ライフサイエンスコーパス: homogenate

1 human plasma but liberated 14 in swine brain homogenate.

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

3 mass in lung homogenate compared to pancreas homogenate.

4 th human lens-epithelial cell lysate or lens homogenate.

5 o inhaled prion-infected or uninfected brain homogenate.

6 l inoculation with Alzheimer's disease brain homogenate.

7 performed within several minutes from sample homogenate.

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

9 data to those obtained from bulk hippocampal homogenate.

10 se activity was measured as Pi from cellular homogenate.

11 exposure to Creutzfeldt-Jakob disease brain homogenate.

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

13 had decreased trypsin-like activity in total homogenate.

14 asured in nasal washes and middle ear tissue homogenate.

15 similar in control and IUGR skeletal muscle homogenate.

16 act that the signals are derived from tissue homogenates.

17 measurement of drug concentration in tissue homogenates.

18 even for mixed solution and in brain tissue homogenates.

19 to detect the other individual ABX in brain homogenates.

20 on and fission were measured in brain tissue homogenates.

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

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

23 hosphopeptides from fractionated whole-heart homogenates.

24 nols was observed in raw broccoli and carrot homogenates.

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

26 uorescence staining of cell and mouse tissue homogenates.

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

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

29 s in bronchoalveolar lavages and lung tissue homogenates.

30 atively resistant to metabolism by rat liver homogenates.

31 the MDM2 in the cancerous mouse brain tissue homogenates.

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

33 present in in vitro digestions of rat brain homogenates.

34 sess primary lung cell migration toward lung homogenates.

35 AMPKalpha, p70 S6 kinase and rpS6 in muscle homogenates.

36 ble label free quantitation of 1 mug protein homogenates.

37 ession in human and mouse LFs and mouse lung homogenates.

38 otein samples from 3xTg-AD mouse model brain homogenates.

39 NOx have differential stability in placental homogenates.

40 the stability of exogenous NOx in placental homogenates.

41 hanol exposure in both N2A cells and rat PFC homogenates.

42 d chronic wasting disease prions in deer-ear homogenates.

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

44 0.4-fold; p = 0.01) mRNA in cervical spinal homogenates, (2) elicited a sustained increase in IL-1be

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

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

47 mal human PrP with amplified urine and brain homogenate achieving the same 100% attack rate, similar

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

49 The normalized spectra of grape homogenates allowed a calibration and validation determi

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

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

52 We performed RNA-sequencing on total homogenate and glial cell populations isolated from mous

53 sampling strategies like LCM and complement homogenate and single-nucleus approaches in human brain.

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

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

56 Analysis of lung homogenates and bronchoalveolar lavage (BAL) fluid showe

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

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

59 )-inflammasome system in atrial whole-tissue homogenates and cardiomyocytes.

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

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

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

63 2, and GSK-3 signaling pathways in placental homogenates and expression of glucose transporter 1 (GLU

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

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

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

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

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

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

70 eactions also in complex biological cellular homogenates and mixture.

71 Normalized spectra of grape homogenates and normalized plus 1st Derivative spectra o

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

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

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

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

76 rared (MIR) spectra of wines and grape berry homogenates and tested MIR's ability to model sensory pr

77 ificantly reduced TH concentration in tissue homogenates and the percent TH-immunoreactive area in th

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

79 Protein expression of FABP1, 3, 4 and 5 (homogenate) and FATP2, 4, and 6 (MVM, BM) was determined

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

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

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

83 soforms was confirmed ex vivo in mouse brain homogenates, and additional in vivo studies in mice show

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

85 (ADLumin-1 and CRANAD-3) in solutions, brain homogenates, and in vivo whole brain imaging.

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

87 ter NAP treatment of intact cells, rat brain homogenates, and purified protein fragments.

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

89 nical studies such as cultured cells, tissue homogenates, and serum.

90 asured in cell lysates, blood samples, liver homogenates, and subcellular fractions by spectroscopy.

91 tides in trypsin-digested human colon tissue homogenates; and a small-molecule drug in human and rat

92 e nature of this inhibition using crude lens homogenate as well as recombinant human aldose reductase

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

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

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

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

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

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

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

100 By 1 week, biofilm-positive human tumor homogenates, but not healthy biopsies, displayed consist

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

102 Purification of tumor homogenates by affinity chromatography on these peptides

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

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

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

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

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

108 Furthermore, plated gastrointestinal tissue homogenate confirmed antibiotic treatment significantly

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

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

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

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

113 to non-neurons (primarily glia) and prenatal homogenate cortex.

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

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

116 Addition of 2 mm ATP to the lysate or homogenate did not decrease the stability of the complex

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

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

119 amic regions of DNAm that would be masked in homogenate DNAm data; expand on the relationship between

120 the conveyor belt system and the use of the homogenate extraction protocol as reference method provi

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

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

123 in were inoculated intracranially with brain homogenate from individual CWD-infected elk of various g

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

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

126 fection experimentally via microinjection of homogenate from these galbut-only flies.

127 Cellular homogenates from 263K-infected cells exhibited prion see

128 uvate oxidation was similar in gastrocnemius homogenates from Acsl1(M) (-/-) and control mice.

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

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

131 naptic changes and apply the method to brain homogenates from an Alzheimer's disease mouse model.

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

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

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

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

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

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

138 determined by PCR method in striatal tissue homogenates from Hdh(Q140) KI mice and in human HD postm

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

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

141 d to nicotine (50 mug/ml), and in whole lung homogenates from mice chronically exposed to nicotine (1

142 (FeNOs), are relatively stable in placental homogenates from normal placentas, and that NO, nitrite

143 FeNOs), are relatively unstable in placental homogenates from normal placentas.

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

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

146 We further show that treatment of brain homogenates from prion-infected mice with sodium lauroyl

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

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

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

150 1B are found in insoluble forms within brain homogenates from such patients.

151 Here we report that while brain homogenates from symptomatic prion-infected mice are hig

152 Polymer extraction from brain homogenates from Syrian hamsters infected with Hyper pri

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

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 and metabolic fate of NOx in human placental homogenates from uncomplicated pregnancies in healthy mo

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

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

159 In lung homogenates harvested 14 days following infection, there

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

161 Islet homogenates immunodepleted with anti-IAPP-specific antib

162 applied to measure siRNA in serum and tissue homogenate in preclinical species.

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

164 P (prolyl-carboxypeptidase) in kidney biopsy homogenates in 11 healthy living kidney donors, and 12 p

165 ed miR-98 levels in LFs in vitro and in lung homogenates in vivo Treatment with anti-miR-98 alone was

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

167 ut not biofilm-negative, human colon mucosal homogenates induced colon tumor formation in 3 mouse col

168 n of fibrillar amyloid-beta-containing brain homogenates induced tau pathology in an NLRP3-dependent

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

170 he decrease of RyR1 protein content in total homogenates is not accompanied by a decrease of Cav1.1 c

171 protocol mimicking isoniazid in lung lesion homogenate (isoniazid C(MAX) = 1,200 ng/ml, T(MAX) = 2.2

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

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

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

175 ize exclusion chromatography of normal brain homogenates (mNBH) were pooled, but neither mNBH nor pre

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

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

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

179 ctivity was also observed in enzyme-enriched homogenates obtained from human Caco-2 cells (IC(50) = 6

180 piked individual oncometabolites from pooled homogenate of FFPE or frozen tissue ranged 86-112%.

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

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

183 Examination of homogenates of atherosclerotic plaque-laden aorta showed

184 ndividuals undergoing screening colonoscopy; homogenates of biofilm-negative colon biopsies from heal

185 ion, PCR or immunoblot results obtained from homogenates of bladder mucosa or whole bladder do not re

186 Finally, homogenates of cells coexpressing DES1 and MFAT catalyze

187 Crude homogenates of chicken retinas rapidly convert all-trans

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

189 Because most measurements of mtDNA use homogenates of complex tissues, little is known about ce

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

191 s in nasal secretions and nasal polyp tissue homogenates of CRSwNP patients receiving dupilumab 300 m

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

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 38% and 58% of that present in total muscle homogenates of fast and slow muscles from wild-type (WT)

198 Homogenates of human biofilm-positive colon mucosa were

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

200 ss spectrometry (LC-MS/MS) analyses on brain homogenates of our newly generated knockin mouse express

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

202 Past molecular studies of MDD employed bulk homogenates of postmortem brain tissue, which obscures g

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

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

205 ther inflammatory processes were measured in homogenates of sinonasal tissues and statistically analy

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

207 0.047) were significantly reduced in muscle homogenates of T2D.

208 of esterase activity was detected when using homogenates of ten egg-laying females per well.

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

210 ong with protein-expression levels in tissue homogenates or cardiomyocytes, were assessed in 265 atri

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

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

213 3-19338E homogenate, P3, and P9; ISU13-22038 homogenate, P3, and P9) were determined.

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

215 CIE-exposed astrocytes, microglia, and total homogenate PFC tissue.

216 e predicted in-vivo steady-state lung lesion homogenate pharmacokinetic profiles.

217 examined tubulin acetylation in whole-tissue homogenate, plasma membrane, and lipid-raft membrane dom

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

219 Cornea and sclera homogenates possessed a measurable amount of nitrate red

220 opment, we sequenced both RNA fractions from homogenate prenatal and adult human postmortem cortex us

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

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

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

224 -specific luciferin-with Pyrosoma atlanticum homogenate produced light.

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

226 oluble fraction, with normalization to total homogenate protein.

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

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

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

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

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

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

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

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

235 Depletion of IgG from nasal homogenates resulted in an increase in CD23-mediated IgE

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

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

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

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

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

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

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

243 While tissue homogenate showed no changes in tubulin acetylation betw

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

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

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

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

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

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

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

251 By application to tissue homogenates spiked with drug compounds, we can demonstra

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

253 et microorganisms, human serum and shellfish homogenate, supporting the potential of detecting norovi

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

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

256 ontrast to the results generated with tissue homogenate, the radiance data was not able to distinguis

257 acetylation for mouse spinal cord and brain homogenate tissue, respectively, as measured by our assa

258 chizophrenia but may be missed in studies of homogenate tissue.

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

260 trite and nitrosothiols react with placental homogenates to form iron nitrosyl complexes.

261 trite and nitrosothiols react with placental homogenates to form iron nitrosyl complexes.

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

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

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

265 urinus-specific qPCR of DNA from total organ homogenates vs.broncho alveolar lavages implicated tight

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

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

268 es were homogenized in acetonitrile, and the homogenate was frozen.

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

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

271 Bovine lung tissue homogenate was selected as a surrogate matrix, and a bio

272 Liver homogenate was used to generate a viable and molecularly

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

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

275 Compared with total homogenate, we observed unique and robust gene expressio

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

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

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

279 files in plasma, lung tissue and lung lesion homogenate were simulated for isoniazid, rifampicin and

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

281 Tissue homogenates were analyzed for complement activation prod

282 Nasal polyp homogenates were collected from patients with grass poll

283 titers in cell culture supernatants and lung homogenates were determined by virus yield assays.

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

285 Carotenoid levels in whole fillet homogenates were not decreased significantly post-challe

286 Gray matter homogenates were prepared from auditory cortex gray matt

287 Retinal homogenates were tested for prion seeding activity.

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

289 sialylation were observed when whole kidney homogenates were used.

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

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

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

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

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

295 itochondria, permeabilized cells, and tissue homogenates with high sensitivity.

296 IgE-containing nasal polyp homogenates with or without IgG depletion were evaluated

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

300 d stability in plasma, liver, and intestinal homogenates yet was readily cleaved to DON in P493B lymp