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Items: 1 to 20 of 67

1.

Identification and analysis of deleterious human SNPs.

Yue P, Moult J.

J Mol Biol. 2006 Mar 10;356(5):1263-74. Epub 2005 Dec 27.

PMID:
16412461
2.
3.
4.

Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms.

Clifford RJ, Edmonson MN, Nguyen C, Buetow KH.

Bioinformatics. 2004 May 1;20(7):1006-14. Epub 2004 Jan 29.

PMID:
14751981
5.

Selective pressures at a codon-level predict deleterious mutations in human disease genes.

Arbiza L, Duchi S, Montaner D, Burguet J, Pantoja-Uceda D, Pineda-Lucena A, Dopazo J, Dopazo H.

J Mol Biol. 2006 May 19;358(5):1390-404. Epub 2006 Mar 15.

PMID:
16584746
6.
7.

Human non-synonymous SNPs: server and survey.

Ramensky V, Bork P, Sunyaev S.

Nucleic Acids Res. 2002 Sep 1;30(17):3894-900.

8.

Predicting deleterious nsSNPs: an analysis of sequence and structural attributes.

Dobson RJ, Munroe PB, Caulfield MJ, Saqi MA.

BMC Bioinformatics. 2006 Apr 21;7:217.

9.

Prediction of deleterious human alleles.

Sunyaev S, Ramensky V, Koch I, Lathe W 3rd, Kondrashov AS, Bork P.

Hum Mol Genet. 2001 Mar 15;10(6):591-7.

PMID:
11230178
10.

Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.

Capriotti E, Arbiza L, Casadio R, Dopazo J, Dopazo H, Marti-Renom MA.

Hum Mutat. 2008 Jan;29(1):198-204.

PMID:
17935148
11.

Identification and structural comparison of deleterious mutations in nsSNPs of ABL1 gene in chronic myeloid leukemia: a bio-informatics study.

George Priya Doss C, Sudandiradoss C, Rajasekaran R, Purohit R, Ramanathan K, Sethumadhavan R.

J Biomed Inform. 2008 Aug;41(4):607-12. doi: 10.1016/j.jbi.2007.12.004. Epub 2007 Dec 31.

12.

Approaches and resources for prediction of the effects of non-synonymous single nucleotide polymorphism on protein function and interactions.

Teng S, Michonova-Alexova E, Alexov E.

Curr Pharm Biotechnol. 2008 Apr;9(2):123-33. Review.

PMID:
18393868
13.

Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.

Reumers J, Conde L, Medina I, Maurer-Stroh S, Van Durme J, Dopazo J, Rousseau F, Schymkowitz J.

Nucleic Acids Res. 2008 Jan;36(Database issue):D825-9. Epub 2007 Dec 17.

16.

Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.

Barenboim M, Masso M, Vaisman II, Jamison DC.

Proteins. 2008 Jun;71(4):1930-9. doi: 10.1002/prot.21838.

PMID:
18186470
17.

Identification and in silico analysis of functional SNPs of the BRCA1 gene.

Rajasekaran R, Sudandiradoss C, Doss CG, Sethumadhavan R.

Genomics. 2007 Oct;90(4):447-52. Epub 2007 Aug 27.

18.

PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease.

Jegga AG, Gowrisankar S, Chen J, Aronow BJ.

Nucleic Acids Res. 2007 Jan;35(Database issue):D700-6. Epub 2006 Nov 16.

20.

Impact of single nucleotide polymorphisms in HBB gene causing haemoglobinopathies: in silico analysis.

George Priya Doss C, Rao S.

N Biotechnol. 2009 Apr;25(4):214-9. doi: 10.1016/j.nbt.2009.01.004. Epub 2009 Jan 21.

PMID:
19429541

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