ライフサイエンスコーパス: Nissl stain

1 tochrome oxidase or stained for cell bodies (Nissl stain).

2 ere depressed with age (PDI and intensity of Nissl staining).

3 tained cellular composition as visualized by Nissl stain.

4 ll brains were stained with Cresyl violet, a Nissl stain.

5 hitecture of the VMH was not recognizable by Nissl stain.

6 ze of mammalian brain regions as revealed by Nissl stains.

7 e defined by histological markers other than Nissl staining.

8 ppaB, protein disulfide isomerase (PDI), and Nissl staining.

9 of neurons in brain sections was examined by Nissl staining.

10 P days) 4 and 6 using cytochrome oxidase and Nissl staining.

11 s determined by MAP2 immunocytochemistry and Nissl staining.

12 eatments were evaluated using cresyl violet (Nissl) staining.

13 orphology were assessed using Cresyl violet (Nissl) staining.

14 roke brain in the same rat was determined by Nissl staining 28 days after surgery.

15 MGV) has cellular laminae visible in routine Nissl stains, allowing a direct comparison of the lamina

16 Nissl stain analyses showed a uniform distribution of ce

17 n of a rhesus and 11 cynomolgus monkeys with Nissl staining and immunohistochemistry for neuron-speci

18 rew's brain, we sectioned brains and applied Nissl staining and NeuN (neuronal nuclei) antibody stain

19 Nissl staining and nicotinamide adenine dinucleotide pho

20 complete (for NF-kappaB) to very minor (for Nissl staining and PDI).

21 Nissl staining and terminal deoxynucleotidyl transferase

22 ent regions of the ganglion cell layer using Nissl staining and tetramethylrhodamine dextran amine ba

23 In this study we used Nissl staining and tyrosine hydroxylase (TH) immunoreact

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

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

26 Neuropathological analyses included Nissl-staining and immunohistochemistry to detect APPs,

27 chitecture of the VMH became recognizable by Nissl stain as GABAergic fibers invaded the nucleus, con

28 in medium, propidium iodide (PI) uptake, and Nissl staining as markers of cell damage.

29 Nissl-stained brain sections of specimens from a previou

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

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

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

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

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

35 ination of Tbr1 and Lmx1a immunolabeling and Nissl staining confirmed the loss of CN neurons from the

36 ach is demonstrated by (i) development of a "Nissl stain" contrast agent for cellular imaging, (ii) v

37 Serial Nissl-stained coronal sections through the medial preopt

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

39 Nissl staining, cytochrome oxidase activity, and neurofi

40 /kg i.p.) also protected against neocortical Nissl-staining deficits.

41 ions and SMI-32 immunohistochemistry than in Nissl stain, especially for area 2 and subdivisions of a

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

43 Visualized by Nissl staining, foetal grafts formed clumps of pyramidal

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

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

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

47 ranule cell axon reorganization and by using Nissl staining, immunocytochemistry, and the optical fra

48 Staining for CO and Nissl stain in layer IV of SI showed a similar range of

49 s of NeuN and DARPP-32 immunoreactivity, and Nissl staining, in the striatum showed no striatal neuro

50 ed SE, bromodeoxyuridine (BrdU) labeling and Nissl staining increased in the rostral forebrain SVZ.

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

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

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

54 nucleus and are not merely artifacts of the Nissl-staining method.

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

56 Nissl staining, NeuN immunocytochemistry, and in situ hy

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

58 2 oscillations cause significant decrease in NISSL-stained neurons (p < 0.05) and induce inflammation

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

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

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

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

63 Nissl staining of retinae from normal adult and 5,7-DHT-

64 a subnuclear cytoarchitectonic parcellation (Nissl stain) of the NST into rostral, intermediate, and

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

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

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

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

69 Using myelin and Nissl stains, plus immunohistochemical staining with the

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

71 Hippocampal sections were processed for Nissl stain, Prox1-immunocytochemistry, GluR2-immunocyto

72 Using Nissl-stained retinal wholemounts and stereological meth

73 d with other histochemical markers including Nissl stains, retrogradely transported fluorescent trace

74 Motoneuronal soma size in Nissl stain revealed the same pattern of results seen wi

75 Nissl stains revealed large striatal lesions in rats rec

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

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

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

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

80 Nissl-stained sections demonstrated that BHK-hCNTF cells

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

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

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

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

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

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

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

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

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

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

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

92 Nissl-stained sections through three cytoarchitectonic s

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

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

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

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

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

98 In Nissl-stained sections, the autoradiographic label corre

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

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

101 Nissl staining showed pronounced tissue body loss with m

102 Histological analyses using Nissl staining showed that in NHPs with the aortic arch

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

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

105 DA cells/section by immunohistochemistry and Nissl staining [TH-labeled cells and thionin-stained cel

106 sparrows (Zonotrichia leucophrys gambelii): Nissl staining, the distribution of acetylcholinesterase

107 re removed after perfusion and processed for Nissl staining, the samples were randomized, and the inv

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

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

110 sed SMI-32 immunohistochemistry, myelin, and Nissl stains to characterize the architecture of the par

111 size of song nuclei have relied primarily on Nissl stains to define the borders of these regions.

112 In this study, Nissl staining was used to investigate whether the marke

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

114 n after 6 hours of ischemia, as evaluated by Nissl staining, was significantly less in HSP70tg mice c

115 NMDA-induced changes in Nissl staining were also different in slices from young

116 Disturbances of Nissl staining were finally evident at 48 h, with nearly