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1 a unique 600-kDa retinoblastoma protein- and calmodulin-binding protein.
2 rly ethylene-responsive gene NtER1 encodes a calmodulin-binding protein.
3 horylation of caldesmon (CaD), an actin- and calmodulin-binding protein.
4 lin and contained an IQ motif found in other calmodulin binding proteins.
5 binding motif was identified for many of the calmodulin-binding proteins.
6 nsmission, we conducted a screen for retinal calmodulin-binding proteins.
7 labeled calmodulin to isolate cDNAs encoding calmodulin-binding proteins.
9 1 through the known transcription activators calmodulin binding protein 60g (CBP60g) and systemic acq
11 inding transcription activators (CAMTA)3 and calmodulin binding protein 60g (CBP60g) together amplify
12 of OsWRKY47; among these two genes encode a Calmodulin binding protein and a Cys-rich secretory prot
16 activation of other beta-granule-associated calmodulin-binding proteins as local [Ca2+]i rises to pr
17 report the identification of the actin- and calmodulin-binding protein caldesmon (CALD1) as a novel
20 ocalization signal (NLS) was detected in the calmodulin-binding protein (CBP) domain and removed by m
21 lin in the presence of Ca2+ and was the only calmodulin-binding protein detected in the absence of Ca
22 homologue of Arabidopsis KCBP (kinesin-like calmodulin binding protein)) exhibited highly processive
24 of protease substrates and Ca(2+)-dependent calmodulin-binding proteins from natural cDNA libraries
25 a clearly identify IQGAP1 as the predominant calmodulin-binding protein in Ca2+-free breast cell lysa
26 ermittent amphetamine altered the content of calmodulin-binding proteins in striatal cytosol or membr
28 granin (Ng) is a brain-specific postsynaptic calmodulin-binding protein involved in synaptic activity
29 ldesmon (Cd) and calponin (Cp) are two actin/calmodulin-binding proteins involved in 'actin-linked' r
33 tors suggest that the total concentration of calmodulin-binding proteins is approximately 2-fold high
36 tion of a cDNA encoding a novel kinesin-like calmodulin-binding protein (KCBP) from Arabidopsis using
37 report the crystal structure of kinesin-like calmodulin-binding protein (KCBP) from potato, which was
42 end-directed microtubule motor kinesin-like calmodulin-binding protein (KCBP) plays a role in tricho
44 f a novel kinesin-like protein (kinesin-like calmodulin-binding protein, KCBP) from Arabidopsis and o
45 ding protein from maize pollen (maize pollen calmodulin-binding protein, MPCBP) was isolated in a pro
46 studies have revealed that a pollen-specific calmodulin-binding protein, No Pollen Germination 1 (NPG
48 g with antisera to caldesmon, a cytoskeletal calmodulin-binding protein of 77 kDa, demonstrated incre
49 associated with the induction of a specific calmodulin-binding protein of about 68 kD (CaM-BP68).
51 calized exclusively to excitatory neurons; a calmodulin-binding protein PCP4; the bone extracellular
52 a missense substitution in PPEF2, encoding a calmodulin-binding protein phosphatase, which we show in
54 the apical and lateral localization of Crag (Calmodulin-binding protein related to a Rab3 GDP/GTP exc
56 nsgenic mice that overexpress neurogranin (a calmodulin-binding protein that facilitates long-term po
57 widely expressed 190-kDa Cdc42-, Rac1-, and calmodulin-binding protein that interacts with F-actin i
58 ne-rich C kinase substrate) is an actin- and calmodulin-binding protein that is expressed in many mam
60 t 10(-5) mol/l [Ca2+]) and competed by other calmodulin-binding proteins that had higher affinity (e.
63 least in part, by four previously identified calmodulin-binding proteins: the TRP and TRPL ion channe
64 3 (also called neurogranin), which encodes a calmodulin binding protein thought to be a neural-specif
65 k tissues and, as one of a growing number of calmodulin-binding proteins to be identified in the nucl
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