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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

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