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1 phosphate receptor and failed to bind to the cation-dependent mannose 6-phosphate receptor.
2 es is mediated by the cation-independent and cation-dependent mannose 6-phosphate receptors.
3 c domains of both the cation-independent and cation-dependent mannose 6-phosphate receptors.
4 hat are recognized by two distinct MPRs: the cation-dependent mannose 6-phosphate receptor and the in
5 lasmic domains of the cation-independent and cation-dependent mannose 6-phosphate receptors and is re
6 30 and Cys34) in the cytoplasmic tail of the cation-dependent mannose 6-phosphate receptor are palmit
7 eceptors, such as the cation-independent and cation-dependent mannose-6-phosphate receptors, are reco
8 lar topology to each other and to the 46 kDa cation-dependent mannose 6-phosphate receptor, assemble
9 n vitro assay that monitors the transport of cation-dependent mannose 6-phosphate receptors between e
10 ydrolases to the lysosome is mediated by the cation-dependent mannose 6-phosphate receptor (CD-MPR) a
11 The 67-amino acid cytoplasmic tail of the cation-dependent mannose 6-phosphate receptor (CD-MPR) c
15 ly endosomes and increased expression of the cation-dependent mannose 6-phosphate receptor (CD-MPR),
16 a glycosylation-deficient form of the bovine cation-dependent mannose 6-phosphate receptor complexed
17 phate receptor (K(D) = 1 microm) than to the cation-dependent mannose 6-phosphate receptor (K(D) = 3
18 r are predicted by sequence alignment to the cation-dependent mannose 6-phosphate receptor to reside
19 ial EH(3) targets Rab, synaptojanin, and the cation-dependent mannose 6-phosphate receptor were used
20 ve form on Niemann-Pick type C membranes, as cation-dependent mannose 6-phosphate receptors were miss
21 structure similar to that of avidin and the cation-dependent mannose 6-phosphate receptor, yet only
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