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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
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
8 development in the New World marmoset monkey Callithrix jacchus is similar to previous reports in Mac
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
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
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
39 experimentally infected the common marmoset (Callithrix jacchus) with diverse strains of Mycobacteriu
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
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
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
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
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