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Items: 1 to 20 of 127

1.

Microarray-based detection of select cardiovascular disease markers.

Witowski NE, Leiendecker-Foster C, Gerry NP, McGlennen RC, Barany G.

Biotechniques. 2000 Nov;29(5):936-8, 940, 942 passim. No abstract available.

PMID:
11084850
2.

Mutant DNA polymerase for improved detection of single-nucleotide variations in microarrayed primer extension.

Kranaster R, Ketzer P, Marx A.

Chembiochem. 2008 Mar 25;9(5):694-7. doi: 10.1002/cbic.200700609. No abstract available.

PMID:
18247447
3.

Minisequencing on oligonucleotide microarrays: comparison of immobilisation chemistries.

Lindroos K, Liljedahl U, Raitio M, Syvänen AC.

Nucleic Acids Res. 2001 Jul 1;29(13):E69-9.

4.

Rapid mapping of zebrafish mutations with SNPs and oligonucleotide microarrays.

Stickney HL, Schmutz J, Woods IG, Holtzer CC, Dickson MC, Kelly PD, Myers RM, Talbot WS.

Genome Res. 2002 Dec;12(12):1929-34.

5.

Accessing single nucleotide polymorphisms in genomic DNA by direct multiplex polymerase chain reaction amplification on oligonucleotide microarrays.

Huber M, Mündlein A, Dornstauder E, Schneeberger C, Tempfer CB, Mueller MW, Schmidt WM.

Anal Biochem. 2002 Apr 1;303(1):25-33.

PMID:
11906147
6.

[Application of oligonucleotide microarray primer extension to detection of p53 single nucleotide polymorphisms].

Wu QH, Ma WL, Zhang B, Guo QY, Li L, Zheng WL.

Ai Zheng. 2005 Jul;24(7):898-902. Chinese.

PMID:
16004824
7.

Dramatic increase in signal by integration of polymerase chain reaction and hybridization on surface of DNA microarray.

Kim KT, Na CH, Yun YM, Hwang TS, Kim SN, Chae CB.

Anal Biochem. 2010 Jan 1;396(1):139-45. doi: 10.1016/j.ab.2009.08.035. Epub 2009 Aug 29.

PMID:
19720042
8.

Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls.

Lohi H, Turnbull J, Zhao XC, Pullenayegum S, Ianzano L, Yahyaoui M, Mikati MA, Quinn NP, Franceschetti S, Zara F, Minassian BA.

Neurology. 2007 Mar 27;68(13):996-1001. Erratum in: Neurology. 2007 Jun 12;68(24):2153. Quinn, NP [added].

PMID:
17389303
9.

Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease.

Folkersen L, van't Hooft F, Chernogubova E, Agardh HE, Hansson GK, Hedin U, Liska J, Syvänen AC, Paulsson-Berne G, Franco-Cereceda A, Hamsten A, Gabrielsen A, Eriksson P; BiKE and ASAP study groups.

Circ Cardiovasc Genet. 2010 Aug;3(4):365-73. doi: 10.1161/CIRCGENETICS.110.948935. Epub 2010 Jun 19. Erratum in: Circ Cardiovasc Genet. 2010 Dec 1;3(6):e5. Paulssson-Berne, Gabrielle [corrected to Paulsson-Berne, Gabrielle].

10.
11.

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Cossée M, Lagier-Tourenne C, Seguela C, Mohr M, Leturcq F, Gundesli H, Chelly J, Tranchant C, Koenig M, Mandel JL.

Neuromuscul Disord. 2009 Apr;19(4):255-60. doi: 10.1016/j.nmd.2009.02.003. Epub 2009 Mar 19.

PMID:
19303295
13.

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array.

Matsuzaki H, Loi H, Dong S, Tsai YY, Fang J, Law J, Di X, Liu WM, Yang G, Liu G, Huang J, Kennedy GC, Ryder TB, Marcus GA, Walsh PS, Shriver MD, Puck JM, Jones KW, Mei R.

Genome Res. 2004 Mar;14(3):414-25. Erratum in: Genome Res. 2004 Apr;14(4):786.

14.

Arrayed primer extension reaction for genotyping on oligonucleotide microarray.

Pullat J, Metspalu A.

Methods Mol Biol. 2008;444:161-7. doi: 10.1007/978-1-59745-066-9_12.

PMID:
18425479
15.

Detection of single base alterations in genomic DNA by solid phase polymerase chain reaction on oligonucleotide microarrays.

Huber M, Losert D, Hiller R, Harwanegg C, Mueller MW, Schmidt WM.

Anal Biochem. 2001 Dec 1;299(1):24-30.

PMID:
11726180
16.

[SNPs typing system for the discovery of the common disease susceptibility genes].

Katashima R, Kato H, Nomura K, Shinohara S, Itakura M.

Tanpakushitsu Kakusan Koso. 2004 Aug;49(11 Suppl):1834-40. Review. Japanese. No abstract available.

PMID:
15377025
17.

Single-nucleotide polymorphism genotyping using microarrays.

Patil N, Nouri N, McAllister L, Matsukaki H, Ryder T.

Curr Protoc Hum Genet. 2001 May;Chapter 2:Unit 2.9. doi: 10.1002/0471142905.hg0209s27.

PMID:
18428273
18.

PCR-product microarray based on polyacrylic acid-modified surface for SNP genotyping.

Shi X, Tang C, Zhou D, Sun J, Lu Z.

Electrophoresis. 2009 Apr;30(8):1286-96. doi: 10.1002/elps.200800450.

PMID:
19382131
19.

Faster, better, cheaper genotyping.

Chicurel M.

Nature. 2001 Aug 9;412(6847):580-2. No abstract available.

PMID:
11493890
20.

Detection of single nucleotide polymorphisms by minisequencing on a polypyrrole DNA chip designed for medical diagnosis.

Ho-Pun-Cheung A, Choblet S, Colineau T, Abaibou H, Zsoldos D, Brengel-Pesce K, Grenier J, Cleuziat P, Lopez-Crapez E.

Lab Invest. 2006 Mar;86(3):304-13.

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