ライフサイエンスコーパス: myo-inositol 1,4,5-trisphosphate

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1 ates, in particular via the second messenger myo-inositol 1,4,5-trisphosphate, and phosphoinositides

2 e of large cholangiocytes by activation of D-myo-inositol 1,4,5-trisphosphate/Ca(2+) /calmodulin-depe

3 locked by neomycin, and is not affected by D-myo-inositol 1,4,5-trisphosphate (D-IP3).

4 A regioisomer of the second messenger D-myo-inositol 1,4,5-trisphosphate [D-Ins(1,4,5)P(3), 1],

5 ability of human Arf1.GDP (Arf1.GDP) to bind myo-inositol (1,4,5)-trisphosphate (I(1,4,5)P(3)), the s

6 itol 1,3,4-trisphosphate (Ins(1,3,4)P3) or D-myo-inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) over 80-

7 ic activity partial agonists at the platelet myo-inositol 1,4, 5-trisphosphate [Ins(1,4,5)P(3)] recep

8 brevicompactum, are potent agonists at the D-myo-inositol-1,4,5-trisphosphate [Ins(1,4,5)P3] receptor

9 platelets but was 40-fold less potent than D-myo-inositol-1,4,5-trisphosphate [Ins(1,4,5)P3].

10 ine)-mediated enhancement of intracellular D-myo-inositol 1,4,5-trisphosphate (IP(3)) and Ca(2+) accu

11 t inhibition of endoplasmic reticulum (ER) d-myo-inositol 1,4,5-trisphosphate (IP(3))-gated calcium r

12 2'-P-cADPR and 1-D-myo-inositol 1,4,5-trisphosphate (IP3) appear to act by

13 Liposomes filled with 100 microM D-myo-inositol 1,4,5-trisphosphate (IP3) enhanced the MEPP

14 Intracellular application of myo-inositol 1,4,5-trisphosphate (IP3, 100 microM) from

15 igh affinity to intestinal SMC; stimulated D-myo-inositol-1,4,5-trisphosphate (IP3) formation, Ca2+ r

16 llular activity of phospholipase C-gamma, by myo-inositol 1,4,5-trisphosphate radioreceptor assay, de

17 phostin A (AdA) is a potent agonist of the d-myo-inositol 1,4,5-trisphosphate receptor (Ins(1,4,5)P3R

18 siently transfected with type I and type III myo-inositol 1,4,5-trisphosphate receptor (IP(3)R) isofo

19 myo-Inositol 1,4,5-trisphosphate receptor (IP3R) degrada

20 ate (8), two analogues of the superpotent 1D-myo-inositol 1,4,5-trisphosphate receptor agonist adenop

21 hostin A (AdA), the most potent agonist of d-myo-inositol 1,4,5-trisphosphate receptors (IP(3)R), is

22 down-regulation of both type I and type III myo-inositol 1,4,5-trisphosphate receptors (IP3Rs).

23 henylborate, a cell-permeant antagonist of D-myo-inositol 1,4,5-trisphosphate receptors, abrogates an

24 The response to KCl or D-myo-inositol 1,4, 5-trisphosphate was not different betw

25 pase C products, namely diacylglycerol and d-myo-inositol 1,4,5-trisphosphate, were identified as pro

26 A variety of inositol phosphates including myo-inositol 1,4,5-trisphosphate, which is a secondary m

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