These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

541 related items for PubMed ID: 23415628

  • 1. Frequency of LCT-13910C/T and LCT-22018G/A single nucleotide polymorphisms associated with adult-type hypolactasia/lactase persistence among Israelis of different ethnic groups.
    Raz M, Sharon Y, Yerushalmi B, Birk R.
    Gene; 2013 Apr 25; 519(1):67-70. PubMed ID: 23415628
    [Abstract] [Full Text] [Related]

  • 2. Frequency of LCT -13910C>T single nucleotide polymorphism associated with adult-type hypolactasia/lactase persistence among Brazilians of different ethnic groups.
    Mattar R, Monteiro MS, Villares CA, Santos AF, Silva JM, Carrilho FJ.
    Nutr J; 2009 Oct 02; 8():46. PubMed ID: 19799794
    [Abstract] [Full Text] [Related]

  • 3. Simultaneous genotyping of the three lactose tolerance-linked polymorphisms LCT -13907C>G, LCT -13910C>T and LCT -13915T>G with Pyrosequencing technology.
    Nilsson TK, Olsson LA.
    Clin Chem Lab Med; 2008 Oct 02; 46(1):80-4. PubMed ID: 18034639
    [Abstract] [Full Text] [Related]

  • 4. 13910C>T and 22018G>A LCT gene polymorphisms in diagnosing hypolactasia in children.
    Tomczonek-Moruś J, Wojtasik A, Zeman K, Smolarz B, Bąk-Romaniszyn L.
    United European Gastroenterol J; 2019 Mar 02; 7(2):210-216. PubMed ID: 31080605
    [Abstract] [Full Text] [Related]

  • 5. Identification of novel genetic variants in the mutational hotspot region 14 kb upstream of the LCT gene in a Mexican population.
    Valencia L, Randazzo A, Engfeldt P, Olsson LA, Chávez A, Buckland RJ, Nilsson TK, Almon R.
    Scand J Clin Lab Invest; 2017 Sep 02; 77(5):311-314. PubMed ID: 28452238
    [Abstract] [Full Text] [Related]

  • 6. The -13914G>A variant upstream of the lactase gene (LCT) is associated with lactase persistence/non-persistence.
    Khabarova Y, Torniainen S, Savilahti E, Isokoski M, Mattila K, Järvelä I.
    Scand J Clin Lab Invest; 2010 Sep 02; 70(5):354-7. PubMed ID: 20509822
    [Abstract] [Full Text] [Related]

  • 7. Comparison of Quick Lactose Intolerance Test in duodenal biopsies of dyspeptic patients with single nucleotide polymorphism LCT-13910C>T associated with primary hypolactasia/lactase-persistence.
    Mattar R, Basile-Filho A, Kemp R, Santos JS.
    Acta Cir Bras; 2013 Sep 02; 28 Suppl 1():77-82. PubMed ID: 23381829
    [Abstract] [Full Text] [Related]

  • 8. Real-time PCR based detection of the lactase non-persistence associated genetic variant LCT-13910C>T directly from whole blood.
    Muendlein A, Leiherer A, Zach C, Brandtner EM, Fraunberger P, Drexel H, Geiger K.
    Mol Biol Rep; 2019 Apr 02; 46(2):2379-2385. PubMed ID: 30790118
    [Abstract] [Full Text] [Related]

  • 9. Analysis of three functional polymorphisms in relation to osteoporosis phenotypes: replication in a Spanish cohort.
    Agueda L, Urreizti R, Bustamante M, Jurado S, Garcia-Giralt N, Díez-Pérez A, Nogués X, Mellibovsky L, Grinberg D, Balcells S.
    Calcif Tissue Int; 2010 Jul 02; 87(1):14-24. PubMed ID: 20390408
    [Abstract] [Full Text] [Related]

  • 10. LCT-22018G>A single nucleotide polymorphism is a better predictor of adult-type hypolactasia/lactase persistence in Japanese-Brazilians than LCT-13910C>T.
    Mattar R, Monteiro Mdo S, Silva JM, Carrilho FJ.
    Clinics (Sao Paulo); 2010 Jul 02; 65(12):1399. PubMed ID: 21340236
    [No Abstract] [Full Text] [Related]

  • 11. The Frequency of the LCT*-13910C>T Polymorphism Associated with Lactase Persistence Diverges among Euro-Descendant Groups from Brazil.
    Boschmann SE, Boldt AB, de Souza IR, Petzl-Erler ML, Messias-Reason IJ.
    Med Princ Pract; 2016 Jul 02; 25(1):18-20. PubMed ID: 26334798
    [Abstract] [Full Text] [Related]

  • 12. The lactase gene -13910T allele can not predict the lactase-persistence phenotype in north China.
    Sun HM, Qiao YD, Chen F, Xu LD, Bai J, Fu SB.
    Asia Pac J Clin Nutr; 2007 Jul 02; 16(4):598-601. PubMed ID: 18042517
    [Abstract] [Full Text] [Related]

  • 13. Brief communication: Effect of nomadic subsistence practices on lactase persistence associated genetic variation in Kuwait.
    Hill SC, Mohammad TR, Kivisild T.
    Am J Phys Anthropol; 2013 Sep 02; 152(1):140-4. PubMed ID: 23913618
    [Abstract] [Full Text] [Related]

  • 14. Lactase persistence genotyping: rapid detection of seven sequence variants in a single tube with melting curve analyses.
    Strand H, Sørensen LK, Ingebretsen OC.
    Clin Chem Lab Med; 2014 Sep 02; 52(9):1277-82. PubMed ID: 24756060
    [Abstract] [Full Text] [Related]

  • 15. Very low frequency of the lactase persistence allele LCT-13910T in the Armenian population.
    Németh S, Kriegshäuser G, Hovhannesyan K, Hayrapetyan H, Oberkanins C, Sarkisian T.
    Ann Hum Biol; 2022 Sep 02; 49(5-6):260-262. PubMed ID: 36129808
    [Abstract] [Full Text] [Related]

  • 16. Polymorphisms of CYP2C19 and CYP2D6 in Israeli ethnic groups.
    Luo HR, Aloumanis V, Lin KM, Gurwitz D, Wan YJ.
    Am J Pharmacogenomics; 2004 Sep 02; 4(6):395-401. PubMed ID: 15651900
    [Abstract] [Full Text] [Related]

  • 17. Lactase persistence/non-persistence genetic variants in irritable bowel syndrome in an endemic area for lactose malabsorption.
    Kumar S, Ranjan P, Mittal B, Singh R, Ghoshal UC.
    J Gastroenterol Hepatol; 2012 Dec 02; 27(12):1825-30. PubMed ID: 22989008
    [Abstract] [Full Text] [Related]

  • 18. Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients.
    Piepoli A, Schirru E, Mastrorilli A, Gentile A, Cotugno R, Quitadamo M, Merla A, Congia M, Usai Satta P, Perri F.
    J Biomol Screen; 2007 Aug 02; 12(5):733-9. PubMed ID: 17478481
    [Abstract] [Full Text] [Related]

  • 19. Effect of C/T -13910 cis-acting regulatory variant on expression and activity of lactase in Indian children and its implication for early genetic screening of adult-type hypolactasia.
    Kuchay RA, Thapa BR, Mahmood A, Mahmood S.
    Clin Chim Acta; 2011 Oct 09; 412(21-22):1924-30. PubMed ID: 21763294
    [Abstract] [Full Text] [Related]

  • 20. Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians.
    Nagy D, Bogácsi-Szabó E, Várkonyi A, Csányi B, Czibula A, Bede O, Tari B, Raskó I.
    Eur J Clin Nutr; 2009 Jul 09; 63(7):909-12. PubMed ID: 19156157
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 28.