Journal of Animal and Veterinary Advances

Year: 2011
Volume: 10
Issue: 7
Page No. 928 - 931

A Comprehensive in silico Analysis of Functional and Structural Impact SNPS in the MC1R Gene

Authors : Chuan-Sheng Zhang, Li-Ying Geng, Zheng-Zhu Liu, Zhi-Xin Fu, Yuan-Fang Gong, Min-Shan Feng, Chen Juan, Qing-Hui Jia, Qiu-Yue Wang, Xie-Rong Liu and Su-Min Pan

References

Bernig, T. and S.J. Chanock, 2006. Challenges of SNP genotyping and genetic variation: Its future role in diagnosis and treatment of cancer. Expert Rev. Mol. Diagn., 6: 319-331.
PubMed  |  

Collins, F.S., L.D. Brooks and A. Chakravarti, 1998. A DNA polymorphism discovery resource for research on human genetic variations. Genome Res., 8: 1229-1231.
PubMed  |  

Griffiths-Jones, S., H.K. Saini, S. van Dongen and A.J. Enright, 2008. miRBase: Tools for microRNA genomics. Nucl. Acids Res., 36: D154-D158.
CrossRef  |  PubMed  |  

Guex, N. and M.C. Peitsch, 1997. SWISS-MODEL and the Swiss-PDB viewer: An environment for comparative protein modeling. Electrophoresis, 18: 2714-2723.
CrossRef  |  PubMed  |  Direct Link  |  

Matichard, E., P. Verpillat, R. Meziani, B. Gerard and V. Descamps et al., 2004. Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure. J. Med. Genet., 41: e13-e13.
PubMed  |  

Ng, P.C. and S. Henikoff, 2003. SIFT: Predicting amino acid changes that affect protein function. Nucl. Acids Res., 31: 3812-3814.
CrossRef  |  Direct Link  |  

Nielsen, M., C. Lundegaard, O. Lund and T.N. Petersen, 2010. CPHmodels-3.0--remote homology modeling using structure-guided sequence profiles. Nucl. Acids Res., 38: W576-W581.
PubMed  |  

Ramensky, V., P. Bork and S. Sunyaev, 2002. Human non-synonymous SNPs: Server and survey. Nucl. Acids Res., 30: 3894-3900.
PubMed  |  

Sherry, S., M. Ward, M. Kholodov, J. Baker, L. Phan, E.M. Smigielski and K. Sirotkin, 2001. dbSNP: The NCBI database of genetic variation. Nucl. Acids Res., 29: 308-311.
PubMed  |  

Sturm, R.A., 2002. Skin colour and skin cancer-MC1R, the genetic link. Melanoma Res., 12: 405-416.
PubMed  |  

Yu, Z., Z. Li, N. Jolicoeur, L. Zhang and Y. Fortin et al., 2007. Aberrant allele frequencies of the SNPs located in microRNA target sites are potentially associated with human cancers. Nucl. Acids Res., 35: 4535-4541.
CrossRef  |  

Yuan, H.Y., J.J. Chiou, W.H. Tseng, C.H. Liu and C.K. Liu et al., 2006. FASTSNP: An always up-to-date and extendable service for SNP function analysis and prioritization. Nucl. Acids Res., 34: W635-W641.
PubMed  |  

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