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1 ct regions along approximately 600 bp of the regulatory sequence.
2 ression in mammalian organisms directly from regulatory sequence.
3 on by blocking access of other RBPs to a key regulatory sequence.
4 nding the mutation define an uncharacterized regulatory sequence.
5 of transcriptional regulation by a specified regulatory sequence.
6 gh a canonical DSX-binding site in the Fmo-2 regulatory sequence.
7 ations of single-nucleotide polymorphisms at regulatory sequences.
8 NAs with retrotransposons and pseudogenes as regulatory sequences.
9 fications, particularly methylation of their regulatory sequences.
10 A activity in vivo and also identifies novel regulatory sequences.
11 rexpress Dyrk1a under the control of its own regulatory sequences.
12 ion in other neurons is mediated by separate regulatory sequences.
13 te TFL1 mimic, even when expressed from TFL1 regulatory sequences.
14 ssion by direct and specific binding to gene regulatory sequences.
15 cilitates interactions between transcription regulatory sequences.
16 ence of polycomb at a subset of CG-dense cis-regulatory sequences.
17 nvolve protein-coding genes, as well as gene regulatory sequences.
18 oters, suggesting an overlap with endogenous regulatory sequences.
19 ing SOC1 heterodimers, are able to bind SOC1 regulatory sequences.
20 e H3K9acS10ph and H3K27acS28ph marks at both regulatory sequences.
21 o produce a map of nearly 300,000 murine cis-regulatory sequences.
22 equence conservation and genomic function of regulatory sequences.
23 ent epigenomic marks can be used to discover regulatory sequences.
24 f target human genome loci such as exons and regulatory sequences.
25 t with DNA have distinct preferences for cis regulatory sequences.
26  expression is controlled by endogenous zeta regulatory sequences.
27 lates independently of the nature of the cis-regulatory sequences.
28 tic MADS domain proteins appear to bind SOC1 regulatory sequences.
29 ly to be the outcome of neutral variation in regulatory sequences.
30 e-scale libraries of systematically designed regulatory sequences.
31 ere wired together by a vast spectrum of cis-regulatory sequences.
32 s technique as a nonbiased screen to isolate regulatory sequences.
33 ts ability to confer this property to linked regulatory sequences.
34 a DNA-BP, to identify putative FOXO1 genomic regulatory sequences.
35 n of the Prmt4 substrate, H3R17, at microRNA regulatory sequences.
36 rry out a genetic analysis of their upstream regulatory sequences.
37 ely in neurons expressing TH transcriptional regulatory sequences.
38 hed by transcription factor (TFs) binding to regulatory sequences.
39 ctions between Drosophila TFs and target cis-regulatory sequences.
40 actions and the specific genomic position of regulatory sequences.
41 the binding of transcription factors to gene regulatory sequences.
42 ing regions, splicing junctions and splicing regulatory sequences.
43 neocortex may involve the evolution of novel regulatory sequences.
44 utations in splice factors, splice sites, or regulatory sequences.
45  with beta-catenin displaced TCF4 from MMP13 regulatory sequences.
46 vertebrate genomes and the function of human regulatory sequences.
47 e binding and functionality of the predicted regulatory sequences.
48  the coordinates of core promoters and other regulatory sequences.
49 nteractions may serve as a marker for active regulatory sequences.
50                  Two of them, named silencer regulatory sequence 1 (SRS1) and SRS2, are located on a
51 sed of Swi4 and Swi6) in the 700-bp upstream regulatory sequence 2 (URS2) promoter region.
52 (TEs) are uniquely equipped to deposit their regulatory sequences across a genome, which could also c
53 t manner and relies on gain/loss of splicing regulatory sequences across the exons.
54 ransposon transcripts, suggesting a class of regulatory sequences acting in trans.
55 asts within anterior fin rays, whereas hand2 regulatory sequences activated expression in these same
56 ease-associated SNPs, appears to behave as a regulatory sequence, affecting the expression of a neigh
57 sative polymorphisms occurring in coding and regulatory sequences alike.
58                                        RSAT (Regulatory Sequence Analysis Tools) is a modular softwar
59                       Although developed for regulatory sequence analysis, these methods can be appli
60 tory elements including a stem-cell specific regulatory sequence and an element that drives reporter
61 , the analysis of the role of a specific DNA regulatory sequence and the interacting proteins in the
62 comprehensive understanding of TF binding to regulatory sequences and allows the characterization of
63                    Hypomethylation of ZNF423 regulatory sequences and BMP2 signaling result in transa
64 ining 30% of all genes that are enriched for regulatory sequences and depleted for genes involved in
65 se of epigenome maps to delineate human gene regulatory sequences and developmental programs.
66                        Accurately predicting regulatory sequences and enhancers in entire genomes is
67 ually all known experimentally validated cis-regulatory sequences and expose a vast trove of novel el
68 ta identify thousands of prospective cardiac regulatory sequences and indicate that multiple TF co-oc
69 es that have been played by many plant-viral regulatory sequences and proteins in the creation of pla
70 harbors essential noncoding RNAs, promoters, regulatory sequences and replication origins.
71   We examine changes in constraints on known regulatory sequences and show that for the Rck1/Rck2, Fk
72 as well as the overlaps with exons, putative regulatory sequences and single-nucleotide polymorphisms
73 gene regulation that restrict access to both regulatory sequences and the underlying template.
74 re assumed to be determined primarily by DNA regulatory sequences and their associated activators, wh
75 ng of interactions between individual distal regulatory sequences and their target genes.
76         Transcription regulators bind to cis-regulatory sequences and thereby control the expression
77 ful platform to develop predictive tools for regulatory sequences and to study their sequence propert
78                                 Diversifying regulatory sequences and using native microalgal coding
79    The ProxTom transgene contained all Prox1 regulatory sequences and was faithfully expressed in LVs
80 rious [5% versus 0.4%] but not more often in regulatory sequences), and certain disease classes.
81 on requires direct binding of TTX-1 to ver-1 regulatory sequences, and is induced in dauers and at hi
82 by exploiting the cryptic activity of extant regulatory sequences, and this may reflect a general mec
83  smaller evolutionary distance) that its cis-regulatory sequence appears unrelated in different speci
84 n and out of regulons through changes in cis-regulatory sequences appears to be a general phenomenon.
85 types to identify which particular genes and regulatory sequences are causal.
86 ets and the binding motifs in associated cis-regulatory sequences are dispersed throughout the hierar
87 slational fusions and to ensure that all cis-regulatory sequences are included, we have used a bacter
88  all eukaryotic species, promoters and other regulatory sequences are more nucleosome-depleted, where
89 rlap is not coincidental; retrovirus-derived regulatory sequences are often used to control cellular
90 ment in which a library of partially mutated regulatory sequences are partitioned according to their
91  non-coding region, indicating that proximal regulatory sequences are sufficient for HPRT1 expression
92  provide evidence that rearrangements in the regulatory sequences around egr4 and mafb genes may acco
93  to UCUAUC in the context of unc-52 intronic regulatory sequences as well as to RNAs containing tande
94 ection correlate better with the presence of regulatory sequences, as predicted by the ENCODE Project
95         Our results demonstrate changes in a regulatory sequence associated with a major body plan tr
96                                              Regulatory sequences at DPP10 and additional loci carrie
97 ations located in cis-acting transcriptional regulatory sequences at the gene junctions of the genome
98 d, a flexible SVM workflow that predicts new regulatory sequences based on the annotation of known CR
99 , or 'unintelligibility', of orthologous cis-regulatory sequences between Molgula and Ciona.
100 mputational RNA-folding landscape as well as regulatory sequence binding data treated with the same f
101 tations identified create cryptic cis-acting regulatory sequence binding sites that drive aberrant OV
102  not alter MyoD binding at myogenic microRNA regulatory sequences but prevents the binding of both my
103 ion are associated with the evolution of cis-regulatory sequences, but it is not known how temporal r
104  sharp peaks at gene promoters and other cis-regulatory sequences, but molecular and cellular phenoty
105                             We show that the regulatory sequences, but not other regions of genes exp
106  thought to be tightly coupled to changes in regulatory sequences, but specific molecular events asso
107 hundreds of thousands of tissue-specific cis-regulatory sequences, but the determinants critical to t
108 coupled with SpDamID reveals co-targeting of regulatory sequences by Notch and Runx1.
109 eering approaches to computationally predict regulatory sequences by using comparative genomics.
110 prinkled throughout the genome are a million regulatory sequences called transcriptional enhancers th
111 nstrate that even a severely constrained cis-regulatory sequence can be significantly rewired over a
112 ructs can increase the efficiency with which regulatory sequences can be assayed, restricting analysi
113    Our data indicates that ancient conserved regulatory sequences can be tested effectively in transg
114 sly thought and that seemingly unrelated cis-regulatory sequences can nonetheless be homologous.
115                Specific DNA demethylation of regulatory sequences can result in upregulation of genes
116 in the methods for discovery of putative cis-regulatory sequences, characterisation of their spatio-t
117 od and combines these with allele frequency, regulatory sequences, chromosomal topological domains, a
118 sed approach to identify frequently used cis-regulatory sequence combinations in the promoter sequenc
119                  In addition, with known cis-regulatory sequence combinations, gene function annotati
120 and selection have shaped variation in a cis-regulatory sequence controlling gene expression by empir
121 these two species, little is known about the regulatory sequences controlling hand2 expression in zeb
122           Together, our results identify new regulatory sequences controlling IE1 and IE2 expression
123             The majority of known TE-derived regulatory sequences correspond to relatively ancient in
124 TCP20 targets, and binding of TCP20 to their regulatory sequences could be confirmed by chromatin imm
125 rthermore, several uncharacterized genes and regulatory sequences demonstrated convergence and thus c
126                       HSV-1 contains no such regulatory sequences, demonstrating different mechanisms
127 ion alteration in cancer cells of the distal regulatory sequences described as super-enhancers.
128  let us use comparative genomics to identify regulatory sequences directing expression in the DVA int
129 e1, H3K27ac, H3K4me3 and H3K9ac), active cis-regulatory sequences (DNA hypersensitivity sites (DHS)),
130            We further demonstrate that adt-2 regulatory sequences drive expression in glial-like and
131                                         nope regulatory sequences drive reporter gene expression in g
132            In BAC transgenic zebrafish, cav1 regulatory sequences drove strong expression in ostensib
133 tion at this site is inhibited by a negative regulatory sequence element, and potentially by the H-NS
134 controlled by proteins that bind directly to regulatory sequence elements and either activate or repr
135 h the transcription factors binding to these regulatory sequence elements and their ability to recrui
136 e caused by mutations in splicing signals or regulatory sequence elements, recent studies have noted
137 which have identical open reading frames and regulatory sequences-encode functional toxin-antitoxin s
138 s in gene expression due to mutations in cis-regulatory sequences (enhancers).
139 protein (GFP)-KOR1 expressed from its native regulatory sequences established that all eight N-glycos
140 ata to computationally identify relevant cis regulatory sequences flanking syn-expressed genes in the
141  distantly related ERVs have been exapted as regulatory sequences for many host genes in a wide range
142              We propose a model in which the regulatory sequences form a hydrophobic core that recipr
143              Our genome-wide Foxa1-bound cis-regulatory sequences from ChIP-Seq and Foxa1/2 candidate
144         We further demonstrate how different regulatory sequences give rise to nucleosome-mediated TF
145 duced (Scr) is directed by an unusually long regulatory sequence harboring diverse cis elements and a
146  regions of noncoding DNA for functional cis-regulatory sequences harboring variation implicated in c
147  novel transgenic rodent model in which Zeb2 regulatory sequence has been disrupted, resulting in a p
148                    Removing nucleosomes from regulatory sequences has been proposed to play a signifi
149                        A large number of cis-regulatory sequences have been annotated in the human ge
150                                      Two cis-regulatory sequences have been identified upstream of th
151                                  Millions of regulatory sequences have been predicted in the human ge
152                                        A cis-regulatory sequence here corresponds to a DNA motif boun
153 ty arises from the coordinated action of two regulatory sequences: (i) a WASP homology 2 (WH2) domain
154                  Moreover, the wealth of new regulatory sequences identified here provides an invalua
155  therefore identified GARRPR as a novel BF-3 regulatory sequence important for fine-tuning the activi
156                   Purified Bil1 bound to the regulatory sequence in Bud6 and triggered NPF effects on
157 t rs2237895 influenced methylation levels of regulatory sequence in fetal pancreas but without demons
158 nd characterize natural variation in the cis-regulatory sequence in the transcription factor CONSTANS
159  immunoprecipitation, STAT1 bound a putative regulatory sequence in the ULK1 5'-flanking region, the
160 oximately 6.9 kb MIR137/MIR2682 and upstream regulatory sequences in 2,610 SZ cases and 2,611 control
161 chloroplast genomes, the number of known DNA regulatory sequences in chloroplast genomes are limited.
162 s proven to be a powerful method for mapping regulatory sequences in cultured cells, chromatin states
163                      However, the cis-acting regulatory sequences in DE and L genes that mediate thei
164 gration, LedPred excels at the prediction of regulatory sequences in Drosophila and mouse datasets co
165 methods to systematically study putative DNA regulatory sequences in intergenic regions near chloropl
166 d comprehensive identification of functional regulatory sequences in mammalian genomes remains a majo
167 equencing, we would like to quickly annotate regulatory sequences in newly-sequenced genomes.
168 use genome have yet to be found, and the cis-regulatory sequences in particular are still poorly anno
169 d describe how core protein circuits and cis-regulatory sequences in promoters integrate with chromat
170  program, as evidenced by induction of gata4 regulatory sequences in regenerating cardiomyocytes.
171  opposes Gli1 activity by binding cis-acting regulatory sequences in the 5' flanking regions of Snai1
172 id not change the DNA-methylation pattern of regulatory sequences in the caspase-8 gene.
173 on factors are adaptor molecules that detect regulatory sequences in the DNA and target the assembly
174 IKE1 (PHL1) were identified to bind to P5CS1 regulatory sequences in the first intron, which carries
175 d discovery and functional assessment of cis-regulatory sequences in the genome.
176 rial ribosomal protein S12 (MRPS12), contain regulatory sequences in their 3'-untranslated region (UT
177 ential of MYC stems from its ability to bind regulatory sequences in thousands of target genes, which
178 ive/repressive function of SMARCA4 at distal regulatory sequences in vivo and support its role in tis
179 show that Hnf1b occupies novel Ngn3 putative regulatory sequences in vivo.
180 , the BAG-1-p50 complex was detected at gene regulatory sequences including the epidermal growth fact
181 , revealed MEF2C motif enrichment within cis-regulatory sequences, including neuron-specific promoter
182 e widespread loss of cytosine methylation at regulatory sequences, including promoter regions of prot
183 ion and contains at least three required cis-regulatory sequences, including the 10-bp motif (5'-GAAA
184 ge part, on the activation and repression of regulatory sequences, including transcriptional enhancer
185 ne the positions from which certain intronic regulatory sequences increase mRNA accumulation, the eff
186 nhibited ERalpha, but not PR binding to both regulatory sequences, indicating that an interaction bet
187                            Understanding how regulatory sequences interact in the context of chromoso
188 ons, and the other subset subdivides the Scr regulatory sequences into independent enhancer access do
189 n FGF19 (ortholog to mouse Fgf15), including regulatory sequences, into the FRGN mice to create FRGN1
190  both biased codon usage and conservation of regulatory sequences involved in mRNA processing, althou
191 ng-distance enhancers is orchestrated by DNA regulatory sequences involving transcription factors and
192 fic single CpG dinucleotide in the ZAP-70 5' regulatory sequence is a highly predictive and reproduci
193    Binding of transcription factors (TFs) to regulatory sequences is a pivotal step in the control of
194 Elucidating the function of highly conserved regulatory sequences is a significant challenge in genom
195                          Activation of gata4 regulatory sequences is also prevented by NF-kappaB sign
196    Prediction of gene expression levels from regulatory sequences is one of the major challenges of g
197 ediction of gene expression levels driven by regulatory sequences is pivotal in genomic biology.
198 antitatively predict TF binding to different regulatory sequences is still limited.
199                               Although these regulatory sequences likely arose in ancient viruses, th
200 H20 or SLC28A3, suggesting that variation in regulatory sequences may affect expression.
201     Characterization of these five PPARgamma regulatory sequences may enable isolation of the transcr
202                                  A conserved regulatory sequence module attached to the AAA+ helicase
203                        The identification of regulatory sequence motifs and the characterization of s
204 gly appreciated that coding sequences harbor regulatory sequence motifs in addition to encoding for p
205  that distinct epigenetic signatures and cis-regulatory sequence motifs predicted to bind putative co
206 ions and 96% of these regions contained NRF2-regulatory sequence motifs.
207 ke; NFE2L2) binding to deoxyribonucleic acid-regulatory sequences near stress-responsive genes.
208 represses excitatory cell fate by binding to regulatory sequences near the Tlx1 and Tlx3 genes to sil
209                     Finally, we observe that regulatory sequences occur at genomic locations correspo
210 nstructed pVASpf containing pf linked to the regulatory sequence of medaka germ gene vasa and generat
211 translocate into adjacent cells, bind to the regulatory sequence of Nkx3.1 target genes and impact th
212 rent DNA methylation patterns within the cis-regulatory sequence of the agn43 gene turn on or off a f
213 ator-1, and RNA polymerase II binding at the regulatory sequence of the SCNN1A gene and also remarkab
214 atures are likely a result of changes at the regulatory sequence of the target genes.
215 tire coding region and flanking intronic and regulatory sequences of 88 genes and 40 microRNAs associ
216 e researcher does not have to guess what the regulatory sequences of a gene are, as tens of thousands
217 sed genes are preferentially found in the 5' regulatory sequences of cis-NAT-encoding genes.
218 clude that FCGR3B deletion juxtaposes the 5'-regulatory sequences of FCGR2C with the coding sequence
219                  Under these conditions, the regulatory sequences of late gene loci were not in close
220 chii, due in part to multiple changes in cis-regulatory sequences of mFAS.
221 ally expressed EGFP under the control of the regulatory sequences of the bHLH transcription factor ge
222 line, where eGFP expression is driven by the regulatory sequences of the embryonic betaH1 hemoglobin
223 through hypermethylation of CpG sites in the regulatory sequences of the gene.
224 cate a dynamic association of Prmt5 with the regulatory sequences of the PPARgamma2 gene that facilit
225 BACH2 peaks overlap with BCL6, including cis-regulatory sequences of the PRDM1 gene.
226    Transgenic reporter strains revealed that regulatory sequences of the transcription factor gene al
227 nd that natural variation in both coding and regulatory sequences of these paralogs responded to a co
228                           Here, we find that regulatory sequences of tph1b, which encodes an enzyme t
229            Furthermore, by altering the gene regulatory sequences on the Rubisco transgenes, cyanobac
230 wo genes in a DGP potentially share the same regulatory sequence, one might expect that they should b
231 s - for example, through the modification of regulatory sequences or chromatin architecture - can lea
232 010 and C. elegans that are likely to encode regulatory sequences or previously unknown ncRNAs.
233 ntisense vivo-morpholinos (vMOs) to mask cis-regulatory sequences or to disrupt splicing factor expre
234 ent have been identified, the distant-acting regulatory sequences orchestrating their in vivo express
235        Monoallelic expression not due to cis-regulatory sequence polymorphism poses an intriguing pro
236 pendent cluster, and more notably, important regulatory sequences present in Borna disease virus but
237 on does not involve the IDRS (iron-dependent regulatory sequence) present in the AtFer1 promoter and
238 ed matching of methylation status of the key regulatory sequences (promoters and CpG islands) to expr
239  that amino acid region 1000-1008 of fV is a regulatory sequence protecting the organisms from sponta
240 Genetic lineage tracing systems based on Wt1 regulatory sequences provided evidence that epicardium-d
241 's expression pattern through changes at its regulatory sequence, rather than changes at the coding s
242  varphiC31 att site positioned adjacent to a regulatory sequence recognized by Tn3 resolvase.
243 cific manner, and we identify the set of cis-regulatory sequences recognized by Wor3.
244 in (FNIII)-like domains, along with a unique regulatory sequence referred to as the M-domain, whose s
245 III (FNIII)-like domains along with a unique regulatory sequence referred to as the MyBP-C motif or M
246 th of genomic data, functional annotation of regulatory sequences remains difficult.
247 minants of differences in cis-regulation for regulatory sequences residing in episomes versus chromos
248      The genetic alteration in this critical regulatory sequence resulted in reduced reporter gene ac
249                              Analysis of Id3 regulatory sequences revealed a novel enhancer, located
250 tion by examining the evolution of important regulatory sequences (short linear motifs) in retained d
251 pregnancy; this might be due to variation in regulatory sequences-some of which are progesterone and
252 -NTR tadpoles the myelin basic protein (MBP) regulatory sequences, specific to mature oligodendrocyte
253                      CPEB is a translational regulatory sequence-specific RNA-binding protein that co
254                              p53 is a master regulatory, sequence-specific transcription factor that
255  is a chromatin feature enriched at gene cis-regulatory sequences such as promoters and enhancers.
256 tionally related genes via binding to shared regulatory sequences, such as the adenylate-uridylate-ri
257 , but its NPF effects were masked by a short regulatory sequence, suggesting that additional factors
258 nt retroviral insertions were used to co-opt regulatory sequences targeted by KDM1A for epigenetic si
259 hosphoserines in an intrinsically disordered regulatory sequence that integrates cellular signaling a
260 nd the alternatively spliced exon 11 contain regulatory sequences that affect insulin receptor splici
261             CTCF-binding locations represent regulatory sequences that are highly constrained over th
262 abidopsis and Brassica to identify conserved regulatory sequences that are responsible for specific e
263 ,638 combinations composed of two to six cis-regulatory sequences that are shared by the two plant sp
264  a powerful approach to the investigation of regulatory sequences that can be applied to other cell t
265 omoter was studied in detail to identify cis regulatory sequences that confer tapetal specific expres
266 few and there are no reports on specific cis regulatory sequences that control tapetal gene expressio
267                                          The regulatory sequences that control the expression of such
268                Enhancer elements are genomic regulatory sequences that direct the selective expressio
269                    Enhancers are genomic cis-regulatory sequences that integrate spatiotemporal signa
270 zation elements identified several candidate regulatory sequences that may be responsible for PB-ER t
271  cartilage development, SoxE, gained new cis-regulatory sequences that subsequently directed its nove
272 ry protein modularity, conversion of one cis-regulatory sequence to another, distribution of binding
273 ast, modular cloning and accommodate diverse regulatory sequences to drive reagent expression.
274 ly interacts with a distinct site in its cis-regulatory sequences to maintain its own expression, and
275 control of the glycine transporter 2 (GLYT2) regulatory sequences to study for the first time the gly
276 rus (MHV), the NTD binds the transcriptional regulatory sequence (TRS) RNA, a conserved hexanucleotid
277 f these ORFs, a single genomic transcription regulatory sequence (TRS) was identified.
278 at orients SL1, SL2, and the transcriptional regulatory sequence (TRS), and this spacer function may
279 inuous transcription involving transcription regulatory sequences (TRSs) located in the 5' leader seq
280 raction of T187 with the 11mer GRE consensus regulatory sequence UGUUUGUUUGU and has significant cons
281 hanism, and maps of hap-ASM and mQTLs reveal regulatory sequences underlying supra- and sub-threshold
282 or exon(s) only, or ultraconserved potential regulatory sequences upstream of PMP22, further supporti
283  the detection of functional conservation of regulatory sequences using predicted occupancy levels of
284                       Such maps can nominate regulatory sequence variants that underlie GWAS signals
285 er (gkm-SVM) that encodes cell type-specific regulatory sequence vocabularies.
286 he search of somatosensory specific genes or regulatory sequences, we mapped the H-2Z1 transgene inse
287 s densely populated with previously unmapped regulatory sequences, which interact in complex ways to
288 ey murine leukemia virus contains inhibitory/regulatory sequences, which prevent export and mediate n
289  by Polycomb-group response elements (PREs), regulatory sequences whose activity depends on the bindi
290 ut the selection of modified transcriptional regulatory sequences with passage facilitated the restor
291 lowing us to identify thousands of genes and regulatory sequences with signatures of adaptive evoluti
292 seudoknots that integrate ligand-binding and regulatory sequences within a single folded domain, the
293 nsight into the complexity of Drosophila cis-regulatory sequences within exon-poor regions, we have u
294 raction between RNA-binding proteins and cis-regulatory sequences within miRNA precursor loops.
295                            Identification of regulatory sequences within non-coding regions of DNA is
296 egy and used it to interrogate 174 candidate regulatory sequences within the 1-Mbp POU5F1 locus in hu
297 iated from the TAD(cPcdh) fringes toward cis-regulatory sequences within the cPcdh locus, counterbala
298 further demonstrated to bind directly to cis-regulatory sequences within the first intron of CSE to a
299                                              Regulatory sequences within the gene, which are subject
300 tion, suggesting the existence of additional regulatory sequences within the locus.

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