1 lls because these surface structures are sub-
light microscopic.
2 Light microscopic analyses have shown that both subunits
3 Light microscopic analyses of male meiosis in these plan
4 Previous
light microscopic analyses of these mice left open quest
5 Double-immunofluorescence and
light microscopic analyses revealed that both group I mG
6 Light microscopic analyses revealed that choline acetylt
7 Unexpectedly,
light microscopic analyses showed a dramatic loss of the
8 Light microscopic analyses showed that labeled axons rea
9 We present here detailed electron and
light microscopic analyses that provide new insight into
10 Both
light microscopic analysis and staining with the pan-neu
11 Light microscopic analysis demonstrated GLY-IR profiles
12 Light microscopic analysis demonstrated that erythrocyte
13 Light microscopic analysis in both Collins- and glycine-
14 Light microscopic analysis indicated that CRF processes
15 Light microscopic analysis of 11 biocytin-filled cells s
16 Light microscopic analysis of detached retinas showed th
17 Light microscopic analysis of ENK and GABA immunoreactiv
18 Light microscopic analysis of the optic nerve, chiasm, a
19 Light microscopic analysis revealed four populations of
20 Light microscopic analysis revealed oval or circular imm
21 Light microscopic analysis revealed prominent kappaOR im
22 Light microscopic analysis shows extensive glomerular di
23 Light microscopic analysis using Neurolucida tracings of
24 cells into mature fiber cells, as judged by
light microscopic analysis.
25 Here, we describe FLASH (fast
light-microscopic analysis of antibody-stained whole org
26 Light-microscopic analysis of semi-thin sections reveale
27 To overcome limitations of conventional
light-microscopic analysis, we used high resolution Rama
28 colocalization in this material at both the
light microscopic and electron microscopic levels sugges
29 ction compartment of these cells at both the
light microscopic and electron microscopic levels.
30 and distorted NMJs were evident at both the
light microscopic and electron microscopic levels.
31 m bovine molar teeth and studied at both the
light microscopic and electron microscopic levels.
32 holaminergic neurons) and examined with both
light microscopic and electron microscopic methods.
33 Animals were perfused and processed for
light microscopic and electron microscopic study of both
34 By integrating
light microscopic and EM data, we estimate that sprouted
35 esting in GLT1 knock-out mice, were used for
light microscopic and EM-ICC.
36 uts from two eyes, although there are subtle
light microscopic and physiological differences.
37 of 8 months of age by routine techniques of
light microscopic and scanning electron microscopy.
38 Light microscopic and ultrastructural analysis revealed
39 and perivascular mesenchymal cells appear by
light microscopic and ultrastructural criteria to be fib
40 ichia coli (EPEC) on the basis of postmortem
light microscopic and, in some cases, microbiological ex
41 In the present study, complimentary
light microscopic anterograde biocytin and retrograde ho
42 Light microscopic anterograde tract-tracing studies have
43 We recently developed a multi-label confocal
light microscopic approach that makes possible the syste
44 We used electron and
light microscopic approaches to unravel the roles of fib
45 g RNAi and is well suited to high-resolution
light microscopic assays.
46 In accord with these results,
light microscopic autoradiography of the rat brain showe
47 e evaluated with receptor binding assays and
light microscopic autoradiography, using 1-2 nM [3H]pire
48 Using
light microscopic autoradiography, we observe heavy labe
49 NTS had neither proteinuria nor significant
light microscopic changes, yet had increased uptake of [
50 t appositions (18/21; 85.7%) selected by our
light microscopic criteria were confirmed as direct cont
51 ns (3/21; 14.3%) selected as contacts by our
light microscopic criteria were in fact separated from t
52 axon/myelin segmentation using a dataset of
light-microscopic cross-sectional images of osmium tetro
53 t selected optical levels for correlation of
light microscopic data and electron microscopic detail.
54 These
light microscopic data suggested that neurons in the PGi
55 Consistent with the
light microscopic data, ultrastructural analysis showed
56 Quantitative
light microscopic densitometry of the superficial dorsal
57 Quantitative
light microscopic densitometry of the superficial dorsal
58 management of thyroid neoplasms is based on
light microscopic diagnosis, but its accuracy and precis
59 vity was seen in processes having a regional
light microscopic distribution comparable to that of kno
60 In this study, we describe the
light microscopic distribution of CGRP immunoreactivity
61 Specificity also was demonstrated by the
light microscopic distribution of KT-LI in sections thro
62 In the present report we have defined the
light microscopic distribution of preganglionic negative
63 ghout the rat brain corresponds to the known
light-microscopic distribution of VGLUT3.
64 Light microscopic double labeling immunocytochemistry fo
65 Light microscopic double-labeling immunoperoxidase exper
66 A semiquantitative
light microscopic evaluation of 1-mum-thick sections inc
67 staining were then compared to the standard
light microscopic evaluation of the biopsies for rejecti
68 degree of deefferentation was quantified via
light microscopic evaluation of the density of OCB fasci
69 ed before histopathology to allow for direct
light microscopic evaluation of the lenses.
70 Physiological and
light microscopic evidence suggest that substance P (SP)
71 We produced
light microscopic evidence that the axons of rostral VLM
72 upporting structures were processed for both
light microscopic examination and immunohistochemical st
73 Light microscopic examination disclosed survival of the
74 Light microscopic examination of adult tissue revealed n
75 Light microscopic examination of an enucleated globe as
76 Light microscopic examination of brain, kidney, and sple
77 Based on
light microscopic examination of Congo red-stained secti
78 re treated with Masson's trichrome stain for
light microscopic examination of muscle fibers (red) and
79 urring inversions, identical at the level of
light microscopic examination of polytene chromosomes, m
80 In the present study,
light microscopic examination of the immunohistochemical
81 Light microscopic examination of the mouse hippocampal f
82 Light microscopic examination of the PIMI and Linplant a
83 Light microscopic examination of the retinas showed that
84 Light microscopic examination revealed free blood island
85 Light microscopic examination revealed that DOX-induced
86 Polarizing
light microscopic examination showed alternating light a
87 Light microscopic examination showed only loss of RGCs a
88 A
light microscopic examination was performed to study the
89 airs of neurones could not be predicted from
light microscopic examination.
90 owed widespread, microvesicular steatosis on
light-microscopic examination, but only electron-microsc
91 Gross pathologic and
light microscopic examinations of each organ, as well as
92 MS, originally characterized on the basis of
light microscopic features, are driven by fundamentally
93 However, this
light microscopic finding does not guarantee that NMDA r
94 ormed and the results were correlated to the
light microscopic findings on traditional hemotoxyin and
95 IVCM and
light microscopic findings suggest that the central corn
96 Light microscopic findings were recorded.
97 gions and dentate gyrus, and, in contrast to
light microscopic findings, in nuclei of a few pyramidal
98 However,
light microscopic histological analysis showed minimal h
99 ult without macular disease were compared to
light microscopic histology from comparable ages.
100 Diagnosis is usually accomplished by
light microscopic identification of spores in body fluid
101 ained or immunohistochemically stained whole
light microscopic images (200 x) were acquired (15.61 TB
102 ll subset of podocytes enabled us to acquire
light microscopic images of podocyte foot processes in u
103 High-speed
light microscopic images of swimming T. primitia cells s
104 Light microscopic images were captured in 32 regions of
105 y of myelinated peripheral nerve fibers from
light microscopic images.
106 non-fluorescence based phenotyping to enable
light microscopic imaging modalities.
107 n be accomplished at low cost, and can allow
light microscopic imaging of cleared tissues, thus enabl
108 By using
light microscopic immunocytochemistry and computer analy
109 Using
light microscopic immunocytochemistry and freeze-fractur
110 We used
light microscopic immunocytochemistry and ultrastructura
111 as localized in normal human brain tissue by
light microscopic immunocytochemistry by using highly sp
112 ned recording of wheel-running activity with
light microscopic immunocytochemistry for vasoactive int
113 Light microscopic immunocytochemistry indicated that exp
114 Light microscopic immunocytochemistry revealed reaction
115 Light microscopic immunocytochemistry revealed that gran
116 Light microscopic immunocytochemistry reveals presenilin
117 Light microscopic immunocytochemistry showed that dying
118 were injected with neurobiotin and shown by
light microscopic immunocytochemistry to be multipolar c
119 MF pathway LENK levels, we used quantitative
light microscopic immunocytochemistry to evaluate LENK l
120 hybridization techniques in combination with
light microscopic immunocytochemistry to show that the t
121 Light microscopic immunocytochemistry using affinity-pur
122 cortex of the rhesus macaque was examined by
light microscopic immunocytochemistry using an antibody
123 Light microscopic immunocytochemistry using antibodies t
124 at caudate putamen, by using immunoblots and
light microscopic immunocytochemistry.
125 ntrol and Huntington's disease (HD) cases by
light microscopic immunocytochemistry.
126 Corneas were fixed and prepared for
light microscopic,
immunohistochemical, and electron mic
127 Here, we used
light microscopic immunohistochemistry and multilabel im
128 Light microscopic immunohistochemistry was performed on
129 Using
light microscopic immunohistochemistry we find that the
130 ked immunosorbent assay and was localized by
light-microscopic immunohistochemistry.
131 Light microscopic immunolocalization was performed with
132 Using
light microscopic immunoperoxidase method, it was identi
133 presence did not seem to correlate with the
light microscopic injury pattern represented by balloone
134 controlled, they are ideal for quantitative
light microscopic investigation of dynamic processes in
135 This
light microscopic investigation provides a detailed qual
136 f the alpha(1F) subunit were examined at the
light microscopic level and by immunohistochemistry.
137 f this model, including visualization at the
light microscopic level and direct analysis of virus pro
138 the frequency of VND was accomplished at the
light microscopic level and validated by ultrastructural
139 Analysis of synaptotagmin labeling at the
light microscopic level during development of the antenn
140 Retinal morphometry was performed at the
light microscopic level in caspase-3 mutant mice from PN
141 ation of ERbeta-immunoreactivity (ir) at the
light microscopic level in many brain regions and the id
142 mmunoreactive processes were apparent at the
light microscopic level in the hypoglossal nucleus, but
143 phosphatase calcineurin was localized at the
light microscopic level in the rat hindbrain and spinal
144 At the
light microscopic level p75(NTR) immunoreactive elements
145 red hippocampal neurons and rat brain at the
light microscopic level showed enrichment of GRIP in GAB
146 e from intracellular labeling studies at the
light microscopic level suggests that a single cochlear
147 trated specific immunoreactivity (IR) at the
light microscopic level throughout the brain, spinal cor
148 Immunostaining was employed at the
light microscopic level to selectively label large myeli
149 t of the light neuropil staining seen at the
light microscopic level was due to the staining of dendr
150 f most collateral branches correlates at the
light microscopic level with dendrites.
151 ection, GluR1 appears as small puncta at the
light microscopic level, and is found in dendritic spine
152 At the
light microscopic level, autoradiography shows cell nucl
153 At the
light microscopic level, both ENK and PNMT varicose proc
154 At the
light microscopic level, dense M2 staining was seen in t
155 At the
light microscopic level, immunolabeling was prominent in
156 At the
light microscopic level, intense immunoreactivity was ap
157 At the
light microscopic level, labeled fibers within the supra
158 letion did not affect lung morphology at the
light microscopic level, nor did it affect the distribut
159 At the
light microscopic level, retrogradely labeled cells were
160 At the
light microscopic level, the anti-TH and anti-DA reveale
161 At the
light microscopic level, the biotin reactivity appears i
162 ptive terms for liver precursor cells at the
light microscopic level, the cells included in these des
163 At the
light microscopic level, the density of vesicular glutam
164 At the
light microscopic level, the distribution pattern and ce
165 At the
light microscopic level, the nob retina appeared to have
166 At the
light microscopic level, the NTS and inferior olive cont
167 At the
light microscopic level, there appeared to be increased
168 At the
light microscopic level, there was light to moderate lab
169 lar colocalization of NR2A/B with NR1 at the
light microscopic level.
170 ed the pattern of mu-ORi at the bright-field
light microscopic level.
171 s primarily due to limited resolution at the
light microscopic level.
172 ot affect growth or tissue morphology at the
light microscopic level.
173 e increased staining density observed at the
light microscopic level.
174 not differ from the wild-type protein at the
light microscopic level.
175 t terminals of any type could be detected at
light microscopic level.
176 ological features of microglial cells at the
light microscopic level.
177 rameter by which to assess plasticity at the
light microscopic level.
178 (GFAP) to label astrocytes were used at the
light microscopic level.
179 ne-sparse interneurons and astrocytes at the
light microscopic level.
180 is interspersed thoroughly with CentC at the
light microscopic level.
181 nd presumptive boutons invest the PPT at the
light microscopic level; (2) at the ultrastructural leve
182 s of photodamaged versus healthy skin at the
light microscopic level; comparison of cell shape and ap
183 ere was no evidence of histopathology at the
light microscopic level; however, ultrastructural studie
184 At the
light-microscopic level, both group I mGluRs are express
185 erular structure was normal at the gross and
light microscopic levels.
186 unolocalization studies at the electron- and
light-microscopic levels supported the conclusion that m
187 d RGS10 protein in rat and mouse brain using
light microscopic (
LM) and electron microscopic (EM) imm
188 t 15-360 min after injury, and processed for
light microscopic (
LM) and electron microscopic (EM) sin
189 the animals were perfused and processed for
light microscopic (
LM) and electron microscopic (EM) vis
190 y against the N-terminal of the 5-HTT at the
light microscopic (
LM) level indicates that the 5-HTT is
191 considerable expense and low throughput, and
light microscopic (
LM) methods, which provide molecular
192 een alga and tissues of the garden pea for a
light microscopic localization of lipid A in these eukar
193 A finding of practical importance is that
light microscopic measurements of boutons were diagnosti
194 Light microscopic measures revealed that a significant d
195 ration was not detected with general purpose
light microscopic methods in previous studies using seve
196 Using
light microscopic methods with immunohistochemistry, ele
197 at would not be detectable by using standard
light microscopic methods.
198 NA fragmentation and the ultrastructural and
light microscopic morphological features of MNs followin
199 In the present study we performed a
light microscopic,
morphometric analysis of identified O
200 Light microscopic observation of NMJs that showed synapt
201 copic, stereologic calculation confirmed the
light microscopic observation.
202 quantitatively along the cochlear spiral via
light-microscopic observation of cochlear wholemounts im
203 Light microscopic observations demonstrated morphologic
204 Light microscopic observations of the basilar papilla st
205 Light microscopic observations of the secretion process
206 Light microscopic observations revealed dense CaMK stain
207 ocytochemistry of rat brain sections shows a
light microscopic pattern that is suggestive of reactivi
208 The most common
light microscopic patterns were diffuse (53%), focal (28
209 Therefore, we applied
light microscopic postembedding immunostaining and optic
210 However, in
light microscopic preparations it was common to observe
211 ices, intracellularly labeled, processed for
light microscopic reconstruction, and compared to GC lay
212 transmission electron microscopic images and
light-microscopic reconstructions.
213 e morphology of these clefts, from the first
light-microscopic report up to recent three-dimensional
214 At
light microscopic resolution, M(2) immunoreactivity (-ir
215 energic fibers in the lesioned hemisphere at
light microscopic resolution; at electron microscopic re
216 Our
light microscopic results show that NOS I, as defined ma
217 Light microscopic retinal morphology was similar in Wt a
218 Using high magnification
light microscopic screening, both qualitative and quanti
219 nylated dextran amine were examined by using
light microscopic serial reconstruction and electron mic
220 n hypothalamus were investigated by means of
light microscopic single- and double-label immunocytoche
221 Light microscopic studies have shown that endomorphin-1
222 Light microscopic studies involving Kit tyrosine kinase
223 Light microscopic studies of BFT-treated monolayers reve
224 In addition,
light microscopic studies of fluorescently tagged protei
225 In aged cats,
light microscopic studies revealed significant decrease
226 Our previous
light microscopic studies suggested that extension of sy
227 Routine
light microscopic studies were performed in a total of 7
228 Consistent with previous
light microscopic studies, alpha2AAR-I was found in peri
229 Opioid receptors have been demonstrated by
light microscopic techniques in fine cutaneous nerves in
230 Using
light microscopic techniques, including retinal whole-mo
231 this copolymerization is well-studied using
light microscopic techniques, structural consequences of
232 removal corresponds to ECM as determined by
light microscopic visualization of the stained protein.