ライフサイエンスコーパス: brevis

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

2 terium adolescentis but not of Lactobacillus brevis.

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

4 oxins produced by the dinoflagellate Karenia brevis.

5 n potentials recorded from abductor pollicis brevis.

6 entials were recorded from abductor pollicis brevis.

7 als were recorded from the abductor pollicis brevis.

8 n potentials recorded from abductor pollicis brevis.

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

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

11 itially coincident with high densities of K. brevis.

12 molecules was investigated in Lactobacillus brevis.

13 entials were recorded from abductor pollicis brevis.

14 tensor digitorum brevis and flexor digitorum brevis.

15 r and naturally produced brevetoxins from K. brevis.

16 roduced by the marine dinoflagellate Karenia brevis.

17 leading edge of the extensor carpi radialis brevis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 00, 152 dolphins died following extensive K. brevis blooms and brevetoxin was detected in 52% of anim

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

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

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

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

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

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

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

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

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

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

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

61 solated from sourdough isolate Lactobacillus brevis E25 was determined.

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

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

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

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

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

67 (2+) release from the SR of flexor digitorum brevis (FDB) fibers, either a ryanodine receptor agonist

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 K. brevis is variably allelopathic to multiple competitors,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 ical representation of the abductor pollicis brevis muscle.

115 ntact fibers from the mouse flexor digitorum brevis muscle.

116 entials were recorded from abductor pollicis brevis muscle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 genases from Pseudomonas ovalis and Bacillus brevis, respectively.

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

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

135 rovisional name "Candidatus Nitrosopelagicus brevis" str.

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

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

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

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

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

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

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

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

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

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

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

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

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