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1  BRIa and BRII with a key component of CCPs, adaptor protein 2.
2 , which have reduced binding to the clathrin adaptor protein-2, a critical regulator of GABA(A)R endo
3 athrin-associated protein adaptor protein 1, adaptor protein 2 and adaptor protein 180 complexes from
4 periments indicate that LMBD1 interacts with adaptor protein-2 and is involved in the unique clathrin
5 mplexes and other endocytic proteins such as adaptor protein 2 (AP-2) and clathrin.
6 pid down-regulation of CD4 via the endocytic adaptor protein 2 (AP-2) complex, a process linked to en
7 th the clathrin-associated, heterotetrameric adaptor protein 2 (AP-2) complex.
8 s internalized from the cell surface via the adaptor protein 2 (AP-2) complex.
9              Inhibition of expression of the adaptor protein 2 (AP-2) or inhibition of clathrin by pi
10 ion through canonical endocytic motifs in an adaptor protein 2 (AP-2)-dependent way.
11 requires palmitoylation for interacting with adaptor protein-2 (AP-2) and AP-3, respectively, for tra
12 e clathrin endocytic machinery, clathrin and adaptor protein-2 (AP-2) in vitro.
13       Depletion of the mu subunits of either adaptor protein-2 (AP-2) or AP-1 using RNAi further prov
14 al cord slices and that it is carried out by adaptor protein-2 (AP-2) via clathrin-mediated endocytos
15 However, no loop-dependent binding of Nef to adaptor protein-2 (AP-2), which is the adaptor protein c
16 f Cell describes the atomic structure of the adaptor-protein 2 (AP-2) core, the portion that makes co
17 , null mutations in subunits of the clathrin adaptor protein 2 (AP2) complex in Caenorhabditis elegan
18  identified as cargo proteins of the classic adaptor protein 2 (AP2) complex of the clathrin-mediated
19                             Heterotetrameric adaptor protein 2 (AP2) complexes, which initiate clathr
20               Here we show that clathrin and adaptor protein 2 (AP2) were part of the LRP6 signalosom
21 ing RNA (siRNA), we found that inhibition of adaptor protein 2 (AP2), which mediates endocytosis of t
22 f predicted to recruit the clathrin adaptor, Adaptor protein 2 (AP2).
23                                              Adaptor protein-2 (AP2), a central component of clathrin
24  reduced association with beta arr-2 and the adaptor protein-2 beta.
25 n 1 binding site and the other involving the adaptor protein 2 binding site.
26 re the ability of Nef to colocalize with the adaptor protein-2 complex (AP-2).
27 rlapping consensus motifs for binding to the adaptor protein-2 complex, and mutation of a tyrosine sh
28 l interfering RNA against the mu2 subunit of adaptor protein 2, dominant negative dynamin construct K
29 ere clathrin interacts with the membrane via adaptor proteins; 2) elongation, where the membrane is t
30   Now, two studies agree that four-phosphate adaptor protein 2 (FAPP2) transfers glucosylceramide (Gl
31  targeting the PI4P effector, four-phosphate adaptor protein 2 (FAPP2).
32                             This motif binds adaptor protein-2 in glutathione S-transferase-uncoverin
33 eimide-sensitive fusion protein-AP2-clathrin adaptor protein 2 inhibitory peptide pep2m occluded LTD
34 , a motif that interacts with mu2 subunit of adaptor protein 2, is critical for the cell motility-pro
35                                          The adaptor protein-2 sigma subunit (AP2sigma2) is pivotal f
36 this receptor is dependent on the binding of adaptor protein 2 to the specific LLKIL motif found with
37 iated endocytosis, as well as association of adaptor protein-2 with clathrin-coated pits.

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