[1] Lysaght, M.J. (2002) Maintenance Dialysis Population Dynamics: Current Trends and Long-Term
Implications. Journal of the American Society of Nephrology, 13, 37-40.
http://jasn.asnjournals.org/content/13/suppl_1/S37.long
[2] (WHR) World Health Rankings. http://www.worldlifeexpectancy.com/world-health-rankings
[3] Gilbertson, D.T., Liu, J., Xue, J.L., Louis, T.A., Solid, C.A., Ebben, J.P. and Collins, A.J. (2005) Projecting
the Number of Patients with End-Stage Renal Disease in the United States to the Year 2015.
Journal of the American Society of Nephrology, 16, 3736-3741.
http://jasn.asnjournals.org/content/16/12/3736.long
http://dx.doi.org/10.1681/ASN.2005010112
[4] Elsharif, M.E. and Elsharif, E.G. (2011) Causes of End-Stage Renal Disease in Sudan: A Single-Center
Experience. Saudi Journal of Kidney Diseases and Transplantation, 22, 373-376.
http://www.sjkdt.org/article.asp?issn=13192442;year=2011;volume=22;issue=2;spage=373;epage=376;aulast=Elsharif
[5] Barsoum, R.S. (2006) Chronic Kidney Disease in the Developing World. New England Journal of Medicine, 354, 997- 999.
http://www.nejm.org/doi/full/10.1056/NEJMp058318
http://dx.doi.org/10.1056/nejmp058318
[6] Mehra, N.K. (2001) Histocompatibility Antigens. Encyclopedia of Life Sciences.
Nature Publishing Group.
http://web.udl.es/usuaris/e4650869/docencia/segoncicle/genclin98/recursos_classe
_%28pdf%29/revisionsPDF/HLA.pdf
[7] Bodmer, W.F. (1987) The HLA System: Structure and Function. Journal of Clinical Pathology,
40, 948-958.
http://jcp.bmj.com/content/40/9/948.full.pdf
http://dx.doi.org/10.1136/jcp.40.9.948
[8] Hassan, M.M., Dowd, A.A., Mohamed, A.H., Mahalah, S.M.O.S., et al. (2014) Computational Analysis
of Deleterious nsSNPs within HLA-DRB1 and HLA-DQB1 Genes Responsible for Allograft Rejection.
International Journal of Computational Bioinformatics and In-Silico Modeling, 3, 562-577.
http://bioinfo.aizeonpublishers.net/content/2014/6/562-577.html
[9] Uricaru, R., Rizk, G., Lacroix, V., Quillery, E., et al. (2015) Reference-Free Detection of Isolated SNPs.
Nucleic Acids Research, 43, e11.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333369/pdf/gku1187.pdf
http://dx.doi.org/10.1093/nar/gku1187
[10] Berno, G., Zaccarelli, M., Goril, C., Tempestilli, M., et al. (2014) Analysis of Single-Nucleotide
Polymorphisms (SNPs) in Human CYP3A4 and CYP3A5 Genes: Potential Implications for the Metabolism of HIV Drugs. BMC Medical Genetics, 15, 76.
http://www.biomedcentral.com/content/pdf/1471-2350-15-76.pdf
http://dx.doi.org/10.1186/1471-2350-15-76
[11] Zhan, X., Dixon, A., Batbayar, N., Bragin, E., et al. (2015) Exonic versus Intronic SNPs: Contrasting
Roles in Revealing the Population Genetic Differentiation of a Widespread Bird Species.
Heredity (Edinb), 114, 1-9.
http://www.nature.com/hdy/journal/v114/n1/pdf/hdy201459a.pdf
http://dx.doi.org/10.1038/hdy.2014.59
[12] Kim, S.K., Park, H.J., Seok, H., Jeon, H.S., et al. (2014) Association Studies of Cytochrome P450, Family 2, Subfamily E, Polypeptide 1 (CYP2E1) Gene Polymorphisms with Acute Rejection in Kidney
Transplantation Recipients. Clinical Transplantation, 28, 707-712.
http://onlinelibrary.wiley.com/doi/10.1111/ctr.12369/pdf
http://dx.doi.org/10.1111/ctr.12369
[13] Ng, P.C. and Henikoff, S. (2001) Predicting Deleterious Amino Acid Substitutions. Genome Research,
11, 863-874.
http://genome.cshlp.org/content/11/5/863
http://dx.doi.org/10.1101/gr.176601
[14] Ramensky, V., Bork, P. and Sunyaev, S. (2002) Human Nonsynonymous SNPs: Server and Survey.
Nucleic Acids Research, 30, 3894-3900.
http://nar.oxfordjournals.org/content/30/17/3894.long
http://dx.doi.org/10.1093/nar/gkf493
[15] Bao, L., Zhou, M. and Cui, Y. (2005) nsSNP Analyzer: Identifying Disease-Associated Nonsynonymous
Single Nucleotide Polymorphisms. Nucleic Acids Research, 33, W480-W482.
http://nar.oxfordjournals.org/content/33/suppl_2/W480.abstract
http://dx.doi.org/10.1093/nar/gki372
[16] Capriotti, E., Fariselli, P., Calabrese and Casadio, R. (2005) Predicting Protein Stability Changes from
Sequences Using Support Vector Machines. Bioinformatics, 2, 54-58.
http://bioinformatics.oxfordjournals.org/content/21/suppl_2/ii54.abstract
http://dx.doi.org/10.1093/bioinformatics/bti1109
[17] Venselaar, H., Beek, T., Kuipers, R.K., Hekkelma, M.L. and Vriend, G. (2010) Protein Structure Analysis
of Mutations Causing Inheritable Diseases. An e-Science Approach with Life Scientist Friendly Interfaces. BMC Bioinformatics, 11, 548.
http://www.biomedcentral.com/1471-2105/11/548
http://dx.doi.org/10.1186/1471-2105-11-548
[18] Gasteiger, E., Hoogland, C., Gattiker, A., Duvaud, S., et al. (2005) Protein Identification and Analysis
Tools on the ExPASy Server. In: Walker, J.M., Ed., The Proteomics Protocols Handbook, Humana Press, 571-607.
http://link.springer.com/protocol/10.1385%2F1-59259-890-0%3A571
http://dx.doi.org/10.1385/1-59259-890-0:571