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1 i retrieval of membrane proteins such as the cation-independent mannose 6-phosphate receptor.
2 , chimeric enzyme with high affinity for the cation-independent mannose 6-phosphate receptor.
3 CD8 protein with the cytoplasmic tail of the cation-independent mannose 6-phosphate receptor.
4 -II binding site on the bifunctional, IGF-II cation-independent mannose 6-phosphate receptor.
5 ceptor and the insulin-like growth factor II/cation-independent mannose 6-phosphate receptor.
6 coprotein 1 and the proton pump, but lacking cation-independent mannose 6-phosphate receptor.
7  alters the steady state localization of the cation-independent mannose 6-phosphate receptor.
8 ith heparan sulfate glycosaminoglycans and a cation-independent mannose-6-phosphate receptor.
9 ion in the intracellular distribution of the cation-independent mannose-6-phosphate receptor.
10 in fractions similar to those containing the cation-independent mannose-6-phosphate receptor.
11 e weak binding of the acid hydrolases to the cation-independent mannose 6-phosphate receptor allows s
12 ters, exhibited a decreased affinity for the cation-independent mannose 6-phosphate receptor and fail
13 lycoprotein receptor, and low amounts of the cation-independent mannose 6-phosphate receptor and the
14 d by oligosaccharide receptors including the cation-independent mannose 6-phosphate receptor and the
15  domain of cargo proteins such as furin, the cation-independent mannose-6-phosphate receptor and in v
16 N is incorporated into cells via sortilin or cation-independent mannose 6-phosphate receptor, and fac
17                                              Cation-independent mannose 6-phosphate receptors are enr
18 or between 0 and 2.5 min, then contained the cation-independent mannose 6-phosphate receptor between
19                  While ectopic expression of cation-independent mannose-6 phosphate receptor blocks a
20                     The cation-dependent and cation-independent mannose 6-phosphate receptors (CD- an
21 o-trans-Golgi network (TGN) transport of the cation-independent mannose 6-phosphate receptor (CI-MPR)
22 usly identified high affinity ligand for the cation-independent mannose 6-phosphate receptor (CI-MPR)
23                                  The 300 kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
24                                  The 300-kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
25                                  The 300 kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
26     The retromer complex, which recycles the cation-independent mannose 6-phosphate receptor (CI-MPR)
27                                  The 300-kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
28                                  The 300-kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
29           This may be because of inefficient cation-independent mannose 6-phosphate receptor (CI-MPR)
30                                  The 300 kDa cation-independent mannose 6-phosphate receptor (CI-MPR)
31                                          The cation-independent mannose 6-phosphate receptor (CI-MPR)
32             Although the distribution of the cation-independent mannose 6-phosphate receptor (CI-MPR)
33                  (iii) Cells transduced with cation-independent mannose 6-phosphate receptor (CI-MPR)
34 leucine motif in the cytoplasmic tail of the cation-independent mannose 6-phosphate receptor (CI-MPR)
35 protein induced a dramatic redistribution of cation-independent mannose 6-phosphate receptor (CI-MPR)
36 ann-Pick type C protein NPC2, a cargo of the cation-independent mannose-6-phosphate receptor (CI-M6PR
37 fR), a component of early endosomes, and the cation-independent mannose-6-phosphate receptor (CI-M6PR
38  disorders, which has been attributed to low cation-independent mannose-6-phosphate receptor (CI-MPR)
39 ffect of adjunctive clenbuterol treatment on cation-independent mannose-6-phosphate receptor (CI-MPR)
40 A), which has been attributed to inefficient cation-independent mannose-6-phosphate receptor (CI-MPR)
41 sport for endosome-to-Golgi retrieval of the cation-independent mannose-6-phosphate receptor (CI-MPR)
42 unsuspected interaction between SNX5 and the cation-independent mannose-6-phosphate receptor (CI-MPR)
43 t mediates the retrograde trafficking of the cation-independent mannose-6-phosphate receptor (CI-MPR)
44                                          The cation-independent mannose-6-phosphate receptor (CI-MPR)
45 omer-mediated endosome-to-Golgi retrieval of cation-independent mannose-6-phosphate receptors (CI-MPR
46 to examine each of 25 ArfGAPs for effects on cation-independent mannose 6-phosphate receptor (CIMPR)
47     In cells with rerouted AP-1, endocytosed cation-independent mannose 6-phosphate receptor (CIMPR)
48 g mDpy-30 levels changes the distribution of cation-independent mannose 6-phosphate receptor (CIMPR)
49 sorting of multiple receptors, including the cation-independent mannose 6-phosphate receptor for lyso
50 n complex that mediates the retrieval of the cation-independent mannose 6-phosphate receptor from end
51   In mammals the extracellular region of the cation-independent mannose-6-phosphate receptor has gain
52 D-MPR) and the insulin-like growth factor II/cation-independent mannose 6-phosphate receptor (IGF-II/
53 g of the retromer cargo, sortilin, SorLA and cation-independent mannose 6-phosphate receptor, in rode
54 ssociated with impaired incorporation of the cation-independent mannose 6-phosphate receptor into cla
55  Recombinant TIP47 binds more tightly to the cation-independent mannose 6-phosphate receptor (K(D) =
56  positive for markers of transport vesicles (cation-independent mannose 6-phosphate receptor), late e
57  endocytic pathway, but not with Rab7 or the cation-independent mannose 6-phosphate receptor, markers
58 te five stable human cell lines deficient in cation-independent mannose 6-phosphate receptors (MPRci)
59 oplasmic domains of the cation-dependent and cation-independent mannose 6-phosphate receptors (MPRs)
60 here was no effect on the trafficking of the cation-independent mannose 6-phosphate receptor or the G
61 grown cells revealed loss of TC II-R but not cation-independent mannose 6-phosphate receptor protein
62 o required for trafficking of an endocytosed cation-independent mannose 6-phosphate receptor reporter
63  AP-5 subunits: all six knockdowns cause the cation-independent mannose 6-phosphate receptor to becom
64 r SNX2 is essential for the retrieval of the cation-independent mannose 6-phosphate receptor to the T
65 embryonic development that is independent of cation-independent mannose 6-phosphate receptor traffick
66 oplasmic GGA1 and GGA3 but not GGA2 bind the cation-independent mannose 6-phosphate receptor very poo
67                                          The cation-independent mannose 6-phosphate receptor was not
68       The late endosomal-prelysosomal marker cation-independent mannose 6-phosphate receptor was not
69      hDNase binds to a column of immobilized cation-independent mannose 6-phosphate receptor, with th

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