ライフサイエンスコーパス: external capsule

1 oligodendrocytes residing in the ipsilateral external capsule.

2 dial edge of the band to its boundary at the external capsule.

3 A (2.5 or 25 nmol) or vehicle (PBS) into the external capsule.

4 ecially in the corpus callosum, cingulum and external capsule.

5 , or laminae, that parallel the curve of the external capsule.

6 lamic radiation, anterior corona radiata, or external capsule.

7 e most pronounced in the corpus callosum and external capsule.

8 s callosum as well as bilateral internal and external capsules.

9 nate fasciculus) as well as the internal and external capsules.

10 ibrotic response displaying an alphaSMA cold external capsule and a long-lasting, inner alphaSMA hot

11 which do not express Tbr1) deviated into the external capsule and amygdala regions, without entering

12 al fasciculi, limbs of the internal capsule, external capsule and cerebellum (p < 0.05, corrected), i

13 Axonal damage was detected in the external capsule and cortex in sections immunostained fo

14 m is a small, elongated nucleus close to the external capsule and deep in the insular cortex.

15 ns of brain including hippocampus, thalamus, external capsule and motor cortex also noted, which were

16 r temporal lobe resection in the ipsilateral external capsule and posterior limb of the internal caps

17 rior and posterior corona radiata, bilateral external capsule and the right superior longitudinal fas

18 pulations of DCX-expressing cells within the external capsule and the surrounding gray matter (claust

19 vision travelling in the white matter of the external capsule and uncinate fasciculus and a perisylvi

20 white matter (corpus callosum, internal and external capsule) and gray matter (cerebral cortex, fron

21 on site, mainly dorsal to the putamen in the external capsule, and below the premotor cortex.

22 FA in parts of the anterior corona radiata, external capsule, and cerebellum (P<0.05, family-wise er

23 the reduced thickness of corpus callosum and external capsule, and decline of mature oligodendrocytes

24 y in the corpus callosum, corona radiata and external capsule, and increased mean diffusivity of the

25 posterior limb of the internal capsule, the external capsule, and the pyramidal tracts and medial le

26 osterior limb of the internal capsule, right external capsule, and the right temporal inferior longit

27 rpus callosum, optic radiation, internal and external capsules, and cerebral peduncles.

28 e dense dorsolateral AGm band that abuts the external capsule, are densest in the dorsolateral striat

29 sed in layers I, II-III and V as well as the external capsule beneath the activated columns.

30 as to the striatum (e.g. striatal bundle and external capsule), but also in long association fiber pa

31 urons whose axons were seen traveling in the external capsule, but not entering the ALa.

32 tial evoked in the BLA by stimulation of the external capsule by 167.3+/-9.7 % of control amplitude.

33 tial evoked in the BLA by stimulation of the external capsule by 186.5+/-10.7% of control amplitude.

34 into the rostral putamen, internal capsule, external capsule, caudate nucleus, and globus pallidus.

35 in OX-42-positive cells in the ependyma, the external capsule, choroid plexus, and meninges.

36 ated neurons in several subcortical regions (external capsule, claustrum, and amygdala).

37 ination was observed in the corpus callosum, external capsule, CP, and dorsal hippocampal commissure

38 LFS (1 Hz, 15 min) of the external capsule (EC) induced a persistent 1.7-fold enha

39 GABAergic neurons in the external capsule (EC) provide feedforward inhibition in

40 rona radiata (CR), internal capsule (IC) and external capsule (EC).

41 rtico-spinal tracts, cingulum fibre bundles, external capsule, forceps minor and major, genu, body an

42 se signals in the anterior temporal pole and external capsule in Swedish subjects upon magnetic reson

43 ala in response to stimulation of either the external capsule (neocortical inputs) or fibers from the

44 anges in morphology in the same axons in the external capsule numerous times over 30 to 60 days, befo

45 Quantification of axonal damage in the external capsule of MAP 5-immunostained sections showed

46 erior temporal lobes (OR: 7.65, p<0.001) and external capsule (OR: 13.32, p<0.001).

47 , beta = -0.01 (P = .03)] corona radiata and external capsule [right FA, beta = 0.01 (P = .03); left

48 ically seen on conventional MR images (e.g., external capsule, thalamic substructures, basal ganglia,

49 ip of grey matter between the insula and the external capsule that densely expresses 5-HT2A receptors

50 of the internal capsule (ALIC and PLIC), the external capsule, the retrolenticular part of the intern

51 ficantly lower FA in the ALIC, the PLIC, the external capsule, the RLIC, the cerebral peduncle, and t

52 ala, we have studied LTP in the pathway from external capsule to the lateral nucleus, a pathway that

53 Anisotropic flow along the external capsule tracts carried GDNF into the anterior a

54 iatum but also insula, internal capsule, and external capsule were associated with higher SN-AI(95) a

55 , GABA(A) IPSPs evoked by stimulation of the external capsule were significantly reduced by CORT appl

56 of betaT4 cells myelinated up to 4 mm of the external capsule, which significantly exceeded that of t

57 alities in the corpus callosum, cingulum and external capsule, with differing severity across epileps

58 the ipsilateral parahippocampal cingulum and external capsule, with smaller effects across most other