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1 ulations and late-born neurons that form the substantia gelatinosa.
2 in the superior cerebellar peduncle and the substantia gelatinosa.
3 for the wiring of local circuitry within the substantia gelatinosa.
4 ation of Abeta fiber-mediated input into the substantia gelatinosa after peripheral inflammation may
5 adhesion molecule (PSA-NCAM) in adult spinal substantia gelatinosa also express the mu-opioid recepto
6 Purkinje cells, and was also observed in the substantia gelatinosa and ventral horn motor neurons of
9 known that C-tactile fibres terminate in the substantia gelatinosa (lamina II) of the spinal cord, vi
11 e neural circuitry in the SDH, including its substantia gelatinosa (lamina II), has an explicit organ
13 d no higher than the middle of the incipient substantia gelatinosa, leaving a clear gap more dorsally
14 stry and whole-cell patch-clamp recording of substantia gelatinosa neurons in slices of rat spinal co
15 depression (LTD) of synaptic transmission in substantia gelatinosa neurons that can be induced by low
16 0.1 msec) produced LTD of EPSP amplitudes in substantia gelatinosa neurons to 41 +/- 10% of control t
18 nsmission in the rat dorsal horn, but mostly substantia gelatinosa, neurons were investigated using c
19 udied and found to be in nerve fibers of the substantia gelatinosa of the dorsal horn and in dorsal r
21 ium-evoked network field oscillations in the substantia gelatinosa of the neonatal rat dorsal horn, a
22 een dorsal root afferents and neurons in the substantia gelatinosa of the spinal cord dorsal horn was
23 Nociceptors in the periphery travel to the substantia gelatinosa of the spinal cord while secondary
25 PSCs) could be evoked in neurones of the rat substantia gelatinosa of the spinal trigeminal nucleus p
27 analyses localized the elevated NT-3 to the substantia gelatinosa (SG) and nucleus of the dorsal hor
28 -12Hz oscillatory activity within rat spinal substantia gelatinosa (SG) has been used to determine th
29 ceptor subtypes is largely restricted to the substantia gelatinosa (SG) in the dorsal horn, with very
32 rotein (GFP) coding sequence labels a set of substantia gelatinosa (SG) neurons (SG-GFP) homogenous i
33 e-cell patch-clamp recordings were made from substantia gelatinosa (SG) neurons in thick adult rat tr
36 twork activity recorded extracellularly from substantia gelatinosa (SG) of young rat spinal cord in v
37 tors (KARs) are expressed in the spinal cord substantia gelatinosa (SG) region, and their activation
38 recognized features in the spinal cord, the substantia gelatinosa (SG) remains among the most enigma
39 tch clamp recordings in slices of guinea-pig substantia gelatinosa (SG), we studied the serotonin (5-
40 e information from the skin epidermis to the substantia gelatinosa (SG, lamina II) of the spinal cord
43 xpress FLI in thoracic laminae I, IIo (outer substantia gelatinosa), Vre (lateral reticulated divisio
44 pha modulates synaptic transmission in mouse substantia gelatinosa was studied using whole-cell patch
45 e rhythmic activity in discrete areas of the substantia gelatinosa which lasted for 5-15 s with a sin
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