ライフサイエンスコーパス: depletion

1 mole fraction of Cl/Na >/= 0.1, 90% chloride depletion).

2 infections due to combined T cell and B cell depletion.

3 N knockout mice, to obtain mdx mice with ApN depletion.

4 we assessed different mouse models for Treg depletion.

5 aling is up-regulated in response to miR-277 depletion.

6 hat the eruptions led to stratospheric ozone depletion.

7 its BK channel function, thereby causing ASL depletion.

8 s exhibited a similar phenotype following RB depletion.

9 t and was completely abolished with monocyte depletion.

10 which was prevented by NK cell or IFN-gamma depletion.

11 TOR rescued MaSCs from Cbl/Cbl-b DKO-induced depletion.

12 failure of disease to recur after CD3 T cell depletion.

13 l capacity, myeloid skewing, and immune cell depletion.

14 d macaques with or without CD8(+) lymphocyte depletion.

15 hese, 129 (64.5%) received an in vivo T-cell depletion.

16 Specific natural killer cell depletion 24 hours pre-acute myocardial infarction signi

17 l atrophy featuring stem and progenitor cell depletion, a phenotype unexpected from the previously re

18 However, neutrophil depletion abrogated protection from death in Nlrp3(-/-)

19 expression increases, whereas targeted DNMT1 depletion abrogates KIT signaling cascade through Sp1/mi

20 Indeed, enforced mitotic bypass through EMI1 depletion abrogates PARP-inhibitor-induced cytotoxicity.

21 ad reduced Cu storage pools in intestine, Cu depletion, accumulation of triglyceride-filled vesicles

22 rotein Tau deficiencies, and report that Tau depletion affects rRNA synthesis, ribonucleotide pool ba

23 al injury and podocytes leads to defects and depletion, albuminuria, and glomerulosclerosis.

24 Unexpectedly, PI(4,5)P2 depletion also caused loss of pre-assembled Gag lattices

25 Such depletion also causes aberrant levels of DNA.

26 20 recipients undergoing alemtuzumab-induced depletion and belatacept/sirolimus immunosuppression wer

27 Further, we observed that 6-ETI induces ATP depletion and cell death accompanied by S phase arrest a

28 ical feature in most cases of ALS is nuclear depletion and cytoplasmic accumulation of the protein TD

29 f action have been proposed, including thiol depletion and generation of hydrogen peroxide and supero

30 oved the pericardial AT and performed B-cell depletion and granulocyte-macrophage colony-stimulating

31 ated under conditions of alveolar macrophage depletion and in mice with a macrophage-specific defect

32 mediate and reversible intracellular glucose depletion and lactate accumulation.

33 ows a Tsodyks-Markram description of vesicle depletion and recovery.

34 l remission was associated with autoantibody depletion and with recovery of conduction block and dist

35 ional as well as blood parameters, leukocyte depletion, and bone marrow hypoplasia.

36 Following sodium depletion, and in the absence of either sucrose or salt,

37 Here, using chemical inhibition, genetic depletion, and overexpression experiments, we show that

38 tically ill patients signified by microbiota depletion, and reestablishment of a physiologic gastroin

39 cating that communal perceptions of resource depletion are closely linked to collective movement deci

40 Meibomian gland obstruction and meibocyte depletion are important components of MGD.

41 lethal in mice, but mice with postnatal CTCF depletion are less well studied.

42 ng all daylight hours, with complete sulfide depletion around midday.

43 somatized the granites, which resulted in Ce depletion as Ce(4+) and enrichment of the remaining REE,

44 B-cell depletion before HDM challenge in HDM-sensitized mice re

45 to respiratory F. tularensis infection, and depletion beginning at 3 days postinfection led to more

46 tion led to more pronounced sensitivity than depletion beginning prior to infection.

47 -deficient mice after cytotoxic T lymphocyte depletion, but also in WSX-1/tristetraprolin double knoc

48 y PLX5622 treatment or peripheral macrophage depletion by clodronate liposome treatment.

49 ntal liver metastases phenocopied neutrophil depletion by reducing liver metastatic colony growth, va

50 stress response (ISR) via sensing amino acid depletion by the eukaryotic initiation factor 2 (eIF2) k

51 onkeys, assessment of safety and target cell depletion by the high- and low-affinity TDBs revealed th

52 Such subsets likely explain why B cell depletion can either ameliorate or exacerbate inflammato

53 1), associates with the kinetochore, and its depletion causes severe defects in karyokinesis, loss of

54 levels of MSN2/MSN4 are increased in glucose-depletion conditions and that during growth in nonprefer

55 Despite eliciting broader B lymphocyte depletion, continuous combo therapy afforded no greater

56 Vitamin B12 depletion decreased de novo dTMP biosynthesis capacity b

57 y, preventing the cross talk by preceding DC depletion decreases MC antigen presenting capacity and T

58 onstitutive activation of Notch1 prevents SC depletion despite Pten deletion.

59 Its depletion destabilizes the pluripotency network and trig

60 crucial component of Orai1 channels, and its depletion disrupts the functional assembly of Orai1 mult

61 A hydration depletion down to 45%, which is close to the minimum hyd

62 Treg depletion during iNKT infusions completely abolished iNK

63 ng recovery from genetically manipulated GSC depletion, E(z) knockdown germ cells also fail to replen

64 The depletion effects are overcome and protein capture rates

65 Silencing MYC expression phenocopied the CSC depletion effects of C1572 and induced senescence in TNB

66 nts demonstrated a critical cutoff point for depletion efficacy, with low-level residual NK cells pro

67 Our quantification of groundwater depletion embedded in the world's food trade is based on

68 cycling of Hg (through 'atmospheric mercury depletion events', or AMDEs) and wet deposition via prec

69 e chemistry has been shown to initiate ozone depletion events, and it has long been hypothesized that

70 PDAC mice with pancreas-specific CXCL12 depletion exhibited diminished SC chemoattraction to pan

71 Interestingly, NK cell depletion experiments demonstrated a critical cutoff poi

72 duction were examined by transwell assay and depletion experiments, respectively.

73 Greater than 99% Wolbachia depletion following 7-day combination of RIF+ABZ also le

74 filing to examine the time-varying substrate depletion from a mixture of 19 amino acids and glucose b

75 WASP depletion from human neutrophils confirms that both prot

76 PPIns depletion from the PM was achieved either by agonist-ind

77 e with ventral tegmental area (VTA) dopamine depletion had attenuated delta activity (1-4 Hz) in the

78 These depletions identified differential actions of ILP7 and I

79 Serotonin depletion impaired the ability of exendin-4, a clinicall

80 Furthermore, Kapbeta2 depletion impaired the growth of cultured medulloblastom

81 ll-like and metastasis signatures, and their depletion impairs the metastatic potential of breast can

82 Furthermore, TBC1D5 depletion in autophagy-deficient cells rescues retromer

83 Here we report that SIRT6 depletion in cardiac as well as skeletal muscle cells pr

84 Antibody-mediated CD4(+) T-cell depletion in HF mice (starting 4 weeks after ligation) r

85 sis indicates unusually low CpG dinucleotide depletion in KYAV compared to other ledanteviruses and r

86 nal, Pdx1-Cre-mediated, pancreatic PAK4 gene depletion in the mouse, verified by loss of PAK4 protein

87 d polypeptide (IAPP) is responsible for cell depletion in the pancreatic islets of Langherans, and fo

88 chanism underlying progressive CD4(+) T cell depletion in vivo.

89 ion of Pax3 mRNA+ cells after satellite cell depletion in young and aged mice suggests that Pax3+ cel

90 eric boundary layer undergoes frequent rapid depletions in ozone and gaseous elemental mercury due to

91 after fasting or salt intake following salt depletion; inactivation increased saline intake after de

92 In contrast, acute 2-AG depletion increased anxiety-like behaviors, which was no

93 Sirt3 depletion increased SOD2 acetylation, elevated mitochond

94 Importantly, TbRAP1 depletion increases the TERRA level, which appears to re

95 MYCN partially reversed the effects of MDM2 depletion, indicating that MYCN is an important MDM2 tar

96 erexpression was reversed by concurrent LSD1 depletion, indicating that tumor-promoting activity of H

97 are hypersensitive to methionine restriction/depletion-induced differentiation and apoptosis, primari

98 Consistently, KDM3A depletion inhibited the growth of subcutaneously implant

99 We show that Usp36 depletion is lethal in preimplantation mouse embryos, wh

100 Therefore, miR-338-3p depletion is necessary and sufficient to disrupt auditor

101 ic adenocarcinoma mouse prostate model, Skp2 depletion leads to a profound repression of prostate tum

102 in mice and provide novel evidence that CTCF depletion leads to overexpression of inflammation-relate

103 PfCRK4 depletion led to a complete block in nuclear division an

104 While ATP depletion led to cell death, over-acetylated tubulin led

105 T cells reduced viral burdens, whereas their depletion led to higher tissue burdens, and CD8(-/-) mic

106 ntrols were transplanted into the antibiotic depletion mice model.

107 By transforming stimulated emission depletion microscopy into a time-resolved ultrafast appr

108 Finally, we used stimulated emission depletion microscopy to analyze how the mutation altered

109 l population but cannot be explained by food depletion nor is it modulated by biogenic amines, which

110 In contrast, about 90% Treg depletion obtained in BAC transgenic Foxp3.LuciDTR4 mice

111 raction molecule 1 (STIM1), upon sensing the depletion of (Ca(2+)) from the endoplasmic reticulum (ER

112 sor, gamma-glutamylcysteine, and significant depletion of 1 other putative metabolite in resistant st

113 losis-specific CD4 T cells, and preferential depletion of a discrete subset of M. tuberculosis-specif

114 Depletion of aCDase also promoted accumulation of cerami

115 echanism of lymphocyte contraction is clonal depletion of activated T cells by cytokine withdrawal in

116 Finally, the depletion of Ag NPs in the growth medium allowed the fun

117 Furthermore, depletion of Ahr, Med1, or Ctcf in Mir122(-/-) hepatocyt

118 siRNA-mediated depletion of AKAP350A caused displacement of both Cep68

119 ongoing acidity loading at the site, and the depletion of Al mineral buffering capacity after approxi

120 permeability, in the context of progressive depletion of all VEGF-A isoforms from the podocytes.

121 Conversely, the depletion of APC leads to a significant decrease in memb

122 Depletion of Atg7, a necessary component of the autophag

123 Purpose Our preclinical work identified depletion of ATR as a top candidate for topoisomerase 1

124 Here, we further demonstrate that depletion of AUF1 abolishes the global interaction of mi

125 However, depletion of BDNF by transfecting lentivirus-derived shB

126 Finally, we observe that depletion of BICD2 in the monocytic cell line THP-1 resu

127 Depletion of biota and trawl penetration into the seabed

128 ss induced by FANCM deficiency, simultaneous depletion of BLM and FANCM, or of BRCA1 and FANCM, leads

129 his phenotype can be rescued by simultaneous depletion of both Satb1 and Satb2, owing to their antago

130 Depletion of butyrate-producing Clostridia, either throu

131 tal nitrogen added), which was linked to the depletion of C11-C20 fatty acids.

132 anticancer strategy, leading to a selective depletion of cancer-relevant proteins after turnover.

133 Subsequent antibody-mediated depletion of CART123 or CART123-CD20 did not impair leuk

134 Depletion of CCR2(+) inflammatory monocytes and pharmaco

135 ciated dysregulation of adaptive immunity by depletion of CD4 Th cells most likely contributes to los

136 Depletion of CD4(+) cells after an established humoral r

137 pletion on GVL versus GVHD and revealed that depletion of CD4+ T cells leads to the upregulation of P

138 onditional knockout), with antibody-mediated depletion of CD4+ T cells.

139 Furthermore, depletion of CD8 and CD4 T cells resulted in loss of ear

140 Depletion of cell surface Sia by neuraminidase treatment

141 e to broadly facilitate robust and long-term depletion of cell-cycle proteins and reveals insights in

142 Reciprocally, depletion of CHIP leads to promotion of tumor growth.

143 Depletion of CTCF was sufficient to induce heart failure

144 iously, depends upon a significant, specific depletion of cyclin B1 and its encoding RNA, which precl

145 Depletion of disassembly factor Prp43 suppresses H2A.Z-m

146 Here we have demonstrated that temporary depletion of donor CD4+ T cells early after hematopoieti

147 Depletion of either LRRC25 or ISG15 abrogates RIG-I-p62

148 PM depletion of either phosphatidylinositol 4-phosphate (Pt

149 ween LIB and LIC and can avoid the excessive depletion of electrolyte during the charge process.

150 Depletion of endothelial-derived MPs from ACS patients r

151 ast, loss of Mll3/4 proteins leads to strong depletion of enhancer Pol II occupancy and eRNA synthesi

152 of RhopH2 expression in cycle one leads to a depletion of essential vitamins and cofactors and decrea

153 s of replicated DNA technique, we found that depletion of FANCM dramatically reduces the replication

154 Conditional depletion of Foxp1 in bone marrow MSCs led to premature

155 f Wnt5a results in cerebellar hypoplasia and depletion of GABAergic and glutamatergic neurons.

156 Finally, we show that postnatal depletion of GLP-1R in the PVN increases food intake and

157 siRNA-mediated depletion of GNB1 (encoding Gbeta1) in murine megakaryoc

158 and smooth muscle, as well as a significant depletion of goblet cell metaplasia and mucus secretion

159 s with PBP2a and PBP2b, and that deletion or depletion of GpsB prevents closure of the septal ring th

160 cell death pathway that was characterized by depletion of GSH and ascorbic acid and accumulation of c

161 Bone marrow progenitor analysis revealed depletion of hematopoietic stem cells and multipotent pr

162 In addition, depletion of HP1gamma in PCa cells not only repressed pr

163 d neutrophils in the lungs of male mice, and depletion of inflammatory monocyte macrophages partially

164 Depletion of inflammatory monocytes, but not DCs or othe

165 ycle arrest and death in cancer cells due to depletion of intracellular GSH and ensuing elevated ROS;

166 ) is a Ca(2+)-entry process activated by the depletion of intracellular stores and has an important r

167 urs by interferon-gamma (IFN-gamma)-mediated depletion of intracellular tryptophan, and some Ct strai

168 o release from nj-SR; however, the degree of depletion of j-SR [Ca(2+) ]SR was smaller than nj-SR [Ca

169 The depletion of KDM3 inhibits tumorigenic growth and chemor

170 Unexpectedly, depletion of KDM3A was capable of reactivating mutated p

171 f these manipulations are fully dependent on depletion of kynurenic acid (KYNA), a neuroinhibitory me

172 Critically, depletion of LARP1 alone in human adult CD34+ bone marro

173 upling via extracellular electric fields and depletion of local sodium ion nanodomains.

174 Pharmacological depletion of MCs granules or prevention of MC degranulat

175 pecific knockout of Yap or antibody-mediated depletion of MDSCs promoted macrophage reprogramming, re

176 ecule inhibition, genetic deletion, or acute depletion of MELK did not significantly affect cellular

177 Depletion of Miwi2-expressing cells results in a transie

178 Depletion of MRE11 and abrogation of its exonuclease act

179 unts of large-scale deletions and a dramatic depletion of mtDNA in the epidermis and showed macroscop

180 a given cellular process have centered upon depletion of mtDNA through chemical or genetic means.

181 Depletion of murine CAFs from PDX restored sensitivity t

182 There is extensive depletion of Mycobacterium tuberculosis-specific CD4+ T

183 Depletion of Myt1l in primary postmitotic neurons de-rep

184 Depletion of NatD suppresses the epithelial-to-mesenchym

185 Here, we investigated how acute depletion of negatively charged PM polyphosphoinositides

186 Depletion of neutrophils, ablation of Adrb1 in haematopo

187 Depletion of NK cells restored the allergen responsivene

188 nsible for such attenuated responses because depletion of NK1.1(+) cells in IP(-/-) mice restored bot

189 Indeed, loss or depletion of NMD factors have been shown to disrupt deve

190 Constitutive depletion of p21-activated kinase 4 (PAK4) in the mouse

191 scued by nucleotide supplementation or after depletion of p53.

192 Genetic depletion of p62 robustly inhibited tumor-initiating fre

193 Depletion of PAQR11 dispersed Golgi organelles and impai

194 Depletion of PDLIM5 resulted in significant reduction in

195 Moreover, depletion of PFKFB4-attenuated cellular biosynthetic act

196 Depletion of PHF11 diminished the ATR signaling response

197 -induced apoptosis and EV71 release, whereas depletion of PinX1 by small interfering RNA promoted apo

198 e sensitive to topoisomerase inhibitors, and depletion of PKCdelta in this subgroup suppresses apopto

199 Targeted depletion of PPM1A by shRNA or inhibition of PPM1A activ

200 Depletion of RAD51 prevents the DNA2/WRN-dependent degra

201 regions together with H2AZ and H3.3 and that depletion of Repo-Man alters the peripheral localization

202 Depletion of RNF146 caused hypersensitivity to LPS-induc

203 ETO-induced block was completely rescued by depletion of SAMHD1 in MDM Concordantly, infection by HI

204 In contrary, depletion of SATB2 inhibited cell proliferation, colony

205 Depletion of satellite cells impaired post-burn recovery

206 Depletion of Smo from osteoblastoid cells is associated

207 In addition, depletion of SMYD5 in human colon and lung cancer cells

208 ing period, which was found to coincide with depletion of solid phase iron in the source zone.

209 eas subject to periodic enhanced UV-B due to depletion of stratospheric ozone.

210 The depletion of sulfur from the surface of this catalyst du

211 Furthermore, antibody-mediated depletion of T cells prevented nasopharyngeal infection

212 itrosopumilus maritimus (AOA) during gradual depletion of TAN (NH3 + NH4+) and O2 .

213 Depletion of TANGO1 in HSCs blocked collagen I secretion

214 Genetic depletion of Tfh cells decreased IgE antibody levels and

215 man erythroid cell differentiation; specific depletion of TH from the culture medium completely block

216 Depletion of the annotated lncRNA, IFNG-AS1, or one IFNG

217 Depletion of the assembly factor Erb1 prevents stable as

218 nal and cell cycle defects was observed upon depletion of the cell cycle inhibitor p21.

219 inhibiting RNA polymerase II termination via depletion of the cleavage/polyadenylation machinery, cir

220 Furthermore, we found that depletion of the commensal genus Neisseria and the speci

221 a non-cell-autonomous fashion in vitro, and depletion of the Hh effector Smoothened (Smo) from strom

222 4K16 acetylation was abolished in cells upon depletion of the histone methyltransferase gene SET-doma

223 late entire glands, including the base, upon depletion of the Lgr5(+) population.

224 Depletion of the memory B-cell compartment contributes t

225 acquired pathogens, and antibiotic-mediated depletion of the microbiota reduces host resistance to i

226 Depletion of the microbiota significantly attenuated ren

227 o study whether these effects were driven by depletion of the microbiota, we performed fecal transpla

228 sing gene targeting and RNAi, we showed that depletion of the nonsense-mediated mRNA decay (NMD) fact

229 Here, we show that depletion of the nuclear export adaptor SRSF1 prevents n

230 rom nephron progenitors results in premature depletion of the progenitors and increased expression of

231 Finally, we demonstrate that depletion of the single Drosophila homolog dBRWD3 result

232 s I, and findings suggest that age-dependent depletion of the SMC5/6 complex in oocytes could contrib

233 get cells for SIV/HIV infection, and massive depletion of these cells is considered a major cause of

234 tumor stroma of breast cancer patients, and depletion of these factors from normal human breast fibr

235 notypic variation, as there is a significant depletion of these genes in annotated gene sets.

236 Genetic depletion of TLR4 or SPAK normalizes hyperactive CSF sec

237 s, excluded from the centromere regions, and depletion of topo-II did not change CENP-A levels.

238 Constitutive activation of mTORC1 by depletion of tuberous sclerosis complex 2 (TSC2) inhibit

239 The RNAi-mediated depletion of UBF diminishes nucleolar localization of Sm

240 alized hits specific for STx2 and found that depletion of UNC50 blocked early endosome-to-Golgi traff

241 ever, neither overexpression nor conditional depletion of wag31 impacted M. tuberculosis susceptibili

242 Depletion of XPA or progerin each significantly restored

243 Deletion of YY1 binding sites or depletion of YY1 protein disrupts enhancer-promoter loop

244 Accordingly, depletion of ZIC2 shifted the balance of bivalent histon

245 Effects of Mff and Drp1 depletion on degradation rates and ubiquitination of Mcl

246 s study, we investigated the effects of Lcn2 depletion on diet-induced obesity, inflammation, and PDA

247 f GVHD to evaluate the effect of CD4+ T cell depletion on GVL versus GVHD and revealed that depletion

248 mpact of meldonium-mediated muscle carnitine depletion on whole-body fuel selection, and muscle fuel

249 phocyte infiltration as expected, reciprocal depletion or inactivation of CD4(+) T lymphocytes decrea

250 X5 mutations (K464A or DeltaCT51), or TRIM37 depletion or mutation, reduce PEX5 abundance by promotin

251 RB action is abrogated either by direct depletion or through inactivation of RB function; howeve

252 e associated with modern stratospheric ozone depletion over Antarctica-plausibly link the Mount Takah

253 Unlike B cell depletion, pan-T cell aplasia is prohibitively toxic.

254 Finally, induced IL-17A depletion peritransplant also enhanced acute GVHD, consi

255 ic cytokine administration and/or lymphocyte depletion prior to oral antigen-specific immunotherapy w

256 The extent to which depletion processes deplete non-EV particles is incomple

257 dings, we propose a model in which ER Ca(2+) depletion promotes the activation of SREBP2 and subseque

258 We report that acute estrogen depletion rapidly disrupts auditory processing in large

259 Here, we show that ER Ca(2+)-store depletion rapidly induces STIM1 phosphorylation at Y361

260 While endogenous Mcl-1 depletion reduced HR and enhanced NHEJ, Mcl-1 overexpres

261 While CD11c+ cell depletion reduced IL-6, IL-1beta, CXCL1, CXCL2 and CXCL1

262 Hilpda depletion reduced resistance against lipid overload and

263 Indeed, TrxR1 depletion reduces myoblasts growth by inducing an early

264 itro ADCC, and in vivo IgG-mediated cellular depletion, regardless of sialylation status.

265 m, whereas hydraulic dredges caused the most depletion, removing 41% of biota and penetrating the sea

266 Otter trawls caused the least depletion, removing 6% of biota per pass and penetrating

267 The upregulation by Ku80 depletion requires Chk1 activation following DNA end-res

268 eq K(+) consistent with K(+) accumulation or depletion, respectively, in the extracellular space, whi

269 Treg depletion resulted in a blip of HIV-1 replication in T c

270 As expected, tRNASec depletion resulted in loss of ribosome density downstrea

271 Mi-2beta depletion resulted in rapid deployment of both a pro-inf

272 Chd1 depletion robustly enhances TDP-43-mediated neurodegener

273 r during somatic cell reprogramming, and its depletion significantly enhances reprogramming efficienc

274 However, monocyte depletion significantly reduced glomerular necrosis and

275 trongly binds to PapMV nanoparticles and its depletion significantly reduces PapMV's interaction with

276 tes was significantly delayed upon microglia depletion, spontaneous and LI-induced axon regeneration

277 C4 depletion started at prodromal phase, and C4 was lowest

278 w to apply mt-Keima with stimulated emission depletion (STED) microscopy, which can potentially provi

279 low toxicity and enable stimulated emission depletion (STED) nanoscopy in neurons, human fibroblasts

280 After Ca(2+) store depletion, STIM1 and Orai couple to each other, allowing

281 horylation, although it is unclear how store depletion stimulates this gating pathway.

282 Amino acid depletion strengthens this interaction, explaining the r

283 RNAi depletion studies confirmed that ESCRT-III proteins, par

284 Adoptive transfer and cell depletion studies demonstrate that DENV-immune CD8(+) T

285 KYNA depletion then leads, in an N-methyl D-aspartate recepto

286 We propose a mechanism in which cholesterol depletion triggers a signaling cascade, culminating with

287 asmic reticulum stress, explaining why SRp55 depletion triggers beta-cell apoptosis.

288 00 unique Tn5 insertions and measured mutant depletion upon exposure to three clinically relevant ant

289 bolished the protective effect of microbiota depletion upon renal I/R injury.

290 Neuron, Chu et al. (2017) show that dopamine depletion using a 6-OHDA model causes a decrease in hype

291 Systemic neutrophil depletion was found to render wild-type mice highly sens

292 f Carrizo citrange revealed that the hormone depletion was linked to the upregulation of CsAOG, invol

293 und that synaptic vesicle pool recovery from depletion was sensitive to high concentrations of EGTA,

294 Moreover, the effect of Nox4 depletion was time-dependent; following six weeks of rep

295 r type (mother) and GVHD prophylaxis (T-cell depletion) were also significant predictors of aGVHD.

296 Interestingly, macrophage depletion with clodronate inhibited the development of c

297 of SSA particles ranged from full to partial depletion, with 24% of SSA particles containing chloride

298 led that Treg loss was primarily due to cell depletion, with minimal evidence of Treg conversion to a

299 It is demonstrated that the proton depletion zone may be constrained and controlled by the

300 y, single particles appear to exhibit target depletion zones near their surface, caused by the high d