ライフサイエンスコーパス: bushy

1 me to allow for the formation of very small, bushy adult plants.

2 culinaris Medik (Leguminosae) is an annual, bushy and herbaceous plant cultivated globally for its e

3 A subset of both bushy and T-stellate cells receives inhibition from an u

4 ajor excitatory projection cell classes, the bushy and T-stellate cells, receive a spatially broad in

5 neurons of the ventral cochlear nucleus, the bushy and T-stellate cells, receive glycinergic inhibiti

6 Spherical bushy, globular bushy, and octopus cells were not labeled.

7 eenhouse conditions, they revealed a stunted bushy appearance that could be rescued by gibberellic ac

8 planes facilitated the formation of upright bushy body plans and enabled the invasion of land.

9 hat for various synthetic stimuli, spherical bushy cell (SBC) activity in the Mongolian gerbil is ren

10 ecific cation current, I(h), was examined in bushy cell bodies and their giant presynaptic terminals

11 e majority of terminals contacting spherical bushy cell bodies in the guinea-pig anteroventral cochle

12 The bushy cell body I(h) showed similar properties to those

13 clude that LVA currents are expressed in the bushy cell body, but are not localized to the excitatory

14 Overall, large regional differences in bushy cell characteristics were not found; however, rost

15 source of input to the LSO that complements bushy cell projections from the ventral cochlear nucleus

16 Kv1 homomers were absent from bushy cell somata (from which the calyx axons arise); in

17 species suggest that the distinction between bushy cell subtypes is not always straightforward.

18 inhibition at the endbulb of Held-spherical bushy cell synapse in the auditory brainstem of juvenile

19 he input (endbulb of Held) output (spherical bushy cell) function.

20 tatory synapse types included AN synapses on bushy cells (AN-BC synapses) and fusiform cells (AN-FC s

21 us, where auditory nerve (AN) fibers contact bushy cells (BCs) at synapses called "endbulbs of Held."

22 hich is formed by auditory nerve fibers onto bushy cells (BCs) in the anteroventral cochlear nucleus.

23 We addressed this by comparing bushy cells (BCs) in the mouse cochlear nucleus with T-s

24 ss this, we studied the effects of mGluRs in bushy cells (BCs) of the mammalian anteroventral cochlea

25 he primary auditory signal from the ear, the bushy cells (BCs) of the ventral cochlear nucleus (VCN).

26 r hearing onset in a subset of low-frequency bushy cells (characteristic frequency< 10 kHz).

27 The spherical bushy cells (SBCs) of the anteroventral cochlear nucleus

28 rons in the cochlear nucleus, e.g. spherical bushy cells (SBCs).

29 a reduction in the somatic size of spherical bushy cells (SBCs).

30 onducted a systematic investigation of mouse bushy cells along the rostral-caudal axis in an effort t

31 in the PVCN and were also found on globular bushy cells and multipolar neurons in the PVCN and AVCN.

32 ly by four brainstem neuron types: spherical bushy cells and planar multipolar neurons of the ipsilat

33 ignalling, as shown for the cochlear nucleus bushy cells and principal neurons in the medial nucleus

34 responses arises mostly in the axons of VCN bushy cells and/or their calyceal terminals rather than

35 VCN neurons (bushy cells), axonal endings of bushy cells at MNTB cells (calyces of Held), and MNTB ne

36 Computer models reveal that slow IPSCs in bushy cells can improve spike timing on the scale of ten

37 that the dynamic AP inhibition in spherical bushy cells closely matches the inhibitory conductance p

38 Finally, bushy cells fired fewer action potentials in response to

39 However, no such spikes were observed in bushy cells from mice after the onset of hearing (>P14).

40 In bushy cells from mice before the onset of hearing (P6-P1

41 In the ventral CN, bushy cells hybridized strongly with Kv3.1 specific prob

42 g voltage- and current-clamp recordings from bushy cells in brain slices from mouse anteroventral coc

43 investigated via patch-clamp recordings from bushy cells in brainstem slices during stimulation of au

44 sions, adjacent to postsynaptic membranes of bushy cells in the cochlear nucleus.

45 ich are formed by auditory nerve fibers onto bushy cells in the cochlear nucleus.

46 fects of CHL at auditory nerve synapses onto bushy cells in the mouse anteroventral cochlear nucleus

47 e-cell patch clamp recordings were made from bushy cells of the anterioventral cochlear nucleus (aVCN

48 silhouette area was determined for spherical bushy cells of the anteroventral cochlear nucleus (AVCN)

49 Spherical and globular bushy cells of the AVCN receive huge auditory nerve endi

50 bit morphological similarities with globular bushy cells of the cochlear nucleus and principal cells

51 These included octopus cells and spherical bushy cells of the cochlear nucleus and principal neuron

52 bodies of the calyces of Held, the globular bushy cells of the cochlear nucleus, expressed somatoden

53 n the parent-cell bodies of the calyces, the bushy cells of the cochlear nucleus.

54 ellularis (NM) neurons, the avian homolog of bushy cells of the mammalian anteroventral cochlear nucl

55 Globular bushy cells project from the VCN to the medial nucleus o

56 at delayed release can drive spikes in older bushy cells provided synchronous release is absent, sugg

57 in synaptic organization of inputs to mouse bushy cells rather than the morphological characteristic

58 acteristics were not found; however, rostral bushy cells received a different complement of axosomati

59 Globular bushy cells reliably and faithfully transfer spike signa

60 ransmit signals along monaural pathways, and bushy cells sharpen the encoding of fine structure and f

61 of a model cell with some of the features of bushy cells to follow high frequency input with temporal

62 N neurons do not project to the LSO, and VCN bushy cells were not filled by these injections.

63 Our results also suggest that noise-exposed bushy cells would remain hyperexcitable for a period aft

64 -unit recordings were made from VCN neurons (bushy cells), axonal endings of bushy cells at MNTB cell

65 act multipolar cells, spherical and globular bushy cells, and octopus cells.

66 principal neurons of the AVCN, the spherical bushy cells, appears to be mediated by an excitatory ami

67 that planar multipolar cells, in addition to bushy cells, are a source of ascending input from the co

68 In cochlear nucleus (CN) bushy cells, ATP increases spontaneous and also acoustic

69 These cell types are bushy cells, bipolar (or fusiform) cells, octopus cells,

70 of the HVA current subtypes are expressed in bushy cells, but there is a strong polarity to their loc

71 ha-dendrotoxin revealed late spikes in older bushy cells, suggesting that postsynaptic activation of

72 Bushy cells, which provide precisely timed spike trains

73 ns arise from multipolar cells and spherical bushy cells.

74 egulation of GluA3 AMPA receptor subunits on bushy cells.

75 fiber and contact the cell body of spherical bushy cells.

76 ce the frequency range of that integrated by bushy cells.

77 fiber terminals contacting cochlear nucleus bushy cells.

78 ement of axosomatic input compared to caudal bushy cells.

79 emically induced mutations that suppress the bushy, determinate growth habit of field tomatoes, we is

80 eeping sickness), carried by tsetse flies in bushy environments, had a significant influence on pasto

81 rphism included brachycephaly, highly arched bushy eyebrows, synophrys, long eyelashes, low-set ears,

82 Spherical bushy, globular bushy, and octopus cells were not labele

83 transitions between filamentous, planar, and bushy growth are mimicked within moss life cycles.

84 sequently cleave in three planes, generating bushy growth.

85 mic astrocytes to cells that have lost their bushy-like morphology because of a reduction of distal f

86 S (P = 0.98); ERL regeneration and decreased bushy loops were associated with a shorter duration of u

87 Hsp70 positive, activated "bushy" microglia and Hsp70 negative, activated "polarize

88 dissociated aVCN neurones and in identified bushy neurones from a cochlear nucleus slice.

89 Bushy, octopus, and T-stellate cells of the ventral coch

90 mEPSCs from bushy, octopus, T-stellate, and tuberculoventral cells h

91 n higher levels of cytokinins, and display a bushy phenotype at late stages of development.

92 of omr1-1 initial transformants exhibited a bushy phenotype at the rosette stage.

93 endogenous cytokinin levels and restores the bushy phenotype to the wild type.

94 ound, the precursor was not cleaved, and the bushy phenotype was not produced.

95 s overexpressing microRNA156 (miR156) show a bushy phenotype, reduced internodal length, delayed flow

96 cells giving rise either to new filaments or bushy shoots are frequently juxtaposed on a single paren

97 Previous studies with tomato bushy stunt tombusvirus (TBSV) in a yeast model host hav

98 Previous work with Tomato bushy stunt tombusvirus (TBSV) in model host yeast has r

99 Tomato bushy stunt tombusvirus (TBSV) is a model virus that can

100 somerases, have been found to inhibit Tomato bushy stunt tombusvirus (TBSV) replication in a Saccharo

101 Previous works with Tomato bushy stunt tombusvirus (TBSV) revealed the recruitment

102 recruited to the replicase complex of Tomato bushy stunt virus (TBSV) and affects asymmetric viral RN

103 be defective interfering (DI) RNAs of tomato bushy stunt virus (TBSV) and have investigated their pot

104 Tomato bushy stunt virus (TBSV) and other tombusviruses encode

105 The VRCs built by Tomato bushy stunt virus (TBSV) are enriched with phosphatidyle

106 Tomato bushy stunt virus (TBSV) cDNA, positioned between a modi

107 Tomato bushy stunt virus (TBSV) co-opts cellular ESCRT (endosom

108 Overall, the works on Tomato bushy stunt virus (TBSV) have revealed intriguing and co

109 onucleases involved in degradation of Tomato bushy stunt virus (TBSV) in a Saccharomyces cerevisiae m

110 and ERG4 affected the replication of Tomato bushy stunt virus (TBSV) in a yeast model host.

111 performed complete RNA replication of Tomato bushy stunt virus (TBSV) in yeast cell-free extracts and

112 Similarly to other (+)RNA viruses, tomato bushy stunt virus (TBSV) induces major changes in infect

113 er of the genus Tombusvirus, of which tomato bushy stunt virus (TBSV) is the type member.

114 lication, we show that replication of Tomato bushy stunt virus (TBSV) leads to the formation of doubl

115 -chloride exchanger in replication of Tomato bushy stunt virus (TBSV) model (+)RNA virus.

116 ed replication of the closely related Tomato bushy stunt virus (TBSV) or Cucumber necrosis virus (CNV

117 rus model host Nicotiana benthamiana, Tomato bushy stunt virus (TBSV) P19 suppressor mutants are very

118 ased assay that the activation of the Tomato bushy stunt virus (TBSV) RdRp requires a soluble host fa

119 atidylethanolamine (PE) vesicle-based Tomato bushy stunt virus (TBSV) replication assay.

120 entify host proteins interacting with Tomato bushy stunt virus (TBSV) replication proteins in a genom

121 Previously we described Tomato bushy stunt virus (TBSV) vectors, which retained their c

122 each host gene on the replication of tomato bushy stunt virus (TBSV), a positive-strand RNA virus of

123 l host genes affecting replication of Tomato bushy stunt virus (TBSV), a small model plant virus, we

124 genes affecting RNA recombination in Tomato bushy stunt virus (TBSV), a small model plant virus.

125 y host genes affecting replication of Tomato bushy stunt virus (TBSV), a small model positive-strande

126 o study the activation of the RdRp of Tomato bushy stunt virus (TBSV), a small tombusvirus of plants,

127 To study the replication of Tomato bushy stunt virus (TBSV), a small tombusvirus of plants,

128 Tomato bushy stunt virus (TBSV), a tombusvirus with a nonsegmen

129 RNA, a model template associated with Tomato bushy stunt virus (TBSV), a tombusvirus, undergoes frequ

130 of gene silencing, the p19 protein of tomato bushy stunt virus (TBSV), that prevents the onset of PTG

131 Using the prototypical tombusvirus, Tomato bushy stunt virus (TBSV), we show that recombinant p33 r

132 ract with the replication proteins of Tomato bushy stunt virus (TBSV), which is a small, plus-strande

133 e of CNV is highly similar to that of Tomato bushy stunt virus (TBSV), with major differences lying o

134 The Tomato bushy stunt virus (TBSV)-encoded p19 protein (P19) is wi

135 such as brome mosaic virus (BMV) and tomato bushy stunt virus (TBSV).

136 fully functional replicase complex of Tomato bushy stunt virus (TBSV).

137 ic virus (TMV), potato virus X (PVX), tomato bushy stunt virus (TBSV)], is inhibited by disruption of

138 ive interfering (DI) RNA templates of tomato bushy stunt virus and a partially purified, RNA-dependen

139 Tomato bushy stunt virus and its cell-to-cell movement protein

140 V has two domains resembling those of tomato bushy stunt virus and Norwalk virus, rather than the exp

141 AtpC did not influence the spread of Tomato bushy stunt virus and Potato virus X.

142 This study on Tomato bushy stunt virus identified and defined three previousl

143 nd its accumulation was enhanced upon Tomato bushy stunt virus infection of two plant species.

144 he mechanical stability of individual tomato bushy stunt virus nanoparticles (TBSV-NPs).

145 e-stranded RNA-binding protein, e.g., tomato bushy stunt virus P19.

146 can efficiently recognize the related Tomato bushy stunt virus promoter sequences, including the minu

147 As (DI-RNAs) of Turnip crinkle virus, Tomato bushy stunt virus, Cucumber necrosis virus, and Potato v

148 ace the CP gene of a different virus, tomato bushy stunt virus, the resulting chimeric viral RNAs wer

149 The Tomato bushy stunt virus-encoded P19 forms dimers that bind dup

150 d enhancement of RNA recombination in Tomato bushy stunt virus.

151 small viral replicon RNA derived from tomato bushy stunt virus.

152 fungus-infecting hypovirus, or p19 of tomato bushy stunt virus.

153 a monopolar (L), medulla intrinsic (Mi, Mt), bushy T (T), transmedullary (Tm), transmedullary Y (TmY)

154 e retinotopic pathway defined by small-field bushy T-cells (T4) demonstrate only weak directional sel

155 owering, these transgenic plants produced a "bushy" tassel with increased lateral branching and spike

156 ction neurons in the CN, including spherical bushy, type I stellate/multipolar, and octopus cells in

157 and ReA patients had predominantly tortuous, bushy vessels; 89% of the RA patients had mainly straigh

158 It has been suggested that a bushy/woodland habitat that harbored tsetse fly constrai