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Items: 14

1.

Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes.

Funk WD, Labat I, Sampathkumar J, Gourraud PA, Oksenberg JR, Rosler E, Steiger D, Sheibani N, Caillier S, Stache-Crain B, Johnson JA, Meisner L, Lacher MD, Chapman KB, Park MJ, Shin KJ, Drmanac R, West MD.

Stem Cell Res. 2012 Mar;8(2):154-64. doi: 10.1016/j.scr.2011.10.001. Epub 2011 Oct 8.

2.

Concise review: Genomic stability of human induced pluripotent stem cells.

Martins-Taylor K, Xu RH.

Stem Cells. 2012 Jan;30(1):22-7. doi: 10.1002/stem.705. Review.

3.

The clinical context of copy number variation in the human genome.

Lee C, Scherer SW.

Expert Rev Mol Med. 2010 Mar 9;12:e8. doi: 10.1017/S1462399410001390. Review.

PMID:
20211047
4.

[DNA polymorphisms].

Suehiro Y, Furuya T, Sasaki K, Hinota Y.

Rinsho Byori. 2013 Nov;61(11):1001-7. Review. Japanese.

PMID:
24450105
5.
6.

[The problem of genomic instability of cultivated human stem cells].

Polianskaia GG.

Tsitologiia. 2014;56(10):697-707. Review. Russian.

PMID:
25711078
7.

[Genomic techniques used in uveal melanoma: a literature review].

Abi-Ayad N, Kodjikian L, Couturier J.

J Fr Ophtalmol. 2011 Apr;34(4):259-64. doi: 10.1016/j.jfo.2010.11.012. Review. French.

9.

Sequence variation at the human ABO locus.

Yip SP.

Ann Hum Genet. 2002 Jan;66(Pt 1):1-27. Review.

10.

Pharmacogenetics: technologies to detect copy number variations.

Dhawan D, Padh H.

Curr Opin Mol Ther. 2009 Dec;11(6):670-80. Review.

PMID:
20072944
11.

The impact of human copy number variation on a new era of genetic testing.

Choy KW, Setlur SR, Lee C, Lau TK.

BJOG. 2010 Mar;117(4):391-8. doi: 10.1111/j.1471-0528.2009.02470.x. Epub 2010 Jan 26. Review.

12.

Safety paradigm: genetic evaluation of therapeutic grade human embryonic stem cells.

Stephenson E, Ogilvie CM, Patel H, Cornwell G, Jacquet L, Kadeva N, Braude P, Ilic D.

J R Soc Interface. 2010 Dec 6;7 Suppl 6:S677-88. doi: 10.1098/rsif.2010.0343.focus. Epub 2010 Sep 8. Review.

13.

Next-generation sequencing of experimental mouse strains.

Yalcin B, Adams DJ, Flint J, Keane TM.

Mamm Genome. 2012 Oct;23(9-10):490-8. doi: 10.1007/s00335-012-9402-6. Epub 2012 Jul 7. Review.

14.

Allele-specific and heritable chromatin signatures in humans.

Birney E, Lieb JD, Furey TS, Crawford GE, Iyer VR.

Hum Mol Genet. 2010 Oct 15;19(R2):R204-9. doi: 10.1093/hmg/ddq404. Epub 2010 Sep 16. Review.

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