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1 laced in a liquid medium released about nine major proteins.
2 servation of tissue structures as well as of major proteins.
5 nterica serovar Typhimurium LT2 encoding the major protein acetyltransferase (Pat) enzyme that, in co
7 tory factor (IRF)-2 was found to be the only major protein, among the IRF family proteins, that bound
8 ll components of paraspeckles including four major proteins and Neat1 displayed a circadian expressio
9 tin, caldesmon, myosin IC, and annexin A2 as major proteins and was noted to exhibit compositional si
10 rate high-level expression of genes encoding major protein antigens in the bovine subspecies of Mycob
11 high-density lipoprotein cholesterol and its major protein, apoAI, are largely influenced by the rate
12 The cardioprotective action of HDL and its major protein, apolipoprotein A-I (apoA-I), is well-esta
13 -established, yet the function of the second major protein, apolipoprotein A-II (apoA-II), is less cl
14 is almost 80% identical to human PRMT1, the major protein arginine methyltransferase activity in mam
18 einuria levels (30-300 ppm) and identify the major proteins associated with the microproteinuria.
20 ll characterized in seeds, and oleosins, the major proteins associated with their surface, were shown
21 s of normal vitreous and plasma detected two major proteins at approximately 35 kDa and approximately
22 otypic subset-specific CLL mAbs, revealing a major protein band at approximately 225 kDa that was ide
23 matography-purified tryptic fragments of the major protein band matched sequences of human and murine
24 organisms revealed consistent labeling of a major protein band of purified HR-LBP at approximately 2
28 However, when cells proliferate, at least 10 major proteins bind directly or indirectly to the 5' cap
30 The bacterial Sec-dependent system is the major protein-biogenic pathway for protein secretion acr
34 ation on the products of 646 genes from four major protein classes (G protein-coupled receptors, nucl
35 Messenger RNA decay mediated by the c-fos major protein coding-region determinant of instability (
37 lization of network modules, which represent major protein complexes in protein-protein interaction a
39 es on human apolipoprotein A-I (apoA-I), the major protein component in high-density lipoproteins, th
42 ion, and with glycoproteins representing the major protein component of biological fluids this makes
43 unctional amyloid protein CsgA, which is the major protein component of curli fibers assembled by ent
50 we show that apolipoprotein A1 (apoA1), the major protein component of high density lipoprotein (HDL
51 ported that apolipoprotein A-I (apoA-I), the major protein component of high density lipoprotein, is
52 been shown to mimic apolipoprotein A-I, the major protein component of high density lipoproteins and
53 operties of apolipoprotein A-I (apoA-I), the major protein component of high density lipoproteins.
58 tified the serine protease HtrA1/PRSS11 as a major protein component of human articular cartilage, wi
61 ng evidence suggests that alpha-synuclein, a major protein component of Lewy bodies (LB), may be resp
62 Mutations in the gene encoding TDP-43-the major protein component of neuronal aggregates character
64 idue islet amyloid polypeptide (IAPP) is the major protein component of the amyloid deposits found in
65 ype 4 pili system homologs, in the T2SS, the major protein component of the central pseudopilus is de
66 unctional amyloid fibres that constitute the major protein component of the extracellular matrix in p
70 et amyloid polypeptide (IAPP, amylin) is the major protein component of the islet amyloid deposits as
76 e region DNA binding protein (TDP-43) is the major protein component of ubiquitinated inclusions foun
77 minal region of apolipoprotein B (apoB), the major protein component of very low-density lipoprotein
78 d that apolipoprotein B (apoB), which is the major protein component of VLDL and LDL, bound PrP(Sc) t
79 ng ACSL3, secretion of apolipoprotein B, the major protein component of VLDL, was inhibited and the l
82 major intrinsic protein that constitutes the major protein component on the symbiosome membrane (SM)
87 we investigated the associations between the major protein components of HDL (apoA1, apoA2, and apoC3
88 ral nervous system depends upon induction of major protein components of myelin, such as peripheral m
90 es produce essential signaling molecules and major protein components of the pial basement membrane d
91 1) and HP1-ORC-associated protein (HOAP) are major protein components of the telomere cap in Drosophi
93 vidin affinity chromatography, and the three major protein components were determined by N-terminal s
94 ibrio cholerae biofilm matrix contains three major protein components, RbmA, Bap1, and RbmC, which ar
95 However, the structural organization of the major proteins composing the lamina is poorly defined.
96 etween amyloid-beta (Abeta) and tau, the two major proteins composing the neuropathological lesions d
97 Plug size was associated with divergence in major protein composition of seminal vesicle fluid, sugg
98 on of the protein.DNA complex (i) effected a major protein conformational change and (ii) was prevent
102 lipid-poor apolipoprotein A-I (apo A-I), the major protein constituent of HDL, and the mature spheric
103 for the structure of apolipoprotein A-I, the major protein constituent of HDL, in its lipid-free and
108 gene encoding myelin protein zero (MPZ), the major protein constituent of peripheral myelin, can caus
114 the structural components of caveolae, their major protein constituents, are the semicarbazide-sensit
116 promiscuous and not exclusive, although the major proteins copurified with PSBS were components of t
119 relationship is at the heart of biology, and major protein deformations are correlated to specific fu
123 in the targeting of substrates to all three major protein degradation pathways in mammalian cells: t
125 at S-nitrosoglutathione reductase (GSNOR), a major protein denitrosylase, provides a key regulatory l
128 oxin (Trx), Trx reductase, and NADPH, is the major protein-disulfide reductase of the cell and has nu
130 ells were found to be composed of only three major proteins: eIF4isoE, which is primarily a cytoplasm
136 mes, novel fusion proteins, and loss of some major protein families including ones associated with ch
145 tep in Cu homeostasis, the properties of the major protein, hCTR1, that mediates Cu uptake, and the s
149 rt by regulating the oligomeric state of the major protein import gate, the TOM complex, and the inne
150 hat at the 144 h time point, the mass of the major protein in ADC-depleted human plasma had an additi
153 Proteolytic breakdown of E-cadherin, the major protein in epithelial cell junctions, has been pro
154 pendent oxidation of apolipoprotein A-I, the major protein in HDL, blocks HDL's ability to remove exc
158 n Parkinson's disease (PD) because it is the major protein in Lewy bodies, and because its gene mutat
160 of 43 kDa (TDP-43) has been recognized as a major protein in normal and pathological ageing, increas
162 n the physicochemical properties of kafirin, major protein in sorghum, and its stability against peps
164 axons, and increasing local synthesis of the major protein in the myelin sheath, myelin basic protein
165 ed their common target antigen to be MrkA, a major protein in the type III fimbriae complex, and show
172 uctural organization and functional roles of major proteins in these organelles can provide critical
173 is study addressed the identification of the major proteins in these secretory vesicles that provide
175 n factor ICBP90 (also known as UHRF1) is the major protein interacting with the MIF microsatellite.
176 ome Organization (HUPO), and is supported by major protein interaction data providers, in particular
178 terize heme detoxification protein, PfHDP, a major protein involved in hemozoin formation, as a novel
180 creased iNOS expression and S-nitrosation of major proteins involved in insulin signaling, thereby re
181 viously identified the genes that encode the major proteins involved in the biosynthesis of M. catarr
184 n of DlgS97, a SAP97 homolog, and one of two major protein isoforms encoded by dlg1 via alternative s
186 plicing of the WT1 transcript generates four major protein isoforms, each having different functional
190 he apolipoprotein E family consists of three major protein isoforms: apolipoprotein E4 (ApoE4), ApoE3
191 he SSeCKS/GRAVIN/AKAP12 gene ("SSeCKS") is a major protein kinase (PK) C substrate that exhibits tumo
192 osphorylation by protein kinase A (PKA), the major protein kinase activated in response to glucose, i
193 of the HIF-alpha network, we identified the major protein kinase C substrate MARCKS (myristoylated a
194 alanine-rich C kinase substrate (MARCKS), a major protein kinase C substrate, binds electrostaticall
197 d not act through Galpha(i/o) or through the major protein kinases activated downstream of G-protein-
198 ults suggest that GSK3beta and CK1/2 are the major protein kinases that contribute to the removal of
199 nt in Schizosaccharomyces pombe contains two major protein kinases, the sensor kinase Rad3 and the ef
200 ed on the conserved sixth region of variable major protein-like sequence expressed (C6)-that were per
201 cence immunoassay (CLIA); and (3) a variable major protein-like sequence, expressed (VlsE) CLIA follo
203 ecently documented that LMP1 induces a third major protein modification by physically interacting wit
206 ic secretion of apolipoprotein-B (apoB), the major protein of atherogenic lipoproteins, is regulated
208 roperties the helices of apoprotein A-I, the major protein of atheroprotective HDL, show promise for
211 e possibility that acrolein might target the major protein of HDL, apolipoprotein A-I (apoA-I), for m
212 lipid-free apolipoprotein A-I (apoA-I), the major protein of HDL, was exposed to MPO or peroxynitrit
219 protein A-I (apoA-I, 243 amino acids) is the major protein of high-density lipoproteins (HDL) that pl
225 plete TbMP18 (band VII), the last unexamined major protein of our purified editing complex, showing i
229 Dsg2 associates with caveolin-1 (Cav-1), the major protein of specialized membrane microdomains calle
235 horylation of connexin 43 (Cx43), one of the major proteins of gap junctions, can adversely impact my
238 A6 (Anx-A5, -A2, and -A6) are quantitatively major proteins of the matrix vesicle nucleational core t
242 ith phorbol myristate acetate revealed three major proteins of ~25, 90, and 100 kDa following chondro
246 that protein disulfide isomerase (PDI), the major protein oxidase of the ER lumen, engages Akita pro
247 literature references and easy links to the major protein (PDB, SWISS-PROT/TrEMBL, PIR-ALN, NCBI Tax
249 have previously reported that PP2A/Balpha, a major protein phosphatase 2A (PP2A) holoenzyme, binds to
251 g a B55delta subunit (PP2A- B55delta) is the major protein phosphatase that acts on model CDK substra
253 dependent kinase (Cdk) 1 while activities of major protein phosphatases, like PP1 and PP2A, appear di
255 ng protein TDP-43 has been identified as the major protein present in the hallmark inclusion bodies o
256 tributes to virulence by degrading MUC2, the major protein present in the small intestinal mucous lay
261 have observed that GC induction of the three major protein products of the Bcl-2 relative Bim (BimEL,
265 data suggest that the CRD may function as a major protein-protein interaction domain of these kinase
267 ave shown that IPSE/alpha-1 (here M-IPSE), a major protein secreted from S. mansoni eggs, can infiltr
276 ion of the fimA and rgpA genes, encoding the major protein subunit of fimbriae and an arginine-specif
277 bits expression of fimA, a gene encoding the major protein subunit of long fimbriae in P. gingivalis;
279 there is considerable variation in PilA, the major protein subunit, both in amino acid sequence and i
280 on, motility, and biofilm formation, and the major protein subunit, PilA, is a promising vaccine cand
282 embrane, but the molecular function of their major protein subunits, the BAR domain-containing protei
283 tical role of STIM1-mediated SOCE and define major protein targets of calcium signaling in neutrophil
284 shift assays showed that C/EBPalpha was the major protein that bound to this site and, consistent wi
285 earance and contained the same complement of major proteins, though only +H2 virions were infectious.
287 an incompletely understood manner from four major proteins to form a homogeneous, transparent extrac
289 l deficits and reduce function of two of the major protein turnover systems: autophagy and proteasome
290 gy 2-containing phosphatase-1 (SHP-1) is the major protein-tyrosine phosphatase that targets two crit
291 t Drosophila centrosomin (cnn) expresses two major protein variants: the centrosomal form (CnnC) and
294 er of the Drosophila eggshell, contains four major proteins (VMPs) that possess a highly conserved "V
295 urface from one of many bloodstream variable major proteins (Vmps) to a unique protein, Vtp (Vsp33).
296 iyamotoi is able to express various variable major proteins (VMPs) to evade humoral immunity and that
298 a time- and cost-effective tool for reducing major proteins, which often interfere with downstream an
299 genomic orientation, and common features of major proteins with human anelloviruses, and PCV2 DNA ma
300 d filling and compensate for the shortage of major proteins with the increased selective accumulation