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Items: 23

1.

SNPSelect: A scalable and flexible targeted sequence-based genotyping solution.

Hogers RCJ, de Ruiter M, Huvenaars KHJ, van der Poel H, Janssen A, van Eijk MJT, van Orsouw NJ.

PLoS One. 2018 Oct 12;13(10):e0205577. doi: 10.1371/journal.pone.0205577. eCollection 2018.

2.

Sequence-based SNP genotyping in durum wheat.

van Poecke RM, Maccaferri M, Tang J, Truong HT, Janssen A, van Orsouw NJ, Salvi S, Sanguineti MC, Tuberosa R, van der Vossen EA.

Plant Biotechnol J. 2013 Sep;11(7):809-17. doi: 10.1111/pbi.12072. Epub 2013 May 3.

3.

Sequence-based genotyping for marker discovery and co-dominant scoring in germplasm and populations.

Truong HT, Ramos AM, Yalcin F, de Ruiter M, van der Poel HJ, Huvenaars KH, Hogers RC, van Enckevort LJ, Janssen A, van Orsouw NJ, van Eijk MJ.

PLoS One. 2012;7(5):e37565. doi: 10.1371/journal.pone.0037565. Epub 2012 May 25.

4.

High-throughput detection of induced mutations and natural variation using KeyPoint technology.

Rigola D, van Oeveren J, Janssen A, Bonné A, Schneiders H, van der Poel HJ, van Orsouw NJ, Hogers RC, de Both MT, van Eijk MJ.

PLoS One. 2009;4(3):e4761. doi: 10.1371/journal.pone.0004761. Epub 2009 Mar 13.

5.

Complexity reduction of polymorphic sequences (CRoPS): a novel approach for large-scale polymorphism discovery in complex genomes.

van Orsouw NJ, Hogers RC, Janssen A, Yalcin F, Snoeijers S, Verstege E, Schneiders H, van der Poel H, van Oeveren J, Verstegen H, van Eijk MJ.

PLoS One. 2007 Nov 14;2(11):e1172.

6.

Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations.

Andrulis IL, Anton-Culver H, Beck J, Bove B, Boyd J, Buys S, Godwin AK, Hopper JL, Li F, Neuhausen SL, Ozcelik H, Peel D, Santella RM, Southey MC, van Orsouw NJ, Venter DJ, Vijg J, Whittemore AS; Cooperative Family Registry for Breast Cancer studies.

Hum Mutat. 2002 Jul;20(1):65-73.

PMID:
12112659
7.

Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues.

Nekhaeva E, Bodyak ND, Kraytsberg Y, McGrath SB, Van Orsouw NJ, Pluzhnikov A, Wei JY, Vijg J, Khrapko K.

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5521-6. Epub 2002 Apr 9.

8.

BRCA1 gene sequence variation in centenarians.

Vijg J, Perls T, Franceschi C, van Orsouw NJ.

Ann N Y Acad Sci. 2001 Apr;928:85-96. Review.

PMID:
11795532
9.

Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours.

Yeh JJ, Lunetta KL, van Orsouw NJ, Moore FD Jr, Mutter GL, Vijg J, Dahia PL, Eng C.

Oncogene. 2000 Apr 13;19(16):2060-6.

10.

Background mutations and polymorphisms in lacZ-plasmid transgenic mice.

Dollé ME, Snyder WK, van Orsouw NJ, Vijg J.

Environ Mol Mutagen. 1999;34(2-3):112-20.

PMID:
10529734
11.

A highly accurate, low cost test for BRCA1 mutations.

van Orsouw NJ, Dhanda RK, Elhaji Y, Narod SA, Li FP, Eng C, Vijg J.

J Med Genet. 1999 Oct;36(10):747-53.

12.

Accurate, high-throughput "snapshot" detection of hMLH1 mutations by two-dimensional DNA electrophoresis.

Smith WM, Van Orsouw NJ, Fox EA, Kolodner RD, Vijg J, Eng C.

Genet Test. 1998;2(1):43-53.

PMID:
10464596
13.

Two-dimensional gene scanning: exploring human genetic variability.

Vijg J, van Orsouw NJ.

Electrophoresis. 1999 Jun;20(6):1239-49. Review.

PMID:
10380764
14.

Characterization of color mutants in lacZ plasmid-based transgenic mice, as detected by positive selection.

Dollé ME, Martus HJ, Novak M, van Orsouw NJ, Vijg J.

Mutagenesis. 1999 May;14(3):287-93.

PMID:
10374996
15.

Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions.

Khrapko K, Bodyak N, Thilly WG, van Orsouw NJ, Zhang X, Coller HA, Perls TT, Upton M, Vijg J, Wei JY.

Nucleic Acids Res. 1999 Jun 1;27(11):2434-41.

16.

Design and application of 2-D DGGE-based gene mutational scanning tests.

Van Orsouw NJ, Vijg J.

Genet Anal. 1999 Feb;14(5-6):205-13.

PMID:
10084116
17.

Critical factors in the performance and cost of two-dimensional gene scanning: RB1 as a model.

Dhanda RK, van Orsouw NJ, Sigalas I, Eng C, Vijg J.

Biotechniques. 1998 Oct;25(4):664-8, 670, 672-5.

18.

Mutational scanning of mitochondrial DNA by two-dimensional electrophoresis.

van Orsouw NJ, Zhang X, Wei JY, Johns DR, Vijg J.

Genomics. 1998 Aug 15;52(1):27-36.

PMID:
9740668
19.

Comprehensive mutational scanning of the p53 coding region by two-dimensional gene scanning.

Rines RD, van Orsouw NJ, Sigalas I, Li FP, Eng C, Vijg J.

Carcinogenesis. 1998 Jun;19(6):979-84.

PMID:
9667734
20.

Rapid design of denaturing gradient-based two-dimensional electrophoretic gene mutational scanning tests.

van Orsouw NJ, Dhanda RK, Rines RD, Smith WM, Sigalas I, Eng C, Vijg J.

Nucleic Acids Res. 1998 May 15;26(10):2398-406.

21.

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.

Marsh DJ, Roth S, Lunetta KL, Hemminki A, Dahia PL, Sistonen P, Zheng Z, Caron S, van Orsouw NJ, Bodmer WF, Cottrell SE, Dunlop MG, Eccles D, Hodgson SV, Järvinen H, Kellokumpu I, Markie D, Neale K, Phillips R, Rozen P, Syngal S, Vijg J, Tomlinson IP, Aaltonen LA, Eng C.

Cancer Res. 1997 Nov 15;57(22):5017-21.

22.
23.

Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene.

Van Orsouw NJ, Li D, van der Vlies P, Scheffer H, Eng C, Buys CH, Li FP, Vijg J.

Hum Mol Genet. 1996 Jun;5(6):755-61.

PMID:
8776589

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