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1                                              We identified 1 392 289, 530 771, and 1 125 231 hospital
2                                              We identified 100% of the germline NF1 mutations and fou
3                                              We identified 1044 patients, among whom 460 (44.1%) rece
4                                Additionally, we identified 12 potential new species among the 76 isol
5                                              We identified 13 randomised controlled trials done in 73
6                                              We identified 13 TAS2R16 residues that contribute to lig
7                    Through RNA-Seq analyses, we identified 137 genes that are missing in chicken, inc
8                        In the PA mouse liver we identified 14 significantly dysregulated miRNAs.
9                                              We identified 14 studies on the topic (distinct by regio
10                                Additionally, we identify 15 tales that are more likely to be predomin
11          Using mass spectrometry approaches, we identified 16 VTPs of the CyHV-3 FL strain.
12 Recipients data from June 2013 to June 2015, we identified 1768 DD livers exported to regional candid
13                                              We identified 19 rotor domains in 10 patients (1.8+/-1.1
14                                              We identify 19 new TGCT risk loci, roughly doubling the
15                                     However, we identified 2 or more missense variants predicted to b
16         Using hierarchical cluster analysis, we identify 21 epidemic clusters, of which 12 were cross
17               In the combined meta-analysis, we identified 22 loci associated at genome-wide signific
18                  Using a circRNA microarray, we identified 226 differentially expressed circRNAs, of
19                                              We identified 235 children with CMA; 66 of these childre
20                                              We identified 238 (XP-EHH) and 213 (XP-CLR) positively s
21                                              We identified 25 new SNP-CAD associations (P < 5 x 10(-8
22                                              We identified 25 new susceptibility loci, 3 of which con
23                                              We identified 26 ancient and more recent polyploidy even
24                                              We identified 265 specimens to species or genus using DN
25                                              We identified 3 mechanisms underlying local progression
26                                              We identified 3 such proteins and show that they interac
27                                              We identified 31 cases of PTLD during the study period.
28                                              We identified 348,462 patients with one of the eligible
29                                              We identified 35 articles, including 7112 respondents.
30                                              We identified 4 host gene expression profiles, among whi
31                                              We identified 402 patients from 233 articles published i
32                                              We identified 411 (198 annotated) and 27 (15 annotated)
33                            During follow-up, we identified 5,462 incident cases of rosacea.
34                                              We identified 50 genes essential for the survival of A.
35                                      Results We identified 51 trials assessing 14 drugs across 15 con
36  In ocular tissues of healthy house finches, we identified 526 total bacterial operational taxonomic
37                               For 2010-2016, we identified 53 national care continua with viral suppr
38                                              We identified 57 articles from 27 countries.
39                                              We identified 57 longitudinal studies exploring the asso
40 mbinant inbred Arabidopsis thaliana genomes, we identified 6502 segregating structural variants.
41                                              We identified 764 genes with at least a 2-fold differenc
42                                              We identified 79 associations influencing 13 primary and
43                                              We identified 89,790 incident PD cases and 118,095 compa
44                                  METHODS AND We identified 905 patients that were married at the time
45                                              We identified 968 patients with brain metastases at the
46                 Using these switching rules, we identified a 3-month and a 6-month cohort of "treatme
47                                              We identified a causal mutation in 1 of 14 genes in 50%
48                                              We identified a centrin-binding site within H. sapiens P
49 urther Palestinian-Jordanian SPG23 pedigree, we identified a complex homozygous 4-kb deletion/20-bp i
50                                  In summary, we identified a conopeptide that targets the nociceptor-
51 f genetics, proteomics and RNA biochemistry, we identified a core set of mRNA m(6) A writer proteins
52 ognize known major antigenic sites in MeV-H, we identified a D4 genotype variant that escapes neutral
53                                              We identified a feedback loop within the NANCI (Nkx2.1-a
54                       Through this analysis, we identified a ferrireductase: six-transmembrane epithe
55                   By whole-exome sequencing, we identified a heterozygous truncating mutation (c.279d
56 e antibodies spanning the dysferlin protein, we identified a highly reproducible jigsaw map of dysfer
57                                       First, we identified a light-sensing B12-binding transcriptiona
58                                              We identified a new set of genes encoding subunits of th
59 eover, by using mutated promoter constructs, we identified a NF-kappaB site as critical in this activ
60                                              We identified a novel 1 bp deletion in YAP1 in a boy wit
61 zation, expression and phylogenetic analyses we identified a novel class of Arabidopsis thaliana poll
62                               In this study, we identified a novel direct interaction between APP and
63  TLR3 and TLR4 ligands as previous reported, we identified a novel group of TRIM genes (TRIM14, 15, 3
64             By using whole-exome sequencing, we identified a novel missense mutation in the binding d
65                                  In summary, we identified a novel pathway for regulation of beta-cat
66            As a validation of this approach, we identified a novel Sertoli cell enhancer upstream of
67                                              We identified a novel splice mutation in IKBKG (c.518+2T
68                                 Furthermore, we identified a novel therapeutic approach in crescentic
69                                 Furthermore, we identified a nuclear export signal (NES) at the N ter
70 ecifically, based on the relative abundance, we identified a panel of 11 proteins to distinguish CRC
71                                   From this, we identified a panel of 6 genes, ALDH1A1, HSP90AB1, KIT
72                                    Moreover, we identified a pathogenic CD8(+) T cell MPO epitope (MP
73                                  Previously, we identified a potent neutralizing antitoxin against Bo
74                                         Here we identified a range of small organic molecules, drugs,
75 ry of 46 656 heparan sulfate hexasaccharides we identified a rare sequence consisting of consecutive
76                                       First, we identified a self-feeding mechanism by which CCL1 pro
77                                        Here, we identified a series of peptides that interact specifi
78                                    Moreover, we identified a significant global decrease in effective
79                                              We identified a small conopeptide of only four amino aci
80                                              We identified a small molecule, AC1903, that specificall
81                                     Overall, we identified a small number of immunodominant regions,
82                               In this study, we identified a special case of cross-order recombinatio
83                                     Instead, we identified a specific set of markers associated with
84                                         Here we identified a two-amino-acid substitution in RORgammat
85                                         Here we identified a Y/F-x-x-Y/L/F-x-Y/F motif, evolutionaril
86                                         Here we identify a brain-region-specific neural progenitor-ba
87                                         Here we identify a complex, nutrient-rich organic coating on
88                                              We identify a conserved region in the Ulp2 C terminus th
89                                         Here we identify a critical role for ETAA1 in this process by
90                                              We identify a distinct C-terminal autoinhibitory four-re
91                                              We identify a functional EptA ortholog responsible for t
92                                         Here we identify a lysosomal switch that enhances germline pr
93                                        Here, we identify a new pathway that acts through NIMA-related
94 pitation with sequencing and RNA sequencing, we identify a novel B-lymphoid program for transcription
95                                        Here, we identify a novel boundary subdividing the mdFP into t
96                                              We identify a novel Myst2-associated protein, the tumour
97                                              We identify a novel susceptibility signal in the immunog
98    Here, using genome-resolved metagenomics, we identify a number of CRISPR-Cas systems, including th
99                                        Here, we identify a presynaptic effector molecule of the Wingl
100                                 By contrast, we identify a pull-push inhibitory circuit in frontal co
101                                Cumulatively, we identify a signaling cascade that provokes structural
102                                Unexpectedly, we identify a subset of genes that adopted increased or
103 cal translation in the cortex of mice, where we identify a subset of mRNAs that are translated in den
104 using gene expression and mutation profiles, we identify a unique subpopulation based on addiction to
105                                              We identified alterations in signaling pathways and prot
106 model and human biopsies of prostate cancer, we identify alterations in tumours affecting the product
107 d healthy controls (both males and females), we identified an abnormally widespread hub formation in
108 nalysis including >300,000 European samples, we identified an additional nine novel loci.
109                                              We identified an atherosclerosis-associated single-nucle
110           To prevent the IPDs caused by ST2, we identified an effective ST2 neoglycoconjugate vaccine
111                                              We identified an FXR-responsive element on the Tgr5 gene
112                   By cDNA library screening, we identified an immune cell-specific, co-stimulatory re
113                             Mechanistically, we identified an interaction between moesin and TGF-beta
114                                              We identified an N-TIMP2 mutant, with five mutations in
115                                        Here, we identified an orphan protein (Plu2236) from Photorhab
116                                         Here we identify an additional motif that drives VE-cadherin
117                                     Finally, we identify an association between high MCAM levels in p
118                               In this study, we identified and characterized IgE-binding proteins fro
119                                              We identified and cloned four AQPs from C. lectularius,
120                                              We identified and confirmed the highly potent antiandrog
121                                        Here, we identified and deleted a polyketide synthase (PKS) ge
122 ogy called CANE developed in our laboratory, we identified and selectively labeled noxious-stimulus-a
123                                        Last, we identified and studied three novel patient XIAP mutat
124                                     Finally, we identify and analyze the conserved syntenic blocks am
125                                         Here we identify and characterise an epigenetic predictor of
126                                     Finally, we identify and compare appropriate tunable-by-doping ma
127                                        Here, we identify and determine that the previously uncharacte
128 n to protect against coronary heart disease; we identified APOC3 homozygous pLoF carriers in our coho
129                                              We identified Arabidopsis pex6 and pex26 mutants by scre
130      These data suggest that the dynamic CGs we identify are not specific to the Col-Cvi recombinant
131 effector spleen tyrosine kinase (SYK), which we identified as an HSP90 client protein.
132                                              We identified associations between the FEV1/FVC ratio an
133      Using genome-wide association analysis, we identify associations between several candidate genes
134                                         Here we identify AUTEN-99 (autophagy enhancer-99), which acti
135                                              We identified autophagy as a pivotal cell response deter
136                                              We identified bacteria from the regurgitant of field-col
137                                              We identified basement membrane (BM) and collagen IV in
138                                              We identified both inflammatory monocytes and tissue-res
139                                              We identified BRPF1 deletions or point mutations in six
140 with strain maps of the developing skeleton, we identify canonical Wnt signalling as a candidate for
141                                        Thus, we identify CATH functional families that are currently
142                                 Importantly, we identified chaperonin containing TCP1 subunit 6A (CCT
143 noparticles to eight tissues simultaneously, we identified chemical properties promoting delivery to
144                                              We identify clusters corresponding to known tetraloop fo
145                                              We identified compounds that match the pharmacophore of
146 as chromatography mass spectrometry (GC-MS), we identified compounds typically associated with plant
147                                 Furthermore, we identified conserved miRNA-targets regulations in the
148                                        Here, we identified core FtsH target proteins in S. aureus.
149                                        Here, we identify dense innervation in the microenvironment of
150                                              We identify discriminatory features, which may be useful
151                        Within this interval, we identified disruptive mutations in two genes.
152                                 Furthermore, we identified distinct epigenetic methylation patterns t
153 rewards and punishments of different nature, we identify distributed neural representation of value,
154        Using Caenorhabditis elegans mutants, we identify DNA repair factors that protect against the
155 o-hybrid protein-protein interaction method, we identified eight novel interaction partners of EGFR,
156                               In this study, we identified elevated levels of matrix metalloproteinas
157                   To elucidate Grh functions we identified embryonic Grh targets by ChIP-seq and gene
158 ding motifs in a machine learning framework, we identify EOR-1 as a unique transcription factor that
159                                              We identify features associated with chiral edge plasmon
160                                              We identified few horizontally transferred genes, but so
161                                              We identify filamentation self-compression scaling strat
162            On the basis of these dimensions, we identified five distinct subtypes of perinatal depres
163                                              We identified five loci associated with emphysema distri
164                                              We identify five factors, including the HIV co-receptors
165        By pharmacologic and genetic studies, we identify FKBP12 as a novel hepcidin regulator.
166                                              We identified Flunarizine - a well-known anti-migraine c
167 ng locally, nationally, and internationally, we identified four communities that each shared a type o
168                                   SYNTHESIS: We identified four issues highlighting the key areas of
169                                        Here, we identified four unique mbf1 genes in the lichenized f
170                                              We identified gene expression signatures and clinical da
171                                         Here we identify gene expression outliers, or individuals sho
172 it neuroblastoma metastasis in vivo Overall, we identify gene expression signatures and candidate the
173 nterneurons to those of more mature neurons, we identified genes important for human interneuron diff
174 e change within a species geographic range), we identified global hotspots of species at risk from cl
175                                              We identified heavy smokers that were resistant (n = 65)
176                                              We identified heterozygous nonsense mutations in four an
177                                              We identified Hhex as a direct target of RUNX1 and FLT3-
178                                              We identified IL-18 as a cytokine that cooperates with a
179 investigate the role of two gtr operons that we identified in the S Typhi genome.
180                                  Previously, we identified increased translocation of the fatty acid
181                                              We identified individual and shared defects in PLP1 mRNA
182                                        Here, we identified inositol-requiring enzyme 1alpha (IRE1alph
183                                     Instead, we identify Insensible (Insb), another neural nuclear No
184  function of these and other p190A segments, we identified interacting proteins by tandem mass spectr
185                                         Here we identified IRAP(+) endosomes as major cellular compar
186                                              We identified less common conservation strategies that h
187 DLK inhibition is only partially protective, we identify leucine zipper kinase (LZK) as cooperating w
188                               In this study, we identified LGR4 as a master controller of Wnt/beta-ca
189 ise many of the elements heavier than iron.) We identify line features in the spectra that are consis
190 on and repair by next-generation sequencing, we identified locations of elongation complexes and tran
191                                              We identified low but escalating risk of severe M. chima
192                                 Furthermore, we identify Maf as a downstream target of the CIC-ETV5 a
193 nsequences of aneuploidy on cell physiology, we identified mechanisms that eliminate aneuploid cells.
194                                     Overall, we identify miR-500a-5p as an oxidative stress response
195                                              We identify molecular pathways and segmentation phenotyp
196                                     Overall, we identified more infections (n = 146) in the denosumab
197                                    In mouse, we identified more than 800 LTRs from ORR1, MT, MT2, and
198                                In this study we identify MRAP2 as a partner of ghrelin-GHSR1a signali
199                                    Moreover, we identify multiple neurite-targeted non-coding RNAs an
200                               In conclusion, we identified mutations in MAPKBP1 as a genetic cause of
201                               In this study, we identify new functional roles of RASSF4.
202                                              We identified nineteen differentially methylated gene re
203  with comprehensive untargeted metabolomics, we identified novel alterations in purine metabolism, gl
204                                              We identified novel and previously reported BMI-related
205  context of a quantum description of solids, we identify novel capabilities for polarization- and pha
206  the fields of genomics and development, and we identify organizational similarities between networks
207                Using bioinformatic analysis, we identified over a thousand of human L1 loci containin
208                                Unexpectedly, we identified PABPN1-dependent ALYREF binding near the 3
209                                              We identified pathogenic mutations in 36 of 204 (17.6%)
210                                              We identified PKC delta and varepsilon as required and s
211              Through forward genetic screens we identified PKL, a gene required for developmental reg
212                               In this study, we identified pleckstrin homology domain and leucine-ric
213                                              We identified predictors of final macular status, and de
214           Utilizing high-throughput screens, we identify prion-curing mutants and engineer "anti-prio
215                                              We identify profound rearrangement in cellular proteosta
216                                     Further, we identify promoters able to drive strong expression in
217                    Using a connectivity map, we identified prostaglandin E1 (PGE1) as a small molecul
218                                 KEY MESSAGE: We identify proteins that associate with the THO core co
219 nse to PD-1 blockade in a mesenchymal tumor, we identified PTEN mutations and reduced expression of g
220         Using the North American power grid, we identified, quantified, and analyzed the set of netwo
221                                 In addition, we identified Rab27 as an important regulator of the int
222  downstream targets and effectors of miR-32, we identified RAC2 as a potential, and clinically releva
223                                              We identify RIPK1 and caspase-8 as linearly ubiquitinate
224                                        Here, we identified seven unrelated individuals affected with
225                                  Using fMRI, we identified several areas of parietal, occipitotempora
226                               In particular, we identified several arginine residues that interact wi
227                                              We identified several different aggregating sites from l
228                                              We identified several genes involved in disease resistan
229 tional modeling and the BiLC reporter assay, we identified several novel small-molecule compounds tha
230                                         Here we identify several acetylation sites of the influenza A
231                                        Here, we identify several novel CO2-dependent changes in the N
232                                              We identify SIAH2, a RING finger E3 ubiquitin ligase ass
233          Using multiple logistic regression, we identified significant associations between whether a
234                                              We identified significant changepoints in all sites and
235                                              We identified significant group differences in striatal
236                                              We identified single-point mutations in the Fc domain (e
237                                Among others, we identified sites catalyzed at faster rates with poten
238 -susceptible gene locus, PSS1 In this study, we identified six candidate PSS1 genes by comparing sing
239                                              We identify six mutational signatures (E1-E6), and Signa
240                                         Here we identify soluble ephrin-B2 (sEphrin-B2) as a new prof
241                                         Here we identify soluble epoxide hydrolase (sEH) as a key enz
242                                 Furthermore, we identified splice variants encoding distinct nuclear
243 chromatography coupled to mass spectrometry, we identified statistically significant differences in t
244                                              We identified substantial differences among CA, AA, and
245                                In this work, we identified suppressor mutations in the M1 protein whi
246                                              We identified surface markers associated with each chrom
247                             Mechanistically, we identified TBK1 as a key regulator of mTORC1 activity
248                                              We identified that HBx K91 and K95 as the key HBx NEDDyl
249                                              We identified that miR-195 was packaged in the extracell
250                                Additionally, we identified that NF-kappaB and MAPK signaling pathways
251                                         Here we identified that the lysine-specific demethylase KDM3A
252                                        Here, we identify that infection of host cells with reovirus c
253 biophysical and crystallographic approaches, we identify that PrimPol possesses two RPA-binding motif
254                                         Here we identify that tumour necrosis factor-alpha (TNFalpha)
255                                              We identified the band gap Eg and phonon cut-off frequen
256                                              We identified the BSs and assessed the effects on transc
257                                        Here, we identified the conserved NK-2 homeobox gene ceh-24 to
258 t interact with ASK1 in the context of NASH, we identified the deubiquitinase tumor necrosis factor a
259                From these empirical studies, we identified the features of interaction patterns assoc
260                                              We identified the following variables as unfavourable pr
261 apillae deposition on the cell wall surface, we identified the GLASSY HAIR 1 (GLH1) gene, which is ne
262 ntegrated analysis of the HIF-alpha network, we identified the major protein kinase C substrate MARCK
263                                              We identified the minimal threshold that the participant
264 urthermore, using a yeast two-hybrid screen, we identified the motor protein Kif15 as a potential int
265                                       First, we identified the optimal NP formulation through compreh
266 olate host receptors for bacterial cdNs, and we identified the oxidoreductase RECON.
267                               In this study, we identified the proliferating cell nuclear antigen (PC
268                                        Here, we identified the spatial, temporal, and amplitude chara
269                                        Thus, we identified the sublateral SIA neurons to control the
270                                         (ii) We identified the variables that impact Env's glycosylat
271                                     Finally, we identify the challenges that the field currently face
272                                        Here, we identify the conserved RNA helicase Aquarius/EMB-4 as
273                                    Moreover, we identify the ditiocarb-copper complex as the metaboli
274  novel ex vivo spinal cord preparation, here we identify the functional organization of muscle and cu
275 and a custom CRISPR/Cas9 screening platform, we identify the H3K9 methyltransferase SETDB1 as a novel
276            Using ex vivo and in vivo models, we identify the Hedgehog (HH) paracrine system as a cand
277                                         Here we identify the Iw1 gene from durum wheat and demonstrat
278                               In this study, we identify the metabolic sensor AMP-activated protein k
279                                              We identify the MuvB protein Lin37 as an essential facto
280 PA has a six-bladed beta-propeller fold, and we identify the region that interacts with PfRh5.
281                  Using an unbiased approach, we identified thousands of genes whose expression was en
282                                              We identified three key components of the Notch pathway,
283                                        Here, we identify TIAM1 as a critical antagonist of CRC progre
284               Using genome-wide association, we identified Tnni3k as one gene that influences variati
285  Besides a predominant Neolithic background, we identify traces of Post-Neolithic Levantine- and Cauc
286 rveillance in reprogramming gene expression, we identified transcriptome-wide binding sites for RNA p
287                                         Here we identify twenty-six DHC-derived features that provide
288                                         Here we identified two classes of unmyelinated sensory neuron
289                                        Here, we identified two conserved residues (R151, I155) in the
290                 Through mutational analysis, we identified two glutamine residues and a beta-hairpin
291               In a forward genetic approach, we identified two Lotus japonicus mutants defective in A
292                                              We identify two bulge-depleted regions on the miRNA stem
293                                              We identify two distinct modes of kinetic stabilization
294                                              We identify two modes of transformation between stereoch
295                                 In addition, we identified up to 161 genes that encode transcriptiona
296                                              We identified viral antigen in multiple organ tissues wh
297                              Among the genes we identified were some with obvious colonization-relate
298                                              We identified women diagnosed with unilateral stage I to
299                                              We identified ZEB1 binding sites within the LIF (stemnes
300                                              We identify zyxin as a regulator of stress fibre mechani

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