLT1).
    Wright EM, Turk E, Hager K, Lescale-Matys L, Hirayama B, Supplisson S, Loo DD.
    Acta Physiol Scand Suppl; 1992 Jan 28; 607():201-7. PubMed ID: 1449065
    [Abstract] [Full Text] [Related]

  • 12. I. Glucose galactose malabsorption.
    Wright EM.
    Am J Physiol; 1998 Nov 28; 275(5):G879-82. PubMed ID: 9815014
    [Abstract] [Full Text] [Related]

  • 13. Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.
    Lam JT, Martín MG, Turk E, Hirayama BA, Bosshard NU, Steinmann B, Wright EM.
    Biochim Biophys Acta; 1999 Feb 24; 1453(2):297-303. PubMed ID: 10036327
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Structure of the human Na+/glucose cotransporter gene SGLT1.
    Turk E, Martín MG, Wright EM.
    J Biol Chem; 1994 May 27; 269(21):15204-9. PubMed ID: 8195156
    [Abstract] [Full Text] [Related]

  • 16. Expression cloning and cDNA sequencing of the Na+/glucose co-transporter.
    Hediger MA, Coady MJ, Ikeda TS, Wright EM.
    Nature; 1994 May 27; 330(6146):379-81. PubMed ID: 2446136
    [Abstract] [Full Text] [Related]

  • 17. [Congential malabsorption of glucose and galactose in 2 brothers].
    Kawakami E, Silvestrini WS, Machado NL, Wehba J, Fagundes Neto U.
    Arq Gastroenterol; 1982 May 27; 19(1):38-43. PubMed ID: 7181724
    [Abstract] [Full Text] [Related]

  • 18. Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.
    Vallaeys L, Van Biervliet S, De Bruyn G, Loeys B, Moring AS, Van Deynse E, Cornette L.
    Eur J Pediatr; 2013 Mar 27; 172(3):409-11. PubMed ID: 22843301
    [Abstract] [Full Text] [Related]

  • 19. Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
    van den Heuvel LP, Assink K, Willemsen M, Monnens L.
    Hum Genet; 2002 Dec 27; 111(6):544-7. PubMed ID: 12436245
    [Abstract] [Full Text] [Related]

  • 20. Intestinal absorption in health and disease--sugars.
    Wright EM, Martín MG, Turk E.
    Best Pract Res Clin Gastroenterol; 2003 Dec 27; 17(6):943-56. PubMed ID: 14642859
    [Abstract] [Full Text] [Related]

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