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1 could produce reactive oxygen species (ROS) normally.
2 , but axonemal microtubules fail to elongate normally.
3 e strain PH-1, while 10 Group 2 mutants grew normally.
4 Sohlh2, meiosis is not affected and proceeds normally.
5 nce of OPCs, perineurial glia exited the CNS normally.
6 well behaved and the computations continuing normally.
7 ssion in myocytes that do not express the AR normally.
8 ed sheep concluded that the animals had aged normally.
10 h a part of the ERK2 D-recruitment site that normally accommodates the hydrophobic sidechains of a ca
11 en as the source of TCA cycle expansion that normally accompanies exercise and imply that impaired TC
15 pathways, foremost being the STAT3 pathway, normally activated by cytokines from the interleukin-2 (
17 25 family member A (Cdc25A) is a phosphatase normally activated during cell division in proliferating
19 l destabilize a D354-R375 salt-bridge, which normally acts as an electrostatic lock to prevent coordi
24 hypothalamic progenitors are not maintained normally and neuronal differentiation is compromised: rx
25 hat Muc4(ko) animals are fertile and develop normally, and adult mice exhibit no overt tissue abnorma
26 , the concept of complementary modulation of normally antagonistically targeted GSK3 substrates offer
29 bilization of the nuclear RNA 7SK, a process normally associated with adult megakaryocytic P-TEFb act
30 oach considering that real-life stimuli come normally associated with competing aversive and appetiti
31 cancers is that they activate genes that are normally associated with distinct developmental states,
34 perfusion decreases in regions of the brain normally associated with the 'default mode' or 'task neg
36 wnregulated the expression of multiple genes normally associated with the response to infection, incl
37 site not susceptible to the immune processes normally associated with tissue injury and wound repair.
43 se of the respiratory CO2 chemoreflex, which normally augments ventilation in response to hypercapnic
45 c-Fos controls blood vessel growth into the normally avascular photoreceptor layer through the infla
46 Pathological neovessels growing into the normally avascular photoreceptors cause vision loss in m
50 ies of water diffusion through tissue, which normally becomes increasingly restricted and anisotropic
51 RNAs by recruiting release factor RF2, which normally binds stop codons to catalyze peptide release.
52 D1 mutants and wild-type (wt) SOD1 exposes a normally buried nuclear export signal (NES)-like sequenc
53 Armc5 heterozygote mice (Armc5+/-) developed normally but at the age of 1 year, their corticosterone
54 nic progenitors lacking Minion differentiate normally but fail to form syncytial myotubes, and Minion
55 Capzb-null stereocilia initially developed normally but later shortened and disappeared; surprising
56 aspase-2 deficient (Casp2(-/-)) mice develop normally but show premature ageing-related traits and wh
57 Plants silenced in NaAGO8 expression grew normally but were highly susceptible to herbivore attack
60 scam(del17) ; Dscam(2J)), RGC axons pathfind normally, but growth from the chiasm toward their target
63 could escape T cell fate constraints imposed normally by a Notch-inductive microenvironment and under
66 ndition characterized by the clouding of the normally clear eye lens brought about by deposition of c
69 ddition, the BRCA2 interacting protein BCCIP normally colocalizes with chromatin bound BRCA2, and upo
71 dis (Nm) is a Gram-negative diplococcus that normally colonizes the nasopharynx and rarely infects th
72 strain sensitivity (dlambda/dH) (compared to normally compacted (NC) unsubstituted CoFe2O4 (CFO)) of
74 ological regions in semantic dementia do not normally contain significant levels of recently proposed
76 ciceptive behavior and cortical activity are normally correlated, this relationship is disrupted in i
78 re isolated from hysterectomy specimens from normally cycling premenopausal women with uterine fibroi
79 nces a later part of the oscillation that is normally damped; when this enhancement crosses perceptua
80 y, our data suggest that autophagic activity normally decreases with age in C. elegans, whereas daf-2
81 nce to heat, flame, and chemical agents that normally degrade conventional macrofibers, high-performa
84 subsequently restart DNA synthesis, which is normally dependent upon HR-mediated resolution of collap
92 nfounding in mediation analysis allowing for normally distributed or Bernoulli distributed exposures,
93 indexed parameters (X/BSA(alpha)) that were normally distributed without residual dependence on BSA.
94 y ICU time (neither of which is likely to be normally distributed) to produce overall LOS distributio
95 f the early Notch-active cells, however, are normally diverted from this fate and increasing lateral
100 function, and fragmentation (fission) of the normally elongated mitochondria indicates loss of their
102 tion, exposing bees to elevated temperatures normally encountered by honey bees during typical activi
106 relatively thick-walled vesicles that do not normally exhibit stimulus-responsive behavior and (ii) i
108 st of gene candidates to the subset that are normally expressed at a given stage or in a given tissue
110 1 (Plk1), a serine/threonine protein kinase normally expressed in mitosis, is frequently up-regulate
112 idarian Nematostella vectensisNvbrachyury is normally expressed in precursors of the pharynx, which s
113 xtraembryonic tissue, the hypoblast, and are normally expressed in the pregastrulation stage epiblast
114 ectopic expression of proteins that are not normally expressed in the red blood cell, leading to sys
117 itro fertilisation (IVF), only about half of normally fertilised human embryos develop beyond cleavag
119 e results reveal that NLRC4 and NLRP3, which normally form distinct inflammasomes, activate an LPC-in
120 teral to neural tube and the somites that is normally formed by PNA-binding proteins that block entry
123 granules marked by chromogranin B, which are normally found in neuronal presynaptic terminals storing
124 stress response including autophagy markers normally found in portacaval anastomosis rats were rever
127 in Notum null mutants, indicating that Notum normally functions to coordinate synaptic structural and
129 models and samples from pregnant women with normally grown and large-for-gestational age infants.
130 d as birth weight below 10th centile) and 94 normally grown fetuses identified in utero and followed-
132 tes are glomerular epithelial cells that are normally growth-arrested because of the expression of cy
133 ited state (4)T1 and the ground state (6)A1 (normally >17,000 cm(-1)) while the latter with f-f trans
137 n response to premature depolarizations that normally helps protect against the formation of ectopic
138 teins by binding galactose residues that are normally hidden below terminal sialic acid residues.
144 in medical applications; its sensitivity is normally in pico-to-micro-molar range, dependent on exog
146 Surprisingly, cuticular ridges at first form normally in the cus2 mutant, but are lost progressively
147 e DeltacheY2 spirochetes are able to survive normally in the Ixodes ticks, mice fed upon by the Delta
149 individuals with GATA2 mutation proliferated normally in vitro, whereas lineage-negative progenitors
151 eries of resonances as the grating couples a normally-incident THz wave to standing surface plasmon w
155 ad to an activated, or primed, state of Env (normally induced after Env interaction with the receptor
157 V pyramidal neurons is induced at +30 ms, a normally ineffective timing interval for t-LTP induction
158 ight, stays high during the night, when mice normally ingest food and when translation is known to be
159 th silencing of hypermethylated genes, which normally inhibit these pathways and are associated with
160 -evoked responses of mitral cells, which are normally inhibited by abGCs, were increased in microglia
165 mor growth through the production of factors normally involved in tissue repair and maintenance.
166 e function is to pump acid into the stomach, normally lack MIST1 and do not perform regulated secreti
167 protects nonobese diabetic (NOD) mice, which normally lack this isotype, from spontaneous development
170 ic rewiring of glycolysis can circumvent the normally lethal effects of oxygen deprivation, a mechani
171 ng the adhesive properties of neurons in the normally lissencephalic mouse cortex leads to the format
173 ollers maintain HIV-1 viremia at low levels (normally <2000 HIV-RNA copies/mL) without antiretroviral
175 lts suggest that a reduction in the currents normally mediated by Ether-a-go-go-Related Gene (ERG) K(
179 . burgdorferi can transform a ubiquitous but normally nonadhesive blood constituent to increase the e
181 tants to express a recoded ARG8(m) when this normally nuclear gene is substituted for ATP8 in mitocho
182 files were imposed, in order to mimic the pH normally obtained in southern-type and northern-type dry
185 aberrant RNAs, UPF1 also degrades specific, normally occurring mRNAs to regulate diverse cellular pr
188 The results indicated that cells could grow normally on plant-produced hOPN as compared to commercia
191 The findings suggest that cortical tissue normally operates as a type I excitable medium but it is
192 ogenlyase (FHL) enzyme from Escherichia coli normally oxidizes formic acid to carbon dioxide and coup
193 ntroduced adjacent to cysteines that are not normally palmitoylated, they became palmitoylation sites
196 EN3 3 (alp3), displaying accumulation of the normally plasma membrane (PM)-localized PEN3-GFP in endo
197 te specificity in favor of l-serine over the normally preferred l-serine-O-sulfate ( approximately 12
199 ing the cells to mechanical stress, which is normally present in wounds, wound healing was impaired.
201 ns is a ubiquitous mucosal commensal that is normally prevented from causing acute or chronic invasiv
202 nput guides the compensatory plasticity that normally prevents the plasticity underlying H-reflex cha
203 ls, which showed that the ABCB4 mutants were normally processed and targeted to the plasma membrane,
205 date NRPS requires TM-modes, so the TE-modes normally produced by integrated lasers cannot be isolate
206 ll autonomous, from loss of alpha3(V) chains normally produced by tumour cells, in which they affect
209 re responsible for a form of PCH with small, normally proportioned cerebellum and should be screened
215 -links (ICLs) and bulky minor groove adducts normally recognized by Fanconi anemia and nucleotide exc
219 , the mechanisms by which LMP1 expression is normally regulated in epithelial cells remain poorly und
221 respiratory motor circuit in bullfrogs that normally remains inactive for several months during the
222 somes, suggesting that many meiotic DSBs are normally repaired by intersister recombination in mice.
223 mpatible non-face objects, including objects normally represented in other parts of inferotemporal co
224 ible backup ('dark' shadow enhancer) that is normally repressed but becomes active in the absence of
225 o the stromogenic path, suggesting that Pax2 normally represses an otherwise inevitable transition be
227 om aldehydes, and considering that aldehydes normally require harsh reaction conditions to take part
229 find that under conditions when TFIIH is not normally required for transcription, Mediator actually r
230 may complement formal diagnosis procedures (normally requiring time, cost-intensive sleep studies an
231 via the induction of a CD8(+) T cell program normally reserved for latent pathogens and persistence i
234 lly localizes to the cytosol or nucleus, PDC normally resides within the mitochondrial matrix where i
237 ork and a lack of termination cytokines that normally restore haematopoietic stem-cell quiescence.
238 orneal infection is that the virus spread is normally restricted to only a small fraction of cells on
239 forced apical localization of Par3, which is normally restricted to tight junctions, is sufficient to
240 e receptors, along with membrane lipids, are normally returned to the plasma membrane to sustain this
241 aboratory, rats exhibit negative affect to a normally rewarding taste cue when it predicts impending
244 of phagocytosis is great enough, for acute, normally self-limiting infections, then (i) antibiotics
248 rugs usurp neural plasticity mechanisms that normally serve reward-related learning and memory, prima
250 successful in inducing remissions, these are normally short-lived, with median response durations of
251 These synapses, called endbulbs of Held, normally show strong depression in voltage-clamp recordi
252 served vision and 38 age- and gender-matched normally sighted controls to determine whether periphera
253 mployment rate vs age- and education-matched normally sighted controls to guide visual disability str
255 enables androgens to drive expression of the normally silent E26 transformation-specific (ETS) transc
260 cular endothelial growth factor (VEGF), that normally stimulate multiple phases of wound healing.
261 with the accompanying loss of fluid, is not normally stimulated by intestinal distension as the meal
263 e MCMV epitope sequence, M57727-734, and the normally subdominant LCMV epitope L2062-2069, indicating
270 riability is due to stochastic conversion of normally symmetric cell divisions to asymmetric and vice
274 lates of utricle hair cells initially formed normally, then degenerated after postnatal day 5; large
275 Moreover, the thickness and total width normally thought to determine the local stiffness, and t
278 peripheral blood mononuclear cells responded normally to all TLR1/2, TLR2/6, TLR4, TLR7, and TLR8 (R8
279 at RyR1 channels from Tric-a KO mice respond normally to cytosolic Ca(2+) , ATP, adenine, caffeine an
280 n by divalent cations, although they respond normally to cytosolic Ca(2+) , ATP, caffeine and luminal
281 However, ULK1-deficient cells responded normally to DMXAA, indicating that AMPK promotes STING-d
289 T1-mTOR pathway, we increased the caliber of normally unmyelinated axons and the expression of numero
291 r and engages in [4 + 2] cycloadditions with normally unreactive azadienophiles including unactivated
292 l1b-/- Il18-/- mutant mice survived and grew normally until adulthood and, at 6 months of age, exhibi
294 Instead, transcription was initiated in normally untranscribed sequences the same distance upstr
295 n of KLF9, an axon growth suppressor that is normally upregulated 250-fold in RGC development, promot
296 amines (PE) by 15-lipoxygenases (15-LO) that normally use free polyunsaturated fatty acids as substra
299 t was recorded in a gait laboratory, walking normally, with 5 degrees and 10 degrees LWIs, toes inwar
300 core IFTB proteins are unable to accumulate normally within Ift56(hop) cilia, including IFT88, IFT81
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