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Items: 1 to 20 of 88

1.

ABSOLUTE cancer genomics.

Van Loo P, Campbell PJ.

Nat Biotechnol. 2012 Jul 10;30(7):620-1. doi: 10.1038/nbt.2293. No abstract available.

2.

Finding genes that underlie cancer using genetic tools.

Carracedo A.

Clin Transl Oncol. 2006 Nov;8(11):771-2. No abstract available.

PMID:
17134962
3.

Analysis of genomic CFTR DNA.

Férec C, Le Maréchal C, Audrézet MP, Farinha CM, Amaral MD, Gallati S, Sanz J, Steiner B, Mouchel N, Harris A, Schwarz MJ.

J Cyst Fibros. 2004 Aug;3 Suppl 2:7-10. Review.

4.

Cancer genomics: technology, discovery, and translation.

Tran B, Dancey JE, Kamel-Reid S, McPherson JD, Bedard PL, Brown AM, Zhang T, Shaw P, Onetto N, Stein L, Hudson TJ, Neel BG, Siu LL.

J Clin Oncol. 2012 Feb 20;30(6):647-60. doi: 10.1200/JCO.2011.39.2316. Epub 2012 Jan 23. Review. Erratum in: J Clin Oncol. 2012 Apr 1;30(10):1149.

PMID:
22271477
5.

Faster, better, cheaper genotyping.

Chicurel M.

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

PMID:
11493890
6.

Overcoming complexities in genetic screening for cancer susceptibility.

Friend SH, Iggo R, Ishioka C, Fitzgerald M, Hoover I, O'Neill E, Frebourg T.

Cold Spring Harb Symp Quant Biol. 1994;59:673-6. No abstract available.

PMID:
7587129
7.

Methods for detection of subtle mutations in cancer genomes.

Dahl C, Ralfkiaer U, Guldberg P.

Crit Rev Oncog. 2006 Jul;12(1-2):41-74. Review.

PMID:
17078206
8.

Mutational analysis of oncogenes and tumor suppressor genes in human cancer using denaturing gradient gel electrophoresis.

Guldberg P, Grønbaek K, Worm J, thor Straten P, Zeuthen J.

Methods Mol Med. 2002;68:125-39. No abstract available.

PMID:
11901498
9.

Mutation analysis of cancer using automated sequencing.

Strickson A, Fidler C.

Methods Mol Med. 2002;68:171-7. No abstract available.

PMID:
11901501
10.

Making the perfect mismatch.

Baumbach L.

Nat Biotechnol. 1997 Apr;15(4):318. No abstract available.

PMID:
9094125
11.

Identifying cancer driver genes in tumor genome sequencing studies.

Youn A, Simon R.

Bioinformatics. 2011 Jan 15;27(2):175-81. doi: 10.1093/bioinformatics/btq630. Epub 2010 Dec 17.

12.

[Molecular diagnostic techniques in oncogenetics].

Beroud C.

Ann Med Interne (Paris). 2001 Sep;152(5):326-31. Review. French.

PMID:
11593145
13.

Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine.

Dias-Santagata D, Akhavanfard S, David SS, Vernovsky K, Kuhlmann G, Boisvert SL, Stubbs H, McDermott U, Settleman J, Kwak EL, Clark JW, Isakoff SJ, Sequist LV, Engelman JA, Lynch TJ, Haber DA, Louis DN, Ellisen LW, Borger DR, Iafrate AJ.

EMBO Mol Med. 2010 May;2(5):146-58. doi: 10.1002/emmm.201000070.

14.
15.

Preventing prejudice in genome profiling.

Maruthappu M, Finlayson AE.

Science. 2013 Apr 19;340(6130):273. doi: 10.1126/science.340.6130.273-a. No abstract available.

PMID:
23599461
16.

Pricey cancer genome project struggles with sample shortage.

Waltz E.

Nat Med. 2007 Apr;13(4):391. Epub 2007 Mar 28. No abstract available.

PMID:
17415360
17.

Mutation scanning methods for the analysis of parasite genes.

Gasser RB.

Int J Parasitol. 1997 Dec;27(12):1449-63. Review.

PMID:
9467731
18.

Nucleic acids in diagnosis (Part II): Genetic testing and screening.

Datar RH.

Natl Med J India. 2001 Mar-Apr;14(2):93-8. Review. No abstract available.

PMID:
11396327
19.

Validation of whole genome amplification for analysis of the p53 tumor suppressor gene in limited amounts of tumor samples.

Hasmats J, Green H, Solnestam BW, Zajac P, Huss M, Orear C, Validire P, Bjursell M, Lundeberg J.

Biochem Biophys Res Commun. 2012 Aug 24;425(2):379-83. doi: 10.1016/j.bbrc.2012.07.101. Epub 2012 Jul 27.

20.

[High-resolution melting analysis for the detection of EGFR mutations in circulating DNA of lung cancer patients].

Zhao J, Peng QX, Yang BH, Lu DR.

Zhonghua Yi Xue Za Zhi. 2011 Mar 15;91(10):674-8. Chinese.

PMID:
21600173
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