ライフサイエンスコーパス: Nissl-stained

1 The density of Nissl-stained and GABA-immunoreactive neurons was high e

2 of all vocal nuclei, as measured using both Nissl-stained and NADPH-d-stained material, as well as t

3 Nissl-stained brain sections of specimens from a previou

4 ion-level asymmetry in the areal fraction of Nissl-stained cell bodies, a finding that differs from p

5 ations, we performed stereologic analyses of Nissl-stained cells in layer III of area DSCF in mustach

6 A higher percentage (relative to Nissl-stained cells) of PV(+) cells compared with CB(+)

7 e marker tyrosine hydroxylase (TH), 60% more Nissl-stained cells, and 40% less norepinephrine transpo

8 a reduction of the counts of TH-positive and Nissl-stained cells.

9 Serial Nissl-stained coronal sections through the medial preopt

10 We found that the Nissl-stained cross-sectional area of the posterodorsal

11 these nuclei could not be identified within Nissl-stained female tissue.

12 and necrosis to neuronal injury in adjacent Nissl-stained, hematoxylin and eosin-stained, and termin

13 ts, epileptic kainate-treated rats had fewer Nissl-stained hilar neurons and fewer somatostatin-immun

14 At 7 d, traumatic brain lesion volumes on Nissl-stained histological sections were significantly s

15 D) interneuron numbers without diminution in Nissl-stained interneuron numbers, indicating loss of GA

16 of the cellular architecture as derived from Nissl-stained material and in terms of the dendritic pro

17 al region (STR) in the human was analyzed in Nissl-stained material to see whether auditory cortex is

18 d boutons were seen in close apposition with Nissl-stained motoneurons in the Vmo, VII, XII and Amb.

19 dehydrogenase (LDH) release measurements and Nissl-stained neuron counts.

20 2 oscillations cause significant decrease in NISSL-stained neurons (p < 0.05) and induce inflammation

21 KA (2.5 nmol) destroyed 43% of Nissl-stained neurons and 70% of choline acetyltransfera

22 ts, an average of approximately one-third of Nissl-stained neurons and one-third of the GABAergic int

23 ficant 32 +/- 11% reduction in the number of Nissl-stained neurons compared with young monkeys.

24 Stereology was used to estimate numbers of Nissl-stained neurons per hippocampus in the granule cel

25 gic criteria in coronal and oblique sections Nissl stained or immunoreacted for neuron-specific nucle

26 reticulospinal (RS) neurons were missing in Nissl-stained or neurofilament-immunostained brain whole

27 sections from each tissue block were either Nissl-stained or stained with antibodies against somatos

28 d stereological estimates of cell numbers in Nissl-stained, paraffin-wax sections of brain, we invest

29 imes, these neurons were swollen and pale in Nissl-stained preparations.

30 Using Nissl-stained retinal wholemounts and stereological meth

31 the overall neuronal density was measured on Nissl stained sections and the proportion of CR+ and PV+

32 g (S) than autumn (A), in both the PG21- and Nissl-stained sections (S:A = 1.9 and 1.7, respectively)

33 dopaminergic cell survival were confirmed in Nissl-stained sections and by quantitation of retrograde

34 temporale and Heschl's gyrus was assessed on Nissl-stained sections by semi-automated microscope imag

35 Nissl-stained sections demonstrated that BHK-hCNTF cells

36 ally toward stereological analyses of thick, Nissl-stained sections for the homotypical cortex of the

37 Interestingly, emulsion-dipped, Nissl-stained sections from schizophrenia and comparison

38 ually dimorphic male nucleus (MN) is seen in Nissl-stained sections from the dorsal preoptic area/ant

39 d koniocellular (K) layers was calculated in Nissl-stained sections from the LGN of adult marmosets (

40 alling near OD column borders are evident in Nissl-stained sections in all layers and in immunoreacti

41 rmine cell density and cortical thickness in Nissl-stained sections of area 46.

42 neuron number and soma size were assessed in Nissl-stained sections of spinal cord segments T17-S1 of

43 differences in DCN organization, we compared Nissl-stained sections of the DCN in five different spec

44 ogical striatal volume analyses performed on Nissl-stained sections revealed that rats transplanted w

45 Analysis of Nissl-stained sections reveals a neuronal population tha

46 used to estimate numbers of granule cells in Nissl-stained sections so that numbers of excitatory syn

47 Nissl-stained sections through three cytoarchitectonic s

48 d somatosensory cortices of the mouse, using Nissl-stained sections to define laminar boundaries.

49 Examination of the hilus in adjacent Nissl-stained sections with the optical dissector reveal

50 In immunolabelled Nissl-stained sections, CR+ neurones constituted an over

51 logical counting procedures on immunoreacted Nissl-stained sections, CR+ neurons were estimated to co

52 In systematic series of Nissl-stained sections, the areas of major forebrain reg

53 In Nissl-stained sections, the autoradiographic label corre

54 a 3D marmoset brain template, generated from Nissl-stained sections.

55 (GLR) of layer III neurons were measured in Nissl-stained sections.

56 lar layer and granule cell layer and loss of Nissl-stained, somatostatin-immunoreactive, and parvalbu

57 ed by alpha-bungarotoxin binding to numerous Nissl-stained structures in CA1 lacunosum/moleculare in

58 esion was confirmed following examination of Nissl-stained tissue sections at all times post-lesion a

59 ution of NeuN-labeled neurons was similar to Nissl-stained tissue, with the exception of some areas w

60 The number of TH+/Nissl-stained was significantly decreased in both Swiss-