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Mismatch repair in mammals
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The development of research tools in the study of myotonic dystrophy: I. CTG trinucleotide repeat expansion; II. DMPK protein functionality; III. Gain of function effect of CUG RNA
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Mechanistic studies of DNA polymerase expansions of trinucleotide repeats associated with neurological disease
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Whole genome amplification from a single cell and mutation analysis of trinucleotide repeats using sperm typing
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Human genetic mapping studies using single sperm typing
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Base mispair extension kinetics and searching for microgene conversion events in the HLA
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Biochemical mechanism of TopBP1 recruitment to sites of DNA damage
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Scanning and catalytic properties of AID with structural comparisons to APOBEC3A
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How phosphorylation affects the biochemical regulation and targeting of activation induced cytidine deaminase (AID)
Chorion gene amplification in Drosophila melanogaster
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DNA methylation inhibitors and epigenetic regulation of microRNA expression
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The role of steroid hormones in the etiology of urologic diseases
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Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome
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The exon-skipping variant RGR-d of the human RGR gene: analysis in human retina and cultured cells
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The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I
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Loss of WRN causes instability of expanded CTG trinucleotide repeats (TNRs)
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Discovery of novel small-molecule compounds with anticancer properties
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Sensing sequence-specific DNA micro-environment with nucleotide-independent nitroxides
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Computational construction and analysis of DNA and RNA
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Functional analyses of androgen receptor structure pertaining to prostate cancer
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X-linked repeat polymorphisms and disease risk: statistical power and study designs
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Interaction of monoclonal antibodies MW1 and PHP1 with huntingtin exon1 protein
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