コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 lifetime of the complex necessary to achieve maximal activation.
2 orylation, synergize functionally to achieve maximal activation.
3 ing increased Ca(2+) sensitivity but reduced maximal activation.
4 All three Nck SH3 domains are required for maximal activation.
5 s the only compound tested that demonstrated maximal activation.
6 cing signals and IFN-gamma are necessary for maximal activation.
7 regulatory factors in addition to SREBPs for maximal activation.
8 rotein combinations show different levels of maximal activation.
9 K required a change to a pH lower than 2 for maximal activation.
10 nd the hydrophobic motif site (Ser-473), for maximal activation.
11 n, indicating these two signals converge for maximal activation.
12 r Ala, highlighting that Trp is required for maximal activation.
13 ess could not be induced, suggesting already maximal activation.
14 ing phosphorylation of the kinase domain and maximal activation.
15 to integrate multiple cooperative inputs for maximal activation.
16 d increases the actin concentration for half-maximal activation.
17 but a length of 10 nucleotides is needed for maximal activation.
18 but not Smad1, significantly contributes to maximal activation.
20 dy, the cGMP concentration required for half-maximal activation (A(50)) of wild-type PKG type Ibeta (
21 ensembles was recruited incrementally, with maximal activation achieved after four laps a day for 4
22 decane, a lipid-solubilizing agent, with 50% maximal activation achieved at approximately 10 microM D
24 equency and amplitude from the location with maximal activation and from the location of the MRS voxe
28 rgoing infection with B. bacilliformis, with maximal activation and translocation to the plasma membr
29 , which requires micromolar calcium for half-maximal activation, and the m-calpain, or calpain II, wh
30 ant Y1771A, BTX shifted the voltage for half-maximal activation approximately 40 mV in the hyperpolar
31 rmed these 4-AP-sensitive currents with half maximal activation at -13.85 +/- 1.17 mV and half maxima
32 activates and inactivates rapidly with half-maximal activation at -18 mV and half-maximal fast inact
33 ctivating and inactivating current with half maximal activation at -27.08 +/- 3.48 mV and -25.51 +/-
35 phosphorylated recombinant enzyme, with half-maximal activation at 0.16 mM, which results in a decrea
37 operative dose-dependent manner, with a half-maximal activation at 0.47 microM and a maximal increase
38 equation with a slope factor of 2.5 and half-maximal activation at 1.6 microM intracellular Ca2+.
46 essentially identical in EPI and ENDO (half-maximal activation at 9-10 mM [Na(+)](i) or approximatel
47 ram in the presence of Ca2+ and reaches half-maximal activation at about 3 x 10(-7) molar free Ca2+,
49 ey (HEK) 293 cells expressing GLIC show half-maximal activation at pH 6, close to the pK(a) of histid
50 IC1 is gated by external protons with a half-maximal activation at pHo 5.6 and a half-maximal inactiv
51 s of REGalpha-gamma chimeras were needed for maximal activation because exchanged carboxyl-terminal s
52 4-yl-PL between membrane leaflets, with half-maximal activation between 20 and 60 microM Ca2+ (satura
54 inactivation by 11 mV, shifts the V(1/2) for maximal activation by 40 mV, and reduces the voltage dep
57 sing discharge to increasing pressures, with maximal activation by crushing or tearing stimuli that c
61 rom both the calcium concentrations for half-maximal activation (Ca(1/2)) and the shift in the calciu
62 e calcium concentration associated with half-maximal activation (Ca(1/2)) of the Ca-ATPase, 290 +/- 1
63 hip revealed an [Ca2+]i required for 50 % of maximal activation (Ca50) of 0.95 +/- 0.08 microM, a Hil
64 reperfusion, the [Ca2+] required for 50% of maximal activation (Ca50) was increased in both intact (
65 ltured in low glucose (LG; 2.5 mm), the half-maximal activation concentration (A(0.5)) of glucose 6-p
68 ncentration, with Hill coefficients and half-maximal activation concentrations very close to the valu
70 Ca50 (-log of [Ca(2+)]free required for half-maximal activation), decreased in McTnT1-44 (alpha-Tm) f
72 rents in the same cell, but the time to half-maximal activation for MagNuM was about two to three tim
73 ween the two choriocarcinoma cell lines, but maximal activation in both cell lines resided within the
74 rotein phosphatases 1 and 2A decreased Ih at maximal activation in hippocampal CA1 pyramidal dendrite
78 [Ca(2+)]free concentration required for half-maximal activation), increased significantly at both sho
80 rease in Ca(2+) spark frequency, with a half-maximal activation (K) of 1.1 micro M, a Hill coefficien
83 ne phosphorylation decreased Ih amplitude at maximal activation (maximal Ih ), without altering HCN1
84 he amount of UreE provided is critical, with maximal activation observed at a concentration equal to
86 d similar concentration dependence with half-maximal activation occurring at 0.02 mol of pigment/mol
87 three Akt isoforms (Akt1 > Akt2 > Akt3) with maximal activation occurring at 2.5 min and returning to
88 ) increased sharply with raised [Ca(2+)](i), maximal activation occurring at a [Ca(2+)](i) of about 1
90 tes; their effects were dose-dependent, with maximal activation of 2.8- and 4.4-fold, respectively.
91 ly p46/54(JNK), p38(MAPK), and ERK-1/2, with maximal activation of 20-, 25-, and 3-fold, respectively
93 r-abl and occurred rapidly, concomitant with maximal activation of a temperature-sensitive mutant of
94 The concentration of GABA producing half-maximal activation of A-type neurons is somewhat less (1
97 trast, Brn-3a and p53 co-operative to induce maximal activation of another p53 target gene encoding t
98 Early-morning exposure to UV also produced maximal activation of ataxia telangiectasia mutated and
100 ads to nearly complete dephosphorylation and maximal activation of BCKDC in heart, muscle, kidneys, a
103 AZ heterogeneity whereby the voltage of half-maximal activation of Ca(2+) influx ranged over approxim
104 and wheat germ calmodulin required for half-maximal activation of Ca(2+)-ATPase were tenfold and fou
105 not change during hypertonic depression, but maximal activation of Ca2+ current shifted to a more neg
106 ble of activating phosphodiesterase, and the maximal activation of calcineurin is reduced by 40% as c
109 jects infused with epinephrine, the ratio of maximal activation of coagulation and maximal activation
112 at 1 microM paraquat was sufficient for half-maximal activation of each reporter fusion within 5 min
113 These studies show that Itk is required for maximal activation of early growth responses 2 and 3 and
117 MAPK family including Erk1/2, JNK, and p38, maximal activation of Erk5 by G-CSF required the C-termi
118 tio of maximal activation of coagulation and maximal activation of fibrinolysis was reduced by >50%.
120 0 minutes after platelet activation, whereas maximal activation of GP IIb/IIIa occurred within the fi
122 show that Sufu plays a positive role in the maximal activation of Hh signaling that defines the vent
123 oncentration of IIC2-delta 3 to achieve half-maximal activation of IC1 was 0.8 and 1.3 microM when st
125 4 and IRS-2 association is also required for maximal activation of IGF-I signalling and cell prolifer
126 atrial myocytes with 10 nM FSCPX reduced the maximal activation of IKAdo by 60% (7.9 +/- 0.2 to 3.2 +
128 iments indicate that GCK is required for the maximal activation of JNK by LPS, lipid A, poly(IC), and
129 cent studies showed that Btk is required for maximal activation of JNK, a family of stress-activated
133 tive in vehicle-treated rats produced a near-maximal activation of LC neurons of rats chronically adm
139 cts independently of its metabolism to allow maximal activation of mTORC1 by growth factors via a mec
140 e and allowing the firing rates required for maximal activation of muscle fibers to be generated by s
142 combined effects of CpG-A plus IL-15 induced maximal activation of NK cells and further enhanced acti
143 al approach for the therapy of AML, aimed at maximal activation of p53-mediated apoptosis by concomit
145 d the Ca(2+) concentration required for half-maximal activation of PDP1 from 3 to 1 microM, but this
147 centration of calmodulin-2 required for half-maximal activation of phosphodiesterase is 2- and 6-fold
149 l phosphorylation of IR or IRS-1 and <50% of maximal activation of PI3K, 2) a novel PI3K-independent
150 phosphorylation of RII subunits, persistent maximal activation of PKA results in a phosphatase-depen
155 d the Ca(2+) concentration required for half-maximal activation of PLCdelta1 from 5.4 to 0.5 microM.
157 GTP loading is similar for IL-8 and C5a, the maximal activation of Raf-1 and B-Raf is approximately 2
158 Depletion of endogenous C/EBPbeta decreased maximal activation of RCAN1-4 expression by calcineurin,
159 duced promoter demethylation is relevant for maximal activation of reelin and GAD67 transcription.
160 mitochondrial signaling complex required for maximal activation of RIG-I-mediated signaling, consisti
164 either Y343 or Y401 is sufficient to mediate maximal activation of STAT5; tyrosine residues Y429 and
167 Phosphorylation at this site is required for maximal activation of the actin-activated Mg2+-ATPase ac
168 K activity has been shown to be required for maximal activation of the canonical Ras/Raf/MEK/ERK Map
170 ession and activates the cIL-6 promoter, and maximal activation of the cIL-6 promoter by vFLIP requir
171 by showing that while TRAF1 is required for maximal activation of the classical NF-kappaB pathway do
175 coccal lipid A was structurally required for maximal activation of the human macrophage TLR4 pathway
176 expression in T cells are also required for maximal activation of the IL-2 gene in FcepsilonRI-stimu
177 uires collaboration with the JNK pathway for maximal activation of the NFLC gene in PC12 cells throug
180 arrestin-interacting domain are required for maximal activation of the p38 mitogen-activated protein
181 with the endogenous Ih, the voltage for half-maximal activation of the PAIH-evoked current was depola
182 n the amount of CaM necessary to obtain half-maximal activation of the PM-Ca-ATPase, indicating that
185 tive regulatory mechanism(s) which prohibits maximal activation of the Ras-dependent signaling events
186 studies identify a novel mechanism by which maximal activation of the rat SREBP-1c gene expression b
187 eosome removal while concurrently inhibiting maximal activation of the same enhancers by recruiting h
188 ly), the calcium concentration at which half maximal activation of the thin filament is achieved can
190 ype II fibers could communicate centrally by maximal activation of their entire pool of presynaptic O
192 tered to cancer patients, and if so, whether maximal activation of these T cells with the combination
194 Y229, as a major amino acid determinant for maximal activation of transcription by AgrA and provides
196 hermore, we found that DOCK1 is required for maximal activation of two HER2 effectors, c-JUN and STAT
197 ease in effective blood volume that leads to maximal activation of vasoconstrictive systems, renal va
198 ease in effective blood volume that leads to maximal activation of vasoconstrictive systems, renal va
201 ftward shift (pCa(50) [change in pCa at half-maximal activation]) of 0.09+/-0.02 pCa units while at 2
202 as assessed as the pCa (-log[Ca2+]) for half-maximal activation, or pCa50, decreased to a greater ext
203 vated by decreasing PO2, with a PO2 for half-maximal activation (P50) not significantly different fro
205 of force, i.e. the [Ca2+] required for half-maximal activation (pCa50) increased from pCa 5.85 +/- 0
206 other members of the cdk family require for maximal activation phosphorylation of a Ser/Thr residue
207 e described by activation curves with a half-maximal activation potential (V ) of -93 mV, slope (k) o
208 did not alter macroscopic desensitization or maximal activation rate and only slightly slowed rapid d
210 by a decrease in agonist affinity, with half-maximal activation rates achieved at 0.77 mM GABA in WT
212 d at the TFIID-TFIIA stage of initiation and maximal activation required the concomitant presence of
215 half-amplitude, 0.5 or 1.0 ms) did not reach maximal activation until the action potential had repola
218 0.55 pA/pF, n = 54; P < .001), yet the half-maximal activation voltage (V0.5), time course of decay,
221 hanges in either HCN conductance or its half-maximal activation voltage resulted in graded changes in
223 acutely isolated neurons gave estimated half-maximal activation voltages of -63 and 12 mV for the two
226 centration of calcium ions required for half-maximal activation was increased in the RVH group: 2.64
230 e, the dose of OKT3 required to achieve half-maximal activation was the same using PMA or different c
231 ose-response curve with little effect on the maximal activation when compared with cells expressing t
232 alue with an additional 40% reduction in the maximal activation when compared with cells expressing t
233 U210, WIN55,212, and anandamide all elicited maximal activation, whereas Delta(9)-THC (56 +/- 6%) cau
234 at the 1-44 region of McTnT is essential for maximal activation, whereas the cardiac-specific 45-74 r
235 y a 1:10 peptide:detergent stoichiometry for maximal activation, whereas the inhibitors are effective
239 ound source is determined by the position of maximal activation within an array of binaural coinciden
240 h was in contrast to the 100% consistency of maximal activation within the traditional fusiform face
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。