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1 a](2+) IM-MS profiles with reduced conformer microheterogeneity.
2 formation on protein glycosylation and their microheterogeneity.
3 es use more than one poly(A) site, excluding microheterogeneity.
4 played human-like conformational freedom and microheterogeneity.
5 lso at work in tumors and may underlie tumor microheterogeneity.
6 llels the progressive decline of the network microheterogeneity.
7     We sought a genetic explanation for this microheterogeneity.
8 carbohydrate analysis to a detailed level of microheterogeneity.
9 inogen 2 is insufficient to account for this microheterogeneity.
10 by O-glycosylation with differing degrees of microheterogeneity; 9 sites of O-mannosylation and 14 si
11     The unusual morphology was attributed to microheterogeneity among Isf molecules.
12                                       Target microheterogeneity and antibody glycan specificity are t
13 th immunoaffinity enrichment detects protein microheterogeneity and can quantify different isoforms.
14 enotyping by FAFLP analysis revealed genetic microheterogeneity and differentiated otherwise "identic
15 logical methods were used to investigate MDL microheterogeneity and function in this species.
16 rgeted quantitative investigation of protein microheterogeneity and is well suited for assessment of
17 ations and genetic variants increase protein microheterogeneity and may play important roles in biolo
18 mass spectrometry enabled us to identify the microheterogeneity and relative abundance of glycans on
19  a structural basis for some of the observed microheterogeneity, and have implications with regard to
20 but complicated by the intricate structures, microheterogeneity, and the limitations of current tools
21 nteracting the detrimental manifestations of microheterogeneity are presented.
22 so avoids additional introduction of protein microheterogeneity as the result of labeling reaction.
23  membrane association by altering structural microheterogeneity at the membrane surface.
24        Overall, the data describe the glycan microheterogeneity at the PSGL-1 N-terminus.
25                           Analysis of glycan microheterogeneity at this site is complicated by the pr
26 anisms providing a window into understanding microheterogeneity, bacterial speciation, and taxonomic
27           In addition, the peptide exhibited microheterogeneity because of differential mono- and dih
28 F-actin recruitment or depletion, so F-actin microheterogeneities cannot explain the deep penetration
29 f metal concentrations can be compromised by microheterogeneity commonly referred to as the "nugget e
30 minogen 2 displays a further well documented microheterogeneity dependent on the N-acetylneuraminic a
31 glycopeptides remains challenging due to the microheterogeneity (different glycoforms attached to one
32 nd IGF1, suggesting that FGF2 amino-terminal microheterogeneity does not alter mitogenic activity.
33   Although distinct regions for the onset of microheterogeneity have previously been proposed, within
34 urther indicated by four mutations and three microheterogeneities in 3,255 nucleotides during 17 days
35                                              Microheterogeneities in glycosylation were characterized
36 ated forms of both enzymes indicate that the microheterogeneity in carbohydrate structure may be resp
37 pture microdissection in revealing molecular microheterogeneity in complex neoplasms.
38 sequencing and by 5' RT-PCR and demonstrated microheterogeneity in GARP polyadenylation by 3' RT-PCR.
39              Even the cleaved trimers showed microheterogeneity in gp41 glycosylation.
40 o P450 provides a novel method for assessing microheterogeneity in heme orientation and raises questi
41 hich limits understanding of the role of MBP microheterogeneity in human physiology and disease.
42 rent in the approach: the widespread genomic microheterogeneity in naturally occurring prokaryotic po
43 l NPCs, and suggested both heterogeneity and microheterogeneity in NUP62 and NUP214 immunolabeling am
44             The altered astrocytes display a microheterogeneity in phenotypes, even neighboring cells
45      We also show that there is considerable microheterogeneity in pJM1-like plasmids from virulent s
46                                      Because microheterogeneity in the amino acid sequence of the var
47 the protonation state of His179 gave rise to microheterogeneity in the aromatic donor molecule bindin
48 ysis of natural Cbs junctions confirmed that microheterogeneity in the macronuclear telomere addition
49 CF) sputum do not address the high degree of microheterogeneity in the rheological properties of the
50 a meningitidis has demonstrated considerable microheterogeneity in the variable region of LOS due to
51                                     Sequence microheterogeneity including point mutations and duplica
52 ed for the determination of the IgG N-glycan microheterogeneity, including MS methods for the analysi
53 served, it appeared that preexisting lateral microheterogeneities led to compositionally distinct tra
54  in non-neoplastic colon cells, and sequence microheterogeneity occurs within individual colonic muco
55 ur data analysis suggested strong macro- and microheterogeneity of 3'/5' end positions of individual
56 od, we compare the mechanical properties and microheterogeneity of actin filament networks containing
57 ifferences in the number of sialic acid, the microheterogeneity of bovine serum apotransferrin glycan
58    Here, we charted in detail the structural microheterogeneity of C9 purified from human blood serum
59 tic ER cisterns provide spatial and temporal microheterogeneity of Ca2+ signalling, acting not only a
60 escribed here can provide information on the microheterogeneity of cancer cell populations in terms o
61    Degradation of the beta-chain resulted in microheterogeneity of cleavage sites at beta Asp 123-Leu
62 r, the technique allowed us to observe glyco-microheterogeneity of FET as well as establish the prese
63                 We have observed the highest microheterogeneity of glycoforms at the N187 site of HPX
64 rtant implications for the role of regulated microheterogeneity of glycosylation in the CNS.
65                         While the structural microheterogeneity of heparin is predominantly biosynthe
66                                 Although the microheterogeneity of native human GALT has long been re
67 with carboxypeptidase B to reduce the charge microheterogeneity of partial Arg32 truncation.
68 spectrometry is essential to determining the microheterogeneity of protein glycosylation.
69         Proteomic analysis mapped structural microheterogeneity of signal peptide cleavage at the ami
70 nt activation of Rho decreases the degree of microheterogeneity of the cytoplasm.
71 ength of DNA influence the microrheology and microheterogeneity of the DNA within the nucleus.
72                                          The microheterogeneity of the linear DNA solutions increases
73 sented for rapid assessment of site-specific microheterogeneity of the two potential N-linked glycosy
74                     To better understand the microheterogeneity of this protein, the 2086 genes from
75 e demonstrate a unique postsynaptic receptor microheterogeneity on chick parasympathetic ciliary gang
76 allenging structures and the fact that their microheterogeneity precludes their isolation in single a
77 lysis provided a detailed view of the glycan microheterogeneity present on the IL9 portion of the rec
78 more than one unique poly(A) site (excluding microheterogeneity sites), and 13% had four or more poly
79 nalysis of recombinant gp120 revealed glycan microheterogeneity sufficient to explain the existence o
80 x glycoproteins that present a wide range of microheterogeneities that requires multiple analytical m
81 15A mutant of MurA was utilized to avoid the microheterogeneity that arises in the wild-type MurA fro
82 nd a microscopic description of the proposed microheterogeneity that exists is still not clearly esta
83 o assess the biological relevance of the IgG microheterogeneities thus providing valuable information
84        This methodology permits glycoprotein microheterogeneity to be evaluated in a time frame of ap
85 geting due to a unique postsynaptic receptor microheterogeneity - under one presynaptic terminal, alp
86         The analysis of site-specific glycan microheterogeneity was illustrated for the CD44 fusion p
87                                              Microheterogeneity was observed in the 16S rRNA gene seq
88              Translated MBP exhibits extreme microheterogeneity with numerous alternative splice vari
89 d modules that facilitates the resolution of microheterogeneity within hard-to-assemble repetitive DN
90             The matrix therefore shows great microheterogeneity, within which numerous microenvironme

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