ライフサイエンスコーパス: ex vivo

1 ated ANP-mediated relaxation of aortic rings ex vivo.

2 spontaneous help for autoantibody production ex vivo.

3 primary bone marrow-derived dendritic cells ex vivo.

4 monocytic THP-1 cells compared with old skin ex vivo.

5 n enhanced response to weak agonist peptides ex vivo.

6 first-trimester placentas infected with ZIKV ex vivo.

7 es of each tissue and could be recapitulated ex vivo.

8 compensatory processes operating in vivo and ex vivo.

9 otocol using Th17 cells expanded only 4 days ex vivo.

10 t bladder cancer cells shed in patient urine ex vivo.

11 reproduced the ILC and NK cell abnormalities ex vivo.

12 on of these peptides was studied in vivo and ex vivo.

13 lial cell angiogenic activities in vitro and ex vivo.

14 the activation of the Ahr signaling pathway ex vivo.

15 two different regions of the mouse, studied ex vivo.

16 copic evaluation to study corneal morphology ex vivo.

17 and impaired SMC outgrowth from aortic rings ex vivo.

18 lly relevant media was assessed in vitro and ex vivo.

19 peripheral myeloid cells, release IL-1alpha ex vivo.

20 although hitherto it has mostly been applied ex vivo.

21 nger Ag-specific CD4(+) T cell proliferation ex vivo.

22 bens core using fast scan cyclic voltammetry ex vivo.

23 8+ T cells reduced direct tumor cell killing ex vivo.

24 cific neoepitopes and tumor reactive T cells ex vivo.

25 died the biological effects of MPs generated ex vivo.

26 inescent TTFL rhythms in SCN slices recorded ex vivo Abrogation of circadian competence in VPAC2 cell

27 tric model, a static intestinal model and an ex vivo absorption model (Ussing chambers).

28 LT(2)R-dependent immunopathology, as well as ex vivo activation of mouse and human platelets.

29 althy prostates, supporting the relevance of ex vivo activity assays to in vivo translation.

30 Ex vivo, addition of the IL-1 receptor antagonist anakin

31 analyzed fibril structures were seeded with ex-vivo amyloid fibrils purified from the explanted hear

32 Ex vivo analysis of inflammatory disease patients' whole

33 We also perform a high-resolution ex vivo analysis of pre-existing and induced SARS-CoV-2-

34 The cells were expanded ex vivo and administered in a single infusion at one of

35 Current ex vivo and animal models of hidradenitis suppurativa (H

36 This reduction was corroborated ex vivo and correlated with decreased TAM density.

37 ed higher peanut-induced basophil activation ex vivo and higher peanut sIgE levels and sIgE/total IgE

38 with a large structural variety of lipidoids ex vivo and identified imidazole-containing lipidoids th

39 s of PSC patients and controls were analyzed ex vivo and in vitro using transwell experiments with ch

40 s from brain and other tissues were measured ex vivo and in vitro.

41 hat induced comparable anticoagulant effects ex vivo and in vivo (tail-bleeding assay and FeCl(3)-ind

42 smooth muscle cells, constricted arterioles ex vivo and in vivo and increased systemic blood pressur

43 no-regulation of miR-21-5p and miR-27a-5p in ex vivo and in vivo cartilage loading models.

44 onstrate its performance and utility by fast ex vivo and in vivo imaging of human skin.

45 Here, using ex vivo and in vivo imaging, we show in Drosophila that

46 ta-cell proliferation in response to glucose ex vivo and in vivo in transplanted glucose-infused rats

47 cally manipulated human and mouse cells, and ex vivo and in vivo rat models, we uncovered a function

48 V RNA (rca-RNA) increased after VOR exposure ex vivo and in vivo received 4 doses of AGS-004 every 3

49 del, and functionally validated by in vitro, ex vivo and in vivo techniques.

50 deficiency of Scd1 accelerated remyelination ex vivo and in vivo.

51 R-Cas system and deliver its components both ex vivo and in vivo.

52 ing to measure cell abundance and cell state ex vivo and in vivo.

53 s inhibited the function of Ae. aegypti ORco ex vivo and repelled adult Asian tiger mosquitoes (Ae. a

54 mediate early gene expression and higher FRs ex vivo and tracked the drop and rebound in ensemble mea

55 nderstanding of HSC self-renewal in vivo and ex vivo, and discusses important advances in ex vivo HSC

56 ophages from mice and humans, polarized them ex vivo, and examined their functional interaction with

57 have smaller myofibers, generate less force ex vivo, and exhibit reduced exercise endurance, associa

58 ing FAO in clinical prostate tumors cultured ex vivo, and identify DECR1, encoding the rate-limiting

59 n induces activation of T cells in in vitro, ex vivo, and in vivo conditions, irrespective of T cell

60 potential of Bald's eyesalve using in vitro, ex vivo, and in vivo models representative of skin or ey

61 B1) and CD15 on brain SHH MB cells in vitro, ex vivo, and in vivo.

62 ratinocytes in vitro and human skin explants ex vivo, and mice in vivo generate microvesicle particle

63 function led to precocious stream departure ex vivo, and stream disruption, morphological changes an

64 In addition, VSMC stiffness (-46.6%) and ex vivo aortic ring contraction force (-40.1%) were lowe

65 hat may additionally participate in altering ex vivo aortic vessel function.

66 tant from the tumor bulk, using a variety of ex vivo approaches.

67 This is promising, but ex-vivo approaches are cumbersome and challenging to tra

68 Readouts included bladder histology and ex vivo assessments of urothelial proliferation, cell cy

69 e model, the correlation between in vivo and ex vivo assessments revealed histological characteristic

70 with histology has important applications in ex vivo atlas building and in modeling the link between

71 d X-linked CGD (X-CGD) patients who received ex vivo autologous CD34(+) hematopoietic stem and progen

72 Ex vivo autoradiography was performed on resected brain

73 ation alters the gene expression response to ex vivo bacterial and viral challenge.

74 Results: PET images and ex vivo biodistribution in immunocompetent mice with [(8

75 Ex vivo biodistribution of (64)Cu-LLP2A was determined b

76 Ex vivo biodistribution studies revealed reversible accu

77 OVCAR-3 OvCa xenografts by dynamic PET/MRI, ex vivo biodistribution, and radiometabolite analysis of

78 ts by in vitro autoradiography, PET imaging, ex vivo biodistribution, metabolite experiments, and rec

79 the dynamic response of 3D printed phantoms, ex vivo biological tissue, and in vivo mouse and rat mod

80 Using a combination of ex vivo bioluminescence and in vivo gene expression, we

81 For ex vivo biopsy samples, diagnostic yield was 100% using

82 ment of PD-1 within the tumor, but not acute ex vivo blockade, partially restored cell couple mainten

83 herefore, we developed and characterized the ex vivo brain slice culture model for CWD, using a trans

84 In the ex vivo breast cancer tissue assay, WISP1 promoted the g

85 (+) T cells from controls respond to opioids ex vivo by increasing cytoplasmic calcium, a novel findi

86 trophils, and epithelial cells was confirmed ex vivo by inflammatory macrophages and in vivo by thiog

87 e media either alone or together with HDL or ex vivo by plasma derived from subjects with familial hy

88 Beyond this, the ex vivo CAA-RBC assay determined the cellular antioxidan

89 In contrast, ex vivo cardiac function in HFD-fed WT mice dropped ~ 50

90 5L1 cKO mice did not display any decrease in ex vivo cardiac workload in response to a HFD.

91 d miR-27a-5p were significantly increased in ex vivo cartilage explants subjected to increasing load

92 In ex vivo CD4(+) T cells from ARV-suppressed individuals,

93 eed for a priori knowledge of tumor antigen, ex vivo cellular manipulation, or cellular manufacture,

94 umbilical cord blood without altering their ex vivo characteristics.

95 trol kidneys; (2) donor kidneys subjected to ex vivo cold ischemia (CI); (3) donor kidneys subjected

96 CD8 T cells showed lower perforin expression ex vivo compared with blood CD8 T cells, with reduced gr

97 spiratory activity were measured in vivo and ex vivo Compared with NOD TLR4(+/+) mice, NOD TLR4(-/-)

98 performed in vivo or alternatively using an ex vivo configuration, where retinas are isolated and tr

99 Ex vivo conjugated ALDC1 also significantly inhibited tu

100 PDX animals, and this signal was matched in ex vivo counts for 2 of 3 models.

101 Ex vivo, crosslinking of alpha2-antiplasmin and fibrin w

102 Although Treg stability during ex vivo culture has improved, methods to assess Treg sta

103 vanced in vitro cell culture models, such as ex vivo culture models or organoids, have also been deve

104 Long-term ex vivo culture offers one approach to increase engraftm

105 ped a cell-free, ligand-based activation and ex vivo culture system for CD19-specific CAR T cells.

106 HT-DBP requires only 24 hours of ex vivo culture, which enables a more immediate study of

107 s adaptive changes that occur with prolonged ex vivo culture.

108 riment 4, tissue secretome was obtained from ex-vivo culture of these paired tissue samples.

109 Here we describe an ex vivo cultured human skin explant model in which we ha

110 of tamoxifen-resistant cell lines as well as ex vivo-cultured ERalpha-positive breast tumors.

111 ells from primary human tumor samples, after ex vivo culturing, and from multiple mouse tumor and vir

112 not normally expressed in mature Tregs, and ex vivo data reveal that forced overexpression of GILZ i

113 ells from controls exposed to mu-OR agonists ex vivo decrease expression of activation markers CD69 a

114 ng activated human memory B cells, activated ex vivo, demonstrating its versatility.

115 yte adhesion, both in vitro and in human LSV ex vivo, demonstrating that this pathway is necessary fo

116 w conditions as well as in the generation of ex vivo derived immune cellular therapeutics.

117 The recent structural elucidation of ex vivo Drosophila Orb2 fibrils revealed a novel amyloid

118 bject-specific gut microbial communities, an ex vivo drug metabolism screen, and targeted and untarge

119 Restoration of normoxic conditions-either ex vivo during NMP or in vivo following transplant-trigg

120 Ex vivo electrophysiological recordings show that nesfat

121 established rat model of alcohol dependence, ex vivo electrophysiology and ISH, provides mechanistic

122 lamp rig for performing high signal-to-noise ex vivo ERGs.

123 Increased reticulocytosis, enhanced ex vivo erythrocyte sickling, and increased erythrocyte

124 For ex vivo evaluation, 15 chylous and five nonchylous study

125 Individualized adoptive transfer of ex vivo expanded CMV-specific CD8+ T cells has provided

126 We ex vivo expanded highly pure NKT cells (mean +/- s.d., 9

127 RISPR/Cas9 system to delete CD38 (CD38KO) in ex vivo expanded peripheral blood NK cells.

128 s following adoptive T cell therapy (ACT) of ex vivo expanded tumor-infiltrating lymphocytes (TILs).

129 Adoptive T cell therapy (ACT) using ex vivo-expanded autologous tumor-infiltrating lymphocyt

130 tions and which protocols effectively induce ex vivo expansion of GZMB(+) B cells.

131 ecause of the paucity of HSCs and the modest ex vivo expansion of HSCs in media that contain poorly d

132 rgeting various BCPs as potential agents for ex vivo expansion of human HSCs.

133 esence of Epo, EpoRm-CAR T cells had greater ex vivo expansion than CAR T cells and killed CD19+ leuk

134 Consistent with this, ex vivo exposure of LSVs to acute arterial WSS promoted

135 be both heterologously seeded using patient ex-vivo fibrils.

136 excellent agreement between the in vivo and ex vivo findings, confirmed with histology.

137 Ex vivo fluorescence imaging after overnight cold exposu

138 m for the expansion of functional mouse HSCs ex vivo for >1 month under fully defined albumin-free co

139 comparable performance has been found in the ex vivo formation of PCO between the two IOLs.

140 Transmission electron microscopy of ex vivo-formed PNAs revealed a propensity of necrotic pl

141 cell lines in vitro and metastases analyzed ex vivo from an autochthonous lung cancer mouse model ha

142 Thus, HT-DBP appears to be an ex vivo functional method with sufficient scale to simul

143 es PNN deposition and increases the power of ex vivo gamma oscillations in conventionally housed mice

144 icosterone-treated mice also display reduced ex vivo gamma power and impaired working memory.

145 Linking ex vivo gene down-regulation with in vivo neuroimaging,

146 approach may therefore prove beneficial for ex vivo gene editing, for enhanced platelet production,

147 Ex-vivo gene therapy using stem cells or T cells transdu

148 erapeutic modalities (combination therapies, ex-vivo gene therapy, and in-vivo gene therapy) for a ta

149 In contrast, adoptive transfer of ex vivo generated MDSC from cytokine-treated bone marrow

150 The ex vivo generation of gastrointestinal organoids from cr

151 Ex-vivo generation of PDO for pharmacotyping may serve a

152 phages could be adoptively transferred after ex vivo genetic modification.

153 agnetic resonance spectra were acquired from ex vivo glioma tissue (n = 16, grades II-IV) to quantify

154 Other ex vivo glycemic correlates occurred more generally in e

155 was developed by using computer simulations, ex vivo heart preparations, and dogs.

156 The most commonly performed procedure was ex vivo hepatectomy (n = 18), followed by ex vivo resect

157 probes showed a significant correlation with ex vivo histology (p < 0.001) and also corresponded well

158 ciferase reporter assays and analysis in the ex vivo HSC assays.

159 ex vivo, and discusses important advances in ex vivo HSC expansion that are providing new biological

160 ed HA and versican production, we studied an ex vivo human bronchial epithelial cell (BEC)/human lung

161 distance of responding neighboring cells in ex vivo human corneas was measured.

162 reduced after 24 h of Ca(2+) chelation in an ex vivo human skin model, suggesting that desmosomal cad

163 include directly administering the peptides ex vivo (i.e., to excised tissue) or in vivo (in animals

164 Cellular responses were assessed using an ex-vivo IFN-gamma enzyme-linked immunospot assay.

165 ed induction of IL-10 but is dispensable for ex vivo IL-10 expression.

166 Finally, we show that ex vivo IL-1alpha release is gasdermin-D dependent, and

167 associated PD-1 signaling, we established an ex vivo imaging approach to investigate the response of

168 rthermore, when administered orally to mice, ex vivo imaging of rhodamine-loaded chitosan nanoparticl

169 In this ex vivo imaging study of coronary artery specimens, the

170 measured by both tissue extraction assay and ex vivo imaging.

171 nment, was topically applied to 90 specimens ex vivo immediately following excision.

172 ed MuV peptides were tested for in vitro and ex vivo immunogenicity.

173 Isolated pulmonary arteries were evaluated ex vivo in a myograph.

174 tochrome c oxidase-negative cells were found ex vivo in biopsies of affected tissues, such as kidney

175 onment in vivo in the db/db mouse islets and ex vivo in C57BL/6J islets exposed to different glucose

176 e glucose uptake and signaling were measured ex vivo in fetal (n = 5-8/group) and juvenile (n = 8/gro

177 f the MAO-A and MAO-B isoforms was confirmed ex vivo in mouse brain homogenates, and additional in vi

178 is demonstrated in vitro in cancer cells and ex vivo in mouse liver.

179 ular interactions in vivo in EAE animals and ex vivo in organotypic hippocampal slice cultures.

180 -13 treatment on ACE2 and TMPRSS2 expression ex vivo in primary airway epithelial cells from particip

181 tumor types could be visualized both in- and ex vivo in thirty subjects.

182 Utilizing an ex vivo infection model, we sought to understand the vir

183 Blood cell populations and ex vivo innate whole blood cytokine responses were measu

184 study, we comprehensively classify human HCs ex vivo, interrogate phenotypic plasticity, and characte

185 in, PCI34051) HDAC inhibitors were evaluated ex vivo (IPAH-PAAF, IPAH-PASMC) and in vivo (rat chronic

186 h automated scanning and imaging software on ex-vivo irradiated human lymphocytes to: a) reconstruct

187 We compared continuous normothermic ex vivo kidney perfusion (NEVKP) with hypothermic anoxic

188 t a novel NMR-based method that measures the ex-vivo kinetics of sCD73 activity with high specificity

189 uction and stability in contraction arrested ex vivo Langendorff heart preparations before and during

190 to ischemia and excitotoxicity in vitro and ex vivo Last, deletion of Bbeta2 rescued excessive strok

191 Ex vivo leukocyte responses to unrelated stimuli and pat

192 VAT ex-vivo lipolysis was increased (p < 0.05) in P-HFHS com

193 In combination with existing methods, the ex vivo lung MGIA may represent an important tool for an

194 urprisingly, they did not correlate with the ex vivo MAIT hyperinflammatory cytokine profile observed

195 Ex vivo, mast cell-mediated histamine release and degran

196 Ex vivo measurements of such multicellular tractions wit

197 Ex vivo measurements revealed a partial correlation betw

198 he cholangiocyte monolayer was comparable to ex vivo measurements, and that cholangiocytes in the dev

199 We also describe novel ex vivo methods based on human cells and tissues, such a

200 he authors use a combination of in vitro and ex vivo methods to show that treatment regimens, includi

201 Ex vivo microCT analysis showed increased radial bone ex

202 ally validate these findings, we utilized an ex vivo model of angiogenesis.

203 We therefore developed a novel ex vivo model using discs of porcine and human cornea an

204 In this ex vivo modeling system, clinically used valve-sparing a

205 t strains of B. miyamotoi using in vitro and ex vivo models and compared this to the response elicite

206 Ex vivo models such as mouse patient-derived xenografts

207 ss the use of various in vitro, in vivo, and ex vivo models to elucidate the contributions of host fa

208 ll death and demyelination both in vitro and ex vivo models.

209 Here we report changes in AFL of ex vivo mouse knee joints, porcine metacarpophalangeal j

210 high-throughput, and large-volume imaging of ex vivo mouse organs.

211 al tails by adapting protocols developed for ex vivo muscle mechanics.

212 We present an optimised ex vivo mycobacterial growth inhibition assay (MGIA) to

213 Using both in vitro and ex vivo neuronal tracing methods, we identified two new

214 The role of ex vivo normothermic perfusion (EVNP) in both organ viab

215 e drugs through the layers and structures of ex vivo nude mouse ear skin and extracted pharmacokineti

216 This effect was observed ex vivo on isolated aortas, but also in vivo on femoral

217 and compare in vivo radiologic imaging with ex vivo optical imaging techniques for assessing hypoxia

218 hanges in heart rate, as measured by ECG and ex vivo optical mapping.

219 n shortening of action potentials in VMs and ex vivo optically mapped Sham hearts.

220 cargoes in beta-cells over other islet cells ex vivo or other cell-types in an organismal context wil

221 Moreover, both in vitro and ex vivo outcomes showed an improved antioxidant profile.

222 Ex vivo patch clamp electrophysiology and immunohistoche

223 Using ex-vivo patch-clamp recordings from up to 55 SCs per mou

224 Our results suggest that in the healthy ex vivo perfused heart, HBP flux does not respond to acu

225 muCT measurements of the ex vivo peri-implant bony structure after 12 weeks follo

226 cant reduction of collagen degradation in an ex vivo pig-skin model.

227 We present the results of an ex vivo pilot study involving 10 cases of biopsy-proven

228 s in a preclinical animal model to design an ex vivo platform that recreates genetic susceptibility t

229 Ex vivo platforms that enable identification of key comp

230 the cumulative insulin transport across the ex vivo porcine buccal tissue (~26% of loaded insulin) w

231 Five ex vivo porcine carotid artery models (n = 6 each) were

232 We measure both as a function of IOP in ex vivo porcine cornea, obtaining values consistent with

233 We also show, by using ex vivo porcine ureter segments and sedated pigs that, w

234 cancerous and non-cancerous tissue was found ex vivo, potentially due to the lower nonlinearity in th

235 In ex vivo preparations from mice of both sexes, we measure

236 ic machine perfusion (NMP) enables optimized ex-vivo preservation of a donor liver in a normal physio

237 Using ex vivo pressure myography, we found that loss of this c

238 utotransplantation (n = 8) and multivisceral ex vivo procedure (n = 7).

239 Ex vivo production of proinflammatory cytokines was high

240 st all 3 proteins with comparable magnitude, ex vivo proliferation, and portions of responding patien

241 ical characteristics of acutely synaptotoxic ex vivo PrPSc derived from the brains of mice dying from

242 ctivated latently HIV-1-infected cells in an ex vivo quantitative viral outgrowth assay.

243 Ex vivo recordings were performed in NAcS D(1) receptor-

244 as ex vivo hepatectomy (n = 18), followed by ex vivo resection and intestinal autotransplantation (n

245 asure the ECS volume fraction (alpha) in the ex vivo retina of male and female mice.

246 Ex vivo retrovirally mediated gene therapy has been show

247 A closer scrutiny in vivo and ex vivo revealed that the 3V wall is not static and is a

248 Direct measurements of intracellular cAMP ex vivo show that Opn5 POA neurons increase cAMP when st

249 automated sample preparation to characterize ex vivo signaling network responses (n = 1764) measured

250 arteries from SMC-specific Gprc5b-KOs showed ex vivo significantly enhanced prostacyclin receptor (IP

251 luation included cross-sectional imaging and ex vivo simulation using printed or virtual 3-dimensiona

252 Ex vivo, single action potentials evoked alkalinizing pH

253 Using ex vivo skin explants from cutaneous MF tumors as well a

254 lonRI expression and addressed this in human ex vivo skin, in vitro Langerhans cells, and IDEC models

255 In addition, ex vivo slice electrophysiology of transgenic Cre-induci

256 ations in vHIP-NAc activity in vivo and used ex vivo slice electrophysiology to identify the mechanis

257 glia behaviors with two-photon microscopy in ex vivo spinal cord slices from CX3CR1-GFP mice compleme

258 ressed higher levels of Pdcd1 mRNA following ex vivo stimulation as well as increased surface levels

259 Here, we used ex vivo stimulation of memory T cells and screening of n

260 Cytokine production capacity after ex vivo stimulation of peripheral blood mononuclear cell

261 Ex vivo stimulation studies using murine peritoneal macr

262 Furthermore, ex vivo stimulation with interferon-gamma induced endoge

263 Following ex vivo stimulation with phorbol myristate acetate/ionom

264 accumbens and medial prefrontal cortex, and ex vivo striatal dopamine reuptake.

265 rks of structural covariance, as measured by ex vivo structural magnetic resonance imaging (MRI).

266 Ex vivo studies revealed that PKC activation acutely dec

267 herapeutic RNA targets, large-animal models, ex vivo studies with human cells/tissues, and new delive

268 The purpose of this ex vivo study is to verify if the material is calculus a

269 in vitro infection of tonsillar Tfh with the ex vivo study of circulating Tfh from HIV-2-infected pat

270 nts with conventionally unresectable tumors, ex vivo surgery can offer effective surgical removal wit

271 Ex vivo surgery may provide a chance at R0 resection for

272 Ex vivo, terlipressin relaxed pulmonary and constricted

273 of treatment-naive lung tumors, coupled with ex vivo testing of PDOs, identifies continuous AXL, TGFb

274 Further, ex vivo testing with human blood and plasma revealed no

275 tive animals; two of these were validated by ex vivo tetramer staining.

276 Flow cytometry and qPCR further analyzed ex vivo the glomerular leukocyte infiltrate during NTN.

277 from acute ischemia/reperfusion (I/R) injury ex vivo, the role of dysferlin in mediating the recovery

278 the response of orthotopically transplanted ex vivo therapy-induced senescent cells to immune checkp

279 ose) polymerase inhibitors both in vitro and ex vivo These findings might pave a way for new syntheti

280 anical tests can quantify corneal elasticity ex vivo, they cannot be used clinically.

281 The in silico analysis was validated ex vivo, through T cell proliferation experiments, provi

282 After the last time point, the ex vivo tissue distribution was measured to corroborate

283 scale (AFM), bulk solution phase (FRAP), and ex vivo tissue experiments.

284 er nonlinearity in the elastic properties of ex vivo tissue.

285 draw parallels between the transcriptomes of ex vivo tissues and in vitro fetal organoids, revealing

286 The discussion focuses primarily on ex vivo tissues, though many considerations are relevant

287 the Foxp3 locus can be epigenetically edited ex vivo to generate stable therapeutic iTregs.

288 Tissues were collected to evaluate ex vivo tracer biodistribution and to perform flow cytom

289 olecular markers in response to sulforaphane ex vivo treatment in PBMCs from healthy donors by real-t

290 We further show that in vivo and ex vivo treatment with S increases activity and expressi

291 e a combination of in situ hybridization and ex vivo two-photon Ca(2+) imaging of the mouse spinal co

292 Antigen stimulation of T cells in ex vivo vaginal tissue cultures triggered antiviral resp

293 Using wire myography, ex vivo vasoreactivity studies were conducted in uterine

294 n vivo imaging system (IVIS), and quantified ex vivo via electron paramagnetic resonance (EPR) spectr

295 zed and particle distribution was quantified ex vivo via EPR spectroscopy.

296 ctivity, (3) autonomous PV GPe neuron firing ex vivo was upregulated, presumably through homeostatic

297 and intestinal autotransplantation (n = 12), ex vivo Whipple procedure and liver autotransplantation

298 Ex vivo whole blood stimulations were performed with mat

299 ell activation by both species, we performed ex vivo whole-blood infection assays and confrontation a

300 ells from pediatric B-ALL patients, cultured ex vivo, with Plk1-targeting siRNNs results in cleavage