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Items: 1 to 20 of 22

1.

Worm variation made accessible: Take your shopping cart to store, link, and investigate!

Snoek LB, Joeri van der Velde K, Li Y, Jansen RC, Swertz MA, Kammenga JE.

Worm. 2014 Jan 1;3(1):e28357. doi: 10.4161/worm.28357. Epub 2014 Mar 6.

2.

Genomic data and disease forecasting: application to type 2 diabetes (T2D).

Sirovich L.

PLoS One. 2014 Jan 17;9(1):e85684. doi: 10.1371/journal.pone.0085684. eCollection 2014.

3.

WormQTLHD--a web database for linking human disease to natural variation data in C. elegans.

van der Velde KJ, de Haan M, Zych K, Arends D, Snoek LB, Kammenga JE, Jansen RC, Swertz MA, Li Y.

Nucleic Acids Res. 2014 Jan;42(Database issue):D794-801. doi: 10.1093/nar/gkt1044. Epub 2013 Nov 11.

4.

Unraveling genomic variation from next generation sequencing data.

Pavlopoulos GA, Oulas A, Iacucci E, Sifrim A, Moreau Y, Schneider R, Aerts J, Iliopoulos I.

BioData Min. 2013 Jul 25;6(1):13. doi: 10.1186/1756-0381-6-13.

6.

UASIS: Universal Automatic SNP Identification System.

Poo DC, Cai S, Mah JT.

BMC Genomics. 2011 Nov 30;12 Suppl 3:S9. doi: 10.1186/1471-2164-12-S3-S9. Epub 2011 Nov 30.

7.

Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.

Roncarati R, Latronico MV, Musumeci B, Aurino S, Torella A, Bang ML, Jotti GS, Puca AA, Volpe M, Nigro V, Autore C, Condorelli G.

J Cell Physiol. 2011 Nov;226(11):2894-900. doi: 10.1002/jcp.22636.

8.

MitoInteractome: mitochondrial protein interactome database, and its application in 'aging network' analysis.

Reja R, Venkatakrishnan AJ, Lee J, Kim BC, Ryu JW, Gong S, Bhak J, Park D.

BMC Genomics. 2009 Dec 3;10 Suppl 3:S20. doi: 10.1186/1471-2164-10-S3-S20.

9.

SNP and mutation data on the web - hidden treasures for uncovering.

Barnes MR.

Comp Funct Genomics. 2002;3(1):67-74. doi: 10.1002/cfg.131.

10.

Identification of functional SNPs in the 5-prime flanking sequences of human genes.

Mottagui-Tabar S, Faghihi MA, Mizuno Y, Engström PG, Lenhard B, Wasserman WW, Wahlestedt C.

BMC Genomics. 2005 Feb 17;6:18.

11.

PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level.

Conde L, Vaquerizas JM, Santoyo J, Al-Shahrour F, Ruiz-Llorente S, Robledo M, Dopazo J.

Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W242-8.

12.

Multiplexed SNP genotyping using the Qbead system: a quantum dot-encoded microsphere-based assay.

Xu H, Sha MY, Wong EY, Uphoff J, Xu Y, Treadway JA, Truong A, O'Brien E, Asquith S, Stubbins M, Spurr NK, Lai EH, Mahoney W.

Nucleic Acids Res. 2003 Apr 15;31(8):e43.

13.

Total C4B deficiency due to gene deletion and gene conversion in a patient with severe infections.

Jaatinen T, Lahti M, Ruuskanen O, Kinos R, Truedsson L, Lahesmaa R, Lokki ML.

Clin Diagn Lab Immunol. 2003 Mar;10(2):195-201.

14.

rSNP_Guide, a database system for analysis of transcription factor binding to DNA with variations: application to genome annotation.

Ponomarenko JV, Merkulova TI, Orlova GV, Fokin ON, Gorshkova EV, Frolov AS, Valuev VP, Ponomarenko MP.

Nucleic Acids Res. 2003 Jan 1;31(1):118-21.

15.

Sequence variation and haplotype structure at the human HFE locus.

Toomajian C, Kreitman M.

Genetics. 2002 Aug;161(4):1609-23.

16.
17.

JSNP: a database of common gene variations in the Japanese population.

Hirakawa M, Tanaka T, Hashimoto Y, Kuroda M, Takagi T, Nakamura Y.

Nucleic Acids Res. 2002 Jan 1;30(1):158-62.

18.

Predicting deleterious amino acid substitutions.

Ng PC, Henikoff S.

Genome Res. 2001 May;11(5):863-74.

19.

Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation.

Prince JA, Feuk L, Howell WM, Jobs M, Emahazion T, Blennow K, Brookes AJ.

Genome Res. 2001 Jan;11(1):152-62.

20.

ALFRED: an allele frequency database for diverse populations and DNA polymorphisms--an update.

Osier MV, Cheung KH, Kidd JR, Pakstis AJ, Miller PL, Kidd KK.

Nucleic Acids Res. 2001 Jan 1;29(1):317-9.

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