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1 Positive selection is detected in the bindin coding region.
2 in solution and binds to DNA within the sbnC coding region.
3 le small open reading frames upstream of the coding region.
4 anslation control and expression of the EPRS coding region.
5 lowing for increased translation of the EPRS coding region.
6 tide divergence in the viral protein 1 (VP1) coding region.
7 levels of translation initiation at the EPRS coding region.
8 ically G-quadruplex-like DNA, within the CTD coding region.
9 recombination sites inside the viral protein-coding region.
10 and LGP2 specifically bound MV nucleoprotein-coding region.
11 sence of the essential MYB activation domain coding region.
12 and a shorter construct containing only the coding region.
13 (pA)d, and another, (pA)p, within the capsid-coding region.
14 ier that prevents reinitiation at the GADD34 coding region.
15 other complex site, (pA)p, within the capsid-coding region.
16 ader region or continues into the downstream coding region.
17 depends on the nucleotide composition of the coding region.
18 elements (PPREs) upstream of the pre-miR-223 coding region.
19 equires sequences in both the 5' UTR and the coding region.
20 d thereby prevents transcription of the corA coding region.
21 and nucleotide sequence analysis of the VP1 coding region.
22 s rise to viable chimeras in the polyprotein coding region.
23 number of ribosomes on the principal protein-coding region.
24 et elements located at the beginning of thiM coding region.
25 mutations occur at similar frequencies as in coding regions.
26 ed because most GWAS SNPs are located in non-coding regions.
27 yses to variants that are in or proximate to coding regions.
28 persed throughout approximately 40 kb of non-coding regions.
29 d powerful linkage analyses, particularly in coding regions.
30 able genome, and that fusion predominates in coding regions.
31 WSA overall but 97% more information for the coding regions.
32 zation of genomic variants in coding and non-coding regions.
33 VP22), US3, US4 (gG), US6 (gD), and US7 (gI) coding regions.
34 ed with the attention focused on the protein coding regions.
35 introduced premature termination codons into coding regions.
36 es across the GAL cluster gene promoters and coding regions.
37 ll splicing events, and 43% of the events in coding regions.
38 llenging due to a lack of annotations in non-coding regions.
39 H3 levels remain relatively constant within coding regions.
40 (gL), UL2, UL4, UL49 (VP22), UL50, and ICP4 coding regions.
41 nections between stimulus-coding and outcome-coding regions.
42 st, generally in the second half of the gene coding regions.
43 ore difficult to study compared with protein-coding regions.
44 not included in the published annotation of coding regions.
45 tral drift or positive selection, similar to coding regions.
46 selection on regulatory elements as well as coding regions.
47 py of the stem-loop between the NS7- and VP1-coding regions.
48 bition of spurious transcription from within coding regions.
49 erns established by SAGA at promoters versus coding regions.
50 unknown function and located outside protein-coding regions.
51 CEs) that predominantly (>99%) reside in non-coding regions.
52 in coding regions and approaching 90% in non-coding regions.
53 asis of the presence of mutations in protein-coding regions.
54 g indicating disease-causing variants in non-coding regions.
55 outside of functionally well-defined protein coding regions.
56 tely predict all or even most of the protein-coding regions.
57 ilized target sites lie predominantly within coding regions.
58 known about cancer-causing mutations in non-coding regions.
59 (s) for reducing misincorporation in protein-coding regions.
60 nslated regions (UTRs), introns, and protein-coding regions.
61 tations and genomic polymorphisms in protein-coding regions.
62 ntified ORFs and pre-existing annotations of coding-regions.
63 ng patient sequence data from within protein coding-regions.
64 ther hand, exon skipping events were rare in coding regions (1%) but enriched in UTRs where they acco
65 of peripheral-blood gene expression included coding regions (11.41x), conserved regions (4.67x), and
67 ulation of peripheral-blood gene expression: coding regions (4.47x), conserved regions (4.51x), and t
68 an especially proficient 'extended FMDV 2A' coding region allows production of two independent prote
70 e expression analysis revealed that this non-coding region alteration is associated with the signific
72 o efficiently capture and amplify the entire coding region and flanking intronic and regulatory seque
73 developed based on the two mutations in the coding region and one in the promoter region and validat
76 m neutrality has been detected in the bindin coding region and suggested in the intron, indicating th
77 iable rhinovirus chimeras in the polyprotein coding region and that recombination hotspots map to non
78 , RTC4 transcription begins near the protein-coding region and the resulting short transcript leader
79 t extends 13 nucleotides into the N-terminal coding region and, when a mRNA structure overlaps or par
80 e methods, reaching 91% balanced accuracy in coding regions and 70% in non-coding regions, while even
81 es and eukaryotes in general - nearly 80% in coding regions and approaching 90% in non-coding regions
82 A majority of these variants reside in non-coding regions and are co-inherited with hundreds of can
83 y-based method, AlignFS, to identify protein-coding regions and correct erroneous frame-shifts, suita
85 LA3 variants were not detected by sequencing coding regions and intron-exon boundaries either in 142
87 5' positioning of the ER-targeting sequence coding regions and is facilitated by the RNA-binding dom
88 Most RA GWAS loci reside outside of protein-coding regions and likely affect distal transcriptional
89 und evidence that this mechanism of using 5' coding regions and particular RBPs to achieve gene-speci
90 association study (GWAS) signals map to non-coding regions and potentially point to non-coding varia
91 T, their distribution between coding and non-coding regions and synonymous-to-non-synonymous mutation
93 curacy of GeneMarkS-T in identifying protein-coding regions and, particularly, in predicting translat
94 s sequences covered 99.3% to 100% of the HCV coding region, and the average coverage was 6,070 reads/
96 codon preference index (CPI) to overlapping coding regions, and use RNAsampleCDS to generate control
97 al gene enhancers, promoters and transcribed coding regions, and was required for transcription initi
102 because indels caused by a single cut in non-coding regions are unlikely to produce a functional knoc
103 ught to identify genetic variants in protein-coding regions associated with subclinical atheroscleros
104 ize the need to interrogate the mutations in coding regions beyond their obvious effects on protein s
105 sible for its recruitment to the promoter or coding regions but, rather, are required to orient its a
106 ic traits or disease do not fall within gene coding regions, but in regulatory regions, rendering the
107 ally enables transcription of its associated coding region by favoring an RNA conformation that seque
110 s and genomic distance, co-localization with coding regions, CpG islands (CGIs), and regulatory eleme
112 replication element (CRE) in the 2C protein-coding region [CRE(2C)] templates the addition of two ur
113 occurs, but RNAP II is absent from the gene-coding region, demonstrating Sas3 and Ada2-dependent his
114 LARP4 mRNA contains a translation-dependent, coding region determinant (CRD) of instability that limi
115 glioma-associated oncogene 1 (GLI1) mRNA by coding region determinant binding protein (CRD-BP) throu
116 is a major criterion for the function of the coding region determinant-binding protein (CRD-BP).
118 tory apparatuses, and the composition of the coding region determines the abundance of mRNAs near the
119 We show that SCA23 mutations in the Dyn A-coding region disrupted peptide secondary structure lead
120 and analysis of high-quality exome (protein-coding region) DNA sequence data for 60,706 individuals
124 ion conditions confirmed that coding and non-coding regions explained aspartic and glutamic acid cons
125 lternative splicing tends to remove parts of coding regions from a longer, major isoform, providing e
128 ophilia B, the large size of the factor VIII coding region has precluded improved outcomes with gene
131 GR-ORF15 cDNA that includes a purine-rich 3'-coding region; however, its effectiveness has recently b
132 ocused their efforts in polymorphisms within coding regions, ignoring those within regulatory regions
133 sociated with cancer risk lie in non-protein-coding regions, implicating regulatory DNA elements as f
134 verning translation initiation at N-terminal coding regions, improving the predictive design of post-
135 3 in nonsyndromic clefting, we sequenced its coding region in 576 Europeans with nsCL/P and 96 with n
136 We detected somatic mutations in protein-coding regions in 140 benign tissue samples representing
139 ted here are previously undiscovered protein-coding regions in exon 1 of hKCNE3 and hKCNE4 that exten
140 during sexual reproduction and mainly in the coding regions in filamentous ascomycetes, involving ade
143 de sequences that target both coding and non-coding regions in spCas9 CRISPR system across human, mou
145 nal analysis of CALM1, CALM2, and CALM3 gene-coding regions, in vitro measurement of CaM-Ca(2+) (Ca)-
146 not only from coding exons but also from non-coding region including core promoters generated by rand
147 acting elements within the N-terminal capsid coding region, including the stem-loop structure (5'SL6)
148 led an abundance of miR target sites in gene coding regions, including several sites pointing to new
149 so identify novel recurrent mutations in non-coding regions, including the 3' region of NOTCH1, which
151 ion of any intergenic or deeply intronic non-coding region, indicating that proximal regulatory seque
152 ries both the causal mutations in the TaPHS1 coding region, indicating that the mis-splicing (+646) m
153 a gene caused by a small deletion in the non-coding region is a novel mechanism, which to the best of
154 this gene has accumulated mutations, so its coding region is unlikely to produce a functional protei
156 t fraction of Pol III transcription from non-coding regions is not subjected to Xist-mediated transcr
157 fying these transcriptional regions from non-coding regions is the first step towards lincRNA recogni
158 ing sequence or for the beginning and end of coding regions, largely explained by target site motifs.
159 on rates have been extensively calibrated in coding regions, leading to the identification of many dr
161 SNPs) (including imputed ones) fall into non-coding regions, making it difficult to associate statist
162 s that functional properties attributed to a coding region may in fact be carried out by an embedded
163 10a miRNA, whose precursor overlaps the KapA-coding region, may account for the oncogenic properties
165 retinoblastoma uncovered a tumor that had no coding-region mutations or focal chromosomal lesions oth
167 elaborate eccentricities, such as scrambled coding regions, nonstandard genetic codes, and convolute
169 interference (RNAi) using the extracellular coding region of a maize zmbri1 complementary DNA knocke
170 ly designed RNA hairpins into the N-terminal coding region of a reporter protein with steadily increa
173 For engineering nuclear male sterility, the coding region of Brassica napus cysteine protease1 (BnCy
176 nymous single nucleotide polymorphism in the coding region of HAB rodents revealed that it caused a h
177 ally conserved RNA structure within the NS5B coding region of hepatitis C virus functions as a cis-re
180 hod to efficiently amplify the entire capsid coding region of human enteroviruses (EVs) including PV.
181 trates that FMRP preferentially binds to the coding region of its targets but also revealed binding a
183 We performed Sanger sequencing of the entire coding region of MPL in 62, and of JAK2 in 49 additional
185 d recombinants throughout the non-structural coding region of poliovirus from dually transfected cell
186 approach to effectively delete an important coding region of Sav1, which increased the editing effic
187 ation efficiency at high salinity map to the coding region of sigH and in the regulatory region of ki
188 METTL3 induces m(6)A modification within the coding region of the associated mRNA transcript, and enh
189 on of expanded CCUG repeat RNAs from the non-coding region of the CCHC-type zinc finger nucleic acid-
191 the GGGGCC hexanucleotide repeat in the non-coding region of the Chromosome 9 open-reading frame 72
193 ition gene, while the analysis of the entire coding region of the FANCM gene in familial index cases
194 URKC c.744C > G (AURKC p.Y248*) occur in the coding region of the gene and are the focus of this stud
195 tion has been constrained in Melanesians the coding region of the MC1R gene was sequenced in 188 indi
196 f oncogenic H-Ras and K-Ras, we replaced the coding region of the murine K-Ras locus with H-Ras(G12V)
201 identified Hoip-responsive sequences in the coding region of the Tm2 mRNA that are essential for Tm2
202 Two haplotype blocks, one upstream to the coding region of UGT2A1 (rs146712414, P = 9.1 x 10(-5);
203 iple evolutionary events in the promoter and coding region of VAC-INVcis-QTL were also detected for A
206 ore than 10 million mutations in the protein-coding regions of 2,735 mutant lines of tetraploid and h
208 A custom panel was designed to cover the coding regions of 81 NSCLC-related genes and 40 ancestry
209 nd fibers condensed up to 10-fold containing coding regions of active genes, constitute the euchromat
210 g resulted in low nucleosome turnover in the coding regions of active genes, stably expressed at inte
214 odel specifically studies the effects of non-coding regions of DNA (in this case, CpG sites) on mappi
215 ential missense and other alterations in the coding regions of every IGF family gene, but the vast ma
216 relation to genetic variation in the protein-coding regions of five genes thought to be important in
217 evealed that RE are extensively spliced into coding regions of gene transcripts yielding thousands of
218 umber variants or point mutations in protein-coding regions of genes contribute to risk, and some of
219 ce of a regular chromatin structure over the coding regions of genes occurs co-transcriptionally via
220 ied 5hmC induction in putative enhancers and coding regions of genes that have pivotal roles in drug
222 hairpin RNAs (dual-shRNA) against different coding regions of HBV delivered by a self-complementary
223 r RNA duplexes, a depletion of duplexes from coding regions of highly translated mRNAs, an unexpected
224 ymous single nucleotide variants (nsSNVs) in coding regions of human genes frequently lead to patholo
226 somes in euchromatic regions, notably in the coding regions of long genes that were expressed at low
227 binding to the 5' untranslated and/or early coding regions of mRNA targets, causing changes in trans
231 exanucleotide expansions, GGGGCC, in the non-coding regions of the C9orf72 gene were found in major f
232 atistical approach to isolate coding and non-coding regions of the cancer genome that appear enriched
234 utations in PIGY can occur in coding and non-coding regions of the gene and cause variable phenotypes
235 s, aberrant enhancer element activity at non-coding regions of the genome is a key driver of tumorige
236 of disease pathogenesis confined to protein-coding regions of the genome may be incomplete because m
237 e contribution of regulatory and non-protein coding regions of the genome, we conducted aggregate tes
238 or somatic point mutations in coding and non-coding regions of the genome, we propose CScape, an inte
243 structural RNA motifs that occur in multiple coding regions of the HCV genome, and we demonstrate tha
244 and copy number variants (CNVs), in the non-coding regions of the human genome can play an important
245 especially chromosomal rearrangements in non-coding regions of the human genome, remains one of the b
249 RGG/RG motif bound G4 structures within the coding regions of the MLL1 and MLL4 mRNAs increasing the
250 cing, our method successfully identified all coding regions of the mouse picobirnavirus for the first
253 lly, basal histone acetylation levels in the coding regions of WRKY33, ORA59, and PDF1.2 are reduced
254 ene containing transcripts, possess long non-coding regions (often >45 kb) and remain chromatin bound
256 protein-centric standpoint; however, protein-coding regions only make up approximately 1% to 2% of th
259 efficiently link the effects of mutations in coding regions or promoter elements in a highly parallel
260 similar technology to deoptimize the capsid-coding region (P1) of foot-and-mouth disease virus (FMDV
261 tudy, a 606-bp fragment (comprising the pncA coding region plus the promoter) was sequenced using Ion
263 nsisting of an sgRNA adjoining a GFP protein coding region produced indels and viral-based GFP overex
264 We propose histone H3 acetylation in the coding region provides rate-limiting control during the
265 r two protein-coding genes and conserved non-coding regions putatively involved in replication and/or
270 atin domains, whereas H1X is associated with coding regions, RNA polymerase II-enriched regions, and
271 Their impact on retrotransposons in non-coding regions shed light on important aspects of mammal
274 mic regions and also showed that defined non-coding regions, such as first introns of genes and regul
275 ed evidence of rearrangements within the CTD coding region, suggesting that DNA instability may play
276 ssociation studies (GWAS), >90% occur in non-coding regions, suggesting a strong regulatory component
278 cluding the polyA tail), including 909 bp of coding region that encoded a polypeptide of 302 amino ac
280 ation study to discover germline variants in coding regions that affect risk for pancreatic cancer, c
282 s in sequences that are repeated within gene coding regions, thereby leading to the synthesis of neoa
284 dramatically increased diversity in the gene coding regions, though obvious blocks were formed on mos
285 plication element (CRE) from the polyprotein coding region to the 3' non-coding region we have furthe
286 ibution of both rare and common variation in coding regions to prostate cancer risk, we sequenced the
288 e translated upstream of the primary protein-coding region (uORFs) and 4% are translated downstream (
290 ntified four patients with MBL2 promoter and coding region variations associated with MBL deficiency
291 e show that editing levels in non-repetitive coding regions vary more between tissues than editing le
292 n, Setting, and Participants: The entire GBA coding region was screened for mutations and E326K in 74
293 of S. cerevisiae GAL promoter alleles or GAL coding regions was sufficient for partial reconstruction
294 the polyprotein coding region to the 3' non-coding region we have further developed a cell-based ass
295 in RNA (shRNA) targeted against the reporter coding region, we have characterized the dynamics of the
296 t mutations and a common risk variant in the coding region, we have identified an important contribut
297 h high CpG/UpA sequences inserted into a non-coding region were similarly replication defective.
299 ed accuracy in coding regions and 70% in non-coding regions, while even higher accuracy may be achiev
300 segment roughly follows that seen within the coding regions, with HLA-B showing the highest ( approxi
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