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1 hod were compared with previous estimates of average molecular weight.
2 with varying compositions at a given number-average molecular weight.
3 ilar despite the 100 kD difference in weight-average molecular weight.
4 determine the absolute value for the number average molecular weight.
5 unctionalized polymers with twice the number average molecular weight.
6 s accuracy consistent with their theoretical average molecular weights.
7 minated polymers at nearly equivalent number average molecular weights.
8 charge state distribution (z = 15+ to 26+), average molecular weight (141.7 to 169.6 kDa), and phosp
9 olesterol, vitamin E, polyethylene glycol of average molecular weight 2,000 or 5,000, N-octyl-oligo-o
10 n reducing ability, but provided the highest average molecular weight ( 7 kDa), followed by commercia
11 ed at t = 30 mins with 150 mg/kg of dextran (average molecular weight 70,000 daltons) as a 5% (weight
12 city (94% rr), and control (predicted number-average molecular weight and 1.14 molecular weight distr
15 ots, a linear correlation between the number-average molecular weight and the monomer conversion, and
17 amolecular polymers is found to decrease the average molecular weight and to enhance ring formation,
21 ly, although empirical relationships between average molecular weights and monomer have been establis
23 id poly(ester ether) prepolymers with number-average molecular weights between 4 and 6 x 10(3) g/mol
25 these NRE oligosaccharides afforded a number-averaged molecular weight consistent with that expected
26 Using a 3-cm-long polysulfone membrane with averaged molecular weight cutoff of 30 kDa in a concentr
27 for charge state deconvolution, monoisotopic/average molecular weight determination and quantitation
29 indicated significant changes in the weight average molecular weight distribution of the control ver
32 ight-averaged molecular weight to the number-averaged molecular weight) for the PEG degradation were
33 g in enzymes that exhibit a decreased weight average molecular weight in comparison to that of the wi
34 Novozym 435 produced polyesters with weight average molecular weights limited to 2900 Da due to prec
38 ion yield, galacturonic acid (GalA) content, average molecular weight (M(w,ave)), intrinsic viscosity
39 monomer-to-initiator ratio 200:1, PHB number-average molecular weights (M(n)) are proportional to con
40 with initial monomer ratios and with number average molecular weights (M(n)) ranging from 1.69 to 2.
43 e x 2.4 mum deep) from relatively low number-average molecular weight (Mn < 3000) polydisperse thin f
44 NMR, GPC, FT-IR, and UV-vis and had a number average molecular weight (Mn) of 24,000 and a polydisper
47 c phthalic acid based polyesters (the number-average molecular weights (Mn) 1770 to 10000 g/mol and s
49 tohumification denoted by an increase in the average molecular weight (MW) and the double bound equiv
51 (cOACOE) in high yield (95%), with a weight-average molecular weight (Mw) of 1.6 kDa and polydispers
53 POPC) complexes, with i = 23-29, and have an average molecular weight (MW) of 38.2 +/- 3.3 kDa at pH
54 total, three different thiol-modified PEGs (average molecular weight (MW), 900, 1500, and 5000 g mol
55 turonic acid content (52-59% w/w) and weight-average molecular weights (Mw, 1.7-3.8 x 10(6)g/mol) com
60 tation equilibrium analysis yielded a weight-average molecular weight of 18811, indicating apoA-V(1-1
64 ant concentrations or with gelatin solution (average molecular weight of 30 kDa) of comparable viscos
65 Hydrodynamic experiments yielded a weight average molecular weight of 34000, indicating apoA-I-(44
66 terminated oligomeric ethylene oxide with an average molecular weight of 350 Da) undergo marked chang
68 (13)C NMR and GPC and found to have a number average molecular weight of 4420 and a polydispersity of
71 s that it provides a firm upper bound on the average molecular weight of DOM, based on the kinetic li
74 f SCs was ca. 186 per brush molecule and the average molecular weight of the brush molecules was ca.
76 years) there is little change in the weight-average molecular weight of the chains, and the levels o
78 I-MS mass spectra pattern indicated that the average molecular weight of the OA fraction ranged betwe
82 to avoid hydrodynamic chain scission (weight-average molecular weights of 400 to 1000 kg/mol) and rev
84 s an important technique to characterize the average molecular weights, oligomer repeat units, and en
87 ite but exhibited a strong relationship with average molecular weight, suggesting that FI might be a
89 itivity index (i.e., the ratio of the weight-averaged molecular weight to the number-averaged molecul
90 to produce PgammaBL materials with a number-average molecular weight up to 30 kg mol(-1) and with co
92 s in addition to the linear nature of number average molecular weight versus conversion plots and mon
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