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Items: 1 to 20 of 124

1.

Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach.

B R, C GP.

PLoS One. 2011;6(9):e24607. doi: 10.1371/journal.pone.0024607. Epub 2011 Sep 13.

2.

Computational and structural analysis of deleterious functional SNPs in ARNT oncogene.

George Priya Doss C, Sethumadhavan R.

Interdiscip Sci. 2009 Sep;1(3):220-8. doi: 10.1007/s12539-009-0042-9. Epub 2009 Aug 7.

PMID:
20640841
3.
4.

Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach.

Doss CG, Sethumadhavan R.

J Biomed Sci. 2009 Apr 24;16:42. doi: 10.1186/1423-0127-16-42.

5.
6.

G6PD-MutDB: a mutation and phenotype database of glucose-6-phosphate (G6PD) deficiency.

Zhao X, Li Z, Zhang X.

J Bioinform Comput Biol. 2010 Dec;8 Suppl 1:101-9.

PMID:
21155022
7.

Computational methods to work as first-pass filter in deleterious SNP analysis of alkaptonuria.

Magesh R, George Priya Doss C.

ScientificWorldJournal. 2012;2012:738423. doi: 10.1100/2012/738423. Epub 2012 Apr 19.

8.

Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach.

George Priya Doss C, Nagasundaram N, Chakraborty C, Chen L, Zhu H.

Hum Genomics. 2013 Apr 5;7:10. doi: 10.1186/1479-7364-7-10.

9.

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
10.

Phenotype prediction of deleterious nonsynonymous single nucleotide polymorphisms in human alcohol metabolism-related genes: a bioinformatics study.

Wang LL, Yang AK, Li Y, Liu JP, Zhou SF.

Alcohol. 2010 Aug;44(5):425-38. doi: 10.1016/j.alcohol.2010.05.009. Epub 2010 Jun 18.

PMID:
20804942
11.

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.

12.

Computational identification and structural analysis of deleterious functional SNPs in MLL gene causing acute leukemia.

George Priya Doss C, Rajasekaran R, Sethumadhavan R.

Interdiscip Sci. 2010 Sep;2(3):247-55. doi: 10.1007/s12539-010-0007-z. Epub 2010 Jul 25.

PMID:
20658337
14.

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
15.

Hemolytic anemias due to erythrocyte enzyme deficiencies.

Jacobasch G, Rapoport SM.

Mol Aspects Med. 1996 Apr;17(2):143-70.

PMID:
8813716
16.

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.

17.

Prediction of deleterious nonsynonymous single-nucleotide polymorphism for human diseases.

Wu J, Jiang R.

ScientificWorldJournal. 2013;2013:675851. doi: 10.1155/2013/675851. Epub 2013 Jan 30. Review.

18.

Red cell enzymopathies as a model of inborn errors of metabolism.

Miwa S, Kanno H, Hirono A, Fujii H.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:112-9. Review.

PMID:
8629088
19.

Prioritization of candidate SNPs in colon cancer using bioinformatics tools: an alternative approach for a cancer biologist.

George Priya Doss C, Rajasekaran R, Arjun P, Sethumadhavan R.

Interdiscip Sci. 2010 Dec;2(4):320-46. doi: 10.1007/s12539-010-0003-3. Epub 2010 Dec 12. Review.

PMID:
21153778
20.

In-Silico Computing of the Most Deleterious nsSNPs in HBA1 Gene.

AbdulAzeez S, Borgio JF.

PLoS One. 2016 Jan 29;11(1):e0147702. doi: 10.1371/journal.pone.0147702. eCollection 2016.

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