1 tion of distance from the center of plaques (
double labeled for A beta peptide and microglia) reveale
2 rase (ChAT) in the geniculate A-laminae were
double labeled for BNOS.
3 number of cells in the SFO, OV and MePO were
double-labeled for both FOS-ir and fluoro-gold.
4 riatopallidal and striatonigral neurons were
double-labeled for both mGluR1a or mGluR5.
5 after a 3-wk survival time, there were cells
double-labeled for BrdUrd and either TuJ1 or neuronal nu
6 and neocortex; some of the latter cells were
double-labeled for BrdUrd and TuJ1.
7 AII amacrine cells also were
double-labeled for calretinin and parvalbumin; however,
8 The proportions of TH cell profiles
double-labeled for ChAT or VIP significantly increased b
9 In sections
double-labeled for CR and mGluR1alpha, the patterns of d
10 s, but not other CRF-containing nuclei, were
double labeled for CRF and PRV.
11 he BSTL as a retrograde tracer, neurons were
double labeled for CTB and PACAP or VIP immunohistochemi
12 -estradiol, the number of perirhinal neurons
double-labeled for ER-beta/GABA was reduced by 28% (P<0.
13 Cells
double labeled for GABA and MOR1 were common in the peri
14 In rats, cells
double labeled for GABA and MOR1 were observed in layers
15 ctory organs were cryosectioned (10 microm),
double-labeled for Galpha(olf), Galpha(q), or PLC140, an
16 They were also
double labeled for GFP and RPE65 or MITF.
17 The majority of these syncytia could be
double labeled for HIV-1 RNA and a dendritic cell marker
18 Tissue sections were also
double labeled for Melan-A and CD34.
19 cetyltransferase-immunoreactive neurons were
double-labeled for mGluR1a-like immunoreactivity.
20 ion was confirmed by the presence of neurons
double-labeled for NADPH-d and Fluoro-Gold.
21 These findings were confirmed in sections
double labeled for NGF and CGRP immunoreactivity.
22 than a third of the cholinergic neurons were
double-labeled for NOS.
23 bunits, 56% of parvalbumin interneurons were
double-labeled for NR2A/2B, and all identified cholinerg
24 ndin-containing striatal matrix neurons were
double-labeled for NR2A/2B.
25 trols and 1 year post-injection retinas were
double labeled for protein kinase C and tyrosine hydroxy
26 elected cases, series of brain sections were
double labeled for PRV-Ba and tyrosine hydroxylase to de
27 mall percentage of F4-80+ microglia are also
double labeled for SHP-1 at early times post-MCAO.
28 ) of mGluR1alpha-immunopositive neurons were
double-labeled for somatostatin.
29 ssue triple labeled for SS, NPY and nNOS, or
double-labeled for SS and nNOS or for SS and NPY.
30 In tissue
double-labeled for SS and nNOs, confocal laser scanning
31 sections from developing rat cerebellum were
double-labeled for TAG-1 and the Purkinje cell-specific
32 cells in the inner nuclear layer (INL) were
double-labeled for TH immunoreactivity.
33 The majority of FG-filled cells
double-labeled for TH were found in the dorsocaudal A10
34 maniculatus, and Peromyscus polionotus, and
double labeled for the expression of ERalpha and AVP imm
35 Hippocampal sections were
double-labeled for the alpha1, alpha4, gamma2, and delta
36 imulus-induced neuronal activation, and were
double-labeled for tyrosine hydroxylase to identify cate