1 y LINC00346 re-expression in KO cells (i.e.,
rescue experiment).
2 3 cap gene were generated in a single marker
rescue experiment.
3 f UNC-73 RhoGEF-2 isoform function in mutant
rescue experiments.
4 ole of this motif in HCV replication in cDNA
rescue experiments.
5 quirements for this function of SV2, we used
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 e phenotypes to BBS knockdown was shown with
rescue experiments.
16 t can be distinguished by their response to "
rescue" experiments.
17 In
rescue experiments,
19,20-DHDP prevented astrocyte loss
18 lidated through in vivo loss of function and
rescue experiments,
3-dimensional immunohistochemistry,
19 In
rescue experiments,
achaete or scute, but not lethal of
20 robing, mutate-and-map studies, and mutation/
rescue experiments all provide strong evidence for the s
21 ing the Psn transcription unit by transgenic
rescue experiments allowed us to localize two of the ess
22 toxin-antitoxins using in vivo toxicity and
rescue experiments along with in vitro interaction exper
23 These
rescue experiments also separate the transcriptional fro
24 Rescue experiments and 3C data confirmed this hypothesis
25 e mechanism behind these phenotypes, we used
rescue experiments and found that Smad5 is unable to res
26 f the phenotype was verified by interspecies
rescue experiments and further mutant analyses.
27 ion serves to reduce gene repair activity in
rescue experiments and in experiments where RAD52 is ove
28 ing Drosophila eye development using in vivo
rescue experiments and in vitro transcriptional regulato
29 Plasmid
rescue experiments and sequence analysis of rearranged p
30 Rescue experiments and the use of two separate hnRNP K M
31 he LIM-homeobox gene Lhx6 is induced by this
rescue experiment,
and gain- and loss-of-function studie
32 Reciprocal
rescue experiments,
and comparison of the effects of the
33 blotting, enzyme measurements, transduction
rescue experiments,
and in vitro calcification assays we
34 ockouts, ES cell differentiation and chimera
rescue experiments,
and tissue-specific inducible knocko
35 Gene knockout strategies, RNAi and
rescue experiments are all employed to study mammalian g
36 By performing such
rescue experiments before and after 30 h of development,
37 In transient, stable, and stable-inducible
rescue experiments,
both wild-type Abeta and Aalpha muta
38 Rescue experiments by ectopic expression of wild-type or
39 ted and assayed their activity in phenotypic
rescue experiments by introducing them as transgenes int
40 Rescue experiments can help to distinguish between devel
41 Through
rescue experiments,
chromatin immunoprecipitation and re
42 and identified TSV by map-based cloning and
rescue experiments,
combined with genetic, cytological a
43 o1 by mapping, and confirmed its function by
rescue experiments,
combined with genetic, cytological a
44 Rescue experiments conducted by injecting mRNAs encoding
45 kdown in zebrafish and report the results of
rescue experiments conducted with full-length and trunca
46 Rescue experiments conducted with mouse otoferlin restor
47 Rescue experiments confirm that the specific combination
48 Furthermore, small-interferring RNA (siRNA)
rescue experiments confirm that the UIMs of S5a are requ
49 henotype of miR-138 knockdown and functional
rescue experiments confirm that TUSC2 is a direct downst
50 Metabolic
rescue experiments confirm the specificity of these effe
51 Phenotypic
rescue experiments confirmed that betaPIX and GIT1 repre
52 Rescue experiments confirmed that HDAC6 mediates the Erg
53 Rescue experiments confirmed that Shh-dependent prolifer
54 In vivo knockdown and
rescue experiments confirmed that the 3' end processing
55 Rescue experiments confirmed that this phenotype was due
56 RNA interference lines and molecular
rescue experiments confirmed the linkage between the bra
57 Rescue experiments confirmed the specificity of the RNA
58 mutant lacking Or22a, along with transgenic
rescue experiments,
confirms the mapping and demonstrate
59 relative efficiencies observed in Bmp ligand
rescue experiments,
conserved chromosomal synteny, and i
60 Rescue experiments coupled with transcriptome analysis a
61 RNA interference, knockout and
rescue experiments demonstrate a critical role for ASIC1
62 etastasis-associated gene uPA and phenotypic
rescue experiments demonstrate that exogenous urokinase
63 Clonal analysis and cell type-specific
rescue experiments demonstrate that Lsd1 functions withi
64 Our
rescue experiments demonstrate that Msk is required in t
65 Cell-specific ablation and
rescue experiments demonstrate that orientation to humid
66 In vivo gain-of-function and
rescue experiments demonstrate that Sema3c is a major do
67 Genetic
rescue experiments demonstrate that this interface is in
68 Genetic
rescue experiments demonstrate, surprisingly, that phosp
69 , as well as RNA-interference and phenotypic-
rescue experiments,
demonstrate that Ofs has eIF4G activ
70 Rescue experiments demonstrated that all neurexins teste
71 Genetic ablation and
rescue experiments demonstrated that Bmi1 is a critical
72 DNA sequence analysis and marker
rescue experiments demonstrated that divE is the C. cres
73 Cell-specific
rescue experiments demonstrated that EGL-15/FGFR acts in
74 Viral
rescue experiments demonstrated that long-term re-expres
75 Rescue experiments demonstrated that miRNA binding and 3
76 Moreover, genetic
rescue experiments demonstrated that PUM binding is requ
77 Rescue experiments demonstrated that RAP domain is requi
78 Mechanistically, metabolic
rescue experiments demonstrated that statins reduce memb
79 Marker
rescue experiments demonstrated that the genetic lesion
80 RNA interference-based knock-down and
rescue experiments demonstrated that the p.P916R mutatio
81 Marker
rescue experiments demonstrated that the UL5 gene from T
82 was reduced in mutants, and cell-autonomous
rescue experiments demonstrated the indispensability of
83 in association was highlighted by functional
rescue experiments demonstrating that a Cobl mutant defi
84 on Noxa up-regulation as confirmed by siRNA
rescue experiments demonstrating that siPMAIP1-based tar
85 ent induced a strong MAD2 downregulation and
rescue experiments depicted it as a key effector in HuR-
86 Phenocopy and
rescue experiments determined that a loss of Vps11 resul
87 Loss-of-function and
rescue experiments determined that l(2)tn is allelic to
88 EphB knockdown and
rescue experiments during different developmental time w
89 In fis1Delta
rescue experiments,
Fis1-E78A causes a novel localizatio
90 A Cdc42 mutant
rescue experiment found that downstream of Cdc42, p21-ac
91 In vivo genetic
rescue experiments further confirm that the lethality of
92 Transgenic
rescue experiments further demonstrate that endodermal E
93 Rescue experiments further demonstrate that periostin fu
94 In vivo transformation
rescue experiments further showed that the reduced DNase
95 d almost exclusively in mouse models, and no
rescue experiments have been reported.
96 ed in neurons, not muscle, and cell-specific
rescue experiments have previously shown that emodepside
97 These gsb alleles, as well as gsb
rescue experiments,
have allowed us to determine which a
98 Additional in vivo marker
rescue experiments identified a 20-kb fragment, encoding
99 Genetic and pharmacological
rescue experiments identified c-Jun as a key substrate o
100 Rescue experiments identified cyclin D1 as the primary t
101 Using in vitro assays and
rescue experiments in autaptic neurons, we show that int
102 Rescue experiments in Bax(fl/fl) mutants supported these
103 nt fusion and leads to a gain-of-function in
rescue experiments in Caenorhabditis elegans unc-18 null
104 We used cross-species
rescue experiments in Cd2ap(KD) zebrafish and in Drosoph
105 However, genetic
rescue experiments in combination with additional geneti
106 We used
rescue experiments in combination with an extensive muta
107 Using
rescue experiments in cultured syntaxin-deficient neuron
108 Rescue experiments in dlp embryos demonstrate that Dlp f
109 Importantly,
rescue experiments in DM1 myoblasts demonstrated that lo
110 Rescue experiments in Dnmt3a/3b double knockout mouse em
111 However,
rescue experiments in Dnmt3a/3b/3l triple-knockout (TKO)
112 Rescue experiments in Drosophila indicate that Wnt signa
113 terization of Trichoplax OGT/OGA and genetic
rescue experiments in Drosophila melanogaster that these
114 etency of the reporter was confirmed by gene
rescue experiments in EGFR-null cells.
115 ation of filopodia in cells as determined by
rescue experiments in fascin-depleted cells.
116 ts with inhibitors of FAK, Src, and PI3K and
rescue experiments in MEFs, we found that the FAK/Src/PI
117 kdown experiments in hematopoietic cells and
rescue experiments in nonhematopoietic cells show that P
118 ncluding locomotor activity, protection, and
rescue experiments in rats, of drug toxicity treatment w
119 Rescue experiments in ret zebrafish embryos expressing t
120 quantitative imaging, electrophysiology, and
rescue experiments in sensory and motor neurons in vivo.
121 equirement, we conducted a series of genetic
rescue experiments in snail mutant embryos.
122 Angiogenic
rescue experiments in ventricular explants, or in primar
123 By employing loss-of-function and
rescue experiments in vitro, we showed that both recepto
124 This is supported by genetic
rescue experiments in which the Ugdh lacrimal gland defe
125 to form 18 S rRNA were assayed by depletion/
rescue experiments in Xenopus oocytes.
126 Finally, in
rescue experiments in zebrafish, all ARL13B allele combi
127 Using mutant and transgenic
rescue experiments in zebrafish, we show that Tbx1 funct
128 pective is strongly supported by "coreceptor
rescue" experiments in which transgenic CD4 coreceptors
129 iR-21-mediated actions was demonstrated by a
rescue experiment,
in which IGFBP3 knockdown in miR-21KD
130 mediated tumorigenesis was demonstrated by a
rescue experiment,
in which silencing FBXO11 in miR-21KD
131 Importantly,
rescue experiments including expression of full length b
132 Rescue experiments increasing AID expression in KI B cel
133 Tissue-specific
rescue experiments indicate a partial requirement in epi
134 Rescue experiments indicate that APM-2/mu2 functions in
135 Rescue experiments indicate that Baboon binding, but not
136 Rescue experiments indicate that catalytic activity and
137 with its expression profile, tissue-specific
rescue experiments indicate that cmpy functions neuronal
138 Moreover, targeted knockdown and
rescue experiments indicate that Col expression is requi
139 ults of the mutation analysis and phenotypic
rescue experiments indicate that LMBD1 interacts with ad
140 Cell-specific
rescue experiments indicate that lsy-2 is required auton
141 Rescue experiments indicate that MCAK centromeric activi
142 rmore, gain and loss of function and genetic
rescue experiments indicate that Nrg1 intracellular sign
143 Moreover,
rescue experiments indicate that re-expression of p54/nr
144 Cell ablation, cell-specific knockdown, and
rescue experiments indicate that secreted semaphorins fr
145 Rescue experiments indicate that Sox2 is downstream of X
146 mozygous mutant plants generated from embryo-
rescue experiments indicated that emp4 also affects gene
147 Inhibition and
rescue experiments indicated that Reelin regulates migra
148 Finally, maternal knockdown and
rescue experiments indicated that the KH domains were es
149 vab-1 mutations; as well as tissue specific
rescue experiments;
indicated that each of these gene pr
150 This
rescue experiment is the second example in which the fun
151 Tissue-specific
rescue experiments,
lesion studies, and neurophysiologic
152 Marker
rescue experiments localized the mutations in one group
153 Genetic
rescue experiments normalized the CD73 and alkaline phos
154 splice variants in vivo, we have performed a
rescue experiment of the Cypher null mutant by replacing
155 Rescue experiments of abi mutants also reveals a physiol
156 ossible mechanism for oscillations in double-
rescue experiments of per(01)-tim(01) mutants.
157 A
rescue experiment on 47 tools that were published from 2
158 Rescue experiments on cultured patient megakaryocytes co
159 provides valuable insight into the chemical
rescue experiments on HCA II mutants.
160 Finally, Zbtb11 mutant
rescue experiments point to a ZBTB11-regulated TP53 requ
161 Rescue experiments point to the early period of polar Dl
162 Genetic
rescue experiments presented evidence that both BMP and
163 First, transgenic
rescue experiments prove that the Sac locus encodes T1R3
164 This is the first time a metal-
rescue experiment provides evidence for inner-sphere div
165 In a
rescue experiment,
rats initiated therapy on Day 21.
166 Rescue experiments relying on viral RNA polymerase-induc
167 Knockdown-
rescue experiments reveal that C18 executes a role that
168 ShRNA knockdown/
rescue experiments reveal that LIMK1 palmitoylation is e
169 Transgenic
rescue experiments reveal that Robo can function in a ce
170 Lentiviral
rescue experiments reveal that such disruption selective
171 Genetic
rescue experiments reveal that Tbx2 and Tbx3 function do
172 Knockout-
rescue experiments reveal that Tmod's interaction with t
173 Finally, a
rescue experiment revealed that YY1-regulated BMP6 expre
174 Inhibition and
rescue experiments revealed that defective MEK/extracell
175 Morpholino-based knockdown and
rescue experiments revealed that MCT8 is strictly requir
176 es in combination with siRNA knockdown-based
rescue experiments revealed that MLN4924 induced the acc
177 Rescue experiments revealed that only the activating but
178 ological inhibitors, dominant negatives, and
rescue experiments revealed that PI3K-C2beta and AKT wer
179 Moreover,
rescue experiments revealed that the decrease in spontan
180 RNA interference
rescue experiments revealed that the NH(2)-terminal four
181 Rescue experiments revealed that the phenotype is caused
182 ent mice, combined with gain-of-function and
rescue experiments,
revealed a specific role for this li
183 and epigenetic analysis, as well as genetic
rescue experiments,
revealed that EZH2 represses neurona
184 Examination of mutant embryos and tetraploid
rescue experiments reveals that abnormal yolk-sac vascul
185 Overexpression of c-MYC in
rescue experiments reversed miR-203-induced growth arres
186 Lastly, deletion-
rescue experiments show that a respiration-defective mut
187 s with unresolved intercellular bridges, and
rescue experiments show that expression of small interfe
188 Rescue experiments show that increased expression of H3
189 Rescue experiments show that only full-length Ensconsin
190 RNAi and
rescue experiments show that PDF from these cells is nec
191 Computational analysis and
rescue experiments show that PTEN (phosphatase and tensi
192 Functional
rescue experiments show that the ability of human LAMP2
193 Rescue experiments show that the isomerase activity of e
194 Metal-ion
rescue experiments show that those at positions 9, 12, a
195 number of neurons, including PVT, transgenic
rescue experiments show that zig-3 can function irrespec
196 In utero
rescue experiments showed that a key function of Magoh i
197 Protein depletion and
rescue experiments showed that EB1 and EB3, but not EB2,
198 Rescue experiments showed that fully functional myosin V
199 Transgenic
rescue experiments showed that Gr5a confers response to
200 Genetic
rescue experiments showed that only the enzymatically ac
201 Cell-autonomous
rescue experiments showed that Sema-1a is involved in as
202 MIG6 and the apoptosis regulator BIM, which
rescue experiments showed were essential to mediate the
203 of two alleles, RNA interference (RNAi) and
rescuing experiments showed that dig-1 encodes a giant m
204 Moreover,
rescue experiments shows that Cenpj mediates the role of
205 02, D132, and D135) by mutagenesis and metal
rescue experiments specified residues that contribute to
206 Furthermore, gain-of-function and
rescue experiments suggest an important regulatory role
207 Rescue experiments suggest brown preadipocytes require t
208 Additional
rescue experiments suggest involvement of the Ras pathwa
209 al adhesion-targeting domain of p130Cas, and
rescue experiments suggest that Ajuba acts upstream of p
210 Transgene
rescue experiments suggest that differences in isoform e
211 Neuron- and muscle-specific
rescue experiments suggest that DYB-1 is required for SL
212 Tissue-specific knockdown and
rescue experiments suggest that epidermally derived Pvf1
213 These
rescue experiments suggest that male and female gametoge
214 Loss-of-function and germ layer-specific
rescue experiments suggest that pannier provides an esse
215 Rescue experiments suggest that Slit is secreted from th
216 Rescue experiments suggest that Spz3 can exert these eff
217 RNAi-
rescue experiments suggest that the CARD, coiled-coil, S
218 Tissue-specific transgenic
rescue experiments suggest that the FN matrix on the sur
219 Mutant
rescue experiments suggest that the H2AZ-like rather tha
220 genetic interactions, expression studies and
rescue experiments suggest that, in normal development,
221 Competition UV cross-link and translation
rescue experiments suggested that LAP inhibits IRES-medi
222 These chemical
rescue experiments support the conclusion that Tyr140 an
223 Rescue experiments support these observations, indicatin
224 ly chromosomes, and have conducted a genetic
rescue experiment that suggests that the edited cDNA is
225 We also show, using a "
rescue" experiment,
that the molecular target of the nit
226 In
rescue experiments,
the transfection of a vector encodin
227 This study analyzes, by genetic
rescue experiments,
the virulence of mutants affecting a
228 show by mosaic analysis and tissue-specific
rescue experiments to act in muscle to affect locomotory
229 We therefore performed cross-species
rescue experiments to compare the functions of murine an
230 in a combination of overexpression and RNAi
rescue experiments to determine the requirement for PAK4
231 hogenic ASFV isolate E70 were used in marker
rescue experiments to identify sequences capable of rest
232 protein depletion coupled with protein-based
rescue experiments to investigate the involvement of per
233 We used cell-autonomous
rescue experiments to show that Ben has a presynaptic ro
234 We used transgene
rescue experiments to show that defects in these dopamin
235 We performed a series of transgenic
rescue experiments to test the spatial, structural, and
236 of overexpression, knockdown, knockout, and
rescue experiments together with transcriptional analyse
237 on of specific gene targets, whereas genetic
rescue experiments unambiguously link Notch 3 function i
238 In addition, our functional
rescue experiment using Jpx-deletion mutant cells shows
239 Collectively, these data, as well as a
rescue experiment using rIL-10 together with rapamycin,
240 Rescue experiments using a GAL4-driven pUAS transgene de
241 Genetic
rescue experiments using an uncleavable form of Robo sho
242 Rescue experiments using concurrent treatment with small
243 Rescue experiments using constitutively active Cdc42 or
244 Rescue experiments using G3BP1 mutants show that phospho
245 Rescue experiments using mRNA bearing Notch repeat 1 mut
246 Rescue experiments using Pard6b mRNA restored cell polar
247 Rescue experiments using RNA interference and transfecti
248 Azide
rescue experiments using the D327G enzyme showed a 30-fo
249 ly indistinguishable images in our phenotype
rescue experiments using the endothelial tube formations
250 assays; results were validated in functional
rescue experiments using transgenes expression in EPCs f
251 Genetic
rescue experiments utilizing FEN1 mutant proteins that r
252 rebroretinal microvessels, performed genetic
rescue experiments,
vascular reactivity analysis, and co
253 Based on transformation
rescue experiments we hypothesize that EGRH-1 in the som
254 Using gene expression analysis and
rescue experiments we show that Alcama functions downstr
255 inding to PTPN14 and using a PTPN14 knockout
rescue experiment,
we demonstrate that the degradation o
256 Through a transgenic
rescue experiment,
we verified that sequence polymorphis
257 In the
rescue experiments,
we confirmed vitamin D and VDR inhib
258 munofluorescence reconstruction imaging, and
rescue experiments,
we demonstrate that the dephosphoryl
259 By performing RNA interference-
rescue experiments,
we demonstrate that these phosphoryl
260 Importantly, using conditional alleles and
rescue experiments,
we demonstrate that ZFP809 is requir
261 Using dominant negative mutants and
rescue experiments,
we demonstrate the functional signif
262 nt analyses, genetic mapping, and transgenic
rescue experiments,
we found that 2Bc function, mediated
263 of Connexin 43 (Cx43) and Cx26 together with
rescue experiments,
we found that gap junctions are disp
264 Using tissue-specific
rescue experiments,
we found that Gr66a-expressing neuro
265 Moreover, through protein depletion and
rescue experiments,
we found that the CNK1/cytohesin int
266 rough mutant analysis, protein depletion and
rescue experiments,
we identify CNK2 as a spatial modula
267 escence analysis, time-lapse microscopy, and
rescue experiments,
we investigate the roles of these 12
268 combination of pharmacological inhibitor and
rescue experiments,
we provide evidence that isoprenoids
269 wing on a combination of pharmacological and
rescue experiments,
we provide evidence that mTOR kinase
270 using an EMSY knock-out line and subsequent
rescue experiments,
we show that EMSY is in most cases p
271 Through
rescue experiments,
we show that specific slo-1 isoforms
272 By cell ablation and cell-specific
rescue experiments,
we show that the ASI chemosensory ne
273 In
rescue experiments,
we showed that in the zebrafish floo
274 In ex vivo culture models and genetic
rescue experiments,
we showed that Shp2 acts downstream
275 he cap genes from several independent marker
rescue experiments were PCR amplified, cloned, and then
276 Rescue experiments were performed by expressing wild-typ
277 tative virulence determinant, in vivo marker
rescue experiments were performed by inoculating swine w
278 An in vivo
rescue experiment with adeno-associated virus serotype 9
279 n (PAR) junctional complex identified by the
rescue experiment with tjp-2/ZO-2 or the PAR complex (pa
280 Moreover,
rescue experiments with a kinase-dead mutant of hRio1 re
281 Rescue experiments with a MOF histone acetyltransferase
282 Marker
rescue experiments with a wild-type IVa2 DNA fragment co
283 Rescue experiments with ASA showed a normalization of th
284 Chemical
rescue experiments with catalytic mutants of Csk demonst
285 Rescue experiments with catalytically inactive mutants o
286 ors can function autonomously, cell-specific
rescue experiments with circadian clock mutants indicate
287 Here, we use a combination of genetic
rescue experiments with CSLD-CESA chimeric proteins, in
288 Rescue experiments with human tau expression restored MT
289 Functional
rescue experiments with Lyn siRNA targeting the 3' UTR i
290 Rescue experiments with Mib1 and Neuralized show further
291 Rescue experiments with mutated KRas 3'UTR showed very s
292 Rescue experiments with mutated transgenes demonstrate t
293 Further observations, including
rescue experiments with nod kinesin-like protein transge
294 ockout mice and chimeric animals, along with
rescue experiments with novel CD24 fusion protein demons
295 In vitro
rescue experiments with purified exosomes and matrix coa
296 Complementation
rescue experiments with RSV-MLV chimeras now map this di
297 Rescue experiments with syntaxin-1 mutants revealed that
298 evels of apical acetylated microtubules, and
rescue experiments with the HDAC6 inhibitor tubacin high
299 Strikingly,
rescue experiments with wild-type HSP70 restored GATA1 e
300 By means of
rescuing experiments with a series of deletion and point