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1 R) and rare codons at the beginning of their coding sequence.
2 ranslated leader and the other is within the coding sequence.
3 in unique positions that did not disrupt the coding sequence.
4 ridine additions both reconstituting crucial coding sequence.
5  determine the impact of the mutation on the coding sequence.
6 s are corrected by reintroduction of a TgDCX coding sequence.
7 te translational derepression of the var2csa coding sequence.
8  allele causes a frame-shifted and truncated coding sequence.
9 tream from the start codon, or 1 kb into the coding sequence.
10 amoxifen-inducible Cre recombinase (CreERT2)-coding sequence.
11 utations in the Gag or reverse transcriptase coding sequence.
12 e transcription from the 3' end of the GAL10 coding sequence.
13 ribosome reinitiation at the downstream CHOP coding sequence.
14 AAV-PHP.B vector carrying the mouse Slc25a46 coding sequence.
15 equired for termination upstream of the ribD coding sequence.
16 or allele frequency of a SNP 3' of the GATA6 coding sequence.
17  the gradient, despite sharing most of their coding sequence.
18 iency increases p63gamma mRNA through APA in coding sequence.
19 , the second in-frame methionine of the TDP2 coding sequence.
20 and in the most conserved portion of protein-coding sequences.
21 d in association studies are located outside coding sequences.
22 ing control features embedded within protein-coding sequences.
23 opy repeats, most of which overlap predicted coding sequences.
24 reby leading to heterogeneity in base-editor coding sequences.
25 genes have been described, all targeting the coding sequences.
26 l tool for the genome-wide detection of AARS coding sequences.
27 rent 3' untranslated regions (3'UTRs) and/or coding sequences.
28 r to that affected by recurrent mutations to coding sequences.
29 create in-frame and frameshift insertions in coding sequences.
30 presentation for complex genomic regions and coding sequences.
31 ons and have the potential to change protein coding sequences.
32 uctures within the N-terminal regions of its coding sequences.
33 ining pause sites were identified in protein-coding sequences.
34 ed by the lack of recognizable mitochondrial coding sequences.
35  adds hundreds of uridines to create protein-coding sequences.
36 ead heterozygous structural variation within coding sequences.
37 ction of cases remain outside of single gene coding sequences.
38 ble to that of missense variation in protein-coding sequences.
39 ing from nutrient limitation shape microbial coding sequences.
40  fails to distinguish between coding and non-coding sequences.
41 haploidized to mask deleterious mutations on coding sequences.
42 d by a Foxp3 enhancer known as conserved non-coding sequence 1 (CNS1)(2-4).
43 including density of ribosomal footprints on coding sequences, 5' leader ribosomal densities, distrib
44  and estimate alpha = 0.135 in human protein-coding sequences, 72% of which is contributed by weakly
45 t adeno-associated virus containing the CRRY coding sequence (AAV-CRRY) into the subretinal space of
46 19-nCoV) RdRp (RNA-dependent RNA polymerase) coding sequence, achieving a detection limit of 0.4 fM w
47 art sites that were sometimes within protein-coding sequences, acquisition of polyadenylation sites,
48 tions are indeed conserved within homologous coding sequences across diverse eukaryotic, bacterial, a
49 fferent codon positions along a transcript's coding sequence affects this self-assembly process.
50                         More than 60% of the coding sequence alleles analyzed were previously unchara
51 which encodes a lung mucin and exhibits more coding sequence alleles than any HLA class I or II gene
52 ker than the selection on the same codons in coding sequences, although the switches between the codo
53 for animal evolution, our recent large-scale coding-sequence analyses from vertebrates and invertebra
54 ased on Freebayes and ExomeDepth to identify coding sequence and copy number variants, respectively,
55 on was found within the HvCslF6 promoter and coding sequence and does not explain variation in (1,3;1
56  evolutionarily plastic both at the level of coding sequence and expression across A. thaliana access
57 for miR-200c seed pairing in their 3'UTR and coding sequence and for genes that were downregulated by
58 f the C-terminal p63 isoforms through APA in coding sequence and mRNA translation and that the p63-PA
59 y genome-wide association studies map to non-coding sequence and their tissue-specific effects influe
60 th a correlation between m6A modification in coding sequences and enhanced translation, particularly
61 ng a combinatorial deletion approach of both coding sequences and enhancers, our work provides new in
62  genes with discernible recent ancestral non-coding sequences and evidence of translation.
63 occur in both protein-coding and non-protein-coding sequences and generate missense, nonsense, splice
64 iptomes (for 27 species in total), predicted coding sequences and identified single copy orthologues
65 ase deletions is preferentially increased in coding sequences and in short rather than long mononucle
66 wn role in ribosomal (rRNA) processing, many coding sequences and intergenic regions appeared to be d
67 c-rearrangement mutational process affecting coding sequences and noncoding regulatory elements and c
68 rrelated with increases in mutation rates in coding sequences and regulatory regions.
69 including disease-linked variants in protein-coding sequences and variants with trans regulatory effe
70 376 other individuals, we identified 244,246 coding-sequence and splice-site ultra-rare variants (URV
71 c copy number can influence gene expression, coding sequence, and zygosity, making them powerful acto
72 in the transcripts of many genes, notably in coding sequences, and identify consensus sites for hydro
73  the translational start codon, depletion in coding sequences, and mixed patterns of enrichment in th
74 l densities, distribution of ribosomes along coding sequences, and ribosome codon occupancies.
75 ty patterns and coverage similarities across coding sequences, and showed that they yield comparable
76 ranslated region between the M and F protein coding sequences, and shown that, for more than half the
77  related species, evidence for ancestral non-coding sequences, and transcription and translation of t
78 vast majority of these novel contigs possess coding sequences, and we have validated their existence
79 ximately 6%), and a high fraction of protein-coding sequence ( approximately 39%) with relatively lon
80          When the regions flanking the miRNA coding sequence are highly methylated, the miRNAs are mo
81 ve in current studies, genes whose wild-type coding sequences are needed for tumor growth are also of
82 ary transcripts of eukaryotic nuclear genes, coding sequences are often interrupted by U2-type intron
83 ensure all single point mutations in protein-coding sequences are selected against while maintaining
84  itself such that point mutations in protein-coding sequences are selected against.
85  create random nucleotide sequences, protein coding sequences are subject to a unique set of constrai
86                       Frameshifts in protein coding sequences are widely perceived as resulting in ei
87   MNase HS regions are therefore on par with coding sequences as annotations that demarcate the funct
88 ae and I. pulchra genomes have many long non-coding sequences between genes, likely driving genome si
89 xpression units, avoiding scars at sensitive coding sequence boundaries.
90 delaying modifier signal does not alter FAN1 coding sequence but is associated with increased FAN1 mR
91  inhibitors that target ribosomes within the coding sequence but not those targeting newly initiated
92 udes not only the duplication or deletion of coding sequences, but also the perturbation of noncoding
93 ally, Rho promotes termination at the end of coding sequences, but it can also terminate transcriptio
94                                     We found coding sequence can affect IME; the same three synthetic
95 ion of an mRNA, despite carrying a canonical coding sequence, can directly cause gene repression.
96 (ORF) of the target gene which truncates the coding sequence (CDS) and targets the corresponding tran
97 a unit from which the extant repetitive AFGP-coding sequence (cds) arose through tandem duplications.
98                    Mechanistically, the pchA coding sequence (CDS) base pairs with the 5' untranslate
99 assessed 24 SNPs located in the 3'UTR or the coding sequence (CDS) of targets.
100 nservation was lost mostly downstream of the coding sequence (CDS), indicating the presence of high s
101 xpressed mRNAs contained a highly structured coding sequence (CDS).
102 icrobial community by cataloging the protein-coding sequences (CDS) present in the metagenome of the
103               Cryptic polyadenylation within coding sequences (CDS) triggers ribosome-associated qual
104     931,698 reads were annotated into 11,676 coding sequences (CDS), which were manually curated into
105 ducing > 190,000 contigs, identifying 18,857 coding sequences (CDS).
106         We find that uORFs are depleted near coding sequences (CDSes) and have initiation contexts th
107 sis of 5'-truncated mRNA ends that mapped to coding sequences (CDSs) of Arabidopsis thaliana, rice (O
108 latory sequences and using native microalgal coding sequences (CDSs) with higher GC content improved
109 s (altORFs) in addition to annotated protein coding sequences (CDSs).
110 aracterized translation outside of canonical coding sequences (CDSs).
111  result from initial non-functionality, with coding sequence changes unnecessary.
112  therefore the requirements for and order of coding sequence changes, expression changes, or gene dup
113  synonymous coding and 2 were non-synonymous coding sequence changes.
114 driven in part by variation in conserved non-coding sequences (CNS).
115    Here we present a protocol for generating coding-sequence-complete genomes, comprising an online p
116 s between the serogroup Y sublineages of all coding sequences, complex genomic regions, intergenic re
117 led CRISPR screening to disrupt NuRD protein coding sequences comprehensively in human adult erythroi
118                                     The AT1R coding sequence contains over 100 nsSNPs; therefore, thi
119 vergence (particularly of highly constrained coding sequence) contributes to convergent phenotypic ev
120 whereas alternative polyadenylation (APA) in coding sequence creates two more C-terminal isoforms p63
121 pinpointing risk factors of disease from non-coding sequence data.
122  in the gland rather than gene death through coding sequence degradation.
123 ted with p16 silencing in the absence of p16 coding sequence deletion and MAX induction restores p16
124 t interact in three dimensional space, while coding sequence duplicates are rare, GC-rich, short, and
125 identify the disruption of exon-proximal non-coding sequences (e.g., the promoter) as functionally co
126 ient function for ATHs and demonstrates that coding sequence evolution can underlie quantitative vari
127                         However, the role of coding sequence evolution remains unresolved.
128 al start codon while the bulk of the protein-coding sequence evolved through a CAG repeat expansion.
129 an clock-dependent AS by binding to exons at coding sequences flanking exons that are more frequently
130 tified an unusual gene in Apicomplexa with a coding sequence for membrane-docking and structure-speci
131  portion of RNA1 5' UTR but extends into the coding sequence for nine nucleotides, thus was missed in
132 n, and the distal part of ALK, including the coding sequence for the entire kinase domain.
133           Because of negative selection, the coding sequence for the prothrombin-binding D1-D2 domain
134 deno-associated viral vectors to deliver the coding sequence for Transmembrane Channel-Like (Tmc) 1 o
135 have leveraged this technology to delete the coding sequences for a known type III effector.
136 or 99% of IMD isolates, including those with coding sequences for MnB, MnC, MnW, and MnY, and the phe
137 -associated virus serotype 10 expressing the coding sequences for the CLN2 gene implicated in late in
138 at specific positions in a set of homologous coding sequences, for example to tune translation rate w
139 o GPA was overcome by expression of the ADF3 coding sequence from the phloem-specific SUC2 promoter,
140 manized for BCRP (hBCRP), in which the mouse coding sequence from the start to stop codon was replace
141 ble and can be warmed-up (gene promoters and coding sequences), from those that remain refractory (ge
142 g domains (MBDs) were deleted from the ATP7B coding sequence, giving rise to the miniATP7B protein (D
143                  HDR-mediated insertion of a coding sequence (green fluorescent protein or CD40L) ups
144 arasite lines, where the P. berghei csp gene coding sequence has been replaced with either full-lengt
145                                          Its coding sequence has further been maintained during all o
146 le for synonymous rare codons farther within coding sequences has not yet been established, several r
147            Rare codons at the 5' terminus of coding sequences have been shown to increase translation
148   Translated regions distinct from annotated coding sequences have emerged as essential elements of t
149 ls built on Arabidopsis thaliana genes or 2) coding sequence homology searches using curated database
150            Analysis of transcription outside coding sequence identifies deregulation of repetitive el
151 ally characterize how these de novo emerging coding sequences impact fitness in budding yeast.
152  Our results support a model in which a uORF coding sequence impacts its regulatory functions by alte
153  analyzed the genetic variation in the FOXP2 coding sequence in 63 chimpanzees, 11 bonobos, 48 gorill
154 through binding at the N-terminal amino acid coding sequence in EXT2 mRNA.
155 coding gene and tRNA overlap with little non-coding sequence in the compact P. rubra genome.
156 osine (m6dA) accumulates along promoters and coding sequences in activated prefrontal cortical neuron
157 y polynucleotide and were located within the coding sequences in both wild type and degradosome mutan
158  supports the role of common variants in non-coding sequences in influencing complex phenotypes throu
159 ed as de novo orphans by tracing them to non-coding sequences in related species.
160 arge number of GGDEF proteins, nearing 1% of coding sequences in some cases, raises the question of w
161                        Comparison of FtsZ2-2 coding sequences in the 1001 Genomes database showed tha
162 leotide tails were mostly located within the coding sequences in the degradosome mutants compared to
163  results shed light on the importance of non-coding sequences in the evolution of the S-locus, and on
164 ic selection coefficients across all protein-coding sequences in the human genome.
165 P mutations are, however, relatively rare in coding sequence, in part because RIP preferentially atta
166               Yet surprisingly, many protein coding sequences include large clusters of synonymous ra
167 lastoid cell lines, we identified 7273 novel coding sequences, including 2442 translated upstream ope
168                              Each gene has a coding sequence insertion/deletion mutation within the S
169 e demonstrate that both gene disruptions and coding sequence insertions are efficiently generated, pr
170 rimarily associated with target sites within coding sequences instead of 3'UTRs.
171 election, followed by integration of the tag-coding sequence into the endogenous locus in zebrafish.
172 o start and stop codons are used to assemble coding sequences into expression units, avoiding scars a
173 e hybrid fragment containing these human non-coding sequences into the mTert locus in mouse embryonic
174 Small non-coding RNAs (ncRNAs) are short non-coding sequences involved in gene regulation in many bio
175      Sequence analysis revealed that the VP2-coding sequence is considerably conserved among FMDV ser
176 f ALAS2 expression, indicating that this non-coding sequence is indispensable for ALAS2 expression in
177 ity and/or translation, while changes in the coding sequences lead to mRNAs encoding distinct protein
178 ve ribosome pausing within the DENV envelope coding sequence, leading to enhanced protein stability.
179 s flanking the initiating AUG codon, protein coding sequence length, and codon usage.
180 vast majority of them are located outside of coding sequences, making it challenging to directly inte
181 However, most of these variants do not alter coding sequences, making it difficult to assign their fu
182 es upstream of the green fluorescent protein-coding sequence markedly reduces the levels of gfp mRNA
183 ntly in cis with the WT allele than the TERT coding sequence mutation.
184          Unexpectedly, the majority of these coding sequence mutations appear not to be the direct pr
185                                 Insulin gene coding sequence mutations are known to cause mutant INS-
186 trains have over an order of magnitude fewer coding sequence mutations outside of duplicated domains
187                    Despite this, with over 5 coding sequence mutations per genome per generation, the
188 n people, with risk variants enriched in non-coding sequences near chondrocyte genes, loci that likel
189    In familial MDS/AML, mutations change the coding sequence of a gene to generate a mutant protein w
190    We then use genome editing to disrupt the coding sequence of a S. rosetta C-type lectin gene, rose
191 l II into transcriptional elongation) to the coding sequence of an active gene, ADH1, independently o
192 vigilin binds to CU-rich regions in the mRNA coding sequence of Apob and other proatherogenic secrete
193  showed that miR-K6-5p directly targeted the coding sequence of CD82 molecule (CD82), a metastasis su
194                                          The coding sequence of CDH3 fits within the packaging limit
195 ucing an in-frame nonsense mutation into the coding sequence of Cre recombinase (nsCre).
196 ort the notion that SNPs in the 3'UTR or the coding sequence of disease-relevant genes may be importa
197                                          The coding sequence of each human pre-mRNA is interrupted, o
198      We show that the transgenes disrupt the coding sequence of endogenous genes in half of the lines
199 nce to missense variation within the protein-coding sequence of genes.
200 eotides, so-called polyA tracks, to the gene coding sequence of interest will decrease translation el
201 ion because overexpression of a noncleavable coding sequence of MYB83 significantly increased plant s
202 fied a number of mutations within the capsid-coding sequence of poliovirus (PV) that were established
203                           A variation in the coding sequence of SlHAK20 was found to be the causative
204 epletion, especially at the beginning of the coding sequence of SMN-specific mRNAs, leading to impair
205 s suggest the existence of an IRES in the 5' coding sequence of TDP2 that translationally regulates e
206 genotype-phenotype differences more than the coding sequence of the fusion gene created.
207 sing a lentivirus containing the full-length coding sequence of the human NR2B subunit.
208  c.1750G > A; p.Gly584Ser variant within the coding sequence of the KCNH2 gene implicated in Long QT
209 apping peptide libraries spanning the entire coding sequence of the norovirus genome.
210  other than previously reported deletions at coding sequence of the ORF8 (open reading frame), spike,
211 The binding site within the beginning of the coding sequence of the prfA gene, which encodes the mast
212                          Changes in both the coding sequence of transcriptional regulators and in the
213 e largest dataset tested, which included all coding sequences of 100 bacterial species.
214 diting and used these discoveries to correct coding sequences of 174 pathogenic transversion SNVs wit
215       Consistently, San1 associates with the coding sequences of active genes to regulate Spt16's abu
216 ntron or when introduced into the 5'-UTR and coding sequences of an intronless construct, demonstrati
217 d by inserting sex-specific introns into the coding sequences of antibiotic-resistance genes.
218 s model is based on mutations in the protein-coding sequences of clock genes.
219 ll-known mutagen, has been maintained within coding sequences of crucial plant and animal genes.
220 r role in fruit ripening in more detail, the coding sequences of FvXTH9 and FvXTH6 were cloned into t
221 nes as well as between selection pressure on coding sequences of genes and their cold responsiveness.
222 led abundant genetic variation affecting the coding sequences of human transcription factors (TFs), b
223  both in promoter regions and throughout the coding sequences of many genes and is particularly enric
224 affecting all parts of the genome, including coding sequences of mating behavior-related genes.
225 egion from within LUR, containing the entire coding sequences of ORF50-encoding reactivation transact
226 fy an average of 14+/-5 somatic mutations in coding sequences of sorted monocyte DNA and the signatur
227 an diseases can be made by exploring the non-coding sequences of the human genome.
228 the potential impact of mutations on the DNA coding sequences of these targets, and compare these res
229 raction reporter to intracellularly fuse the coding sequences of two interacting proteins and next-ge
230 ences on the papaya X chromosome and protein-coding sequences on the S. latifolia X chromosome, our m
231                 Thus, the importance of uORF coding sequences on their regulatory functions remains l
232       Some elements have preferences for non-coding sequence or for the beginning and end of coding r
233 nor the implications of DTU on their protein coding sequences or functions, are currently well unders
234              We provide evidence for a novel coding sequence, ORF-Y, that overlaps the POLG ORF.
235 ion-elongation kinetics along a transcript's coding sequence plays an important role in the maintenan
236 on targeting, and also incorporates domains, coding sequence position, U6 termination (TTT), restrict
237  encode multiple, often undescribed, protein-coding sequences, potentially increasing the diversity o
238 y activating transcription, altering protein-coding sequences, producing noncoding RNAs, and even sup
239  ligands and receptors exhibit similarity of coding sequences, protein structures, and chromosomal po
240                 SgrS binding within the purR coding sequence recruits the RNA chaperone Hfq to direct
241 on of gene structure by using the lengths of coding sequence regions and dinucleotide percentages to
242 s located adjacent to UGA codons, additional coding sequence regions necessary for efficient producti
243 r have largely focused on genes, whereas non-coding sequences remain relatively unexplored.
244 -fold repetitive B1 gene, and more recently, coding sequence Rep 529 has been preferred, as it was re
245     We hypothesise that these modules in non-coding sequence represent distinct cis-regulatory loci t
246                  ATHs and the ancestral-like coding sequences rescued sensory organ fate in atonal mu
247 ce genes that do not disrupt the target gene coding sequence, resulting in easy and flexible gene tag
248 orA) or no T (porA) at the 3' end of the gfp coding sequence revealed that both the transcript level
249       Phylogenetic analysis of mitochondrial coding sequences revealed accelerated rates of sequence
250 re, variants creating uORFs that overlap the coding sequence show signals of selection equivalent to
251 opsis thaliana lines expressing the effector-coding sequence showed altered expression levels of defe
252             Further analysis of the AraEXLB8 coding sequences showed high conservation across the Ara
253        More than 75% of these 104 genes have coding sequences small enough to be packaged efficiently
254                    To remove rRNA and enrich coding sequences, subtractive hybridization procedures h
255 NA identified several mutations in the opsin coding sequence, suggesting the loss of cone cell functi
256 iolate these parametric assumptions for such coding sequences, suggesting that a non-parametric appro
257 er, we show that when placed downstream of a coding sequence, sxRNA can be used to switch "ON" transl
258 ating more relaxed constraint on the FtsZ2-2 coding sequence than on those of FtsZ2-1 or FtsZ1-1 Our
259 re uncharacterized and encompass one or more coding sequences that are actively transcribed.
260 rmatic analyses to identify putative protein-coding sequences that are specific to mosquito genomes.
261  3'UTRs that results in species-specific non-coding sequences that may contribute to bacterial divers
262 est that in addition to allelic variation of coding sequence, the heterogenous nature of the tetraplo
263                     In comparison to protein coding sequences, the impact of mutation and natural sel
264                          Compared to protein coding sequences, there are many challenges associated w
265                                       In the coding sequence, these mutations are found in multiple l
266             Although SMN2 maintains the same coding sequence, this gene cannot compensate for the los
267 mutant mice reconstituted the otoferlin cDNA coding sequence through recombination of the 5' and 3' c
268 e resolution of sexual conflict over protein coding sequences, thus contributing to the long-term mai
269 en the TMPRSS2 promoter sequence and the ERG coding sequence (TMPRSS2:ERG) in urine, noninvasive scre
270 o acid change in the hexose transporter HXT7 coding sequence to be responsible for the evolved phenot
271 earrangement of the TERT gene juxtaposes the coding sequence to strong enhancer elements, leading to
272  the Waxy1 chloroplast targeting the peptide coding sequence to the Pgd1 and Pgd2 open reading frames
273 ession and the contribution of a 3' terminal coding sequence to this process.
274  of Cpf1 by approximately threefold in human coding sequences to one cleavage site per approximately
275 dentified by in silico changing the C57BL/6J coding sequences to the SPRET/Ei sequences, converting t
276 ith the AXR1 promoter and either AXR1 or AXL coding sequences) to further study the extent of functio
277                                  Compared to coding sequences, untranslated regions of the transcript
278                             A non-synonymous coding sequence variant (c.2 T > C; p.1Met?) found in VD
279                                          Two coding sequence variants in the APOL1 gene (G1 and G2) e
280 erized RP were completely screened for TRNT1 coding sequence variants, and a second family was identi
281     Through DNA genotyping, we tested 54,003 coding-sequence variants covering 13,715 human genes in
282                             We show that non-coding sequence variation at the FRO2 locus leads to var
283  emerging findings regarding the role of non-coding sequence variation offer opportunities for unders
284 ic specificity, and interprets the action of coding sequence variations in proteins, people and popul
285                            Drosophila atonal coding sequence was endogenously replaced with that of a
286  gene-targeting approach where the mouse PrP coding sequence was replaced with elk or deer PrP, we sh
287 uced ribosome accumulation on the 5' side of coding sequences was cycloheximide-dependent.
288 fected by recurrent mutations disrupting non-coding sequences was similar to that affected by recurre
289 ed on Jug r 1, Jug r 3, and Jug r 4 allergen-coding sequences, was set up and validated.
290 1 RNA element that partially overlaps the PR coding sequence, we identified a novel function of the P
291 om which fragment antigen-binding nucleotide coding sequences were cloned as a single chain into a le
292 al genome and nuclear intergenic and protein-coding sequences were obtained by direct sequencing of g
293 tional ability of a luciferase reporter gene coding sequence when it is preceded by multiple tyrosine
294 d rare SVs that disrupt or duplicate protein-coding sequence, which suggests that genes that are high
295  erroneously annotated as containing protein-coding sequences, which over time have propagated to cre
296 a specific fragment of the Sola l 7 allergen coding sequence with appropriate RNA probes designed and
297 rooxidans species comprising of 6926 protein coding sequences with 23.04% (1596) core genes, 46.13% (
298  (>=99.4% shared core genome, >=99.6% shared coding sequence) with priority AMR were found in birds o
299 8) per base pair per generation in autosomal coding sequence, with a corresponding non-crossover gene
300 atial orientation of regular repeats of rDNA coding sequences within the nucleoli.

 
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