ライフサイエンスコーパス: -depleted

1 DJ-1-depleted cells displayed increased levels of glycated DN

2 The enhanced calcium cycling in the HAX-1-depleted heart was mediated through increases in the cal

3 Microarray analysis of HO-1-depleted and control EC exposed to VEGF identified cycli

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

5 Consistent with this model, MCL-1-depleted cells had a reduced frequency of IR-induced BRC

6 uction of stalled replication forks in MCL-1-depleted cells, there was a decreased ability to subsequ

7 8-1 rescues impaired secretion in syntaxin-1-depleted PC12 cells and the lethality and lethargy of un

8 in 1, was particularly inhibited in ataxin-3-depleted human cell lines and mouse primary neurons, and

9 Using MASP-3-depleted human serum, serum from 3MC patients, and Masp1

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

11 ion of the Abl effector Enabled (Ena) in abl-depleted embryos suppressed the abl phenotype, consisten

12 ight F-actin patch at the tip, whereas actin-depleted neurites never elongated, even though they stil

13 hat an enzymatic release of payload from ADC-depleted human plasma at 144 h was able to account for a

14 s only one enriched protein in the 144 h ADC-depleted and antipayload immunoprecipitated plasma sampl

15 t only reversed sensitization to BSIA in AE2-depleted H69 cholangiocytes but even completely prevente

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

17 Accordingly, tensin silencing in AMPK-depleted fibroblasts impedes enhanced cell spreading, tr

18 f differential regulation in HSF1-naive and -depleted cells, our results suggest that a large majorit

19 Ectopic expression of AnxA8 in AnxA8-depleted cells led to decreased neuronal marker staining

20 aded THP-1 cells with the participants' apoB-depleted plasma.

21 bating human macrophage foam cells with apoB-depleted serum.

22 In response to injury, AQP3-depleted colonic epithelial cells showed defective lamel

23 inhibition of nucleotide synthesis in ARID1B-depleted cells results in re-establishment of senescence

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

25 ATR-depleted or patient-derived ATR-SS cells form cilia of s

26 BD2-depleted urine samples from bladder infected mice suppor

27 Dynamic imaging revealed that beta1-depleted cells lacked the ability to sustain protrusions

28 ioenergetic defects that we observed in BMI1-depleted cells, for example, mitochondrial respiration,

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

30 e, followed by approximately 50 kyr of (13)C-depleted carbon injection.

31 d with rapid and massive injections of (13)C-depleted carbon into the ocean-atmosphere system, reflec

32 period within the PETM of longer-term (13)C-depleted carbon release.

33 scopy of (13)C-TBBPA residues bound to (13)C-depleted HA suggested that in the presence of delta-MnO2

34 p Pacific as a major reservoir of this (14)C-depleted carbon, its extent and evolution still need to

35 es (Delta(14)C) suggest the release of (14)C-depleted CO2 from old carbon reservoirs.

36 sical complement pathway using TNT003 or C1q-depleted serum significantly reduced adhesion of monocyt

37 with the C3-inhibitor compstatin Cp40, in C3-depleted human serum, or when purified properdin is appl

38 , carbonated zone; and (3) a more porous, Ca-depleted inner zone.

39 esicle docking and evoked exocytosis in CAPS-depleted cells, showing that CAPS residence on vesicles

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

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

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

43 indlimb tissue, CD34Exo, but not the CD34Exo-depleted conditioned media, mimicked the beneficial acti

44 nza virus split vaccine in CD4KO mice or CD4-depleted WT mice equivalent to those in intact WT mice,

45 ed immunocompetent mice and unvaccinated CD4-depleted mice remained persistently infected with P. mur

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

47 SIV-infected CD8-depleted macaques treated with natalizumab either early

48 escues the meiotic resumption defect of Cdh1-depleted oocytes.

49 CDK18-depleted cells accumulate in early S-phase, exhibiting r

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

51 CD3(+)TCRalphabeta(+) and CD19(+) cell-depleted haploidentical or mMUD HSCT is a practical and

52 ls were able to colonize testes of germ cell-depleted mice after transplantation.

53 although not completely protected, mast cell-depleted mice displayed less organ atrophy and fibrosis

54 te cell-wild-type (SC-WT) and satellite cell-depleted (SC-Dep) mice (8 weeks of age) were randomized

55 ensity in both young and aged satellite cell-depleted diaphragm muscle (P < 0.05), which may compensa

56 nsity was maintained in young satellite cell-depleted mice regardless of running, although it was mod

57 l-replete) or tamoxifen (Tam, satellite cell-depleted) treated at 4 months of age and were then allow

58 Patients with leukemia who receive a T cell-depleted allogeneic stem cell graft followed by postpone

59 Last, we demonstrate that T cell-depleted human PBMCs exposed to UV-HSV-1 provide a survi

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

61 h transplantation of a "mega-dose" of T cell-depleted peripheral blood hematopoietic progenitor cells

62 activity following haplo-mismatched, T cell-depleted stem cell transplantations for the treatment of

63 tion-free conditioning regimen with a T-cell-depleted graft to eliminate radiation exposure and minim

64 f samples collected from controls and T-cell-depleted macaques after rVSV-EBOV vaccination and EBOV c

65 All grafts were CD34-selected/T-cell-depleted using the CliniMacs CD34 columns (Miltenyi).

66 ce but not in immunocompromised or Treg cell-depleted mice.

67 ghted the importance of the portlandite (CH)-depleted zone and the surface dissolution zone in the CO

68 use through the carbonated zone to form a CH-depleted zone.

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

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

71 Our data indicate that in CK-depleted plants exposed to As(V), transcript levels of A

72 be reduced approximately twofold in clathrin-depleted cells as a whole and approximately fivefold in

73 roteoglycans present in the type VI collagen-depleted matrices.

74 lowing administration of PapMV to complement-depleted mice.

75 ve imaging of meiotic divisions in condensin-depleted cells showed repeated nuclear stretching and co

76 In condensin-depleted cells, a chromosome condensation defect was mos

77 CPEB1-depleted mammary cells become metastatic to the lung fol

78 Here, we show that CPEB1-depleted mammary epithelial cells alter their gene expre

79 -enriched HMLER-shEcad cells over breast CSC-depleted HMLER cells.

80 ction reveal transformation from Cu2 S to Cu-depleted phases, along with CuI formation.

81 nriched bone marrow cells into septic Cx3cr1-depleted mice prevented kidney damage and promoted mouse

82 ore, raising serum calcium levels in Cyp27b1-depleted mice directly increased FGF23 levels and indire

83 n splenectomized, Rag-1(-/-), or CD11c(+) DC-depleted mice.

84 erve regeneration was also delayed in the DC-depleted corneas.

85 phenotype was nonglaucous and beta-diketone-depleted.

86 mikimotoi were set up in L1 medium (+P), DIP-depleted L1 medium (-P) and ATP-replacing-DIP medium (AT

87 ctivity under simulated healthy and dopamine-depleted conditions.

88 us in brain slices from control and dopamine-depleted mice.

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

90 g GPe neurons, restores movement in dopamine-depleted mice and attenuates pathological activity of ba

91 Importantly, in dopamine-depleted striatum, a widespread population of iSPNs, whi

92 to restore promoter-proximal pausing to DSIF-depleted Drosophila nuclear extracts.

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

94 Volatile-element-depleted bodies such as the Moon were expected to be enr

95 rescued the endoreplication defects in Elg1-depleted nurse cells.

96 ELMO1-depleted macrophages showed a time-dependent increase in

97 s in both compartments (exosomes and exosome-depleted media (EDM)) of the conditioned media.

98 hECTs with exosome-enriched, but not exosome-depleted, fractions of the hMSC secretome recapitulated

99 The exosome-depleted supernatant of ML had no effect on in vitro and

100 recovered from control but not C-NHEJ factor-depleted cells, providing important mechanistic insights

101 Genes altered in FAM46C-depleted cells were enriched for signaling pathways regu

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

103 restore EPA-induced Ucp1 expression in Ffar4-depleted cells, implicating that Ffar4 signaling activit

104 i, results in reduced NET production in FlnA-depleted neutrophils.

105 Gut flora-depleted mice expressed lower levels of F4/80 and chemok

106 ol BM monocytes, BM monocytes from gut flora-depleted mice had decreased migratory capacity toward CX

107 e of chem163S, which was undetectable in FXI-depleted plasma and markedly enhanced in platelet-rich p

108 Moreover, FXII-depleted AD mice showed better cognitive function than u

109 tibiotic-treated donors to germ-free or germ-depleted mice.

110 (P) signaling cascade, was diminished in GIV-depleted cells, suggesting that GIV is required to estab

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

112 thods, glycopeptide-enriched and beta-glucan-depleted products were each prepared from Brewer's and B

113 promoters of beta-oxidation genes in glucose-depleted conditions, and in vivo reporter gene analysis

114 by enhanced phagocytosis of Klebsiella GPVI-depleted mice showed increased lung hemorrhage during in

115 Despite higher bacterial loads, GPVI-depleted mice showed reduced platelet numbers, platelet

116 GR-depleted preadipocytes show adipogenesis defects 1 week

117 Mechanistically, MMR deficiency in K-H-depleted cells was a consequence of reduced stability of

118 In H1-depleted animals, ectopic expression of Elba2 rescues th

119 e somatic tissues and similar to those of H1-depleted roots.

120 27Ac-rich chromatin and inaccessible H3K27Ac-depleted MaLR-enriched chromatin.

121 lings fed either bovine blood or haemoglobin-depleted serum.

122 urce of haem since, feeding with haemoglobin-depleted serum led to aborted embryogenesis.

123 sfer and the upshift in the Em of QA HCO3(-)-depleted PSII also showed diminished light-induced (1)O2

124 ization and greater lipid oxidation in HDAC3-depleted muscles, a fuel switch caused by the activation

125 d to HemW was actively transferred to a heme-depleted, catalytically inactive nitrate reductase, rest

126 to preferentially stimulate oxidized or heme-depleted, but not native sGC.

127 molecular alterations observed in the HOXA5-depleted cells.

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

129 her in ConA-treated control mice than in HSC-depleted mice.

130 ConA was administered i.v. to control or HSC-depleted mice; hepatic histopathology and cytokines/chem

131 ls were markedly reduced in ConA-treated HSC-depleted mice compared with control mice.

132 HSCs into cycle, was well tolerated by HSPC-depleted mice and did not induce expansion of the small

133 Only upon 5-fluorouracil treatment was HSPC-depleted bone marrow compromised in reconstituting hemat

134 Whereas AID levels were not altered in Id3-depleted activated B cells, the expression of a subset o

135 In vitro, Id3-depleted B cells displayed a defect in class switch reco

136 In contrast, in IFT20-depleted cells, PDGFRalpha localizes aberrantly to the p

137 studies, and when ApoC-III-rich or ApoC-III-depleted lipoproteins were injected into mice.

138 Perfusion of C1-inhibitor-depleted plasma over glomerular endothelial cells promot

139 Supplementation of choline to inositol-depleted growth medium led to decreased TAG synthesis in

140 or ((58)Fe)-labelled ferrous sulfate in iron-depleted (serum ferritin </=25 mug/L) women aged 18-40 y

141 s HLIIIA and HLIVA ESTUs codominated in iron-depleted areas of the Pacific Ocean, CRD1 and the yet-to

142 ruginosa mutants defective in growth in iron-depleted media and find that gene PA2374, proximal to th

143 INTERPRETATION: In iron-depleted women, providing iron supplements daily as divi

144 At the end of the study, comparison of iron-depleted patients and controls showed ferritin levels 71

145 tional iron status measures.Seventy-two iron-depleted, nonanemic Chinese women [serum ferritin (sFer)

146 ssion of iron-containing proteins under iron-depleted conditions.

147 to differentiation culture conditions, Kdm5b-depleted adult NSCs migrated from neurospheres with incr

148 hat we also observed in experimentally KIF14-depleted cells.

149 However, in women with a Lactobacillus-depleted, high-diversity VM, significantly less correlat

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

151 Transcriptomic analysis of LDB1-depleted beta cells revealed the collapse of the termina

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

153 In addition, LIMCH1-depleted HeLa cells exhibited a decrease in the number o

154 RNA was obtained, as expected, from the LK14-depleted population, but was also in sIgkappa(+) splenoc

155 effects are blunted in SHP-null mice or LSD1-depleted mice.

156 selection patterns in non-CD8(+) lymphocyte-depleted animals were characterized by sequential popula

157 odel with SIV-infected non-CD8(+) lymphocyte-depleted macaques also provides a unique opportunity to

158 CD8(+) lymphocyte-depleted macaques infected with simian immunodeficiency

159 MacroH2A1-depleted HCC cells also exhibited reduced proliferation,

160 PPARgamma-deficient and macrophage-depleted mice presented decreased IL-10-mediated myeloid

161 In macrophage-depleted animals, the infusion of macrophages cultured i

162 Notably, zinc- and manganese-depleted portions of the biofilm repress the production

163 protein mice) transplantation in bone marrow-depleted IL10KO mice (IL10KO chimeric mice) reduced tran

164 is a complex process in which the melanocyte-depleted interfollicular epidermis is repopulated by mel

165 get proteins that are, or can be, methionine-depleted.

166 observed this contribution under methionine-depleted conditions, unexpectedly, we found that serine

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

168 er Solar System composition toward a (26)Mg*-depleted and (54)Cr-enriched component.

169 rom vehicle-gavaged NOD donors to microbiota-depleted C57BL/6 recipients was sufficient to induce soc

170 ibited by abGCs, were increased in microglia-depleted mice.

171 vate ratio at the injury cortex of microglia-depleted animals at 7 days post-injury remained unchange

172 Zeb2, and Snail2 are upregulated, and miRNA-depleted CDs undergo partial epithelial-to-mesenchymal t

173 Concomitantly, MITF-depleted cells display larger number of invadopodia and

174 unts mostly for the above phenotypes in MITF-depleted cells.

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

176 to generate Parkin-expressing, mitochondria-depleted cells from scratch in 23 d, as well as offer a

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

178 Mitofilin-depleted MICOS detaches from SAM while remaining MICOS w

179 NP overexpression rescues furrowing in MKlp2-depleted cells in an INCENP-actin binding-dependent mann

180 Reconstituting RELMalpha in CD301b(+) MNP-depleted animals restored body weight and normoglycemia.

181 Monocyte-depleted PBMCs were treated with phytohemagglutinin for

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

183 d degradation of HIF-1alpha in partial mtDNA-depleted cells.

184 that miR-663 was down-regulated in the mtDNA-depleted Rho(0) line.

185 a result of this secretory blockade, Munc18c-depleted acini unexpectedly activated a component of the

186 we found that pancreatic acini from Munc18c-depleted mice (Munc18c(+/-)) and human pancreas (lenti-M

187 CCK-8 levels to mimic pancreatitis, Munc18c-depleted (Munc18c(+/-)) mouse acini exhibited a reductio

188 affecting pluripotency, suggesting that Myc-depleted stem cells enter a state of dormancy similar to

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

190 ng that N deposition in the region is (15) N-depleted, these data suggest that the increased foliar [

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

192 matin immunoprecipitation assays from NAP1L1-depleted cells showed LANA-mediated recruitment of NAP1L

193 ies the formation of a complementary (142)Nd-depleted reservoir that either is hidden in the deep Ear

194 eptor constitutive activity in neurofibromin-depleted cells.

195 icient, lymphocyte-deficient, and neutrophil-depleted murine hosts revealed that neutrophil-phage syn

196 of K. pneumoniae is preserved in neutrophil-depleted mice, monocyte depletion or TNF deficiency impa

197 Protection from IRI in neutrophil-depleted WT recipients was sustained by repopulation wit

198 juice) compared with placebo intake (nitrate-depleted beetroot juice) on vascular and platelet functi

199 otal lipids, respectively, grown in nitrogen-depleted conditions.

200 cularity, increased CTL infiltrate, and Nrp1-depleted BMDM adopted a more antitumorigenic phenotype r

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

202 Most genes have a nucleosome-depleted region at the promoter and an array of regularl

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

204 s binding, while the well-defined Nucleosome-Depleted Regions (NDRs) marked the genes crucial for cel

205 es occupies previously designated nucleosome-depleted regions around transcription start sites and tr

206 that bivalent regions have fewer nucleosome-depleted regions and transcription factor-binding sites

207 chromatin, with faster repair in nucleosome-depleted regions, and slower repair and higher mutation

208 utionarily conserved signature of nucleosome-depleted regions around transcription start/termination

209 ur findings show that regulatory, nucleosome-depleted chromatin and elevated transcription shape the

210 In yeast, significant nucleosome-depleted regions are found, which facilitate transcripti

211 es (TSSs) are bordered by a small nucleosome-depleted region, but lack the stereotypic downstream nuc

212 and elevated transcription within nucleosome-depleted chromatin.

213 mplying that the west Pacific was a nutrient-depleted environment and that oligotrophy may have facil

214 igher than in iron-rich coastal and nutrient-depleted oligotrophic waters, and were dominated by amph

215 ce of relatively young, very dense, nutrient-depleted water during the LGM (18 ky to 21 ky ago).

216 These stratified nutrient-depleted regions are expected to expand with future warm

217 t and dry soil moisture conditions to (18) O-depleted water vapour (c. - 200 per thousand) at high re

218 .5 mumol mol(-1) indicate the presence of O2-depleted water.

219 ed a reduction of viral endocytosis in OBSL1-depleted cells.

220 The ORC1 or ORC2-depleted cells replicate with decreased chromatin loadin

221 exhibit diminished H3K9 methylation in ORCA-depleted cells, suggesting a role for ORCA in recruiting

222 on the in vitro peptic digestion of ovomucin-depleted egg white was investigated.

223 e zones (AMZs), which constitute huge oxygen-depleted regions in the tropical oceans.

224 ions, usually produced by microbes in oxygen-depleted environments.

225 m amyloid P replenishment of serum amyloid P-depleted acute respiratory distress syndrome broncho-alv

226 expression profiling of p53-mutated and p53-depleted cancer cells, we identified ectonucleoside trip

227 f methylation-deficient p53 mutants into p53-depleted NTera2 cells results in elevated expression of

228 ve role for the microbiome, treatment of pDC-depleted neonates with the microbial-derived metabolite

229 proteomics and informatic analyses of PEAK1-depleted PDAC cells, we defined protein translation, cyt

230 Finally, expression profiling of PEDF-depleted fibroblasts revealed induction of IL8, SERPINB2

231 utant was significantly reduced in phosphate-depleted medium, while growth was only marginally affect

232 Under phosphate-depleted conditions some bacteria utilise phosphite and

233 compared with Pin1-null fibroblasts or PIN1-depleted hepatoma cells.

234 , but not to the extent observed in platelet-depleted mice, and lung bleeding was not significantly d

235 Plekhg5-depleted cultured motoneurons show defective axon growth

236 Furthermore, in PNN-depleted adults as well as in juveniles, MD caused an im

237 Such Porcn-depleted mice have normal intestinal morphology but are

238 reover, orthotopic implantation of PR55alpha-depleted pancreatic cancer cells into nude mice resulted

239 has been mostly injected back into pressure-depleted oil-producing reservoirs for enhanced oil recov

240 eversed spontaneous differentiation of PRMT7-depleted mouse ESCs.

241 ry chain supercomplex assembly in prohibitin-depleted neurons.

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

243 ivo studies demonstrating that in Tum/RacGAP-depleted S2 Drosophila cells, Pav/kinesin-6 exhibits sev

244 likely the primary source of the radiocarbon-depleted CO2 released to the atmosphere during the last

245 Neurite outgrowth defects of RBM4-depleted neurons were rescued by RBM4-induced exon 9-lac

246 Subsequently, utilizing the RF1-depleted E. coli strain C321.DeltaA, we could produce ma

247 n from both simulated and real ribosomal RNA-depleted (rRNA-depleted) RNA-seq datasets.

248 Pol I with the rRNA gene is reduced in RPS19-depleted cells.

249 n profiles from both polyA-selected and rRNA-depleted libraries.

250 ulated and real ribosomal RNA-depleted (rRNA-depleted) RNA-seq datasets.

251 ripts in expression quantification from rRNA-depleted RNA-seq data showed substantial increased accur

252 In particular, rRNA-depleted libraries sample a broader fraction of the tran

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

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

255 stering tumor cell survival within the serum-depleted tumor microenvironment.

256 ophores are able to outcompete diatoms in Si-depleted waters, which can contribute to the formation o

257 t and successful congression, whereas in Ska-depleted cells, detached kinetochores remain in a futile

258 VFV replication was severely reduced in Skp1-depleted cells when PKR was present.

259 progression, and the loss of E2F1 in SmgGDS-depleted cells provides an explanation for previous repo

260 al truncation and branching phenotype in Smn-depleted zebrafish.

261 Smurf2-depleted cells exhibited a reduced ability to resolve DN

262 Introducing Topo IIalpha into Smurf2-depleted cells rescued this phenomenon.

263 helial tumor cells coxenografted with Snail1-depleted fibroblasts originated tumors with lower invasi

264 ha-SNAP with Stim1 and Orai1, and alpha-SNAP-depleted cells show faster and less constrained mobility

265 ed in Sirt3-knockout (Sirt3(-/)(-)) and SOD2-depleted (SOD2(+/)(-)) mice in response to low dose of a

266 Sodium-depleted animals develop an appetite for aversive concen

267 ng strongly drives sodium appetite in sodium-depleted mice, whereas a role for kappa (KOR) and delta

268 gnaling was not detected, at least in sodium-depleted mice.

269 oalescence that promote homogeneous, species-depleted landscapes; and (g) deliberate culture and rele

270 e presynaptic structures in betaIII spectrin-depleted neurons make shaft synapses that exhibit increa

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

272 In SPOPL-depleted cells, endosomes are enlarged and fail to acqui

273 Finally, RNA sequencing of ST18-depleted tumors before involution revealed down-regulati

274 toichiometry in the plasma membrane of store-depleted cells.

275 tiviral expression of NICD1 or HES1 in STRAP-depleted tumor cells reversed the CSC phenotype.

276 fter reconstitution into the relevant subset-depleted population.

277 acks an explanation for the origin of sulfur-depleted organic matter in the deep ocean and cannot ade

278 Gene expression profiling of SYNCRIP-depleted cells demonstrated a loss of the MLL and HOXA9

279 ranscription decreases for genes in the Taf1-depleted, Taf1-enriched, TATA-containing, and TATA-less

280 By contrast, ER/Golgi defects in Tango1-depleted cells persist in the absence of bulky cargo, sh

281 In TbRAP1-depleted cells, expression of excessive TbRNaseH1, which

282 RNA levels and proliferation defects in TERT-depleted cells.

283 Control and Treg-depleted EF4.1 mice were immunized, and the extent of th

284 hat B-cell lymphopoiesis is impaired in Treg-depleted mice, yet this reduced B-cell lymphopoiesis is

285 ic and allogeneic transplantation using Treg-depleted mice as recipients.

286 reduced ROS and preserved viability of TRPM2-depleted cells, however, failed to restore ATP levels.

287 Splicing activity in the U1-depleted extract can be reconstituted by the galectin-3-

288 These UGCG-depleted cells show reduced levels of gangliosides and s

289 USP7-depleted cells also fail to elongate nascent daughter st

290 ency resolution, Utx-null mouse ESCs and UTX-depleted NT2/D1 cells displayed defects in RA-driven cel

291 istent with these results, we found that Ver-depleted telomeres form RPA and gammaH2AX foci, like the

292 entrifugation in the preparations of vesicle-depleted FBS (vdFBS) commonly utilized in the studies of

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

294 Patients with vessel-depleted necks and failed reconstructions require altern

295 their crystallization, confirming a volatile-depleted lunar interior source with homogeneous delta(66

296 end data set used to detect LGT in Wolbachia-depleted B. malayi (p-value: <2e-16).

297 WRN-depleted fibroblasts, although remaining largely viable,

298 genes that are required for viability of WRN-depleted cells after hydroxyurea treatment, and identifi

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

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