ライフサイエンスコーパス: gelatinosa

1 ed MOR internalization in the rat substantia gelatinosa.

2 ing of local circuitry within the substantia gelatinosa.

3 d late-born neurons that form the substantia gelatinosa.

4 erior cerebellar peduncle and the substantia gelatinosa.

5 eta fiber-mediated input into the substantia gelatinosa after peripheral inflammation may contribute

6 lecule (PSA-NCAM) in adult spinal substantia gelatinosa also express the mu-opioid receptor.

7 lls, and was also observed in the substantia gelatinosa and ventral horn motor neurons of the spinal

8 plants, other traits being distinctive of T. gelatinosa, and perhaps related to its symbiotic lifesty

9 the transcriptome of axenically cultured T. gelatinosa by using Illumina sequencing technology.

10 Oscillatory behaviour in the substantia gelatinosa could potentially play a role in the processi

11 vokes oscillatory activity in the substantia gelatinosa in vitro.

12 related to Paracoccus denitrificans and Rc. gelatinosa is related to Ps. cepacia.

13 C-tactile fibres terminate in the substantia gelatinosa (lamina II) of the spinal cord, virtually all

14 The substantia gelatinosa (lamina II) of the spinal dorsal horn contain

15 rcuitry in the SDH, including its substantia gelatinosa (lamina II), has an explicit organization in

16 perficial laminae, especially the substantia gelatinosa (lamina II).

17 than the middle of the incipient substantia gelatinosa, leaving a clear gap more dorsally.

18 gesting that the desiccation tolerance of T. gelatinosa mostly relies on constitutive mechanisms.

19 ole-cell patch-clamp recording of substantia gelatinosa neurons in slices of rat spinal cord in vitro

20 (LTD) of synaptic transmission in substantia gelatinosa neurons that can be induced by low-frequency

21 roduced LTD of EPSP amplitudes in substantia gelatinosa neurons to 41 +/- 10% of control that lasted

22 Loading substantia gelatinosa neurons with Ca2+ chelator BAPTA also blocked

23 n the rat dorsal horn, but mostly substantia gelatinosa, neurons were investigated using conventional

24 ound to be in nerve fibers of the substantia gelatinosa of the dorsal horn and in dorsal root ganglio

25 ntrated in the outer layer of the substantia gelatinosa of the dorsal horn.

26 network field oscillations in the substantia gelatinosa of the neonatal rat dorsal horn, a lamina inv

27 root afferents and neurons in the substantia gelatinosa of the spinal cord dorsal horn was examined b

28 rs in the periphery travel to the substantia gelatinosa of the spinal cord while secondary and tertia

29 n, cerebellar Purkinje cells, and substantia gelatinosa of the spinal cord.

30 be evoked in neurones of the rat substantia gelatinosa of the spinal trigeminal nucleus pars caudali

31 axon terminals in lamina II (the substantia gelatinosa) of spinal cord.

32 uences of 5S ribosomal RNAs from Rhodocyclus gelatinosa, Rhodobacter sphaeroides, and Pseudomonas cep

33 ocalized the elevated NT-3 to the substantia gelatinosa (SG) and nucleus of the dorsal horn.

34 latory activity within rat spinal substantia gelatinosa (SG) has been used to determine the impact of

35 ypes is largely restricted to the substantia gelatinosa (SG) in the dorsal horn, with very low level

36 The spinal substantia gelatinosa (SG) is a major termination region for unmyel

37 The spinal substantia gelatinosa (SG) is known to be involved in the manipulat

38 ) coding sequence labels a set of substantia gelatinosa (SG) neurons (SG-GFP) homogenous in morpholog

39 h-clamp recordings were made from substantia gelatinosa (SG) neurons in thick adult rat transverse sp

40 The substantia gelatinosa (SG) of the dorsal horn of the spinal cord is

41 The substantia gelatinosa (SG) of the spinal dorsal horn shows signific

42 ity recorded extracellularly from substantia gelatinosa (SG) of young rat spinal cord in vitro.

43 are expressed in the spinal cord substantia gelatinosa (SG) region, and their activation has a capac

44 features in the spinal cord, the substantia gelatinosa (SG) remains among the most enigmatic of cent

45 ecordings in slices of guinea-pig substantia gelatinosa (SG), we studied the serotonin (5-HT)- and no

46 on from the skin epidermis to the substantia gelatinosa (SG, lamina II) of the spinal cord.

47 ventral or inner region of spinal substantia gelatinosa (SG; lamina II(i)) is a heterogeneous sublami

48 The spinal substantia gelatinosa (SG; lamina II) is a major synaptic zone for

49 ally) showed prion protein in the substantia gelatinosa, spinothalamic tracts, posterior columns and

50 um, Rhodobacter sphaeroides, and Rhodocyclus gelatinosa), the cyanobacteria [Anacystis nidulans, Micr

51 approach to a common member of the genus, T. gelatinosa, to investigate the alteration of gene expres

52 in thoracic laminae I, IIo (outer substantia gelatinosa), Vre (lateral reticulated division), VII (la

53 es synaptic transmission in mouse substantia gelatinosa was studied using whole-cell patch clamp and

54 s (DRPs), which are highly diversified in T. gelatinosa, whereas Late Embryogenesis Abundant Proteins

55 activity in discrete areas of the substantia gelatinosa which lasted for 5-15 s with a single promine