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1 Viscerofugal neurons were also labeled by biotinamide.
2 identified and intracellularly stained with biotinamide.
3 ed rats and filled them juxtacellularly with biotinamide.
4 s processed for the visualization of HRP and biotinamide.
5 axons were then intracellularly stained with biotinamide.
6 N of anesthetized rats and were labeled with biotinamide.
7 otor presympathetic neurons were filled with biotinamide and analyzed for the presence of tyrosine hy
8 cellular method, we labeled these cells with biotinamide and determined whether the recorded neurons
9 dividually filling the recorded neurone with biotinamide and observing expression of GAD67 mRNA by in
10 SNA, we juxtacellularly labeled neurons with biotinamide and subsequently reconstructed their somas a
12 esthetized rats and filled individually with biotinamide by using a juxtacellular labeling method.
13 siologically characterized BOTZ neurons with biotinamide by using a juxtacellular labeling method.
14 ns were recorded in the rVRG and filled with biotinamide by using the juxtacellular labeling techniqu
17 barosensitive, bulbospinal RVLM neurons with biotinamide following electrophysiological characterizat
18 ly passed Lucifer yellow and N-(2-aminoethyl)biotinamide hydrochloride (neurobiotin); in contrast, He
22 neurons could be classified as C1 cells, the biotinamide-labeled cells were processed for detection o
24 5 +/- 4.7% (n = 6), and 24 +/- 4% (n = 7) of biotinamide-labeled extrinsic axons in myenteric ganglia
26 d extrinsic varicosities; only 1 +/- 0.3% of biotinamide-labeled extrinsic varicosities contained alp
27 immunoreactivity coexisted in 15 +/- 1.4% of biotinamide-labeled extrinsic varicosities; only 1 +/- 0
32 barosensitive bulbospinal cells labeled with biotinamide were examined for phenylethanolamine N-methy
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