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1  share the same architecture on the basis of sequence homology.
2  SKI/SNO/DAC domain, despite lacking obvious sequence homology.
3 high structural similarity despite their low sequence homology.
4 tilis, SpaI, despite the lack of significant sequence homology.
5  the Holliday junctions to the boundaries of sequence homology.
6 oup was highly variable and not predicted by sequence homology.
7 or genes and estimate their likelihoods from sequence homology.
8 nnel analog) without sharing any significant sequence homology.
9 nuclease YbeY, even though they do not share sequence homology.
10 to four clusters based on gene structure and sequence homology.
11 tail genes even in the absence of detectable sequence homology.
12 r features, MFS transporters share only weak sequence homology.
13  humans on the basis of their high degree of sequence homology.
14 nt beta-galactosidase showed high amino acid sequence homology.
15 ors, respectively, despite their significant sequence homology.
16 ATX1-Like Copper Chaperone (CCH), share high sequence homology.
17  some annotations are solely on the basis of sequence homology.
18 an array of cell-surface receptors that lack sequence homology.
19 a melanogaster, and Mus musculus revealed no sequence homology.
20 ntiporter NhaA, despite having no detectable sequence homology.
21 AD51 paralogue genes have been identified by sequence homology.
22 ring transcription initiation despite little sequence homology.
23 fferent very long chain lengths despite high sequence homology.
24  fact that the human and rat forms share 99% sequence homology.
25 hibitor sensitivity profiles despite lacking sequence homology.
26 istance protein families, despite a very low sequence homology.
27 itiator, TbORC1/CDC6, has been identified by sequence homology.
28 d nature of their functional commonality and sequence homology.
29  factor-beta superfamily sharing 89% protein sequence homology.
30 gly than GC-rich duplexes, regardless of the sequence homology.
31  discrimination of miRNA sequences with high sequence homology.
32  discrimination of miRNA sequences with high sequence homology.
33 ow the efficiency of repair is influenced by sequence homology.
34 classified by their receptor specificity and sequence homology.
35 183, -96 and -182, is also a miR family with sequence homology.
36  lipid kinases, despite the absence of clear sequence homology.
37 ures are unknown, but they share significant sequence homologies.
38  termed SMASH, for short multiply aggregated sequence homologies.
39  were annotated as motility-related based on sequence homologies.
40                                  Despite low sequence homology (48.2%-77.3% similarity), all ortholog
41                                          Low sequence homology (88% average pairwise identity) and fr
42 re a family of proteins with no structure or sequence homology, able to elicit a sweet sensation in h
43 A nucleoprotein filaments efficiently locate sequence homology across genomic DNA remains unclear.
44               LlaBIII shares >95% amino acid sequence homology across its first three protein domains
45                                      Despite sequence homology across the PAR isoforms, discovery of
46                                     Based on sequence homology, AdPLA is part of a small family of ac
47                       BESs were searched for sequence homology against known databases.
48 m the identification of short regions of DNA sequence homology, also known as microhomology, at chrom
49                                 Despite high sequence homology among different deer species, a fallow
50                         Considering the high sequence homology among DNA of H. pylori isolated from s
51 roperties of short length, low abundance and sequence homology among family members, it is difficult
52 omoter using the following methodologies: 1) sequence homology among several mammalian species, 2) DN
53          Because of the substantial level of sequence homology among sodium channels, our data also i
54                                     However, sequence homology among them is limited.
55                                              Sequence homology among viruses and ability of T cells t
56 RFs) and does not require linkers, adaptors, sequence homology, amplification or mutation (domesticat
57 thermal denaturation, biochemical assays and sequence homology analysis all strongly support defects
58                                              Sequence homology analysis revealed a potential canonica
59 ue of the mouse Rosa26 locus through genomic sequence homology analysis.
60  conserved enhancers in the absence of overt sequence homologies and over extensive evolutionary dist
61  predict organismal metabolic networks using sequence homology and a global metabolic network constru
62       Sister chromatids provide near-perfect sequence homology and are therefore the preferred templa
63 2 cytotoxic factors exhibited 50% amino acid sequence homology and bound to the same receptor, they c
64                          TssL and TssM share sequence homology and characteristics with two component
65 of M. silvestris and eukaryotic Tdms have no sequence homology and contrasting characteristics.
66                                  EF-P shares sequence homology and crystal structure with eIF5A, but
67                                              Sequence homology and domain modeling suggest that Teb1
68           EptC shares significant amino acid sequence homology and domain structure with the MukB pro
69        FcepsilonR1gamma and CD247 share high sequence homology and form disulphide-linked homodimers
70 genases, with which they share only moderate sequence homology and from which they are distinguished
71 he depupylase Dop share close structural and sequence homology and have a common evolutionary history
72 ve markedly different patterns of evolution; sequence homology and negative selection were highest in
73 or open pan-genomes and share generally high sequence homology and number of core genes including vir
74                    Despite sharing up to 78% sequence homology and overlapping expression profiles in
75                                 We performed sequence homology and phylogenetic analyses, and carried
76                                              Sequence homology and phylogenetic analysis indicated th
77 prehensive systems-scale analysis of genomic sequence homology and phylogenetic relationships among C
78 immunoglobulin-like fold, despite sharing no sequence homology and possessing different disulfide lin
79 ase, where the synaptic joints either locate sequence homology and progress to a post-synaptic joint,
80                                     Based on sequence homology and secondary structure prediction, we
81  They can be divided in two classes based on sequence homology and the presence of an insertion withi
82 at this effect is largely independent of DNA sequence homology and thus cannot be explained by non-al
83 y to other profilins correlated with overall sequence homology, and 2 immunodominant epitope regions
84 like canonical Rap1 effectors despite little sequence homology, and disruption of the binding strongl
85 ubtle structural similarities independent of sequence homology appear to sustain operational equivale
86 e bat-associated viruses because of its high sequence homology (approximately 90% in most genes) to i
87                                           By sequence homology Aq793 is a member of the PcrA/UvrD/Rep
88 l set of gene expression data in addition to sequence homologies are instrumental in the assignment o
89 st that not all Pooideae grass epitopes with sequence homology are cross-reactive.
90 llowed differentiation of proteins with high sequence homology as evidenced by de novo sequencing of
91                                      Despite sequence homology at the active site and biophysical pro
92                               In first step, sequence homology-based genetic analysis of a set of 50
93                        A major limitation of sequence homology-based identification for highly diverg
94                 The low levels of amino acid sequence homology between E3-19K proteins suggest that t
95                    Given the high amino acid sequence homology between fish enzymes, a 3-D structure
96                                 In addition, sequence homology between frog and mammalian Cerberus is
97                 Capitalizing on the complete sequence homology between human and mouse in the heparin
98                                  Despite the sequence homology between RON and MET receptor tyrosine
99 e and RRV proteins; we identified regions of sequence homology between RRV and enolase.
100 trategy that was based on the high degree of sequence homology between S1P(1) and S1P(2).
101                    The unexpected nucleotide sequence homology between SLE patient-derived autoantibo
102                                        Thus, sequence homology between T cell epitopes of 2 self-prot
103                     However, on the basis of sequence homology between the 5 Ebolavirus species, we h
104 ial collaboration in actin assembly, but low sequence homology between the Basic domains of Drosophil
105                                     The high sequence homology between the D3R and D2R, especially wi
106 tor has been challenging because of the high sequence homology between the D3R and the dopamine D2 re
107                 These methods, which rely on sequence homology between the ends of DNA parts, have be
108 vidual antigenic regions correlated with the sequence homology between the MVA- and DNA Gag-encoded i
109 rved from bacteria to man, despite a lack of sequence homology between the resolvases.
110 ly, SNGD-mediated gene editing requires long-sequence homology between the target gene and repair tem
111 y, EigenTHREADER does not depend directly on sequence homology between the target protein and entries
112                                       Strong sequence homology between the three ORMDL genes and ORMD
113 : the similarity in action suggests that the sequence homology between the two compounds might have a
114                              Despite the low sequence homology between the two enzymes (29% identity)
115 en co-expressed in COS-7 cells, despite high sequence homology between the two enzymes.
116 ne coupling subunits do not share an obvious sequence homology between the two transporter families.
117                              Despite limited sequence homology between the vertebrate and Drosophila
118 ghly challenging owing to the glutamate-site sequence homology between these proteins.
119 hbor" serotype O55:H7 revealed a high degree sequence homology between these two serotypes.
120 esponses were rarely elicited when there was sequence homology between vaccine immunogen and endogeno
121 d that MdmX, an Mdm2 family member with high sequence homology, binds adenine nucleotides with simila
122 composed of several isoforms that share high sequence homology but differ in functional characteristi
123 tional modeling, we studied ORs sharing high sequence homology but with different response properties
124 ide bonds are quite diverse and share little sequence homology, but all contain a CXXC catalytic acti
125  (RecA-ssDNA) filament searches a genome for sequence homology by rapidly binding and unbinding doubl
126 d developed an acute HBV infection with 100% sequence homology, compared with HBV inoculum.
127 s from known antibody crystal structures and sequence homology comparison indicates that non-consensu
128                   The confounding effects of sequence homology, complexity of competing cleavages and
129 ering, presence of H275Y mutation, and viral sequence homology confirmed nosocomial transmission of o
130                              As predicted by sequence homology, CT189/190 are the two subunits of DNA
131                    Evolutionary analysis and sequence homology data revealed P450 family blooms in oo
132 paya lines resistant to PRSV isolates in the sequence-homology-dependent manner have been developed i
133                                              Sequence homology diagrams were constructed to compare e
134 n of CER2 as a BAHD acyltransferase based on sequence homology does not fit with CER2 catalytic activ
135                        Thus, despite limited sequence homology, Drosophila and vertebrate APCs exhibi
136 M2) are functional analogs, they have little sequence homology, except for a conserved HXXXW motif, w
137  pathogen specific with minimum interspecies sequence homology for the design of Flavivirus vaccines.
138 le identification of natural LHE proteins by sequence homology from genomic and metagenomic sequence
139                          Despite significant sequence homologies, functional differences between the
140 putational approaches based, for example, on sequence homology, gene co-expression and phylogenetic p
141                                        While sequence homology has been a standard to annotate metabo
142                                              Sequence homology identified the pyridoxal phosphate-dep
143                         Detailed analysis of sequence homology identifies canonical TIR motifs as wel
144                              The notion that sequence homology implies functional similarity underlie
145 itope in the CH3 domain of hFc that has high sequence homology in all four hIgG isotypes (hIgG(1-4)),
146 , of which 3,761 are novel with little or no sequence homology in any existing databases.
147 or netrin-domain-containing proteins display sequence homology in structurally important regions of A
148 e virulent P18 strain shows a high degree of sequence homology in the bisegmented genome between the
149               The two transporters share 40% sequence homology in the C-terminal transmembrane region
150 rison of the resulting peptides showed large sequence homology in the phosphopeptides released by try
151             The six clones demonstrated some sequence homology in the region 2600-2605 and incorporat
152 B-cell receptors (BCRs) with a high level of sequence homology in the variable domains of the heavy a
153                          Despite substantial sequence homology in their core domains, nTop1 and mitoc
154                 PLN and SLN have significant sequence homology in their transmembrane regions, sugges
155  identify analogous folds where little or no sequence homology information is.
156  that makes use of both network topology and sequence homology information, based upon the observatio
157                                 Inference of sequence homology is inherently an evolutionary question
158                                     This low sequence homology is the result of the inclusion of diso
159 ften persists throughout evolution even when sequence homology is undetectable, As macromolecules can
160 on of two DNA sequences that contain limited sequence homology, lie in inverted orientation, and are
161 , bacterial and mammalian PPATs share little sequence homology, making the enzyme a potential target
162 tionic amino acid transporters (CATs) due to sequence homology, may represent system c.
163                        We notice significant sequence homology of AIM2(PYD) with the hydrophobic patc
164 conservation of neural expression and strong sequence homology of all CORL proteins suggests that thi
165                             Despite the high sequence homology of the two domains, a network of large
166         Our data indicate that due to linear sequence homology, part of the MOG35-55-specific T cell
167                                         Gene sequence homology predicts that the sioxanthin biosynthe
168 ufficient coverage (<20x read depth) or high sequence homology (pseudogenes) are complemented by ampl
169 cue model for SV with breakpoints located in sequence homology regions.
170 Is of Colias and the silkmoth, but no intron sequence homology remains.
171 tion tools RepeatMasker and Censor depend on sequence homology search tools such as cross_match and B
172          For allergen identification protein sequencing, homology search and mass spectrometry were a
173                                              Sequence homology searches were performed to extend ZU5-
174 and are classified into four groups based on sequence homology (SEPT2, SEPT3, SEPT6, and SEPT7 groups
175 f these proteins, which share no discernible sequence homology, share a striking structural similarit
176 t to the Toll/IL-1R domain of TLR10 with low sequence homology, substantial differences were observed
177                            Despite a lack of sequence homology, the genes are aligned in a head-to-ta
178                          Consistent with the sequence homology, the GK subunits adopt the same overal
179  two enzymes share approximately 50% protein sequence homology, the membrane topology of VKOR is stil
180                    Thus, despite low overall sequence homology, the production of infectious virus is
181      Although the RSKs have a high degree of sequence homology, their functional differences in cance
182      Although calbindin and S100B have a low sequence homology, they seem to activate IMPase-1 in a s
183  Dscam and vertebrate Pcdh proteins share no sequence homology, they seem to underlie similar strateg
184 AChR subtypes (M1-M5) share a high degree of sequence homology, they show pronounced differences in G
185         Furthermore, PHF2 shares significant sequence homology throughout the entire region, includin
186                        SSGP-71 proteins lack sequence homologies to other proteins, but their structu
187 TP0326, the sole protein in T. pallidum with sequence homology to a Gram-negative OMP, belongs to the
188 es significant structural similarity but not sequence homology to a group of enzymes that bind to and
189                                              Sequence homology to a putative yeast thiamine (vitamin
190                                              Sequence homology to A1cf, the RNA-binding subunit of th
191 he green alga Chlamydomonas reinhardtii with sequence homology to animal cryptochromes and (6-4) phot
192           Gp1.7 is unusual in that it has no sequence homology to any known nucleotide kinase, it has
193                         TcpF has no apparent sequence homology to any known protein.
194  gene, RteC, did not have primary amino acid sequence homology to any known proteins in the databases
195 d executor type R genes show no considerable sequence homology to any known R genes.
196 d executor type R genes show no considerable sequence homology to any known R genes.
197 proteins (LipA and LipB) that had amino acid sequence homology to bacterial adhesins and structural h
198   Furthermore, this domain has been shown by sequence homology to be present in all bacterial L-serin
199  identified, but human FIZZ2 has significant sequence homology to both rodent FIZZ2 (59%) and FIZZ1 (
200                    CLDs have high degrees of sequence homology to cathelin, a protein isolated from p
201 (CD99L2) is a membrane protein with moderate sequence homology to CD99, which initiates cell aggregat
202 bout half of the components of the TCPM show sequence homology to components of the previously analys
203 ator of Cdk1 and Cdk2 that has no amino acid sequence homology to cyclins, are sterile and display me
204                           EnvD showed strong sequence homology to dienelactone hydrolases from other
205 f approximately 70 amino acids and have high sequence homology to each other (>85% identity).
206 ces cerevisiae MTase Yjr129c, which displays sequence homology to FAM86A, is a functional FAM86A orth
207 ar domains KL1 and KL2, each of which shares sequence homology to glycosyl hydrolases.
208 a class of vertebrate proteins that exhibits sequence homology to innexins, the invertebrate gap junc
209 embers of a tick protein family bearing high sequence homology to Japanin are also likely to bind cho
210 ammaherpesvirus 68 (MHV68) ORF73 (mLANA) has sequence homology to Kaposi's sarcoma-associated herpesv
211 affinity M. sexta GABA transporter with high sequence homology to known mammalian GABA transporters,
212 r short (2-100 amino acids) peptides with no sequence homology to known proteins.
213        One of these miRNAs, miR-J8, has seed sequence homology to members of the cellular miR-17/20/1
214  segment of the LRRK2 kinase domain based on sequence homology to mixed-lineage kinases.
215                  SynCaK displays significant sequence homology to MthK, a calcium-dependent potassium
216    Based on its cytoskeletal association and sequence homology to myelin P2 (FABP8), it has been sugg
217 ng the Crenarchaeota branch, and bear little sequence homology to other DNA polymerase families.
218                           This region has no sequence homology to other known fibrinogen binding prot
219 al virus proteins display very low levels of sequence homology to other proteins listed in the public
220 ew major allergen was isolated, which showed sequence homology to peritrophins, which contain chitin-
221                                     Based on sequence homology to pilins in Gram-negative bacteria, C
222                               SdbA shows low sequence homology to previously identified oxidoreductas
223 r analysis" yielded heavy chains with little sequence homology to previously identified VRC01 class h
224 he hidden Markov model library that provides sequence homology to SCOP structural domains remains unc
225 hiseptica, plrS, the product of which shares sequence homology to several NtrY-family sensor kinases
226 potassium conductance domains that show high sequence homology to the bacterial TrkA family of K(+) t
227 rminal domain (AP7C) that exhibits imperfect sequence homology to the C subclass of the intracellular
228 nsmembrane-helix (6-TM) domain, which has no sequence homology to the canonical tetrameric K(+) chann
229 e, and the core herpesvirus genes had strong sequence homology to the corresponding KSHV genes.
230 92 aa protein that contains a domain showing sequence homology to the glycosyl hydrolase motif in the
231 to-inhibitory domain within Snf2h that bears sequence homology to the H4 tail, abolishes the linker-l
232                          These proteins have sequence homology to the N-terminal domain (NTD) of the
233                                Despite close sequence homology to the protease cathepsin L, the silic
234  associated with metabolosomes (PduL) has no sequence homology to the PTAC ubiquitous among fermentat
235 cludes a rhodanese-fold in accordance to its sequence homology to the rhodanese family of sulfurtrans
236 cific sgRNA is not uniquely defined by exact sequence homology to the target site, thus unintended of
237 elanogaster alpha7 (Dalpha7) has the closest sequence homology to the vertebrate alpha7 subunit and i
238                   Despite showing no primary sequence homology to TNF family cytokines, UL141 binds t
239                                     Based on sequence homology to TNF-alpha, now a total of 19 member
240    Despite previous failure in detecting any sequence homology to ubiquitin, the folded state was det
241 des a single-pass transmembrane protein with sequence homology to vertebrate Cysteine-rich transmembr
242 s capable of recognizing extremely divergent sequence homology, we identified a MYRF protein domain d
243                                     Based on sequence homology, we identified a single M. polymorpha
244                                     Based on sequence homology, we identify IPLA-1 as the closest C.
245  proteins of these viruses show the greatest sequence homology, we tested hyperimmune antisera prepar
246              A strong genome colinearity and sequence homology were observed between MneRV2 and RRV26
247 eyi (Hd-CDT), which share limited amino acid sequence homology, were directly compared.
248 omyces lactis Hsv2, which shares significant sequence homologies with its three Saccharomyces cerevis
249                            BM2 shares little sequence homology with AM2, except for a conserved HxxxW
250 NM; and (iii) the LnmJ-SH domain, sharing no sequence homology with any other enzymes catalyzing C-S
251 ciparum SSB (Pf-SSB) shares a high degree of sequence homology with bacterial SSB proteins but differ
252 protease and signaling inhibitor TIKI shares sequence homology with bacterial TraB/PrgY proteins, inh
253 se, but further work revealed that it shared sequence homology with beta-lactamase/metallo-beta-lacta
254 system, we discovered an adhiron that shared sequence homology with C3 and abolished C3-induced prolo
255         One adhiron (A6) was found to have a sequence homology with C3 and studied further.
256 r protein KIAA0157, which shares significant sequence homology with CCDC98.
257                                     ClsC has sequence homology with ClsA and ClsB, which all belong t
258                            They often shared sequence homology with co-expressed genes and contained
259                            They share a high sequence homology with cyclotides but are biosynthetical
260 d3 is presumed to be palmitoylated, based on sequence homology with Drd2, but the functional attribut
261 he two O. tsutsugamushi isolates shared >99% sequence homology with each other, reflecting the consis
262  The HLA-DR-presented GNS peptide has marked sequence homology with epitopes from sulfatase proteins
263                      LsbB shares significant sequence homology with five other leaderless bacteriocin
264 rhodopsins from cryptophyte algae show close sequence homology with haloarchaeal rhodopsin proton pum
265 cus contains more than 50 genes sharing high sequence homology with hexose transporters in Saccharomy
266 ne viral miRNA, miR-K12-11, shares 100% seed sequence homology with hsa-miR-155, an oncogenic human m
267 S27, UL33, and UL78, which present important sequence homology with human chemokine receptors.
268                              Despite limited sequence homology with human GLTP, we recently showed th
269 ingolipids between membranes and has limited sequence homology with human glycolipid transfer protein
270 the deduced Cq-IGFBP was shown to share high sequence homology with IGFBP family members from both in
271               Although it has low amino acid sequence homology with known 2-oxoglutarate-dependent di
272 acterized protein, Vp1659, which shares some sequence homology with LcrV from Yersinia.
273 ound ubiquitin ligase that bears significant sequence homology with mammalian Hrd1 and mediates stero
274 ntial to viral transcription and that shares sequence homology with members of the paramyxoviruses an
275  (DENV1 to -4), which share a high degree of sequence homology with one another.
276 erotypes (DENV1 to -4) which share 67 to 75% sequence homology with one another.
277 of the S1 helix, as a consequence of its low sequence homology with other Kv family members.
278                                 S2 shares no sequence homology with other retroviral factors known to
279 NS1 C-terminal residues 305-311, which share sequence homology with Plg residues 590-597.
280                             Hp0267 shares no sequence homology with previously characterized ADDs, ye
281  we demonstrate that NUCKS1 shares extensive sequence homology with RAD51AP1 (RAD51 associated protei
282 , an essential initiation factor, having 21% sequence homology with RatA.
283                      ICMT has no discernible sequence homology with soluble methyltransferases, and a
284 vel ORFs, which we name cylc-1 and -2, share sequence homology with stathmins and encode small, very
285  (H1N1) virus exhibits hemagglutinin protein sequence homology with the 1918 pandemic influenza virus
286 imensional models of MdtB and MdtC, based on sequence homology with the AcrB transporter, also suppor
287                           It exhibits strong sequence homology with the bacteriophage T7 gene 4 prote
288                  Remarkably, Us3 displays no sequence homology with the cellular kinase Akt, yet dire
289       Restriction enzymes share little or no sequence homology with the exception of isoschizomers, o
290 nfected with HCV that had more than 95% NS5B sequence homology with the HCV strains of the 3 case pat
291 erminal domain (C domain) shares significant sequence homology with the OmpA-like family of peptidogl
292 d, and P4 proteins of WMoV exhibited limited sequence homology with the orthologous proteins of other
293 PLR1) was identified in Arabidopsis based on sequence homology with the protein in yeast.
294 e inserted, as the position is determined by sequence homology with the recombination primers.
295             Although StnA has no significant sequence homology with the reported alpha/beta-fold hydr
296         Class C methylases share significant sequence homology with the RS enzyme, HemN, and may bind
297             The endogenous protein has 88.0% sequence homology with the theoretically predicted Gly m
298 acy by up to 40% for species which have high sequence homology within their genus.
299 eptors ERalpha and ERbeta share considerable sequence homology yet exert opposite effects on breast c
300 alcium channel, has three isoforms with >65% sequence homology, yet the isoforms differ in their func

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