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1 tly studied words produced activity in three neuroanatomically and functionally dissociable neural po
2 n choice that can be doubly dissociated both neuroanatomically and neurochemically at the level of th
3 g" and eating are systematically mapped in a neuroanatomically and neurochemically interactive manner
4 aracterized by a lower fractional anisotropy neuroanatomically associated with localized reduced grey
5 ures relate to cognition and augment classic neuroanatomically based predictions about cognitive and
6 of tau pathology from the injection site to neuroanatomically connected brain regions, and these tau
7 se, the development of tau pathology follows neuroanatomically connected pathways, suggesting that ab
8 anterior cingulate gyrus, which are regions neuroanatomically connected with limbic structures, are
11 nt induces CRE-mediated gene expression in a neuroanatomically differentiated pattern and further elu
13 ns of the dopamine system are carried out by neuroanatomically discrete subgroups of dopamine neurons
15 be decomposed into three computationally and neuroanatomically distinct factors that were evident in
17 ndbrain, boundaries separate molecularly and neuroanatomically distinct segments called rhombomeres.
18 the existence of two longitudinally defined, neuroanatomically distinct, and clinically relevant phen
20 ter the anesthetic dose of ketamine that was neuroanatomically identical to that produced by the suba
21 ower-law scaling behavior is a pervasive but neuroanatomically inhomogeneous property of neuronal dyn
22 first report of a hypothalamic brain region neuroanatomically integrated with song control circuitry
23 njection and functional mapping procedure to neuroanatomically localize and neurochemically character
24 The present study was conducted in order to neuroanatomically localize the effects of (+)-HA966 upon
27 ve microarray profiling of approximately 900 neuroanatomically precise subdivisions in two individual
33 onal and glial tau-immunoreactive lesions in neuroanatomically specific nuclei in the basal ganglia,
35 , by using neurocomputational simulations in neuroanatomically structured models of the perisylvian l
36 meta-analytic results support an elegant and neuroanatomically viable model of the salience of negati
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