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1 ate cortex of the common marmoset (Callithrx jacchus).
2 er in the retina of the marmoset (Callithrix jacchus).
3 d lesions in the common marmoset (Callithrix jacchus).
4 ignals in awake marmoset monkeys (Callithrix jacchus).
5 istening female marmoset monkeys (Callithrix jacchus).
6 ted species, the common marmoset (Callithrix jacchus).
7 ted species, the common marmoset (Callithrix jacchus).
8 a New World monkey, the marmoset (Callithrix jacchus).
9 lateral sulcus in five marmosets (Callithrix jacchus).
10 iatal sections from the marmoset (Callithrix jacchus).
11 ll lymphomas of common marmosets (Callithrix jacchus).
12 ections from the common marmoset (Callithrix jacchus).
13 n regions of the common marmoset (Callithrix jacchus).
14 lion cells in the common marmoset Callithrix jacchus.
15 the retina of the common marmoset Callithrix jacchus.
16 idate for the in vivo proof of concept in C. jacchus.
17 ive inhibitor of 17beta-HSD1 from Callithrix jacchus.
18 al neurons in the common marmoset Callithrix jacchus.
19 from the LGN of adult marmosets (Callithrix jacchus; 10 trichromatic females; 2 dichromatic females;
21 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey with a hearing range simila
24 eys, such as the common marmoset (Callithrix jacchus), a species of growing interest as a primate mod
25 xtraction in the common marmoset (Callithrix jacchus), a vocal primate species, by measuring pitch di
26 rld primate, the common marmoset (Callithrix jacchus), across the entire hearing frequency range.
28 neration of transgenic marmosets (Callithrix jacchus), an important nonhuman primate model in neuroph
29 ly supports the classification of Callithrix jacchus and C. geoffroyi into the jacchus group, and C.
30 A. nancymaae, but not marmoset (Callithrix jacchus), APOBEC3G was partially downregulated by HIV-1
31 cortex of awake marmoset monkeys (Callithrix jacchus) are capable of firing in a sustained manner ove
32 itory cortex of marmoset monkeys (Callithrix jacchus) are sensitive to auditory feedback during vocal
34 y of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneous (s.c.), and intranasal ex
35 al cortex in the common marmoset (Callithrix jacchus) by using intracortical microstimulation and an
36 mans, we tested common marmosets (Callithrix jacchus) by using intranasal infection and monitoring fo
37 at family, termed Platy-1, in the Callithrix jacchus (common marmoset) genome that arose around the t
38 The GH gene cluster in marmoset, Callithrix jacchus, comprises eight GH-like genes and pseudogenes a
39 a diverse TCRB repertoire is generated in C. jacchus despite the limited polymorphism of class I MHC
40 whether hyperhexosemic marmosets (Callithrix jacchus) develop characteristic retinal vascular lesions
41 man primate (the common marmoset, Callithrix jacchus) following four systemic injections of 30 mg/kg
42 equencing of the common marmoset (Callithrix jacchus) genome and a growing demand for alternatives to
43 equencing of the common marmoset (Callithrix jacchus) genome offers the opportunity to explore the ge
44 Callithrix jacchus and C. geoffroyi into the jacchus group, and C. argentata and C. mauesi into the a
45 The New World marmoset monkey (Callithrix jacchus) has a relatively short gestational period compa
47 e, the New World common marmoset (Callithrix jacchus) has taken a seminal position in neurobiological
49 itory cortex of marmoset monkeys (Callithrix jacchus), in which the firing rate of a neuron is a mono
51 in the New World marmoset monkey Callithrix jacchus is similar to previous reports in Macaca and hum
53 roglodytes) and common marmosets (Callithrix jacchus), left-handed individuals are less likely than r
54 up to 61 neurons in the marmoset (Callithrix jacchus) middle temporal area to a sequence of direction
56 olution of NWMs in the lineage leading to C. jacchus Platy-1 appears to have reached its amplificatio
57 orld monkey, the common marmoset (Callithrix jacchus), produced a persistent impairment on visual dis
58 (Cebus apella, Aotus azarae, and Callithrix jacchus) representing three of the seven platyrrhine cla
59 of A1 neurons in awake marmosets (Callithrix jacchus) responded to rapid time-varying CI stimulation
60 l belt of awake marmoset monkeys (Callithrix jacchus) showed significant changes in firing rates in r
61 us oedipus) and common marmosets (Callithrix jacchus), species known to differ in temporal discountin
62 ammatory disorders are characteristics of C. jacchus that create a useful model system for the study
64 ral gyrus of the common marmoset (Callithrix jacchus) to 1) compare the functional organization of AI
65 striatum of a primate (marmoset; Callithrix jacchus) using fast-scan voltammetry at a carbon-fiber m
66 in the brain of common marmosets (Callithrix jacchus) using in situ hybridization, immunocytochemistr
67 Thus, using the marmoset monkey Callithrix jacchus we characterize here a new neurobiological model
68 recordings from awake marmosets (Callithrix jacchus), we validate several model predictions, includi
72 enty-four adult common marmosets (Callithrix jacchus) were followed with regular behavioural tests fo
73 primates, adult marmoset monkeys (Callithrix jacchus) were injected with BrdU and perfused 2 hr or 3
74 ddle aged adult common marmosets (Callithrix jacchus) were injected with BrdU and perfused 3 weeks la
75 the adult common marmoset monkey (Callithrix jacchus) were modified by extensive exposure to altered
76 ular, the common marmoset monkey (Callithrix jacchus) with a relatively short life span is an ideal m
78 lly infected the common marmoset (Callithrix jacchus) with diverse strains of Mycobacterium tuberculo
79 We inoculated common marmosets (Callithrix jacchus) with the objective of developing a small nonhum
80 mine whether the common marmoset (Callithrix jacchus) would be an appropriate model to assess vaccine
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