ライフサイエンスコーパス: preparation from

1 Brainstem-spinal cord preparations from 1- to 3-day-old neonates were studied

2 Islet preparations from 102 human pancreatic islet isolations

3 We optically mapped left ventricular wedge preparations from 12 failing native hearts and 2 rejecte

4 chromatography tandem MS analyses of drusen preparations from 18 normal donors and five AMD donors i

5 ed the ascending contraction in 15 % of oral preparations (from 26 preparations, 18 animals) and the

6 ted for MAP by PCR and culture in buffy coat preparations from 28 individuals with Crohn's disease, n

7 Whole-mount cochlear preparations from 3-week- to 2-month-old CGRPalpha-EGFP

8 Coronary-perfused, isolated whole-atrial preparations from 33 normal dogs were studied.

9 An efficient 10-step preparation from 4-methoxypyridine of (2R,3R,4R)-2-aceta

10 while the lowest value was noted for soybean preparations (from 49.6% to 60.8%).

11 Spinal cord/brainstem preparations from 5- to 8-day-old rats, maintained in vi

12 recorded from CA3 pyramidal cells in a slice preparation from 6-month-old male APP/PS1 mice, and stud

13 ped coronary-perfused left ventricular wedge preparations from 6 human end-stage failing hearts (F) a

14 Heavy membrane preparations from 697 lymphoblastoid cells contain a tig

15 Membrane preparations from 81-176 mutants defective in any of the

16 ility of starch was observed for adzuki bean preparations (from 91.6% to 95.5%), while the lowest val

17 id-phase simplifies the procedure for glycan preparation from a complex mixture and can be a powerful

18 Using a medullary slice preparation from a neonatal mouse, including the site of

19 rotein, porin A (PorA), no PorA and membrane preparations from a mutant with no LPS (LpxA(-)).

20 -time PCR with greater consistency than with preparations from a QIAamp DNA Blood minikit.

21 iffered across four donors and between three preparations from a single donor.

22 to document the associations of purified TG preparations from a variety of tissues (human red cells,

23 ide gel electrophoresis (PAGE) of junctional preparations from a variety of vertebrate sources has an

24 apical muscle, tube foot and cardiac stomach preparations from A. rubens.

25 Plasma membrane preparations from activated monocytes also induced mesan

26 ies were conducted in an in vivo spinal cord preparation from adult mice; thoracic levels were target

27 swimming in an ex vivo carapace-spinal cord preparation from adult turtles (Trachemys scripta elegan

28 In an ex vivo carapace-spinal cord preparation from adult turtles (Trachemys scripta elegan

29 An in vitro brainstem-spinal cord preparation from adult turtles was used to test the hypo

30 toneurons in an ex vivo carapace-spinal cord preparation from adult turtles, we demonstrate that irre

31 ed with those from young mice, intact T cell preparations from aged mice had impaired proliferative r

32 isingly, the fictive patterns of the in situ preparations from ALI pups retained these characteristic

33 ailable starting materials due to their easy preparation from aliphatic aldehydes through spontaneous

34 psulated B. anthracis Ames (WT) or a control preparation from an isogenic B. anthracis Ames strain th

35 he sigma1 affinity was tested using membrane preparations from animal (guinea pig) and human origin.

36 e analog was increased compared with similar preparations from animals immunized with control gp120,

37 ergen-induced contractions were increased in preparations from animals subjected to intranasal IL-33

38 evoked greater excitatory input in B31/32 in preparations from animals that had received paired train

39 (AxlA) was purified from a commercial enzyme preparation from Aspergillus niger, and the encoding gen

40 nd are competitive with optimized commercial preparations from Aspergillus and Trichoderma.

41 performed with commercial beta-galactosidase preparations from Aspergillus oryzae, Kluyveromyces lact

42 Ex vivo skin/nerve preparations from Atoh1(CKO) animals demonstrate complet

43 amics in an ex vivo intact SAN/atrial tissue preparation from atrial-specific NCX knockout (KO) mice.

44 hosphate termini and occurred with whole RNA preparations from bacteria but not from eukaryotes.

45 Incubation of crude seed LOX preparations from Birte and the LOX-2-null mutant showed

46 ulating activities of different polyphenolic preparations from black chokeberry fruits: crude extract

47 n to the rRNA-depletion protocol for library preparation from blood RNA effectively reduces highly ab

48 atients' serum/plasma, which requires sample preparation from blood, hence hampering the turnaround t

49 virus and recombinant hemagglutinin protein preparations from both lineages raised hemagglutination-

50 Preparations from both pilocarpine and kainate models of

51 atch-clamp recordings from acute spinal cord preparations from both rat and mouse.

52 inolyl (4) with a crude cholesterol esterase preparation (from bovine pancreas) yielded highly enanti

53 ylamide gel separations of enriched membrane preparations from bovine and human lenses.

54 and ETO/MTG8 cofractionate in nuclear matrix preparations from brains of DRPLA transgenic mice.

55 ynthesized in Escherichia coli and cell wall preparations from C. cellulovorans.

56 We show, in an in vitro slice preparation from C57BL/6 male mice, that a dopamine (DA)

57 that basement membrane extracted NC1 domain preparations from Caenorhabditis elegans, Drosophila mel

58 skin and seeds residue remaining after pulp preparation from camu-camu (Myrciaria dudia).

59 electrophysiology recordings in murine slice preparations from CB1 receptor-null mice and green fluor

60 m, we developed a novel unfolded hippocampus preparation, from CD1 mice of either sex, which preserve

61 tocol, which describes procedures for sample preparation from cell monolayers and cell pellets, can b

62 e presence of host contaminants, using viral preparations from cell culture supernatant, allantoic fl

63 Highly washed membrane preparations from cells of the hyperthermophilic archaeo

64 ring long-term storage, cryopreserved nuclei preparations from chicken lung were used to optimize ATA

65 chimeric mouse model, B2G1 and polyclonal Ig preparations from clinical HPA-1a-specific sera reduced

66 Colonic epithelial preparations from co-infected mice showed increased expr

67 se, and pyruvate kinase were evaluated using preparations from commercial sources and human HepG2 cel

68 In membrane preparation from control brainstem tissues, Western blot

69 DNase activity not associated with identical preparations from control cells.

70 tly, we performed an additional sci-ATAC-seq preparation from cultured hippocampal neurons (899 high-

71 n addition, these responses did not occur in preparations from Cx30-deficient mice or with purinergic

72 Slice preparations from D1 or D2 receptor knock-out mouse embr

73 osynthesis in vitro is catalysed by membrane preparations from developing fenugreek seed endosperms.

74 lement chemical ingredient in separating TCM preparation from different manufacturers and batches wit

75 comparative analysis of the responses to Ag preparations from different mycobacterial species reveal

76 Other enzyme preparations from different sources, such as beta-glucur

77 Here we show that antigen preparations from divergent H7 strains are able to induc

78 ith multiphoton confocal microscopy in slice preparations from dopamine-deficient (DD) and reserpine-

79 n expression in homogenates or mitochondrial preparations from DRG.

80 t enables direct analysis without any sample preparation from dried blood, plasma, and urine.

81 IF-enriched cytoskeletal preparations from dynamitin-overexpressing cells contain

82 s, E. faecalis, or S. aureus, (iii) sacculus preparations from each strain, or (iv) culture fluid con

83 Independent RNA preparations from eight normal and eight scrapie-infecte

84 (3)H]1,25D(3) revealed negligible binding in preparations from either female or male KOs.

85 Peptide antibiotic (halocin) preparations from euryarchaeal halophilic strains S8a, G

86 uptake by examining this process in neuronal preparations from FAAH(-/-) mice and in the presence of

87 ees C by incubating whole cell or microsomal preparations from FAAH-expressing cells with AAMCA.

88 ior-lateral left ventricular free wall wedge preparations from failing (n=5) and nonfailing (n=5) hum

89 etermine N* for nine prior Ir(0) nanocluster preparations from five different [(1,5-COD)Ir(+)]n [anio

90 Irradiated cells or membrane preparations from fresh or frozen tumor tissue can be us

91 llularly recorded action potentials in three preparations from frog: skeletal muscle, cardiac muscle

92 n are structurally compromised, and filament preparations from fully matured 3- to 5-day-old adult fl

93 ti-Gal and other IgM Abs in fresh splenocyte preparations from GalT(-/-) and (for non-Gal specificiti

94 in vertebrate nerve terminals, nerve-muscle preparations from garter snake (Thamnophis sirtalis) wer

95 In striatal slice preparations from GluClalphabeta-expressing animals, IVM

96 annels (SOCCs) in OPCs and acute brain slice preparations from golli knock-out and golli-overexpressi

97 aging of isolated OPCs and acute brain slice preparations from golli KO and golli J37 overexpressing

98 tic anion in FeFbpA-X species in periplasmic preparations from Gram-negative bacteria.

99 cording and calcium imaging using wholemount preparations from guinea pig and mouse gallbladder.

100 A was detected in small and large intestinal preparations from guinea pigs.

101 Both proteins were present in APC preparations from haploid cells arrested in G(1), S, and

102 ochondria from apoptotic cells but identical preparations from healthy cells were inactive.

103 typhlonius Ag, but not when cultured with Ag preparations from Helicobacter pylori, various non-helic

104 Results based on preparations from HepG2 cells showed that L-nucleoside a

105 lly to PAS-positive channels in histological preparations from highly aggressive primary uveal melano

106 Nuclear preparations from histone H4 heterozygotes contained les

107 hythmias in Langendorff-perfused whole heart preparations from homozygous KCNE1-/- mice compared to w

108 odies, fibrinogen was undetectable in plasma preparations from homozygous mutant fish.

109 s on sound production, in an isolated larynx preparation from horseshoe bats.

110 Sample preparation from human and plant specimens is a time-con

111 te for casein kinase 2, a contaminant in our preparation from human embryonic kidney cells.

112 t lysate gel (hPLG), an extracellular matrix preparation from human platelets able to support the pro

113 Analysis of enriched mitochondrial membrane preparations from human cells yielded identification of

114 the coronary-perfused left ventricular wedge preparations from human hearts with end-stage nonischemi

115 In hippocampal slices and intact hippocampal preparations from immature CLM-1 mice, increases in [Cl(

116 Retinal whole-mount preparations from infant and adult rhesus monkeys (Macac

117 ative capacity of enriched splenocyte T-cell preparations from infected animals following stimulation

118 rane modifications using crude mitochondrial preparations from infected Drosophila cells.

119 In a radioligand assay, IgG preparations from infected mice specifically inhibited [

120 RNA preparations from infected/uninfected cells and patient

121 mulate in vitro amplification of PrPres, RNA preparations from invertebrate species do not.

122 CoA thioesterase activity in skeletal muscle preparations from iPLA 2beta-null mice is significantly

123 sed to protease-active extracellular protein preparations from isogenic mutants of P. gingivalis.

124 Preparation from iZON column; however, had a broader siz

125 rforming RNA immunoprecipitation of the mRNA preparation from JSE1880 using a mutant RNase III protei

126 bited one positive band, which was absent in preparations from KO mice.

127 w that mitotic neuroblasts from brain squash preparations from larvae heteroallelic for the two Chrom

128 Microsomal preparations from leaves of these mutants showed around

129 We performed experiments in brain slice preparations from Long-Evans rats to investigate the abi

130 Pheromone preparations from loss-of-function mutants of daf-22, a

131 f bovine serum albumin has been addressed in preparations from low to high solids.

132 inhibition of MYPT1 phosphorylation found in preparations from LPS-treated animals.

133 arabinosyltransferase assay using a membrane preparation from M. smegmatis expressing Rv3792 and synt

134 -labeling techniques in the entorhinal slice preparation from macaque monkeys to investigate the morp

135 we present an enhanced in vitro brain slice preparation from male Wistar rat cortical slices that in

136 sl, immunocytochemical, and plastic-embedded preparations from mature specimens.

137 echanisms, we developed an in vitro cochlear preparation from Meriones unguiculatus that affords opti

138 on was performed in coronary perfused atrial preparations from MI (n=5) and controls (n=4).

139 lease during this period, we used a cochlear preparation from mice of either sex at P4, P6-P7, and P9

140 orferi were obtained from primary lymphocyte preparations from mice challenged with each of the three

141 Lymphocyte preparations from mice challenged with stock infectious

142 In ex vivo preparations from mice of both sexes, we measured MC and

143 ed in spontaneously rhythmic medullary slice preparations from mice.

144 , released during the washing step of surimi preparation from minced fish, that causes environmental

145 Sample preparation from minute amounts of serum was performed i

146 Retinal flat preparations from monkey and cat were stained with methy

147 receptor proteins were expressed in membrane preparation from morphine-tolerant rats.

148 d hyperflagellated, and sheared cell protein preparations from motN contained more flagellin than pre

149 osylation can be detected in intact arterial preparations from mouse and that eNOS S-nitrosylation is

150 ically localized to mitochondria in synaptic preparations from mouse brain.

151 e, we investigated the potential of vascular preparations from mouse retina to undergo myogenesis whe

152 protein, the authors prepared outer segment preparations from mouse retinas.

153 After symptom onset, a higher percentage of preparations from mSOD1 mice exhibited bursting, and the

154 generated by chemically skinned single fiber preparations from Mtm1delta4 muscle were largely preserv

155 Studies in Langendorff heart preparations from mutant TR-beta(1) transgenic animals r

156 wed chromosomal rereplication, and metaphase preparations from mutant zebrafish embryos revealed rere

157 cyclase activity in purified plasma membrane preparations from N18TG2 neuroblastoma cells.

158 The remaining ADP kinase activity in preparations from ndk::km cells, which varies between pr

159 used an intact, ex vivo somatosensory system preparation from neonatal mice to allow intrasomal recor

160 atory neurons in an in vitro medullary slice preparation from neonatal mice.

161 In a medullary slice preparation from neonatal rat (postnatal days 0-4) gener

162 g an isolated in vitro brainstem-spinal cord preparation from neonatal rat in which the respiratory a

163 motor behavior, breathing, using an in vitro preparation from neonatal rat that generates respiratory

164 n an isolated in vitro brainstem-spinal cord preparation from neonatal rat, we report that the locomo

165 mplex (preBotC) in rhythmically active slice preparations from neonatal C57BL/6 mice.

166 ly reduced in isolated brainstem-spinal cord preparations from neonatal Lmx1b(f/f/p) mice and complet

167 ted modulation by using isolated spinal cord preparations from neonatal mice in which locomotor-relat

168 ice and completely blocked in perfused brain preparations from neonatal rats treated with selective a

169 ordings in the preBotzinger Complex in slice preparations from neonatal rodents and tested for pacema

170 clamp recordings from neurons in acute slice preparations from neonatal wild-type and hSOD1(G93A) mic

171 Using an in vitro brainstem slice preparation from newborn mice, we found that intracellul

172 Therefore the RNA content of TAC preparations from Nicotiana tabacum was determined using

173 ber of peptides that are not seen in similar preparations from nonautoimmune C3H animals.

174 in coronary perfused left ventricular wedge preparations from nonfailing (n=6) and failing (n=5) hum

175 AN was optically mapped in coronary-perfused preparations from nonfailing human hearts (n = 4, age 54

176 s after the infection, whereas the same cell preparation from normal mice produced interferon gamma (

177 AN was optically mapped in coronary perfused preparations from normal canine hearts (n=17).

178 f the RVLM presympathetic neurons in in situ preparations from normal rats and rats submitted to a me

179 In preparations from normal rats SNAP or l-arginine did not

180 iferations of autologous CD4 T cells, unlike preparations from normals or those with other lung disea

181 was observed in a PS I reaction center core preparation from Nostoc punctiforme.

182 t histamine release increased in washed cell preparations from omalizumab- but not placebo-treated su

183 regularity of feeding motor output found in preparations from operantly trained animals.

184 ioned culture medium (SECM), but not similar preparations from other bacteria, enhanced human beta-de

185 ng 33 previously described proteins in HIV-1 preparations from other cell types.

186 ranes and has the potential to be applied to preparations from other tissues.

187 at the ratio of MT1-MMP to TIMP2 in membrane preparations from PAF-stimulated HUVEC is 1.6:1, approxi

188 ted analogues of oroidin by cell-free enzyme preparations from PAI-producing sponges.

189 y polymeric forms of vWf compared to control preparations from patients with corresponding, localized

190 e, the gene expression pattern in lymph node preparations from patients with mantle cell lymphoma (MC

191 Cytospin preparations from peritoneal exudate cells (PECs) 48 hrs

192 tions, using sarcoplasmic reticulum-enriched preparations from phospholamban-deficient and wild-type

193 Microsomal preparations from Pichia cells expressing AtGALT2 incorp

194 hnique was tested using cryopreserved nuclei preparations from pig tissues, resulting in NFR that wer

195 Protease preparations from plant (papain and bromelain) and funga

196 rom abattoirs, was hydrolysed using protease preparations from plant (papain and bromelain) and funga

197 Four protease preparations from plant and fungal sources (papain, brom

198 sis of a low-molecular-weight heparin (LMWH) preparation from porcine heparin.

199 RNA preparations from porcine liver, retina, and Muller cell

200 ghly complex peptide mixture (outer membrane preparation from Psuedemonas aeruginosa) was efficiently

201 P1 [Ca2+]i responses were observed mainly in preparations from rabbits on a low-salt diet and were co

202 eved by affinity chromatography of a protein preparation from rat brain on immobilized C16-serinol.

203 NR2C and NR3A subunits in a purified myelin preparation from rat brain.

204 rol permeabilities in mitochondrial membrane preparations from rat brain, liver, and kidney and from

205 formed in 96-well microplates using membrane preparations from rat liver as a source of ASGP-R and Cy

206 rude 20S and 26S and purified 20S proteasome preparations from rat liver as well as proteasome activi

207 Synaptoneurosomal preparations from rat pre-frontal cortex were obtained a

208 nerve as well as skeletal muscle in isolated preparations from rat.

209 ared with rats on 0.3% NaCl diet, glomerular preparations from rats on 8.0% NaCl diet contained more

210 y culture of hippocampal neurons and ex vivo preparations from rats to study the function of proBDNF

211 fluidic device which includes on-chip sample preparation from raw samples.

212 treatment with protic acid, and independent preparation from reaction of [NBu(4)][LCuOH] with H(2)O(

213 RNA preparations from resected menisci (n = 12) were subject

214 Examination of cell wall polysaccharide preparations from RGP1 and RGP2 knockout mutants showed

215 , our data also indicate that commercial LTA preparations from S. aureus, B. subtilis, and S. sanguis

216 d Schizosaccharomyces pombe, but not zymosan preparations from S. cerevisiae.

217 The two extract preparations from sardine by-product (viscera and by-pro

218 applied this technique to total nucleic acid preparations from scrapie-infected and control brain.

219 al precursor cells when added to neurosphere preparations from sedentary mice.

220 A total of 220 virus-enriched preparations from serially collected fecal samples from

221 rve injury-induced ectopic in an ex vivo DRG preparation from SNL rats.

222 Experiments were performed in PSII membrane preparations from spinach in the presence of electron ac

223 Thus, brain preparations from spinophilin-null mice demonstrate enha

224 vestigates the effect of exclusion of copper preparations from spray programs for disease control in

225 ed Rac1 and AMPK activation both in arterial preparations from statin-treated mice as well as in cult

226 urthermore, recombinant ICAM bound to an OMP preparation from strain 1128f+, which expresses P5, but

227 Purified capsular polysaccharide preparations from Streptococcus pneumoniae that are used

228 The results presented here show that gp140 preparations from suitable isolates can adopt a compact,

229 Cardiac muscle preparations from Tg-Delta43 mice demonstrate reduced fo

230 Using sorted DA neuron preparations from TH-eGFP mice we found that DA neurons

231 t activity of POAH neurons in a tissue slice preparation from the adult male rat, in response to temp

232 study that distinguishes the effects of site preparation from the antecedent logging.

233 hesis of marine terpenoids and enables their preparation from the corresponding terrestrial terpenes.

234 c in this polysaccharide, while carbohydrate preparation from the epaB mutant did not contain rhamnos

235 les have been introduced at the time of film preparation from the gels or afterward by sorption after

236 unctional mosaic, using an intact epithelial preparation from the mouse, in which odor responses of m

237 In an ex vivo brain preparation from the pond turtle Trachemys scripta elega

238 Valerian is an herbal preparation from the roots of Valeriana officinalis used

239 In a slice preparation from the spinal cord of the adult turtle, we

240 xtend the theory of double-quantum coherence preparation from the strong coupling/small CSA limit to

241 vitro using an isolated brainstem-cerebellum preparation from the turtle by pairing trigeminal and au

242 Pretreatment with a preparation from the whole root of American ginseng had

243 The binding of [3H]muscimol to membrane preparations from the brain of the bullfrog, Rana catesb

244 Specifically, in slice preparations from the CA1 region of the hippocampus, KCN

245 Electrophysiological recordings of slice preparations from the CeA showed that binge-like ethanol

246 Previous proteomic analysis of the PSII preparations from the cyanobacterium Synechocystis sp PC

247 a altogether; moreover, sheared-cell protein preparations from the fliC mutant lacked a 30-kDa band c

248 Twenty-five commercial ginseng preparations from the genera Panax or Eleutherococcus we

249 sed lamellar structure, ex vivo and in vitro preparations from the hippocampus have provided experime

250 In organotypic preparations from the hippocampus of juvenile mice, stim

251 nhibition of root elongation, and microsomal preparations from the ilr2-1 mutant exhibit enhanced ATP

252 sceptible Escherichia coli host with plasmid preparations from the isolate generated a transformant f

253 f mGAT1-GFP at presynaptic structures in CNS preparations from the knock-in mice.

254 oth single myocytes and multicellular muscle preparations from the rat heart.

255 motor neurons recorded in reduced, in vitro preparations from the same animals.

256 rphisms was confirmed by using different DNA preparations from the same isolate or by repeated runs f

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

258 Skinned myofibre preparations from the TG hearts indicate a decrease in c

259 how that CACCs can be activated in VNO slice preparations from the TRPC2-/- mice and this activation

260 The preparations from the virulent strain of M. arthritidis

261 Retrovirus preparations from these lines killed target cells effici

262 In both live and fixed brain preparations from these mice, detailed microanatomical f

263 through plethysmography, then formed in situ preparations from these pups and recorded their 'fictive

264 Here we report that a particulate preparation from this layer (pLL) strongly inhibits the

265 s that are immunologically related to an LPS preparation from this organism.

266 Striatal preparations from this animal had an impaired capacity t

267 mocellum as compared with purified cellulase preparations from this organism in controlled experiment

268 Thick filament preparations from those muscles show that although the Z

269 logical activity of five different laminarin preparations from three different commercial sources.

270 Findings were validated against neurosphere preparations from three independent Down's syndrome fetu

271 and the CysLT1 receptor has been in membrane preparations from tissues enriched for this receptor.

272 taryl and adipoyl phosphonates on the enzyme preparations from tissues with varied DHTKD1 expression

273 ially purified, RNA-dependent RNA polymerase preparation from tombusvirus-infected plants, revealed t

274 Conversely, in preparations from trained animals, experimental suppress

275 iosulfonate hydrobromide (MTSEA) in membrane preparations from transfected cells.

276 We used rhythmic in vitro transverse slice preparations from transgenic mice where neurons expressi

277 rounding the opaque cells that was absent in preparations from translucent strains.

278 In glial plasmalemmal vesicle (GPV) preparations from treated rats, insulin prevented the in

279 Western blotting of tubule preparations from trp and trpl mutants revealed a correl

280 nt terminals, we used the ex vivo skin-nerve preparation from Trpa1(+/+), Trpa1(+/-), and Trpa1(-/-)

281 response is generated in in vitro brainstem preparations from turtles by pairing a weak conditioned

282 ted five lots of commercially available IVIG preparations from two different suppliers for polyomavir

283 Dye injections in slice preparations from undamaged BP explants identified cell

284 studied in an in vitro bladder-pelvic nerve preparation from untreated or cyclophosphamide (CYP) tre

285 ign that separates variance caused by sample preparation from variance due to analytical equipment.

286 Lamina propria preparations from WASP-deficient mice demonstrated eleva

287 Tricin was recently discovered in lignin preparations from wheat (Triticum aestivum) straw and su

288 Using a recently developed whole-brain preparation from which "fictive" vocalizations are readi

289 e C, are important for IPC in isolated heart preparations from wild-type (WT) and CFTR knockout (CFTR

290 activation responses of skinned ventricular preparations from wild-type (WT) and homozygous cMyBP-C

291 bovine thyroglobulin, and several invertase preparations from wild-type and mutant yeast strains.

292 ions from motN contained more flagellin than preparations from wild-type cells.

293 Cytokine treatment of tracheal ring preparations from wild-type mice resulted in a profound

294 Typically, NSTs are studied in microsomal preparations from wild-type or mutant lines; however, in

295 also evaluated in OS-enriched vs OS-depleted preparations from WT and Rom-1-/- retinas.

296 more abundant than those detected in similar preparations from WT or V337M transfectants.

297 ed with in vitro assays utilizing microsomal preparations from yeast overexpressing the respective ge

298 assays performed with purified CNV replicase preparations from yeast revealed critical roles for thre

299 ena robustly responded to 1,25(OH)(2)D(3) in preparations from young birds, older animals no longer r

300 Membrane preparations from young donors were permeable to protein