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Similar articles for PubMed (Select 10493873)

1.

Universal DNA microarray method for multiplex detection of low abundance point mutations.

Gerry NP, Witowski NE, Day J, Hammer RP, Barany G, Barany F.

J Mol Biol. 1999 Sep 17;292(2):251-62.

PMID:
10493873
2.

Ligase detection reaction/hybridization assays using three-dimensional microfluidic networks for the detection of low-abundant DNA point mutations.

Hashimoto M, Hupert ML, Murphy MC, Soper SA, Cheng YW, Barany F.

Anal Chem. 2005 May 15;77(10):3243-55.

PMID:
15889915
3.
4.

A universal microarray for detection of SARS coronavirus.

Long WH, Xiao HS, Gu XM, Zhang QH, Yang HJ, Zhao GP, Liu JH.

J Virol Methods. 2004 Oct;121(1):57-63.

PMID:
15350733
5.

Approaching real-time molecular diagnostics: single-pair fluorescence resonance energy transfer (spFRET) detection for the analysis of low abundant point mutations in K-ras oncogenes.

Wabuyele MB, Farquar H, Stryjewski W, Hammer RP, Soper SA, Cheng YW, Barany F.

J Am Chem Soc. 2003 Jun 11;125(23):6937-45.

PMID:
12783546
6.

Microarrays assembled in microfluidic chips fabricated from poly(methyl methacrylate) for the detection of low-abundant DNA mutations.

Wang Y, Vaidya B, Farquar HD, Stryjewski W, Hammer RP, McCarley RL, Soper SA, Cheng YW, Barany F.

Anal Chem. 2003 Mar 1;75(5):1130-40.

PMID:
12641233
7.
8.

An endonuclease/ligase based mutation scanning method especially suited for analysis of neoplastic tissue.

Huang J, Kirk B, Favis R, Soussi T, Paty P, Cao W, Barany F.

Oncogene. 2002 Mar 14;21(12):1909-21.

9.

Development of a PCR/ligase detection reaction/nanogold-based universal array approach for the detection of low-abundant DNA point mutations.

Yi P, Lu W, Guo J, Liu Q, Chen Z, Han J, Li L.

Cell Biochem Biophys. 2011 Dec;61(3):629-36. doi: 10.1007/s12013-011-9248-7.

PMID:
21847634
10.

Multiplex PCR/LDR for detection of K-ras mutations in primary colon tumors.

Khanna M, Park P, Zirvi M, Cao W, Picon A, Day J, Paty P, Barany F.

Oncogene. 1999 Jan 7;18(1):27-38.

11.

Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA.

Thomas G, Sinville R, Sutton S, Farquar H, Hammer RP, Soper SA, Cheng YW, Barany F.

Electrophoresis. 2004 Jun;25(10-11):1668-77.

PMID:
15188256
12.

Needle-in-a-haystack detection and identification of base substitution mutations in human tissues.

Wilson VL, Wei Q, Wade KR, Chisa M, Bailey D, Kanstrup CM, Yin X, Jackson CM, Thompson B, Lee WR.

Mutat Res. 1999 Aug;406(2-4):79-100.

PMID:
10479725
13.

Mutation detection in K-ras, BRCA1, BRCA2, and p53 using PCR/LDR and a universal DNA microarray.

Favis R, Barany F.

Ann N Y Acad Sci. 2000 Apr;906:39-43. Review.

PMID:
10818594
14.

Diagnosis of HNF-1alpha mutations on a PNA zip-code microarray by single base extension.

Song JY, Park HG, Jung SO, Park J.

Nucleic Acids Res. 2005 Feb 1;33(2):e19.

15.

PCR-free mutation detection of BRCA1 on a zip-code microarray using ligase chain reaction.

Girigoswami A, Jung C, Mun HY, Park HG.

J Biochem Biophys Methods. 2008 Apr 24;70(6):897-902. doi: 10.1016/j.jprot.2008.01.005. Epub 2008 Jan 18.

PMID:
18276013
16.

Ligase-based detection of mononucleotide repeat sequences.

Zirvi M, Nakayama T, Newman G, McCaffrey T, Paty P, Barany F.

Nucleic Acids Res. 1999 Dec 15;27(24):e40.

17.

Development of multiplex reverse transcription-ligase detection reaction-polymerase chain reaction (MRLP) mediated universal DNA microarray for diagnostic platform.

Wang P, Guo Y, Cheng J, Dong Q, Ding X, Guo J, Jiang Y.

Biosens Bioelectron. 2011 Apr 15;26(8):3719-24. doi: 10.1016/j.bios.2011.02.027. Epub 2011 Feb 22.

PMID:
21397486
18.

Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction.

Battistella S, Damin F, Chiari M, Delgrosso K, Surrey S, Fortina P, Ferrari M, Cremonesi L.

Clin Chem. 2008 Oct;54(10):1657-63. doi: 10.1373/clinchem.2008.107870. Epub 2008 Aug 14.

20.

Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome.

Rouleau E, Lefol C, Bourdon V, Coulet F, Noguchi T, Soubrier F, Bi├Ęche I, Olschwang S, Sobol H, Lidereau R.

Hum Mutat. 2009 Jun;30(6):867-75. doi: 10.1002/humu.20947.

PMID:
19224586
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