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1 tive, a channel that is otherwise anesthetic insensitive.
2 e calcium-sensing RCK domain are practically insensitive.
3 )-OT response in mOTR and hOTR cells was PTX insensitive.
4 e level of initial release, i.e. are release insensitive.
5 tients with hereditary UC susceptibility are insensitive.
6 he best-studied receptors is BRASSINOSTEROID INSENSITIVE 1 (BRI1) in Arabidopsis (Arabidopsis thalian
7 defective in the BR-receptor BRASSINOSTEROID INSENSITIVE 1 (BRI1).
8 r FLAGELLIN SENSING 2 (FLS2)-BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (BAK1) complex, and in
9  on the plant protein kinase brassinosteroid insensitive 1-associated kinase 1 (BAK1) conformational
10 munity, Arabidopsis thaliana BRASSINOSTEROID INSENSITIVE 1-associated receptor kinase 1 (BAK1) and so
11 activity of GSK3-like kinase BRASSINOSTEROID-INSENSITIVE 2 (BIN2), a key repressor of brassinosteroid
12 nknown biochemical activity, called ethylene-insensitive 2 (EIN2); and transcription factors such as
13  alpha/beta-fold hydrolase receptor KARRIKIN INSENSITIVE 2 (KAI2) and the F-box protein MORE AXILLARY
14 sion of an ethylene signaling gene, ETHYLENE INSENSITIVE 2 (ZmEIN2), co-segregated with a decreased s
15 w, winter-long upregulation of VERNALIZATION INSENSITIVE 3 (VIN3)(5-7), a PHD protein that functions
16 master transcriptionactivator EIN3 (Ethylene Insensitive 3)-mediated transcriptional activation plays
17  LEAFY COTYLEDON 1/2 (LEC1/2), ABSCISIC ACID INSENSITIVE 3, FUSCA 3 and WRINKLED 1 is upregulated in
18 ICE1 binds to and inhibits expression of ABA INSENSITIVE 3.
19                                Abscisic acid-insensitive 5 (ABI5) is an essential and conserved plant
20 responsive genes and the accumulation of ABA Insensitive 5 (ABI5), causing mutant plants with ABA-ins
21 educed transcript abundance of ABSCISIC ACID-INSENSITIVE 5 (ABI5), which encodes an activator of FLC
22 -fluorodeoxyglucose, (11)C-methionine and pH-insensitive (64)Cu-labelled nanoparticles.
23 anescens) lines: wild type and abscisic acid-insensitive (abi1) with functionally impaired stomata.
24                             In contrast, CoA-insensitive Acot2 could provide a constitutive siphon fo
25 ender a metalens achromatic and polarization-insensitive across nearly the entire visible spectrum fr
26 ding effect on the treatment of chemotherapy-insensitive aggressive B-cell non-Hodgkin lymphoma (B-NH
27                                       The pH-insensitive alanine resonance was used as a reference.
28 rridden in plants that contain a photoperiod-insensitive allele of Ppd-1, which hastens the completio
29         Here mutations in the KAI2 (KARRIKIN INSENSITIVE) alpha/beta-fold hydrolase and the MAX2 (MOR
30                 To test for both devaluation insensitive and devaluation sensitive Pavlovian conditio
31 iagnosing bloodstream infections (BSIs), are insensitive and limited by prolonged time to results.
32 d bone scintigraphy, are recognized as being insensitive and nonspecific for response monitoring in a
33 strained heptamethine cyanine is temperature-insensitive and significantly extended at moderately ele
34  the non-desensitizing current was amiloride insensitive and voltage dependent.
35 elf-adhesive, breathable, flexible, moisture-insensitive, and able to maintain their accuracy under s
36 ays of A. solani inoculated SA-deficient, JA-insensitive, and wild type plant lines.
37              The paracellular pathway was pH-insensitive at pH 6.0 vs. pH 7.4 and was equally permeab
38          We show that these CIAO (cross-over insensitive ATG-out) vectors virtually eliminate leak ex
39 s to compare the performance of arrival-time-insensitive (ATI) and arrival-time-sensitive (ATS) compu
40 ed that Hellinger distance is not only class-insensitive but also translation-invariant.
41 (2+) chelation or overexpression of a Ca(2+)-insensitive CaM mutant, reduced coupling, which is consi
42 hibitory receptor expression, and interferon-insensitive CAR T cells enable combinatorial therapy wit
43 -complete responders of CC patients and CDDP-insensitive CC cell lines with CDDP-sensitive group.
44 f a T cell and show that checkpoint blockade-insensitive CD8 T cells can be induced to respond to che
45 herins, and require coupling to pull Cxcl12a-insensitive cells along.
46 ondary targeted approach to render otherwise insensitive cells, sensitive to a targeted therapeutic.
47    Heterologous expression of unc-7 in touch-insensitive chemosensory neurons confers ectopic touch s
48 n-sensitive rat TRPV1 (rTRPV1) and capsaicin-insensitive chicken TRPV1 (cTRPV1) exposed to a series o
49                            Wild-type and AZD-insensitive Chlamydomonas strains were treated with TOR-
50 specifically disrupted by deleting rapamycin-insensitive companion of target of rapamycin (Rictor), e
51 ion (TG) that includes Rictor, the rapamycin-insensitive complex-2 of mTOR (mTORC2), and genes involv
52 human mucosal epithelial cell types: insulin-insensitive corneal epithelial cells and insulin-sensiti
53 ht the possibility of developing photoperiod-insensitive crops by adjusting the allelic combination o
54 t well described and is derived largely from insensitive culture techniques.
55 in-coated gelation films also show thickness-insensitive deep-blue emission with respect to the refer
56 ature or shade reduced the stability of a GA-insensitive DELLA allele in Arabidopsis thaliana Further
57 P1 enhanced the degradation of normal and GA-insensitive DELLA alleles when coexpressed in Nicotiana
58 f yeast MTHFR to create a series of feedback-insensitive, deregulated mutants.
59    Present impedance provides a specific but insensitive diagnostic.
60                 Mainstay serologic tests are insensitive during the acute phase of infection and are
61                                  Serology is insensitive during the first days to weeks of infection,
62 teins mediated by a GA-activated GIBBERELLIN-INSENSITIVE DWARF1 (GID1) receptor.
63 a target of gibberellin receptor GIBBERELLIN INSENSITIVE DWARF1 (GID1)-promoted proteasomal destructi
64  of grain yield by up to 30% compared to the insensitive elite barley allele.
65  the normalized capacitance as a temperature-insensitive extrinsic variable to measure strain.
66                                 Mechanically-insensitive fibers were also detected in lingual afferen
67 f Galpha(i2) deficient (Gnai2 (-/-)) and RGS-insensitive Galpha(i2) (Gnai2 (G184S/G184S)) BMDMs.
68 d dosage responses than do putatively dosage-insensitive gene groups, suggesting that constraints on
69 ne expressing cyclic adenosine monophosphate-insensitive HCN4 channels.
70                        In addition, the AITC-insensitive highveld mole-rat exhibited overexpression o
71                           The glucocorticoid-insensitive hyperrresponsiveness in isolated human airwa
72                Current laboratory testing is insensitive in early infection, the stage at which appro
73 , because spontaneous release becomes Ca(2+)-insensitive in Syb1(lew/lew)Syb2 (-/-) NMJs, our finding
74 res and soil moisture levels were remarkably insensitive in terms of their J(max25 degrees C) and V(c
75 Both receptors induced pertussis-toxin (PTX) insensitive inhibition of cyclic AMP (cAMP) levels in ma
76            In hippocampal slices, picrotoxin-insensitive inhibitory synaptic currents exhibited fast
77 me encodes three BEN-solo proteins including Insensitive (Insv), Elba1 and Elba2 that possess activit
78 mics: the charge relaxation time as a strain-insensitive intrinsic variable to measure absolute tempe
79 2+)-dependent inactivation in the previously insensitive isoform.
80                             We used polarity-insensitive k-means clustering to segment resting-state
81 plant line compared to the wild type and JA- insensitive line.
82 es, and that these neurons present direction-insensitive, linear voltage integration, suggesting they
83 ted inflorescence development of photoperiod-insensitive lines is promoted by advanced seasonal expre
84 chemical genetics screening to identify DFPM-insensitive loci by monitoring the activity of ABA-induc
85 erscreening strategy to generate an L-lysine insensitive LysG-based biosensor.
86 cyte studies using the ubiquitous amantadine-insensitive M2 S31N variant, the current block showed fa
87 ly and affected the organization of estrogen-insensitive MCF10A cells in 3D collagen matrix by influe
88 l tissues, the corneal epithelium is insulin insensitive, meaning it does not require insulin for glu
89 n undiluted serum with desensitization is an insensitive measure of effectiveness.
90 ing-feeding cycle in nutrient-sensitive and -insensitive mice.
91 ic airways disease (AAD) model and a steroid-insensitive model combining ovalbumin-induced AAD with C
92           Here we demonstrate that rapamycin-insensitive mTORC1 signaling via 4E-BP1 is a critical pa
93 ,5-triazine (RDX) have been updated with the insensitive munition (IM) 2,4-dinitroanisole (DNAN).
94      3-Nitro-1,2,4-triazol-5-one (NTO) is an insensitive munition compound (MC) that has replaced leg
95 of 2,4-dinitroanisole (DNAN), a component of insensitive munitions formulations, by mineral-bound Fe(
96 (NTO) is one of the main ingredients of many insensitive munitions, which are being used as replaceme
97    AF2ER is an AF-2 disrupted estradiol (E2)-insensitive mutant ERalpha, but AF-1-dependent transcrip
98 ytes expressing wild-type SERCA2b or a redox-insensitive mutant in which C674 is replaced by serine (
99 ffects to recapitulate the phenotype of a JA-insensitive mutant lacking the COI1 receptor.
100 ly, we generated knockin mice carrying Cl(-)-insensitive mutant WNK4.
101                             An abscisic-acid-insensitive mutant, abi1, showed altered sensitivity to
102                      Ethylene- and cytokinin-insensitive mutants were partly insensitive to germinati
103 ient and wild type plants, but not in the JA-insensitive mutants.
104    Ion substitutions revealed that amiloride-insensitive NaCl responses depended on Cl(-) rather than
105 into slow inactivation compared with menthol-insensitive neurons.
106 y polarization transfer (DEPT) and refocused insensitive nuclei enhanced by polarization transfer (RI
107 of these axons do not need to be temperature-insensitive or highly restricted, but coordinating the t
108 ated signaling pathways for survival and are insensitive, or rapidly evolve resistance, to selective
109 e presence of IL-4 to become potent, steroid-insensitive, pathogenic effector cells in asthmatic pati
110                        By contrast, androgen-insensitive PC3 and DU145 cells displayed clear nuclear
111 cue the PIF4 level in addition to the thermo-insensitive phenotype of spaQ, suggesting that the SPA1
112 efore defining PGA as a potentially "steroid-insensitive" phenotype that requires exploration of alte
113 ive 5 (ABI5), causing mutant plants with ABA-insensitive phenotypes during seed germination and seedl
114 fully complements both picloram and chlorate insensitive phenotypes of pic30-3.
115  overexpression of ABI5 could rescue the ABA-insensitive phenotypes of pifq mutants in the dark.
116 in stability/activity by inducing proteasome-insensitive polyubiquitination.
117 unders were minimized by using an arrhythmia-insensitive-rapid (AIR) cardiac T1 mapping pulse sequenc
118 receptor signaling but involves the CLAVATA3 INSENSITIVE RECEPTOR KINASE (CIK) family co-receptors, w
119 d an AAV vector that uses mutant "cross-over insensitive" recognition sites combined with an "ATG-out
120 ductant appears to be dissipated via cyanide-insensitive respiration.
121 sed mammalian or snake TRP channels in light-insensitive retinal cones in a mouse model of retinal de
122 ), a peptide ligand, and its receptors, RGF1 INSENSITIVEs (RGIs), a clade of five leucine-rich-repeat
123 zed by Na(+)-sensitive eticlopride and Na(+)-insensitive risperidone correspond to different degrees
124  Cl(-), not Na(+), generates these amiloride-insensitive salt taste responses.
125 erminant of taste transduction for amiloride-insensitive salt taste.SIGNIFICANCE STATEMENT Sodium and
126 KRAS(G12C) is maintained in its active, drug-insensitive state by epidermal growth factor receptor an
127 morphology and converts them into a nutrient insensitive state that is coupled to endoplasmic reticul
128 d also efficiently ablate the growth of drug-insensitive stem-like cells as well as therapy resistant
129 n protein stability than in partial androgen insensitive syndrome (PAIS).
130 e bradycardia and AV block, but the atropine-insensitive tachycardia and PVCs were abolished by the b
131 t assay methods for milk oxidases are either insensitive, tedious or not cost-effective.
132 ith the production of cold-induced and light-insensitive TIM isoforms facilitate EYA accumulation in
133 f stool remains the gold standard but can be insensitive, time-consuming, and difficult to maintain c
134 he potentiometric response of the MC3-ISM is insensitive to [Formula: see text] or changes in pH.
135 ome and demonstrate how dendritic spines are insensitive to a brief period of novel sensory experienc
136 nterestingly, jazD and jazD phyB plants were insensitive to a chemical inhibitor of Trp biosynthesis,
137 of DvABCB1 by RNAi which rendered WCR larvae insensitive to a Cry3A toxin.
138 , we observe that certain capsid mutants are insensitive to a Nup62-mediated nuclear pore complex blo
139 d that myoblasts from the D2 background were insensitive to a specific small molecule inhibitor of DU
140 ed muscarinic acetylcholine receptor that is insensitive to acetylcholine.
141 )] (i) Because catalytically-inactive BTK is insensitive to active-site BTK inhibitors, the mechanism
142          This lifetime change was relatively insensitive to added glycerol up to 60%, suggesting that
143  uPlm that are both catalytically active and insensitive to alpha2-AP inhibition.
144 unctional in mood and anxiety disorders, are insensitive to alterations in area 14 activity as is the
145 1N) in the influenza A M2 channel renders it insensitive to amantadine (AMT) and rimantadine (RMT) bl
146 s arginine residue rendered mTORC1 signaling insensitive to amino acid starvation and are found frequ
147 e arousal-induced memory boosting effect was insensitive to amisulpride but was sensitive to proprano
148 urthermore, GNE551-evoked pain is relatively insensitive to antagonist treatment.
149 orms constitutively active channels that are insensitive to ATP or the antagonist suramin, suggesting
150 e of the agg1agg2 Ggamma double-mutant, were insensitive to Ca(o) .
151  mutation of these interactions renders Eag1 insensitive to calmodulin inhibition.
152 oforms, whereas HCN1 and HCN3 are relatively insensitive to cAMP.
153  pocket in these Env mutants renders the Env insensitive to CD4 binding.
154 udies suggest that GluN2B-type receptors are insensitive to CDI.
155                                This value is insensitive to changes in ATP and CYT-19 concentration a
156 ation site specific activity that is largely insensitive to changes in NMDA receptor-mediated neurotr
157 r to reversion for this adduct is relatively insensitive to changes in solvent while the adduct forme
158 emission rate (86 +/- 8 mug m(-2) h(-1)) was insensitive to changes in the ACH because its large indo
159 iscal characteristics of this MOF family are insensitive to changes in the metal cation, which enable
160 f cancers arise due to p53 mutations and are insensitive to chemotherapeutic treatments that activate
161 with a rigid alkyne linker rendering a probe insensitive to cis-trans isomerization.
162          Symbiotic nitrogen fixers-which are insensitive to climatic controls on decomposition (compa
163 whereas ACC inhibition renders waiting times insensitive to confidence-modulating attributes of visua
164 +) release from an intracellular compartment insensitive to CPA; (iii) only Thg is able to activate C
165 f TYROSYL-DNA PHOSPHODIESTERASE 1 (TDP1) are insensitive to CPT, and only the wss1A tdp1 double mutan
166 formed at the top surface, which is not only insensitive to depth-dependent inhomogeneities but also
167 e wave dynamics, but that these dynamics are insensitive to details of cellular activation.
168           However, previous studies were too insensitive to determine whether semantic representation
169 h superoxide (O(2) (*-)) production, must be insensitive to deuteration, and yields a predicted (16)O
170 spatial localisation of the outcome which is insensitive to devaluation.
171  and electronic bandgaps that are relatively insensitive to disorder.
172 udies suggest that viral genome packaging is insensitive to DNA sequence and fluctuations in packagin
173 ~4 angstrom, as manifest by kinetics largely insensitive to E(app).
174 d E2-induced events, making GREB1 completely insensitive to E2 induction.
175  of clinical rating scales; these scales are insensitive to early degenerative changes that underlie
176 -forming organic reactivity, were relatively insensitive to early drought conditions but decreased by
177 rs evolved (genetically or culturally) to be insensitive to efficacy because people tend not to rewar
178 that these variants render the eIF2B complex insensitive to eIF2 phosphorylation, which occurs under
179 -scales prior to burial in sediments and are insensitive to elevated (14)C concentrations following n
180 pressed functional KI GlyRs that were rather insensitive to ethanol when compared with WT GlyRs.
181 in a heteromeric alpha2beta receptor that is insensitive to ethanol.
182 nd nuclear transitions(7), which are largely insensitive to external perturbations and reach waveleng
183          Emergence of such a pattern, albeit insensitive to extrinsic factors, requires a balance bet
184  in HsSAS-6, whose substitutions rendered it insensitive to FBXW7-mediated degradation and control of
185 n addition, the ATN framework was relatively insensitive to frontotemporal lobar degeneration, and th
186                                sAC, which is insensitive to G-protein modulation but responsive to Ca
187  triple mutant was extremely dwarf and fully insensitive to GA.
188 nd cytokinin-insensitive mutants were partly insensitive to germination-inhibition.
189 omosome-integrated native lac is shown to be insensitive to Gyrase overexpression, even at critically
190  as opposed to its pattern and amplitude, is insensitive to hydrogeological and nucleation parameters
191                          Macrophages (MPhis) insensitive to IFN-gamma (MIIG) mice have MPhis, monocyt
192 thermophotovoltaic efficiency becomes nearly insensitive to increasing cell bandgap or decreasing emi
193                         Channel activity was insensitive to inhibitors of the adenine nucleotide tran
194            Although metabolic tissues become insensitive to insulin in the setting of obesity, a numb
195                      These microsensors were insensitive to interfering redox molecules and surpassed
196 by the fate is determined quite early and is insensitive to intracellular noise.
197 he membrane orientation of Ras is relatively insensitive to its bound guanine nucleotide and activati
198 proliferation, but rendered these phenotypes insensitive to KLF9 and ROS.
199 esult of Ku inhibition, as Ku-null cells are insensitive to Ku-DBi's.
200                         p53 mutant cells are insensitive to LDIR and outcompete wild-type cells follo
201 iers: those for which the carrier density is insensitive to Li adsorption, and those whose density de
202 e variogram underlying OK is global and thus insensitive to local data variation.
203 ol intoxication and reduced anxiety, and are insensitive to local manipulations of signaling in the B
204 ases, a subset of mammary spheroids remained insensitive to local matrix stiffness.
205   In contrast, Lhb expression was relatively insensitive to loss of endogenous GnRH and continuous tr
206 rom the fou2 mutant, harboring TPC1 channels insensitive to luminal Ca(2+), can be excited fully by e
207                                  The loss is insensitive to magnetic field but increases for excited
208 al and spin transitions that are first-order insensitive to magnetic field fluctuations, enabling opt
209 rain-induced resistance switching process is insensitive to magnetic fields.
210        The Trichoplax channel was relatively insensitive to mammalian Ca(V)2 channel blockers omega-a
211                Although the rho1 receptor is insensitive to many anesthetic drugs that modulate the h
212 , defined as 'stiff' dimensions, while it is insensitive to many others ('sloppy' dimensions).
213           Modelling shows that the design is insensitive to MIEC material choice with channels about
214 more differentiated fates and rendering them insensitive to mitogenic factors such as Notch.
215 y on large and uncertain corrections and are insensitive to most of the Universe's volume and probabl
216                           Stylet neurons are insensitive to nectar-specific sugars and respond to glu
217 ASE4 (DGK4) grow slower and become partially insensitive to NO-dependent growth inhibition and re-ori
218                POU3F3 is an intronless gene, insensitive to nonsense-mediated decay, and 13 individua
219 um responses to glutamate but are relatively insensitive to norepinephrine.
220 rmed C-N network, yielding a stable compound insensitive to O(2) and H(2)O.
221                                      CyBA is insensitive to OCl(-), NO, NO(2)(-), NO(3)(-), tBuOOH, O
222                          The procedures were insensitive to other behaviors, including jumping and se
223 e compounds, in contrast to pyridomycin, are insensitive to overexpression of InhA in Mycobacterium t
224 stomatal reopening, and TARK1 OE plants were insensitive to P syringae pathovar tomato strain DC3118
225 that persons lacking functional Na(V)1.7 are insensitive to pain, has spurred considerable effort to
226       Furthermore, this linear dependency is insensitive to particle size variation within 20-200 nm
227 n is, unusually for RiPP biogenesis, largely insensitive to perturbations of the leader portion of th
228                                 Sorption was insensitive to pH changes except for PFOSB; PFOSB underw
229                Membrane disruption by VLP is insensitive to pH, but unassembled capsid protein and AR
230                                 Lapronic was insensitive to physiological pH and temperature and did
231  three allelic pic30 mutants are selectively insensitive to picolinate herbicides, while pic30-3 is a
232 , we show that a memory selectivity bias was insensitive to propranolol but sensitive to amisulpride,
233                                     Subjects insensitive to punishment are afraid of aversive events,
234 epletion of extracellular Ca(2+); these were insensitive to quaternary ammonium block.
235 ighly sensitive to rapid TFIID depletion and insensitive to rapid SAGA depletion.
236  that the second phase of RhoA activation is insensitive to rapid turning off of the receptor and is
237 adrenergic receptors, respectively, and were insensitive to reverse-mode NCX blockade (KB-R7943).
238  activation of RagC and RagD GTPases, but is insensitive to RHEB activity induced by growth factors.
239 rom infant mice were predominantly immature, insensitive to RORgamma-inducing bacterial cues and to I
240 within 3 h of its activation, stomata become insensitive to ROS and open.
241          In comparison, they were relatively insensitive to S-cone CD.
242         Moreover, the DeltaFolvam7 mutant is insensitive to salt and osmotic stresses and hypersensit
243              By contrast MITF(Low) cells are insensitive to SCD inhibition.
244  the histone H4 tail and appeared relatively insensitive to sequence differences on either side of th
245                            Since CD19 CAR is insensitive to serum IgG, we designed various combinator
246 ganoids lacking p53 mutation and p53 LOH are insensitive to SOAT1 loss, indicating a potential therap
247 e mechanism; it renders autoreactive B cells insensitive to stimulation by self-antigen, whereas Toll
248 e mass spectrometry, makes the gates largely insensitive to stoichiometric imbalances in the inputs,
249 s and elastic modulus of the four films were insensitive to strain rate changes.
250      The fuscanodin biosynthetic enzymes are insensitive to substrate concentration and operate in a
251 dual TRIM21 on a stress-fibre subset that is insensitive to substrate stiffness.
252  after binding the poly(A) tail, PABP became insensitive to suppression by PAIPs and efficiently acti
253 ed integrated emissivity (epsilon(int) ), is insensitive to temperature (|depsilon(int) /dT| ~ 10(-4)
254 l voltage-dependent equilibria are virtually insensitive to temperature.
255  4 (ACTN4) causes its binding kinetics to be insensitive to tension.
256 ope peak, which is a robust measure of mass, insensitive to the aforementioned natural and technical
257          ULP1a mutants are salt tolerant and insensitive to the BR inhibitor, brassinazole.
258              BRAF mutant TCC cell lines were insensitive to the BRAF inhibitor vemurafenib, with IC(5
259 entional imaging methods are destructive and insensitive to the buried device geometries, preventing
260 where the patient's immune system has become insensitive to the cancer cells.
261 endogenous phosp27-CDK4-CycD1 complexes were insensitive to the CDK4-targeting drug palbociclib.
262 activation produced by these agents and were insensitive to the channel blocker mecamylamine.
263                                      PIXE is insensitive to the chemical environment, but coupled wit
264 concentration of an active CaM-binding TF is insensitive to the concentration of any other CaM-bindin
265 r is a fundamental physical feature which is insensitive to the details of the network generation.
266 ults of biodiversity experiments are largely insensitive to the exclusion of unrealistic communities
267 ion, while the neutral exciton state remains insensitive to the ferromagnet.
268 vels than the peripheral rate-place code and insensitive to the harmonic relationships among frequenc
269 377V/V388I mutant or SALL4 G416A mutant were insensitive to the inhibitory effects of thalidomide, le
270 text] This energy partition is approximately insensitive to the ion-to-electron temperature ratio [Fo
271 h autobiographical recall periods (which are insensitive to the moment-to-moment content of retrieval
272 GAT107, and B-973B responses were relatively insensitive to the noncompetitive antagonist mecamylamin
273 d that accuracy and precision are relatively insensitive to the number of replicated assignments for
274  from mice of either sex, an effect that was insensitive to the PKA inhibitors (H-89, KT270) but that
275 ive species, such that decomposition becomes insensitive to the presence of (SiOH)(4).
276 y slight cooling, although sugar neurons are insensitive to the same mild stimulus.
277              On the other hand, the N400 was insensitive to the sharing or distribution of the two in
278 also that the degree of shielding is largely insensitive to the specific glycoform.
279  show that most polyspermy-derived seeds are insensitive to the triploid block suppressor admetos.
280  a small safe operating space exists that is insensitive to the type of policy implementation, while
281 can polymers, before exposure rendered cells insensitive to this effect.
282 ar features, malignant clones are frequently insensitive to traditional AML chemotherapeutic agents.
283                                              Insensitive to transverse fluctuations, our measurements
284  Whereas the behavior of CYP 19A1 was rather insensitive to truncation of the TM-helix, mutations in
285 tosol avoid inflammasomes(1-6) and are often insensitive to type I interferons (IFN-I), but are restr
286  and explains why the KCNQ1 channel alone is insensitive to up to 1 mM mefenamic acid.
287 among high ITN users is consistently low and insensitive to variation in mosquito exposure.
288 nce of J-coupling, and (c) can be relatively insensitive to variations in B0, T2 and B1.
289                         Results were largely insensitive to variations in in-hospital mortality, age
290 erence ligand and produces a ranking that is insensitive to variations in the concentration of indivi
291  are able to maneuver through narrow spaces, insensitive to wall-targeting antibiotics, and capable o
292   However, this intramembrane enzyme becomes insensitive to warfarin inhibition in vitro, preventing
293  it is information-rich, minimally invasive, insensitive to water background and requires little to n
294  mixed with wild-type tumor cells, IFN-gamma-insensitive tumor cells indeed grow out, which depends u
295 erefore mediated by the MCRC but becomes RAP-insensitive under DFO treatment, with concomitantly decr
296 , GPR65, and GPR68 pH sensing and provide pH-insensitive variants that should be valuable for assessi
297 requires diacylglycerol (DAG) but is Ca(2+) -insensitive, which are characteristics of the novel grou
298  found that Phi6 RdRp is largely temperature insensitive, while PV and HRV-C RdRps replication kineti
299                        A novel, polarization insensitive, wide-angle and broadband electromagnetic me
300 thyl ether); and (5) the reaction is largely insensitive with respect to common hydrosilane reductant

 
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