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Journal of Human Genetics|November 19, 2002
SNP alleles in human disease and evolutionBarkur S ShastryJournal of Human Genetics|November 28, 2001
Molecular and cell biological aspects of Alzheimer diseaseB S ShastryMolecular Medicine Reports|April 8, 2011
Common polymorphisms of the CFH, LOC 387715/ARMS2 and HTRA1 genes may not influence the intra-familial variability of X-linked juvenile retinoschisisBarkur S ShastryMolecular Medicine Reports|April 9, 2011
Copy number variation and susceptibility to human disorders (Review)Barkur S ShastryIUBMB Life|October 14, 2000
Hereditary degenerative retinopathies: optimism for somatic gene therapyB S ShastryComparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology|September 1, 1995
Overexpression of genes in health and sickness. A bird's eye viewB S ShastryJournal of Cell Science|March 1, 1996
Transcription factor IIIA (TFIIIA) in the second decadeB S ShastryMethods in Molecular Biology (Clifton, N.J.)|September 22, 2009
SNPs: impact on gene function and phenotypeBarkur S ShastryInternational Journal of Molecular Medicine|February 13, 2003
SNPs and haplotypes: genetic markers for disease and drug response (review)Barkur S ShastryPageof 1,346