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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.
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.
48 m the identification of short regions of DNA sequence homology, also known as microhomology, at chrom
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
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
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
63 2 cytotoxic factors exhibited 50% amino acid sequence homology and bound to the same receptor, they c
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
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,
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
88 l set of gene expression data in addition to sequence homologies are instrumental in the assignment o
90 llowed differentiation of proteins with high sequence homology as evidenced by de novo sequencing of
104 ial collaboration in actin assembly, but low sequence homology between the Basic domains of Drosophil
106 tor has been challenging because of the high sequence homology between the D3R and the dopamine D2 re
108 vidual antigenic regions correlated with the sequence homology between the MVA- and DNA Gag-encoded i
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
113 : the similarity in action suggests that the sequence homology between the two compounds might have a
116 ne coupling subunits do not share an obvious sequence homology between the two transporter families.
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
127 s from known antibody crystal structures and sequence homology comparison indicates that non-consensu
129 ering, presence of H275Y mutation, and viral sequence homology confirmed nosocomial transmission of o
132 paya lines resistant to PRSV isolates in the sequence-homology-dependent manner have been developed i
134 n of CER2 as a BAHD acyltransferase based on sequence homology does not fit with CER2 catalytic activ
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
140 putational approaches based, for example, on sequence homology, gene co-expression and phylogenetic p
145 itope in the CH3 domain of hFc that has high sequence homology in all four hIgG isotypes (hIgG(1-4)),
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
150 rison of the resulting peptides showed large sequence homology in the phosphopeptides released by try
152 B-cell receptors (BCRs) with a high level of sequence homology in the variable domains of the heavy a
156 that makes use of both network topology and sequence homology information, based upon the observatio
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
164 conservation of neural expression and strong sequence homology of all CORL proteins suggests that thi
168 ufficient coverage (<20x read depth) or high sequence homology (pseudogenes) are complemented by ampl
171 tion tools RepeatMasker and Censor depend on sequence homology search tools such as cross_match and B
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
179 two enzymes share approximately 50% protein sequence homology, the membrane topology of VKOR is stil
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
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
191 he green alga Chlamydomonas reinhardtii with sequence homology to animal cryptochromes and (6-4) phot
194 gene, RteC, did not have primary amino acid sequence homology to any known proteins in the databases
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 (
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
206 ces cerevisiae MTase Yjr129c, which displays sequence homology to FAM86A, is a functional FAM86A orth
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,
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.
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-
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
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
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
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
245 proteins of these viruses show the greatest sequence homology, we tested hyperimmune antisera prepar
248 omyces lactis Hsv2, which shares significant sequence homologies with its three Saccharomyces cerevis
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
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
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
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
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
281 we demonstrate that NUCKS1 shares extensive sequence homology with RAD51AP1 (RAD51 associated protei
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
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
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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