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Our DSIP is synthesized to meet high standards of purity and quality, providing a reliable material for investigating complex physiological and cellular mechanisms in a controlled research environment
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
References Uribe PM, Kawas LH, Harding JW, Coffin AB
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This binding activates c-Met phosphorylation, which turns on the HGF receptor and triggers a series of signalling events
