1 3 cap gene were generated in a single marker
rescue experiment.
2 f UNC-73 RhoGEF-2 isoform function in mutant
rescue experiments.
3 ole of this motif in HCV replication in cDNA
rescue experiments.
4 quirements for this function of SV2, we used
rescue experiments.
5 e phenotypes to BBS knockdown was shown with
rescue experiments.
6 s confirmed by gene knockdown and pyrimidine
rescue experiments.
7 these with gfp reporters and tissue-specific
rescue experiments.
8 in pigment granule biogenesis in transgenic
rescue experiments.
9 sh between these possibilities, we performed
rescue experiments.
10 -specific mutagenesis together with chemical
rescue experiments.
11 within a 6.4 kb genomic region by transgenic
rescue experiments.
12 ccount when interpreting the results of Mn2+
rescue experiments.
13 of the relative rates and yields of chemical
rescue experiments.
14 tion, as demonstrated by immunodepletion and
rescue experiments.
15 t can be distinguished by their response to "
rescue" experiments.
16 In
rescue experiments,
achaete or scute, but not lethal of
17 robing, mutate-and-map studies, and mutation/
rescue experiments all provide strong evidence for the s
18 ing the Psn transcription unit by transgenic
rescue experiments allowed us to localize two of the ess
19 toxin-antitoxins using in vivo toxicity and
rescue experiments along with in vitro interaction exper
20 These
rescue experiments also separate the transcriptional fro
21 e mechanism behind these phenotypes, we used
rescue experiments and found that Smad5 is unable to res
22 f the phenotype was verified by interspecies
rescue experiments and further mutant analyses.
23 ion serves to reduce gene repair activity in
rescue experiments and in experiments where RAD52 is ove
24 ing Drosophila eye development using in vivo
rescue experiments and in vitro transcriptional regulato
25 Plasmid
rescue experiments and sequence analysis of rearranged p
26 Rescue experiments and the use of two separate hnRNP K M
27 he LIM-homeobox gene Lhx6 is induced by this
rescue experiment,
and gain- and loss-of-function studie
28 Reciprocal
rescue experiments,
and comparison of the effects of the
29 blotting, enzyme measurements, transduction
rescue experiments,
and in vitro calcification assays we
30 ockouts, ES cell differentiation and chimera
rescue experiments,
and tissue-specific inducible knocko
31 Gene knockout strategies, RNAi and
rescue experiments are all employed to study mammalian g
32 By performing such
rescue experiments before and after 30 h of development,
33 In transient, stable, and stable-inducible
rescue experiments,
both wild-type Abeta and Aalpha muta
34 Rescue experiments by ectopic expression of wild-type or
35 ted and assayed their activity in phenotypic
rescue experiments by introducing them as transgenes int
36 Rescue experiments can help to distinguish between devel
37 Through
rescue experiments,
chromatin immunoprecipitation and re
38 o1 by mapping, and confirmed its function by
rescue experiments,
combined with genetic, cytological a
39 and identified TSV by map-based cloning and
rescue experiments,
combined with genetic, cytological a
40 Rescue experiments conducted by injecting mRNAs encoding
41 kdown in zebrafish and report the results of
rescue experiments conducted with full-length and trunca
42 Rescue experiments conducted with mouse otoferlin restor
43 Rescue experiments confirm that the specific combination
44 Furthermore, small-interferring RNA (siRNA)
rescue experiments confirm that the UIMs of S5a are requ
45 Metabolic
rescue experiments confirm the specificity of these effe
46 Phenotypic
rescue experiments confirmed that betaPIX and GIT1 repre
47 Rescue experiments confirmed that HDAC6 mediates the Erg
48 Rescue experiments confirmed that Shh-dependent prolifer
49 In vivo knockdown and
rescue experiments confirmed that the 3' end processing
50 Rescue experiments confirmed that this phenotype was due
51 RNA interference lines and molecular
rescue experiments confirmed the linkage between the bra
52 Rescue experiments confirmed the specificity of the RNA
53 mutant lacking Or22a, along with transgenic
rescue experiments,
confirms the mapping and demonstrate
54 relative efficiencies observed in Bmp ligand
rescue experiments,
conserved chromosomal synteny, and i
55 Rescue experiments coupled with transcriptome analysis a
56 RNA interference, knockout and
rescue experiments demonstrate a critical role for ASIC1
57 etastasis-associated gene uPA and phenotypic
rescue experiments demonstrate that exogenous urokinase
58 Clonal analysis and cell type-specific
rescue experiments demonstrate that Lsd1 functions withi
59 Our
rescue experiments demonstrate that Msk is required in t
60 Cell-specific ablation and
rescue experiments demonstrate that orientation to humid
61 In vivo gain-of-function and
rescue experiments demonstrate that Sema3c is a major do
62 Genetic
rescue experiments demonstrate that this interface is in
63 Genetic
rescue experiments demonstrate, surprisingly, that phosp
64 , as well as RNA-interference and phenotypic-
rescue experiments,
demonstrate that Ofs has eIF4G activ
65 Rescue experiments demonstrated that all neurexins teste
66 Genetic ablation and
rescue experiments demonstrated that Bmi1 is a critical
67 DNA sequence analysis and marker
rescue experiments demonstrated that divE is the C. cres
68 Cell-specific
rescue experiments demonstrated that EGL-15/FGFR acts in
69 Viral
rescue experiments demonstrated that long-term re-expres
70 Rescue experiments demonstrated that RAP domain is requi
71 Mechanistically, metabolic
rescue experiments demonstrated that statins reduce memb
72 Marker
rescue experiments demonstrated that the genetic lesion
73 RNA interference-based knock-down and
rescue experiments demonstrated that the p.P916R mutatio
74 Marker
rescue experiments demonstrated that the UL5 gene from T
75 was reduced in mutants, and cell-autonomous
rescue experiments demonstrated the indispensability of
76 in association was highlighted by functional
rescue experiments demonstrating that a Cobl mutant defi
77 on Noxa up-regulation as confirmed by siRNA
rescue experiments demonstrating that siPMAIP1-based tar
78 Phenocopy and
rescue experiments determined that a loss of Vps11 resul
79 Loss-of-function and
rescue experiments determined that l(2)tn is allelic to
80 EphB knockdown and
rescue experiments during different developmental time w
81 In fis1Delta
rescue experiments,
Fis1-E78A causes a novel localizatio
82 A Cdc42 mutant
rescue experiment found that downstream of Cdc42, p21-ac
83 In vivo genetic
rescue experiments further confirm that the lethality of
84 Transgenic
rescue experiments further demonstrate that endodermal E
85 Rescue experiments further demonstrate that periostin fu
86 In vivo transformation
rescue experiments further showed that the reduced DNase
87 d almost exclusively in mouse models, and no
rescue experiments have been reported.
88 ed in neurons, not muscle, and cell-specific
rescue experiments have previously shown that emodepside
89 These gsb alleles, as well as gsb
rescue experiments,
have allowed us to determine which a
90 Additional in vivo marker
rescue experiments identified a 20-kb fragment, encoding
91 Genetic and pharmacological
rescue experiments identified c-Jun as a key substrate o
92 Rescue experiments identified cyclin D1 as the primary t
93 Using in vitro assays and
rescue experiments in autaptic neurons, we show that int
94 Rescue experiments in Bax(fl/fl) mutants supported these
95 nt fusion and leads to a gain-of-function in
rescue experiments in Caenorhabditis elegans unc-18 null
96 However, genetic
rescue experiments in combination with additional geneti
97 We used
rescue experiments in combination with an extensive muta
98 Using
rescue experiments in cultured syntaxin-deficient neuron
99 Rescue experiments in dlp embryos demonstrate that Dlp f
100 Importantly,
rescue experiments in DM1 myoblasts demonstrated that lo
101 Rescue experiments in Drosophila indicate that Wnt signa
102 terization of Trichoplax OGT/OGA and genetic
rescue experiments in Drosophila melanogaster that these
103 etency of the reporter was confirmed by gene
rescue experiments in EGFR-null cells.
104 ation of filopodia in cells as determined by
rescue experiments in fascin-depleted cells.
105 ts with inhibitors of FAK, Src, and PI3K and
rescue experiments in MEFs, we found that the FAK/Src/PI
106 kdown experiments in hematopoietic cells and
rescue experiments in nonhematopoietic cells show that P
107 ncluding locomotor activity, protection, and
rescue experiments in rats, of drug toxicity treatment w
108 Rescue experiments in ret zebrafish embryos expressing t
109 quantitative imaging, electrophysiology, and
rescue experiments in sensory and motor neurons in vivo.
110 equirement, we conducted a series of genetic
rescue experiments in snail mutant embryos.
111 By employing loss-of-function and
rescue experiments in vitro, we showed that both recepto
112 This is supported by genetic
rescue experiments in which the Ugdh lacrimal gland defe
113 to form 18 S rRNA were assayed by depletion/
rescue experiments in Xenopus oocytes.
114 Finally, in
rescue experiments in zebrafish, all ARL13B allele combi
115 Using mutant and transgenic
rescue experiments in zebrafish, we show that Tbx1 funct
116 pective is strongly supported by "coreceptor
rescue" experiments in which transgenic CD4 coreceptors
117 iR-21-mediated actions was demonstrated by a
rescue experiment,
in which IGFBP3 knockdown in miR-21KD
118 mediated tumorigenesis was demonstrated by a
rescue experiment,
in which silencing FBXO11 in miR-21KD
119 Importantly,
rescue experiments including expression of full length b
120 Rescue experiments increasing AID expression in KI B cel
121 Tissue-specific
rescue experiments indicate a partial requirement in epi
122 Rescue experiments indicate that APM-2/mu2 functions in
123 Rescue experiments indicate that Baboon binding, but not
124 Rescue experiments indicate that catalytic activity and
125 with its expression profile, tissue-specific
rescue experiments indicate that cmpy functions neuronal
126 Moreover, targeted knockdown and
rescue experiments indicate that Col expression is requi
127 ults of the mutation analysis and phenotypic
rescue experiments indicate that LMBD1 interacts with ad
128 Cell-specific
rescue experiments indicate that lsy-2 is required auton
129 rmore, gain and loss of function and genetic
rescue experiments indicate that Nrg1 intracellular sign
130 Moreover,
rescue experiments indicate that re-expression of p54/nr
131 Cell ablation, cell-specific knockdown, and
rescue experiments indicate that secreted semaphorins fr
132 Rescue experiments indicate that Sox2 is downstream of X
133 mozygous mutant plants generated from embryo-
rescue experiments indicated that emp4 also affects gene
134 Inhibition and
rescue experiments indicated that Reelin regulates migra
135 vab-1 mutations; as well as tissue specific
rescue experiments;
indicated that each of these gene pr
136 This
rescue experiment is the second example in which the fun
137 Tissue-specific
rescue experiments,
lesion studies, and neurophysiologic
138 Marker
rescue experiments localized the mutations in one group
139 Genetic
rescue experiments normalized the CD73 and alkaline phos
140 splice variants in vivo, we have performed a
rescue experiment of the Cypher null mutant by replacing
141 Rescue experiments of abi mutants also reveals a physiol
142 ossible mechanism for oscillations in double-
rescue experiments of per(01)-tim(01) mutants.
143 Rescue experiments on cultured patient megakaryocytes co
144 provides valuable insight into the chemical
rescue experiments on HCA II mutants.
145 Finally, Zbtb11 mutant
rescue experiments point to a ZBTB11-regulated TP53 requ
146 Rescue experiments point to the early period of polar Dl
147 Genetic
rescue experiments presented evidence that both BMP and
148 First, transgenic
rescue experiments prove that the Sac locus encodes T1R3
149 This is the first time a metal-
rescue experiment provides evidence for inner-sphere div
150 In a
rescue experiment,
rats initiated therapy on Day 21.
151 Rescue experiments relying on viral RNA polymerase-induc
152 Knockdown-
rescue experiments reveal that C18 executes a role that
153 ShRNA knockdown/
rescue experiments reveal that LIMK1 palmitoylation is e
154 Transgenic
rescue experiments reveal that Robo can function in a ce
155 Lentiviral
rescue experiments reveal that such disruption selective
156 Genetic
rescue experiments reveal that Tbx2 and Tbx3 function do
157 Inhibition and
rescue experiments revealed that defective MEK/extracell
158 Morpholino-based knockdown and
rescue experiments revealed that MCT8 is strictly requir
159 es in combination with siRNA knockdown-based
rescue experiments revealed that MLN4924 induced the acc
160 Rescue experiments revealed that only the activating but
161 ological inhibitors, dominant negatives, and
rescue experiments revealed that PI3K-C2beta and AKT wer
162 Moreover,
rescue experiments revealed that the decrease in spontan
163 RNA interference
rescue experiments revealed that the NH(2)-terminal four
164 Rescue experiments revealed that the phenotype is caused
165 ent mice, combined with gain-of-function and
rescue experiments,
revealed a specific role for this li
166 and epigenetic analysis, as well as genetic
rescue experiments,
revealed that EZH2 represses neurona
167 Examination of mutant embryos and tetraploid
rescue experiments reveals that abnormal yolk-sac vascul
168 Overexpression of c-MYC in
rescue experiments reversed miR-203-induced growth arres
169 Lastly, deletion-
rescue experiments show that a respiration-defective mut
170 s with unresolved intercellular bridges, and
rescue experiments show that expression of small interfe
171 Rescue experiments show that increased expression of H3
172 Computational analysis and
rescue experiments show that PTEN (phosphatase and tensi
173 Functional
rescue experiments show that the ability of human LAMP2
174 Rescue experiments show that the isomerase activity of e
175 Metal-ion
rescue experiments show that those at positions 9, 12, a
176 number of neurons, including PVT, transgenic
rescue experiments show that zig-3 can function irrespec
177 In utero
rescue experiments showed that a key function of Magoh i
178 Protein depletion and
rescue experiments showed that EB1 and EB3, but not EB2,
179 Rescue experiments showed that fully functional myosin V
180 Transgenic
rescue experiments showed that Gr5a confers response to
181 Cell-autonomous
rescue experiments showed that Sema-1a is involved in as
182 MIG6 and the apoptosis regulator BIM, which
rescue experiments showed were essential to mediate the
183 of two alleles, RNA interference (RNAi) and
rescuing experiments showed that dig-1 encodes a giant m
184 Moreover,
rescue experiments shows that Cenpj mediates the role of
185 02, D132, and D135) by mutagenesis and metal
rescue experiments specified residues that contribute to
186 Furthermore, gain-of-function and
rescue experiments suggest an important regulatory role
187 Additional
rescue experiments suggest involvement of the Ras pathwa
188 al adhesion-targeting domain of p130Cas, and
rescue experiments suggest that Ajuba acts upstream of p
189 Transgene
rescue experiments suggest that differences in isoform e
190 Neuron- and muscle-specific
rescue experiments suggest that DYB-1 is required for SL
191 Tissue-specific knockdown and
rescue experiments suggest that epidermally derived Pvf1
192 These
rescue experiments suggest that male and female gametoge
193 Loss-of-function and germ layer-specific
rescue experiments suggest that pannier provides an esse
194 Rescue experiments suggest that Slit is secreted from th
195 Rescue experiments suggest that Spz3 can exert these eff
196 RNAi-
rescue experiments suggest that the CARD, coiled-coil, S
197 Tissue-specific transgenic
rescue experiments suggest that the FN matrix on the sur
198 Mutant
rescue experiments suggest that the H2AZ-like rather tha
199 genetic interactions, expression studies and
rescue experiments suggest that, in normal development,
200 Competition UV cross-link and translation
rescue experiments suggested that LAP inhibits IRES-medi
201 These chemical
rescue experiments support the conclusion that Tyr140 an
202 Rescue experiments support these observations, indicatin
203 ly chromosomes, and have conducted a genetic
rescue experiment that suggests that the edited cDNA is
204 We also show, using a "
rescue" experiment,
that the molecular target of the nit
205 In
rescue experiments,
the transfection of a vector encodin
206 This study analyzes, by genetic
rescue experiments,
the virulence of mutants affecting a
207 show by mosaic analysis and tissue-specific
rescue experiments to act in muscle to affect locomotory
208 We therefore performed cross-species
rescue experiments to compare the functions of murine an
209 in a combination of overexpression and RNAi
rescue experiments to determine the requirement for PAK4
210 hogenic ASFV isolate E70 were used in marker
rescue experiments to identify sequences capable of rest
211 protein depletion coupled with protein-based
rescue experiments to investigate the involvement of per
212 We used cell-autonomous
rescue experiments to show that Ben has a presynaptic ro
213 We used transgene
rescue experiments to show that defects in these dopamin
214 We performed a series of transgenic
rescue experiments to test the spatial, structural, and
215 on of specific gene targets, whereas genetic
rescue experiments unambiguously link Notch 3 function i
216 Collectively, these data, as well as a
rescue experiment using rIL-10 together with rapamycin,
217 Rescue experiments using a GAL4-driven pUAS transgene de
218 Genetic
rescue experiments using an uncleavable form of Robo sho
219 Rescue experiments using constitutively active Cdc42 or
220 Rescue experiments using G3BP1 mutants show that phospho
221 Rescue experiments using mRNA bearing Notch repeat 1 mut
222 Rescue experiments using Pard6b mRNA restored cell polar
223 Rescue experiments using RNA interference and transfecti
224 Azide
rescue experiments using the D327G enzyme showed a 30-fo
225 assays; results were validated in functional
rescue experiments using transgenes expression in EPCs f
226 Genetic
rescue experiments utilizing FEN1 mutant proteins that r
227 Based on transformation
rescue experiments we hypothesize that EGRH-1 in the som
228 Using gene expression analysis and
rescue experiments we show that Alcama functions downstr
229 Through a transgenic
rescue experiment,
we verified that sequence polymorphis
230 munofluorescence reconstruction imaging, and
rescue experiments,
we demonstrate that the dephosphoryl
231 By performing RNA interference-
rescue experiments,
we demonstrate that these phosphoryl
232 Importantly, using conditional alleles and
rescue experiments,
we demonstrate that ZFP809 is requir
233 Using dominant negative mutants and
rescue experiments,
we demonstrate the functional signif
234 nt analyses, genetic mapping, and transgenic
rescue experiments,
we found that 2Bc function, mediated
235 of Connexin 43 (Cx43) and Cx26 together with
rescue experiments,
we found that gap junctions are disp
236 Using tissue-specific
rescue experiments,
we found that Gr66a-expressing neuro
237 Moreover, through protein depletion and
rescue experiments,
we found that the CNK1/cytohesin int
238 rough mutant analysis, protein depletion and
rescue experiments,
we identify CNK2 as a spatial modula
239 escence analysis, time-lapse microscopy, and
rescue experiments,
we investigate the roles of these 12
240 combination of pharmacological inhibitor and
rescue experiments,
we provide evidence that isoprenoids
241 wing on a combination of pharmacological and
rescue experiments,
we provide evidence that mTOR kinase
242 using an EMSY knock-out line and subsequent
rescue experiments,
we show that EMSY is in most cases p
243 Through
rescue experiments,
we show that specific slo-1 isoforms
244 By cell ablation and cell-specific
rescue experiments,
we show that the ASI chemosensory ne
245 In
rescue experiments,
we showed that in the zebrafish floo
246 In ex vivo culture models and genetic
rescue experiments,
we showed that Shp2 acts downstream
247 he cap genes from several independent marker
rescue experiments were PCR amplified, cloned, and then
248 Rescue experiments were performed by expressing wild-typ
249 tative virulence determinant, in vivo marker
rescue experiments were performed by inoculating swine w
250 n (PAR) junctional complex identified by the
rescue experiment with tjp-2/ZO-2 or the PAR complex (pa
251 Moreover,
rescue experiments with a kinase-dead mutant of hRio1 re
252 Rescue experiments with a MOF histone acetyltransferase
253 Marker
rescue experiments with a wild-type IVa2 DNA fragment co
254 Rescue experiments with ASA showed a normalization of th
255 Chemical
rescue experiments with catalytic mutants of Csk demonst
256 Rescue experiments with catalytically inactive mutants o
257 ors can function autonomously, cell-specific
rescue experiments with circadian clock mutants indicate
258 Rescue experiments with human tau expression restored MT
259 Functional
rescue experiments with Lyn siRNA targeting the 3' UTR i
260 Rescue experiments with Mib1 and Neuralized show further
261 Rescue experiments with mutated KRas 3'UTR showed very s
262 Rescue experiments with mutated transgenes demonstrate t
263 Further observations, including
rescue experiments with nod kinesin-like protein transge
264 ockout mice and chimeric animals, along with
rescue experiments with novel CD24 fusion protein demons
265 In vitro
rescue experiments with purified exosomes and matrix coa
266 Complementation
rescue experiments with RSV-MLV chimeras now map this di
267 Rescue experiments with syntaxin-1 mutants revealed that
268 By means of
rescuing experiments with a series of deletion and point