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Items: 1 to 20 of 137

1.

High-resolution melting analysis using unlabeled probe and amplicon scanning simultaneously detects several lactase persistence variants.

Janukonyté J, Vestergaard EM, Ladefoged SA, Nissen PH.

Scand J Clin Lab Invest. 2010 Dec;70(8):535-40. doi: 10.3109/00365513.2010.522251. Epub 2010 Oct 28.

PMID:
21028949
2.

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;52(9):1277-82. doi: 10.1515/cclm-2014-0123.

PMID:
24756060
4.

Pitfalls in LightCycler diagnosis of the single-nucleotide polymorphism 13.9 kb upstream of the lactase gene that is associated with adult-type hypolactasia.

Weiskirchen R, Tag CG, Mengsteab S, Gressner AM, Ingram CJ, Swallow DM.

Clin Chim Acta. 2007 Sep;384(1-2):93-8. Epub 2007 Jun 16.

PMID:
17651714
5.

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;70(5):354-7. doi: 10.3109/00365513.2010.491554.

PMID:
20509822
6.

Evaluation of a novel reverse-hybridization StripAssay for typing DNA variants useful in diagnosis of adult-type hypolactasia.

Tag CG, Oberkanins C, Kriegshäuser G, Ingram CJ, Swallow DM, Gressner AM, Ledochowski M, Weiskirchen R.

Clin Chim Acta. 2008 Jun;392(1-2):58-62. doi: 10.1016/j.cca.2008.03.006. Epub 2008 Mar 18.

PMID:
18396155
7.

A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?

Ingram CJ, Elamin MF, Mulcare CA, Weale ME, Tarekegn A, Raga TO, Bekele E, Elamin FM, Thomas MG, Bradman N, Swallow DM.

Hum Genet. 2007 Feb;120(6):779-88. Epub 2006 Nov 21.

PMID:
17120047
8.

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. doi: 10.1016/j.gene.2013.01.049. Epub 2013 Feb 13.

PMID:
23415628
9.

Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group.

Ingram CJ, Raga TO, Tarekegn A, Browning SL, Elamin MF, Bekele E, Thomas MG, Weale ME, Bradman N, Swallow DM.

J Mol Evol. 2009 Dec;69(6):579-88. doi: 10.1007/s00239-009-9301-y. Epub 2009 Nov 24.

PMID:
19937006
10.

Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients.

Bernardes-Silva CF, Pereira AC, de Fátima Alves da Mota G, Krieger JE, Laudanna AA.

Clin Chim Acta. 2007 Nov-Dec;386(1-2):7-11. Epub 2007 Jul 19.

PMID:
17706627
11.

Diagnosis of genetic predisposition for lactose intolerance by high resolution melting analysis.

Delacour H, Leduc A, Louçano-Perdriat A, Plantamura J, Ceppa F.

Ann Biol Clin (Paris). 2017 Feb 1;75(1):67-74. doi: 10.1684/abc.2016.1210.

PMID:
28132945
12.

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;12(5):733-9. Epub 2007 May 3.

PMID:
17478481
13.

The causal element for the lactase persistence/non-persistence polymorphism is located in a 1 Mb region of linkage disequilibrium in Europeans.

Poulter M, Hollox E, Harvey CB, Mulcare C, Peuhkuri K, Kajander K, Sarner M, Korpela R, Swallow DM.

Ann Hum Genet. 2003 Jul;67(Pt 4):298-311. Erratum in: Ann Hum Genet. 2005 Jul;69(Pt 4):499.

PMID:
12914565
14.

Combination of real-time PCR and sequencing to detect multiple clinically relevant genetic variations in the lactase gene.

Brasen CL, Frischknecht L, Ørnskov D, Andreasen L, Madsen JS.

Scand J Clin Lab Invest. 2017 Feb;77(1):60-65.

PMID:
27937006
15.

Lactose intolerance: lactose tolerance test versus genotyping.

Ridefelt P, Håkansson LD.

Scand J Gastroenterol. 2005 Jul;40(7):822-6.

PMID:
16109658
16.

Evaluation of a new DNA test compared with the lactose hydrogen breath test for the diagnosis of lactase non-persistence.

Högenauer C, Hammer HF, Mellitzer K, Renner W, Krejs GJ, Toplak H.

Eur J Gastroenterol Hepatol. 2005 Mar;17(3):371-6.

PMID:
15716664
17.

Hydrogen breath testing versus LCT genotyping for the diagnosis of lactose intolerance: a matter of age?

Kerber M, Oberkanins C, Kriegshäuser G, Kollerits B, Dossenbach-Glaninger A, Fuchs D, Ledochowski M.

Clin Chim Acta. 2007 Aug;383(1-2):91-6. Epub 2007 May 10.

PMID:
17574225
18.

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus.

Garritano S, Gemignani F, Voegele C, Nguyen-Dumont T, Le Calvez-Kelm F, De Silva D, Lesueur F, Landi S, Tavtigian SV.

BMC Genet. 2009 Feb 17;10:5. doi: 10.1186/1471-2156-10-5.

19.
20.

Lactose digestion and the evolutionary genetics of lactase persistence.

Ingram CJ, Mulcare CA, Itan Y, Thomas MG, Swallow DM.

Hum Genet. 2009 Jan;124(6):579-91. doi: 10.1007/s00439-008-0593-6. Epub 2008 Nov 26.

PMID:
19034520

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