ライフサイエンスコーパス: homogenate

1 performed within several minutes from sample homogenate.

2 tivity to detect a new TBPV in a single tick homogenate.

3 se activity was measured as Pi from cellular homogenate.

4 human plasma but liberated 14 in swine brain homogenate.

5 exposure to Creutzfeldt-Jakob disease brain homogenate.

6 ined to be 4.89 +/- 0.19 nmol min(-1) mL(-1) homogenate.

7 HF samples from endocardial left ventricular homogenate.

8 eed supernatant and pellet of frontal cortex homogenate.

9 nd tested for their affinity toward AD brain homogenate.

10 respectively, using [(3)H]5 on rat striatum homogenate.

11 n vivo in both the effusion fluid and bullar homogenate.

12 atory coronavirus (PRCV) in turbinate tissue homogenate.

13 ified via fluorometric assay of whole vessel homogenate.

14 NA copy number (40%) were detected in muscle homogenate.

15 mass in lung homogenate compared to pancreas homogenate.

16 o inhaled prion-infected or uninfected brain homogenate.

17 l inoculation with Alzheimer's disease brain homogenate.

18 act that the signals are derived from tissue homogenates.

19 mixed into a range of scrapie-positive brain homogenates.

20 ilar to what we observed with chicken-retina homogenates.

21 atively resistant to metabolism by rat liver homogenates.

22 the MDM2 in the cancerous mouse brain tissue homogenates.

23 correlated well with LC-MS/MS in whole brain homogenates.

24 present in in vitro digestions of rat brain homogenates.

25 sess primary lung cell migration toward lung homogenates.

26 ed enzyme, membrane preparations, and tissue homogenates.

27 aling proteins relative to undamaged retinal homogenates.

28 nt in mouse and rat retina, brain, and liver homogenates.

29 (18)F-l-FEHTP were detected in the xenograft homogenates.

30 sed risk of senescence, and the use of liver homogenates.

31 cubations with wild-type heart mitochondrial homogenates.

32 ty to disaggregate PrP(Sc) in infected brain homogenates.

33 on and fission were measured in brain tissue homogenates.

34 mpus/entorhinal cortex of non-AD human brain homogenates.

35 ly to amyloid plaque-rich, NFT-poor AD brain homogenates.

36 measurement of drug concentration in tissue homogenates.

37 hosphopeptides from fractionated whole-heart homogenates.

38 nols was observed in raw broccoli and carrot homogenates.

39 was found in mouse and rat retina and brain homogenates.

40 even for mixed solution and in brain tissue homogenates.

41 uorescence staining of cell and mouse tissue homogenates.

42 Employing AD homogenates, [(18)F]-9, a PET tracer demonstrates superi

43 0.4-fold; p = 0.01) mRNA in cervical spinal homogenates, (2) elicited a sustained increase in IL-1be

44 mouse urine, blood serum, kidney, and liver homogenates 30 min after injection.

45 lated differences were found in hypothalamic homogenates, a focus on specific brain structures using

46 g) gel electrophoresis of Wistar rat retinal homogenates after 10 hours of 10,000 lux (4200 degrees K

47 ted virus (MARV/Ang-MA) recovered from liver homogenates after 24 serial passages in severe combined

48 In membrane homogenates, AMC20: demonstrated picomolar affinity at D

49 exposed statically to intact fillet and fish homogenate and dynamically by rolling with cut fillet cu

50 ondrial, and nuclear proteins from rat liver homogenate and resolved by two-dimensional electrophores

51 ssed immunohistochemically to identify brain homogenate and the disease-associated isoform of the pri

52 has been investigated in vivo, on olive leaf homogenate and, in vitro with pure oleuropein and other

53 FZD expression was analyzed in lung homogenates and alveolar epithelial type II (ATII) cells

54 TNF-alpha, IL-1beta, and chemokines in lung homogenates and bronchoalveolar lavage fluid; however, P

55 ventional lipid extraction of excised tissue homogenates and by mapping the spatial distribution and

56 y genes differ in expression in whole tissue homogenates and cell cultures, with female Cyp expressio

57 lmonary Th1-type cytokine production in lung homogenates and classical macrophage activation as evide

58 hemicals in male Sprague-Dawley rat liver S9 homogenates and compared the rates to those measured by

59 ble protein complexes from hippocampal brain homogenates and cultured hippocampal neurons from Spragu

60 n liver tissue, calibration by spiked tissue homogenates and droplet deposition was found to provide

61 2, and GSK-3 signaling pathways in placental homogenates and expression of glucose transporter 1 (GLU

62 sease (CWD)-infected white-tailed deer brain homogenates and found that lipid extraction enabled RT-Q

63 hibition of active caspase-3 and -8 in liver homogenates and in a cell-free system in vitro.

64 on levels of AMPAR subunits (GluA1/2/3/4) in homogenates and in postsynaptic density fractions from s

65 cient lung B-cell migration toward COPD lung homogenates and induced lung B cells to up-regulate lymp

66 d and tested in the vitreous humor, RPE cell homogenates and intact RPE cells.

67 elated with lipophilicity, directly in brain homogenates and inversely in the oils, in agreement with

68 rmined in bronchoalveolar lavage fluid, lung homogenates and lung mononuclear cells ex vivo.

69 ed the infectivity of prion-containing brain homogenates and of prion-infected cerebellar organotypic

70 in synaptic compartment (P3) in dorsal horn homogenates and presynaptic met-enkephalin-containing bo

71 TFV-DP concentrations in tissue homogenates and rectal lymphocytes were highly correlate

72 In contrast, proteinase K-treated AD homogenates and Sarkosyl-soluble AD fractions were unabl

73 er molecular weight oligomers-in total brain homogenates and synaptoneurosomal preparations failed to

74 sarcosine(1), isoleucine(8) Ang II) in brain homogenates and tissue sections prepared from rats given

75 At E18.5, dams were killed and placental homogenates and trophoblast plasma membrane (TPM) vesicl

76 tabolites, were compared in nerve terminals, homogenate, and cortex of anesthetized rats with and wit

77 odified posttranslationally in the cell-free homogenate, and directly attached to the glass surface w

78 f subsequent AMPAR potentiators in rat brain homogenate, and PF-04701475 (8a), a prototype used to ex

79 ctivities were determined in gingival tissue homogenates, and ABL was evaluated with histometric meas

80 lcium activated 3 (CLCA3) expression in lung homogenates, and ELISA of Muc5ac in BAL fluid.

81 olecular weight, insoluble material in brain homogenates, and neuronal inclusions throughout the CNS

82 ture with recombinant human (rh)-SLPI, liver homogenates, and plasma derived from AALF patients in th

83 se levels were determined in gingival tissue homogenates, and receptor activator of nuclear factor-ka

84 in mast cells compared with uncinate tissue homogenates, and responses were significantly inhibited

85 parent compound was confirmed in rat kidney homogenates, and the prodrug was shown to be an active v

86 (PMCA) uses PrP(Sc) in prion-infected brain homogenates as an initiating seed to convert PrP(C) and

87 a wide range of half-lives in rat intestinal homogenate at pH 6.5 (<30-1732 min) with differences of

88 gent was diluted into scrapie-infected brain homogenates at 1% (vol/vol).

89 rmed with single cell samples because tissue homogenates average the biochemical composition of many

90 paration of standard curves of spiked tissue homogenates, based on the drilling of holes in a block o

91 ion constant]) was determined using in vitro homogenate binding assays in human, monkey, and rat cere

92 V-1451, by fluorescence, autoradiography and homogenate binding assays with homologous and heterologo

93 lipid, PC, and disaturated PC in lung tissue homogenate, bronchoalveolar lavage fluid, and lung LB wa

94 tivity is similarly detectable in blastocyst homogenates but not those of two-cell or morula stage em

95 heral blood mononuclear cells and lymph node homogenates, but only the wild-type virus was found in t

96 Purification of tumor homogenates by affinity chromatography on these peptides

97 ophage populations were isolated from kidney homogenates by fluorescence-activated cell sorting for w

98 nd an analysis of their metabolism in tissue homogenates by gel electrophoresis.

99 e inhibitor was purified from salivary gland homogenates by reverse-phase HPLC and identified by mass

100 ulk oils, using the Rancimat test, and brain homogenates, by measuring malondialdehyde (MDA) levels a

101 cement investigations were extended to apple homogenate characterized by high chemical diversity.

102 resulting in a higher molecular mass in lung homogenate compared to pancreas homogenate.

103 uman serum, insect hemolymph and mouse brain homogenates, confirming this technique as a powerful pro

104 Fifth, tracheal homogenates contained NAADP-binding sites of high affini

105 Inoculation of brain homogenates containing Abeta aggregates into susceptible

106 with high affinity to human AD brain cortex homogenates containing abundant NFTs but bound poorly to

107 y, intraperitoneal inoculation of pancreatic homogenates containing IAPP aggregates into transgenic m

108 The SR fraction of heart homogenate contains mitochondria with extensive SR assoc

109 m the same animals and unseeded normal brain homogenate controls (n = 116 of 117) remained negative.

110 Third, tracheal homogenates could synthesize NAADP by base exchange from

111 Examination of liver homogenates demonstrated efficient FXN LNP uptake in hep

112 (Tg) mice, intracerebral injections of brain homogenates derived from older Tg mice exhibiting alpha-

113 nt-insoluble Abeta1-40 or Abeta1-42 in brain homogenates did not reveal significant between-group dif

114 ranasal inoculation with mock-infected brain homogenate, different strains of prion-infected brain ho

115 enesis, we inoculated infected chicken liver homogenate directly into the intestine of cats by use of

116 Rabbit brain homogenate, either unseeded or seeded in vitro with dise

117 Coral homogenates exhibited some of the highest cAMP productio

118 highly populated PLB state in cardiac tissue homogenates), followed by 2P-PLB, then P17-PLB.

119 and metastasis, were down-regulated in cell homogenates following cystatin C uptake.

120 Muc1 tyrosine phosphorylation in mouse lung homogenates following P. aeruginosa infection.

121 of 3.16 and 57.7 CFU/ml of lymph node tissue homogenate for IMS-PCR and IMS-culture, respectively).

122 ein forms prions, we examined 14 human brain homogenates for transmission to cultured human embryonic

123 full-length ratio of gammaENaC compared with homogenate from patients on no medication (n=5).

124 By immunoblotting, kidney cortex homogenate from patients treated with angiotensin II typ

125 We incubated prion positive 10% brain homogenate from terminally sick mice infected with the R

126 ponding to the analysis of a 2 ng aliquot of homogenate from the 6 ng cell lysate.

127 Here, we demonstrate that total homogenates from AD brain induce soluble U1-70K from con

128 23:Gfap-luc) mice were inoculated with brain homogenates from aged Tg(APP23) mice, BLI detected the a

129 ion of SOD1 in human post-mortem spinal cord homogenates from ALS and non-ALS subjects.

130 Tissue homogenates from antibiotic-treated mice induced IgG rea

131 and galanin was increased in serum and liver homogenates from BDL rats.

132 By contrast, homogenates from brains of APPSwePSEN1dE9 mice failed to

133 ucted with (3)H-MK-6240 in tissue slices and homogenates from cognitively normal and AD human brain d

134 OE4 compared with APOE2/APOE3 in hippocampal homogenates from EFAD transgenic mice (expressing five f

135 Crude muscle homogenates from exposed larvae did not display any appa

136 vels, and related metabolite levels in brain homogenates from five neurodevelopmental mouse models of

137 n and nitrogen stable isotopes), in egg pool homogenates from five selected colony sites across the G

138 ormed after intracerebral injection of brain homogenates from human tauopathies into nontransgenic mi

139 urements of NFATc3 and c4 in the hippocampal homogenates from injured and sham rats sacrificed at the

140 In whole-brain and spinal cord homogenates from mice expressing Galphao RGSi subunits,

141 Protein arrays of liver homogenates from patients with acetaminophen-induced acu

142 ition by protease inhibitors in whole sputum homogenates from patients with CF before and after treat

143 th-1 mRNA expression was increased in tissue homogenates from patients with CRSwNP compared with cont

144 , and etanercept were incubated with mucosal homogenates from patients with IBD or activated recombin

145 We previously reported that brain homogenates from prion-infected mice induced cytokine pr

146 rmed using 6xHis-rMERTK(571-999) and protein homogenates from rat RPE/choroid.

147 nstrate that CWD prions can amplify in brain homogenates from several species sympatric with cervids,

148 Mouse heart homogenates from sham-procedure mice contained high mRNA

149 whereas the same mice inoculated with brain homogenates from spontaneously ill TgM83(+/+) mice devel

150 s in susceptible transgenic mice using brain homogenates from sporadic or heritable (Arctic and Swedi

151 1B are found in insoluble forms within brain homogenates from such patients.

152 ificantly reduced in isolated HPCs and liver homogenates from TF(flox/flox)/albumin-Cre mice (HPC(Del

153 Egg pool homogenates from the Channel-Shelter (C-S) Island (Lake

154 we first quantified PAK by immunoblotting in homogenates from the parietal neocortex of subjects with

155 In hippocampal homogenates from THY-Tau22 mice and cortex homogenates o

156 Furthermore, incubation of mitochondrial homogenates from transgenic myocardium expressing iPLA(2

157 we inoculated the TgM83(+/-) mice with brain homogenates from two pathologically confirmed MSA cases.

158 ortional to the amount of PP1cdelta in total homogenates from wild-type or MYPT1-deficient tissues.

159 roxidation (assay B) were evaluated in liver homogenates from Wistar rats by the thiobarbituric acid

160 ng the GST-MYPT1 fragment as a ligand and SM homogenates from WT and telokin KO mice as a source of e

161 In lung homogenates harvested 14 days following infection, there

162 s in Mecp2 knock-out mice using brain tissue homogenates have revealed only subtle changes in gene ex

163 Islet homogenates immunodepleted with anti-IAPP-specific antib

164 PI3K activity was measured in retinal homogenates immunoprecipitated with an anti-PY antibody.

165 indiscriminate rapid bulk transport of brain homogenate in the nasal cavity results in immediate entr

166 fragment in the insoluble fraction of tissue homogenate in the severe AD group versus the control gro

167 h leverages high-throughput data from tissue homogenates in a novel iterative statistical framework.

168 We serially passaged their brain homogenates in mice and cultured cells.

169 reased in nasal secretion and mucosal tissue homogenates in patients with chronic rhinosinusitis, and

170 entrations of inflammatory mediators in lung homogenates increased early in infection in contrast wit

171 utoimmune encephalomyelitis induced with CNS homogenate, indicating that the DCs are able to modulate

172 ally to ME7-inoculated mice and normal brain homogenate-injected (NBH) controls.

173 o- to three-fold reduction in renal cortical homogenate insulin receptor-beta among knockout mice com

174 (RAVV) from infected scid BALB/c mouse liver homogenates into immunocompetent BALB/c mice results in

175 ation was induced by clarified scrapie brain homogenates lacking PrPres.

176 e absence of any alterations in total tissue homogenate levels of these proteins.

177 approaches based on analysis of whole-tumor homogenates may be inaccurate.

178 stimated variations in sialylation in tissue homogenates might be simply the result of a changed cell

179 of prion-infected brain homogenate, or brain homogenate mixed with India ink.

180 Neither endogenous Hsp90 present in the homogenate nor unmodified and fully active recombinant H

181 1 protein, which is contrary to heart tissue homogenate not detectable in frozen tissue sections of m

182 isolated cardiomyocytes, whereas in cardiac homogenates, NTG inhibited xanthine oxidoreductase activ

183 l homogenates from THY-Tau22 mice and cortex homogenates obtained from Alzheimer patients, ADx215 con

184 prostatitis in Balb/C mice was induced by a homogenate of reproductive tissues of male rats.

185 rast to in vitro aggregated synthetic Abeta, homogenates of Abeta deposits containing HSCs induced ce

186 Examination of homogenates of atherosclerotic plaque-laden aorta showed

187 Finally, homogenates of cells coexpressing DES1 and MFAT catalyze

188 Crude homogenates of chicken retinas rapidly convert all-trans

189 and p-ERK1/2 activity in the renal cortical homogenates of cKO-PT-Mfn2 mice.

190 "dilution problem" associated with assaying homogenates of complex tissues.

191 Here, we present a novel methodology using homogenates of cultured cells for rapid estimation of fu

192 Profiles of cytokines detected in lung homogenates of DeltaT-vaccinated mice were indicative of

193 example, whole-body imaging, a set of tissue homogenates of different tissue types (lung, liver, kidn

194 In total lung homogenates of Epac1(-/-) mice, MUC5AC and matrix remode

195 Homogenates of esophageal biopsy specimens from 11 subje

196 Homogenates of esophageal tissues from patients with eos

197 Brain homogenates of ill Tg(BVPrP) mice transmitted disease to

198 antiinflammatory cytokines, respectively, in homogenates of lung from LP-treated mice were suggestive

199 ured by real-time quantitative PCR on tissue homogenates of patients with CRSwNP (n = 21) and healthy

200 EET levels were measured in tissue homogenates of rat liver, kidney, and aorta, using an en

201 r necrosis factor-alpha and interleukin-6 in homogenates of rectal tissue were measured by ELISA.

202 citrate and calcium sulphate to 100g of raw homogenates of spinach to determine whether calcium woul

203 0.047) were significantly reduced in muscle homogenates of T2D.

204 and the (15)epsilon for NADH eukNR from cell homogenates of the marine diatom Thalassiosira weissflog

205 erial colonization was determined by plating homogenates onto MacConkey agar, and immunofluorescence

206 for quantitation of protein carbonylation in homogenates or purified proteins.

207 e, different strains of prion-infected brain homogenate, or brain homogenate mixed with India ink.

208 fully detected in spiked adult Aedes aegypti homogenate over a broad dynamic range with high sensitiv

209 3-19338E homogenate, P3, and P9; ISU13-22038 homogenate, P3, and P9) were determined.

210 enome sequences of six viruses (ISU13-19338E homogenate, P3, and P9; ISU13-22038 homogenate, P3, and

211 Culture of healthy monocytes with AALF liver homogenates, plasma, or rhSLPI induced monocytes with st

212 Photolysis of sea urchin egg homogenates preincubated with [(32)P-5N(3)]NAADP resulte

213 paring the effect of alcohol in SN and total homogenate preparations from the same samples.

214 Neither the tissue culture medium nor a homogenate prepared from VZV-infected neurons produced a

215 receptor subtypes were measured in membrane homogenates prepared from HEK293 cells expressing human

216 However, homogenates prepared from whole SIRT5(-/-) liver did sho

217 utologous pulsing with tg(sm/p22phox) aortic homogenates promoted DCs of tg(sm/p22phox) mice to stimu

218 le to small molecule antioxidants and tissue homogenates, proved to be efficient for thiol-type antio

219 drilling of holes in a block of frozen liver homogenate, providing easy cryo-slicing and good quantit

220 ulation with both donor and recipient spleen homogenates, providing initial evidence of similar trans

221 d PFASs were found in both liver and carcass homogenate ranging from approximately 50% in 3M foam up

222 rge amounts of infected and uninfected brain homogenate rapidly cross the nasal mucosa and enter the

223 Tiron added to muscle homogenates reduced ROS production in vitro.

224 ivity, and we measure this in a bovine liver homogenate reference sample for 20 drugs representing im

225 hold true for drug doped in the bovine liver homogenate reference sample, except for fluticasone, nic

226 activity in mitochondrially-enriched tissue homogenates, requiring at least 50 mg skeletal muscle, a

227 ine (PBS) and 1.3pg/ml in mouse brain tissue homogenate, respectively.

228 revealed that exposure of HK cells to brain homogenate resulted in increased numbers of detectable l

229 ain-2, but not calpain-1, treatment of brain homogenates resulted in PTEN degradation.

230 spiked with Creutzfeldt-Jakob disease brain homogenate, resulting in a coarse granular perinuclear P

231 Inhalation of infected brain homogenate results in transepithelial transport of prion

232 PAGE examination of irradiated tadpole brain homogenate revealed labeled protein, identified by mass

233 Radioligand binding to brain homogenates revealed multiple binding components with di

234 Finally, evaluation of brain homogenates revealed that HFD-shaped microbiota increase

235 as identified for the first time in biota in homogenate samples of fish by liquid chromatography-quad

236 Liver and carcass homogenate samples were analyzed for 20 PFASs using LC-M

237 Western blotting of rodent retina and brain homogenates showed a single 123-kDa band.

238 At the end point, retinal homogenates showed a substantial overexpression of BDNF

239 of patients' fibroblasts and skeletal muscle homogenates showed decreased levels of mutant LRPPRC pro

240 Whole brain homogenates showed normal levels of DISC1 protein, but d

241 In vivo analysis of gene expression in lung homogenates shows that PrrF-mediated regulation of genes

242 Compared to cortical homogenates, small molecular weight oligomeric species w

243 surrogate tissue sections from blank tissue homogenate spiked with compounds.

244 c tissue model consisting of a set of tissue homogenates spiked with a range of different drug concen

245 he presence of (40k)PEG in plasma and tissue homogenates suggests the degradation of PEGylated protei

246 In nonexposed crude muscle homogenates, TCS decreased the binding of [(3)H]PN20-110

247 dissociation was observed in skeletal muscle homogenates that contained 0.43 microM myoplasmic FKBP12

248 ghly stable heterodimer in human spinal cord homogenates that was resistant to dissociation by boilin

249 d ribosomes can be captured from mouse brain homogenates, thereby enriching directly for the mRNAs ex

250 ase treatment abolished the ability of brain homogenate to reconstitute the propagation of both mouse

251 In vitro exposure of untreated liver homogenates to apocynin led to a dose-dependent inhibiti

252 rophobic substances in largely aqueous liver homogenates, to determine biotransformation rates at low

253 H2S production from mouse liver homogenate under aerobic conditions in the presence of c

254 d spatial parameters of prion-infected brain homogenate uptake following inhalation and to test the h

255 ROS concentration was measured in lung homogenates using OxiSelect ROS assay kit.

256 eptide degradation in blood plasma and liver homogenates versus an unstapled counterpart.

257 ing affords, the number of brains in a fixed homogenate volume can be increased to concentrate the sa

258 The matrix effect from mouse brain tissue homogenate was also studied and the immunosensor showed

259 tissue, while the unbound fraction in brain homogenate was around 1.5%.

260 Each portion of brain homogenate was divided into two parts, one for determina

261 Infected or uninfected brain homogenate was identified adhering to M cells, passing b

262 se and polygalcturonase activities in tomato homogenate was investigated by subjecting identically tr

263 ding to human embryonic kidney cell (HEK293) homogenate was measured in a small-scale dialysis appara

264 To test this hypothesis, CWD-positive brain homogenate was mixed with montmorillonite clay (Mte), ly

265 A small drop of infected or uninfected brain homogenate was placed below each nostril, where it was i

266 Liver homogenate was used to generate a viable and molecularly

267 e seeding activity of Abeta-containing brain homogenates was considerably reduced by alpha-syn, and A

268 Cytokine production in eye tissue homogenates was measured by ELISA.

269 histochemistry and the amount of TF in tumor homogenates was measured by enzyme-linked immunosorbent

270 ysis of the harvested tumor and organ/tissue homogenates was performed to determine doxorubicin conce

271 f phosphorylated MYPT1 in telokin-null ileum homogenates was restored to nonphosphorylated MYPT1 leve

272 wly synthesized compounds using brain tissue homogenate, we selected the most active inhibitor and sh

273 ext-generation sequencing of infected tissue homogenates, we assembled a contiguous 174-kb genome seq

274 Using human hippocampal homogenates, we found that ADAM10 removal from the plasm

275 sessment of angiotensin metabolism in kidney homogenates, we identified neprilysin (NEP) to be a majo

276 of prions, larger amounts of infected brain homogenate were transported paracellularly across the re

277 The tissue homogenates were also used in a characterization of vari

278 Tissue homogenates were analyzed for complement activation prod

279 For all samples, fruit homogenates were analyzed in ATR-FTIR using the same met

280 Likewise, A2AP levels in plasma and lung homogenates were elevated in mice infected with B. pseud

281 All the supernatants of the homogenates were monitored for pH.

282 Gray matter homogenates were prepared from auditory cortex gray matt

283 Retinal homogenates were tested for prion seeding activity.

284 Myocardial homogenates were used for assessment of PKG activity, cG

285 ssociated forms from mouse and hamster brain homogenates were used to seed RT-QuIC-induced fibrilliza

286 sialylation were observed when whole kidney homogenates were used.

287 ar to that induced by scrapie-infected brain homogenates, whereas purified full-length CyPA was a poo

288 ases 3, 8, 9, and 12 increased in TAA tissue homogenates, whereas tissue inhibitors of metalloprotein

289 entified from 50 ng of Xenopus laevis zygote homogenate, which is comparable with an offline sample p

290 We isolate nuclei at 4 degrees C from tissue homogenates, which cause minimal damage.

291 proteomic analysis of light-damaged retinal homogenates, which induced Muller glia proliferation whe

292 lasmic and synaptic fractions of spinal cord homogenates, which was attenuated by PKC inhibitor chele

293 reactivity for met-enkephalin in dorsal horn homogenates, which was dose-dependently attenuated by se

294 e show that treatment of infected oat tissue homogenate with sodium sulfite reduces transmission of t

295 In brain homogenates with Abetao, the interaction of PrP(C) and m

296 in vitro after seeding rabbit and dog brain homogenates with classical BSE were studied.

297 Treatment of brain homogenates with purified calpain-1 and calpain-2 trunca

298 te with detergent-insoluble Tau levels as AD homogenates with reduced levels of these components were

299 sTMT labeling method, we treated whole-heart homogenates with the S-nitrosylating agent S-nitrosoglut

300 eleasing 5-PP-InsP5 in mammalian cell/tissue homogenates within a few minutes and can be used to rele