Tissue-specific insulator function at H19/Igf2 revealed by deletions at the imprinting control region.The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11.An assessment of molecular pathways of obesity susceptible to nutrient, toxicant and genetically induced epigenetic perturbation.Genomic imprinting mechanisms in mammals.Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.Maternal vitamin D depletion alters DNA methylation at imprinted loci in multiple generations.Genetic and haplotype diversity among wild-derived mouse inbred strains.Nutrigenomics, the Microbiome, and Gene-Environment Interactions: New Directions in Cardiovascular Disease Research, Prevention, and Treatment: A Scientific Statement From the American Heart Association.Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.Rescue of the mouse DDK syndrome by parent-of-origin-dependent modifiers.ZFP57: KAPturing DNA methylation at imprinted loci.Intergenerational response to the endocrine disruptor vinclozolin is influenced by maternal genotype and crossing scheme.Extensive polymorphism in the plasmodium vivax merozoite surface coat protein MSP-3alpha is limited to specific domainsImpact of vitamin D depletion during development on mouse sperm DNA methylation
P50
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P50
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American geneticist
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wetenschapper
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հետազոտող
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Folami Ideraabdullah
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Folami Y Ideraabdullah
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Folami Y Ideraabdullah
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