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Items: 1 to 20 of 134

1.

In silico analysis of Single Nucleotide Polymorphisms (SNPs) in human BRAF gene.

Hussain MR, Shaik NA, Al-Aama JY, Asfour HZ, Khan FS, Masoodi TA, Khan MA, Shaik NS.

Gene. 2012 Oct 25;508(2):188-96. doi: 10.1016/j.gene.2012.07.014. Epub 2012 Jul 21.

PMID:
22824468
2.

In silico analysis of single nucleotide polymorphism (SNP) in human TNF-α gene.

Dabhi B, Mistry KN.

Meta Gene. 2014 Aug 24;2:586-95. doi: 10.1016/j.mgene.2014.07.005. eCollection 2014 Dec.

3.

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
4.

Computational identification of significant missense mutations in AKT1 gene.

Shanthi V, Rajasekaran R, Ramanathan K.

Cell Biochem Biophys. 2014 Nov;70(2):957-65. doi: 10.1007/s12013-014-0003-8.

PMID:
24809327
5.

Impacts of Nonsynonymous Single Nucleotide Polymorphisms of Adiponectin Receptor 1 Gene on Corresponding Protein Stability: A Computational Approach.

Saleh MA, Solayman M, Paul S, Saha M, Khalil MI, Gan SH.

Biomed Res Int. 2016;2016:9142190. doi: 10.1155/2016/9142190. Epub 2016 May 15.

6.

Computational and structural investigation of deleterious functional SNPs in breast cancer BRCA2 gene.

Rajasekaran R, Doss GP, Sudandiradoss C, Ramanathan K, Rituraj P, Sethumadhavan R.

Sheng Wu Gong Cheng Xue Bao. 2008 May;24(5):851-6.

PMID:
18724707
7.

Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.

Phani NM, Acharya S, Xavy S, Bhaskaranand N, Bhat MK, Jain A, Rai PS, Satyamoorthy K.

Gene. 2014 Feb 25;536(2):247-53. doi: 10.1016/j.gene.2013.12.026. Epub 2013 Dec 27. Erratum in: Gene. 2014 Apr 15;539(2):285. Kapaettu, Satyamoorthy [corrected to Satyamoorthy, Kapaettu].

PMID:
24378235
8.

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.

9.

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.

10.

An integrated in silico approach to analyze the involvement of single amino acid polymorphisms in FANCD1/BRCA2-PALB2 and FANCD1/BRCA2-RAD51 complex.

Doss CG, Nagasundaram N.

Cell Biochem Biophys. 2014 Nov;70(2):939-56. doi: 10.1007/s12013-014-0002-9.

PMID:
24817641
11.

A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.

Wang LL, Li Y, Zhou SF.

Drug Metab Dispos. 2009 May;37(5):977-91. doi: 10.1124/dmd.108.026047. Epub 2009 Feb 9.

12.

In silico analysis of single nucleotide polymorphism (SNPs) in human β-globin gene.

Alanazi M, Abduljaleel Z, Khan W, Warsy AS, Elrobh M, Khan Z, Al Amri A, Bazzi MD.

PLoS One. 2011;6(10):e25876. doi: 10.1371/journal.pone.0025876. Epub 2011 Oct 20.

13.

In silico analysis of nonsynonymous single nucleotide polymorphisms of the human adiponectin receptor 2 (ADIPOR2) gene.

Solayman M, Saleh MA, Paul S, Khalil MI, Gan SH.

Comput Biol Chem. 2017 Jun;68:175-185. doi: 10.1016/j.compbiolchem.2017.03.005. Epub 2017 Mar 14.

PMID:
28359874
15.

Application of a BRAF pyrosequencing assay for mutation detection and copy number analysis in malignant melanoma.

Spittle C, Ward MR, Nathanson KL, Gimotty PA, Rappaport E, Brose MS, Medina A, Letrero R, Herlyn M, Edwards RH.

J Mol Diagn. 2007 Sep;9(4):464-71. Epub 2007 Aug 9.

16.

Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.

Nakken S, Alseth I, Rognes T.

Neuroscience. 2007 Apr 14;145(4):1273-9. Epub 2006 Oct 19. Review.

PMID:
17055652
17.

A new insight into structural and functional impact of single-nucleotide polymorphisms in PTEN gene.

George Priya Doss C, Rajith B.

Cell Biochem Biophys. 2013 Jun;66(2):249-63. doi: 10.1007/s12013-012-9472-9.

PMID:
23161105
18.

Investigation of V600E BRAF mutation in papillary thyroid carcinoma in the Polish population.

Brzeziańska E, Pastuszak-Lewandoska D, Wojciechowska K, Migdalska-Sek M, Cyniak-Magierska A, Nawrot E, Lewiński A.

Neuro Endocrinol Lett. 2007 Aug;28(4):351-9.

PMID:
17693984
19.

Functional genomics based prioritization of potential nsSNPs in EPHX1, GSTT1, GSTM1 and GSTP1 genes for breast cancer susceptibility studies.

Masoodi TA, Rao Talluri V, Shaik NA, Al-Aama JY, Hasan Q.

Genomics. 2012 Jun;99(6):330-9. doi: 10.1016/j.ygeno.2012.04.006. Epub 2012 May 1.

20.

Human malignant melanoma: detection of BRAF- and c-kit-activating mutations by high-resolution amplicon melting analysis.

Willmore-Payne C, Holden JA, Tripp S, Layfield LJ.

Hum Pathol. 2005 May;36(5):486-93.

PMID:
15948115

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