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1 he identities of PKC, annexin I, annexin IV, annexin VI, and annexin VII were confirmed by Western bl
2                            Here we show that annexin VI bound to the NH2-terminal 28-kD portion of me
3 es of coated pits, one of which requires the annexin VI-dependent activation of a cysteine protease t
4                                              Annexin VI-dependent budding is accompanied by the loss
5       Other annexins, such as annexin IV and annexin VI, do not exhibit this binding.
6                             Translocation of annexin VI from the membrane during exposure to t-butyl
7                                   In the SC, annexin VI has the most striking distribution.
8 mbrane spectrin is as effective as cytosolic annexin VI in supporting coated pit budding.
9 well characterized genes including those for annexin VI, interleukin-4 and protein kinase C-beta.
10                                              Annexin VI is differentially expressed by sensory neuron
11                                              Annexin VI is not required for the budding of these new
12                  Previously we reported that annexin VI is required for the budding of clathrin-coate
13 e analysis reveals that mud-1 corresponds to annexin VI; mud-3 corresponds to rat PC3, mouse TIS21; m
14 easable intracellular calcium, that bound to annexin VI on the inner surface of the plasma membrane.
15       Recent electron microscopic studies of annexin VI revealed that the protein's two core domains
16 When the mutant is compared to the wild-type annexin VI, subtle differences are seen at the site of t
17       Finally, microinjection of a truncated annexin VI that inhibits budding in vitro has the same e
18 the Ca(2+)-dependent binding of CRHSP-28 and annexin VI, together with their colocalization in the ap
19 it suggests a mechanism for participation of annexin VI translocation that may underlie the alteratio
20 ossibly a higher calcium binding affinity of annexin VI upon phosphorylation.
21         The interaction between CRHSP-28 and annexin VI was demonstrated by coimmunoprecipitation and
22 a(2+)-sensitive phospholipid-binding protein annexin VI was purified from rat pancreas as a CRHSP-28-
23 6D in the flexible connector region of human annexin VI) was determined to 2.65 A resolution.
24  B, ninjurin1, Ref1, calpastatin, HDJ-2, and annexin VI) were expressed in B-lineage ALL cells at hig
25 onfirmed a dual localization of CRHSP-28 and annexin VI, which appeared in a punctate pattern in the
26  enhanced the colocalization of CRHSP-28 and annexin VI within regions of acini immediately below the

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