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1 m mRNAs containing the DICE (differentiation control element).
2 (controlling element), and peripheral plant (controlled element).
3 As, the miRNA synthesis rate is the dominant control element.
4 Bcl-6, which is a candidate site for such a control element.
5 gene by binding specifically to the internal control element.
6 rger than the minimal experimentally defined control element.
7 er these opposing elements form the intronic control element.
8 uggesting a possible repressor role for this control element.
9 ored the use of DNA copy number as a circuit control element.
10 ts polymerization by removing the inhibitory control element.
11 (3 cases) by using cinchonine as the chiral control element.
12 The E-Box is a widely used DNA control element.
13 ancer and at least one other transcriptional control element.
14 the 3'-UTR of COX-2 as a major translational control element.
15 )-end turnover in addition to being an actin control element.
16 he recently identified proteasome-associated control element.
17 of Nanos mRNA, which contains a translation control element.
18 inone methide as an important stereochemical control element.
19 e RNAP III terminator as an information-rich control element.
20 nic mice using a chondrocyte-specific Col2a1 control element.
21 me hypertrophic chondrocyte-specific Col10a1 control element.
22 aline phosphatase using light as an external control element.
23 e first insight into a damage-based archaeal control element.
24 generation without additional integration of control elements.
25 proper regulation of complex transcriptional control elements.
26 ome cases overriding that of transcriptional control elements.
27 (SIs) to limit the action of transcriptional control elements.
28 g strategy for constructing programmable RNA control elements.
29 ation about the context specificity of these control elements.
30 nesis, but little is known of the cis-acting control elements.
31 trongly suggesting interaction between these control elements.
32 he gene, its promoter or at the upstream cis-control elements.
33 sive tissue specificities and interdigitated control elements.
34 the understanding and application of genetic control elements.
35 its, nucleic acid detection systems and gene control elements.
36 ry domains, defined by a gene and its linked control elements.
37 the apoE gene was mediated via distinct gene control elements.
38 d enhancers, which function as accessibility control elements.
39 re facilitated the approximation of intronic control elements.
40 nstrain interactions between transcriptional control elements.
41 conformation analysis in discovering new cis control elements.
42 f new types of biosensor devices and genetic control elements.
43 reat majority of which are not near exons or control elements.
44 the recruitment of MED25 to transcriptional control elements.
45 tin loops to immobilized RNA polymerases and control elements.
46 whereas others did not, and represent novel control elements.
47 ented in consideration of steric and dipolar control elements.
48 ily identified the known splicing signals as control elements.
49 identify oligomers that comprise cis -acting control elements.
50 pression and antisense transcription as dual control elements.
51 icity of DNA methylation at these imprinting control elements.
52 ion of the rat TRIII gene to assess possible control elements.
53 osage by overexpressing Dlk1 from endogenous control elements.
54 cture as well as incorporation of allosteric control elements.
55 is regulated by magnesium-responsive genetic control elements.
56 litate communication between transcriptional control elements.
57 sassembly of trans host factors with cis RNA control elements.
58 ssembly strategy for this class of RNA-based control elements.
59 far focusing on using hydrogen bonds as the controlling element.
60 survival--is so inefficient, and to identify controlling elements.
61 te the formation of adjacent gene expression controlling elements.
62 uster have identified a 320-bp amplification control element (ACE3) required for amplification, as we
64 river lines utilizing common transcriptional control elements affect germline recombination rates.
66 ycline transactivator (TTA) acts as an inert control element and does not contribute to phenotypes un
68 -components are embedded among the hindbrain control elements and are highly diverged between species
72 s), recombining various post-transcriptional control elements and screening for the desired relative
73 inserted between eukaryotic transcriptional control elements and stably incorporated into the P. pas
74 nscription by pairing promoters with distant control elements and to orchestrate intrachromosomal rec
75 eocenters were used as removable atropisomer control elements and were installed by using a highly en
76 s of two subsystems: the central controller (controlling element), and peripheral plant (controlled e
77 pha3 gene via a cis-acting positive/negative control element, and the T-cell-specific CD8alpha gene v
78 tern is controlled by a number of long-range control elements, and is reflected in the severe homozyg
79 and foreign promoters, and to show that Bmp5 control elements are capable of rescuing phenotypic effe
83 croarray on some tumor tissue and select the control element associated with the greatest amount of g
84 a establish a bioresource that links genetic control elements associated with normal immune traits to
85 ous TFs that are distributed along tRNA gene control elements, beginning upstream of the transcriptio
87 that could find application as novel genetic-control elements, biosensor components or precision swit
88 H2B and H2A.Z are all acetylated at the cis-control elements but H3 remains unacetylated except at t
89 xpression, H4 acetylation appears at the cis-control elements but not at the Lys gene or its promoter
90 e increase the regulatory range of the Rnt1p control elements, by modifying a critical region for enz
92 three types of function: (i) conformational control elements comprising an RNA switch, (ii) self-fun
94 bility of cation-pi interactions to act as a controlling element decreases when Lewis acids coordinat
95 nslated region elements: the differentiation control elements (DICE) in Lox mRNA and the pyrimidine-r
96 l A beta oligomerization and show that these controlling elements differ between A beta 40 and A beta
97 a relatively simple array of transcriptional control elements, divided into proximal and distal regio
99 level, indicating the presence of a negative control element downstream of the P(3) promoter sequence
102 expression patterns, and the transcriptional control elements ("enhancers") that govern them, remain
103 ima et al. (2018) discover early replicating control elements (ERCEs), a new type of cis-acting eleme
104 nd the necessity of these "early replication control elements" (ERCEs) was validated by deletions and
105 nds that do not bind to this RNA replication control element fail to induce plasmid loss in vivo, whe
106 These results prove that the IG-DMR is a control element for all imprinted genes on the maternal
107 thylated region (IG-DMR) that is a candidate control element for an imprinted domain on distal mouse
109 ts allow for the use of light as an external control element for pharmacological activity, which can
110 B12, and that it likely serves as a genetic control element for regulating expression of the 25-gene
111 electrostatic interaction provides a unique control element for selective C-H functionalization.
113 f O-GlcNAc on Ser/Thr residues, is a dynamic control element for transcription repression, protein de
114 ion (OriP) has been implicated as a critical control element for viral transcription, as well as vira
115 fering membrane properties, suggesting novel control elements for biological and amyloid regulation o
116 trategy for quantitatively tailoring genetic control elements for broader integration within biologic
117 f the supporting ligand points to key ligand control elements for further extending the known tetrava
119 ecognized by RNA polymerase III in which all control elements for initiation are located in the 5'-fl
120 erface of the lipid bilayer are suggested as control elements for insertional depth and orientation o
122 upport a model where S12 and S13 function as control elements for the more ancient rRNA- and tRNA-dri
123 ctam intermediate not only serves as the key controlling element for pyrrolidine stereochemistry but
125 resence of the Delta(5)-unsaturation are key controlling elements for the formation of the natural ca
126 e their protein counterparts, these RNA gene control elements form highly specific binding pockets fo
127 cagon gene through activation of a conserved control element found between nucleotides -77 to -51.
128 ne methyltransferase overrides accessibility control element function and cripples V(D)J recombinatio
129 complexes compensated for the accessibility-control element function of a promoter but not an enhanc
130 th previous studies of these transcriptional control elements, GFP was strongly and specifically expr
131 commitment is to characterize the cis-acting control elements governing the expression of CD4 and CD8
132 a rise in H3 acetylation throughout the cis-control elements; H4 and H2B acetylation remain substant
137 s grown under iron limitation bound the iron control elements (ICE) within the promoters of blr7895 a
138 l requires (i) suitably proportioned movable control elements, (ii) a method for operating them on de
139 he largely ignored amino-terminal helix is a control element in AsLOV2's light-activated conformation
141 aster transcriptional regulator is a central control element in Caulobacter cell cycle progression an
142 ctivity by remote protecting groups and as a control element in enzymic processes for glycosidic bond
144 to a metal is often a key driving force and control element in many important reactions including as
145 tline the molecular polaron's potential as a control element in phononic circuitry architecture.
150 esults suggest that TSPAN33 represents a new control element in the development of inflammation by ma
152 The response regulator Spo0A is the master control element in the initiation of sporulation in Baci
153 al candidate factors that recognize the MPEX control element in the Muscle creatine kinase (MCK) prom
154 resented data suggest that CcpA is a central control element in this important developmental process
156 r method is able to identify transcriptional control elements in a gene specific manner that reflect
160 ogenous Ig light chain (IgL) transcriptional control elements in GCV/SHM in the chicken B cell line D
161 in (ori) shares a common theme with many DNA control elements in having multiple binding sites for on
162 mma-globin gene under beta-globin regulatory control elements in hematopoietic stem cells (HSCs) resu
163 on of artificial networks of transcriptional control elements in living cells represents a new fronti
165 viruses have been postulated to function as control elements in RNA replication, transcription, and
166 f reports on 5' terminal posttranscriptional control elements in spleen necrosis virus and human foam
167 enting these engineered RNA molecules as key control elements in synthetic genetic networks are highl
170 to the Igkappa locus, known transcriptional control elements in the Iglambda locus lack functional N
171 upstream of Nrl, we identified putative cis-control elements in the Nrl promoter/enhancer region by
172 on the molecular axle act as strict kinetic control elements in the self-assembly, thereby dictating
175 re the dominant class of ligands and the key controlling element in asymmetric homogeneous transition
176 n germline and points to a possible deletion-controlling element in the beta-globin gene separate fro
177 ecombination reactions and, in some cases, a controlling element in transcription and the initiation
178 evealed evidence for peptide determinants as controlling elements in LacdiNAc biosynthesis, we report
180 ed the presence of potential tissue-specific control elements including a consensus sequence found in
181 at least 5 distinct types of functional cis-control elements, including a binding site for the Notch
182 so describe a complex series of hierarchical control element interactions that orchestrate CD4 expres
183 been integrated with an adjacent araC-P(BAD) control element into the bacterial chromosome allows dyn
185 n channels, suggesting that beta2Glu155 is a control element involved in coupling ligand binding to c
186 phase transition via the Site II cell cycle control element is distinct from E2F-dependent mechanism
191 al level and that cis-acting transcriptional control elements mediating fauA iron repressibility resi
192 s satisfy the prediction of the cassette and controlling element models that genetic information is t
194 able radiopharmaceuticals, discusses quality control elements needed to optimize the study, summarize
195 Acetylation is thus concentrated at the cis-control elements, not at the Lys gene or its immediate p
197 HIF-2alpha expression in keratinocytes is a control element of both tissue perfusion and systemic ar
198 sotope-controlled selectivity (ICS), a novel control element of chemical reactivity where a molecular
200 The results obtained indicated that the Agr control element of the sed promoter resides within the -
201 geted sequences function as distantly-acting control elements of antisense long non-coding RNAs, whic
203 , and that these proteins serve as molecular control elements of bacterial programmed cell death.
205 dy has important implications for unraveling control elements of high-order genome structure and func
206 l GTPases have recently emerged as important control elements of many stages of vesicular trafficking
207 , and further fine mapping revealed that the control elements of mutation frequency reside within the
209 n a specific immune cell lineage, based upon control elements of the colony stimulating factor 1 rece
215 LQT1-AS) represents an additional imprinting control element or center in the human 11p15.5 and mouse
217 ly, we found no evidence for transcriptional control elements or transcriptional initiation in the in
220 ation of proximal and distal transcriptional control elements permits lineage-specific and elevated b
221 individual models to identify the potential control elements predictive of the expression of each ge
223 sites of intrinsic flexibility within a DNA control element provide hinges for its protein-directed
224 he M. tuberculosis enzyme lacks a C-terminal control element recently uncovered in E. coli gyrase and
225 ment, termed DICE (Downstream Immunoglobulin Control Element), reduces in vivo activity in B cells.
226 gical systems, and their levels are critical control elements, reflecting the interplay between trans
227 s via the introduction of specific structure control elements responsible for binding analyte molecul
228 on in skeletal muscles, we characterized the control elements responsible for the positionally restri
230 A breakdown of the steric and electronic control elements shows that a gearing effect in the tran
231 hput in vivo Screening PLatform for Intronic Control Elements (SPLICE) to identify 125 unique ISRE se
232 -Src occurs through distinct transcriptional control elements such as the serum response element (SRE
233 TR of human APP contains several interesting control elements, such as an acute box element, a CAGA b
234 of Bcl-2 and Bcl-xL expressed under similar control elements supports the model that antiapoptotic B
235 -loops within the nanos 3' UTR translational control element (TCE) act independently to direct transl
236 RNA is mediated by a bipartite translational control element (TCE) in its 3' untranslated region.
237 is mediated by a 90-nucleotide translational control element (TCE) in the nos 3' untranslated region
238 nos (nos) mRNA by a cis-acting Translational Control Element (TCE) in the nos 3'UTR is critical for a
239 We previously identified a novel TGF-beta control element (TCE) in the promoters of SMC differenti
241 )6GG] and a transforming growth factor-beta1 control element (TCE) that are required for alpha-SMA ex
242 a conserved transforming growth factor-beta control element (TCE) within the 5'-region of the smooth
244 e this secondary structure, or translational control element (TCE), that provide the 15 nucleotides r
245 n, the natural Smcp mRNA contains a positive control element that counteracts the inhibition of trans
246 (SNV) contains a unique posttranscriptional control element that facilitates Rev/Rev-responsive elem
247 tions likely harbors a cis-acting imprinting control element that is necessary for establishing and/o
248 their scaffolds, which acts as an endocyclic control element that promotes intramolecular hydrogen bo
249 macroscopic valve is a device with a movable control element that regulates the flow of gases or liqu
250 ted region at exon 1A contains an imprinting control element that specifically regulates Gnas and com
251 results identify a novel posttranscriptional control element that uses a conserved cellular export me
252 ecently characterized Hoxb13 transcriptional control elements that are active in prostate luminal epi
253 tches are widespread metabolite-sensing gene control elements that are typically found in the 5' untr
254 circuit design is the number of independent control elements that can be combined together in a sing
255 witching oligonucleotides (SSOs) are genetic control elements that can be used to specifically contro
260 boswitches are metabolite-responsive genetic control elements that reside in the untranslated regions
262 ive to stereochemical features of the chiral controlling element that combines a CH-pai interaction b
263 posttranscriptionally regulated by multiple controlling elements that impede translation, including
264 ila and gene silencing in maize mediated by "controlling elements" (that is, transposable elements) l
265 adenylation requires a far-upstream splicing control element, the negative regulator of splicing (NRS
266 e G-rich strands of two such transcriptional control elements, the 5'-S1 nuclease-hypersensitive sile
267 avior called "optomotor response." As neural control elements, the large tangential horizontal system
268 genes contain core promoters with two basal control elements, the TATA box and the pyrimidine-rich i
270 and smooth-muscle genes that lack known SRF control elements, thus further expanding the breadth of
271 the down-regulation of CTLA-4 as a possible control element to enhance early T cell expansion throug
272 tor (UBF), which interacts with the upstream control element to facilitate the assembly of the transc
273 met several obstacles: one is lack of a good control element to regulate replication, and the other i
274 uences act as a distinct posttranscriptional control element to stimulate gag RNA nuclear export and
275 potential for eIF4E and other translational control elements to mediate myc's transforming functions
276 other regions of the Bmp5 gene for potential control elements, to confirm the location of several ele
277 h findings of others that methylation within control elements typically negatively correlates with ge
278 cts that illustrate that the transcriptional control elements used by both pathways are contained wit
279 ably from novel native orthogonal biological control elements using quantitatively in-context charact
281 ntrolling RNA3 production (distal subgenomic control element) was identified 1.5 kb upstream, at nt 1
282 translation of ccnd1 mRNA, a G1/S checkpoint control element, was impaired by microinjection of ccnd1
284 lored region and to identify potential novel control elements, we physically mapped the most D-distal
285 ther potential positive- and negative-acting control elements were identified in area II after mutati
287 is catalyst, are demonstrated to be powerful control elements when operating in combination in comple
289 nsgenesis, and have identified two important control elements which reside about 9 kb upstream at the
290 intact human genes with all their long-range controlling elements which might give high levels of tis
291 Motion of the ring is influenced by several control elements whose force-generating capability is ba
292 strategy to identify communities of related control elements with a penalized regression approach, w
294 scriptional regulation is often specified by control elements within mRNA 3'- untranslated regions (3
296 acid sequences; the evolution of expression control elements within the protein coding sequence of r
299 as determined by alleles at the X chromosome controlling element (Xce), a locus defined genetically b