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Items: 1 to 20 of 455

1.
2.

Enhanced high density oligonucleotide array-based sequence analysis using modified nucleoside triphosphates.

Hacia JG, Woski SA, Fidanza J, Edgemon K, Hunt N, McGall G, Fodor SP, Collins FS.

Nucleic Acids Res. 1998 Nov 1;26(21):4975-82.

3.
4.

Effect of oligonucleotide probes substituted by deoxyinosines on the specificity of SNP detection on the DNA microarray.

Qian X, Pu D, Liu B, Xiao P.

Electrophoresis. 2015 Jan;36(2):263-70. doi: 10.1002/elps.201400324. Epub 2014 Dec 22.

PMID:
25347966
5.

Detection of a single base substitution in a single cell using the LightCycler.

Pals G, Young C, Mao HS, Worsham MJ.

J Biochem Biophys Methods. 2001 Jan 30;47(1-2):121-9.

PMID:
11179768
6.

Oligonucleotide microarray based detection of repetitive sequence changes.

Hacia JG, Edgemon K, Fang N, Mayer RA, Sudano D, Hunt N, Collins FS.

Hum Mutat. 2000 Oct;16(4):354-63.

PMID:
11013446
7.

Strong position-dependent effects of sequence mismatches on signal ratios measured using long oligonucleotide microarrays.

Rennie C, Noyes HA, Kemp SJ, Hulme H, Brass A, Hoyle DC.

BMC Genomics. 2008 Jul 3;9:317. doi: 10.1186/1471-2164-9-317.

8.

ATM mutations in Italian families with ataxia telangiectasia include two distinct large genomic deletions.

Cavalieri S, Funaro A, Porcedda P, Turinetto V, Migone N, Gatti RA, Brusco A.

Hum Mutat. 2006 Oct;27(10):1061.

PMID:
16941484
9.
10.

Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.

Durocher F, Labrie Y, Soucy P, Sinilnikova O, Labuda D, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Ouellette G, Pichette R, Plante M, Tavtigian SV, Simard J.

BMC Cancer. 2006 Sep 29;6:230.

11.

Low density DNA microarray for detection of most frequent TP53 missense point mutations.

Rangel-López A, Maldonado-Rodríguez R, Salcedo-Vargas M, Espinosa-Lara JM, Méndez-Tenorio A, Beattie KL.

BMC Biotechnol. 2005 Feb 15;5:8.

12.

Genotyping African haplotypes in ATM using a co-spotted single-base extension assay.

Jain M, Thorstenson YR, Faulkner DM, Pourmand N, Jones T, Au M, Oefner PJ, White KP, Davis RW.

Hum Mutat. 2003 Sep;22(3):214-21.

PMID:
12938086
13.
15.

Inactivation of the ATM gene in T-cell prolymphocytic leukemias.

Stoppa-Lyonnet D, Soulier J, Laugé A, Dastot H, Garand R, Sigaux F, Stern MH.

Blood. 1998 May 15;91(10):3920-6.

16.
17.

Design and evaluation of Actichip, a thematic microarray for the study of the actin cytoskeleton.

Muller J, Mehlen A, Vetter G, Yatskou M, Muller A, Chalmel F, Poch O, Friederich E, Vallar L.

BMC Genomics. 2007 Aug 29;8:294.

18.

Discrimination of single nucleotide mutation by using a new class of immobilized shared-stem double-stranded DNA probes.

Bai Y, Lin D, Han Q, Jia Y, Tu J, Luo J, Ge Q, Zhang D, Lu Z.

J Biomed Nanotechnol. 2011 Oct;7(5):640-7.

PMID:
22195481
20.

Detection of known mutations in hypertrophic cardiomyopathy using oligonucleotide microarrays assisted by improved base stacking hybridization.

Wang D, Li Y, Zhang R, Jiang D, Ma X, Zhou Y, Cheng J.

Biotechnol Lett. 2003 Oct;25(19):1613-8.

PMID:
14584916

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