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1 iption activator capable of binding a unique recognition sequence.
2 ed at two critical positions within the CTCF recognition sequence.
3 target cytosine and frameshifting of the DNA recognition sequence.
4 e second recognizes the 3' half (CGC) of the recognition sequence.
5 th rates as a function of the quality of the recognition sequence.
6 to occur independently of a specific peptide recognition sequence.
7 ransferred to different positions in the RNA recognition sequence.
8 l that also correspond to helix 1 of the LC7 recognition sequence.
9 veral complementary miRs harboring the PDE4D recognition sequence.
10 ffinity as a monomer to a single copy of its recognition sequence.
11 ein dissociates from the DNA or it finds the recognition sequence.
12  FokI (GGATG 9/13) and cleaves closer to the recognition sequence.
13  site and a single monomer covers the entire recognition sequence.
14 A towards the stationary enzyme bound at the recognition sequence.
15  TATA box but not a transcription factor IIB recognition sequence.
16 heir interactions with opposite sides of the recognition sequence.
17 ax6 from binding the consensus paired domain recognition sequence.
18 itinated directly by APC/C(Cdh1) via a novel recognition sequence.
19  displacement of NKX3.1 from its cognate DNA recognition sequence.
20 ater molecules for the last 2 nt in the core recognition sequence.
21 ein and decreased binding to its cognate DNA recognition sequence.
22 econd monomer that remains detached from the recognition sequence.
23 ion of the protein to the binding of its DNA recognition sequence.
24 de substrate that mimics the PLpro replicase recognition sequence.
25 rs even when the DNA does not contain an ETS recognition sequence.
26 fied a GC-rich, inverted 14 bp repeat as the recognition sequence.
27 asmic Cu(+) homeostasis and its putative DNA recognition sequence.
28 l share a common motif that matches the YBX1 recognition sequence.
29 osylase) excises unmethylated bases from its recognition sequence.
30 f the reporter by reengineering the protease recognition sequence.
31 owing transient HOXA9 binding to its cognate recognition sequence.
32 se genes are active but also revealing their recognition sequences.
33 sm were sub-cloned to test for viability and recognition sequences.
34 ias 24% of integrations near endogenous Gal4 recognition sequences.
35 mbining gene segments and their flanking RAG recognition sequences.
36 d between leading and trailing 12-nucleobase recognition sequences.
37  of motifs, corresponding to Hox and Pbx-Hox recognition sequences.
38 display limited diversity in their preferred recognition sequences.
39 ect repeats, which presumably contain kinase recognition sequences.
40 gma(E) dependent based on consensus promoter recognition sequences.
41 heir aligned amino-acid residues and aligned recognition sequences.
42 re length of coding regions only at specific recognition sequences.
43 WM motif to also inhibit binding to Hox-only recognition sequences.
44 P49 and P35 also differ in their RSL caspase recognition sequences.
45 alpha gene promoter that served as the NFAT3 recognition sequences.
46 exhibit the largest variation from consensus recognition sequences.
47 exes of lambda Cro repressor with varied DNA recognition sequences.
48 ition sequences, CBF promoters also have Myb recognition sequences.
49  its inability to bind cognate paired domain recognition sequences.
50 A elements bearing marked similarity to STAT recognition sequences.
51 tic reactions, paradoxically involving short recognition sequences.
52  types through evolutionary innovation of TF recognition sequences.
53 y selective natural and unnatural amino acid recognition sequences.
54 o bind to probes containing the putative IHF recognition sequences.
55 ily with regards to the composition of their recognition sequences.
56  genes, and methylome analysis reveals their recognition sequences.
57 or two sortase A enzymes that have different recognition sequences.
58 ry code specifying transcription factor (TF) recognition sequences.
59 hosphodiester linkage in the pentapyrimidine recognition sequence 5'-(C/T)+5 C+4 C+3 T+2 T+1 p / N(-1
60 hosphodiester linkage in the pentapyrimidine recognition sequence 5'-(C/T)+5C4+C3+T+2T+1p \N-1 using
61 combination with the bases flanking the core recognition sequence 5'-CGY M6A: G-3'.
62 loop translocation rightward of the specific recognition sequence 5'-CTnGAyG-3' as written (where n i
63  seen with the Escherichia coli DnaG primase recognition sequence 5'-d(CTG)-3'.
64 -7 nucleotides) downstream of the asymmetric recognition sequence 5'-GCCGC-3'.
65        NotI from Nocardia otitidis-caviarum (recognition sequence 5'-GCGGCCGC-3') has been cloned, th
66                                     The NarI recognition sequence (5'-G1G2CG3CN-3') is the most vulne
67 ificity at four of the six base pairs of the recognition sequence (5'-TCCRAC-3').
68 ificity changes at the first position of the recognition sequence (5'-TCCRAC-3').
69 gher affinity for DNA containing the primase recognition sequence (5'-TGGTC-3') than for DNA lacking
70           Complexes formed by five different recognition sequences (5'-GGCCNNNNNGGCC-3'), with differ
71 rent forms of modified cytosine within their recognition sequence, 5'-GCG(T/G)GGGCG-3'.
72 article discusses an unusually short protein recognition sequence, 5'CG, which is read by multiple DN
73 al potential substrates contained the IPTase recognition sequence A36A37A38 in the anticodon loop, on
74         The nuclear myosin II is tethered to recognition sequence AGCTCC (-39/-34) in the intercellul
75 e should happen specifically at the enzyme's recognition sequence, an unknown proportion of cleavage
76 e human enzyme to recognize part of the core recognition sequence and activate the enzyme for catalys
77 mutational analysis of RCC1 defined the NRMT recognition sequence and enabled the identification of n
78 ion endonuclease that cuts an unusually long recognition sequence and exhibits allosteric self-modula
79 a-673 residue lies within the beta-secretase recognition sequence and is part of the amyloid-beta (Ab
80 e results define the SigB promoter consensus recognition sequence and members of the SigB regulon.
81              MmeI cuts DNA 20 bases from its recognition sequence and modifies just one DNA strand fo
82 ic Bcl2 family protein, which have the KXTQT recognition sequence and neuronal nitric oxide synthase
83                               Nos shifts the recognition sequence and promotes repression complex for
84 ) that methylates a specific base within the recognition sequence and protects DNA from cleavage by t
85  now show that this threshold depends on the recognition sequence and scales linearly with the dissoc
86 ified using a nicking endonuclease with 7-bp recognition sequence and Sequenase version 2.0 in the pr
87            Codon selection, releasing factor recognition sequence and specific introns and 3' untrans
88 ing binding specificity outside the core GGA recognition sequence and the mode of action of Ets post-
89  induce DNA double-strand breaks at specific recognition sequences and can promote efficient introduc
90 folds that include Ag(+)-ions or Hg(2+)-ions recognition sequences and the replication tracks that yi
91 tative cargo, Swallow, which share the KXTQT recognition sequence, and addresses the apparent paradox
92 ction endonucleases cleave DNA outside their recognition sequences, and are therefore particularly us
93 The method involves the conjugation of a DNA recognition sequence (aptamer) to the catalytic DNAzyme,
94 ng virulence factors, that have a C terminal recognition sequence are attached to Gly5 on the peptido
95  MmeI and delineates which base pairs of the recognition sequence are more amenable to alterations th
96                                 Although DNA-recognition sequences are among the most important chara
97 one within nuclear factor-kappaB (NF-kappaB) recognition sequences are identical, homodimers of c-Rel
98 d that functional mammalian microRNA (miRNA) recognition sequences are located preferentially in the
99 lained partially by the presence of fewer GR recognition sequences, arguing for the existence of addi
100 pin B8 demonstrated that both the P4-P1 RXXR recognition sequence as well as the P1'-P5' sequence are
101       The PAX5 fusion products bound to PAX5 recognition sequences as strongly as wild-type PAX5 and
102 B. burgdorferi, nor are any sigma28 promoter recognition sequences associated with the motility genes
103 al selectivities dominated by the respective recognition sequences associated with the scaffolds.
104 development resulted in mutations at the ZFN recognition sequence at frequencies as high as 0.2 mutat
105  though simple, requires that nicking enzyme recognition sequence be present in the target DNA.
106 ding FokI, interact with two copies of their recognition sequence before cutting DNA.
107 rent specificity groups, where the preferred recognition sequence between these groups can differ at
108 vels of the transcription factor recombinant recognition sequence binding protein at Jkappa site (RBP
109 ow that the transcription factor recombinant recognition sequence binding protein at the J(kappa) sit
110 aled that ET increased levels of recombinant recognition sequence binding protein at the Jkappa site
111 utant triggered up-regulation of recombinant recognition sequence-binding protein at the Jkappa site
112 ly increases the length and diversity of DNA-recognition sequence by reusing DBDs from the same famil
113 nd CLOCK suppressed binding of GR to its DNA recognition sequences by acetylating multiple lysine res
114 e human papillomavirus by immobilizing short recognition sequences by amidation or thiol-maleimide re
115 of plasmid DNA, designed to contain the MerR recognition sequence, by a simple temperature trigger.
116 ion of a coumarin fluorophore onto a peptide recognition sequence called LAP1.
117   Recent evidence identified a novel AhR DNA recognition sequence called the nonconsensus xenobiotic
118 r longer target strands, the position of the recognition sequence can be designed in a way that a sma
119  show that specific residues in the protease recognition sequence can differentially modulate the eff
120  high false positive rates; functional miRNA recognition sequences can be as short as six nucleotides
121          A nondegradable Iqg1p (lacking this recognition sequence) can suppress the myo1Delta phenoty
122                               Apart from Myc recognition sequences, CBF promoters also have Myb recog
123 was shown to specifically bind its consensus recognition sequence (CGGGTAA, -166 to -160) in the DGK1
124 ximal activity on DNA with two copies of its recognition sequence, cleaving both sites concertedly.
125 the flgE or napA promoter and includes a Fur recognition sequence common to the H. pylori pfr and sod
126 fected with an Ebola virus lacking the furin recognition sequence compared to those infected with wil
127 nscription factors, Pdx1 binds to a core DNA recognition sequence containing the tetranucleotide 5'-T
128                                     The BcgI recognition sequence contains one adenine in each strand
129 r how the interaction of gamma with specific recognition sequences coordinates directional DNA transl
130 he two forms of p53 bound to a consensus DNA recognition sequence could not be distinguished and were
131 ligomers by Watson-Crick base pairing of the recognition sequences creates linear or cyclic arrays of
132 he substitutions and a polypeptide consensus recognition sequence deduced from the results.
133 vates Thioflavin T fluorescence and a target recognition sequence designed to interact in a molecular
134 eation peptide sequence, an effector caspase recognition sequence, DEVD, and a flanking optically act
135 active site is positioned initially near the recognition sequence, distant from its downstream target
136                            Matalpha1 and its recognition sequence diverged most dramatically in the c
137 insertion of 31 amino acids in the caspase-3 recognition sequence DMQD.
138 NA tail might form upon encounter of a "Chi" recognition sequence during unwinding of DNA by the RecB
139 re separate constructs with their own unique recognition sequences, ERT2-GAL4 is compatible with the
140                                              Recognition sequences exhibit a periodic purine-pyrimidi
141 nylation assay, peptide probe 3 with a RLRGG recognition sequence exhibited the highest activity, wit
142 incubations with recombinant phosphotyrosine-recognition sequences expressed as GST-fusion proteins.
143 -based reporter was designed to contain a LF recognition sequence flanked by the FRET pair formed by
144 enzymes at two distant, inversely orientated recognition sequences followed by helicase-catalysed ATP
145 ion, asparagine (N) in the canonical N-X-S/T recognition sequence for carbohydrate attachment was cha
146 t adjacent ends of a linker that encoded the recognition sequence for caspase-3.
147 hly conserved sequence homologous to the DNA recognition sequence for CBF1 (CSL/RBP-Jkappa/Su(H)/LAG1
148                                The consensus recognition sequence for GSK3 (Ser(76)/Ser(80)) is evolu
149  domain, we first investigated the preferred recognition sequence for TBX22.
150 he circular nucleic acid template includes a recognition sequence for the analyte DNA (the Tay-Sachs
151 in promoter CACCC site, indicating a broader recognition sequence for the EKLF consensus binding site
152 ey are enriched in TAATTA, which is also the recognition sequence for the homeodomain DNA-binding mod
153 ing of the mini-Mu transposon to introduce a recognition sequence for the restriction enzyme MlyI.
154 e algorithm enumerates all possible extended recognition sequences for 16S rRNA and then chooses thos
155   Our data reveal unanticipated diversity in recognition sequences for chaperones; establish a sequen
156 rates for each protease created by appending recognition sequences for ClpCP or ClpXP to the green fl
157  sequence more strongly than to the usual AT recognition sequences for curved minor groove agents.
158 encodes an expansive repertoire of conserved recognition sequences for DNA-binding proteins that near
159 ognition domain (CRD) as well as LDV and RGD recognition sequences for integrin binding.
160                        Specifically, epitope recognition sequences for the 2F5, 4E10, and 447-52D ant
161  systematically perturb transcription factor recognition sequences, frequently alter allelic chromati
162 id reporter that included predicted miR-196a recognition sequence from ANXA1 3'-untranslated region c
163              NusG protects T residues of the recognition sequence from permanganate oxidation, and th
164 nosine and cytidine residues within the HhaI recognition sequence GCGC experience motions on a much s
165 rs of the five genes conform to the proposed recognition sequence GNCCN9GGNG, where N is any nucleoti
166 ts both sites upstream and downstream of the recognition sequence, hydrolyzing eight phosphodiester b
167          The presence of M(1)dG in the EcoRI recognition sequence impaired the ability of the enzyme
168 U0126 decreased NF-kappaB binding to its DNA recognition sequence, implicating the MAPK pathway in NF
169                  The binding of EcoR1 to the recognition sequence in DNA appears as a rapid increase
170 stin-like polypeptide (ELP) fused to a short recognition sequence in E. coli, we show robust and high
171  of at least one physiological miR-107 miRNA recognition sequence in the 3'-UTR of BACE1 mRNA.
172     The IDOL FERM domain binds directly to a recognition sequence in the cytoplasmic tails of lipopro
173                      We identified an NKX6.1 recognition sequence in the distal region of the HNF1alp
174 eover, we identified an Akt/protein kinase B recognition sequence in the PML-binding domain of MOZ pr
175 f mice (MVM) first binds to a simple cognate recognition sequence in the viral origins, comprising tw
176 ly than the wild-type enzyme to the specific recognition sequence in vitro, and show even greater pre
177  pTypeI, which contains all of the 27 Type-I recognition sequences in a 248-bp DNA fragment.
178                    Variants with 2F5 or 4E10 recognition sequences in gp41 retained replication compe
179                        ICE1 binds to the Myc recognition sequences in the CBF3 promoter.
180 onstant for the binding of active FNR to its recognition sequences in the DNA.
181          Tailup was shown to bind to two DNA recognition sequences in the dorsal vessel enhancer of t
182  represent only a small minority of the CTCF recognition sequences in the human genome.
183 protein interacts with ICE1 and binds to Myb recognition sequences in the promoters of CBF genes.
184 NA is the paucity of structural data for DNA recognition sequences in their free (unbound) state.
185 d T3 enzymes, elements in or near the enzyme recognition sequence influenced their activity and requi
186 rs independently of DNA binding at NF-kappaB recognition sequences, instead binding with SMAD family
187                         An artificial I-SceI recognition sequence integrated into genomic DNA was ana
188                  By incorporating additional recognition sequences into the DNA linkers, defined hete
189                  Transfer of the TMV Pumilio recognition sequences into the genome of potato virus X
190            Further, we find that the Gas5 SR-recognition sequence is conserved among haplorhines, wit
191 t that the specificity of HscA for the LPPVK recognition sequence is determined in part by steric obs
192 ry wild type cells if the xylosyltransferase recognition sequence is disrupted.
193 cognition element for LARC, and the LARC DNA-recognition sequence is essential for the enhancement of
194 ambda-development in vivo and a specific IHF recognition sequence is found within cos.
195                            An HIV-1 protease recognition sequence is inserted into one of the surface
196                               Since the THAP recognition sequence is short, and will occur many times
197 s referred to as the AP2 domains and its DNA recognition sequence is still unknown.
198 he assembly of DnaA complexes at chromosomal recognition sequences is affected by the tight binding o
199  possessing the complete Survivin and INCENP recognition sequence, is required for the composition of
200 nd that to cleave a DNA with one copy of its recognition sequence, it has to act in trans, bridging t
201 o cellular proteins fused to a 13-amino acid recognition sequence (LAP), catalyzed by a mutant of the
202  new general method for the determination of recognition sequences longer than three bases for mRNA i
203  considerably from that of its bacteriophage recognition sequence, loxP.
204 bstrates bearing a five amino acid sortase A recognition sequence (LPETG).
205                                  The sortase recognition sequence, LPXTG (for Streptococcus aureus so
206 genes does not resemble a sigma 70 consensus recognition sequence; moreover, it is upstream of two ge
207 athic helix, without requiring a cholesterol recognition sequence motif.
208 th three different C-terminal target protein recognition sequence motifs by CD, fluorescence, and hig
209 es, computational approaches based on kinase recognition sequence (motifs) from known substrates, pro
210 ed enzymes hydrolyzed just one strand of the recognition sequence, nicking the DNA rather than cleavi
211 ntroduction of the methylation site into the recognition sequence of a restriction endonuclease, and
212 rresponding methylases, determination of the recognition sequence of a Type-I restriction enzyme is a
213 DNA at specific sites in the vicinity of the recognition sequence of C.BclI.
214 t codons that closely resemble the consensus recognition sequence of Escherichia coli integration hos
215                       Here, we determine the recognition sequence of LlaBIII (5'-TnAGCC-3', where the
216 ide, pKID-Abl, was designed to incorporate a recognition sequence of the Abl kinase.
217 1 and other mycotoxins by replacing the core recognition sequence of the aptamer.
218  and C-X3-C contexts in the C-G1-G2-C-G3-C-C recognition sequence of the NarI restriction enzyme were
219 '-CTCG(1)G(2)CG(3)CCATC-3' that contains the recognition sequence of the NarI Type II restriction end
220 at variability results in alterations to the recognition sequence of this R-M system.
221 PROTACS is a novel approach of tagging small recognition sequences of a specific E3 ubiquitin ligase
222 nd with the advent of PacBio sequencing, the recognition sequences of DNA methyltransferases (MTases)
223                                 The splicing recognition sequences of exon 3 are less favorable than
224                                  Because the recognition sequences of miRNAs for their targets are sh
225  one either side of the site, to release the recognition sequence on a short DNA fragment; 34 bp long
226                                      The LC7 recognition sequence on IC and its interface with LC7 ar
227 uence partially overlaps the light chain LC7 recognition sequence on IC, raising questions about the
228 rget a region upstream of the FIP/BIP primer recognition sequences on opposite strands, substantially
229 cal data, a model of ComAC bound to the ComA recognition sequences on the srfA promoter has been deve
230 e-strand breaks (DSBs) at each copy of their recognition sequence, one either side of the site, to ex
231 lized to two variants of the canonical KIN10 recognition sequence, one in each of its two AP2 DNA bin
232 st of the genes identified have specific AHR recognition sequences, only seven genes were altered exc
233 led with the ability to introduce a CAAX-box recognition sequence onto almost any protein, this metho
234                                 No consensus recognition sequence or structure has been identified fo
235 f proteins and/or noncoding RNAs to specific recognition sequences or secondary structures within mRN
236                                      The FGE recognition sequence, or aldehyde tag, can be inserted i
237        Here we show that Ste5 and Ste20 have recognition sequences, or "docking" sites, for the G1/S
238  Numerous peptide ligands including protease recognition sequences, peptides mediating protein-protei
239 dation of the influence of target length and recognition sequence position on the sensorial performan
240 anyang (NY) cattle, which are located in the recognition sequences (potential cis-acting elements) of
241 hat cleavage takes place outside the (5)mCpG recognition sequence, predominantly 4-17 bp upstream of
242 purified Nanog-Sox2 complex identified a DNA recognition sequence present in multiple overlapping Nan
243 age targets contain a proline-rich consensus recognition sequence, Pro-Pro-Ser-Pro, residing in the v
244         One of the important elements of the recognition sequence, pTyr-Xxx-Xxx-Gln, is glutamine.
245                The diversity of recovered HD recognition sequences raises important questions about t
246 ed HpaII sequences (Cm5CGG), but its precise recognition sequence remains undefined.
247 GTACNTNNNY) was significantly different from recognition sequences reported for Topo IIA from other o
248 cal modification of PS A1 does not alter the recognition sequence responsible for an MHCII-mediated,
249 a series of truncations, we define a minimum recognition sequence (RS) that is necessary and sufficie
250 y requires both clefts to be filled with its recognition sequence: SfiI has low activity when bound t
251 two conserved prolines of the PXXP consensus recognition sequence show more absorptions than there ar
252 endency, with peptide probe 4 with an LRLRGG recognition sequence showed the fastest rate ( t 1/2 = 0
253                            A putative mTORC1-recognition sequence sits within a flexible loop C-termi
254 haracterization of siRNA binding, target RNA recognition, sequence-specific cleavage and product rele
255                     Mutations within the Sp1 recognition sequence specifically eliminated binding of
256 inds to an imperfect direct repeat COUP-TFII recognition sequence (termed hereafter proxDR) in the pr
257 igh affinity to a broader range of NF-kappaB recognition sequences than did wild-type p65 homodimers.
258           We show that mutations in the Elba recognition sequence that eliminate Elba binding in nucl
259  a picolyl azide (pAz) derivative to a 13-aa recognition sequence that has been genetically fused ont
260 inJ dimer at a single inverted repeat of its recognition sequence that overlaps with the -10 promoter
261 fluorogenic DNA-binding dye to the caspase-3 recognition sequence that renders the dye nonfunctional.
262  induced by the mutation(s) unmasked a furin recognition sequence that was used for cleavage.
263 ely regulate Rv0081 expression by binding to recognition sequences that either partially or completel
264 rocessivity for facilitating encounters with recognition sequences that modify enzyme function during
265 -glutamate-serine-threonine-rich proteolytic recognition sequence, the absence of which has previousl
266  ability to bind the consensus paired domain recognition sequence; the others were unable or only par
267 fine their orientation and register on their recognition sequences, thereby allowing us to define the
268 anscriptional inhibitors binding similar DNA recognition sequences, they have opposite biologic effec
269  recognition at three positions within their recognition sequences through correlations between their
270 unctions (HJs) that contain specific protein-recognition sequences to report protein-DNA interactions
271 es together, their binding to the respective recognition sequences triggers the nicking/polymerizatio
272   The resulting MazF-bs(can) gained a 6-base recognition sequence, UACAUA, for RNA cleavage instead o
273  cells, with the 3' guanine of the HIF-1 DNA recognition sequence uniformly targeted.
274 one of these trinucleotides were known to be recognition sequences used by other microbial primases.
275 ptin and the removal of the calpain-cleavage recognition sequence, via site-directed mutagenesis, abo
276                  The SigG consensus promoter recognition sequence was identified as GCGNGT-N15-18-CGA
277                                An asymmetric recognition sequence was identified, 5'-CTnGAyG-3' (wher
278  target genes regulated by EcfO, and an EcfO recognition sequence was identified.
279 erase-encoding gene (hpt) was flanked by ZFN recognition sequences was constructed.
280 FP) coding sequence (gfp) was flanked by ZFN recognition sequences was used to produce transgenic tar
281            In contrast to canonical protease recognition sequences, we show that IsdG is targeted for
282 ks and flanking 5'- and 3'-single-strand DNA recognition sequences were combined in buffer solution.
283 l methylation patterns corresponding to nine recognition sequences were detected (26695, 3; J99-R3, 6
284  plasmids'), each containing a unique Type-I recognition sequence, were also constructed using pMECA,
285  methyltransferase flips the second C in the recognition sequence, while the endonuclease flips both
286 s an engineered mutation in the conserved PC recognition sequence, while the PC furin cleaves 50 kDa
287 plementarily to the middle nucleotide of the recognition sequence, while the third nucleotide, an ade
288  required sub-cloning to differentiate their recognition sequences, while four MTase genes that were
289 ubstantially faster than the canonical DDDDK recognition sequence, widely used for protein purificati
290                         TFs target their DNA-recognition sequences with high specificity by binding w
291 ed oligonucleotide containing the target DNA recognition sequence, with a methylene blue tag close to
292                   The Elba factor binds to a recognition sequence within a Fab-7 subelement that has
293 F binding and dissociation dynamics at their recognition sequence within duplex DNA, single nucleosom
294 ned rapidly by simply replacing the enzyme's recognition sequence within the generic labeled molecule
295                We identified consensus Egr-1 recognition sequences within proximal and distal regions
296 tion site and that mutation of the consensus recognition sequences within these sites ablated their t
297 Areas I and II, despite the absence of Egr-1 recognition sequences within this promoter segment, sugg
298 gether with the presence of caspase cleavage recognition sequences within virally encoded proteins, w
299 was possible to match MTase genes with MTase recognition sequences without further sub-cloning.
300        These DNA modules were encoded so the recognition sequences would uniquely associate through W

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