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Items: 1 to 20 of 56

2.

Analysis of two mutations in the MTHFR gene associated with mild hyperhomocysteinaemia--heterogeneous distribution in the South African population.

Scholtz CL, Odendaal HJ, Thiart R, Loubser L, Hillermann R, Delport R, Vermaak WJ, Kotze MJ.

S Afr Med J. 2002 Jun;92(6):464-7.

PMID:
12146133
3.

Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos.

Zetterberg H, Regland B, Palmér M, Ricksten A, Palmqvist L, Rymo L, Arvanitis DA, Spandidos DA, Blennow K.

Eur J Hum Genet. 2002 Feb;10(2):113-8.

4.

SNP genotyping with fluorescence polarization detection.

Kwok PY.

Hum Mutat. 2002 Apr;19(4):315-23. Review.

PMID:
11933186
5.

Real-time multiplex PCR assays.

Wittwer CT, Herrmann MG, Gundry CN, Elenitoba-Johnson KS.

Methods. 2001 Dec;25(4):430-42. Review.

PMID:
11846612
6.

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, Tyring SK, Matalon RK.

Am J Med Genet. 2002 Jan 15;107(2):162-8.

PMID:
11807892
7.

The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans.

Rosenberg N, Murata M, Ikeda Y, Opare-Sem O, Zivelin A, Geffen E, Seligsohn U.

Am J Hum Genet. 2002 Mar;70(3):758-62.

8.

Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase.

Yamada K, Chen Z, Rozen R, Matthews RG.

Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):14853-8.

10.
11.

Emerging homogeneous DNA-based technologies in the clinical laboratory.

Foy CA, Parkes HC.

Clin Chem. 2001 Jun;47(6):990-1000. Review.

13.

Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease.

Meisel C, Cascorbi I, Gerloff T, Stangl V, Laule M, Müller JM, Wernecke KD, Baumann G, Roots I, Stangl K.

Atherosclerosis. 2001 Feb 15;154(3):651-8.

PMID:
11257266
14.

Melting curve analysis of SNPs (McSNP): a gel-free and inexpensive approach for SNP genotyping.

Akey JM, Sosnoski D, Parra E, Dios S, Hiester K, Su B, Bonilla C, Jin L, Shriver MD.

Biotechniques. 2001 Feb;30(2):358-62, 364, 366-7.

PMID:
11233605
15.
17.

Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation.

Prince JA, Feuk L, Howell WM, Jobs M, Emahazion T, Blennow K, Brookes AJ.

Genome Res. 2001 Jan;11(1):152-62.

18.

Ethnic differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Israeli populations.

Pollak RD, Friedlander Y, Pollak A, Idelson M, Bejarano-AchacheI, Blumenfeld A.

Genet Test. 2000;4(3):309-11.

PMID:
11142765
20.

Direct polymerase chain reaction from whole blood without DNA isolation.

Nishimura N, Nakayama T, Tonoike H, Kojima K, Kato S.

Ann Clin Biochem. 2000 Sep;37 ( Pt 5):674-80.

PMID:
11026521
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