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1 e OR subfamilies in two species of marmoset (Callithrix).
2 t C. pygmaea should be included in the genus Callithrix.
3 , Alouatta gamma is inactive at term, and in Callithrix, gamma(1) is down-regulated fetally, whereas
4 e to hawk calls, in 18 Geoffroy's marmosets (Callithrix geoffroyi).
5  novel repeat family, termed Platy-1, in the Callithrix jacchus (common marmoset) genome that arose a
6 ates strongly supports the classification of Callithrix jacchus and C. geoffroyi into the jacchus gro
7                                              Callithrix jacchus is an outbred New World primate chara
8 development in the New World marmoset monkey Callithrix jacchus is similar to previous reports in Mac
9                  Using the nonhuman primate, Callithrix jacchus jacchus (common marmoset), we show th
10              Thus, using the marmoset monkey Callithrix jacchus we characterize here a new neurobiolo
11 e auditory cortex of awake marmoset monkeys (Callithrix jacchus) are capable of firing in a sustained
12  in the auditory cortex of marmoset monkeys (Callithrix jacchus) are sensitive to auditory feedback d
13 gth TRPML3 channel from the common marmoset (Callithrix jacchus) at an overall resolution of 2.9 A.
14 athogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneous (s.c.), and in
15 rontoparietal cortex in the common marmoset (Callithrix jacchus) by using intracortical microstimulat
16 ses like humans, we tested common marmosets (Callithrix jacchus) by using intranasal infection and mo
17 vestigated whether hyperhexosemic marmosets (Callithrix jacchus) develop characteristic retinal vascu
18 of a non-human primate (the common marmoset, Callithrix jacchus) following four systemic injections o
19  both the sequencing of the common marmoset (Callithrix jacchus) genome and a growing demand for alte
20       The sequencing of the common marmoset (Callithrix jacchus) genome offers the opportunity to exp
21               The New World marmoset monkey (Callithrix jacchus) has a relatively short gestational p
22                         The common marmoset (Callithrix jacchus) has garnered interest recently as a
23  past decade, the New World common marmoset (Callithrix jacchus) has taken a seminal position in neur
24 sponses of up to 61 neurons in the marmoset (Callithrix jacchus) middle temporal area to a sequence o
25 rld monkeys (Cebus apella, Aotus azarae, and Callithrix jacchus) representing three of the seven plat
26 population of A1 neurons in awake marmosets (Callithrix jacchus) responded to rapid time-varying CI s
27  the lateral belt of awake marmoset monkeys (Callithrix jacchus) showed significant changes in firing
28 n the temporal gyrus of the common marmoset (Callithrix jacchus) to 1) compare the functional organiz
29 ains of the striatum of a primate (marmoset; Callithrix jacchus) using fast-scan voltammetry at a car
30 s examined in the brain of common marmosets (Callithrix jacchus) using in situ hybridization, immunoc
31                  Six adult common marmosets (Callithrix jacchus) were acclimated to light, comfortabl
32                          Juvenile marmosets (Callithrix jacchus) were divided into two experimental g
33          Twenty-four adult common marmosets (Callithrix jacchus) were followed with regular behaviour
34 young to middle aged adult common marmosets (Callithrix jacchus) were injected with BrdU and perfused
35 s of adult primates, adult marmoset monkeys (Callithrix jacchus) were injected with BrdU and perfused
36 neurons in the adult common marmoset monkey (Callithrix jacchus) were modified by extensive exposure
37   In particular, the common marmoset monkey (Callithrix jacchus) with a relatively short life span is
38                            Marmoset monkeys (Callithrix jacchus) with bilateral transections of the a
39 experimentally infected the common marmoset (Callithrix jacchus) with diverse strains of Mycobacteriu
40              We inoculated common marmosets (Callithrix jacchus) with the objective of developing a s
41    To determine whether the common marmoset (Callithrix jacchus) would be an appropriate model to ass
42 ural vocal exchanges in the common marmoset (Callithrix jacchus), a highly vocal New World primate.
43 equency of 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey with a hearing r
44 the visual topography of V1 in the marmoset (Callithrix jacchus), a small diurnal monkey.
45                         The common marmoset (Callithrix jacchus), a small-bodied New World primate, o
46  World monkeys, such as the common marmoset (Callithrix jacchus), a species of growing interest as a
47 for pitch extraction in the common marmoset (Callithrix jacchus), a vocal primate species, by measuri
48 ocal New World primate, the common marmoset (Callithrix jacchus), across the entire hearing frequency
49 ccessful generation of transgenic marmosets (Callithrix jacchus), an important nonhuman primate model
50              A. nancymaae, but not marmoset (Callithrix jacchus), APOBEC3G was partially downregulate
51  in the auditory cortex of marmoset monkeys (Callithrix jacchus), in which the firing rate of a neuro
52 zees (Pan troglodytes) and common marmosets (Callithrix jacchus), left-handed individuals are less li
53 n the New World monkey, the common marmoset (Callithrix jacchus), produced a persistent impairment on
54 ins (Saguinus oedipus) and common marmosets (Callithrix jacchus), species known to differ in temporal
55 single-unit recordings from awake marmosets (Callithrix jacchus), we validate several model predictio
56 nuclear layer in the retina of the marmoset (Callithrix jacchus).
57 ic and CI signals in awake marmoset monkeys (Callithrix jacchus).
58  spinal cord lesions in the common marmoset (Callithrix jacchus).
59 passively listening female marmoset monkeys (Callithrix jacchus).
60 losely related species, the common marmoset (Callithrix jacchus).
61 losely related species, the common marmoset (Callithrix jacchus).
62 aeus), and a New World monkey, the marmoset (Callithrix jacchus).
63 ank of the lateral sulcus in five marmosets (Callithrix jacchus).
64 etry in striatal sections from the marmoset (Callithrix jacchus).
65 aneous B cell lymphomas of common marmosets (Callithrix jacchus).
66  striatal sections from the common marmoset (Callithrix jacchus).
67 riatal brain regions of the common marmoset (Callithrix jacchus).
68             The GH gene cluster in marmoset, Callithrix jacchus, comprises eight GH-like genes and ps
69                            Common marmosets (Callithrix jacchus, n = 18) were trained to discriminate
70 ising spontaneously in the New World primate Callithrix jacchus, the common marmoset.
71 etinal ganglion cells in the common marmoset Callithrix jacchus.
72 e cells in the retina of the common marmoset Callithrix jacchus.
73  and selective inhibitor of 17beta-HSD1 from Callithrix jacchus.
74 inner retinal neurons in the common marmoset Callithrix jacchus.
75 ed sections from the LGN of adult marmosets (Callithrix jacchus; 10 trichromatic females; 2 dichromat
76 rs, we show here that chimerism in marmoset (Callithrix kuhlii) twins is not limited to blood-derived
77 ng that without the pygmy marmoset the genus Callithrix would be paraphyletic.

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