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1 etization at saturation (M(s)) value of 53.0 emu g(-1) from SQUID measurement.
2 ion Ms, measured at 5 K, has a value of 92.0 emu/g for x=0.15.
3 he value of chi(m) T for 3delta approaches 0 emu.K.mol(-1) consistent with formation of a gapped stat
4 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
5 hile showing a magnetization change of 0.015 emu/g.
6 ation magnetic moment of h-CBN reaches 0.033 emu g(-1) at 300 K, which is three times that of as-prep
7  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 yed a saturation magnetization reaching 1.09 emu/g.
9 ity of ~30 Oe, a remnant magnetization of 10 emu.Oe/mol, and a canting angle of 0.5 degrees .
10 , and remnant magnetizations of 9075 and 102 emu.Oe/mol, respectively.
11  and is close to the calculated value of 116 emu/g for the stoichiometric compound (x=0).
12 zation of PASP-IO nanoparticles is about 117 emu/g of iron, and the measured r2 and r2* are 105.5 and
13 oop with a remanent magnetization about 0.14 emu/g and coercive field about 1.8 Tesla (at room temper
14 re shows good magnetic susceptibility (180.2 emu/g).
15 hows a very small static magnetic moment ( 2 emu/cm(3)).
16  base composites reach 1.908 S cm(-1), 28.20 emu g(-1), 16.66 emu g(-1) and 3604.79 Oe, respectively.
17 V), and a large enough magnetic moment (~200 emu/cc), all of which can be tuned by varying the oxygen
18 gnetization of Fe(3)O(4)/CS adsorbent was 25 emu g(-1) and the magnet could easily separate the adsor
19 saturation magnetization (Ms) reaching 17.28 emu/g, remanence (Mr) at 0.29 emu/g, and coercivity (Hc)
20 reaching 17.28 emu/g, remanence (Mr) at 0.29 emu/g, and coercivity (Hc) of 13.71 G.
21  saturation magnetization (Ms) value of 48.3 emu g(-1).
22     The large saturation magnetization (96.3 emu/g) of the synthesized nanoparticles allows fast sepa
23 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
24  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
25 Curie-Weiss behavior for T > 20 K (C = 0.376 emu K mol(-1) and theta = +5.7 K) consistent with local
26 amagnetic behavior, with chiTIP = 6 x 10(-4) emu mol(-1), but its charge transport behavior, with sig
27 usceptibility, chip approximately 4.5x10(-4) emu/mol and is assigned a resonating valence bond (RVB)
28 f the remnant magnetization from 1200 to 400 emu.G/mol, indicating a net antiferromagnetic interactio
29 s with saturation magnetizations of up to 42 emu/g microparticle.
30  M-H loop with remanent magnetization of 3.5 emu/cm(3) was observed at room temperature, and it retai
31 and increases magnetization from 4.7 to 65.5 emu/g.
32 an any current ultrasmall iron oxide NPs (>5 emu g(-1)) reported to date, hence ensuring the low r2 (
33 durability, and high magnetic saturation (59 emu g(-1)), which can effectively catalyze pentyl valera
34 reach 1.908 S cm(-1), 28.20 emu g(-1), 16.66 emu g(-1) and 3604.79 Oe, respectively.
35 e for the magnetism at 300 K (chi(M)T = 0.67 emu.K.mol(-1), u(eff) = 2.31 u(B)), and detectable by pa
36 ses gradually with x and has a value of 60.7 emu/g for x=0.86.
37 nd saturated magnetic moment (M(s) ) of 88.7 emu g(-1) , the highest value reported for SmCo(5) NPs.
38 ctive is to examine the mRNA expression of 7 emu adipokine genes (eFABP4, eSCD1, eAdipoQ, eAdipoR1, e
39 ith H(c) over 15 kOe and M(s) reaching 127.9 emu g(-1) .
40 a high saturation magnetization (Ms) of 48.9 emu/g, which allows it to be attracted rapidly to a magn
41  high TC (700 K) and high magnetization (5.9 emu/g).
42 Back and abdominal fat tissues from 11 adult emus were biopsied at four time points (April, June, Aug
43 mples were collected from each of four adult emus (2 males, 2 females; 5-6 years old) that were free
44                             The two affected emus were found to be homozygous for a 2-bp deletion, 10
45                Three normal and two affected emus were studied for nucleotide sequence covering the e
46 mel, crocodile, emu, kangaroo), emu eggs and emu oil.
47  in food sources available to the Australian emu, beginning about the time of human colonization; a c
48 ontiguous sequence from the kiwi, cassowary, emu and two tinamou genera.
49 etry (LC-QQQ) in raw meat (camel, crocodile, emu, kangaroo), emu eggs and emu oil.
50                                    Dromaius (emu) eggshell occur frequently in deposits from >100 ka
51 required for limb proliferation in the early emu wing bud.
52 esis, forward genetic screens isolated eight emu (enhancer of the nuclear migration defect of unc-84)
53                                The embryonic emu skin lacks sufficient cells to enact feather formati
54 chromosome-level genome assembly of a female emu, and estimated the tempo of chromosome evolution acr
55 eather primordia, are lost in the flightless emu and ostrich, though via different developmental rout
56                    Carbon isotopes in fossil emu (Dromaius novaehollandiae) eggshell from Lake Eyre,
57                       Unlike the human gene, emu NAGLU appeared to be highly polymorphic: 19 variatio
58  joints of two extant dinosaurs (guineafowl, emu) and, through comparison with in vivo kinematics, fi
59  identify gene markers that may help improve emu fat production.
60                    Vitamin D(3) was found in emu meat and calamari/squid (range 0.5-1.0 mug/100 g).
61                    Vitamin D(2) was found in emu products and some kangaroo samples.
62 chanisms underlying forelimb heterochrony in emu embryos.
63  can be applied to improve fat production in emus.
64    The availability of mutation screening in emus now permits early detection of MPS IIIB in breeding
65  raw meat (camel, crocodile, emu, kangaroo), emu eggs and emu oil.
66                         Samples of kangaroo, emu, squid/calamari and lobster/crayfish were collected
67 molecular basis, the sequences of the normal emu NAGLU cDNA and gene were determined by PCR-based app
68                 In Dromaius novaehollandiae (emu), a progressive neurologic disease was recently disc
69 ctly influence the fatty acid composition of emu fat.
70 , we analyze the genome and transcriptome of emu (Dromaius novaehollandiae) and confirm that most gen
71 is known about the GI microbial diversity of emus.
72 of intestinal microbiota on the nutrition of emus and indirectly influence the fatty acid composition
73                       The vestigial wings of emus are a striking illustration of morphological evolut
74 ake), birds (chicken, duck, pigeon, ostrich, emu and zebra finch), early postnatal marsupial mammals
75                          Ratites (ostriches, emus, rheas, cassowaries, and kiwis) are large, flightle
76                                    The other emu mutations potentially represent other components of
77 alluses; and in two outgroups, Paleognathae (emus) and Crocodilia (alligators).
78                However, in the paleognathous emu, the neognathous pattern was not observed, such that
79  its large body size and low metabolic rate, emus have a relatively simple gastroinstetinal (GI) trac
80                The small-sized and gene-rich emu microchromosomes have frequent inter-chromosomal con
81                                          The emu cecal microbiome has more genes than SI segments inv
82                                          The emu timing circuits showed the ancestral (plesiomorphic)
83                                          The emu W is demarcated into a highly heterochromatic region
84 rnum and wing size in a flightless bird, the emu.
85                                 However, the emu forelimb fails to subsequently proliferate.
86 o the LPM, occur at equivalent stages in the emu and chick.
87  significantly lower Fgf10 expression in the emu forelimb.
88 ificially increasing Fgf10 expression in the emu LPM induces ectodermal Fgf8 expression and a limb bu
89 latory elements near Fgf10 and Sall-1 in the emu wing, and the Sall-1 enhancer activity is dependent
90 iological data on the timing circuits in the emu, Dromaius novaehollandiae, and compare these results
91 tites (flightless paleognaths, including the emu and ostrich) often coincide with reduced wings.
92     Using predictive gait simulations of the emu (Dromaius novaehollandiae), we resolve this paradox
93  microbiota of different compartments of the emu intestines via gut samples and not fecal samples.
94 atite birds, only less than one-third of the emu W Chromosome regions have lost homologous recombinat
95  pathway as a factor in the evolution of the emu's stunted wings.
96                     It was observed that the emu NAGLU gene is structurally similar to that of human
97       This expression bias suggests that the emu sex chromosomes have become masculinized, even in th
98                                        Three emus and one rhea produced a wheel-turning innovation, m
99 remains that exhibit mass spectra similar to emu whole blood.
100                                   The unique emu forelimb expression of Nkx2.5, previously associated