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1 traced PdPN and lateral MeApd outputs using biotinylated dextran amine.
2 the Bartha strain of pseudorabies virus, and biotinylated dextran amine.
3 allidothalamic projections were labeled with biotinylated dextran amine.
4 acers Phaseolus vulgaris leucoagglutinin and biotinylated dextran amine.
5 ism-reared owls by retrograde labeling using biotinylated dextran amine.
6 labeled by injections of the neuronal tracer biotinylated dextran amine.
7 inations from the contralateral cortex using biotinylated dextran amine.
8 r cortex neurons with the anterograde tracer biotinylated dextran amine.
9 inin conjugated to horseradish peroxidase or biotinylated dextran amines.
11 lowing retrograde tracer injection into SSN (biotinylated dextran amine 3K or Fluorogold), labeled pe
13 h was visualized by anterograde tracing with biotinylated dextran amine and by immunohistochemistry w
14 ximately 350 microns diameter) injections of biotinylated dextran amine and cholera toxin B to determ
17 njecting small amounts of sensitive tracers (biotinylated dextran amine and cholera toxin subunit B)
21 This study utilized anterograde transport of biotinylated dextran amine and Phaseolus vulgaris leucoa
22 the zebra finch, using in vivo injections of biotinylated dextran amine and verification of projectio
23 keys (Macaca mulatta) received injections of biotinylated dextran amine and wheat germ agglutinin con
24 cleus (NRT) were studied after injections of biotinylated dextran amine and wheat germ agglutinin con
25 xically injected with the anterograde tracer biotinylated dextran amine, and biotinylated dextran ami
26 tion of biocytin, extracellular injection of biotinylated dextran amine, and immunohistochemistry wit
27 h the anterograde tracers (3) H-amino acids, biotinylated dextran amine, and Phaseolus vulgaris leuco
28 solateral amygdala with a small injection of biotinylated dextran amine, and revealed the anterograde
29 cellular injections of the tracers biocytin, biotinylated dextran amine, and wheat germ agglutinin co
30 ee tracers were utilized: tritiated leucine, biotinylated dextran amine, and wheat germ agglutinin co
31 losely examine this assumption, we performed biotinylated dextran amine anterograde tracing studies i
32 e contralateral side, was investigated using biotinylated dextran amine as an anterograde tracer.
34 s, the chorda tympani nerve was labeled with biotinylated dextran amine at 3, 7, 14, 30, and 60 days
35 a focal injection (<100 nl) of a mixture of biotinylated dextran amine (BDA) and (3)H-leucine was ma
36 sory cortical areas, the anterograde tracers biotinylated dextran amine (BDA) and fluoro-ruby (FR) we
37 sory cortical areas, the anterograde tracers biotinylated dextran amine (BDA) and fluoro-ruby (FR) we
38 omatosensory cortex, the anterograde tracers biotinylated dextran amine (BDA) and fluoro-ruby (FR) we
40 sensorimotor cortex, the anterograde tracers biotinylated dextran amine (BDA) and fluororuby (FR) wer
41 um was studied by using axonal labeling with biotinylated dextran amine (BDA) and identifying patch a
42 on in rats by injecting anterograde tracers, biotinylated dextran amine (BDA) and Phaseolus vulgaris-
43 globus pallidus (GP) were studied using the biotinylated dextran amine (BDA) anterograde tracing met
44 onally, inefficient extrinsic tracers such a biotinylated dextran amine (BDA) are used to label regen
47 lation by combining anterograde transport of biotinylated dextran amine (BDA) following injections in
49 DMH-NPY neurons using the anterograde tracer biotinylated dextran amine (BDA) in lactating rats and D
51 ons were labeled by injections of the tracer biotinylated dextran amine (BDA) in the dorsal lateral g
52 ned by filling these cells retrogradely with biotinylated dextran amine (BDA) injected into the visua
54 owed to survive > or =45 days, at which time biotinylated dextran amine (BDA) injections were made in
55 ected the high-resolution anterograde tracer biotinylated dextran amine (BDA) into 126 sites centered
58 gle injections of the neuroanatomical tracer biotinylated dextran amine (BDA) into different tonotopi
59 heir synaptic targets, we made injections of biotinylated dextran amine (BDA) into layer 3 of macaque
60 llowing injections of the anterograde tracer biotinylated dextran amine (BDA) into layers 2-5 of each
62 rograde tracing, we made small injections of biotinylated dextran amine (BDA) into SI barrel cortex.
65 llowing injections of the anterograde tracer biotinylated dextran amine (BDA) into the heterotopic co
67 injected the highly sensitive axonal tracer biotinylated dextran amine (BDA) into the left nodose ga
68 ere that injection of the anterograde tracer biotinylated dextran amine (BDA) into the medial preopti
69 Focal injections of the tracers biocytin or biotinylated dextran amine (BDA) into the MGV labeled th
71 adult rhesus monkeys underwent injections of biotinylated dextran amine (BDA) into the right motor co
72 ospinal projections were traced by injecting biotinylated dextran amine (BDA) into the sensorimotor c
73 y injecting horseradish peroxidase (HRP) and biotinylated dextran amine (BDA) into the utricular macu
74 ed with anterograde tract-tracing, either by biotinylated dextran amine (BDA) labeled with immunogold
75 e labeled using the anterograde transport of biotinylated dextran amine (BDA) or Phaselous leucoagglu
76 herefore, we combined peroxidase labeling of biotinylated dextran amine (BDA) or Phaseolus vulgaris-l
78 e injected the superior colliculus (SC) with biotinylated dextran amine (BDA) to backfill retinal axo
79 ron microscope after retrograde transport of biotinylated dextran amine (BDA) to identify dendrites o
80 horetic injections of the anterograde tracer biotinylated dextran amine (BDA) to investigate intra-SC
81 ng a double labeling method of anterogradely biotinylated dextran amine (BDA) tracing combined with r
94 ities of the anterograde/ retrograde tracer, biotinylated dextran amine (BDA) were injected into loca
95 hat project to the CNIC, focal injections of biotinylated dextran amine (BDA) were made into differen
96 jections (approximately 1 mm in diameter) of biotinylated dextran amine (BDA) were placed in differen
97 ade transganglionic labeling techniques with biotinylated dextran amine (BDA) were used to examine th
98 atches, we combined anterograde transport of biotinylated dextran amine (BDA) with immunogold-silver
99 vulgaris leucoagglutinin and the second with biotinylated dextran amine (BDA) with Vector slate grey
100 s of RTN-Phox2b neurons were traced by using biotinylated dextran amine (BDA), and many BDA-ir bouton
101 munohistochemistry, anterograde tracing with biotinylated dextran amine (BDA), and retrograde tracing
102 g from the nodose ganglion was achieved with biotinylated dextran amine (BDA), and the MOR was detect
103 cers such as horseradish peroxidase (HRP) or biotinylated dextran amine (BDA), but large percentages
104 tal projection neuron type or the other with biotinylated dextran amine (BDA)-3000 molecular weight.
114 atal terminals were labeled anterogradely by biotinylated dextran amine (BDA)10k injection into the c
115 ons of the anterogradely transported form of biotinylated dextran amine (BDA; 10,000 molecular weight
118 ant terminal was labeled after injections of biotinylated dextran amines (BDA) in seven auditory cort
119 asoleus vulgaris-leucoagglutinin (PHA-L) and biotinylated dextran amines (BDA)] tracers were employed
121 ied by means of the anterograde transport of biotinylated dextran-amine (BDA) delivered to incisions
122 discrete unilateral injections of the tracer biotinylated dextran-amine (BDA) into the ventrolateral
123 ods: iontophoretic injections of biocytin or biotinylated dextran-amine (BDA) were made into the guin
124 all iontophoretic injections of anterograde (biotinylated dextran amine; BDA) and retrograde (cholera
125 ed injections of cholera toxin subunit B and biotinylated dextran amine directly into the nucleus.
129 rminals in layer 2/3 labeled by tracing with biotinylated dextran amine formed synapses with PV-negat
130 DMX by anterograde transport of the tracer, biotinylated dextran-amine from injection deposits confi
132 eurons were labeled with the neuronal tracer biotinylated dextran amine in mice ranging in age from p
133 ections of Biocytin and rhodamine-conjugated biotinylated dextran amine in the medial geniculate body
135 ade focal injections of a retrograde tracer, biotinylated dextran amine, in different parts of the IC
136 ear nucleus by using retrograde transport of biotinylated dextran amine injected into restricted but
137 tally reconstructed 68 rat CFs labeled using biotinylated dextran amine injected into the inferior ol
139 By using slice preparations, extracellular biotinylated dextran amine injections demonstrated a den
140 were first retrogradely labeled by injecting biotinylated dextran amine into a restricted region of t
141 t germ agglutinin-horseradish peroxidase, or biotinylated dextran amine into area 17 (V1), area 18 (V
142 racers Phaseolus vulgaris-leucoagglutinin or biotinylated dextran amine into selected forebrain struc
143 In a previous study, we made injections of biotinylated dextran amine into the CNIC of the gerbil a
147 ctions to "rUva" resulted from injections of biotinylated dextran amine into the lateral pontine nucl
148 C connections by extracellular injections of biotinylated dextran amine into the lateral pulvinar of
149 r small injections of the anterograde tracer biotinylated dextran amine into the primary motor cortex
150 cing CST projections following injections of biotinylated dextran amine into the sensorimotor cortex,
151 eriments, we injected the anterograde tracer biotinylated dextran amine into the spinal trigeminal nu
153 oeruleus and subcoeruleus, and injections of biotinylated dextran amines into these noradrenergic nuc
155 the injection of the neuronal tract tracers biotinylated dextran amine or Fast blue into PMv DFL.
158 o acids, Phaseolus vulgaris-leucoagglutinin, biotinylated dextran amine, or Fluoro-Ruby) were injecte
159 tions of Phaseolus vulgaris leukoagglutinin, biotinylated dextran amine, or rhodamine-labeled dextran
160 ns rats received iontophoretic injections of biotinylated dextran amine, Phaseolus vulgaris leucoaggl
161 grade tracer biotinylated dextran amine, and biotinylated dextran amine-positive corticostriatal fibe
162 , primarily a retrograde tracer (n = 15), or biotinylated dextran amine, primarily an anterograde tra
163 ctions into the LP of the anterograde tracer biotinylated dextran amine resulted in heavy anterograde
165 different kinds of neuroanatomical tracers (biotinylated dextran amines, rhodamine-linked dextran am
166 ich we injected the superior colliculus with biotinylated dextran amine to backfill the geniculate br
167 also injected the medullary dorsal horn with biotinylated dextran amine to determine the secondary tr
169 ventral pallidum, anterogradely transported biotinylated dextran amine was evaluated in sections pro
171 urface of the brainstem in vitro, and either biotinylated dextran amine was injected extracellularly
173 s were observed after the anterograde tracer biotinylated dextran amine was injected into the neonata
177 ular axons labeled anterogradely by means of biotinylated dextran amine were examined by using light
182 5) of the anterograde tracers Fluoro-Ruby or biotinylated dextran amine were made into gracile, resul
184 ons of Phaseolus vulgaris leucoagglutinin or biotinylated dextran amine were made into the LC or nucl
186 tions of the anterograde tracers biocytin or biotinylated dextran amine were made into the MGV of you
187 racers Phaseolus vulgaris-leucoagglutinin or biotinylated dextran amine were performed in various cor
189 ticle-conjugated cholera toxin B-subunit and biotinylated dextran amine, were placed in subdivisions
190 dish peroxidase, and the anterograde tracer, biotinylated dextran amine, were used to label dorsal ro
191 projections were studied in adult cats using biotinylated dextran amines, wheat germ agglutinin conju
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