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2 midine and of spermine and is metabolized by methylthioadenosine phosphorylase, an enzyme missing in
3 ix metalloproteinase-1, histone deacetylase, methylthioadenosine phosphorylase, and vascular endothel
4 rolase, purine nucleoside phosphorylase, and methylthioadenosine phosphorylase are required for Nrk-i
6 so studied for co-deletion of the contiguous methylthioadenosine phosphorylase gene, and this was det
8 cture of Sulfolobus solfataricus 5'-deoxy-5'-methylthioadenosine phosphorylase II (SsMTAPII) in compl
9 rexpression of metabolism-related gene MTAP (methylthioadenosine phosphorylase) in SSM resulted in re
10 lian purine nucleoside phosphorylase but not methylthioadenosine phosphorylase is responsible for mam
13 ticular, the gene for the enzyme 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP) and the genes o
15 d Ado cleavage activity was identified as 5'-methylthioadenosine phosphorylase (MTAP) based on its bi
16 ncies, we discovered that loss of the enzyme methylthioadenosine phosphorylase (MTAP) confers a selec
18 denosylmethionine (AdoMet) salvage enzyme 5'-methylthioadenosine phosphorylase (MTAP) has been implic
24 ependent growth and defects in expression of methylthioadenosine phosphorylase (MTAP), a key enzyme i
27 r suppressor gene p16INK4A and deficiency of methylthioadenosine phosphorylase (MTAP), both located o
28 study how methionine salvage pathway enzyme methylthioadenosine phosphorylase (MTAP), frequently del
36 nt plants that expressed either MTN or human methylthioadenosine phosphorylase (which metabolizes MTA
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