コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 id sequence ATTQWKTSAA and confirmed HM-3A a novel protein.
2 structure-function relationships and create novel proteins.
3 f Syn5 includes a number of genes coding for novel proteins.
4 plex morphologies without the acquisition of novel proteins.
5 tive enzymes, and other effectors, including novel proteins.
6 ned thus far, lin-8 and lin-15A, both encode novel proteins.
7 , corresponding to 29 known allergens and 61 novel proteins.
8 n function correlates with immunogenicity of novel proteins.
12 i defective genes rde-10 and rde-11 encode a novel protein and a RING-type zinc finger domain protein
14 proteins, as well as the potential roles of novel proteins and MAPKs in the polarity establishment r
17 bind to host RNA polymerase (RNAP): gp79, a novel protein, and gp36, a distant homolog of sigma(70)
22 alysis, fluorescent protein fusions revealed novel proteins at organelle interfaces such as plastid s
24 for expression of TLT35 in E. coli make this novel protein-based fusion inhibitor a promising candida
25 highly conserved OLF domain, and suggests a novel protein-based hypothesis for glaucoma pathogenesis
26 for inducible expression of LPG, applying a novel protein-based system that allows controlled degrad
32 imental optimization were used to generate a novel protein called BINDI that binds BHRF1 with picomol
34 uence of the amino acid substitutions in the novel protein candidates for direct input into epitope e
40 discovery and intracellular location of six novel proteins (cingulins) that are integral components
41 t the association of this network with three novel protein clusters involved in cell wall biogenesis,
42 enome contains a rich resource of shared and novel protein coding genes, a significantly higher amoun
44 olution map enabled the identification of 14 novel protein coding regions as well as 44 potential nov
45 of transcripts from RNA-sequencing revealed novel protein-coding and long noncoding RNAs (lncRNAs).
50 prised 28,294 expressed, annotated genes, 78 novel protein-coding genes, and 567 putative long interg
51 analysis enabled us to discover a number of novel protein-coding regions, which includes translated
52 er rigorous data filtering, 51 (presumptive) novel protein-coding transcripts, 5326 long and 679 smal
57 the yeast PKM2 homolog, Pyk1, is a part of a novel protein complex named SESAME (Serine-responsive SA
58 ere, we demonstrate that RAD51C is part of a novel protein complex that contains PALB2 and BRCA2.
59 ite stages of Plasmodium and it is part of a novel protein complex with an overall composition overla
60 lear mRNPs and DBC1 (ZIRD)) as subunits of a novel protein complex--named DBIRD--that binds directly
61 lts presented here identify and validate two novel protein components of the putative tRNA translocon
65 , we have now identified and characterized a novel protein contact between the Y-family DNA polymeras
66 hila, is regulated in somatic cells by Yb, a novel protein containing an RNA helicase-like motif and
71 y unknown RNA segment (segment 7) encoding a novel protein designated VP7 was discovered in WFBV.
72 disA-1 abolishes the localization of the novel protein DisAp to T. thermophila striated fibers (k
75 tor inhibitor-1 (PAI-1) gene that recruits a novel protein-DNA complex responsible for TCDD-inducible
76 m GM12878 and K562 cells and identified many novel protein-DNA interactions in segmental duplication
85 or chemotherapy or vaccination, the need for novel protein expression platforms has become a pressing
87 er take place between 8-10 h of IVF, and the novel protein failed to inhibit G9a activity in time, re
88 us proteins help in functional annotation of novel protein families and in improving annotations of w
89 and draft genomes reveal a 10.5% increase in novel protein families as a function of phylogenetic div
90 al complexity enables us to rapidly identify novel protein families found in new genomes and to perfo
92 rminal domain of wild-type TnsE identified a novel protein fold including a central V-shaped loop tha
96 nique biophysical traits, such as exhibiting novel protein folds and unusually high carbohydrate affi
99 randomly selected and deleted, revealing two novel proteins, FTL_1548 and FTL_1709, which are require
102 t LNA and GNA in the application of learning novel protein functional knowledge, the two produce very
104 proteins can be helpful in understanding how novel protein functional sites evolved on an ancient pro
105 roteolysis by calpains potentially generates novel protein functions, it is important to understand h
107 ession of the cell-cycle inhibitor p16 and a novel protein homologous to Scp3, a synaptonemal complex
108 e Electrophile Response Element (EpRE) and a novel protein, human homolog of Xenopus gene which Preve
111 Recently in our laboratory, we identified a novel protein in C. elegans involved in dietary choleste
112 This approach allowed the identification of novel proteins in E. oleoabundans, including two photopr
113 resent in a unique TIM complex consisting of novel proteins in T. brucei and is critical for mitochon
114 ially, we demonstrated for a subset of these novel proteins (including cullin1, ephexin, potassium ch
115 dition to Ago2 and PCBP2, identified several novel proteins, including IGF2BP1, hnRNP L, DHX9, ADAR1,
116 works present at the glial-leading edge, and novel proteins, including members of the Prohibitin fami
117 nd in authentic LBs in PD as well as several novel proteins, including the microtubule affinity-regul
119 roxyanilino)methylidene]naphthalen-2-one), a novel protein interaction inhibitor of replication prote
121 ss of complex formation, thus validating the novel protein interaction mode in the 14-3-3beta.ChREBP
125 -tune binding specificities or change/create novel protein interactions is a common task in structure
127 ion plays in promoting signal amplification, novel protein interactions, and protein turnover has pro
128 or genome-wide PPI studies and has uncovered novel protein interactions, providing new insight into p
130 ating Wnt signalling and identify Axin1 as a novel protein interactor of the widely-expressed gamma-P
132 2A), through a yeast two-hybrid system, as a novel protein involved in the stabilization of VEGFR-2 b
136 Determining the structure and function of a novel protein is a cornerstone of many aspects of modern
138 generated from human SMN genes and reveals a novel protein isoform predicted to be stably expressed d
141 ication, and mass spectrometry to identify a novel protein, KHARON1 (KH1), which is important for the
145 cerol (DAG) content leading to activation of novel protein kinase C (PKC) resulting in decreased insu
146 hodology allows the development of potential novel protein kinase C delta (PKCdelta) analogues for be
151 amely, diacylglycerol-triggers activation of novel protein kinases C with subsequent impairments in i
153 ated 'rpL22-like short') that would encode a novel protein lacking the C-terminal ribosomal protein s
154 ning 160,000 compounds is a useful source of novel protein ligands by identifying a non-covalent synt
155 nsional structures, and ultimately to design novel protein-like architectures with properties unprece
161 n's C-terminal domain binds lipids through a novel protein motif, permitting complexin to inhibit spo
163 sembly of large symmetrical structures and a novel protein nanoparticle for encapsulation and cargo d
164 e show that root gravitropism depends on the novel protein, NEGATIVE GRAVITROPIC RESPONSE OF ROOTS (N
170 POT1 in Arabidopsis fueled the evolution of novel protein-nucleic acid interactions and the migratio
172 In this study, we demonstrate that Tda2 is a novel protein of the endocytic machinery necessary for n
173 ve reported previously the identification of novel proteins of Mycobacterium tuberculosis by the immu
175 draft H. bacteriophora genome sequence were novel proteins of unknown function lacking homologs in C
176 amina analogue NUP-1, represents a cohort of novel proteins operating at the nuclear periphery of try
177 rograming is often accomplished by designing novel protein or RNA parts that respond to specific smal
178 gulated in spinal cords of ALS patients, the novel protein oxidative resistance 1 (Oxr1) protects neu
182 Gfi1 and neutrophil elastase and detected a novel protein, PFAAP5 (also known as N4BP2L2), interacti
187 might exhibit phase behaviour and to design novel protein polymers consisting of biologically active
188 This work provides new insights into the novel protein-primed mechanism of calicivirus VPg-depend
189 ion and characterization of a 628-amino acid novel protein, printor, that interacts with torsinA.
192 abeled antibodies, we show that two of these novel proteins, products of genes 53 and 54, are part of
194 TLC1 and -2 subunits, and here we describe a novel protein-protein interaction between SPTLC1 and the
196 es of the PRL-1.Peptide 1 complex revealed a novel protein-protein interaction whereby a sequence mot
197 ding domain of p53; and (iv) it stimulates a novel protein-protein interaction with the E2-ubiquitin
199 also to bioinformaticans seeking to predict novel protein-protein interactions based on the DDIs.
200 ic binding partners for PRRG4 and identified novel protein-protein interactions for the protein.
201 The ability to rationally design the site of novel protein-protein interactions is an important step
209 nvelope membrane where it possibly confers a novel protein quality control mechanism for chloroplast
210 s nuclear ribonucleoprotein C (hnRNP C) as a novel protein recruited to higher molecular mass fractio
217 hat they copurify with each other and with a novel protein, RNA-DIRECTED DNA METHYLATION 1 (RDM1), fo
218 CLAM provides a useful tool to discover novel protein-RNA interactions and RNA modification site
219 ction of the Rho-GAP Rga7 are regulated by a novel protein, Rng10, during cytokinesis in fission yeas
222 design-free methods can be used to generate novel protein scaffolds that are tailor-made for catalys
227 r crystal structure determination to explore novel protein sequence space and structure-based functio
229 ments have contributed to the acquisition of novel protein sequences during primate and human evoluti
233 hat Skb1 forms nodes by interacting with the novel protein Slf1, which is a limiting factor for node
235 these newly identified conserved residues, a novel protein splicing mechanism that includes a second
236 of this CHIP-SirT6 interaction represents a novel protein-stabilizing mechanism and defines an inter
237 protein extensions, 231 exon extensions, 192 novel protein start sites, 19 novel translational frames
238 Rosetta has been used to accurately design a novel protein structure, predict the structure of protei
239 effective tool for engineering and design of novel protein structures (including naturally knotted pr
247 of drug-dependent plasticity and uncovering novel protein targets in the reward circuit may lead to
248 lso investigated the possible mechanisms and novel protein targets involved in rapamycin-induced pres
249 ion of the 6K gene, yielding production of a novel protein, termed transframe (TF), comprised of a C-
251 vides fundamental structural insights into a novel protein that has undergone multiple biochemical an
255 continuous alpha-helical linker to design a novel protein that self assembles into a 750 kDa, 225 A
256 synMuv gene lin-56 and found it to encode a novel protein that shares a THAP-like C(2)CH motif with
258 slation from antisense CCG repeats generates novel proteins that accumulate in ubiquitinated inclusio
259 e, we used a systematic approach to identify novel proteins that are involved in cancerous EGFR signa
261 biochemical insights into IRES function and novel proteins that function as alternate met-tRNA(i)(me
262 e RNA interference (RNAi) screen to discover novel proteins that function in the replication stress r
263 nity purification and LC-MS/MS to search for novel proteins that interact with R7-RGS heterotrimers i
264 retrieval, included the GET complex and two novel proteins that likely function similarly in membran
274 This is critical for designing and screening novel protein therapeutics and for understanding their p
277 e finishing of large genomes and analysis of novel proteins they encode typically require cloning of
279 The present study delineates a number of novel proteins, TLR3-related pathways, and cellular phen
280 powerful ChIP-MS technique and discovered a novel protein, TRIM24, enriched on OCT4-, SOX2-, and NAN
281 in two affected individuals we identified a novel protein-truncating mutation in the C12orf65 gene,
282 UNC80 protein that bridges NALCN to a large novel protein UNC79 in the same complex, and the last am
283 Deep sequencing of CMG0 and CMG28 revealed novel protein variants in the hypothetical genes TC0237
285 ased on these novel transcripts, at least 36 novel proteins were detected from shotgun proteomics dat
286 GABA receptor subunits and gephyrin, several novel proteins were isolated in association with NL2.
287 ediated transcription, suggesting that these novel proteins were putative SBP-AR-interacting proteins
288 T cell targets for both known allergens and novel proteins, which may inform future diagnostics and
290 oducts: ribosomal component RpL22-like and a novel protein with a role distinct from RpL22-like.
293 ntly differ from their yeast homologues, and novel proteins with high homology to CORVET/HOPS subunit
295 aled the existence of several genes encoding novel proteins with unknown functions, one of which is t
296 ry glands produce a small number of abundant novel proteins with yet unknown functions, in addition t
298 e and frequency was comparable for known and novel proteins, with 15 antigens (nine of which were nov
299 that facilitate the de novo generation of a novel protein within an ancestral ORF have remained poor
300 homologous region in IL-22, we engineered a novel protein (Z13-IL22-2) that contains the MPER epitop
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。