ライフサイエンスコーパス: -depleted

1 In dynamin 1-depleted MPCs by RNAi, alpha-tubulin showed a dispersed

2 Postirradiation, MCL-1-depleted cells exhibited decreased gamma-H2AX foci, decr

3 Interestingly, NRP-1-depleted patient-derived GBM xenografts substantially pr

4 scriptome profiling of IL-1 receptor (IL-1R)-depleted senescent cells indicates that IL-1 controls th

5 ncer-associated thrombus formation in CLEC-2-depleted mice was significantly inhibited, suggesting th

6 d stability, was diminished in the kindlin-2-depleted cells.

7 ed viral and cellular translation in RPLP1/2-depleted cells using ribosome profiling and found that r

8 ion changes were partially relieved in Ki-67-depleted hTERT-RPE1 cells by codepletion of the Rb check

9 human anti-ADAMTS13 autoantibody in ADAMTS13-depleted plasma resulting in an average interassay coeff

10 moter activity and elevated Myc mRNA in AGO1-depleted animals requires RNA polymerase II transcriptio

11 ng the virulence of P. aeruginosa in albumin-depleted versus albumin-rich infection sites and an unde

12 n and pluripotent gene upregulation in Ash2l-depleted pluripotent stem cells.

13 nregulated under acidic conditions, and ASS1-depleted cancer cells maintained a higher intracellular

14 metabolism, we studied the response of ATAD5-depleted cells to several genotoxic agents.

15 We further show that ATAD5-depleted cells are sensitive to poly(ADP)ribose polymera

16 lpha in the cytosol was not affected in ATG7-depleted cells, suggesting a defect in the translocation

17 n1, an actin-depolymerizing protein, in ATG7-depleted cells.

18 Modulating protein turnover in ATM-depleted cells also has an adverse effect on the DNA bas

19 ces membrane tension and does so even on ATP-depleted cell membranes where this occurs despite reduct

20 Our measurements with the ATP-depleted cells reveal that the diffusion dynamics of the

21 We have shown previously that ATXN3-depleted or pathogenic ATXN3-expressing cells abrogate p

22 nd complement 3 protein (in apolipoprotein B-depleted plasma).

23 macrophage foam cells with apolipoprotein B-depleted plasma.

24 ditionally, we show that ILC2s from basophil-depleted mice express reduced amounts of the receptor fo

25 ILC2 responses from control but not basophil-depleted mice, and basophils were sufficient to directly

26 PD-L1 upregulation in BER-depleted cells requires ATR/Chk1 kinase activities, demo

27 n of RAD51 degradation restores HRR in BRCA1-depleted cells.

28 LC8 alleviated the hypersensitivity of BRCA1-depleted cells to ionizing radiation and PARP inhibition

29 We identify two bulge-depleted regions on the miRNA stem, located approximatel

30 ) faster than (13) CO(2) resulting in (13) C-depleted biomass, enabling the use of delta(13) C values

31 Instead, in BIF OM occurs with (13)C-depleted carbonate and apatite, implying OM oxidation oc

32 (13)C-depleted carbonate carbon isotope compositions and low c

33 On the other hand, (13)C-depleted sn-2-hydroxyarchaeol potentially derived from A

34 e accept the more disputed evidence of (13)C-depleted zircon deposits.

35 ence for reduced BER efficiency in lamin A/C-depleted cells (Lmna null MEFs and lamin A/C-knockdown U

36 bosome stability is not affected in C6orf203-depleted cells, mitoribosome profiling analysis revealed

37 substrates from BiP observed in the calcium-depleted ER and suggest a mechanism for tuning ER qualit

38 Conversely, in the calcium-depleted ER, relative acceleration of ADP-to-ATP exchang

39 Senescent beta-catenin-depleted hepatocytes in aged mice create an inflammatory

40 egative breast cancer cells and that CBFbeta-depleted cells undergo a mesenchymal to epithelial trans

41 In addition, we observed that in Cbl-depleted cells there was enhanced entry after infection.

42 erately enhanced compared to that in the Cbl-depleted cells, suggesting that the Cbl-Nectin-1 interac

43 greater at 80% among TCRalphabeta(+)/CD19(+)-depleted and CB transplants versus 40% to 60% among the

44 hout serotherapy and TCRalphabeta(+)/CD19(+)-depleted grafts produced comparable survival rates of ar

45 fts: 30 T-cell receptor (TCR) alphabeta/CD19-depleted grafts, 43 cord blood (CB) grafts (72% with no

46 A combined approach of alphabetaTCR-CD19-depleted stem cell transplantation, enabling immunosuppr

47 s is demonstrated by the finding that CD301b-depleted mice exhibit delayed wound closure in vivo, whi

48 was shed were significantly increased in CD4-depleted compared to control-treated animals.

49 CD8 T cells, which has been observed in CD4-depleted humans.

50 Salmonella-infected, CD4-depleted 129X1/SvJ mice remained chronically colonized f

51 Consistent with previous reports, CD4-depleted mice lost control of virus replication in persi

52 We discovered that inactivated CD47-depleted mouse melanoma cells can protect mice from mela

53 CD8(-/-) mice and CD8-depleted C57BL/6 mice demonstrated significant protectio

54 Moreover, CDK20-depleted cells display impaired cell proliferation, defe

55 xp3 transcription factor; and dendritic cell-depleted CD11c-Cre iDTR mice.

56 seen during the acute infection: immune cell-depleted, long-term-infected mice display severe gait an

57 NK cell-depleted PBMCs had increased ADE as compared to whole PB

58 pe mice, Rag1 knockout mice, and T(reg) cell-depleted DEREG mice.

59 opionate were abrogated in regulatory T cell-depleted angiotensin II-infused mice, suggesting the eff

60 T cell-depleted HCT recipients from January 1, 2012 through Sep

61 In cultures with T cell-depleted lymphoid tissues, retinol enhanced Treg inducti

62 However, CD8(+) T cell-depleted mice displayed no protection against the hetero

63 of splenocytes from these regulatory T cell-depleted mice resulted in increases in gamma interferon

64 In addition, tumor-bearing mice given T-cell-depleted allo-BMT (allo-TCD-BMT) failed to develop GvHD

65 this increase in activity is lost in cenexin-depleted cells.

66 In contrast, reinstating cGAS in cGAS-depleted HD cells activates cGAS activity and promotes i

67 imulated numerically the evolution of the CH-depleted zone and the dissolution of the cement surfaces

68 ons and to regulate the expression of CG/CHG-depleted transposons.

69 ranes by increasing the fraction of the Chol-depleted phase.

70 RNAs and active Polymerase II, are chromatin-depleted and represent the main sites of detectable tran

71 Viral entry in CIN85-depleted cells was only moderately enhanced compared to

72 d functional decline in wild type and Clec9a-depleted mice lacking DC cross-priming function.

73 proteomic experiments with clpC1- and clpP2-depleted Mtb cells suggested that the ClpC1P1P2 complex

74 es remain energetically favorable in cohesin-depleted cells, potentially as a result of the phase sep

75 om structures observed in individual cohesin-depleted cells as intermediate states along a folding pa

76 As-received AN-102, Cs-depleted effluent, and sRF eluate fractions were compreh

77 TCs as they flow through the device, and CTC-depleted blood is returned back to the mouse via the shu

78 ds of genes differentially expressed in CTCF-depleted cells, among which MYC and a number of MYC targ

79 pathology, are capable of innervating the DA-depleted striatum.

80 njection of recombinant DAZL protein in DAZL-depleted oocytes rescues the translation and maturation

81 Additionally, DDIAS-depleted cells are deficient for homologous recombinatio

82 experiments under ATP, DIP-replete, and DIP-depleted conditions.

83 Mitochondrial DNA-depleted RPE cells demonstrated enhanced aerobic glycoly

84 sal striatum of dopamine-intact and dopamine-depleted rats during two brain states, respectively defi

85 cortex improves motor functions in dopamine-depleted male mice.

86 studies, these data suggest that in dopamine-depleted mice abnormally correlated and temporally offse

87 and activation, we report that, in dopamine-depleted mice, (1) D2 dopamine receptor expressing stria

88 We found that, in dopamine-depleted mice, (1) the firing rate of D2-SPNs was elevat

89 y involved in the motor deficits of dopamine-depleted mouse models of Parkinson's disease, where cell

90 tivity in response to L-DOPA in the dopamine-depleted parkinsonian brain.

91 lohydrolase-1, bilaterally into the dopamine-depleted putamen, induced a significant, dose-dependent

92 1 and 3.6 fold, respectively, compared to E2-depleted mice.

93 ck protein 90 (HSP90) are increased in eEF2K-depleted human cells as well as in eEF2K-knockout (eEF2K

94 X17-containing endosomes were larger in EHD1-depleted cells than in WT cells, suggesting that EHD1 de

95 Ribosome profiling of an eIF5A-depleted strain reveals a global elongation defect, with

96 However, other defects in Eip1p-depleted cells suggest additional roles.

97 ole moieties to saturate the highly electron-depleted, benzimidazole- and tetrazole-bearing meso-posi

98 d Frizzled (Fzd) levels were reduced in emc1-depleted embryos, while NCC defects could be rescued wit

99 sistently, similar phenomena occur in energy-depleted cells by DNP at 30 degrees C.

100 t-or-famine existence in an otherwise energy-depleted habitat.

101 sembly intermediates that accumulated in Era-depleted Escherichia coli cells using quantitative mass

102 t abilities to rescue MDC formation in ERMES-depleted strains and are incapable of rescuing MDC forma

103 afficking of ATF6alpha to the Golgi in ERp18-depleted cells.

104 immature WPBs from either BLOC-2 or exocyst-depleted endothelial cells lacked high-molecular weight

105 As expected, EXOSC10-depleted oocytes have impaired endomembrane components i

106 of the transcription factor E2F1 in cyclin F-depleted cells.

107 Sister chromatid cohesion is intact in FACT-depleted cells, although chromosome segregation failure

108 Escherichia coli MG1655 and virulence factor-depleted E. coli C600 strains with enteropathogenic Shig

109 hanistically, we demonstrated that, in FANCM-depleted ALT cells, BRCA1 and BLM help to resolve the te

110 Furthermore, Fbw7-depleted human mesenchymal stem cells and primary mouse

111 In vivo, FBXL7-depleted cancer cells form tumours with a high metastati

112 re for metasediments derived from K-feldspar-depleted rocks that were abundant crustal components on

113 Reintroduction of SCFAs to fiber-depleted mice had protective effects on the development

114 scued the axon pathfinding defects of Fignl1-depleted larvae.

115 Adoptive transfer of Gas6-depleted BMM s failed to clear PMNs in lungs following L

116 EB) downstream of TLR4 compared to their GIV-depleted counterparts.

117 Examination of the Kupffer's vesicle in Gle1-depleted zebrafish revealed compromised ciliary beating

118 Saccharomyces cerevisiae growing in glucose-depleted medium, the re-availability of glucose leads to

119 sponse to mitochondrial dysfunction in GRSF1-depleted cells.

120 ince they are inevitably contaminated with H-depleted byproducts.

121 ison of chromatin structure in normal and H1-depleted CD8(+) T cells reveals that H1-mediated chromat

122 gnificantly upregulated in RNF20- and H2Bub1-depleted FTE cells and imparted upon these cells an enha

123 ns contributes only modestly to the H3K36me2-depleted state at CGI-associated gene promoters and is d

124 at IAV multiplication was augmented in HDAC4-depleted cells and abated in HDAC4-supplemented cells.

125 f host anti-IAV response was abated in HDAC4-depleted cells and augmented in HDAC4-supplemented cells

126 nm diameter) were fabricated from hemoglobin-depleted mice erythrocyte-ghosts and doped with Indocyan

127 the defective DNA damage response of HNRNPD-depleted cells.

128 eation at the centrosome; accordingly, Hook2-depleted cells have reduced astral microtubules and spin

129 l mice, which were strongly minimized in HSC-depleted mice.

130 The resulting class I-depleted mice exhibited a significant reduction in the n

131 Post-IVIG PANDAS sera and IgG-depleted baseline sera did not alter the activity of str

132 nd electron microscopy analysis of ESCRT-III-depleted cells with a mathematical model, we show that u

133 ood was then transferred into two non-immune-depleted RMs, where progeny SHIV-A showed increased repl

134 The implantation of beta3-integrin-depleted tumor cells led to a dramatic decrease in the g

135 addition, the implantation of beta3-integrin-depleted tumors elicited an abscopal immunotherapeutic e

136 d to alter phosphate transport in intestinal-depleted Slc34a2-deficient mice.

137 omic signature that is indicative of an iron-depleted gut niche.

138 ude that CTX-induced disease creates an iron-depleted metabolic niche in the gut, which selectively p

139 mechanism of action (i.e., requiring an iron-depleted state) and due to differences in interpretative

140 adjusted Mueller-Hinton broth (BMD) and iron-depleted cation-adjusted Mueller-Hinton broth (ID-BMD),

141 e growth advantage conferred by pMB2 in iron-depleted media.

142 A method to prepare iron-depleted CAMHB (ID-CAMHB) has been described by the Clin

143 ron might play an important role in the iron-depleted Southern Ocean by enhancing the biological pump

144 that the vertebrate host is a uniformly iron-depleted environment to invading microbes.

145 can suppress cyclin D1 expression in JARID2-depleted cells.

146 ddition, we show that primary cilia in KIF14-depleted cells are defective in response to HH pathway a

147 ns and rescues integrin trafficking in KIF1C-depleted cells.

148 uced apoptosis in Nutlin-3A-treated, FLIP(L)-depleted cells, albeit to a lesser extent than in caspas

149 increase endothelial permeability in MYLK-L-depleted EC and Mylk-L(-/-) lungs, thus demonstrating th

150 Mylk-L(-/-) endothelial cells (EC) or MYLK-L-depleted human EC.

151 f nuclear probes between wild-type and lamin-depleted MCF-10A cells revealed that lamin A/C, but not

152 ression of Kras(G12D) were crossed with Lcn2-depleted animals and fed isocaloric diets with varying a

153 Lineage tracing confirmed that LDB1-depleted, insulin-negative beta cells express NEUROG3 bu

154 perform transcriptome analysis of linc00899-depleted cells and identify the neuronal microtubule-bin

155 tion of key cell cycle regulators in lincNMR-depleted cells like the key dNTP synthesizing enzymes RR

156 antoic Membrane (CAM) in vivo model, lincNMR-depleted tumors are significantly smaller.

157 letion of mtDNA-encoded proteins and a lipid-depleted metabolic phenotype, suggesting that the cytopl

158 h, pathogen thalli become increasingly lipid-depleted; they subsequently tend to become entirely abor

159 ct of a PE diet on FAM; in contrast to lipid-depleted starved animals, PE-fed caterpillars maintain l

160 cyte-specific overexpression of Yap in Llgl1-depleted embryos ameliorated pericardial effusion and re

161 lar sclerosis, mixed cellularity, lymphocyte-depleted or lymphocyte-rich HL), which account for the m

162 ective adherent and tight junctions in Lztr1-depleted endothelial cells are caused by dysregulation o

163 se(lo), and IL10(lo)); the use of macrophage-depleted bone marrow abrogated the GvT effects.

164 hese findings, the expression profile of MDK-depleted tumors was enriched in key indicators of a good

165 and produced at least one complementary melt-depleted reservoir that is now recognized as the upper-m

166 macrophages mimics the phenotype of METTL14-depleted macrophages.

167 nd stabilization of miRNP components in Mfn2-depleted mammalian cells.

168 Gnotobiotic colonization of microbiome-depleted dams with a limited consortium of bacteria prev

169 olon, similar to that observed in microbiota-depleted mice.

170 al contents in antibiotic-induced microbiota-depleted (AIMD) and control mice showed significant vari

171 Microglia-depleted mice in contrast to nondepleted mice were prote

172 endrocyte progenitor cells (OPCs), microglia-depleted mice, and conditional OPC-specific peroxisome p

173 s and use of STAT3 knockout and mitochondria-depleted cells.

174 culture conditions to maintain mitochondrial-depleted cells for up to 30 d with minimal loss of viabi

175 Consistently, in MsrB2-depleted cells, F-actin levels are decreased in ICBs, an

176 itochondrial electron transport chain, mtDNA-depleted cells still maintain mitochondria and many mito

177 urden upon orthotopic implantation of MUC5AC-depleted pancreatic cancer cells.

178 lk1 itself (self-priming) increased in MYPT1-depleted cells showing that MYPT1 provides a molecular l

179 e, preferential volatilization of delta(15)N-depleted compounds (especially ammonia) contributes to f

180 ((15)N-enriched) and deep reservoirs ((15)N-depleted) differ significantly.

181 s to the occurrence of phosphorus-bearing, N-depleted surface waters, which encourages N2 fixation, t

182 Na(+)-depleted mice showed robust preferences to "light taste"

183 transcriptome and proteome analyses of NatB-depleted mutants suggested a function of NatB in multipl

184 ndent nuclear functions and sensitized NBAT1-depleted cells to genotoxic drugs.

185 Nckap1-depleted tumors displayed fibrotic stroma with increased

186 sitization of CXCR2(-/-) mice and neutrophil-depleted WT mice induced both hapten-reactive CD4 and CD

187 Compared to vaccinated controls, neutrophil-depleted mice had higher lung bacterial burdens, increas

188 Sera from neutrophil-depleted mice had less antipneumococcal IgG2c and IgG3,

189 and (3) 2C7 remained effective in neutrophil-depleted mice and in mice treated with PMX205, a C5a rec

190 D4 T cells producing IFN-gamma in neutrophil-depleted WT mice was eliminated by s.c. injection of act

191 ated during DNFB sensitization of neutrophil-depleted WT mice treated with anti-IL-12 mAb or neutroph

192 ce treated with anti-IL-12 mAb or neutrophil-depleted IL-12(-/-) mice.

193 mice received an equivalent dose of nitrate-depleted BRJ (BRJ-) or normal drinking water.

194 J were compared with both 'placebo' (nitrate-depleted) BRJ as well as water to control for potential

195 Mice were subjected to a nitrate/nitrite-depleted diet for 2 wk, then supplemented with sodium ni

196 fic conditions; at a high challenge dose, NK-depleted mice displayed lower viremia and liver damage a

197 , adding activated NK cells back into the NK-depleted-PBMCs or to purified monocytes decreased ADE.

198 encing to characterize neurogenesis by Notch-depleted striatal astrocytes in vivo.

199 isingly, in the non-neurogenic cortex, Notch-depleted astrocytes also initiated neurogenesis.

200 onsistent down-regulation across three NR2F2-depleted ALT+ cell lines.

201 hage populations of wild-type mice with Nrp1-depleted bone marrow-derived macrophages (BMDM) confers

202 Most yeast genes have a nucleosome-depleted region (NDR) at the promoter and an array of re

203 eukaryotes are characterized by a nucleosome-depleted region (NDR), which appears to be flanked upstr

204 ll-positioned nucleosomes flank a nucleosome-depleted region (NDR).

205 the region upstream of TSSs in a nucleosome-depleted state while simultaneously protecting this acce

206 SMAD2 can bind pre-acetylated nucleosome-depleted sites.

207 KO ESCs, whereas unmethylated and nucleosome-depleted CpG islands were enriched for CTCF sites that r

208 ich explains how INO80 can define nucleosome-depleted regions in the absence of other factors(2).

209 ng complex (Ino80C) can establish nucleosome-depleted regions (NDRs) in reconstituted chromatin, and

210 els the +1 nucleosome to generate nucleosome-depleted regions during gene activation(9).

211 distance between heterochromatic nucleosome-depleted regions (NDRs), which is predicted to affect lo

212 sequencing (ATAC-seq) identifies nucleosome-depleted (open) chromatin, which harbors potentially act

213 we defined a specific nucleosome/nucleosome-depleted region structure that restricts HO activation t

214 istone marks, CTCF binding sites, nucleosome-depleted regions, and transcriptome profiling, we identi

215 We found that the nucleosome-depleted region (NDR) near CTCF is asymmetrically locate

216 MBD9 is preferentially bound to nucleosome-depleted regions at the 5' ends of genes containing high

217 osomes and this signal, have wide nucleosome-depleted regions, and are more enriched for core promote

218 unusually low bendability within nucleosome-depleted regions upstream of transcription start sites (

219 broblasts into iPSCs using Gatad2a-Mbd3/NuRD-depleted and highly efficient reprogramming systems.

220 the fast-growing S. mutans creates nutrient-depleted regions that affect the survival and metabolic

221 nutrient condition, whereas in the nutrient-depleted state, BAX binds to SNAP23 to form a ternary BA

222 rocess that becomes activated under nutrient-depleted conditions, like amino acid (AA) starvation.

223 localization at the lysosome under nutrient-depleted conditions.

224 dded in kerogenous shales rich in delta(18)O-depleted glendonites suggests both the onset of sharp th

225 OCRL-depleted human cells proliferated more slowly and about

226 gly, these results were not observed in OMA1-depleted non-tumorigenic MCF10A mammary epithelial cells

227 The ORC5-depleted cells show normal chromatin binding of MCM2-7 a

228 t and anti-inflammatory activity of ovomucin-depleted egg white (OdEW) after in vitro gastrointestina

229 servation of ethylene accumulation in oxygen-depleted soils.

230 ageing faecal material, under moist, oxygen-depleted conditions, now requires more attention in stud

231 ndex); SvO(2) yielded washout time of oxygen-depleted blood, rate of resaturation, and maximum SvO(2)

232 r fermentation to remain active under oxygen-depleted conditions.

233 Conversely, p85beta-depleted cells are less sensitive to these inhibitors.

234 -lives were significantly decreased in PARP1-depleted cells.

235 lenge after 2-hour exposures to DE, particle-depleted DE (PDDE), or filtered air.

236 Transfer of PCSK6-depleted cardiomyocyte secretome resulted in decreased e

237 Nascent RNA Bru-seq analysis of PDI-depleted cells revealed a decrease in transcription of g

238 as an internal peptide surrogate in peptide-depleted environments stabilizing empty MHC I and impedi

239 , PG-depleted, and mechanically injured + PG-depleted cartilage samples (n = 33) were imaged in a mix

240 Intact, PG-depleted, and mechanically injured + PG-depleted cartila

241 eliant only on TCR dwell time in phosphatase-depleted cell contacts constrained in area by cell topog

242 egulation of the Mg(2+) content in polyamine-depleted cells and suggest that elevated Mg(2+) can supp

243 Passaging CVB3 in polyamine-depleted cells generated a mutation in capsid protein VP

244 In polyamine-depleted cells, bunyaviruses produce an overabundance of

245 mutant rescues this inhibition in polyamine-depleted cells.

246 no acid that promotes infection of polyamine-depleted cells.

247 so exhibited reduced attachment to polyamine-depleted cells, suggesting that polyamines may facilitat

248 sis of cell dynamics in chimeric and protein-depleted primordia shows that Cxcl12a-sensing and cadher

249 ain mutant interacting with GEF-H1 in VE-PTP-depleted endothelial cells reduced GEF-H1 activity and r

250 In PTPN23-depleted tumors, we detected hyperphosphorylation of the

251 HBs, colocalized with HBc in the ER of Rab5B-depleted cells, suggesting that HBV envelopment occurs n

252 , loss of AKT-S473 phosphorylation in RABL6A-depleted cells was the result of increased protein phosp

253 stored phosphorylation of AKT-S473 in RABL6A-depleted cells, whereas PP2A reactivation using a specif

254 non by showing that restoration of radiation-depleted resident macrophages through prorepair paracrin

255 e, and respiration of relatively radiocarbon-depleted (i.e., older) substrate contributes to carbon e

256 h recombination focused in gene-rich, repeat-depleted regions near chromosome ends.

257 In addition, retromer-depleted cells displayed more rapid Bax activation and a

258 activity in HIV-1 virions produced from RHA-depleted cells.

259 identifies riboSNitch-enriched or riboSNitch-depleted non-coding elements across tumors.

260 used an in vitro assay combining a ribosome-depleted rabbit reticulocyte lysate and ribosomes prepar

261 o methods for preparing ribosomal RNA (rRNA)-depleted sequencing libraries for RNA-Seq of whole blood

262 been developed to detect circRNAs from rRNA-depleted RNA-seq data based on back-splicing junction-sp

263 tio-based correction was applied to the rRNA-depleted estimates.

264 RSC-depleted cells exhibit low levels of elongating Pol II a

265 these target genes were upregulated in Rspo2-depleted explants.

266 nization and angiogenic sprouting in Rudhira-depleted cells.

267 ite precipitation in the presence of a (34)S-depleted pore water sulfide reservoir, via closed system

268 e water-deprived but not under food- or salt-depleted conditions, indicating that the hedonic value o

269 Under SAM-depleted conditions, H3K9 mono-methylation preserves het

270 imilar GOF phenotype when expressed in Shoc2-depleted MCF10A cells.

271 or genetic inhibition of MYC activity in SMS-depleted CRC cells dramatically induces Bim expression a

272 In xenograft-based studies, SNX27-depleted cell lines showed prolonged survival of SCID mi

273 Transcriptomic analysis of a spermidine-depleted B. subtilis speD mutant uncovered a nitrogen-,

274 a genome-wide CRISPRi screen in sphingolipid-depleted human cells and identified hypersensitive mutan

275 fter reconstitution into the relevant subset-depleted population.

276 hat the increase of light fluxes in symbiont-depleted tissue promoted by reflection of the incident l

277 whose add-back rescues autophagy in YAP/TAZ-depleted cells.

278 red levels of miR-15a/16-1 and MYO1C in TFEB-depleted cells cause increased expression of plasma memb

279 In Top1-depleted cells, DSBs also accumulate at TTS, leading to

280 m the nucleus and cytosol of control and TPR-depleted cells, we provide evidence that TPR is required

281 Moreover, in TPR-depleted cells reporter mRNAs generated from short trans

282 SGs that assemble in TRAPP-depleted cells are smaller and are no longer able to rec

283 1 depletion reduces telomere fusions in TRF2-depleted cells due to defects in ATM-dependent checkpoin

284 aling rescued telomere fusion events in TRF2-depleted SMCHD1 knockout cells.

285 RLPs as postlipolytic partially triglyceride-depleted particles derived from chylomicrons and VLDL th

286 the lithosphere was, at least locally, ultra-depleted at the time of diamond formation, as opposed to

287 ate, a metabolite produced by the vancomycin-depleted gut bacteria, abrogated the vancomycin effect.

288 utilized in a series of patients with vessel-depleted neck anatomy.

289 In VPS13A-depleted cells, ER-mitochondria contact sites are decrea

290 In VPS13A-depleted mammalian cells lipid droplet numbers are incre

291 A similar phenotype was observed in WAPL-depleted cells.

292 N-WASP-depleted cells do not recognize lysophosphatidic acid gr

293 on of differentiation, a proportion of Whsc1-depleted embryonic stem cells remain entrapped in a plur

294 In the presence of Wnt5A-depleted MDSC, tumor-infiltrating lymphocytes expressed

295 ail to rescue the viability phenotype of WRN-depleted MSI-H cancer cells.

296 Microarray analysis of IRE1alpha- and XBP1-depleted cells, validation using RNA cleavage assays, an

297 xyloglucan was allowed to bind to xyloglucan-depleted onion walls, CBM76 labelling gave positive evid

298 )-induced EC migration was diminished in YY1-depleted human umbilical vein endothelial cells (HUVECs)

299 ly at heterochromatic regions normally H2A.Z-depleted in wild-type plants.

300 ification of conformational changes in Zelda-depleted Drosophila embryos; (3) patient-specific aberra