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2 f 0.05 emu g(-1) at H = 2 T at 300 K (0.0006 emu g(-1) for FeOOH/WMSN-PEG), which is 2 orders of magn
3 shows very low magnetization (M(z)) of 0.05 emu g(-1) at H = 2 T at 300 K (0.0006 emu g(-1) for FeOO
8 zation of PASP-IO nanoparticles is about 117 emu/g of iron, and the measured r2 and r2* are 105.5 and
11 base composites reach 1.908 S cm(-1), 28.20 emu g(-1), 16.66 emu g(-1) and 3604.79 Oe, respectively.
13 The large saturation magnetization (96.3 emu/g) of the synthesized nanoparticles allows fast sepa
14 ures, with magnetization (M(S)) values of 30 emu/g (1.63 mu(B)/f.u.) and 33 emu/g (1.79 mu(B)/f.u.) f
15 values of 30 emu/g (1.63 mu(B)/f.u.) and 33 emu/g (1.79 mu(B)/f.u.) for the ODA- and OLA-capped nano
16 amagnetic behavior, with chiTIP = 6 x 10(-4) emu mol(-1), but its charge transport behavior, with sig
17 usceptibility, chip approximately 4.5x10(-4) emu/mol and is assigned a resonating valence bond (RVB)
18 f the remnant magnetization from 1200 to 400 emu.G/mol, indicating a net antiferromagnetic interactio
21 an any current ultrasmall iron oxide NPs (>5 emu g(-1)) reported to date, hence ensuring the low r2 (
22 durability, and high magnetic saturation (59 emu g(-1)), which can effectively catalyze pentyl valera
25 a high saturation magnetization (Ms) of 48.9 emu/g, which allows it to be attracted rapidly to a magn
29 in food sources available to the Australian emu, beginning about the time of human colonization; a c
32 esis, forward genetic screens isolated eight emu (enhancer of the nuclear migration defect of unc-84)
35 The availability of mutation screening in emus now permits early detection of MPS IIIB in breeding
36 molecular basis, the sequences of the normal emu NAGLU cDNA and gene were determined by PCR-based app
38 , we analyze the genome and transcriptome of emu (Dromaius novaehollandiae) and confirm that most gen
44 iological data on the timing circuits in the emu, Dromaius novaehollandiae, and compare these results
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