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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                        Spinal cord/brainstem preparations from 5- to 8-day-old rats, maintained in vi
11 ped coronary-perfused left ventricular wedge preparations from 6 human end-stage failing hearts (F) a
12                               Heavy membrane preparations from 697 lymphoblastoid cells contain a tig
13                                     Membrane preparations from 81-176 mutants defective in any of the
14 id-phase simplifies the procedure for glycan preparation from a complex mixture and can be a powerful
15                      Using a medullary slice preparation from a neonatal mouse, including the site of
16 rotein, porin A (PorA), no PorA and membrane preparations from a mutant with no LPS (LpxA(-)).
17 -time PCR with greater consistency than with preparations from a QIAamp DNA Blood minikit.
18 iffered across four donors and between three preparations from a single donor.
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
21 apical muscle, tube foot and cardiac stomach preparations from A. rubens.
22                              Plasma membrane preparations from activated monocytes also induced mesan
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
25           In an ex vivo carapace-spinal cord preparation from adult turtles (Trachemys scripta elegan
26            An in vitro brainstem-spinal cord preparation from adult turtles was used to test the hypo
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
36 nd are competitive with optimized commercial preparations from Aspergillus and Trichoderma.
37 performed with commercial beta-galactosidase preparations from Aspergillus oryzae, Kluyveromyces lact
38                           Ex vivo skin/nerve preparations from Atoh1(CKO) animals demonstrate complet
39 amics in an ex vivo intact SAN/atrial tissue preparation from atrial-specific NCX knockout (KO) mice.
40 hosphate termini and occurred with whole RNA preparations from bacteria but not from eukaryotes.
41                 Incubation of crude seed LOX preparations from Birte and the LOX-2-null mutant showed
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-
44                                              Preparations from both pilocarpine and kainate models of
45 atch-clamp recordings from acute spinal cord preparations from both rat and mouse.
46                                          VP1 preparations from both virus isolates contained heteroge
47 inolyl (4) with a crude cholesterol esterase preparation (from bovine pancreas) yielded highly enanti
48 ylamide gel separations of enriched membrane preparations from bovine and human lenses.
49 and ETO/MTG8 cofractionate in nuclear matrix preparations from brains of DRPLA transgenic mice.
50 ynthesized in Escherichia coli and cell wall preparations from C. cellulovorans.
51                We show, in an in vitro slice preparation from C57BL/6 male mice, that a dopamine (DA)
52  that basement membrane extracted NC1 domain preparations from Caenorhabditis elegans, Drosophila mel
53  skin and seeds residue remaining after pulp preparation from camu-camu (Myrciaria dudia).
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
58                       Highly washed membrane preparations from cells of the hyperthermophilic archaeo
59 chimeric mouse model, B2G1 and polyclonal Ig preparations from clinical HPA-1a-specific sera reduced
60                           Colonic epithelial preparations from co-infected mice showed increased expr
61 se, and pyruvate kinase were evaluated using preparations from commercial sources and human HepG2 cel
62                                           In preparations from competent pneumococcal cultures a prot
63                                  In membrane preparation from control brainstem tissues, Western blot
64 DNase activity not associated with identical preparations from control cells.
65 n addition, these responses did not occur in preparations from Cx30-deficient mice or with purinergic
66                                        Slice preparations from D1 or D2 receptor knock-out mouse embr
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
69                                 Other enzyme preparations from different sources, such as beta-glucur
70                    Here we show that antigen preparations from divergent H7 strains are able to induc
71 ith multiphoton confocal microscopy in slice preparations from dopamine-deficient (DD) and reserpine-
72 n expression in homogenates or mitochondrial preparations from DRG.
73 t enables direct analysis without any sample preparation from dried blood, plasma, and urine.
74                     IF-enriched cytoskeletal preparations from dynamitin-overexpressing cells contain
75 s, E. faecalis, or S. aureus, (iii) sacculus preparations from each strain, or (iv) culture fluid con
76                              Independent RNA preparations from eight normal and eight scrapie-infecte
77 (3)H]1,25D(3) revealed negligible binding in preparations from either female or male KOs.
78 ved very little attention in the study of F1 preparations from eukaryotic cells.
79                 Peptide antibiotic (halocin) preparations from euryarchaeal halophilic strains S8a, G
80 uptake by examining this process in neuronal preparations from FAAH(-/-) mice and in the presence of
81 ees C by incubating whole cell or microsomal preparations from FAAH-expressing cells with AAMCA.
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
84                 Irradiated cells or membrane preparations from fresh or frozen tumor tissue can be us
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
89                            In striatal slice preparations from GluClalphabeta-expressing animals, IVM
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
92 tic anion in FeFbpA-X species in periplasmic preparations from Gram-negative bacteria.
93 cording and calcium imaging using wholemount preparations from guinea pig and mouse gallbladder.
94 A was detected in small and large intestinal preparations from guinea pigs.
95            Both proteins were present in APC preparations from haploid cells arrested in G(1), S, and
96 ochondria from apoptotic cells but identical preparations from healthy cells were inactive.
97 typhlonius Ag, but not when cultured with Ag preparations from Helicobacter pylori, various non-helic
98 ) with IC(50) values using receptor membrane preparations from Helix aspersa.
99                             Results based on preparations from HepG2 cells showed that L-nucleoside a
100 lly to PAS-positive channels in histological preparations from highly aggressive primary uveal melano
101                                      Nuclear preparations from histone H4 heterozygotes contained les
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
104 odies, fibrinogen was undetectable in plasma preparations from homozygous mutant fish.
105 s on sound production, in an isolated larynx preparation from horseshoe bats.
106 te for casein kinase 2, a contaminant in our preparation from human embryonic kidney cells.
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(
111                          Retinal whole-mount preparations from infant and adult rhesus monkeys (Macac
112 ative capacity of enriched splenocyte T-cell preparations from infected animals following stimulation
113 rane modifications using crude mitochondrial preparations from infected Drosophila cells.
114                  In a radioligand assay, IgG preparations from infected mice specifically inhibited [
115                                          RNA preparations from infected/uninfected cells and patient
116        In vitro studies in isolated membrane preparations from insect cells infected with MDR1-expres
117 mulate in vitro amplification of PrPres, RNA preparations from invertebrate species do not.
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
121 bited one positive band, which was absent in preparations from KO mice.
122 w that mitotic neuroblasts from brain squash preparations from larvae heteroallelic for the two Chrom
123                               Soluble enzyme preparations from leaves catalyzed the divalent metal io
124                                   Microsomal preparations from leaves of these mutants showed around
125      We performed experiments in brain slice preparations from Long-Evans rats to investigate the abi
126                                    Pheromone preparations from loss-of-function mutants of daf-22, a
127 f bovine serum albumin has been addressed in preparations from low to high solids.
128 inhibition of MYPT1 phosphorylation found in preparations from LPS-treated animals.
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
133                           Intestinal peptide preparations from MAT-/- mice had decreased antimicrobia
134 sl, immunocytochemical, and plastic-embedded preparations from mature specimens.
135 echanisms, we developed an in vitro cochlear preparation from Meriones unguiculatus that affords opti
136 on was performed in coronary perfused atrial preparations from MI (n=5) and controls (n=4).
137 orferi were obtained from primary lymphocyte preparations from mice challenged with each of the three
138                                   Lymphocyte preparations from mice challenged with stock infectious
139 d, perfused, thick ascending limb/glomerulus preparations from mice, under baseline conditions, has b
140 ed in spontaneously rhythmic medullary slice preparations from mice.
141 , released during the washing step of surimi preparation from minced fish, that causes environmental
142                                 Retinal flat preparations from monkey and cat were stained with methy
143 receptor proteins were expressed in membrane preparation from morphine-tolerant rats.
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
146 ically localized to mitochondria in synaptic preparations from mouse brain.
147 e, we investigated the potential of vascular preparations from mouse retina to undergo myogenesis whe
148  protein, the authors prepared outer segment preparations from mouse retinas.
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
151                 Studies in Langendorff heart preparations from mutant TR-beta(1) transgenic animals r
152 wed chromosomal rereplication, and metaphase preparations from mutant zebrafish embryos revealed rere
153 cyclase activity in purified plasma membrane preparations from N18TG2 neuroblastoma cells.
154         The remaining ADP kinase activity in preparations from ndk::km cells, which varies between pr
155 used an intact, ex vivo somatosensory system preparation from neonatal mice to allow intrasomal recor
156 atory neurons in an in vitro medullary slice preparation from neonatal mice.
157                         In a medullary slice preparation from neonatal rat (postnatal days 0-4) gener
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
161 mplex (preBotC) in rhythmically active slice preparations from neonatal C57BL/6 mice.
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
166            Using an in vitro brainstem slice preparation from newborn mice, we found that intracellul
167             Therefore the RNA content of TAC preparations from Nicotiana tabacum was determined using
168 ber of peptides that are not seen in similar preparations from nonautoimmune C3H animals.
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 (
172 AN was optically mapped in coronary perfused preparations from normal canine hearts (n=17).
173 f the RVLM presympathetic neurons in in situ preparations from normal rats and rats submitted to a me
174                                           In preparations from normal rats SNAP or l-arginine did not
175 iferations of autologous CD4 T cells, unlike preparations from normals or those with other lung disea
176  was observed in a PS I reaction center core preparation from Nostoc punctiforme.
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.
180  regularity of feeding motor output found in preparations from operantly trained animals.
181 ioned culture medium (SECM), but not similar preparations from other bacteria, enhanced human beta-de
182 ng 33 previously described proteins in HIV-1 preparations from other cell types.
183 ranes and has the potential to be applied to preparations from other tissues.
184 at the ratio of MT1-MMP to TIMP2 in membrane preparations from PAF-stimulated HUVEC is 1.6:1, approxi
185 ted analogues of oroidin by cell-free enzyme preparations from PAI-producing sponges.
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
188                                     Cytospin preparations from peritoneal exudate cells (PECs) 48 hrs
189 tions, using sarcoplasmic reticulum-enriched preparations from phospholamban-deficient and wild-type
190                                   Microsomal preparations from Pichia cells expressing AtGALT2 incorp
191 detected in intestinal brush border membrane preparations from pigs with adhesive phenotypes but not
192                                     Protease preparations from plant (papain and bromelain) and funga
193 rom abattoirs, was hydrolysed using protease preparations from plant (papain and bromelain) and funga
194                                Four protease preparations from plant and fungal sources (papain, brom
195 sis of a low-molecular-weight heparin (LMWH) preparation from porcine heparin.
196                                          RNA preparations from porcine liver, retina, and Muller cell
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
199 fold higher than that observed with the same preparations from rabbits.
200 eved by affinity chromatography of a protein preparation from rat brain on immobilized C16-serinol.
201  NR2C and NR3A subunits in a purified myelin preparation from rat brain.
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
205                            Synaptoneurosomal preparations from rat pre-frontal cortex were obtained a
206 nerve as well as skeletal muscle in isolated preparations from rat.
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
209 fluidic device which includes on-chip sample preparation from raw samples.
210                                          RNA preparations from resected menisci (n = 12) were subject
211      Examination of cell wall polysaccharide preparations from RGP1 and RGP2 knockout mutants showed
212 , our data also indicate that commercial LTA preparations from S. aureus, B. subtilis, and S. sanguis
213 d Schizosaccharomyces pombe, but not zymosan preparations from S. cerevisiae.
214                              The two extract preparations from sardine by-product (viscera and by-pro
215 applied this technique to total nucleic acid preparations from scrapie-infected and control brain.
216 al precursor cells when added to neurosphere preparations from sedentary mice.
217                A total of 220 virus-enriched preparations from serially collected fecal samples from
218 rve injury-induced ectopic in an ex vivo DRG preparation from SNL rats.
219  Experiments were performed in PSII membrane preparations from spinach in the presence of electron ac
220                                  Thus, brain preparations from spinophilin-null mice demonstrate enha
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
223             Purified capsular polysaccharide preparations from Streptococcus pneumoniae that are used
224   The results presented here show that gp140 preparations from suitable isolates can adopt a compact,
225                               Cardiac muscle preparations from Tg-Delta43 mice demonstrate reduced fo
226                       Using sorted DA neuron preparations from TH-eGFP mice we found that DA neurons
227 t activity of POAH neurons in a tissue slice preparation from the adult male rat, in response to temp
228 study that distinguishes the effects of site preparation from the antecedent logging.
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
232                          A "crude" cellulase preparation from the fungus Trichoderma reesei served as
233 les have been introduced at the time of film preparation from the gels or afterward by sorption after
234          We have employed the excised cilium preparation from the grass frog (Rana pipiens) to measur
235 unctional mosaic, using an intact epithelial preparation from the mouse, in which odor responses of m
236                          In an ex vivo brain preparation from the pond turtle Trachemys scripta elega
237                        Valerian is an herbal preparation from the roots of Valeriana officinalis used
238                                   In a slice preparation from the spinal cord of the adult turtle, we
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
241                          Pretreatment with a preparation from the whole root of American ginseng had
242      The binding of [3H]muscimol to membrane preparations from the brain of the bullfrog, Rana catesb
243                       Specifically, in slice preparations from the CA1 region of the hippocampus, KCN
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
247               Twenty-five commercial ginseng preparations from the genera Panax or Eleutherococcus we
248 sed lamellar structure, ex vivo and in vitro preparations from the hippocampus have provided experime
249                               In organotypic preparations from the hippocampus of juvenile mice, stim
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
252 f mGAT1-GFP at presynaptic structures in CNS preparations from the knock-in mice.
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
255 oth single myocytes and multicellular muscle preparations from the rat heart.
256  motor neurons recorded in reduced, in vitro preparations from the same animals.
257 rphisms was confirmed by using different DNA preparations from the same isolate or by repeated runs f
258 effect of alcohol in SN and total homogenate preparations from the same samples.
259                             Skinned myofibre preparations from the TG hearts indicate a decrease in c
260 how that CACCs can be activated in VNO slice preparations from the TRPC2-/- mice and this activation
261                                          The preparations from the virulent strain of M. arthritidis
262                                   Retrovirus preparations from these lines killed target cells effici
263                 In both live and fixed brain preparations from these mice, detailed microanatomical f
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 ially purified, RNA-dependent RNA polymerase preparation from tombusvirus-infected plants, revealed t
273                               Conversely, in preparations from trained animals, experimental suppress
274 iosulfonate hydrobromide (MTSEA) in membrane preparations from transfected cells.
275   We used rhythmic in vitro transverse slice preparations from transgenic mice where neurons expressi
276 rounding the opaque cells that was absent in preparations from translucent strains.
277          In glial plasmalemmal vesicle (GPV) preparations from treated rats, insulin prevented the in
278                   Western blotting of tubule preparations from trp and trpl mutants revealed a correl
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
282                      Dye injections in slice preparations from undamaged BP explants identified cell
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.
285                               Lamina propria preparations from WASP-deficient mice demonstrated eleva
286     Tricin was recently discovered in lignin preparations from wheat (Triticum aestivum) straw and su
287       Using a recently developed whole-brain preparation from which "fictive" vocalizations are readi
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.
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

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