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1 sent protein aggregates that contain several blood proteins.
2 ytic activity may influence cross-linking of blood proteins.
3 ed from fragments of extracellular matrix or blood proteins.
4 state-of-the-art methods available mostly on blood proteins.
5 of proteases working collectively to degrade blood proteins.
8 These initial efforts were centered around blood protein adsorption on biomaterials and related mec
9 T cells to peptide-MHC complexes, results in blood protein Ags having a profound effect on thymic T c
14 s in our understanding of control of soluble blood proteins and blood cell receptors by functional di
17 gested that alterations in brain structures, blood proteins and inflammation potentially contribute t
18 whether DNA is either bound to aggregates of blood proteins and lipid micelles or intrinsically assoc
19 ics of this versatile interface, interfering blood proteins and potential interferences associated wi
20 t a >25 million-fold excess of contaminating blood proteins and represents a 4 order of magnitude imp
21 lead to undesired peptide interactions with blood proteins and self-aggregation due to exposed hydro
22 strongly conserved among vitamin K-dependent blood proteins and, in addition to a high relative conte
26 ise the integrity of this barrier, and allow blood proteins as large as albumin to gain access to the
29 results demonstrate that dynamic changes in blood proteins associated with disease severity can pote
30 evaluated the association between a panel of blood proteins at initial presentation of bacteremia and
31 -PSMA-1007 demonstrated significantly higher blood protein binding and bone uptake than the other tra
38 ls that predict TEG curve outputs from input blood protein concentrations, to facilitate treatment de
40 we aimed to determine whether levels of cord blood proteins differ between the offspring of asthmatic
41 gut extracts, while in vitro fluorescent and blood protein digestion assays revealed important substr
45 ion has been paid to serum albumin, the main blood protein, even though blood disposal is a severe pr
49 , in which brain tissue becomes permeable to blood proteins, extravascular fibrin deposition correlat
54 y quenching with acetonitrile to precipitate blood proteins followed by analysis on an LC-electrospra
55 ales have access to human hosts that provide blood proteins for egg development, conspecific males th
57 entation of various extracellular matrix and blood proteins generates antiangiogenic substances that
60 oach is demonstrated through the assays of a blood protein human alpha-thrombin and an oncoprotein hu
61 arriers, degradation of hemoglobin and other blood proteins, immune evasion, and activation of inflam
63 nces allowed the extravasation of endogenous blood proteins, including albumin and immunoglobulin, as
64 omparative functional multiomics showed that blood proteins induce distinct receptor-mediated transcr
66 and binding.Von Willebrand factor (VWF) is a blood protein involved in clotting and is proposed to be
67 g genes encoded stress response proteins and blood proteins involved in coagulation that were differe
69 However, direct capillary electrophoresis of blood proteins is challenging due to its high content of
70 We show that initial degradation of host blood proteins is ordered, occasionally redundant, and s
73 PGSs for common complex diseases and traits, blood protein levels, and brain and other organ morpholo
78 in reversing inactivation by the mixtures of blood proteins, membrane lipids, and fatty acids studied
80 illebrand factor, an ultralarge concatemeric blood protein, must bind to platelet GPIbalpha during bl
85 cts from reactions with nucleophilic loci of blood proteins, particularly Cys34 of human serum albumi
88 concentrations of a billion times lower than blood proteins, poses a significant challenge for early
91 ib showed a wider spectrum of cardiovascular blood protein reduction, but the protein reduction effec
92 ciated with cardiovascular risks, we studied blood proteins related to inflammation and cardiovascula
94 (SWCNT) and use it against a panel of human blood proteins, revealing a specific corona phase that r
95 Willebrand factor (VWF), a large multimeric blood protein, senses changes in shear stress during ble
97 lar dynamics simulations to demonstrate that blood proteins such as bovine fibrinogen (BFG) can absor
100 von Willebrand factor (VWF) is a multimeric blood protein that acts as a mechanical probe, respondin
102 of inhibitory proteoglycans is induced by a blood protein that leaks in the CNS after vasculature ru
103 We focus on the complement system of ~40 blood proteins that bind microbes, nanoparticles, and me
104 ource for investigation of the immunology of blood proteins that could support therapeutic targeting
105 We also identified a temporal signature of blood proteins that was significantly different at early
106 siological changes, allowing them to utilize blood protein to develop eggs: clearing excess fluid, di
107 our knowledge, this is the first study with blood proteins to show that, in addition to the aromatic
108 sed of tryptic peptides from human and mouse blood proteins using high-resolution time-of-flight mass
111 function of the mechanosensitive, multimeric blood protein von Willebrand factor (VWF) is dependent o
112 acid (bis-ANS) to hydrophobic pockets in the blood protein von Willebrand factor (VWF) is enhanced up
116 the unique optical anisotropy properties of blood proteins, which undergo structural alterations at
117 ssociations of 368 inflammatory-related cord blood proteins with birth weight or BWR and with early l