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1 r PtdIns(4,5)P2, by tagging the PH domain of phospholipase C delta 1 (PLC-delta 1) with the green flu
2 rated the interaction between DLC1-START and Phospholipase C delta 1 (PLCD1) or Caveolin-1, and the c
3 a somatic p.S745L (c.2234 G > A) mutation in phospholipase C delta 1 (PLCD1), a proposed tumor suppre
4 ition by the default PI(4,5)P2 lipid sensor, phospholipase C delta 1 pleckstrin homology domain (PLC
5                       The 2.4-A structure of phospholipase C delta 1 reveals a multidomain protein in
6 ies, which encodes phosphoinositide-specific phospholipase C delta 1 subunit, a key enzyme in phospho
7 raction of the pleckstrin homology domain of phospholipase C delta 1 with PtdIns(4,5)2 combined with
8 te [PI(4,5)P2] hydrolysis catalyzed by human phospholipase C-delta 1 (PLC-delta 1) in model membranes
9                          Here we report that phospholipase C-delta(1) accumulates in the nucleus at t
10 cell cycle-dependent compartmentalization of phospholipase C-delta(1) and support the idea that relat
11                                          The phospholipase C-delta(1) PH domain shows a 10-fold prefe
12   Like certain PH domains (such as that from phospholipase C-delta(1)), the Hrs-1 FYVE domain specifi
13 ion within the pleckstrin homology domain of phospholipase C-delta(1), which disables high affinity p
14 (-1)) than the pleckstrin homology domain of phospholipase C-delta (13 s(-1)).
15  X-ray crystal structure of the C2 domain of phospholipase-C-delta and phylogenetic analysis clarifie
16 rance of the PI(4,5)P2-specific PH domain PH-phospholipase C delta-EGFP at the PM after Ca(2+) ionoph
17  a knockout of the plc-4 gene, which encodes phospholipase C-delta in C. elegans, and demonstrated th
18 o structural information now available for a phospholipase C delta isozyme.
19 ogy (PH)-green fluorescent protein (GFP) and phospholipase C delta (PLC delta)-PH-GFP both first conc
20  marginally changed the dissociation rate of phospholipase C-delta, suggesting that additional electr