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1 e of thermal noise and clock jitter or clock skew.
2 ing of the demise dependent on the amount of skew.
3 ines significantly with increasing sex ratio skew.
4 rences in survival increasing with sex ratio skew.
5 creases in trait variance and distributional skew.
6 low abundance sites is contributing to these skews.
7 icate that parasite distribution is markedly skewed.
8 croL/min, with the distribution being highly skewed.
9 ution is shown by electron micrographs to be skewed.
10 f flow voids vs size of the voids was highly skewed.
11 ly if emissions across facilities are highly skewed.
12 tes and countries around the world is highly skewed.
13 ndicating the lack of requirement for clonal skewing.
14 lowance, at intervention week 1) in either a skewed (10 g at breakfast, 20 g at lunch, and 60 g at di
15 ultiple mechanisms through which hypoxia can skew a population's size distribution toward smaller ind
16 litude (peak and area) and timing (phase and skew, a measure of burst shape) when animals ran on leve
17 in intensity, with local regions of high GC skew, a sequence feature known to form unique secondary
19 al appearance, transcriptional profiling, Ab skewing, Ab repertoire, and secretory response to stimul
20 umber of publications is the question of how skewed allelic expression should be for it to be designa
21 ged, they were metabolically reprogrammed to skew allergic inflammation from eosinophilic T helper ce
22 e results strongly suggest selection-induced skewing alters B-1a cell-derived natural Ab, which may i
23 downregulation in mouse hippocampal neurons skews AMPAR composition towards non GluA2-containing Ca(
24 ion, male bonobos have a higher reproductive skew and a stronger relationship between dominance rank
27 onors with axial-rich substituents contained skew and boat conformations, and three-state models were
28 ormation near gene promoters with strong G/C skew and propensity to form G-quadruplex in non-template
29 x-changing) fish, the sex ratio is typically skewed and biased towards the 'first' sex, while reprodu
30 ur process-based, statistical approach gives skewed and complex probability distributions (single mod
31 stribution that becomes gradually positively skewed and sapwood density increases while the theoretic
36 t mice, we found that S6K2 loss reduces Th17 skewing and increases regulatory T cell differentiation
39 clining populations, but the causes of these skews and their consequences for local population demogr
40 ed increased T-cell activation, naive T-cell skewing, and elevated serum CXCL9 and CXCL10 levels.
42 ficant chronic immune activation, phenotypic skewing, and inflammation driven by years of continuous
43 n a laser pulse is initially incident with a skew angle relative to the channel axis, the laser and a
46 ed and is not due to underlying cytoskeletal skewing, as is the case in other known, phenotypically s
49 They further suggest that public TCR can skew autoimmune susceptibility, and that subsets of publ
50 cient CD8 T cells expanded normally but were skewed away from MPECs with resultant poor development o
53 autologous lymphocytes, led to Th1 response skewing, based on significantly higher levels of IFN-gam
54 y rounded shape, demonstrating a pathway for skewed BLiP size distributions that recapitulate 3D morp
56 ing of IdoA is present in (1)C4-chair, (2)SO-skew boat, and less frequently, in (4)C1-chair conformat
58 er, microbiome compositional data are highly skewed, bounded in [0,1), and often sparse with many zer
59 of both genes correlated with X-inactivation skewing but no significant association with age-adjusted
60 itative analysis of bioimaging data is often skewed by both shading in space and background variation
61 nally used to represent the mean) was highly skewed by outliers, exceeding the 97(th) percentile at s
63 that, under anxiety, decision making may be skewed by salient and conflicting environmental stimuli
65 further confirmed that the Treg-DC-mediated skewed CD4(+) naive T cell polarization resulted from de
67 n rejection, establishing organ tolerance by skewing CD4 T helper polarization away from a proinflamm
70 whether helminthes prevent T cell priming or skew clonal recruitment and effector differentiation is
75 l immunomodulator that provides early type 1-skewed cytokine production to control the parasite load
77 with production of proinflammatory and TH17-skewing cytokines, resulting in a TH17 immune response w
78 mizes assay artifacts of drug metabolism and skewed DAR profiles that may result from the prolonged i
80 rated and characterized mature retinoic acid-skewed dendritic cells (DC-RAs) and assessed their abili
82 shed a transcriptional profile that strongly skewed differentiation toward Th2, led to decreased surv
84 tory response or increased T cell activation/skewing display a more impaired behavioral profile than
85 rmal distribution; the Bhut Jolokia showed a skewed distribution and the Jalapeno peppers showed a ve
88 years of follow-up, but its gradually right-skewed distribution suggested a subpopulation with marke
90 lenges for statistical analysis, including a skewed distribution, excess zero values, and occasional
92 ed population of healthy cells, we show that skewed distributions of incubation periods emerge for a
93 on from flares suggests the need to consider skewed distributions when assessing flare impacts global
94 bacterial morphological diversity is likely skewed due to an experimental focus on pathogens and ind
95 mbalance featuring pathogenic Th1- and Th2/0-skewed effector responses and reduced immunosuppressive
96 mission categories and explicit treatment of skewed emissions at both component and facility levels.
97 to PI may include specific IgE, Th2 cytokine skewing, eosinophils, activation of the complement, and
99 with CVID with secondary complications and a skewed follicular helper T-cell differentiation in defin
101 ities calculated for various symmetrical and skewed gambles served to define formally the direction o
104 , fueled by complement imbalance and therapy-skewing genetic variance, underscore the need for more c
106 tion of pathogens and inflammatory cytokines skews hematopoiesis toward myeloid development, although
107 hematopoietic stem and progenitor cells, and skewed hematopoietic development to the B cell/myeloid l
112 mycin-dependent induction of T helper type 2-skewed immune polarization, M2 macrophage infiltration,
113 on of fibroblast activation, T helper type 2-skewed immune polarization, M2 macrophage infiltration,
114 stand how differential immunity to influenza skews immune responses toward coinfecting bacteria and d
115 rast to a non-classical monocyte-mediated M2-skewed immunosuppression by the Asian-lineage ZIKV infec
116 gnant women's blood led to an exacerbated M2-skewed immunosuppression of non-classical monocytes in c
117 egnant patients showed elevated levels of M2-skewed immunosuppressive cytokines and pregnancy-complic
118 We could reproduce the observed cellular skew in both wild-type embryos and embryos with distorte
121 aminating agents, explains the well-known GC skew in microbial genomes, and suggests the APOBEC3 fami
122 n attractiveness, but is rapidly balanced by skew in the offspring distribution of highly attractive
127 These transcription factor profiles were skewed in HIV-infected individuals where the proportion
133 ment microtubules with reduced protofilament skew, indicating that Mal3 adjusts interprotofilament in
134 classical/intermediate monocyte-mediated M1-skewed inflammation by the African-lineage ZIKV infectio
136 onal iNKT alterations were associated with a skewed iNKT-TCR repertoire with a selective reduction of
143 entified by positive nucleotide distribution skew jumps overlap with origins identified by ini-seq an
144 Variable, Diversity, and Joining genes, and skewed length distribution of the TRB and TRA complement
147 eceptor (Fgfr) and ERK pathways reversed the skewed lineage specification of Klf5 KO blastocysts.
148 lf5 KO and overexpressing blastocysts showed skewed lineage specification phenotypes, similar to FGF4
149 These data indicate expression of IRAK-M skews lung macrophages toward an alternatively activated
150 ; 3) Ly6C(neg) macrophages, originating from skewed Ly6C(pos) cells, actively proliferated; and 4) la
154 mice contained Ly-6C(low) macrophages with a skewed M2-prone gene expression signature, increased col
159 le i) promotes macrophage proliferation, ii) skews macrophages toward a cyto-destructive phenotype, a
160 sease had highly variable and often markedly skewed maturation phenotypes, including CD4/CD8 ratio re
161 ts with CVID with immune dysregulation had a skewed memory CD4 T-cell differentiation toward a CXCR3(
162 wide range of effects in B cells, including skewed memory cell differentiation, compromised B cell f
163 ngs demonstrate that the rs874040(CC) allele skews memory T cells toward a pro-inflammatory phenotype
165 g the demonstration that AHR down-regulation skews monocytes toward macrophage differentiation, sJIA
167 edback inhibition from surviving neurons may skew neuronal regeneration towards ablated cell types.
168 ng parameters and considered both normal and skew normal distributions of the measurement noise.
169 n MINDD0(1/2) and using a function suited to skewed normal distributions, regressions were developed
170 he flank/core difference is not explained by skewed nucleotide content, replication timing, nucleosom
172 IFN-gamma expression, help for CD8 CTLs, and skewing of dendritic cell (DC) subsets toward CD8a DCs,
173 showed that Ssa1 directly promotes early M2 skewing of lung mononuclear phagocytes during the innate
175 cle promotes recruitment, proliferation, and skewing of macrophages toward a cyto-destructive phenoty
186 es in temperature and CO2 in the recent past skew our observed responses to multiple drivers of chang
187 ncerned that this narrow approach might have skewed our understanding of CMV-specific immunity at old
188 covering from past disturbances, potentially skewing our interpretations of forest dynamics and our u
189 ipulations, Dnmt3a+/- mice developed myeloid skewing over time, and their hematopoietic stem/progenit
190 dition, we observed that FKBP4 favored a Th1-skewed phenotype with MalphaSyn but strongly supported a
192 ted by maternal factors (cART and HIV-1) and skews physiological immune responses toward inflammation
193 d gene expression signatures indicative of a skewed polarization in the phenotype of monocytes and ne
194 crophage profile is further supported by the skewed polarization of monocyte-derived macrophages from
196 evealed that Zbtb16(lu/lu)HSCs had a lineage-skewing potential from lymphopoiesis toward myelopoiesis
198 est modelers consider heavy-tailed, downward-skewed probability distributions, such as the skewed Stu
199 d CD16(+) monocytes generate Mvarphis with a skewed proinflammatory profile by virtue of their high a
200 em cell (HSC) exhaustion and myeloid-lineage skewing promote oncogenic transformation of hematopoieti
202 contrasts with the predominantly high female skew reported for offspring at most rookeries around the
204 ying molecular mechanism responsible for the skewed selection of autoreactive B1a cells remains uncle
205 ults showed some data processing methods can skew sequence-based biodiversity measurements from corre
206 that such a free RNA end coupled with a G/C-skewed sequence is necessary and sufficient to induce R-
207 nd that PCR stochasticity is the major force skewing sequence representation after amplification of a
208 for the deletion develop normally but with a skewed sex ratio, one male per litter, revealing its sex
209 ed asymmetries in life history or behaviour (skewed sex ratio, sex-biased dispersal, and sex-specific
210 Small populations may be more likely to have skewed sex ratios if sex differences in survival, recrui
211 success and the extent of male reproductive skew should be lower in bonobos than in chimpanzees [1].
213 ied, we find that GRMs typically have highly skewed singular values, and we prove that the many small
216 kewed probability distributions, such as the skewed Student [Formula: see text] used here, when makin
217 In such lattices, eigenmode pairs come in skew-symmetric pairs with oppositely signed eigenvalues.
219 ition in CD4(+)CD8(+) thymocytes resulted in skewed T cell repertoire, contributing to a reduction in
222 s from the ANRS CODEX cohort showed a highly skewed TCR repertoire that was characterized by a predom
223 tients with impaired BEC properties showed a skewed Th2-type secretion profile (high IL-4/IFN-gamma r
224 his generates concern regarding the possible skew that can be introduced by the inherent bias in the
226 Therefore, lineage-specific effects of IL-10 skew the cytokine dependency of Th17 cell development re
228 d recombinant and hypoallergenic vaccines to skew the immune response from IgE to IgG4 and regulation
230 functional virus-specific CD8(+) TILs could skew the results of prognostic or diagnostic TIL assays.
231 thymic selection in young versus adult mice skew the TCR repertoire, and the relatively higher self-
233 ith previous findings on sway anisotropy, FG skewed the direction of the GVS-evoked GRF vector toward
234 nd that the lack of dual TCRalpha expression skewed the insulin-specific thymocyte population toward
235 ght loss and lowered respiration in mice and skewed the mice toward carbohydrate-dependent metabolism
236 1 and PD-L2 expression on MHCII(lo) DCs, and skewed the Treg-Th17 balance in favor of Foxp3(+) Tregs
237 ns such as ARVs can induce metabolic stress, skewing the cell's immune response and restricting (cell
238 sion and during chronic obesity, permanently skewing the immune system to a proinflammatory phenotype
239 (Mfge8), in directing cardiac remodeling by skewing the inflammatory response after myocardial infar
241 CD56(dim)CD57(+)NKG2C(+) NK cell population, skewing the NK cell repertoire in favor of cytotoxic res
243 nputs from both the Imd and Toll pathways by skewing the transcriptional output of the NF-kappaB dime
246 ite-level methane emission rates were highly skewed; the highest emitting 10% of sites (including two
251 hat the immune response is muted and not yet skewed to a Th2 type response that is associated with ch
252 t epidermal growth factor (EGF) signaling is skewed to favor migration over proliferation via noncano
255 changes in function and structure, including skewing to myeloid lineages, lower reconstitution potent
256 LOS biosynthetic genes indicated significant skewing to specific alleles, dependent on the disease ou
258 tients with active cGVHD, cTFH phenotype was skewed toward a highly activated profile with predominan
259 suggested that the early immune response is skewed toward a Th2 response that would hamper the devel
260 eceiving stressed immune cells had microglia skewed toward an anti-inflammatory, neuroprotective M2-l
261 cells resulted in a CD8(+) T cell population skewed toward an effector memory T phenotype that was as
262 (-/-) BM chimeras, monocytes and neutrophils skewed toward BCAP(-/-) origin, showing a competitive ad
263 al equilibrium of the A3B active site loops, skewed toward being closed, controls enzymatic activity
266 ostatic balance of the epithelial barrier is skewed toward loss of differentiation, reduced junctiona
268 ncy spectrum of high-scoring SVs is strongly skewed toward lower frequencies, suggesting that they ar
269 Macrophage populations were reduced and skewed toward M2 polarization in injured livers of Hrg(-
270 absence of PP5 the MSC lineage allocation is skewed toward osteoblasts and away from lipid accumulati
272 periphery, the few CD4 T cells present were skewed toward RORgammat(+) IL-17-producing Th17 cells, l
273 pecially in sheltered areas, whereas loss is skewed toward southerly aspects and lower latitudes.
275 iana), were unique in showing NLR expression skewed toward the shoot across multiple phylogenetically
276 Furthermore, cells within the anterior pole skewed toward the trunk along their long axis relative t
277 n response to renal IRI, RMP populations are skewed toward those derived from inflammatory monocyte p
278 mmatory transcriptional programming, and (3) skewing toward a T helper (Th)/T cytotoxic (Tc)17 transc
285 ive VDJ rearrangement, there was significant skewing toward the incorporation of proximal VH gene seg
286 ockout (DKO) iNKT cells displayed pronounced skewing toward the NKT17 lineage, with increased DNA met
287 he T cell-to-MDSC balance, associated with a skewing toward type 2 immunity, may predict bladder tumo
290 ing CD11c(+) cells; their differentiation is skewed towards an effector memory phenotype and grafts a
292 the overall ACCORD-BP participant sample was skewed towards participants with less predicted benefit
293 netics of skin pigmentation has been largely skewed towards populations of European ancestry, imparti
294 eptors, decreased functional capacity, and a skewed transcriptional profile, which are only partially
297 w a proallergic inflammatory environment can skew Treg cells toward a pathogenic phenotype that aggra
298 atures suppress endogenous immune responses, skewing tumor growth data and the severity of graft vers
299 he distribution of serum periostin was right skewed with a mean (SD) periostin of 51.2 (11.9) ng/mL,
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