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1 ) was found in all products except camel and kangaroo.
2 ematics and kinetics of hopping red and grey kangaroos.
4 tudy should benefit both the endangered tree kangaroo and humans with immunosuppressive disorders tha
5 ll species tested except simian primates and kangaroo and that retroposons are common to a wide range
6 supial species (two macropodiformes, the red kangaroo and the parma wallaby, and a vombatiform, the k
7 Isolates of MAC organisms from affected tree kangaroos and from their environment had no common restr
8 he largest extant species of marsupials, the kangaroos and wallabies, have a very different reproduct
9 human RPE-1, approximately 80% in PtK2 (rat kangaroo), and approximately 25% in mouse cells, and thi
12 l care, consisting of support for lactation, kangaroo care, and routine developmental therapies, or t
13 ortunistic in humans and other mammals, tree kangaroos commonly develop primary progressive disease w
15 ntained a breeding colony of Matschie's tree kangaroos (Dendrolagus matschiei) since 1975 with a docu
21 d the genomic structure and evolution of the kangaroo endogenous retrovirus (KERV) in the marsupial g
22 relative copy number and distribution of the kangaroo endogenous retrovirus in the Macropus genus.
23 Our data indicate that amplification of the kangaroo endogenous retrovirus occurred in a lineage-spe
26 terization of a novel retrotransposon called kangaroo from the multicellular green alga, Volvox carte
28 tury New Guinean dingoes, a mid-19th-century kangaroo hound, and 33 contemporary dingoes from across
29 ver, from the well-researched and endangered Kangaroo Island echidna population, we understand that t
30 For many cell types, however, including rat kangaroo kidney PtK(1) cells, the MI does not increase d
34 99 kg who were assigned to receive immediate kangaroo mother care (intervention) or conventional care
35 of the key biological pathways through which kangaroo mother care (KMC) improves health outcomes in l
37 (within 1 h), neonatal bag-mask ventilation, kangaroo mother care (KMC), and antibiotics for clinical
39 ta for evidence-based interventions, such as Kangaroo Mother Care and care seeking for newborn infect
40 between-group difference favoring immediate kangaroo mother care at 72 hours was not significant.
41 0 and 1.799 kg, those who received immediate kangaroo mother care had lower mortality at 28 days than
42 an those who received conventional care with kangaroo mother care initiated after stabilization; the
48 s study, we created a three-dimensional (3D) kangaroo musculoskeletal model, integrating 3D motion ca
49 ucted fluorescence microscopy studies on rat kangaroo (PtK) and human (RPE1) cells dividing in the pr
50 otivated its division in 1997 into the agile kangaroo rat (AKR, D. agilis, 2N = 62) in the north of i
51 he effects of a keystone engineer, the giant kangaroo rat (Dipodomys ingens), on plants, invertebrate
52 orth of its range in California, and Dulzura kangaroo rat (DKR, D. simulans, 2N = 60) to the south, w
53 eparated the effects of burrow creation from kangaroo rat density and found that kangaroo rats increa
55 he Mojave Desert in North America, Merriam's kangaroo rat Dipodomys merriami and the sidewinder rattl
56 njection into the cytoplasm of single living kangaroo rat kidney cells (PtK2 cells), the MB hybridize
57 ht adult and captive-born adult and juvenile kangaroo rats (Dipodomys heermanni arenae) to a live sna
59 r data from a 17-year study of banner-tailed kangaroo rats (Dipodomys spectabilis) to quantify the re
61 objective was to determine if the tendons of kangaroo rats (k-rat), small bipedal animals that can ju
62 akes have heat sensing organs (pits) and the kangaroo rats have fur-lined cheek pouches that allow fo
63 ion from kangaroo rat density and found that kangaroo rats increased the diversity and abundance of o
64 condition over the entire study, indicating kangaroo rats offset decreases in energy intake through
71 citation, thermoregulation, breast-feeding, "kangaroo" [skin-to-skin] care, care of the small baby, a
72 collagen as a benchmark, we apply our novel kangaroo tail tendon collagen as an alternative collagen
73 ge and return could be a key factor enabling kangaroos to achieve energetic benefits at faster hoppin
74 supial suborder Macropodiformes (present-day kangaroos, wallabies, and related macropodoids), to the
76 immune reactivity in apparently healthy tree kangaroos was 3- to 6-fold lower than in humans and othe
77 f marsupials, the macropodids (wallabies and kangaroos), with placentation lasting beyond the 2 to 4