ライフサイエンスコーパス: substantia gelatinosa

1 pioid-induced MOR internalization in the rat substantia gelatinosa.

2 for the wiring of local circuitry within the substantia gelatinosa.

3 ulations and late-born neurons that form the substantia gelatinosa.

4 in the superior cerebellar peduncle and the substantia gelatinosa.

5 ation of Abeta fiber-mediated input into the substantia gelatinosa after peripheral inflammation may

6 adhesion molecule (PSA-NCAM) in adult spinal substantia gelatinosa also express the mu-opioid recepto

7 Purkinje cells, and was also observed in the substantia gelatinosa and ventral horn motor neurons of

8 Oscillatory behaviour in the substantia gelatinosa could potentially play a role in t

9 potassium evokes oscillatory activity in the substantia gelatinosa in vitro.

10 known that C-tactile fibres terminate in the substantia gelatinosa (lamina II) of the spinal cord, vi

11 The substantia gelatinosa (lamina II) of the spinal dorsal h

12 e neural circuitry in the SDH, including its substantia gelatinosa (lamina II), has an explicit organ

13 ted over superficial laminae, especially the substantia gelatinosa (lamina II).

14 d no higher than the middle of the incipient substantia gelatinosa, leaving a clear gap more dorsally

15 stry and whole-cell patch-clamp recording of substantia gelatinosa neurons in slices of rat spinal co

16 depression (LTD) of synaptic transmission in substantia gelatinosa neurons that can be induced by low

17 0.1 msec) produced LTD of EPSP amplitudes in substantia gelatinosa neurons to 41 +/- 10% of control t

18 Loading substantia gelatinosa neurons with Ca2+ chelator BAPTA a

19 nsmission in the rat dorsal horn, but mostly substantia gelatinosa, neurons were investigated using c

20 udied and found to be in nerve fibers of the substantia gelatinosa of the dorsal horn and in dorsal r

21 were concentrated in the outer layer of the substantia gelatinosa of the dorsal horn.

22 ium-evoked network field oscillations in the substantia gelatinosa of the neonatal rat dorsal horn, a

23 een dorsal root afferents and neurons in the substantia gelatinosa of the spinal cord dorsal horn was

24 Nociceptors in the periphery travel to the substantia gelatinosa of the spinal cord while secondary

25 al forebrain, cerebellar Purkinje cells, and substantia gelatinosa of the spinal cord.

26 PSCs) could be evoked in neurones of the rat substantia gelatinosa of the spinal trigeminal nucleus p

27 DRG) and on axon terminals in lamina II (the substantia gelatinosa) of spinal cord.

28 analyses localized the elevated NT-3 to the substantia gelatinosa (SG) and nucleus of the dorsal hor

29 -12Hz oscillatory activity within rat spinal substantia gelatinosa (SG) has been used to determine th

30 ceptor subtypes is largely restricted to the substantia gelatinosa (SG) in the dorsal horn, with very

31 The spinal substantia gelatinosa (SG) is a major termination region

32 The spinal substantia gelatinosa (SG) is known to be involved in th

33 rotein (GFP) coding sequence labels a set of substantia gelatinosa (SG) neurons (SG-GFP) homogenous i

34 e-cell patch-clamp recordings were made from substantia gelatinosa (SG) neurons in thick adult rat tr

35 The substantia gelatinosa (SG) of the dorsal horn of the spi

36 The substantia gelatinosa (SG) of the spinal dorsal horn sho

37 twork activity recorded extracellularly from substantia gelatinosa (SG) of young rat spinal cord in v

38 tors (KARs) are expressed in the spinal cord substantia gelatinosa (SG) region, and their activation

39 recognized features in the spinal cord, the substantia gelatinosa (SG) remains among the most enigma

40 tch clamp recordings in slices of guinea-pig substantia gelatinosa (SG), we studied the serotonin (5-

41 e information from the skin epidermis to the substantia gelatinosa (SG, lamina II) of the spinal cord

42 The ventral or inner region of spinal substantia gelatinosa (SG; lamina II(i)) is a heterogene

43 The spinal substantia gelatinosa (SG; lamina II) is a major synapti

44 owed clinically) showed prion protein in the substantia gelatinosa, spinothalamic tracts, posterior c

45 xpress FLI in thoracic laminae I, IIo (outer substantia gelatinosa), Vre (lateral reticulated divisio

46 pha modulates synaptic transmission in mouse substantia gelatinosa was studied using whole-cell patch

47 e rhythmic activity in discrete areas of the substantia gelatinosa which lasted for 5-15 s with a sin