Pages that link to "Q74350934"
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The following pages link to Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets (Q74350934):
Displaying 12 items.
- CpG island methylation in human lymphocytes is highly correlated with DNA sequence, repeats, and predicted DNA structure (Q21563462) (← links)
- DNA triplet repeat expansion and mismatch repair (Q26996542) (← links)
- Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect (Q34145956) (← links)
- The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome (Q34275676) (← links)
- Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis (Q34446513) (← links)
- Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? (Q35433625) (← links)
- Mechanisms of DNA Damage, DNA Hypomethylation, and Tumor Progression in the Folate/Methyl-Deficient Rat Model of Hepatocarcinogenesis (Q35579915) (← links)
- Murine DNA cytosine C5-methyltransferase: in vitro studies of de novo methylation spreading (Q38349941) (← links)
- Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs (Q38351157) (← links)
- The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)n (Q38352689) (← links)
- Structure and dynamics of three-way DNA junctions: atomic force microscopy studies (Q39584318) (← links)
- Modelling studies on neurodegenerative disease-causing triplet repeat sequences d(GGC/GCC)n and d(CAG/CTG)n (Q77536532) (← links)