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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 21407263)

  • 1. Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.
    Mądry E; Fidler E; Sobczyńska-Tomaszewska A; Lisowska A; Krzyżanowska P; Pogorzelski A; Minarowski Ł; Oralewska B; Mojs E; Sapiejka E; Marciniak R; Sands D; Korzon-Burakowska A; Kwiecień J; Walkowiak J
    Eur J Hum Genet; 2011 Jul; 19(7):748-52. PubMed ID: 21407263
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.
    Mądry E; Krasińska B; Drzymała-Czyż S; Sands D; Lisowska A; Grebowiec P; Minarowska A; Oralewska B; Mańkowski P; Moczko J; Walkowiak J
    Eur J Hum Genet; 2012 Oct; 20(10):1092-5. PubMed ID: 22453291
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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; 519(1):67-70. PubMed ID: 23415628
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lactose intolerance, lactose malabsorption and genetic predisposition to adult-type hypolactasia in patients after restorative proctocolectomy.
    Walkowiak J; Fidler-Witoń E; Glapa A; Paszkowski J; Borejsza-Wysocki M; Miśkiewicz-Chotnicka A; Banasiewicz T; Lisowska A
    Acta Biochim Pol; 2019 May; 66(2):173-175. PubMed ID: 31137035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles.
    Terlizzi V; Castaldo G; Salvatore D; Lucarelli M; Raia V; Angioni A; Carnovale V; Cirilli N; Casciaro R; Colombo C; Di Lullo AM; Elce A; Iacotucci P; Comegna M; Scorza M; Lucidi V; Perfetti A; Cimino R; Quattrucci S; Seia M; Sofia VM; Zarrilli F; Amato F
    J Med Genet; 2017 Apr; 54(4):224-235. PubMed ID: 27738188
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.
    Petrova NV; Kashirskaya NY; Saydaeva DK; Polyakov AV; Adyan TA; Simonova OI; Gorinova YV; Kondratyeva EI; Sherman VD; Novoselova OG; Vasilyeva TA; Marakhonov AV; Macek M; Ginter EK; Zinchenko RA
    BMC Med Genet; 2019 Mar; 20(1):44. PubMed ID: 30898088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adult-type hypolactasia and lactose malabsorption in Poland.
    Mądry E; Lisowska A; Kwiecień J; Marciniak R; Korzon-Burakowska A; Drzymała-Czyż S; Mojs E; Walkowiak J
    Acta Biochim Pol; 2010; 57(4):585-8. PubMed ID: 21152447
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 28 Suppl 1():77-82. PubMed ID: 23381829
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 77(5):311-314. PubMed ID: 28452238
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lactose Intolerance Assessed by Analysis of Genetic Polymorphism, Breath Test and Symptoms in Patients with Inflammatory Bowel Disease.
    Nardone OM; Manfellotto F; D'Onofrio C; Rocco A; Annona G; Sasso F; De Luca P; Imperatore N; Testa A; de Sire R; Biffali E; Castiglione F
    Nutrients; 2021 Apr; 13(4):. PubMed ID: 33919766
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 13910C>T and 22018G>A
    Tomczonek-Moruś J; Wojtasik A; Zeman K; Smolarz B; Bąk-Romaniszyn L
    United European Gastroenterol J; 2019 Mar; 7(2):210-216. PubMed ID: 31080605
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence and trends in adult-type hypolactasia in different age cohorts in Central Sweden diagnosed by genotyping for the adult-type hypolactasia-linked LCT -13910C > T mutation.
    Almon R; Engfeldt P; Tysk C; Sjöström M; Nilsson TK
    Scand J Gastroenterol; 2007 Feb; 42(2):165-70. PubMed ID: 17327935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.
    Chaima S; Sondess HF; Khedija B; Ahmed M; Taieb M
    Ann Biol Clin (Paris); 2020 Jun; 78(3):314-318. PubMed ID: 32540817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
    Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
    Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 412(21-22):1924-30. PubMed ID: 21763294
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Improving diagnosis of adult-type hypolactasia in patients with abdominal complaints.
    Haberkorn BC; Ermens AA; Koeken A; Cobbaert CM; van Guldener C
    Clin Chem Lab Med; 2011 Sep; 50(1):119-23. PubMed ID: 21936609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lactase Non-Persistence Genotyping: Comparison of Two Real-Time PCR Assays and Assessment of Concomitant Fructose/Sorbitol Malabsorption Rates.
    Enko D; Pollheimer V; Németh S; Pühringer H; Stolba R; Halwachs-Baumann G; Kriegshäuser G
    Clin Lab; 2016; 62(4):727-30. PubMed ID: 27215094
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 46(2):2379-2385. PubMed ID: 30790118
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Description of rare mutations and a novel variant in Brazilian patients with Cystic Fibrosis: a case series from a referral center in the Bahia State.
    Mota LR; de Melo Filho VM; de Castro LL; Garcia DF; Terse-Ramos R; Toralles MBP; de Lima RLLF; Souza EL
    Mol Biol Rep; 2018 Dec; 45(6):2045-2051. PubMed ID: 30232781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.