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1 proteins on its surface that have structural similarities to a protein crucial for invasion of red bl
2 m Chryseobacterium meningosepticum, indicate similarities to a superfamily phosphate diesterase [Xant
4 l structure for HopBA1 and found that it has similarity to a class of proteins that includes esterase
5 ndem repeat domain that shares high sequence similarity to a non-syntenic zebrafish analog, cat7l Def
6 y N-terminal domain that has high structural similarity to a recently discovered motif present in sev
7 ith an extended series of PAMs with chemical similarity to A-867744, TBS-516, and TQS suggests that a
9 drug-target prediction based on topological similarity with a heterogeneous network, and may be read
12 graded, displaying some superficial chemical similarities to abiotic meteoritic organic matter) are r
15 rough a disulfide bond, revealing structural similarities with ADP regulation in the human ACOT12 thi
18 tudy, ORF52 shares functional and structural similarities with alphaherpesvirus VP22, underscoring th
21 , whereas the C-terminal domain has sequence similarity to an FMN-dependent family of nitroreductase
24 designing polymers which have no structural similarities to antifreeze proteins but reproduce the sa
27 genase of S. thermoautotrophicus have little similarity to anything found in draft genome sequences,
28 f TGSQA expression, a tulip gene with a high similarity to Arabidopsis APETALA1 Gene Ontology enrichm
31 ly secreted proteins shared highest sequence similarity with archaeal and fungal enzymes, which peak
32 base crAssphage genome showed no significant similarity to available protein sequences, precluding cl
34 roteins specific to Lh VLPs possess sequence similarities with bacterial secretion system proteins.
37 enetic cause, despite clinical and molecular similarity to bone morphogenetic protein receptor type 2
39 N1-Src is poorly understood and its high similarity to C-Src has made it difficult to delineate i
41 to identify proteins in kinetoplastids with similarity to canonical outer kinetochore proteins, sugg
44 ted phosphoproteins with greatest functional similarity to CDK2 substrates, particularly proteins inv
48 share morphological, biochemical, or genetic similarities with classic necrosis, necroptosis, parthan
50 class-I aminoacyl-tRNA synthetases with high similarities to consensus amino acid sequences of human
52 o exist filter sequences based on nucleotide similarity to contaminants and risk eliminating sequence
54 is of ergothioneine in EgtB shows structural similarities to cysteine dioxygenase which transfers two
57 reening based on protein interaction profile similarity to discover new targets for molecules, includ
60 domain in HgGLAND18 contains unique sequence similarity to domains of an immunosuppressive effector o
61 but lower levels in the mPFC; a pattern with similarities to dopamine dysbalance in schizophrenia.
63 from chemoinformatics (i.e., pharmacological similarity with drugs of known fetal effect) and empiric
64 ermore, the PHP-exonuclease shows a striking similarity to E. coli endonuclease IV, which provides cl
65 s and their siblings had more vocal sequence similarity with each other than with non-sibling infants
66 plant evolution and exhibits more functional similarity with eIF4G than with eIFiso4G1 during Omega-m
67 dynein arm assembly factors show structural similarities to either Tah1 or Pih1, the other two compo
71 Leptospira licerasiae-which shares sequence similarity to eukaryotic CNG and HCN channels-in the pre
75 ences for attractive faces result from their similarity to facial prototypes, the categorical central
78 Although FLNb shows high amino acid sequence similarity with FLNa, we reveal that only FLNa, but not
79 ark, sleep/wake and meal schedule, which has similarities to flying west or sleeping in the daytime a
80 matics predictions that suggested structural similarity to folliculin, the Birt-Hogg-Dube syndrome tu
81 ed by the upper and lower jaws, bearing some similarity to fossil traces interpreted as footprints.
82 ngle nanoparticle level, which reveal marked similarities to foundational principles of polymerizatio
83 ated mechanism of dissociation, which shares similarities with fragment types produced in electron de
84 hway in Catharanthus roseus showing distinct similarity to gamma-tocopherol C-methyltransferases was
85 es in the gymnosperm Pinus taeda shared some similarities with gbM genes in Amborella trichopoda.
87 for these traits in pigeonpea have sequence similarity to genes functionally characterized in other
89 which identified a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homolo
90 -HLA-F bound to the inhibitory LIR1 revealed similarities to high-affinity recognition of the viral M
91 xhibit striking qualitative and quantitative similarities with histology (e.g., using Sholl analysis)
92 lade HD-Zip I TFs share significant sequence similarities with homologous genes from other plants, th
94 resource due to their incidence and striking similarities to human cancers, sharing similar clinical
98 pecialization of platelets shares remarkable similarities with human-engineered unmanned aerial vehic
99 40-amino acid peptide showing high sequence similarity to human (93%), mouse (93%), and Xenopus (88%
100 lls with NOTCH overexpression, and molecular similarity to human tumors was observed, demonstrating t
104 rson's correlation analysis, and peak height similarity to identify ion adducts, duplicate peak repor
106 to widespread human exposure, and structural similarities with known endocrine disruptors, concerns h
107 ule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure-a
108 cterial fucose-specific lectins that have no similarity to known bacterial fucose-binding proteins, b
112 x-bladed beta-propeller fold bearing limited similarity to known paramyxoviral attachment glycoprotei
113 virus (ASFV) genome do not have significant similarity to known proteins and have not been studied e
114 d similarity and 3D pharmacophoric and shape similarity to known selective tau aggregate binders iden
119 in the Vi antigen biosynthesis locus shares similarity with LpxL, an acyltransferase from lipid A bi
120 ls and showed transcriptional and phenotypic similarities to lymphoid Tfh cells, and hence representi
122 The structure of this domain revealed high similarity to mammalian deubiquitinases with a unique al
124 Rapid embryogenesis, together with genetic similarities with mammals, and the desire to reduce mamm
125 tistical method to quantify a CRM's sequence similarity to many different training sets of CRMs, and
126 responses in mammalian cells and surprising similarities with mechanisms in yeast that deal with DSB
130 IDH1 mice showed many molecular and clinical similarities to muIDH1 human gliomas, including a 100-fo
131 demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from div
132 lass 27 myosin, TgMyoF, which has structural similarity to myosin V, the prototypical cargo transport
134 Individuals with 22q11DS share overarching similarities with ND individuals in psychosis symptoms a
135 tion patterns, time of emergence and genetic similarity to Near Eastern populations are highly sugges
137 not NKT2 and NKT17 cells, had transcriptome similarity to NK cells and were also similar to other IF
139 disorder with clinical and histopathological similarity to OB, represents the leading cause of long-t
140 interference that bears striking conceptual similarity to oligoadenylate signalling in mammalian inn
141 arranged on a hexagonal grid based on their similarity to one another in the original genomic space
143 axonomic units showed the strongest sequence similarity to Ophiocordyceps, Verticillium, Pseudallesch
144 teraction and its structural and fingerprint similarities to other compounds belonging to the differe
145 odel for cell walls in general, as it shares similarities with other cell wall proteomes while also c
146 sease burden profiles differed; India showed similarities with other developing countries (around 50%
148 aucoma is a chronic disease that shares many similarities with other neurodegenerative disorders of t
150 udomonas FliD exhibits unexpected structural similarity to other flagellar proteins at the domain lev
154 ture and immature ZIKV have demonstrated its similarity with other known flaviviruses such as dengue
157 ions) are discussed on the basis of observed similarities with our studied terrestrial chemistry.
158 share a surprising degree of transcriptional similarity with pancreatic beta cells, and expression of
160 a sulfated peptide named RaxX, which shares similarity to peptides in the PSY (plant peptide contain
161 value-based decisions, explain the apparent similarity to perceptual decisions, and predict conditio
162 errhenate, an anion of great physicochemical similarity to pertechnetate, both having uses in nuclear
163 ositional role for Hofstenia muscle and this similarity with planarians suggests mesodermal muscle or
164 n the GREENC and CANTATA databases indicated similarity with plant long non-coding RNAs (lncRNAs) inv
165 1OHI3M) and that IGMT5, a gene with moderate similarity to previously characterized IGMTs, encodes th
166 oducts being published today bear structural similarity to previously published compounds, and that t
167 vated abundance of a cyanomyophage with high similarity to previously sequenced isolates known to inf
168 epidemic (Makona) shares significant genetic similarity with previously identified variants (Kikwit a
169 ic characteristics of these cells, and their similarities to primary islet alpha and beta cells, are
171 Thy1(+)LSK cells share significant molecular similarities with primary CD34(+) cells from PMF patient
172 and bulk expression profiling revealed their similarity to primary ALL cells isolated from pediatric
173 ides cluster products, reporting of sequence similarity to proteins encoded in experimentally charact
176 subphenotypes or if Cpc-PH shares molecular similarities to pulmonary arterial hypertension (PAH).
178 ggering a signaling cascade that shares some similarities to responses to well-known elicitors such a
179 The transcription profiles reveal extensive similarity to retrograde signaling initiated by partial
180 larity to S. halichoeri CCUG 48324(T), 97.9% similarity to S. canis ATCC 43496(T), and 97.8% similari
181 rRNA gene sequencing analysis revealed 98.6% similarity to S. halichoeri CCUG 48324(T), 97.9% similar
188 lly occurring neurodegenerative disease with similarities to some forms of amyotrophic lateral sclero
189 te its remarkable architectural and sequence similarities to spider silk fibroins, indicating that AS
190 ies a novel immunodeficiency with phenotypic similarities to STAT3 hyper-IgE syndrome caused by loss
191 distal to the imatinib binding pocket, show similarities to structural transitions involved in kinas
192 first recognized behavioral addiction, with similarities to substance use disorders but without the
195 icate that, although SynDIG4 shares sequence similarity with SynDIG1, it might act through a unique m
196 otic GVHD has clinical and histopathological similarities with systemic sclerosis, an autoimmune dise
200 The modulation by serotonin has qualitative similarities with that for a decrease in stimulus contra
202 mponent (270-450 ms) was found, which showed similarities with that of prior studies on auditory and
203 obic oxidation of aldehydes shares important similarities with that one of the recently revisited ben
204 ident in the zebrafish gut mucosa, in marked similarity to that found in the intestine of mammals.
207 n alpha1A/betaIII microtubules shows overall similarity to that of heterogeneous brain microtubules,
209 he stepwise mechanism of the reduction shows similarities to the Birch reduction known from organic c
211 Arabidopsis (Arabidopsis thaliana) that has similarities to the cysteine-rich zinc-binding domain of
212 atio of 31 +/- 9 and demonstrated structural similarities to the gray matter distribution on conventi
215 otype of indeterminate PALF shares important similarities to the hyperinflammatory state characterist
217 P surface and spike-tip protein, p40, reveal similarities to the needle-tip invasin proteins SipD and
222 Together, WarA and WarB have structural similarities with the bifunctional Escherichia coli lipo
223 m tens of thousands of 12-ns stimuli and the similarities with the conventional stimulation prove VGS
224 tive analyses reveal sequence and structural similarities with the distant Acidobacteria LexA protein
226 ceptor that shares structural and functional similarities with the family of atypical chemokine recep
227 fied pathway suggests intriguing mechanistic similarities with the initial mitochondrial-mediated ste
228 ce: Inflammatory pathways of psoriasis share similarities with the mechanisms identified in atheroscl
230 newly identified shear-NO oscillator shares similarities with the well-known Van der Pol oscillator,
231 signature of the pseudogap that bears close similarity to the analogous studies of the pseudogap in
233 pts a 6-bladed beta-propeller structure with similarity to the classic sialidase fold, but it has no
234 ea directly track the gradient of perceptual similarity to the conditioned stimulus in healthy indivi
235 rsion model coupled with PCA-LDA showed high similarity to the designed microbiota structure, with no
236 ably, the pyridine synthases show structural similarity to the elimination domain of lanthipeptide de
238 ized peptidomimetics that bear no structural similarity to the established TLR4 ligand, lipopolysacch
240 intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular compositio
242 high sequence (48% identity) and structural similarity to the GRE-type glycerol dehydratase from Clo
243 portion of the active site shows structural similarity to the GTP-binding site of MoaA, suggesting t
244 of a four-alpha-helix bundle with structural similarity to the high mobility group box, a domain that
247 psis, no predicted proteins with significant similarity to the known ADPR cyclases have been reported
249 ore accurate incidence maps showing a closer similarity to the observed incidence distribution, and p
250 l proteins that have no and distant sequence similarity to the ones used for training, receptively.
251 ower replicative ability as well as a higher similarity to the population consensus (in this case HIV
252 rtical topography, individual stability, and similarity to the primate AR organization link ARC1 to t
255 ost all eubacteria and plants, with sequence similarity to the RecA strand exchange protein and a rol
257 hybrid-like structure containing regions of similarity to the structures of BoNT/A1 and BoNT/F5.
259 spectra of driver genes in cancer show high similarity to the tissue-specific ASC mutation spectra,
260 gh expression of epithelial cell markers and similarity to the transcriptome for intrapulmonary airwa
261 n hair cells by negative pressure, with some similarity to the transduction current, persists in TMC
262 ion corresponded to increased neural pattern similarity with the average pattern associated with that
264 y, an internal region of Mcc shares sequence similarity with the central domain of the prion protein,
265 otein of HAdV-C5 contains a region of strong similarity with the clip region of the known portal prot
268 Phylogenetic analysis demonstrated high similarity with the ELO of Tribolium castaneum and Droso
269 era of a snail AChBP, which has 71% sequence similarity with the extracellular ligand-binding domain
270 gent H5N6 viruses, which share high sequence similarity with the human isolate A/Guangzhou/39715/2014
271 been proposed that reconcile the Earth-Moon similarity with the inferred heterogeneous nature of Ear
272 lity, resident species with a high catabolic similarity with the invader efficiently reduced the inva
273 is a dynamical phase transition that shares similarity with the plastic depinning transition occurri
275 ts is assessed by comparing the kernel-based similarity with the similarity in the trait using a scor
277 ngal dockerin and scaffoldin domains have no similarity to their bacterial counterparts, yet several
279 alogs, but the toxin does not share sequence similarity with these nucleases and lacks the characteri
281 me of ccr1 ProSNBE:CCR1 still exhibited many similarities to those of ccr1 mutants, regardless of the
283 files in diabetic versus healthy dogs shared similarities with those reported in human T1D (e.g., alt
284 hat the protein shares intriguing structural similarity to ToxA from the wheat pathogen Pyrenophora t
285 lative to untreated rat liver shows striking similarity with toxicant-exposed cells in vivo, indicati
289 ions during singing correlated with acoustic similarity to tutor syllables, suggesting a process of o
290 ons of Izumo1 display significant structural similarities to two proteins expressed by the invasive s
293 d contigs with predicted amino acid sequence similarities to viruses in the nonredundant protein data
299 the Y in all species examined, yet sequence similarity to YG2 is not detectable in the genome of a m
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