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Items: 15

1.

Genetic differences among ethnic groups.

Huang T, Shu Y, Cai YD.

BMC Genomics. 2015 Dec 21;16:1093. doi: 10.1186/s12864-015-2328-0.

2.

A novel catechol-O-methyltransferase variant associated with human disc degeneration.

Gruber HE, Sha W, Brouwer CR, Steuerwald N, Hoelscher GL, Hanley EN Jr.

Int J Med Sci. 2014 May 15;11(7):748-53. doi: 10.7150/ijms.8770. eCollection 2014 May 15.

3.

A TNF variant that associates with susceptibility to musculoskeletal disease modulates thyroid hormone receptor binding to control promoter activation.

Kiss-Toth E, Harlock E, Lath D, Quertermous T, Wilkinson JM.

PLoS One. 2013 Sep 19;8(9):e76034. doi: 10.1371/journal.pone.0076034. eCollection 2013 Sep 19.

4.

Long span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons.

Yao F, Ariyaratne PN, Hillmer AM, Lee WH, Li G, Teo AS, Woo XY, Zhang Z, Chen JP, Poh WT, Zawack KF, Chan CS, Leong ST, Neo SC, Choi PS, Gao S, Nagarajan N, Thoreau H, Shahab A, Ruan X, Cacheux-Rataboul V, Wei CL, Bourque G, Sung WK, Liu ET, Ruan Y.

PLoS One. 2012;7(9):e46152. doi: 10.1371/journal.pone.0046152. Epub 2012 Sep 28.

5.

Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases.

Gorlova OY, Ying J, Amos CI, Spitz MR, Peng B, Gorlov IP.

J Bioinform Comput Biol. 2012 Apr;10(2):1241008. doi: 10.1142/S0219720012410089.

6.

ComB: SNP calling and mapping analysis for color and nucleotide space platforms.

Souaiaia T, Frazier Z, Chen T.

J Comput Biol. 2011 Jun;18(6):795-807. doi: 10.1089/cmb.2011.0027. Epub 2011 May 12.

7.

Domain altering SNPs in the human proteome and their impact on signaling pathways.

Liu Y, Tozeren A.

PLoS One. 2010 Sep 23;5(9):e12890. doi: 10.1371/journal.pone.0012890.

8.

5'-UTR G-quadruplex structures acting as translational repressors.

Beaudoin JD, Perreault JP.

Nucleic Acids Res. 2010 Nov;38(20):7022-36. doi: 10.1093/nar/gkq557. Epub 2010 Jun 22.

9.

A time for atlases and atlases for time.

Livneh Y, Mizrahi A.

Front Syst Neurosci. 2010 Feb 22;3:17. doi: 10.3389/neuro.06.017.2009. eCollection 2010 Feb 22.

10.

Metabolic syndrome components in murine models.

Lawson HA, Cheverud JM.

Endocr Metab Immune Disord Drug Targets. 2010 Mar;10(1):25-40. Review.

11.

High frequency of hotspot mutations in core genes of Escherichia coli due to short-term positive selection.

Chattopadhyay S, Weissman SJ, Minin VN, Russo TA, Dykhuizen DE, Sokurenko EV.

Proc Natl Acad Sci U S A. 2009 Jul 28;106(30):12412-7. doi: 10.1073/pnas.0906217106. Epub 2009 Jul 15.

12.

Positional conservation and amino acids shape the correct diagnosis and population frequencies of benign and damaging personal amino acid mutations.

Kumar S, Suleski MP, Markov GJ, Lawrence S, Marco A, Filipski AJ.

Genome Res. 2009 Sep;19(9):1562-9. doi: 10.1101/gr.091991.109. Epub 2009 Jun 22.

13.

LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.

Chang HW, Chuang LY, Chang YJ, Cheng YH, Hung YC, Chen HC, Yang CH.

BMC Genet. 2009 Jun 6;10:26. doi: 10.1186/1471-2156-10-26.

14.

Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses.

Fullwood MJ, Wei CL, Liu ET, Ruan Y.

Genome Res. 2009 Apr;19(4):521-32. doi: 10.1101/gr.074906.107. Review.

15.

Problems and solutions for estimating indel rates and length distributions.

Cartwright RA.

Mol Biol Evol. 2009 Feb;26(2):473-80. doi: 10.1093/molbev/msn275. Epub 2008 Nov 28.

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