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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 105 (1995), S. 209-219 
    ISSN: 1432-1106
    Keywords: Inferior temporal cortex ; Neurons ; Visual interactions ; Matching task ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Macaque monkeys were trained to determine whether shapes or colors of two visual stimuli were the same or different (matched/non-matched). Two stimuli were presented at different locations while the monkey fixated a small spot. In one paradigm, two stimuli were presented simultaneously for 0.5 s (Sml-SO task). In the other paradigm, one of the stimuli was turned on 0.5 s before the onset of another stimulus, then the two stimuli were present for the following 0.5 s (Scc SO task). The aim of the later task was to analyze the responses of TE neurons to a single presentation of each stimulus and the effects of successive onsets of two stimuli. Of 232 responsive neurons tested in both tasks, 143 showed a significant selectivity between paired stimuli (termed ‘selective neurons’). During the Sml-SO task, some selective neurons showed a larger response to the different (non-matched) stimuli than to the double optimal stimuli (matched), even though one of the different stimuli was inhibitory. This effect was more prominent in neurons that showed a smaller response to the double presentations of the optimal stimulus than to the single presentation. Since another group of selective neurons showed smaller responses for the different stimuli, the average response amplitudes were similar between the identical and the different stimuli. During the Scc-SO task, when the optimal stimulus was turned on after the non-optimal stimulus (non-matched), the response to the second stimulus was mostly enhanced above the response level to the single presentation of the first stimulus. Since the responses to the second stimulus identical to the first stimulus tended to decrease, the difference in the responses between the matched and non-matched stimuli became significantly larger in the Scc-SO task. The reaction times of the monkeys were shorter during the Scc-SO task than the Sml-SO task. These changes in response amplitude between the different and the identical stimuli were not prominent in the non-selective neurons. These results suggest that non-linear interactions between two different stimuli play an important role in the discrimination of groups of visual stimuli, particularly in successive analysis.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: A 20-kDa DNA-binding protein that binds the AT-rich sequences within the promoters of the brain-specific protein kinase C (PKC) γ and neurogranin/RC3 genes has been characterized as chromosomal nonhistone high-mobility-group protein (HMG)-I. This protein is a substrate of PKC α, β, γ, and δ but is poorly phosphorylated by PKC ε and ζ. Two major (Ser44 and Ser64) and four minor phosphorylation sites have been identified. The extents of phosphorylation of Ser44 and Ser64 were 1:1, whereas those of the four minor sites all together were 〈30% of the major one. These PKC phosphorylation sites are distinct from those phosphorylated by cdc2 kinase, which phosphorylates Thr53 and Thr78. Phosphorylation of HMG-I by PKC resulted in a reduction of DNA-binding affinity by 28-fold as compared with 12-fold caused by the phosphorylation with cdc2 kinase. HMG-I could be additively phosphorylated by cdc2 kinase and PKC, and the resulting doubly phosphorylated protein exhibited a 〉 100-fold reduction in binding affinity. The two cdc2 kinase phosphorylation sites of HMG-I are adjacent to the N terminus of two of the three predicted DNA-binding domains. In comparison, one of the major PKC phosphorylation sites, Ser64, is adjacent to the C terminus of the second DNA-binding domain, whereas Ser44 is located within the spanning region between the first and second DNA-binding domains. The current results suggest that phosphorylation of the mammalian HMG-I by PKC alone or in combination with cdc2 kinase provides an effective mechanism for the regulation of HMG-I function.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1615-2573
    Keywords: Negative feedback ; Transfer function ; Exercise
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In exercise training, precise control of exercise intensity would maximize the training efficacy while minimizing risks. To adjust work rate, heart rate (HR) has been used as a measure of exercise intensity. Thus, we developed a servo-controller of HR using a cycle ergometer. After estimating the transfer function from work rate to HR, we optimized feedback parameters for achieving a quick and stable HR response by means of a computer simulation. We then examined the performance of the servo-controller of HR in 55 healthy volunteers. We set the target HR at 60% and 75% of the age-predicted maximum HR. Times required for HR to reach 90% of the target HR were 136 ± 33 and 137 ± 22s in the respective protocols. Standard deviations of the steady-state difference between the target and measured HRs were 2.5 ± 0.6 and 3.8 ± 1.1 beats/min. We conclude that the developed servo-controller makes it possible to precisely regulate HR and, thereby, exercise intensity.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1615-2573
    Keywords: Cardiac bradyarrhythmias ; Diurnal rhythm ; Suprachiasmatic nucleus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ambulatory EGG and EEG recordings were recorded under a 14/10-h light-dark illumination schedule using rats. The rats consisted of two groups: a suprachiasmatic (Sch) lesioned group (n=5) and a normal control group (n=5). Bilateral Sch nuclei were lesioned electrically (DC, 2.5 mA, 30 s for each) using a pair of platinum electrodes 0.3 mm in diameter. After recovery from surgery, recordings of ECGs (leads I, II, and III) and EEGs from the cortex and the left dorsal hippocampus were continued for 6 days. Diurnal periodicity in bradyarrhythmia (sinoatrial block, atrioventricular block) and heart rate was analyzed by the least square fit of 24-h cosines. Significant diurnal rhythm was observed in control rats, whereas Sch-lesioned rats showed no significant diurnal rhythm. The integrity of the Sch nuclei, therefore, is necessary for the generation and/or the expression of diurnal periodicity in bradyarrhythmia in rats.
    Type of Medium: Electronic Resource
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  • 6
    Publication Date: 2017-01-06
    Description: Nature Physics 13, 30 (2017). doi:10.1038/nphys3895 Authors: Daichi Hirobe, Masahiro Sato, Takayuki Kawamata, Yuki Shiomi, Ken-ichi Uchida, Ryo Iguchi, Yoji Koike, Sadamichi Maekawa & Eiji Saitoh Quantum spin fluctuation in a low-dimensional or frustrated magnet breaks magnetic ordering while keeping spin correlation. Such fluctuation has been a central topic in magnetism because of its relevance to high-Tc superconductivity and topological states. However, utilizing such spin states has been quite difficult. In a one-dimensional spin-1/2 chain, a particle-like excitation called a spinon is known to be responsible for spin fluctuation in a paramagnetic state. Spinons behave as a Tomonaga–Luttinger liquid at low energy, and the spin system is often called a quantum spin chain. Here we show that a quantum spin chain generates and carries spin current, which is attributed to spinon spin current. This is demonstrated by observing an anisotropic negative spin Seebeck effect along the spin chains in Sr2CuO3. The results show that spin current can flow even in an atomic channel owing to long-range spin fluctuation.
    Print ISSN: 1745-2473
    Electronic ISSN: 1745-2481
    Topics: Physics
    Published by Springer Nature
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  • 7
    Publication Date: 2017-06-23
    Description: The Journal of Organic Chemistry DOI: 10.1021/acs.joc.7b00841
    Print ISSN: 0022-3263
    Electronic ISSN: 1520-6904
    Topics: Chemistry and Pharmacology
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  • 8
    Publication Date: 2014-07-22
    Description: Background: Microinjection of clustered regulatory interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9)-related RNA and DNA into fertilized eggs is a novel approach for creating gene-modified mice. Blastocysts obtained just before implantation may be appropriate for testing the fidelity of CRIPSR/Cas9-mediated genome editing because they can be individually handled in vitro and obtained 3 days after microinjection, thus allowing researchers to check mutations rapidly. However, it is not known whether indel mutations caused by the CRISPR/Cas9 system can be reproducibly detected in embryos. In this study, we assessed the detection of CRISPR/Cas9-induced mutations in embryos. Results: T7 endonuclease I was more effective than Surveyor nuclease for detecting mutations in annealed fragments derived from 2 plasmids, which contained nearly identical sequences. Mouse fertilized eggs were microinjected with CRISPR/Cas9-related RNA/DNA to examine whether non-homologous end joining-mediated knockout and homologous recombination-mediated knockin occurred in the endogenous receptor (G protein-coupled) activity modifying protein 2 (Ramp2) gene. Individual blastocysts were lysed to obtain crude DNA solutions, which were used for polymerase chain reaction (PCR) assays. T7 endonuclease I-based PCR and sequencing analysis demonstrated that 25-100% of the embryos were knockout embryos and 7-57% of the embryos were knockin embryos. Our results established that crude DNA from a single blastocyst was an appropriate template for Whole genome amplification and subsequent assessment by PCR and the T7 endonuclease I-based assay. Conclusions: The single blastocyst-based assay was useful for determining whether CRISPR/Cas9-mediated genome editing worked in murine embryos.
    Electronic ISSN: 1472-6750
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Published by BioMed Central
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