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1 ing of local circuitry within the substantia gelatinosa.
2 d late-born neurons that form the substantia gelatinosa.
3 erior cerebellar peduncle and the substantia gelatinosa.
4 eta fiber-mediated input into the substantia gelatinosa after peripheral inflammation may contribute
6 lls, and was also observed in the substantia gelatinosa and ventral horn motor neurons of the spinal
7 plants, other traits being distinctive of T. gelatinosa, and perhaps related to its symbiotic lifesty
12 C-tactile fibres terminate in the substantia gelatinosa (lamina II) of the spinal cord, virtually all
14 rcuitry in the SDH, including its substantia gelatinosa (lamina II), has an explicit organization in
17 gesting that the desiccation tolerance of T. gelatinosa mostly relies on constitutive mechanisms.
18 ole-cell patch-clamp recording of substantia gelatinosa neurons in slices of rat spinal cord in vitro
19 (LTD) of synaptic transmission in substantia gelatinosa neurons that can be induced by low-frequency
20 roduced LTD of EPSP amplitudes in substantia gelatinosa neurons to 41 +/- 10% of control that lasted
22 n the rat dorsal horn, but mostly substantia gelatinosa, neurons were investigated using conventional
23 ound to be in nerve fibers of the substantia gelatinosa of the dorsal horn and in dorsal root ganglio
25 network field oscillations in the substantia gelatinosa of the neonatal rat dorsal horn, a lamina inv
26 root afferents and neurons in the substantia gelatinosa of the spinal cord dorsal horn was examined b
27 rs in the periphery travel to the substantia gelatinosa of the spinal cord while secondary and tertia
29 be evoked in neurones of the rat substantia gelatinosa of the spinal trigeminal nucleus pars caudali
31 uences of 5S ribosomal RNAs from Rhodocyclus gelatinosa, Rhodobacter sphaeroides, and Pseudomonas cep
33 latory activity within rat spinal substantia gelatinosa (SG) has been used to determine the impact of
34 ypes is largely restricted to the substantia gelatinosa (SG) in the dorsal horn, with very low level
37 ) coding sequence labels a set of substantia gelatinosa (SG) neurons (SG-GFP) homogenous in morpholog
38 h-clamp recordings were made from substantia gelatinosa (SG) neurons in thick adult rat transverse sp
42 are expressed in the spinal cord substantia gelatinosa (SG) region, and their activation has a capac
43 features in the spinal cord, the substantia gelatinosa (SG) remains among the most enigmatic of cent
44 ecordings in slices of guinea-pig substantia gelatinosa (SG), we studied the serotonin (5-HT)- and no
46 ventral or inner region of spinal substantia gelatinosa (SG; lamina II(i)) is a heterogeneous sublami
48 um, Rhodobacter sphaeroides, and Rhodocyclus gelatinosa), the cyanobacteria [Anacystis nidulans, Micr
49 approach to a common member of the genus, T. gelatinosa, to investigate the alteration of gene expres
50 in thoracic laminae I, IIo (outer substantia gelatinosa), Vre (lateral reticulated division), VII (la
51 es synaptic transmission in mouse substantia gelatinosa was studied using whole-cell patch clamp and
52 s (DRPs), which are highly diversified in T. gelatinosa, whereas Late Embryogenesis Abundant Proteins
53 activity in discrete areas of the substantia gelatinosa which lasted for 5-15 s with a single promine
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