1 ins within the I-II loop were then mapped by
deletion analysis.
2 oligotyping, biochemical testing, or genomic
deletion analysis.
3 hese elements were authenticated by mutation/
deletion analysis.
4 and p79, using a yeast two-hybrid screen and
deletion analysis.
5 tributions to nucleosome positioning through
deletion analysis.
6 fine the promoter region upstream of idsA by
deletion analysis.
7 ion of this sequence is validated by in vivo
deletion analysis.
8 which we confirmed experimentally by serial
deletion analysis.
9 gPHO4, and CgMSN5 in the PHO pathway through
deletion analysis.
10 By
deletion analysis,
a region between nucleotides -145 and
11 Sequence and
deletion analysis allowed us to map LamR binding to two
12 (iii) The
deletion analysis also revealed that residues 596-638, w
13 Deletion analysis also reveals a functional requirement
14 tart site, which we identified by sequential
deletion analysis and by comparison of human and mouse g
15 Deletion analysis and characterization of the purified B
16 Deletion analysis and FR-alpha/SV40 promoter chimeras sh
17 Deletion analysis and generation of transgenic worms com
18 y, by combining the results from the somatic
deletion analysis and genetic linkage analysis, we were
19 Deletion analysis and mRNA reporter assays show that a c
20 Interestingly,
deletion analysis and mutation of the hypoxia responsive
21 Deletion analysis and mutational studies were done to ma
22 Deletion analysis and NMR spectroscopy revealed that an
23 Deletion analysis and point mutagenesis demonstrate that
24 Deletion analysis and point mutations indicate that pres
25 ntragenic PTEN mutations be offered clinical
deletion analysis and promoter-mutation analysis, respec
26 Deletion analysis and site-directed mutagenesis identifi
27 Here we employ 5' and 3'
deletion analysis and site-directed mutagenesis of the a
28 Sequential
deletion analysis and site-directed mutagenesis of the I
29 regulatory regions function in the same way,
deletion analysis and site-directed mutagenesis of the O
30 A combination of
deletion analysis and site-directed mutagenesis revealed
31 Deletion analysis and site-directed mutagenesis revealed
32 We identified the NLS of LEDGF/p75 through
deletion analysis and site-directed mutagenesis.
33 s characterized by footprinting experiments,
deletion analysis and site-directed mutagenesis.
34 This site was confirmed by
deletion analysis and specific detection with a custom-g
35 Deletion analysis and the activity of hybrid promoter co
36 Through a combination of pull-down assays,
deletion analysis,
and isothermal titration calorimetry,
37 Random-linker insertion mutagenesis,
deletion analysis,
and site-directed mutagenesis of hydr
38 of hypoxia-responsive genes, COX-2 promoter
deletion analysis,
and site-directed mutagenesis, we ide
39 gene were cloned by PCR and characterized by
deletion analysis by using a reporter assay.
40 Promoter
deletion analysis,
by particle-bombardment transient tra
41 Promoter
deletion analysis characterizes a putative RA-responsive
42 nteraction with its binding partners through
deletion analysis,
co-immunoprecipitation, two-hybrid as
43 Site-specific mutagenesis and
deletion analysis confirm that the hydrophobic residues
44 ' genetic elements of the dbpBA operon using
deletion analysis,
coupled with luciferase reporter assa
45 Deletion analysis defined a 25 kb fragment in the RAD50
46 Deletion analysis defined the 5' upstream HS cluster reg
47 Deletion analysis defined the minimal binding motif of t
48 amping and confocal microscopy, coupled with
deletion analysis,
demonstrate that MMP23-PD suppresses
49 Deletion analysis demonstrated that binding to the minim
50 Deletion analysis demonstrated that removal of the regio
51 Previously,
deletion analysis demonstrated that several effectors ha
52 Further,
deletion analysis demonstrated that TAZ binds to the NH(
53 osidase reporter in a proportional manner, a
deletion analysis demonstrated that the AOX1 5'UTR conta
54 with MET1 in vitro and in vivo, and further
deletion analysis demonstrated that the carboxyl-termina
55 A
deletion analysis demonstrated that the low affinity was
56 Extensive
deletion analysis demonstrated that the majority of sile
57 This
deletion analysis demonstrated that the Pen-2 cytosolic
58 r constructs, reverse transcriptase PCR, and
deletion analysis demonstrated that the UpxYs do not aff
59 Deletion analysis demonstrates a critical role for the R
60 Furthermore, systematic
deletion analysis demonstrates that N-terminal amino aci
61 of VR occurs within a (G/C)(14) element, and
deletion analysis demonstrates that the reaction is inde
62 Moreover, this pX
deletion analysis demonstrates that WT pX function is mo
63 Deletion analysis determined that the essential elements
64 Promoter
deletion analysis,
electrophoresis mobility shift assays
65 he assay proved as accurate as the reference
deletion analysis for all 192 isolates and detected and
66 ing site-directed mutagenesis and systematic
deletion analysis from the 5' and the 3' ends of the PAP
67 Deletion analysis further established that the cell line
68 Promoter
deletion analysis further indicates that enhancer elemen
69 Deletion analysis further refined FSN-1 binding to a con
70 Structure-based
deletion analysis further shows the presence of a Wnt si
71 Deletion analysis,
fusion proteins, and point mutations
72 ere isolated, identified and genotyped using
deletion analysis,
Hain(R) Genotype MTBC, spoligotyping
73 ce of each region in gene expression through
deletion analysis has been hampered by the cellular requ
74 5'- and 3'-
deletion analysis has identified the minimal region requ
75 teins is a key element of these circuits and
deletion analysis has implicated the conserved C-termina
76 Large-scale gene
deletion analysis has shown that over 80% of the ~6200 p
77 Deletion analysis,
heterologous promoter assays, and sit
78 Deletion analysis identified a 14-amino acid GRTH sequen
79 Promoter
deletion analysis identified a 280 bp segment of the BON
80 Deletion analysis identified a cyclic AMP receptor prote
81 Deletion analysis identified a dominant-inhibitory segme
82 Deletion analysis identified a Rhox5-responsive element
83 Deletion analysis identified a short segment of 10 amino
84 Deletion analysis identified a short stretch between nuc
85 Deletion analysis identified amino acids 730-758 of hTRP
86 Deletion analysis identified an octamer binding site tha
87 s were identified in the RNase-L 3'-UTR, and
deletion analysis identified positive and negative regul
88 The Nmp4/CIZ promoters are autoregulated and
deletion analysis identified regions that drive P(1) and
89 Sequential
deletion analysis identified that a 250 bp DNA fragment
90 Deletion analysis identified the differentiation-respons
91 Deletion analysis identified the region between residues
92 Deletion analysis identified the second domain (D2) with
93 Deletion analysis identified the Tie2 binding motif to b
94 Deletion analysis identified three elements correspondin
95 A previous
deletion analysis identified two ~100 bp fragments that
96 5'
deletion analysis implied a second upstream positive reg
97 Promoter
deletion analysis in 293T, BaF3, BaF3-p210, and K562 cel
98 Deletion analysis in HoxB BAC reporters reveals that the
99 Deletion analysis in Mt demonstrated that papA5 is requi
100 Systematic
deletion analysis in S. aureus RN6390 is consistent with
101 Deletion analysis in vivo, chemical cross-linking, and m
102 Finally, genetic
deletion analysis in yeast supported the role of a MEK-l
103 Functional
deletion analysis,
in situ mutagenesis and electromobili
104 spoligotyping and MIRU-VNTR, the addition of
deletion analysis increased the number of distinct patte
105 Biochemical mutagenesis and
deletion analysis indicate that this region mediates int
106 Deletion analysis indicated that independent domains of
107 Gene
deletion analysis indicated that only the cel3B gene pro
108 Deletion analysis indicated that promoter constructs lac
109 Deletion analysis indicated that the C-terminal coiled-c
110 Domain
deletion analysis indicated that the N-terminal domain o
111 Deletion analysis indicated that the noncoding exon 1 re
112 Deletion analysis indicated that the Rpt1 and Rpt2 motif
113 Furthermore, promoter
deletion analysis indicated that the sequence up to -543
114 Deletion analysis indicated that TPRs 2-6 of OGT interac
115 Deletion analysis indicates that both the N-terminal DED
116 prescreening followed by gene sequencing and
deletion analysis is feasible and may be desirable.
117 Deletion analysis is used to demonstrate important roles
118 Instead, by
deletion analysis it was discovered that a 46-bp region,
119 Promoter
deletion analysis lead to the identification of a potent
120 Deletion analysis led to the discovery of a novel protei
121 Deletion analysis localized the complementing activity (
122 Limited proteolysis, mass spectrometry and
deletion analysis localized the dRP lyase active site to
123 Progressive
deletion analysis located the SM22 responsive region of
124 Deletion analysis mapped p53-mediated repression to the
125 Deletion analysis mapped the centrosomal localization si
126 Functional
deletion analysis mapped the oxidative stress response e
127 Deletion analysis mapped the PIAS-interacting domain of
128 Deletion analysis mapped the SIRT1-binding domain of cor
129 Deletion analysis mapped this bend to amino acids 611 to
130 rected mutagenesis, DNase I footprinting and
deletion analysis of 5276 bp of 5' proximal -1b flanking
131 Through
deletion analysis of a -907/+70-bp 5' upstream region of
132 In frame
deletion analysis of Asc10 was used to identify a second
133 ith the corresponding MRE11 orthologues, and
deletion analysis of AtNBS1 defines a region towards the
134 By
deletion analysis of beta(2Deltag), we have now identifi
135 A
deletion analysis of Bir1 identified two regions importa
136 Prediction based
deletion analysis of both the promoter elements confirme
137 Deletion analysis of C/EBPalpha indicated that the C ter
138 Deletion analysis of CBS indicates that the C-terminal r
139 By
deletion analysis of cluster 19-1, the largest genomic d
140 Deletion analysis of CSP41 suggests that the specificity
141 Deletion analysis of CXCR4 promoter identified a seven-b
142 cids 1182-1186 and 69-73, respectively), and
deletion analysis of DRIP150 showed that regions contain
143 Extensive
deletion analysis of DRIP205 shows that multiple domains
144 Deletion analysis of EBNA3C identified a motif within am
145 A
deletion analysis of elements within the transcript reve
146 Deletion analysis of Gli1 indicated that multiple domain
147 Deletion analysis of green fluorescent protein (GFP)-ERK
148 Our 5'
deletion analysis of HOXA9 promoter shows that NF-kappaB
149 (b)
Deletion analysis of human osteocalcin and bone sialopro
150 Deletion analysis of Ins2 promoter identifies a sequence
151 Deletion analysis of IRAK4 indicates the essential struc
152 Clonal
deletion analysis of OPN promoter-luciferase constructs
153 Deletion analysis of p39 showed that muskelin binds to t
154 Deletion analysis of Pmga using single-copy Pmga-gusA re
155 Deletion analysis of POP2 revealed that the first alpha-
156 Deletion analysis of prolamine RNA sequences indicates t
157 Deletion analysis of Redbeta revealed that removal of ju
158 Deletion analysis of RhlR indicated that the N-terminal
159 Based on a
deletion analysis of RID to determine the minimal functi
160 Nevertheless,
deletion analysis of Rns demonstrated that the first 60
161 Deletion analysis of SPT5 supports our biochemical data,
162 Deletion analysis of the 3' end of dctD identified the m
163 Progressive
deletion analysis of the 3,221-bp sequence revealed that
164 Deletion analysis of the 5' flanking, approximately 3.0
165 Deletion analysis of the 5' UTR(COX4) revealed the prese
166 Using DNA
deletion analysis of the 5'-flanking region of promoter
167 Deletion analysis of the alpha2-subunit reveals that the
168 We performed a detailed
deletion analysis of the C-terminal region of Qin (amino
169 Deletion analysis of the CDK4 promoter revealed a 231-bp
170 Scanning
deletion analysis of the cytoplasmic domain (FlhAc) demo
171 Nase I footprinting analysis, coupled with a
deletion analysis of the farAB promoter region, indicate
172 A
deletion analysis of the fra-1 promoter revealed that se
173 Deletion analysis of the human gene identified an intron
174 Deletion analysis of the key DNA binding elements in the
175 Deletion analysis of the long and conserved 3'-UTR has r
176 Deletion analysis of the m-Tnk1 promoter reveals the pre
177 utation testing by full sequencing and large
deletion analysis of the MLH1, MSH2, and MSH6 genes was
178 Deletion analysis of the Npr1 promoter and luciferase as
179 Detailed
deletion analysis of the NtPMT1a gene promoter showed th
180 Deletion analysis of the ORF1 IRES indicates that RNA st
181 Deletion analysis of the PKCdelta promoter mapped the Na
182 Using
deletion analysis of the previously defined INO promoter
183 Deletion analysis of the PrfA regulon and complementatio
184 Deletion analysis of the promoter region revealed that b
185 The 5' and 3'
deletion analysis of the PTTG flanking region and electr
186 We performed promoter
deletion analysis of the rat CYP3A9 promoter and identif
187 Deletion analysis of the region indicates the presence o
188 Deletion analysis of the RPL27 promoter in transgenic pl
189 Deletion analysis of the sigmaNS RNA binding domain and
190 Deletion analysis of the sku genes indicated that all Ku
191 Deletion analysis of the tethering arms provides strong
192 Deletion analysis of the upstream sequence reveals that
193 Deletion analysis of the various functional domains of A
194 Deletion analysis of the vrg6 promoter identified the up
195 Deletion analysis of this intervening DNA segment has no
196 Deletion analysis of TLS-ERG in both mouse L-G myeloid p
197 Deletion analysis of transgenic embryos reduced this fra
198 Here we use a comparative
deletion analysis of two family members (ETR-3 and CELF4
199 In this work, we show through
deletion analysis of unmodified E. coli tRNA(Phe) that t
200 We performed a systematic
deletion analysis of YopM in Yersinia pseudotuberculosis
201 In spite of multiple episodes of set
deletion, analysis of the ratio of silent substitutions
202 suppressor mutation sites, binding data, and
deletion analysis onto the FliM(M) surface defines regio
203 23 in K-12, similar to results of the nested-
deletion analysis performed with EHEC.
204 Mutation and
deletion analysis permitted isolation and identification
205 t E47 is phosphorylated in vitro by p38, and
deletion analysis predicts that the critical amino acid(
206 Deletion analysis reveal a requirement for the N-termina
207 Subsequent mutation/
deletion analysis revealed a progesterone receptor half-
208 Deletion analysis revealed that a CsgB molecule missing
209 Promoter-
deletion analysis revealed that NF-kappaB was a necessar
210 Last,
deletion analysis revealed that non-NRRE sequences locat
211 Deletion analysis revealed that stimulation of endocytos
212 Genomic
deletion analysis revealed that strains of Mycobacterium
213 Deletion analysis revealed that the ability to activate
214 Deletion analysis revealed that the binding site is loca
215 Deletion analysis revealed that the core promoter activi
216 Deletion analysis revealed that the leader sequence or t
217 Deletion analysis revealed that the lethal effect of dep
218 Deletion analysis revealed that the luminal region of AT
219 Deletion analysis revealed that the N- and C-terminal mo
220 Deletion analysis revealed that the responsive region fo
221 Deletion analysis revealed that there are two potential
222 Deletion analysis revealed that three different ORF34 do
223 Deletion analysis revealed that transactivation involves
224 Electrophoretic mobility shift assay and
deletion analysis revealed three C/EBP binding sites tha
225 Deletion analysis revealed two classes of rhythmic V2a i
226 Deletion analysis revealed two DNA fragments from -2,725
227 Deletion analysis revealed two sites in the CTR of soybe
228 Deletion analysis reveals that relatively short regulato
229 Systematic
deletion analysis reveals that targeting activity is spr
230 Deletion analysis reveals that the EGF repeats and the t
231 Deletion analysis reveals that the Myo19 tail is necessa
232 A domain
deletion analysis reveals the molecular anatomy of Spt4/
233 Based on in vivo
deletion analysis,
sequences upstream of nucleotide -83
234 nal studies in combination with domain-based
deletion analysis show that the cytosolic KinA forms a h
235 Upstream promoter
deletion analysis showed that a 200- and 412-bp region o
236 Deletion analysis showed that binding of Smad3 to ICD4 w
237 Deletion analysis showed that sequences located up to 75
238 Deletion analysis showed that the CTP transferase domain
239 Deletion analysis showed that the Dlx3 interacting domai
240 Deletion analysis showed that the last C-terminal 10 ami
241 Deletion analysis showed that the leucine zipper domain
242 Deletion analysis showed that the N-terminal 198 of 403
243 Deletion analysis showed that the only genes essential f
244 several Smad binding sites in the promoter;
deletion analysis showed that the region between -274 an
245 Domain
deletion analysis showed that the sterile alpha-motif of
246 Deletion analysis showed that the tRNA(Ser) TPsiC stem-l
247 Deletion analysis shows that that the first 125 amino ac
248 Deletion analysis shows that the caspase-like domain of
249 Domain
deletion analysis shows that the N-terminal DNA-binding
250 Deletion analysis shows that the N-terminal domain of Cl
251 5'-
deletion analysis,
site-directed mutagenesis, and transa
252 5'-
deletion analysis,
site-directed mutagenesis, and transa
253 ll isolates were further characterized using
deletion analysis,
spoligotyping and MIRU-VNTR analysis.
254 Deletion analysis suggested that the N-terminal 67 and C
255 by E2F1 in transient transfections; further,
deletion analysis suggested that the region spanning the
256 Promoter
deletion analysis suggests that ligand-specific receptor
257 Deletion analysis suggests that the 2C central and C-ter
258 Although
deletion analysis supported the requirement of binding s
259 compare these hypotheses in the context of a
deletion analysis that further explores the biphasic dyn
260 IS1 transcription, we carried out a promoter
deletion analysis that identified three regions required
261 This study describes a
deletion analysis that investigates which parts of YidC
262 We demonstrate by
deletion analysis that the extension contributes to DNA
263 It was previously shown by
deletion analysis that the N terminus of Phd was require
264 Through
deletion analysis,
the dimerization interface was mapped
265 By 5'
deletion analysis,
the element(s) responsible for this i
266 By
deletion analysis,
the region between nucleotides -296 t
267 ent lesions, we carried out a candidate gene
deletion analysis to identify genes whose mutation confe
268 sed a reverse yeast two-hybrid selection and
deletion analysis to identify NSI mutants that failed to
269 sed a reverse yeast two-hybrid selection and
deletion analysis to identify NSP mutants that were impa
270 In this study, we performed a
deletion analysis to identify the critical sequences in
271 the present study, we performed a systematic
deletion analysis to identify the signal required for tr
272 Finally, we used domain
deletion analysis to investigate the function of the C-t
273 Deletion analysis to map the IN-binding domain on RT rev
274 ed in SK-N-SH cells were shown by 5'- and 3'-
deletion analysis to play a crucial role in both cell li
275 We used a
deletion analysis to search for functional RNA domains w
276 Here, we use
deletion analysis to show that the LN domain region of n
277 was accomplished in Bacillus subtilis, where
deletion analysis uncovered two cis-elements within the
278 B12-responsive element has been localized by
deletion analysis using a reporter gene assay to a 70-bp
279 Therefore, we used VP40
deletion analysis,
virus-like particle-release assays, a
280 Deletion analysis was facilitated by an improved method
281 ectional promoter activity in a model plant,
deletion analysis was performed for seven rice promoters
282 ificial chromosome (BAC)-based reporter gene
deletion analysis was performed in transgenic mice.
283 Germline PTEN mutation/
deletion analysis was performed.
284 ation scanning, including promoter and large
deletion analysis,
was performed for all subjects.
285 Using
deletion analysis,
we also identify a novel N-terminal d
286 Through
deletion analysis,
we demonstrated that the alpha-(1-->2
287 Through mutation and
deletion analysis,
we have analyzed which specific domai
288 Through a
deletion analysis,
we have identified a cis-acting eleme
289 Using
deletion analysis,
we have identified the PELP1 COOH-ter
290 Through promoter
deletion analysis,
we have mapped a distal E-box element
291 Using promoter
deletion analysis,
we identified a region 1.1 kb upstrea
292 Combined with
deletion analysis,
we identified DNA elements as short a
293 By
deletion analysis,
we identified splicing silencers loca
294 By dissecting its promoters with progressive
deletion analysis,
we identified the sequence between -1
295 Through
deletion analysis,
we identify an active region responsi
296 Using
deletion analysis,
we show that part of this purine-rich
297 By
deletion analysis,
we show that the binding of soluble f
298 rapid amplification of cDNA ends (RACE) and
deletion analysis were used to identify the disA promote
299 all-angle x-ray scattering (SAXS) and domain
deletion analysis were used to obtain solution structura
300 f alanine-scanning, limited proteolysis, and
deletion analysis,
which show that the two reactions dep