ライフサイエンスコーパス: biotinylated dextran amine

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.

10 Injection of the anterograde tracer, biotinylated dextran amine 10K (BDA10K), into PVN or NTS

11 lowing retrograde tracer injection into SSN (biotinylated dextran amine 3K or Fluorogold), labeled pe

12 For the present study, biotinylated dextran amine, an anterograde tracer, was i

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

15 In one of these three monkeys, biotinylated dextran amine and cholera toxin subunit b w

16 In the present study, biotinylated dextran amine and cholera toxin subunit B w

17 njecting small amounts of sensitive tracers (biotinylated dextran amine and cholera toxin subunit B)

18 Biotinylated dextran amine and fluorescent carbocyanine

19 Injections of biotinylated dextran amine and Fluoro-Gold in the ICX re

20 We used biotinylated dextran amine and Phaseolus vulgaris leucoa

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 monkeys of either sex were injected with the biotinylated dextran amine anterograde tracer either in

32 losely examine this assumption, we performed biotinylated dextran amine anterograde tracing studies i

33 e contralateral side, was investigated using biotinylated dextran amine as an anterograde tracer.

34 Using biotinylated dextran-amines as tracer, we observed promi

35 s, the chorda tympani nerve was labeled with biotinylated dextran amine at 3, 7, 14, 30, and 60 days

36 a focal injection (<100 nl) of a mixture of biotinylated dextran amine (BDA) and (3)H-leucine was ma

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

39 In one group of rats, 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

45 We made small injections of biotinylated dextran amine (BDA) as an anterograde trace

46 By using biotinylated dextran amine (BDA) as anterograde tracer,

47 lation by combining anterograde transport of biotinylated dextran amine (BDA) following injections in

48 Thus, we injected biotinylated dextran amine (BDA) in CRNs to study their

49 DMH-NPY neurons using the anterograde tracer biotinylated dextran amine (BDA) in lactating rats and D

50 After iontophoretic deposits of biotinylated dextran amine (BDA) in the area of the rVRG

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

53 Gross biocytin/biotinylated dextran amine (BDA) injections into the SG

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

56 Injections of biotinylated dextran amine (BDA) into Av labeled both af

57 Following injections of biotinylated dextran amine (BDA) into cortical area 17,

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

61 Injection of biotinylated dextran amine (BDA) into physiologically id

62 rograde tracing, we made small injections of biotinylated dextran amine (BDA) into SI barrel cortex.

63 We injected biotinylated dextran amine (BDA) into single vibrissal '

64 Injections of biotinylated dextran amine (BDA) into the dorsal cochlea

65 llowing injections of the anterograde tracer biotinylated dextran amine (BDA) into the heterotopic co

66 Injections of biotinylated dextran amine (BDA) into the InC anterograd

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

70 Injection of biotinylated dextran amine (BDA) into the PVH produced c

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

77 Injections of biotinylated dextran amine (BDA) that included this caud

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

82 ated to wheat germ agglutinin (WGA-HRP) with biotinylated dextran amine (BDA) transport.

83 Iontophoretic injection of 10% biotinylated dextran amine (BDA) unilaterally into the V

84 Biotinylated dextran amine (BDA) was initially iontophor

85 The anterograde tracer biotinylated dextran amine (BDA) was injected into the l

86 An anterograde tracer, biotinylated dextran amine (BDA) was injected into the r

87 Biotinylated dextran amine (BDA) was injected into the r

88 Biotinylated dextran amine (BDA) was injected into the s

89 The anterograde tracer biotinylated dextran amine (BDA) was injected into the v

90 An anterograde tracer, biotinylated dextran amine (BDA) was iontophoresed bilat

91 Thus, biotinylated dextran amine (BDA) was iontophoretically i

92 Tracing with biotinylated dextran amine (BDA) was used to assess intr

93 Biotinylated dextran amine (BDA) was used to label the c

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.

105 is 10-fold more efficient than tracing with biotinylated dextran amine (BDA).

106 has distinct advantages over the widely used biotinylated dextran amine (BDA).

107 seolus vulgaris-leuocoagglutinin (PHA-L) and biotinylated dextran amine (BDA).

108 eir projections using the anterograde tracer biotinylated dextran amine (BDA).

109 AC by using choleratoxin subunit B (CTB) and biotinylated dextran amine (BDA).

110 TN was revealed using the anterograde tracer biotinylated dextran amine (BDA).

111 hy1-YFP-H mice and fluorescence of mini-ruby biotinylated dextran amine (BDA).

112 to the accumbens with the anterograde tracer biotinylated dextran amine (BDA).

113 Using biotinylated dextran amine (BDA)/biocytin injections, we

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

116 Then, biotinylated dextran amine (BDA; 10,000 MW) was injected

117 We deposited biotinylated dextran amine (BDA; 3,000 MW), a retrograde

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

120 d in a ratfish, Hydrolagus colliei, by using biotinylated dextran amines (BDA, 3,000 MW).

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.

126 We used neural tract tracers (biotinylated dextran amines, fluorescein- and rhodamine-

127 Injections of biotinylated dextran amine-fluorescein into the nBIC at

128 LC colocalization of biotinylated dextran amine, following CAmy or PLH inject

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

131 Ganglion cells were labeled with biotinylated dextran amine in four embryos.

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

134 DMH projections determined by injections of biotinylated dextran amine in the mouse DMH.

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

138 Biotinylated dextran amine injected into the primary AC

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

144 To address this issue, we injected biotinylated dextran amine into the cochlear nucleus or

145 Injections of biotinylated dextran amine into the CPA resulted in nume

146 r neurons with an extracellular injection of biotinylated dextran amine into the DCN of rats.

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

152 Injections of the anterograde tracer biotinylated dextran amine into the wMCx revealed direct

153 oeruleus and subcoeruleus, and injections of biotinylated dextran amines into these noradrenergic nuc

154 e severed roots into the SC could be seen by biotinylated dextran amine labeling.

155 d from specific pulvinar domains by means of biotinylated dextran amine microinjections and compared

156 the injection of the neuronal tract tracers biotinylated dextran amine or Fast blue into PMv DFL.

157 Deposits of either biotinylated dextran amine or Phaseolus vulgaris leucoag

158 ade LC labeling after forebrain injection of biotinylated dextran amine or viral tracer.

159 o acids, Phaseolus vulgaris-leucoagglutinin, biotinylated dextran amine, or Fluoro-Ruby) were injecte

160 tions of Phaseolus vulgaris leukoagglutinin, biotinylated dextran amine, or rhodamine-labeled dextran

161 ns rats received iontophoretic injections of biotinylated dextran amine, Phaseolus vulgaris leucoaggl

162 grade tracer biotinylated dextran amine, and biotinylated dextran amine-positive corticostriatal fibe

163 , primarily a retrograde tracer (n = 15), or biotinylated dextran amine, primarily an anterograde tra

164 ctions into the LP of the anterograde tracer biotinylated dextran amine resulted in heavy anterograde

165 Anterograde tracing with biotinylated dextran amine revealed that the RST axons r

166 different kinds of neuroanatomical tracers (biotinylated dextran amines, rhodamine-linked dextran am

167 ich we injected the superior colliculus with biotinylated dextran amine to backfill the geniculate br

168 also injected the medullary dorsal horn with biotinylated dextran amine to determine the secondary tr

169 The retrograde tracer biotinylated dextran amine was deposited in the PAF unil

170 ventral pallidum, anterogradely transported biotinylated dextran amine was evaluated in sections pro

171 In these experiments, biotinylated dextran amine was injected directly into th

172 urface of the brainstem in vitro, and either biotinylated dextran amine was injected extracellularly

173 Biotinylated dextran amine was injected into the dorsal

174 s were observed after the anterograde tracer biotinylated dextran amine was injected into the neonata

175 The neuroanatomical tract tracer biotinylated dextran amine was injected into the PMv han

176 Biotinylated dextran-amine was deposited into physiologi

177 In addition, an anterograde tracer (biotinylated dextran amine) was iontophorized into the c

178 ular axons labeled anterogradely by means of biotinylated dextran amine were examined by using light

179 In adulthood, injections of biotinylated dextran amine were made either in the micro

180 Unilateral deposits of biotinylated dextran amine were made in AAF to retrograd

181 Injections of biotinylated dextran amine were made into AGm in normal

182 Injections of biotinylated dextran amine were made into AGm in normal

183 5) of the anterograde tracers Fluoro-Ruby or biotinylated dextran amine were made into gracile, resul

184 Injections of biotinylated dextran amine were made into several cortic

185 ons of Phaseolus vulgaris leucoagglutinin or biotinylated dextran amine were made into the LC or nucl

186 Injections of biotinylated dextran amine were made into the medullary

187 tions of the anterograde tracers biocytin or biotinylated dextran amine were made into the MGV of you

188 racers Phaseolus vulgaris-leucoagglutinin or biotinylated dextran amine were performed in various cor

189 Small injections of biotinylated dextran amine were placed in the ventral pa

190 ticle-conjugated cholera toxin B-subunit and biotinylated dextran amine, were placed in subdivisions

191 dish peroxidase, and the anterograde tracer, biotinylated dextran amine, were used to label dorsal ro

192 projections were studied in adult cats using biotinylated dextran amines, wheat germ agglutinin conju