ライフサイエンスコーパス: tissue extract

1 ed considerably more versican in the injured tissue extract.

2 with unrelated proteins in an unfractionated tissue extract.

3 the response of metabolite ions in rat brain tissue extract.

4 r demonstrated to assign molecules in a worm tissue extract.

5 radioactive, sensitive assay of MCD in crude tissue extract.

6 properties of granuloma-inducing sarcoidosis tissue extracts.

7 undance was detected in primary colon cancer tissue extracts.

8 n vivo spectrum were confirmed in studies of tissue extracts.

9 y can be immunodepleted from prostate cancer tissue extracts.

10 oid of 3-OST-1 enzyme activity in plasma and tissue extracts.

11 nzyme activity peaked at 12 h in hippocampal tissue extracts.

12 adenosine, even in complex mixtures such as tissue extracts.

13 with amino acids, orphan ligands, serum, and tissue extracts.

14 of D-AKAP2 was characterized by using mouse tissue extracts.

15 e, and sesquiterpenes are detectable only in tissue extracts.

16 idized to oxindole-3-acetic acid by Zea mays tissue extracts.

17 lysates, hepatic subcellular fractions, and tissue extracts.

18 xogenously to supernatant fluids of the null tissue extracts.

19 rate of synthesis of glutathione in cell and tissue extracts.

20 rformed with excellent recovery in different tissue extracts.

21 the mutant allele in total RNA derived from tissue extracts.

22 action of SATB1 and CDP in several different tissue extracts.

23 fication of dTPP II activity from Drosophila tissue extracts.

24 n assay to search for regulators in cell and tissue extracts.

25 rocessing were present in seven of seven AAA tissue extracts.

26 ve proform in all tumor cell lines and tumor tissue extracts.

27 d cleavage of its in vivo substrate titin in tissue extracts.

28 used them to identify authentic proteins in tissue extracts.

29 red by analysis of glutamate enrichment from tissue extracts.

30 measurement of glutamate C4 enrichment from tissue extracts.

31 activity in murine macrophage and human lung tissue extracts.

32 ns was confirmed by Western blot analysis of tissue extracts.

33 72 recognize a >200-kDa protein in cell and tissue extracts.

34 ms are translated as proteins in human brain tissue extracts.

35 es screening of the FFA composition in crude tissue extracts.

36 chromatography (LC)-MS/MS results from brain tissue extracts.

37 d to assess gene and protein expression from tissue extracts.

38 substances and other peroxidases present in tissue extracts.

39 y characterized in liver, brain, and adipose tissue extracts.

40 cromolecular complexes directly from cell or tissue extracts.

41 ilar substrate specificity in worm and mouse tissue extracts.

42 detect endogenous SphK activity in cell and tissue extracts.

43 to endogenous protein complexes from animal tissue extracts.

44 pidly measured in minimally prepared cell or tissue extracts.

45 easure the amounts of these species in brain tissue extracts.

46 fic cleavage was confirmed by digestion with tissue extracts.

47 lipid mass spectral profiles from crude lung tissue extracts.

48 in tumors and by (1)H MRS in cell and tumor tissue extracts.

49 t message for ERG2 and 3 in whole myometrial tissue extracts.

50 antibody in a variety of cultured cells and tissue extracts.

51 of apoptosis in live mice, whole organs and tissue extracts.

52 bstantial levels of IGF-1:TTC in spinal cord tissue extracts.

53 sugar phosphate standards into complex plant tissue extracts.

54 the pellet after low speed centrifugation of tissue extracts.

55 of monoglyceride regioisomers directly from tissue extracts.

56 ological samples, such as serum, plasma, and tissue extracts.

57 ions from the separation of complex neuronal tissue extracts.

58 nd cyclin A as determined by Western blot of tissue extracts.

59 for analyzing telomerase activity in cell or tissue extracts.

60 ysis of metabolites in biological fluids and tissue extracts.

61 nt from results obtained using HPLC-MS/MS of tissue extracts.

62 dependent pterin ring reduction was found in tissue extracts.

63 tic tool of the antioxidant capacity in leaf tissue extracts.

64 rin in alpha-actinin immunoprecipitates from tissue extracts.

65 n account for all such activity in mammalian tissues extracts.

66 trated increased CCR5 protein in hippocampal tissue extracts 32 hours after lesioning.

67 We have isolated from tissue extracts a distinct and abundant mammalian Pol II

68 Forty-one percent of the tissue extracts, amplified by the PCR reacted positively

69 st existing tools using a human glioblastoma tissue extract and illustrate its ability to automatical

70 de cocktail was spiked into a complex native tissue extract and quantified by unscheduled multiple re

71 recognized multiple bands of 240-110 kDa in tissue extracts and collagenous bands of 150-140 kDa in

72 profiling procedures involve the analysis of tissue extracts and consequently lack cellular or subcel

73 End-stage ADPKD renal tissue extracts and cyst fluids were assayed for time-de

74 azine induced HIF-1alpha and VEGF protein in tissue extracts and elevated plasma VEGF levels.

75 Their effects were evaluated in muscle tissue extracts and freshly dissociated SM cells.

76 ge of terpenoid metabolites in complex plant tissue extracts and is independent of retention time, ab

77 This study was performed on medial tissue extracts and primary cultures of VSMCs of human t

78 o enzymes could be coimmunoprecipitated from tissue extracts and proposed functional interactions bet

79 Immunoprecipitation analysis of tissue extracts and proximity ligation assays in dissoci

80 two parts: the preparation of cell cytosolic/tissue extracts and the detection of total glutathione (

81 is stably associated with other proteins in tissue extracts and the first nuclear receptor shown to

82 The results were confirmed in tissue extracts and were in line with the predictions ma

83 esent a systematic analysis of a sample set (tissue extracts), and the utility of a simple correlatio

84 Both HO-1 and HO-2 were present in the IAS tissue extracts, and both enzymes were localized in the

85 ctins, is present in numerous cell lines and tissue extracts, and is expressed on the cell surface.

86 ve PRMT1 activity from RAT1 extracts, murine tissue extracts, and purified rat liver FDH preparations

87 oreover, in contrast to earlier views, MT in tissue extracts appears to be less stable than T.

88 Tissue extracts are treated with subunit-specific probes

89 t, kidney, brain, liver, and skeletal muscle tissue extracts as examples.

90 ysically associated with each other in maize tissue extracts, as demonstrated by reciprocal coimmunop

91 The assay is useful with crude tissue extracts, as demonstrated by the determination of

92 MSA can be measured in tissue extracts at 0.04 nmol (equivalent to 2 microM).

93 K, which is ubiquitously expressed in normal tissue extracts but is absent from many tumor cell lines

94 thiopropyl resin was employed to debulk the tissue extract by selectively removing a substantial fra

95 osomal DNA fragmentation was investigated in tissue extracts by agarose gel electrophoresis.

96 hange factor, in neuronal cells and in brain tissue extracts by co-immunoprecipitation and co-localiz

97 ntification of hundreds of lipids species in tissue extracts by direct-infusion MS, localization of l

98 between immunohistochemistry and analysis of tissue extracts by enzyme immunoassay.

99 Analysis of lung washings and colon tissue extracts by Western blotting in the unreduced sta

100 A complete reduced folate pool analysis of a tissue extract can be obtained in less than 2 h once a s

101 However, coeluting components in tissue extracts can interfere with ionization at the int

102 metabolite analysis, enzyme assays with WRC tissue extracts, cloning, and functional characterizatio

103 High resolution 13C NMR spectra of tissue extracts confirmed that the exogenous lactate did

104 e of approximately 8-kDa was also evident in tissue extracts containing the 225-kDa form.

105 RA synovial tissue extracts demonstrated elevated levels of MMP-9 an

106 Analysis of ischemic wound tissue extracts demonstrated significantly reduced expre

107 dostatin levels in either serum or carcinoma tissue extracts did not change in cathepsin S- or cystat

108 leveraged direct proteomic analysis of tumor tissue extracts, differential feature selection characte

109 In Western blot analyses of whole-tissue extracts, Egr-1 protein levels were shown to be i

110 -LC-MS analysis of a proteolytic digest of a tissue extract, equivalent to a sample size of approxima

111 Northern hybridization and immunoblotting of tissue extracts found keratocan distribution to be more

112 versal of the pH of an adult rat hippocampal tissue extract from 10.5 to 7.4 led to an almost complet

113 genes, was found to be coexpressed mainly in tissue extracted from breast and ovarian cancers, but al

114 tical neurons treated with Abeta or cortical tissue extracts from 12-month-old APPswe/PS1dE9 transgen

115 nanograms of SF per milligram of protein) in tissue extracts from 166 breast cancers and correlated t

116 t detect the BK or JC polyomaviruses in lung tissue extracts from 33 patients with IPF by using real-

117 I-MS approach was successfully used on tumor tissue extracts from a K-ras transgenic mouse model of l

118 ptide sequencing from complex neuroendocrine tissue extracts from a marine model organism, Callinecte

119 we studied adipogenesis by liver and adipose tissue extracts from a polar bear and three synthetic mi

120 ently activated by native proteases in aorta tissue extracts from ApoE(-)/(-), but not from normal mi

121 rin-B co-immunoprecipitates with InsP(3)R in tissue extracts from brain, heart, and lung.

122 Tissue extracts from FDH(+/+), FDH(+/-), and FDH(-/-) mi

123 ect and purify the lumican core protein from tissue extracts from human donors 6 to 89 years of age.

124 e protease responsible for processing Shh in tissue extracts from human stomach.

125 -DNA excision activity as judged by assay of tissue extracts from knockout mice as well as by the res

126 Ex vivo measurements of tissue extracts from liver, kidney, and tumor indicated

127 Tissue extracts from Minpp1-deficient mice lacked detect

128 ermine the GL-3 concentrations in plasma and tissue extracts from normal individuals and patients and

129 atasets of serum, urine, cortex, and stomach tissue extracts from the rats were analysed by multivari

130 Tissue extracts from the RV of 20 patients were assayed

131 Reaction rates with tissue extracts from two grasses were linear for at leas

132 een applied to cells grown in culture and to tissue extracts from young and old animals.

133 lecular mass of 28 kD on western analysis of tissue extracts from zinnia, forsythia (Forsythia suspen

134 STR2-EGFP, or AdEGFP as well as ex vivo with tissues extracted from mice.

135 oxide dismutase and catalase were assayed in tissue extracts generated from fresh human trabecular me

136 NP tissue extracts had significantly more anti-basement mem

137 ed proteomic analyses performed on cartilage tissue extracts identified the serine protease HtrA1/PRS

138 Screening of tissue extracts in a cell line engineered to overexpress

139 nd cellular fibronectin mRNAs in whole-liver tissue extracts in both models.

140 duced AMPK phosphorylation at Thr172 in lung tissue extracts, increased protein content and cell coun

141 Tissue extracts incubated with reduced thioredoxin are t

142 sis of D2 ubiquitination driven by different tissue extracts indicated that D2 ubiquitination in the

143 n of ABBP-1 from an active apoB mRNA editing tissue extract inhibits its editing activity.

144 on of a P450 enzyme system with cofactor and tissue extract is done under a mixture of (18)O(2)/(16)O

145 t the low pH used for peptide isolation from tissue extracts, is even more active than QL9 in cytotox

146 e detected on immunoblots of mouse cytosolic tissue extracts; it was most highly expressed in spleen,

147 s from contact lenses, had no equivalents in tissue-extracted mucins.

148 cal production of antibodies was measured in tissue extracts, nasal lavage fluid, and sera by using m

149 OSM expression was measured in tissue extracts, nasal secretions, and bronchoalveolar l

150 precipitates with the beta(2)-AR in cell and tissue extracts, nucleating a signaling complex that inc

151 Myocardial tissue extracts obtained 24 hours after CCPA treatment w

152 A was detected in all animals from pulmonary tissue extracts obtained at necropsy.

153 legans, but has not been detected in several tissue extracts of Mus musculus.

154 An ELISA of tissue extracts of normal prostate, high-grade prostatic

155 demonstrated with heart and hindlimb muscle tissue extracts of rats infused with [2,4,6,8-13C4]-octa

156 cyclododecadiene, while in liver and adipose tissues extracts only a single monohydroxy-pentabromocyc

157 y known phosphoinositide present in cell and tissue extracts or produced in kinase and phosphatase as

158 n for distinguishing these isozymes in crude tissue extracts or subcellular fractions; that is, activ

159 induced DNA damage in mouse liver and testis tissue extracts prepared at regular intervals over the c

160 Therefore tissue extracts prepared for chemical analysis are not a

161 utility of the assay was demonstrated using tissue extracts prepared from a group of taxonomically d

162 nd mass spectrometry analysis of Gb4Cer from tissue extracts remains challenging.

163 iated apoB mRNA editing activity of in vitro tissue extracts requires the presence of Hsp70/ABBP-2.

164 Western blotting of tissue extracts revealed a diffuse smear with a mean siz

165 Northern analysis of rat tissue extracts showed that rat msrA mRNA is present in

166 Analysis of tissue extracts spiked with steroids revealed that most

167 mum catalytic activity of aconitase in total tissue extracts, suggesting that a cytosolic isoform of

168 de (oxidized + reduced forms) was noted from tissue extracts, suggesting that the loss in contrast as

169 ion-PCR analysis of RNA isolated from rabbit tissue-extracted T. pallidum additionally showed that tp

170 show that IAA-RP (i) is present in brain and tissue extracts that exhibit I-R activity; (ii) is prese

171 Although both MMP were detected in tissue extracts, the differences in expression levels an

172 In some lung tissue extracts, the eicosanoid metabolites 5-oxo-eicosa

173 In whole-tissue extracts, the expression of IL-32 protein was sig

174 the physiological range and the metabolizing tissues extract their required oxygen from blood at a lo

175 normalized to the DNA content of the various tissue extracts to approximate normalization to the numb

176 assess the metabolites found in biofluids or tissue extracts to define a metabolic profile that descr

177 56 PCR-based assays performed robotically on tissue extracts to determine simultaneously the presence

178 led casein, meat myofibrillar and connective tissue extracts to explore their effects on meat structu

179 e and measure the viscoelastic properties of tissue extracts to provide the first force-velocity curv

180 TSG-6 was present in arthritic joint tissue extracts together with the heavy chains of inter-

181 ngly, only a six-line signal was detected in tissue extracts under these conditions.

182 BA, glutamate and glutamine were assessed in tissue extracts using (13)C-edited (1)H nuclear magnetic

183 Analysis of the tissue extracts using acid precipitation demonstrated th

184 ds on processed and stained liver tissues or tissue extracts using current standard analytical techni

185 avior of Gbeta(5), RGS7, RGS9, and Galpha in tissue extracts using immunoprecipitation and convention

186 ication of endogenous substrates of P450s in tissue extracts using metabolomic and isotopic labeling

187 spartate was measured at five time points in tissue extracts using scintillation counting and 13C nuc

188 Accumulation of cAMP in the tissue extract was determined by radioimmunoassay (RIA).

189 and cyclic adenosine monophosphate (cAMP) in tissue extracts was measured by radioimmunoassay, IP3 pr

190 melanogenic activities of individual adipose tissue extracts was noted.

191 Using this method to fractionate soluble tissue extracts, we identified the muscle isoform of pho

192 phonate referred to as FP-biotin, with crude tissue extracts, we quickly and with high sensitivity de

193 The sample detection limits in in vivo tissue extracts were 100 pg and 5 pg on-column for LC/MS

194 Tissue extracts were also analyzed by MALDI wide-isolati

195 Culture media, digestion supernatants, and tissue extracts were assayed for sulfated glycosaminogly

196 The KCa stimulatory effects of target tissue extracts were blocked by a neutralizing pan-TGFbe

197 As samples, both model proteins and tissue extracts were employed.

198 Tissue extracts were examined for ERK activation by phos

199 Murine tissue extracts were found to contain pepstatin-inhibita

200 Tissue extracts were found to influence the LC-MS/MS res

201 ogenous nitrotyrosine-containing proteins in tissue extracts were poor substrates.

202 Tissue extracts were prepared and analyzed for protease

203 teral nephrectomy was performed and cortical tissue extracts were prepared.

204 striatal tissue was homogenized to generate tissue extracts which were added to E14.5 ventral mesenc

205 d investigated the function of TSLP in nasal tissue extracts with a bioassay based on activation of h

206 nd less ROS in their roots apices (tested in tissue extracts with Amplex Red).

207 of FDH activity in RAT1 cells and in murine tissue extracts with antibody to FDH does not diminish t

208 ted to be useful in identifying reactions in tissue extracts with orphan human P450s.

209 ith wide-isolation MS/MS for analysis of the tissue extracts with scan-by-scan COC-to-COC-d(3) normal

210 of HNA and HNE were confirmed by spiking the tissue extracts with synthetic metabolites and finally b

211 Incubation of human brain postmortem tissue extracts with urocortin and urotensin resulted in

212 s telomerase detection in mammalian cell and tissue extracts with very low telomerase activity levels

213 vo sequencing of neuropeptides directly from tissue extract without any genomic information.