ライフサイエンスコーパス: brevis

1 ways are present in squid ORNs (Lolliguncula brevis).

2 uman skin mites (Demodex folliculorum and D. brevis).

3 roduced by the marine dinoflagellate Karenia brevis.

4 leading edge of the extensor carpi radialis brevis.

5 ced by the 'red tide' dinoflagellate Karenia brevis.

6 oxins produced by the dinoflagellate Karenia brevis.

7 terium adolescentis but not of Lactobacillus brevis.

8 n potentials recorded from abductor pollicis brevis.

9 entials were recorded from abductor pollicis brevis.

10 als were recorded from the abductor pollicis brevis.

11 n potentials recorded from abductor pollicis brevis.

12 esis in bloom-forming dinoflagellate Karenia brevis.

13 results from high concentrations of Karenia brevis.

14 ted more robust metabolism in response to K. brevis.

15 e transporter (BbMAT), from the bacterium B. brevis.

16 itially coincident with high densities of K. brevis.

17 molecules was investigated in Lactobacillus brevis.

18 entials were recorded from abductor pollicis brevis.

19 tensor digitorum brevis and flexor digitorum brevis.

20 r and naturally produced brevetoxins from K. brevis.

21 ng the Alonso cultivar and Levilactobacillus brevis 0944 for onion fermentation.

22 vestigated, including 2 isolates of Bacillus brevis, 4 isolates of Bacillus licheniformis, 2 isolates

23 Six different muscles (abductor pollicis brevis, abductor digiti minimi, biceps brachii, tibialis

24 ps brachii, tibialis anterior, extensor dig. brevis, abductor hallucis) were measured every 3 months

25 Employing Lactobacillus brevis ADH, it was possible to achieve the synthesis of

26 eus muscles (1DI) and abductor digiti minimi brevis (ADMB) muscles for index and little fingers, resp

27 silactobacillus fermentum, Levilactobacillus brevis, Agrilactobacillus composti, Lacticaseibacillus p

28 isode was attributed to a persistent Karenia brevis algal bloom or 'red tide' centered in Southwest F

29 The impact of K. brevis allelopathy on competitor physiology was reflecte

30 e had opportunity to evolve resistance to K. brevis, allelopathy disrupted energy metabolism and impe

31 produced by the marine dinoflagellate Karina brevis, an organism associated with 'red tide' blooms in

32 her isolated from the dinoflagellate Karenia brevis, an organism well-known to produce complex polycy

33 terosseous, but not in the abductor pollicis brevis and abductor digit minimi muscles, was reduced to

34 ound to increase the cyanide tolerance of L. brevis and Escherichia coli.

35 oleus, tibialis anterior, extensor digitorum brevis and flexor digitorum brevis.

36 linity increased cellular toxin quotas in K. brevis and hypothesized that brevetoxins serve a role in

37 sure to blooms of the dinoflagellate Karenia brevis and its neurotoxin, brevetoxin (PbTx).

38 ns namely Lactobacillus casei, Lactobacillus brevis and Lactobacillus plantarum were microencapsulate

39 In contrast to E. coli, Bacillus brevis and Mycobacterium smegmatis Dps:DNA complexes, in

40 evis tendon tears in five, and both peroneus brevis and peroneus longus tendon tears in two.

41 MR imaging enabled detection of peroneus brevis and peroneus longus tendon tears.

42 o abundant bacteria of the rumen (Prevotella brevis and Prevotella ruminicola).

43 esence of the brevetoxin 1 from Ptychodiscus brevis and the pyrethroid RU51049, positive allosteric e

44 mediated ecological interactions between K. brevis and two diatom competitors, Asterionellopsis glac

45 ccus, Lactobacillus plantarum, Lactobacillus brevis and unclassified Lactobacillus were predominant i

46 Lacticaseibacillus casei, Levilactobacillus brevis, and Propionibacterium freudenreichii resulted in

47 Saccharomyces cerevisiae, Levilactobacillus brevis, and Pseudomonas fluorescens were exemplarily use

48 first dorsal interosseous, abductor pollicis brevis, anterior tibialis and triceps surae.

49 ions of the right and left abductor pollicis brevis (APB) and flexor carpi radialis (FCR) muscles in

50 amplitude vibration to the abductor pollicis brevis (APB) muscle of eight healthy volunteers for 15 m

51 tic stimulation (TMS) from abductor pollicis brevis (APB), first dorsal interosseous (FDI), and abduc

52 t dorsal interosseus, FDI; abductor pollicis brevis, APB; and abductor digiti minimi, ADM) in order t

53 he harmful algal bloom (HAB) species Karenia brevis, are essential when assessing the toxicological p

54 study we uncover two genes in Lactobacillus brevis ATCC 367, tstT and tstR, encoding for a rhodanese

55 of LVIS553, a MarR member from Lactobacillus brevis ATCC367.

56 mples of seawater collected during a Karenia brevis bloom in Manasota, Florida, were nebulized into a

57 , and those stranding in the absence of a K. brevis bloom, these data, taken together with the absenc

58 ns died in the absence of an identifiable K. brevis bloom; however, 100% of the tested animals were p

59 , although the diatom that co-occurs with K. brevis blooms (A. glacialis) exhibited more robust metab

60 00, 152 dolphins died following extensive K. brevis blooms and brevetoxin was detected in 52% of anim

61 y be a result of its frequent exposure to K. brevis blooms in the Gulf of Mexico.

62 and adverse impacts during at least some K. brevis blooms.

63 arding mechanisms for toxin production in K. brevis by providing an explanation for toxin production

64 in sound spectrum levels and increase in K. brevis cell concentrations also coincided with decreased

65 The assay allowed analysis of 400 L. brevis cells isolated from 1L of beer, which fits the "a

66 Addition of glucose to L. brevis cells loaded with [(14)C]TMG promotes efflux and

67 Live images of K. brevis cells were also examined to assess changes in cel

68 equency bands spanning 0.172-20 kHz after K. brevis cells were opportunistically sampled near the sta

69 se to osmotic stress in three of the four K. brevis clones examined.

70 ium butyricum abundance, while Lactobacillus brevis, Clostridium bolteae and Dialister invisus increa

71 In vivo qRT-PCR experiments performed in L. brevis confirmed that the divergently transcribed genes

72 ay challenges with lysed cultures of Karenia brevis (crude brevetoxin), pure brevetoxin-2, brevetoxin

73 DNA sequences specific exclusively to L. brevis DNA and RNA were selected and used for probe and

74 zyme, both made to be highly specific for L. brevis DNA.

75 solated from sourdough isolate Lactobacillus brevis E25 was determined.

76 the preservation of their extensor digitorum brevis (EDB) muscle seen on MRI and the response of cult

77 tration ([Ca(2+)](rest)) in flexor digitorum brevis (FDB) and vastus lateralis prepared from heterozy

78 In flexor digitorum brevis (FDB) fibers isolated from JP45-CASQ1-CASQ2 tripl

79 ur method to isolated mouse flexor digitorum brevis (FDB) fibers that are embedded in 10 mg/mL Matrig

80 verexpressed Rad and Rem in flexor digitorum brevis (FDB) fibers via in vivo electroporation and exam

81 Myotubes, adult flexor digitorum brevis (FDB) fibers, and sarcoplasmic reticulum skeletal

82 (2+) release from the SR of flexor digitorum brevis (FDB) fibers, either a ryanodine receptor agonist

83 We used Flexor Digitorum Brevis (FDB) isolated from young (~2-months old) and old

84 To this end, short flexor digitorum brevis (FDB) muscle fibers from 5-7- and 21-24-month-old

85 luorescent protein (GFP) in flexor digitorum brevis (FDB) muscle fibres from adult mouse.

86 ing paper, we reported that flexor digitorum brevis (FDB) muscle fibres from S100A1 knock-out (KO) mi

87 vement currents in isolated flexor digitorum brevis (FDB) muscle fibres from wild-type and S100A1 kno

88 hesized that denervation in flexor digitorum brevis (FDB) muscle from ageing mice is more extensive t

89 ngle intact fibres from the flexor digitorum brevis (FDB) muscle from the mouse.

90 ciated from the fast-twitch flexor digitorum brevis (FDB) muscle or in small bundles from the slow-tw

91 in dissociated fibres from flexor digitorum brevis (FDB) muscle using the whole-cell patch clamp con

92 etal muscle fibers from the flexor digitorum brevis (FDB) muscle were obtained from 5-7-, 14-18-, or

93 res from predominantly fast flexor digitorum brevis (FDB) muscle, but did in FDB fibres expressing ex

94 issociated from adult mouse flexor digitorum brevis (FDB) muscles and maintained in culture without o

95 digitorum longus (EDL) and flexor digitorum brevis (FDB) muscles of normal and mdx mice.

96 nterestingly, the intrinsic flexor digitorum brevis (FDB) muscles of the foot are identical to the FD

97 sients in adult dissociated flexor digitorum brevis (FDB) skeletal muscle fibers and human embryonic

98 Ca(2+) transients in mouse flexor digitorum brevis (FDB) skeletal muscle fibres under voltage clamp,

99 Flexor digitorum brevis (FDB)muscles were transfected by in vivo electrop

100 diaphragm and limb muscle (flexor digitorum brevis [FDB]) preparations were used to determine the re

101 (ECCE) in both adult mouse flexor digitorum brevis fibers and primary myotubes.

102 keletal myotubes, and adult flexor digitorum brevis fibers TCS depresses electrically evoked ECC with

103 harge movement densities in flexor digitorum brevis fibers.

104 Isolated mouse flexor digitorum brevis fibres showed a rapidly developing, reversible an

105 One such species, Karenia brevis, forms nearly annual blooms that threaten coastal

106 Single-strain cultures of Levilactobacillus brevis, Fructilactobacillus sanfranciscensis, Companilac

107 initiation module PheATE (GrsA) of Bacillus brevis gramicidin S synthetase catalyzes the activation,

108 e-domain (ATE) initiation module of Bacillus brevis gramicidin S synthetase equilibrates the Calpha c

109 beer spoilage bacterial cells Lactobacillus brevis have been detected by the electrochemical sandwic

110 Thus, Karenia brevis, in addition to producing toxins that adversely a

111 growth of one such bacterium, Lactobacillus brevis, in the presence of fructose induces the synthesi

112 Karenia brevis is the dominant toxic red tide algal species in t

113 BxmR from the cyanobacterium Osciliatoria brevis is the first characterized ArsR protein that sens

114 K. brevis is variably allelopathic to multiple competitors,

115 PEC disc extracts of brevetoxin-producing K. brevis (isolate SP3) cultures, LC/MS analysis yielded th

116 aberus giganteus) and termites (Cryptotermes brevis, Kalotermes flavicollis) identifies these flagell

117 is a naturally occurring product of Bacillus brevis known to form ion channels in synthetic and natur

118 ort the in vivo application of Lactobacillus brevis (Lb)NOX(1), a bacterial water-forming NADH oxidas

119 ater-forming NADH oxidase from Lactobacillus brevis (LbNOX) as a genetic tool for inducing a compartm

120 ssion of the NADH oxidase from Lactobacillus brevis (LbNOX)(13) targeted to the mitochondria or cytos

121 imilar to that recently observed in other K. brevis metabolites, though the "interrupted" polyether s

122 Five Demodex brevis mites were found among the 422 Demodex specimens.

123 aracterization of one of them, Brevibacillus brevis monoamine transporter (BbMAT), from the bacterium

124 xcitability of the relaxed abductor pollicis brevis muscle (APB) at various intervals during a moveme

125 nger (sensory studies) and abductor pollicis brevis muscle (motor studies).

126 sion of miR-19b-3p in mouse flexor digitorum brevis muscle enhances contraction-induced glucose uptak

127 cay of Ca(2+) transients in flexor digitorum brevis muscle fibers during repetitive stimulation.

128 Here, we used flexor digitorum brevis muscle fibers from transgenic mice with muscle-sp

129 recorded simultaneously in flexor digitorum brevis muscle fibers of adult mice, using the whole-cell

130 onitor SR luminal Ca(2+) in flexor digitorum brevis muscle fibers to determine the mechanism of dimin

131 ai1 were delivered into the flexor digitorum brevis muscle in live mice and knockdown of Orai1 elimin

132 mes) was delivered to the extensor digitorum brevis muscle of 3 subjects with documented SGCA mutatio

133 bres were isolated from the flexor digitorum brevis muscle of mice and intracellular NO production wa

134 K.hSGCA injected into the extensor digitorum brevis muscle was conducted.

135 us muscles, six originated from the peroneus brevis muscle, and all seven inserted onto the calcaneus

136 evoked at the contralateral flexor pollicis brevis muscle.

137 entials were recorded from abductor pollicis brevis muscle.

138 ical representation of the abductor pollicis brevis muscle.

139 ntact fibers from the mouse flexor digitorum brevis muscle.

140 EPs) simultaneously in the extensor pollicis brevis muscles bilaterally, was applied at different lat

141 e intact muscle fibres from flexor digitorum brevis muscles from young (2-6 months) and old (23-30 mo

142 st CSQ1 was introduced into flexor digitorum brevis muscles using electroporation.

143 dine receptor disruption in flexor digitorum brevis myofibers isolated from ferlin mutant mice.

144 eletal muscle cells (murine flexor digitorum brevis myofibers) and confocal imaging to detect and cal

145 leading edge of the extensor carpi radialis brevis (n = 4), prominent radial recurrent vessels (n =

146 cells by overexpression of the Lactobacillus brevis NADH oxidase LbNOX increased the translation rate

147 isolated from a foot muscle (flexor hallucis brevis) of the rat; the muscle contains approximately 90

148 n that inducer exclusion and expulsion in L. brevis operates via a multicomponent signal transduction

149 either expressed in a low copy plasmid in L. brevis or as a single copy chromosomal insertion in Baci

150 leading edge of the extensor carpi radialis brevis, or prominent radial recurrent vessels; signal in

151 rages are a good medium for the growth of L. brevis POM, and L. plantarum (TR-71, TR-14), observing h

152 Lactobacillus brevis POM, and Lactobacillus plantarum (TR-7, TR-71, TR

153 Lactobacillus brevis POM, and Lactobacillus plantarum (TR-7, TR-71, TR

154 skeletal muscle fibers from flexor digitorum brevis (predominantly fast-twitch).

155 Ingestion of shellfish contaminated with K. brevis produces neurotoxic shellfish poisoning (NSP) in

156 n the N. viennensis and "Ca Nitrosopelagicus brevis" proteomes.

157 oem formation and differentiation defects in brevis radix (brx) and octopus (ops) mutants are similar

158 iated Arabidopsis proteins OCTOPUS (OPS) and BREVIS RADIX (BRX) display shootward and rootward polar

159 For example, in Arabidopsis thaliana, the BREVIS RADIX (BRX) gene is required for continuous root

160 ation requires plant-specific genes, such as BREVIS RADIX (BRX) in Arabidopsis thaliana roots.

161 ted perturbed protophloem development of the brevis radix (brx) mutant.

162 SE ASSOCIATED WITH BRX (PAX); its inhibitor, BREVIS RADIX (BRX); and PHOSPHATIDYLINOSITOL-4-PHOSPHATE

163 ASYMMETRY IN THE STOMATAL LINEAGE (BASL) and BREVIS RADIX family (BRXf) proteins is required for asym

164 larity module marked by interacting BASL and BREVIS RADIX-LIKE 2 (BRXL2) proteins in Arabidopsis.

165 , the stomatal lineage cell polarity marker, BREVIS RADIX-LIKE 2 (BRXL2), exhibited no significant ex

166 d BRXL4, a shoot-specific protein related to BREVIS RADIX.

167 KK, and Cer-s/ HvBRX-Solo, encoding a single BREVIS-RADIX (BRX) domain protein.

168 in fish populations in response to a Karenia brevis red tide harmful algal bloom by examining sound s

169 me from specific gut bacteria (Lactobacillus brevis) regulates locomotor behavior through carbohydrat

170 genases from Pseudomonas ovalis and Bacillus brevis, respectively.

171 ane of nuclei isolated from flexor digitorum brevis skeletal muscle fibers of adult mice.

172 In contrast, the K. brevis SP1 clone, which has a consistently low brevetoxi

173 rovisional name "Candidatus Nitrosopelagicus brevis" str.

174 ellular toxin concentrations in five Karenia brevis strains from different geographic locations.

175 o low-salinity stress in any of the eight K. brevis strains we tested, including three used in the or

176 neurosis entheses and 89.5% of flexor digiti brevis tendon entheses were unremarkable.

177 ere seen in four patients, isolated peroneus brevis tendon tears in five, and both peroneus brevis an

178 calcaneus, peroneus longus tendon, peroneus brevis tendon; and cuboid bone.

179 Karenia brevis, the major HAB dinoflagellate in the Gulf of Mexi

180 health is directly impacted by blooms of K. brevis through consumption of shellfish contaminated by

181 entative lactic acid bacterium Lactobacillus brevis transports galactose and the nonmetabolizable gal

182 d while recording from the abductor pollicis brevis, using a paired pulse TMS paradigm with subthresh

183 Median CMCT to abductor pollicis brevis was 14.8 ms (range 8.8-27.4 ms).

184 molecular mechanism of inducer control in L. brevis, we have cloned the genes encoding the HPr(Ser) k

185 looms of the red-tide dinoflagellate Karenia brevis, which produces potent neurotoxins that negativel

186 In the K. brevis Wilson clone, cells responded quickly to hypoosmo

187 , L. rhamnosus (WJ-LR), L. casei (WJ-LC), L. brevis (WJ-LB) and Pediococcus pentosaceus (WJ-PP).