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1  smallest dynactin subunit, was isolated and microsequenced.
2 lamide gel electrophoresis, and NH2-terminal microsequenced.
3 ansfer membrane, the 30,000 m.w. protein was microsequenced.
4 isolated from these libraries can be readily microsequenced.
5 zed p62 subunit of dynactin was isolated and microsequenced.
6 CBF2 activity was biochemically purified and microsequenced.
7  kinase 1 (CmCPK1), was cloned using peptide microsequences.
8 protein by affinity purification and peptide microsequencing.
9 s of three tryptic peptides were obtained by microsequencing.
10 ed, purified, and finally subjected to Edman microsequencing.
11 tides were analyzed by mass spectrometry and microsequencing.
12 nd protein kinases, as determined by protein microsequencing.
13 d through photoaffinity labeling and protein microsequencing.
14 ach band were analyzed by mass spectrometric microsequencing.
15 age, the purified proteins were suitable for microsequencing.
16 fied by gel electrophoresis and subjected to microsequencing.
17 s of the Sec6-Sec8-Sec15 complex for peptide microsequencing.
18 ng over 70 amino acids identified by peptide microsequencing.
19 ]halothane, and subjected to proteolysis and microsequencing.
20 e first 10 amino acids determined by protein microsequencing.
21 should be compatible with both MALDI-TOF and microsequencing.
22  (35)S-labeled C2GnT-M was established using microsequencing.
23 ure liquid chromatography and amino-terminal microsequencing.
24 een isolated and subjected to amino-terminal microsequencing.
25 ed from the retina, was confirmed by protein microsequencing.
26  be authentic betaB(2)-crystallin by protein microsequencing.
27 ere identified by phosphopeptide mapping and microsequencing.
28 acting proteins by affinity purification and microsequencing.
29 f three N-terminal residues, as confirmed by microsequencing.
30                          Electrophoresis and microsequencing allowed us to identify 20 proteins.
31 mor cell lines prescreened for probable LOH, microsequence alterations of MMAC1 were detected in 12 (
32 nding protein by far-Western blotting and by microsequence analyses of a 34-kDa protein purified by E
33                                              Microsequence analyses of delta demonstrate that this li
34                                              Microsequence analyses of H3 from Tetrahymena, yeast, an
35                                 SDS-PAGE and microsequence analyses revealed that the Mr 64,000 fgl2
36 The 35-kDa protein was identified by peptide microsequence analysis as the human thioesterase II (hTE
37  approach facilitates sample preparation for microsequence analysis at low picomole level.
38                                      Peptide microsequence analysis by capillary high-performance liq
39                                              Microsequence analysis obtained after limited proteolysi
40 e protein which was originally identified by microsequence analysis of a 67.8 kDa protein spot (pI 5.
41                                              Microsequence analysis of LCRF yielded an amino acid seq
42                                              Microsequence analysis of peptides derived from the 100-
43                                              Microsequence analysis of the E1B2 antigen revealed that
44                    Affinity purification and microsequence analysis of the proteins in the doublet id
45                                    Automated microsequence analysis of the purified enzymes establish
46                                        Edman microsequence analysis of the subunits after import perm
47                                              Microsequence analysis of this approximately 80-kDa poly
48                                              Microsequence analysis of two polypeptide components of
49 ors from HeLa nuclear extract and amino acid microsequence analysis performed.
50                                              Microsequence analysis revealed that OE-1 recognized hum
51                                Purification, microsequence analysis, and cross-blotting experiments i
52 10 protein was gel isolated and subjected to microsequence analysis, and the gene was cloned.
53      The primary structure was determined by microsequence analysis, mass spectrometry, and C-termina
54 hase-high performance liquid chromatography, microsequence analysis, mass spectrometry, and immunocyt
55 axima (pumpkin) phloem exudate and, based on microsequence analysis, the cDNA encoding CmPS-1 was clo
56       This identification, initially made by microsequence analysis, was verified by showing that (i)
57 that mimics the effector domain of Rab3A and microsequence analysis, we found calmodulin to be a majo
58 H and the 125-kDa glycoprotein to amino acid microsequence analysis.
59 fic components were identified using peptide microsequence analysis.
60                                      Through microsequencing analysis and chromatin immunoprecipitati
61 ermination, endoglycosidase sensitivity, and microsequencing analysis as a porcine homologue of CD58.
62                               In this study, microsequencing analysis of the radiolabeled downstream
63                    N-terminal and C-terminal microsequencing analysis showed the expected unique term
64 s band was subsequently shown by Western and microsequencing analysis to comprise both the carboxylas
65 terminal amino acid sequence was obtained by microsequencing analysis, and full-length clones were ob
66           By immunoprecipitation and protein microsequencing analysis, we have identified a major cel
67 tide mapping, site-directed mutagenesis, and microsequencing analysis, we identified two major sites
68 ctive protein spot (MW: 44 kDa, pI: 4.5) was microsequenced and the related cDNA was cloned yielding
69  the protein was revealed by automated Edman microsequencing and a computer database search.
70                                      Peptide microsequencing and confirmatory mutagenesis identified
71 cleavage sites were identified by N-terminal microsequencing and electrospray mass spectrometry, and
72                                              Microsequencing and immunoblot analysis revealed that th
73 Analysis of the phosphopeptides by automated microsequencing and manual Edman degradation identified
74 hoto-cross-linking in TnC were determined by microsequencing and mass spectrometry following enzymati
75 ross-linking site for both TnC mutants using microsequencing and mass spectrometry following proteoly
76 Carcinus maenas, was determined by automated microsequencing and MS, and was almost identical to that
77                                      Protein microsequencing and peptide mapping of wild-type and mut
78 itory protein that was identified by peptide microsequencing and protein database analysis as troponi
79  of the pollen oleosins can be identified by microsequencing and specific immunoblotting.
80                         Following N-terminal microsequencing and subsequent isolation of the correspo
81                    PY proteins identified by microsequencing and Western blotting include Cbl, STAT3,
82 s a mixture of alpha- and beta-synucleins by microsequencing and Western blotting.
83 affinity chromatography and characterized by microsequencing and Western blotting.
84 bioactive and intermediate CART molecules by microsequencing and/or high performance liquid chromatog
85 re able to serendipitously purify, partially microsequence, and clone human copine III.
86 n-regulated proteins, FegA, was purified and microsequenced, and a reverse genetics approach was used
87 ne of these spots at pH 5.7 was subsequently microsequenced, and five partial amino acid sequences we
88 e methylesterase-1 (PME-1), was purified and microsequenced, and its cDNA was cloned.
89  amino terminus of cauliflower RPB5 that was microsequenced, and shows 42 and 53% amino acid sequence
90                     The purified protein was microsequenced, and the sequence information was used to
91     Both proteins were identified by peptide microsequencing, and a complementary DNA encoding the hi
92 ization tandem mass spectrometry, N-terminal microsequencing, and immunoblotting with specific antibo
93 elution with the BIR3 binding peptide AVPIA, microsequencing, and mass spectrometry.
94                         Limited proteolysis, microsequencing, and sedimentation analyses indicate tha
95 in was purified and identified by N-terminal microsequencing as heat shock protein 60 (Hsp60).
96 eins labeled in this assay was identified by microsequencing as HSP25, purified as a recombinant prot
97  using 2-dimensional gels and amino-terminal microsequencing as one of a select few [35S]methionine p
98  and its identification by mass spectrometry microsequencing as pregnancy-associated plasma protein-A
99   To this end we purified and identified via microsequencing ATF2 as a major URE- bound and CREB-asso
100 the distribution and subsequent targeting of microsequences by the mutation mechanism.
101                                              Microsequencing by mass spectroscopy and Western blot an
102 s were identified from tryptic digests using microsequencing by tandem mass spectrometry and database
103  Structures were established by NH2-terminal microsequencing, cross-link analysis, electrospray mass
104                                              Microsequence data from phloem-purified 31 kDa protein w
105                      On the basis of protein microsequence data, we conclude that the synthesis of th
106 s, direct [(14)C]halothane photolabeling and microsequencing demonstrated dominant labeling of W9, le
107                                      Protein microsequencing established 3alpha5alpha-P inhibitable p
108 subunits on analytical SDS-PAGE, and protein microsequencing establishes that the GABA(A)R-modulating
109    Purified LRBP was subjected to N-terminal microsequencing followed by homology search, which revea
110 The results obtained from fragmented protein microsequencing have suggested that autocrine motility f
111 novel mass spectrometry strategy and peptide microsequencing identified 33 known proteins, many of wh
112                                      Protein microsequencing identified one of the SH3-binding protei
113                                      Protein microsequencing identified the 90-kDa protein as mitocho
114                     Purification and partial microsequencing identified the protein as an adenine nuc
115                                              Microsequencing identified this protein as the glycolyti
116                                      Peptide microsequencing identified this protein as the product o
117                                              Microsequencing identified this protein as vasodilator-s
118                                              Microsequencing identified three serine residues, each o
119                               The results of microsequencing, immunochemical analysis of 2D-PAGE blot
120 rmined using epitope-defined antibodies, and microsequencing indicated that K18 cleavage occurs at a
121              Immunoaffinity purification and microsequencing indicated that the core peptide of the S
122 ry analysis of peptide fragments and peptide microsequencing, indicates that Cdc37 is comprised of th
123 ve the following primary structures by Edman microsequencing: IWLTALKFLGKHAAKHLAKQQLSKL-NH2 for lycot
124 e VP16 activation domain followed by peptide microsequencing led to the identification of ARC92 as a
125               It is highly desirable to have microsequencing methods that can be used to precisely id
126 found that the SHM mutability hierarchies on microsequence motifs (i.e., SHM hot/cold spots) are most
127 re purified to homogeneity as ascertained by microsequencing of 14-17 N-terminal amino acids.
128                                              Microsequencing of a 17-amino acid peptide of this polyp
129                                              Microsequencing of a p180 peptide revealed 92% identity
130  protein, caveolin-2, was identified through microsequencing of adipocyte-derived caveolin-enriched m
131 ify of the purified protein was confirmed by microsequencing of an endoproteinase glutamic acid-C fra
132                                              Microsequencing of an internal peptide derived from puri
133        By using mass spectroscopy and direct microsequencing of CNBr fragments of phospho-moesin, the
134                                              Microsequencing of cyanogen bromide fragments of purifie
135                                              Microsequencing of DIPP revealed a 'MutT' domain, which
136                                              Microsequencing of five peptides derived from purified p
137                                      Protein microsequencing of fragments isolated from proteolytic d
138                                              Microsequencing of its two tryptic peptides revealed two
139                      Information gained from microsequencing of oligopeptides obtained by tryptic dig
140                                   Amino acid microsequencing of one of these proteins led to the iden
141                                              Microsequencing of partially purified p18 identified it
142                                              Microsequencing of peptide fragments from a cyanogen bro
143                                              Microsequencing of peptides derived from a 50-kDa paxill
144                                              Microsequencing of peptides derived from purified rat pp
145                                              Microsequencing of Src-phosphorylated caveolin revealed
146                                              Microsequencing of the 50-kDa band yielded an amino-term
147                                 Furthermore, microsequencing of the 95 kDa protein yielded 13 peptide
148                                              Microsequencing of the isolated peptide-beads revealed t
149                                              Microsequencing of the most prominent COM crystal-bindin
150 d sequences with those obtained from peptide microsequencing of the purified complex components.
151                             Purification and microsequencing of the strongest band (88 kDa) demonstra
152 n (KuAg) as documented by partial amino acid microsequencing of tryptic digests and immunologic react
153                                              Microsequencing of tryptic peptides from the two protein
154                                   Amino acid microsequencing of two cyanogen bromide-generated peptid
155 hich were successfully identified by protein microsequencing or matrix-assisted laser desorption ioni
156 tic oligopeptide that was not represented in microsequenced peptides of the trans-factor) also recogn
157                                              Microsequencing proved that this protein is the lymphocy
158                                              Microsequencing provided unique peptide sequences of app
159                          Consistent with the microsequencing results pMS100 failed to complement a tr
160 unoaffinity purification of this protein and microsequencing revealed homology to sheep CD58 as well
161                                      Peptide microsequencing revealed that p140 is probably identical
162                                      Protein microsequencing revealed that R-[(3)H]mTFD-MPAB did not
163                                              Microsequencing revealed that the 47 kDa BAF is identica
164                                      Peptide microsequencing revealed that the enriched protein was E
165                                      Peptide microsequencing revealed that the purified protein was v
166 ize exclusion chromatography, and subsequent microsequencing revealed that they are the zeta isoform
167         These polypeptides were purified and microsequenced, revealing that p58/53 is identical to th
168 beads from the library and subjected them to microsequencing, revealing the sequence of the unreacted
169                                      Protein microsequencing reveals that one constituent of this com
170                                              Microsequencing reveals that protease-accessible regions
171                                              Microsequencing showed it to be human endonuclease G, an
172                The sequence was confirmed by microsequencing six peptides of mature REJ and by Wester
173                         We have compared the microsequence specificity of mutations introduced during
174                                              Microsequencing studies identified the GM35 Ag as human
175 ing of Nef function, we used biochemical and microsequencing techniques to isolate and identify Nef-a
176 ain their amino acid sequences using protein microsequencing techniques.
177  we demonstrated by protein purification and microsequencing that ribosomes of maize (Zea mays L.) co
178        We demonstrated by immunoblotting and microsequencing that the EspD protein is secreted via th
179 minus was determined for the beta-subunit by microsequencing the protein purified from etiolated maiz
180 liquid chromatography, together with protein microsequencing, the protein was identified as heregulin
181 igen was purified by immunoprecipitation and microsequenced; the peptides sequenced showed 100% homol
182 S-4 from human embryonic kidney 293 cells by microsequencing through mass spectrometry.
183 rain) G2 and G1 proteins were established by microsequencing to be equivalent to aa 525 and 1046, res
184 lypeptides (12, 32 and 38 kDa) were found by microsequencing to be identical to parts of the predicte
185 ely with two polypeptides that were shown by microsequencing to be the alpha- and beta-subunits of Ac
186 romatography and SDS-PAGE and found by using microsequencing to be the protein flagellin.
187 olypeptide was purified and shown by peptide microsequencing to be the Torpedo ortholog of the small
188 esent in this construct and was subjected to microsequencing to confirm its identity and the site of
189      It is now routine using automatic Edman microsequencing to determine the primary structure of pe
190 his particle and performed mass spectrometry microsequencing to determine their identities.
191 ach of which was subjected to the N-terminal microsequencing to identify the cleavage sites.
192 l I-like ectodomain followed by SDS-PAGE and microsequencing using electrospray (ISI-Q-TOF-Micromass)
193                                   N-terminal microsequencing was performed to simultaneously confirm
194 nous moesin, which was identified by peptide microsequencing, was dependent on phosphatidylglycerol (
195 ed by [(3)H]AziPm were identified by protein microsequencing, we found propofol-inhibitable photolabe
196 ombination of mutational analysis and direct microsequencing, we have determined that this cysteine p
197  chromatographic purification and subsequent microsequencing, we have identified ERSF as TFII-I.
198 by tandem mass spectrometry (TMS), and novel microsequences were identified that indicated a previous
199 protein was subjected to tryptic mapping and microsequencing, which was followed by molecular cloning

 
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