ライフサイエンスコーパス: emu

1 ion Ms, measured at 5 K, has a value of 92.0 emu/g for x=0.15.

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

4 yed a saturation magnetization reaching 1.09 emu/g.

5 ity of ~30 Oe, a remnant magnetization of 10 emu.Oe/mol, and a canting angle of 0.5 degrees .

6 , and remnant magnetizations of 9075 and 102 emu.Oe/mol, respectively.

7 and is close to the calculated value of 116 emu/g for the stoichiometric compound (x=0).

8 zation of PASP-IO nanoparticles is about 117 emu/g of iron, and the measured r2 and r2* are 105.5 and

9 re shows good magnetic susceptibility (180.2 emu/g).

10 hows a very small static magnetic moment ( 2 emu/cm(3)).

11 base composites reach 1.908 S cm(-1), 28.20 emu g(-1), 16.66 emu g(-1) and 3604.79 Oe, respectively.

12 saturation magnetization (Ms) value of 48.3 emu g(-1).

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

19 s with saturation magnetizations of up to 42 emu/g microparticle.

20 and increases magnetization from 4.7 to 65.5 emu/g.

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

23 reach 1.908 S cm(-1), 28.20 emu g(-1), 16.66 emu g(-1) and 3604.79 Oe, respectively.

24 ses gradually with x and has a value of 60.7 emu/g for x=0.86.

25 a high saturation magnetization (Ms) of 48.9 emu/g, which allows it to be attracted rapidly to a magn

26 high TC (700 K) and high magnetization (5.9 emu/g).

27 The two affected emus were found to be homozygous for a 2-bp deletion, 10

28 Three normal and two affected emus were studied for nucleotide sequence covering the e

29 in food sources available to the Australian emu, beginning about the time of human colonization; a c

30 ontiguous sequence from the kiwi, cassowary, emu and two tinamou genera.

31 Dromaius (emu) eggshell occur frequently in deposits from >100 ka

32 esis, forward genetic screens isolated eight emu (enhancer of the nuclear migration defect of unc-84)

33 Carbon isotopes in fossil emu (Dromaius novaehollandiae) eggshell from Lake Eyre,

34 Unlike the human gene, emu NAGLU appeared to be highly polymorphic: 19 variatio

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

37 In Dromaius novaehollandiae (emu), a progressive neurologic disease was recently disc

38 , we analyze the genome and transcriptome of emu (Dromaius novaehollandiae) and confirm that most gen

39 Ratites (ostriches, emus, rheas, cassowaries, and kiwis) are large, flightle

40 The other emu mutations potentially represent other components of

41 alluses; and in two outgroups, Paleognathae (emus) and Crocodilia (alligators).

42 The emu timing circuits showed the ancestral (plesiomorphic)

43 rnum and wing size in a flightless bird, the emu.

44 iological data on the timing circuits in the emu, Dromaius novaehollandiae, and compare these results

45 It was observed that the emu NAGLU gene is structurally similar to that of human

46 This expression bias suggests that the emu sex chromosomes have become masculinized, even in th

47 remains that exhibit mass spectra similar to emu whole blood.