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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
11 ped coronary-perfused left ventricular wedge preparations from 6 human end-stage failing hearts (F) a
14 id-phase simplifies the procedure for glycan preparation from a complex mixture and can be a powerful
19 to document the associations of purified TG preparations from a variety of tissues (human red cells,
20 ide gel electrophoresis (PAGE) of junctional preparations from a variety of vertebrate sources has an
23 ies were conducted in an in vivo spinal cord preparation from adult mice; thoracic levels were target
24 swimming in an ex vivo carapace-spinal cord preparation from adult turtles (Trachemys scripta elegan
27 toneurons in an ex vivo carapace-spinal cord preparation from adult turtles, we demonstrate that irre
28 ed with those from young mice, intact T cell preparations from aged mice had impaired proliferative r
29 psulated B. anthracis Ames (WT) or a control preparation from an isogenic B. anthracis Ames strain th
30 Da and 15 kDa by electroelution of a protein preparation from an SDS-PAGE gel and analysis of the fra
31 he sigma1 affinity was tested using membrane preparations from animal (guinea pig) and human origin.
32 e analog was increased compared with similar preparations from animals immunized with control gp120,
33 ergen-induced contractions were increased in preparations from animals subjected to intranasal IL-33
34 evoked greater excitatory input in B31/32 in preparations from animals that had received paired train
35 (AxlA) was purified from a commercial enzyme preparation from Aspergillus niger, and the encoding gen
37 performed with commercial beta-galactosidase preparations from Aspergillus oryzae, Kluyveromyces lact
39 amics in an ex vivo intact SAN/atrial tissue preparation from atrial-specific NCX knockout (KO) mice.
42 atients' serum/plasma, which requires sample preparation from blood, hence hampering the turnaround t
43 virus and recombinant hemagglutinin protein preparations from both lineages raised hemagglutination-
47 inolyl (4) with a crude cholesterol esterase preparation (from bovine pancreas) yielded highly enanti
52 that basement membrane extracted NC1 domain preparations from Caenorhabditis elegans, Drosophila mel
54 electrophysiology recordings in murine slice preparations from CB1 receptor-null mice and green fluor
55 m, we developed a novel unfolded hippocampus preparation, from CD1 mice of either sex, which preserve
56 tocol, which describes procedures for sample preparation from cell monolayers and cell pellets, can b
57 e presence of host contaminants, using viral preparations from cell culture supernatant, allantoic fl
59 chimeric mouse model, B2G1 and polyclonal Ig preparations from clinical HPA-1a-specific sera reduced
61 se, and pyruvate kinase were evaluated using preparations from commercial sources and human HepG2 cel
65 n addition, these responses did not occur in preparations from Cx30-deficient mice or with purinergic
67 osynthesis in vitro is catalysed by membrane preparations from developing fenugreek seed endosperms.
68 comparative analysis of the responses to Ag preparations from different mycobacterial species reveal
71 ith multiphoton confocal microscopy in slice preparations from dopamine-deficient (DD) and reserpine-
75 s, E. faecalis, or S. aureus, (iii) sacculus preparations from each strain, or (iv) culture fluid con
80 uptake by examining this process in neuronal preparations from FAAH(-/-) mice and in the presence of
82 ior-lateral left ventricular free wall wedge preparations from failing (n=5) and nonfailing (n=5) hum
83 etermine N* for nine prior Ir(0) nanocluster preparations from five different [(1,5-COD)Ir(+)]n [anio
85 llularly recorded action potentials in three preparations from frog: skeletal muscle, cardiac muscle
86 n are structurally compromised, and filament preparations from fully matured 3- to 5-day-old adult fl
87 ti-Gal and other IgM Abs in fresh splenocyte preparations from GalT(-/-) and (for non-Gal specificiti
88 in vertebrate nerve terminals, nerve-muscle preparations from garter snake (Thamnophis sirtalis) wer
90 annels (SOCCs) in OPCs and acute brain slice preparations from golli knock-out and golli-overexpressi
91 aging of isolated OPCs and acute brain slice preparations from golli KO and golli J37 overexpressing
97 typhlonius Ag, but not when cultured with Ag preparations from Helicobacter pylori, various non-helic
100 lly to PAS-positive channels in histological preparations from highly aggressive primary uveal melano
102 tions (RT-PCR) were performed with total RNA preparations from HLE-B3 cells using sense and antisense
103 hythmias in Langendorff-perfused whole heart preparations from homozygous KCNE1-/- mice compared to w
107 t lysate gel (hPLG), an extracellular matrix preparation from human platelets able to support the pro
108 Analysis of enriched mitochondrial membrane preparations from human cells yielded identification of
109 the coronary-perfused left ventricular wedge preparations from human hearts with end-stage nonischemi
110 In hippocampal slices and intact hippocampal preparations from immature CLM-1 mice, increases in [Cl(
112 ative capacity of enriched splenocyte T-cell preparations from infected animals following stimulation
118 CoA thioesterase activity in skeletal muscle preparations from iPLA 2beta-null mice is significantly
119 sed to protease-active extracellular protein preparations from isogenic mutants of P. gingivalis.
120 rforming RNA immunoprecipitation of the mRNA preparation from JSE1880 using a mutant RNase III protei
122 w that mitotic neuroblasts from brain squash preparations from larvae heteroallelic for the two Chrom
125 We performed experiments in brain slice preparations from Long-Evans rats to investigate the abi
129 arabinosyltransferase assay using a membrane preparation from M. smegmatis expressing Rv3792 and synt
130 -labeling techniques in the entorhinal slice preparation from macaque monkeys to investigate the morp
131 we present an enhanced in vitro brain slice preparation from male Wistar rat cortical slices that in
132 ty were 2-4-fold higher in purified receptor preparations from malignant breast tissue as compared to
135 echanisms, we developed an in vitro cochlear preparation from Meriones unguiculatus that affords opti
137 orferi were obtained from primary lymphocyte preparations from mice challenged with each of the three
139 d, perfused, thick ascending limb/glomerulus preparations from mice, under baseline conditions, has b
141 , released during the washing step of surimi preparation from minced fish, that causes environmental
144 d hyperflagellated, and sheared cell protein preparations from motN contained more flagellin than pre
145 osylation can be detected in intact arterial preparations from mouse and that eNOS S-nitrosylation is
147 e, we investigated the potential of vascular preparations from mouse retina to undergo myogenesis whe
149 After symptom onset, a higher percentage of preparations from mSOD1 mice exhibited bursting, and the
150 generated by chemically skinned single fiber preparations from Mtm1delta4 muscle were largely preserv
152 wed chromosomal rereplication, and metaphase preparations from mutant zebrafish embryos revealed rere
155 used an intact, ex vivo somatosensory system preparation from neonatal mice to allow intrasomal recor
158 g an isolated in vitro brainstem-spinal cord preparation from neonatal rat in which the respiratory a
159 motor behavior, breathing, using an in vitro preparation from neonatal rat that generates respiratory
160 n an isolated in vitro brainstem-spinal cord preparation from neonatal rat, we report that the locomo
162 ly reduced in isolated brainstem-spinal cord preparations from neonatal Lmx1b(f/f/p) mice and complet
163 ice and completely blocked in perfused brain preparations from neonatal rats treated with selective a
164 ordings in the preBotzinger Complex in slice preparations from neonatal rodents and tested for pacema
165 clamp recordings from neurons in acute slice preparations from neonatal wild-type and hSOD1(G93A) mic
169 in coronary perfused left ventricular wedge preparations from nonfailing (n=6) and failing (n=5) hum
170 AN was optically mapped in coronary-perfused preparations from nonfailing human hearts (n = 4, age 54
171 s after the infection, whereas the same cell preparation from normal mice produced interferon gamma (
173 f the RVLM presympathetic neurons in in situ preparations from normal rats and rats submitted to a me
175 iferations of autologous CD4 T cells, unlike preparations from normals or those with other lung disea
177 ffinity labelled in vitro in plasma membrane preparations from oat (Avena sativa L.) aleurone and fro
178 t histamine release increased in washed cell preparations from omalizumab- but not placebo-treated su
179 eive a range of doses of T cell-replete cell preparations from one of the above three cell sources.
181 ioned culture medium (SECM), but not similar preparations from other bacteria, enhanced human beta-de
184 at the ratio of MT1-MMP to TIMP2 in membrane preparations from PAF-stimulated HUVEC is 1.6:1, approxi
186 y polymeric forms of vWf compared to control preparations from patients with corresponding, localized
187 e, the gene expression pattern in lymph node preparations from patients with mantle cell lymphoma (MC
189 tions, using sarcoplasmic reticulum-enriched preparations from phospholamban-deficient and wild-type
191 detected in intestinal brush border membrane preparations from pigs with adhesive phenotypes but not
193 rom abattoirs, was hydrolysed using protease preparations from plant (papain and bromelain) and funga
197 ghly complex peptide mixture (outer membrane preparation from Psuedemonas aeruginosa) was efficiently
198 P1 [Ca2+]i responses were observed mainly in preparations from rabbits on a low-salt diet and were co
200 eved by affinity chromatography of a protein preparation from rat brain on immobilized C16-serinol.
202 rol permeabilities in mitochondrial membrane preparations from rat brain, liver, and kidney and from
203 formed in 96-well microplates using membrane preparations from rat liver as a source of ASGP-R and Cy
204 rude 20S and 26S and purified 20S proteasome preparations from rat liver as well as proteasome activi
207 ared with rats on 0.3% NaCl diet, glomerular preparations from rats on 8.0% NaCl diet contained more
208 y culture of hippocampal neurons and ex vivo preparations from rats to study the function of proBDNF
212 , our data also indicate that commercial LTA preparations from S. aureus, B. subtilis, and S. sanguis
215 applied this technique to total nucleic acid preparations from scrapie-infected and control brain.
219 Experiments were performed in PSII membrane preparations from spinach in the presence of electron ac
221 ed Rac1 and AMPK activation both in arterial preparations from statin-treated mice as well as in cult
222 urthermore, recombinant ICAM bound to an OMP preparation from strain 1128f+, which expresses P5, but
224 The results presented here show that gp140 preparations from suitable isolates can adopt a compact,
227 t activity of POAH neurons in a tissue slice preparation from the adult male rat, in response to temp
229 tion of arachidonic acid with a crude enzyme preparation from the colon samples, revealed the formati
230 hesis of marine terpenoids and enables their preparation from the corresponding terrestrial terpenes.
231 c in this polysaccharide, while carbohydrate preparation from the epaB mutant did not contain rhamnos
233 les have been introduced at the time of film preparation from the gels or afterward by sorption after
235 unctional mosaic, using an intact epithelial preparation from the mouse, in which odor responses of m
239 xtend the theory of double-quantum coherence preparation from the strong coupling/small CSA limit to
240 vitro using an isolated brainstem-cerebellum preparation from the turtle by pairing trigeminal and au
242 The binding of [3H]muscimol to membrane preparations from the brain of the bullfrog, Rana catesb
244 Electrophysiological recordings of slice preparations from the CeA showed that binge-like ethanol
245 Previous proteomic analysis of the PSII preparations from the cyanobacterium Synechocystis sp PC
246 a altogether; moreover, sheared-cell protein preparations from the fliC mutant lacked a 30-kDa band c
248 sed lamellar structure, ex vivo and in vitro preparations from the hippocampus have provided experime
250 nhibition of root elongation, and microsomal preparations from the ilr2-1 mutant exhibit enhanced ATP
251 sceptible Escherichia coli host with plasmid preparations from the isolate generated a transformant f
253 table by the fluorographic assay in membrane preparations from the mutants, and comparison of the seq
254 se tissue and in gastrocnemius/soleus muscle preparations from the obesity-resistant A/J and C57BL/Ks
257 rphisms was confirmed by using different DNA preparations from the same isolate or by repeated runs f
260 how that CACCs can be activated in VNO slice preparations from the TRPC2-/- mice and this activation
267 mocellum as compared with purified cellulase preparations from this organism in controlled experiment
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 ially purified, RNA-dependent RNA polymerase preparation from tombusvirus-infected plants, revealed t
275 We used rhythmic in vitro transverse slice preparations from transgenic mice where neurons expressi
279 nt terminals, we used the ex vivo skin-nerve preparation from Trpa1(+/+), Trpa1(+/-), and Trpa1(-/-)
280 response is generated in in vitro brainstem preparations from turtles by pairing a weak conditioned
281 ted five lots of commercially available IVIG preparations from two different suppliers for polyomavir
283 studied in an in vitro bladder-pelvic nerve preparation from untreated or cyclophosphamide (CYP) tre
284 ign that separates variance caused by sample preparation from variance due to analytical equipment.
286 Tricin was recently discovered in lignin preparations from wheat (Triticum aestivum) straw and su
288 entrations of Ba2+ were needed to depolarize preparations from which the submucosal and myenteric pac
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.
294 Typically, NSTs are studied in microsomal preparations from wild-type or mutant lines; however, in
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
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