ライフサイエンスコーパス: be depleted of

1 inhibitors for PKC, but retained when cells were depleted of 12-myristate 13-acetate (PMA)-inducible

2 sitions, whereas the 16 O-labeled nucleotide is depleted of 13C.

3 Plasma samples were depleted of 14 high abundance proteins with a multi

4 nambiguous picture has emerged where tumours are depleted of 5hmC compared to corresponding normal ti

5 DKO ESCs remained pluripotent but were depleted of 5hmC and caused developmental defects i

6 wed by washing out the ligand, the membranes were depleted of 90% of the cannabinoid receptor binding

7 Often even large remote protected areas are depleted of a substantial proportion of their verteb

8 Using CM that had been depleted of aFGF and/or bFGF and subsequently recon

9 to stem-loop IV RNA affinity chromatography were depleted of all detectable PCBP2.

10 icrobiomes of mice treated with levofloxacin were depleted of all phyla with the exception of Firmicu

11 Kidney eluate that was depleted of alpha3(IV)NC1 antibodies still reacted t

12 Circulating T cells were depleted of alpha4beta7+ cells by immunomagnetic se

13 P. haemolytica when bovine immune serum that was depleted of anti-PlpE antibodies was used as the sou

14 A small fraction of the genome that was depleted of any H3 lysine 4 methylation was enriched

15 tent with this idea, BK polyomavirus genomes are depleted of APOBEC3B-preferred target motifs and enr

16 s LCAT activity in buffer and in plasma that is depleted of apolipoprotein B lipoproteins by selectiv

17 But in vivo, when cells are depleted of ATP by the addition of sodium azide and

18 Madin-Darby canine kidney (MDCK) cells were depleted of ATP by incubation with a mitochondrial

19 T-cell (DN-T) infiltration of the MZ, which was depleted of B cells.

20 virus (SIV) replication, six rhesus monkeys were depleted of B cells by intravenous infusion of ritu

21 CD8+ IPE Tregs were depleted of B7-2+ and CTLA-4+ T cells and assayed f

22 sion of IL-4, IL-13, and MCPT8 or that could be depleted of basophils or eosinophils, be deficient in

23 undesirable concentrated salt solution after being depleted of bodily sodium despite never having tas

24 beta2 microglobulin-deficient mice that have been depleted of both CD4+ and NK cells prolongs surviva

25 emonstrate this, we fertilized eggs that had been depleted of both XTcf3 and the maternal transcripti

26 The bookmarked pol II is depleted of both serine-2 and serine-5 phosphorylatio

27 s, hair follicles failed to form when dermis was depleted of both GFP(+) CD133(+) and GFP(-) CD133(+)

28 mice, whereas peripheral lymph nodes (pLNs) were depleted of both B and T cells and recirculating B

29 d CD4:CD8 ratio in mesenteric lymph node and were depleted of both CD4(+) and CD8(+) intestinal epith

30 phtheria toxin receptor-expressing mice that were depleted of both dendritic cells and alveolar macro

31 ibition, and DRMs from K6-null keratinocytes were depleted of both keratin and Src.

32 t these mice were highly susceptible if they were depleted of both types of T cells.

33 The DH sites were depleted of bulk nucleosomes and were tightly assoc

34 When the sarcoplasmic reticulum (SR) was depleted of Ca(2+) by preexposure to 10 mmol/L caffe

35 mained after the sarcoplasmic reticulum (SR) was depleted of Ca2+, suggesting that it is not a conseq

36 cells but did not activate them until stores were depleted of Ca2+.

37 e 250 K of photosystem II samples which have been depleted of calcium or chloride or treated with flu

38 Hearts from exercised Dsg2 (mut/mut) mice were depleted of calpastatin (CAST), an endogenous CAPN1

39 xidized, and the RyR2 macromolecular complex was depleted of calstabin2.

40 tive selection, and late-replicating regions are depleted of cancer driver genes, although enriched f

41 ose least preferred had whole body odor that was depleted of carboxylic acids among other compounds a

42 s retained on the surface of cells that have been depleted of Cbl; and (iii) that in cells infected w

43 ferentiate from blood mononuclear cells that were depleted of CD14+ cells or from isolated CD19+ cell

44 -treated APCs, even when the DO11.10 T cells were depleted of CD25+ cells before their in vitro stimu

45 8+, CD2+, CD5+, and CD1+ lymphoid cells (all were depleted of CD3+ cells) as well as CD33+ (but CD15

46 ell-deficient muMT mice unless those animals are depleted of CD4 and CD8 T cells at the time of chall

47 The livers of ob/ob mice are depleted of CD4-positive natural killer cells, compo

48 Additionally, RSV-infected mice were depleted of CD4 or CD8 T cells following acute RSV

49 fected intranasally and, 42 days later, they were depleted of CD4(+) and CD8(+) cells.

50 Mice were depleted of CD4(+) T cells and infected with P. mur

51 tavirus infection in IgA knockout mice, mice were depleted of CD4(+) T cells or CD8(+) T cells.

52 n, not only the gut but also the lung mucosa were depleted of CD4(+) T cells, which suggests that ear

53 r of tolerance failed when lymph nodes cells were depleted of CD4(+)CD25(+) T cells.

54 Mice were depleted of CD4+ T cells and inoculated intratrache

55 Control mice were depleted of CD4+ T cells but did not receive Pneumo

56 e, an additional group of vaccinated animals were depleted of CD4+ T cells during challenge.

57 Groups of cynomolgus macaques were depleted of CD4+ T, CD8+ T, or CD20+ B cells before

58 in vivo significance of these findings, mice were depleted of CD4+CD25+ T cells before sham or burn i

59 Initially, recovering T cells were depleted of CD45RA+/CD45RO(-) "naive-like" cells, w

60 f macaques immunized under normal conditions was depleted of CD8(+) T cells prior to challenge exposu

61 ) and from unexposed control subjects (n=12) were depleted of CD8 T cells and were infected with macr

62 BALB/c mice were depleted of CD8 T cells using anti-CD8 Ab treatment

63 s in measles virus clearance, rhesus monkeys were depleted of CD8(+) lymphocytes by monoclonal anti-C

64 Alternatively, animals that were depleted of CD8(+) lymphocytes exhibited greater va

65 was not found to be impaired when these mice were depleted of CD8(+) T cells with an anti-CD8 monoclo

66 so more strongly (P = 10(-7)) when cultures were depleted of CD8(+) T cells.

67 e the mechanism of rejection, recipient rats were depleted of CD8+ cells by treatment with OX-8 mAbs

68 When perforin -/- or perforin +/+ mice were depleted of CD8+ T cells by administration of an an

69 The adult mouse bone marrow population that is depleted of cells expressing any of a panel of lineag

70 s unlabelled toxin, but was blocked if cells were depleted of cellular ATP by the addition of sodium

71 ting units (CRU, > or = 1 per 55 cells), but are depleted of CFCs, day 8 and day 12 CFU-S (171 +/- 8,

72 Cells that are depleted of CH-ILKBP undergo extensive apoptosis des

73 ld type and various mutants of human SO that are depleted of chloride.

74 s rapidly degraded by proteasomes when cells are depleted of cholesterol, and its degradation is inhi

75 ause they are cholesterol auxotrophs and can be depleted of cholesterol by growth in delipidated seru

76 ronment in which purified membrane fragments were depleted of cholesterol with methyl-beta-cyclodextr

77 Cells infected with H pylori were depleted of cholesterol, which reduced IFNG signali

78 ontain endothelial nitric-oxide synthase and were depleted of cholesterol.

79 V replication-competent transgenic mice that are depleted of circulating HBsAg, via either spontaneou

80 1-2 x 10(10) pPBPC/kg into baboons that had been depleted of circulating anti-alphaGal and complemen

81 Importantly, mice that were depleted of circulating neutrophils with NIMP-R14 r

82 eover, genes with redundant enhancer domains are depleted of cis-acting genetic variants that disrupt

83 bout why genes associated with human disease are depleted of cis-eQTLs (cis-expression quantitative t

84 When organoids were depleted of cKit(+) cells using a toxin-conjugated

85 d terminals had far fewer synaptic vesicles, were depleted of coated vesicles, and had a larger plasm

86 g integral membrane and soluble forms of PAM were depleted of copper using bathocuproinedisulfonic ac

87 on of ataxin-7 assembles a SAGA complex that is depleted of critical proteins that regulate the abili

88 Human cells that are depleted of Cul4, DDB1 (damage-specific DNA-binding

89 s injected intragraft with gouty SF that had been depleted of CXCL16 during PMN transfer showed a sig

90 n contrast to mats, microinvertebrates' guts were depleted of Cyanobacteria and differentially enrich

91 L68Q epididymal fluid that was depleted of cystatin C amyloids, however, did not im

92 ity; the exocrine pancreas died in mice that were depleted of DCs and challenged with caerulein or L-

93 All mice with pancreatitis that were depleted of DCs died from acinar cell death within

94 phtheria toxin receptor-expressing mice that were depleted of dendritic cells.

95 the four groups, only euthymic animals that were depleted of donor antigen showed a loss of toleranc

96 7 weeks later, and were either untreated or were depleted of donor cells with anti-donor class I (Dd

97 in which chimera (B10.A-->B10) spleen cells were depleted of donor-type cells ex vivo, adoptively tr

98 substantia nigra in Parkinson's disease (PD) is depleted of dopaminergic neurons and contains fibrill

99 significantly diminished in neurons that had been depleted of dynein heavy chain, whereas the occurre

100 ions, Madin-Darby canine kidney (MDCK) cells were depleted of E-cadherin by RNA interference.

101 n of the tyrosine kinase in samples that had been depleted of EGF.

102 he role of eIF4H in Vhs activity, HeLa cells were depleted of eIF4H or other proteins by transfection

103 ated from naive young male donors, which had been depleted of either IL-4 or IL-10, were transferred

104 To test this idea, mice were depleted of either CD4(+) or CD8(+) T-cell populati

105 Experimental mice were depleted of either CD4(+) T cells or both CD4(+) an

106 indeed dependent upon CD4+ T cell help, mice were depleted of either CD4+ or CD8+ cells before immuni

107 e of host immunity in Tyzzer's disease, mice were depleted of either neutrophils, natural killer cell

108 of gut microbiota and is abolished when mice are depleted of endogenous commensal microbiota by antib

109 added to rabbit reticulocyte lysate that has been depleted of endogenous hsp70, purified wheat germ a

110 e neuronal cultures of either sex, which had been depleted of endogenous SV2A to mimic the homozygous

111 cell protein 0 (ICP0) or glycoprotein C (gC) were depleted of endogenous CD8+ or CD45+ cells and cult

112 hages and hydrolyzed in lysosomes, the cells were depleted of energy by treatment with sodium azide a

113 onal movement continued even after the cells were depleted of energy.

114 stores activity to nuclear extracts that had been depleted of essential factors by binding to Rb.

115 R-driven template in HeLa cell extracts that were depleted of essential factors by addition of RNA ol

116 ur analysis revealed that infiltrated tumors are depleted of favorable PBRM1 mutations and enriched f

117 sis defects in procyclic T. brucei that have been depleted of FLA1 by RNA interference.

118 If overconfluent cells are depleted of Fox-2, the switch from IIIc to IIIb is a

119 impaired glucose-induced insulin secretion, are depleted of Foxo1 and MafA, and include a Neurogenin

120 s accumulate immunosuppressive monocytes and are depleted of functional cytotoxic T cells, characteri

121 ed complex was absent in membranes which had been depleted of G proteins by treatment with alkaline b

122 Cells that had been depleted of GADD45gamma by transfection of short ha

123 binding significantly increased when decorin was depleted of GAGs, which by themselves had no affinit

124 Regions favoring fixation are depleted of genes and evolutionarily conserved eleme

125 he telomeres and centromeres of chromosomes, are depleted of genes, and are enriched for cancer-speci

126 Surprisingly, they are depleted of glycerolipid metabolites and free fatty

127 Fibres in single units were depleted of glycogen by repetitive stimulation, and

128 These ATG9A vesicles are depleted of Golgi proteins and enriched in BAR-domai

129 K site phosphorylation and GRK5 levels while being depleted of GRK2 and GRK6.

130 solated from Bcl-2-overexpressing cells that were depleted of GSH became sensitive to AP24-induced DN

131 otoxicity was enhanced when the Hep G2 cells were depleted of GSH.

132 The POAG JCT is depleted of HA and has an accumulation of CS, which m

133 differentiation and fusion, C2C12 myoblasts were depleted of Has2 by siRNA and induced to differenti

134 cell lines that either overexpress hDaxx or are depleted of hDaxx expression by the use of short hai

135 dded capsules; thus, once a localized region is depleted of healing agent, further repair is preclude

136 ere also cultured in vitreous humor that had been depleted of heparin-binding growth factors.

137 but were markedly decreased in B6 mice that were depleted of hepatic and splenic macrophages and DCs

138 e, obtained within seven days of ARDS onset, was depleted of high abundance proteins and labeled for

139 t1, contains acetylated H3 tail domains, and is depleted of histone H1.

140 highly transcribed ribosomal genes, known to be depleted of histones.

141 Active genes were depleted of histones at promoters and were enriched

142 (ii) when the voltage was positive, the film was depleted of holes becoming more insulating, the elec

143 p19K suppression of CTL lysis in vitro, mice were depleted of IFN-gamma and inoculated with gp19K mut

144 ubmitted to peanut oral immunotherapy (POIT) were depleted of IgG4 and retested in inhibition assays.

145 ecruitment defect persisted when donor cells were depleted of IL-10+ cells.

146 Examples are modified flours that have been depleted of immunogenic gluten epitopes, degradatio

147 , contains full-length FasL protein, and can be depleted of infectivity by immunoadsorption with anti

148 core of tyrosine phosphorylated proteins and are depleted of integrins at the plasma membrane.

149 uce NO, or NO-generating astrocytes that had been depleted of intracellular GSH by 87% following incu

150 Cells were depleted of intracellular glutathione either by the

151 hidonic acid, and 2) WY-14,643-treated cells were depleted of intracellular GSH.

152 RP2, bind IREs with high affinity when cells are depleted of iron, inhibiting translation of some tra

153 se of nitric oxide, because NONOate that had been depleted of its nitric oxide content had no effect.

154 e cells is observed when the plasma membrane is depleted of its support, the cortical actin network.

155 CF1 was depleted of its endogenous nucleotide by treatment w

156 al type of olfactory sensillum in Drosophila was depleted of its sole abundant Obp, it retained a rob

157 olic abnormalities were prevented when liver was depleted of KCs.

158 RESEARCH DESIGN AND Rats were depleted of KCs by administration of gadolinium chl

159 dlin-2, and we found that when SH-SY5Y cells are depleted of kindlin-2, they exhibit pronounced spind

160 btained in previous studies in which neurons were depleted of kinesin-5 (also called Eg5 or Kif11), a

161 is indistinguishable from embryos that have been depleted of known subunits of the anaphase-promotin

162 When DBA/2 mice syngenic for the tumor were depleted of leukocytes by cyclophosphamide administ

163 Polycomb sites are depleted of LINE repeats but enriched for SINEs and

164 cent segments of the human X chromosome that are depleted of LINE1 and enriched for SINE elements, pr

165 SP cells isolated from UCB that had been depleted of lineage-committed cells (Lin(-) UCB) co

166 The SSC(lo)ALDH(br) population was depleted of lineage-committed cells, 40-90% pure for

167 spacing, either very short or very long, and are depleted of linker histone (H1).

168 ans serotype b than an LJP IgG fraction that was depleted of LPS-reactive antibodies but contained an

169 els of the enzyme GSNO reductase (GSNOR) and are depleted of lung S-nitrosothiols (SNOs).

170 The transcribed regions of most active genes are depleted of macroH2A1, often in sharply localized do

171 , rats with AIA, and arthritic rats that had been depleted of macrophages.

172 , the tissue mixture containing fungal cells is depleted of mammalian RNA by centrifugation, followed

173 Although Pysap1(-) sporozoites are depleted of many of these important transcripts, the

174 When the d6 progeny are depleted of mature macrophages and residual CD34+ pr

175 Because these nonadherent cells are depleted of mature NK cells and T cells, but appear

176 Bone marrow harvested from the kidney donor was depleted of mature alloantigen-presenting cells and

177 on were also observed when donor bone marrow was depleted of mature T lymphocytes, indicating that IL

178 sponses were followed in wild-type mice that were depleted of mature B cells by anti-CD20 before or d

179 nd immunoblotting showed that absorbed serum was depleted of MBL-C.

180 At the level of late endosomes, they are depleted of membrane-stabilizing lipids like cholest

181 Integrator complex for premature termination are depleted of METTL3, suggesting a potential antagonis

182 Notably, 1,482 genes have regions that are depleted of missense variants despite being tolerant

183 tory bulb was profoundly reduced in size and was depleted of mitral neurons and oligodendrocytes, and

184 tissue/cell types, whereas genes near eQTLs are depleted of most functional annotations, show relaxe

185 ique composition, and MICOS enrichment sites are depleted of mtDNA and matrix proteins and contain hi

186 ially of the bladder, breast, and kidney, to be depleted of mtDNA, relative to matched normal tissue.

187 human 143B TK(-) osteosarcoma cells that had been depleted of mtDNA (rho(0)) or not (wt).

188 HepG2 cells were depleted of mtDNA to make rho zero cells, before th

189 o(0) SH-SY5Y and rho(0) A431 cell lines that were depleted of mtDNA.

190 In vitro, human LS174T goblet-like cells were depleted of mucus and had elevated levels of MUC2 m

191 ic biopsy specimens exposed to G. duodenalis were depleted of mucus, and in vivo mice infected with G

192 Identifying regions of the genome that are depleted of mutations can distinguish potentially de

193 nd oligodendrocytes, and its efferent tracts were depleted of myelin.

194 CD8+ T cells from adults with DS are depleted of naive subsets and enriched for different

195 tting, the CD34(-) fraction of the allograft was depleted of naive T cells by using magnetic CD45RA b

196 e combined immunodeficient (scid) mouse that was depleted of NE with 6-hydroxydopamine before reconst

197 nly the outer bilayer leaflet of the vesicle is depleted of negatively charged fluorescent lipids, wh

198 T, whereas 5-HT axons in the rest of the NAc are depleted of neurotransmitter.

199 ed severe combined immunodeficient mice that were depleted of neutrophils as compared with controls.

200 To test this hypothesis, mice were depleted of neutrophils by treatment with anti-Gr-1

201 igs with primary C. caviae ocular infections were depleted of neutrophils by using rabbit antineutrop

202 Female C57BL/6 mice were depleted of neutrophils using anti-Gr-1 monoclonal

203 knockout (FcgammaRIIB KO) mice and mice that were depleted of neutrophils with the MAb RB6, whereas 7

204 role in limiting acute JHMV infection, mice were depleted of neutrophils.

205 colitis in Rag-deficient recipients that had been depleted of NK cells was tested.

206 mor cells grew more rapidly in mice that had been depleted of NK cells, we analyzed the effects of th

207 umor-protective immunity in all animals that were depleted of NK cells in vivo.

208 MA cells alone, were injected into mice that were depleted of NK cells, the mice developed an increas

209 cells were obtained from immunized mice that were depleted of NK cells.

210 Therefore, B6 mice were depleted of NK/NKT cells with anti-asialo GM1 or an

211 Cy and IL-12 therapy in CD1d(-/-) mice that were depleted of NK1.1(+) cells.

212 ghly enriched for the expression of KIR3DL1, are depleted of NKp46, and respond poorly to major histo

213 in muscle tissues and found that these genes are depleted of nucleosomes at promoters and gene bodies

214 use embryonic fibroblasts the coding segment is depleted of nucleosomes, which instead cover the RSS,

215 sociation of VC results in subcomplexes that are depleted of one or more subunits and lack ATPase act

216 Mid-Hct (n = 39) and low-Hct (n = 60) groups were depleted of one third and one half of their circula

217 phosphate-buffered saline (PBS) or S. aureus were depleted of overabundant proteins and subjected to

218 Isolated CSCs were depleted of PAF1 using the CRISPR/Cas9 system.

219 HeLa cell extracts that had been depleted of PCBP2 by passage over a PV stem-loop IV

220 However, we have found that when bone marrow is depleted of pDC, the IFN-alpha produced in response t

221 ures of embryonic spinal cord cells that had been depleted of PDGFR alpha-expressing cells by antibod

222 Plasma IgG from one healthy adult was depleted of pepsin agglutinators and generic anti-F(

223 uring transcriptional repression, retrogenes are depleted of permissive chromatin marks without an ob

224 In Ifitm3(-/-) B cells, lipid rafts were depleted of PIP3, which resulted in the defective e

225 plexes preassembled on immobilized templates were depleted of pol III after a single round of RNA syn

226 cific iTregs in the retina whether the mouse was depleted of pre-existing, circulating Tregs.

227 arrow mononuclear cells, whereas CD34- cells were depleted of progenitors.

228 Genomic loci of piRNA biogenesis are depleted of protein-coding genes and tend to overlap

229 ion may be reduced in cell-free systems that are depleted of PTB and restored by reconstitution of ly

230 fect was exacerbated in macrophages that had been depleted of Rab1B by short hairpin RNA (shRNA) trea

231 revious observations using extracts that had been depleted of RCC1 only, extracts lacking both RanBP1

232 th the recombinant fusion protein, such sera were depleted of reactivity against 48 kD OGDC-E2 when p

233 developed in approximately 60% of mice that were depleted of regulatory CD4+ T cells and then subjec

234 When the S-30 extract used was depleted of release factor 2, Arg(12)-TnaC-tRNA(Pro)

235 ner with Piwi-interacting RNAs (piRNAs) that are depleted of repeat sequences, which raises questions

236 positive SP cells, and the residual SP cells were depleted of repopulating cells in a transplant assa

237 Samples were depleted of RF by column-based affinity absorption

238 ing of infected cell RNA that has physically been depleted of ribosomal and mitochondrial RNA followe

239 We found that in strains that are depleted of Rnr1, RER-deficient, and harbor an rNTP-

240 Immature subunits that are depleted of Rps0 protein that contain the 20S rRNA p

241 If rats are depleted of RT6.1+ regulatory T-cells before KRV inf

242 efs of the United States Virgin Islands have been depleted of scleractinian corals, leaving abundant

243 These vesicles appeared to be depleted of secretory cargo.

244 Relative to non-AA samples, AA samples were depleted of sequences from the genus Bacteroides Ph

245 Male Sprague-Dawley rats were depleted of serotonin on postnatal days (PND) 10-20

246 When H2.35 cells were depleted of serum, the expression of SNAT3 was incr

247 nditions whereby the streptococcal cells can be depleted of SGP, thus avoiding the problem of constru

248 to normal vaginal epithelial cells, BV cells were depleted of sialylated N- and O-glycans, with under

249 a and cystic fibrosis, where the airways may be depleted of SNOs.

250 ive concentrations of sodium in animals that are depleted of sodium.

251 In the first experiment, rats were depleted of sodium by treatment with furosemide 24

252 Rats were depleted of sodium with the diuretic furosemide thr

253 rates transcriptionally active nuclei, which are depleted of soluble factors required for the nuclear

254 he three species experiencing high mortality were depleted of starch.

255 biquitinated and rapidly degraded when cells are depleted of sterols.

256 in an Insig-binding conformation when cells were depleted of sterols.

257 crucial for the function of an organism will be depleted of such variants in natural populations, whe

258 In contrast, CD34-BM cells were depleted of such activities at the cell doses teste

259 nc transporter-3 (ZnT3) knockout mice, which are depleted of synaptic vesicle zinc, to assess the con

260 in C. elegans are severely uncoordinated and are depleted of synaptic vesicles, possibly because of a

261 Bone marrow was depleted of T cells by agglutination with soybean le

262 The allograft was depleted of T cells to reduce the risk of severe gra

263 Female DBA/2 mice were depleted of T cells (n = 10) or regulatory T cells

264 within 21 days of challenge even though they were depleted of T cells.

265 sions were significantly more severe if mice were depleted of T(reg) before infection.

266 significant proportion of the infused grafts were depleted of T-lymphocytes; 6 diseases account for 7

267 he growth cones, but the axons and their MTs are depleted of tau.

268 the CD4-deficient Ag-specific TCR repertoire was depleted of TCRs that demonstrated low-affinity bind

269 r using HeLa cell nuclear extracts that have been depleted of TFIIA.

270 At TATA-box-containing promoters, which are depleted of TFIID, a +1 nucleosome was positioned to

271 -bound regions that span an AT-rich core and are depleted of the canonical histone H3.

272 spectrometry show that Dot1-deficient cells are depleted of the global H3K79 methylation mark.

273 nt longevity studies combined; all but three are depleted of the life-shortening alleles in older Bio

274 Strikingly, we find that msk-null mutants are depleted of the snRNP assembly factor, survival moto

275 The vesicles produced (50-80 nm in diameter) are depleted of the trans Golgi marker sialyltransferase

276 redox reaction or contacted with Teflon that was depleted of the electronic surface charge could be r

277 PS II that was depleted of the OEC did not give the peak at 0.2 V.

278 to rebind to photosystem II membranes which were depleted of the 17-kDa component.

279 lysates from T. brucei procyclic cells that were depleted of the cognate endogenous ligase by RNA in

280 and a similar delay was observed when cells were depleted of the histone acetyltransferase CBP.

281 e show that mice produced less IgE when they were depleted of the neurotransmitter norepinephrine (NE

282 Germ-free (GF) mice, which are depleted of their resident microbiota, are the gold

283 The animals were depleted of their CD8(+) T lymphocytes and then cha

284 Immunized mice were depleted of their macrophages by dichloromethylene

285 Bovine articular cartilage explants were depleted of their matrix by trypsin digestion, foll

286 ARPE-19 retinal pigment epithelial cells were depleted of their mitochondrial (mt)DNA by passagin

287 Animals were depleted of their preexisting gut microbiota and th

288 Interestingly, oil produced by 2-PW was depleted of toluene, the preferred electron donor fo

289 We find that lincRNA promoters are depleted of transcription factor (TF) binding sites,

290 sfected into IMR-32 neuroblastoma cells that were depleted of transcription factor NRF2 by RNA interf

291 Consequently, archaeal genomes are depleted of transcriptional regulators found in othe

292 Nuclear extracts were depleted of U1 snRNP with a concomitant loss of spl

293 are intact and proteolytically active, they are depleted of ubiquitin conjugates, Rad23, and Dsk2.

294 Their lymph node cells were depleted of V beta 6(+)CD4(+) cells and were unresp

295 time than those reconstituted with PBMC that were depleted of Vdelta2 T cells.

296 When mice were depleted of Vgamma4(+) cells, clinical disease scor

297 Indeed, brain phospholipids are depleted of vulnerable polyunsaturated fatty acyl ch

298 In the regions that are depleted of water, the bilayers can fuse.

299 erum and three nonsensitized patients, which was depleted of XNA (HLA-IgG), did not react to human or

300 When cells are depleted of YaeT or YfiO, levels of all outer membra