ライフサイエンスコーパス: serpentine

1 dehydration of hydrous minerals, principally serpentine.

2 at attributes relative to inferred shifts to serpentine.

3 odifier Knickkopf and the chitin deacetylase Serpentine.

4 ts accumulated up to 3-fold higher levels of serpentine.

5 re designed and 3D printed in titanium as 2D serpentine, 3D spiral, and 3D serpentine columns, of equ

6 uited to overcome the multiple challenges of serpentine adaptation.

7 t point to a polygenic, multitrait basis for serpentine adaptation.

8 , providing numerous candidate mutations for serpentine adaptation.

9 We first demonstrate that serpentine-adapted plants exhibit dramatically altered e

10 concentrator designs (a rectangular maze, a serpentine and a filament-filled helix, the last perform

11 ptation, we pooled DNA from individuals from serpentine and nonserpentine soils and sequenced each 'g

12 tion of bare environments preceded shifts to serpentine, and may serve as an evolutionary precursor t

13 the dynamics of experimental communities of serpentine annual plants.

14 Alstonine and serpentine are pentacyclic indoloquinolizidine alkaloids

15 (WB), the boron atoms are linked in parallel serpentine arrays, with tungsten atoms in between.

16 Serpentine barrens represent extreme hazards for plant c

17 The stretchable device features a serpentine bilayer of gold mesh and gold-doped graphene

18 Subsequent to the evolution of a serpentine body and carnivory, snakes evolved a highly s

19 between tooth and bone, periosteal reaction, serpentine bone resorption, abscess formation, and root

20 njection of a specific inhibitor of the cAR1 serpentine cAMP receptor almost completely prevents the

21 ry rapidly by extracellular cAMP through the serpentine cAMP receptor cAR1, with Dd-STAT tyrosine pho

22 y cAMP pulses, a process that is mediated by serpentine cAMP receptors (cARs).

23 The chemoattractant cAMP, acting through serpentine cAMP receptors, results in a rapid and transi

24 , double layer) engender fluid flow within a serpentine channel containing a long array of the asymme

25 t moderate sample consumption by employing a serpentine channel design, resulting in a dead time of l

26 A serpentine channel has been patterned with a sol-gel fil

27 The total volume of the sample serpentine channel used for the microdialysis was 1 micr

28 The turns in the serpentine channel were asymmetrically tapered to minimi

29 ography (MEKC) separations in a 19.6-cm-long serpentine channel, the peptides were rapidly sampled in

30 th plasmid DNA continuously flowed through a serpentine channel, the side walls of which also serving

31 mic microdialyzer utilizing two mirror-image serpentine channels, which sandwich a regenerated cellul

32 iched between two chips having micromachined serpentine channels.

33 We use a novel mAb specific for serpentine chemokine-like receptor 1 (CMKLR1) to evaluat

34 ypical Ni bearing phases (i.e., two types of serpentines, chlorite, smectite, goethite, and hematite)

35 ots indicated higher efficiencies for the 3D serpentine chromatographic columns with higher aspect ra

36 r results to a previous study of independent serpentine colonizations in the closely related diploid

37 Use of the 3D serpentine column at a higher flow rate, as compared to

38 Gradient RPLC separations with the 3D serpentine column resulted in an average 15% and 82% (8

39 Isocratic RPLC separations with the 3D serpentine column resulted in an average 23% and 245% (8

40 titanium as 2D serpentine, 3D spiral, and 3D serpentine columns, of equal length and i.d.

41 l plates as compared to the 3D spiral and 2D serpentine columns, respectively.

42 capacity as compared to the 3D spiral and 2D serpentine columns, respectively.

43 Serpentine cord formation in BACTEC 12B medium was evalu

44 In defined circumstances, serpentine cording and cross-barring can be used for rap

45 Mycobacterium tuberculosis often exhibits serpentine cording when grown in liquid medium, whereas

46 and examined for the presence or absence of serpentine cording.

47 irulence is correlated with the formation of serpentine cords, a morphology that was first noted by K

48 ish, which involves the formation of massive serpentine cords, abscesses, and rapid larval death.

49 R variant involved the massive production of serpentine cords, absent during S-variant infection, and

50 A problem with failure by serpentine dehydration is that the volume change accompa

51 paration channels are chemically etched in a serpentine design to 21-cm total length.

52 extended ion path lengths and using compact serpentine designs.

53 LHR showed that this rate is dictated by the serpentine domain and the cytoplasmic tail.

54 difference in rate is dictated mostly by the serpentine domain.

55 e receptors and interact with the receptor's serpentine domain.

56 ) based on wavy-structured Kapton film and a serpentine electrode on stretchable substrates is presen

57 Microfluidic devices with a 23 cm long, serpentine electrophoretic separation channel and integr

58 in Mimulus guttatus and the closely related, serpentine endemic Mimulus nudatus, and compare them to

59 o genes putatively involved in adaptation to serpentine environments, IREG1 and NRAMP4, whereas no su

60 the field ("bareness"), which is greater in serpentine environments, is conserved across soil-type s

61 promotes lumenal secretion of Vermiform and Serpentine, extracellular matrix modifier proteins that

62 er mass transport at U-turns of the tortuous serpentine flow channel of the cell.

63 Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrust

64 wingless/wnt morphogens that are detected by serpentine fz receptors.

65 Serpentine Galphai-linked receptors support rapid adhesi

66 actin bundles zippered together or exhibited serpentine gliding along the coverslip.

67 manipulated plant diversity in a California serpentine grassland and found that many plant species f

68 between tooth and bone, periosteal reaction, serpentine grooving surrounding teeth (considered a sign

69 ic rocks produces serpentinites, composed of serpentine group minerals and varying amounts of brucite

70 the colony morphology and abolished classic serpentine growth (cording), the most profound effect of

71 bidopsis arenosa adapted to a multichallenge serpentine habitat in the Austrian Alps.

72 e of Mg(OH)2 (brucite), Mg2CO3 and iron-rich serpentine have all been proposed to exist on the surfac

73 Chemoattractant receptors of the serpentine, heterotrimeric Galphai protein-linked family

74 etermining the root-specific accumulation of serpentine in C. roseus plants.

75 red to control the presence of Knickkopf and Serpentine in the extracellular matrix.

76 tracheal size-control proteins Vermiform and Serpentine in the tracheal lumen.

77 These results suggest that amorphization of serpentine is an unlikely mechanism for generating deep-

78 restricted to the vicinity of the medulla's serpentine layer and found throughout the medulla; (b) n

79 rge ventral scales suggesting characteristic serpentine locomotion, yet retains small prehensile limb

80 Haphazardly arranged serpentine low-signal-intensity structures, often associ

81 gous mutations in the coding sequence of the serpentine melanocortin 4 receptor (MC4R) are the most f

82 zygous mutations in the coding region of the serpentine Melanocortin 4 receptor are the most common g

83 example, glauconite-nontronite), Fe- and Mg-serpentine, Mg-Fe-Ca-carbonate and probable Fe-sulphide

84 with diffractive optics was combined with a serpentine microfluidic channel geometry designed to pro

85 al and petrological models show the dominant serpentine mineral is antigorite.

86 However, the frictional strengths of serpentine minerals are too high to satisfy the limitati

87 lc is forming as a result of the reaction of serpentine minerals with silica-saturated hydrothermal f

88 microfluidic mixers: a Y channel mixer, a 3D serpentine mixer, and a vortex mixer.

89 In the serpentine mixer, OCT image analysis revealed that the m

90 d velocity profiles at various points in the serpentine mixer.

91 agar was thought to improve traction for the serpentine movement of the S. hyodysenteriae and for the

92 ing plants growing on serpentine (S) and non-serpentine (NS) soils, respectively.

93 more closely match the color of their native serpentine or nonserpentine soil type than the opposing

94 Serpentine, or linear irregular, vessels were most commo

95 ential fields and moved losslessly through a serpentine path including 44 "U" turns using TWs.

96 compression and multiple passes through the serpentine path provides the basis for a highly desirabl

97 ely 1094 m over 81 passes through the 13.5 m serpentine path) and was facilitated by the introduction

98 (trapped) cells ahead of them by choosing a serpentine path.

99 ion induced sequential muscle activation via serpentine-patterned muscle circuits, leading to coordin

100 onolayers were first formed through a single serpentine poly(dimethylsiloxane) microchannel; (ii) a s

101 ext of substantial gene flow from nearby off-serpentine populations of A. arenosa, as well as from A.

102 cluding fusiform/dolichoectatic, dissecting, serpentine, posttraumatic, mycotic and giant aneurysms w

103 Recently, a serpentine protein Smoothened (Smo) has been proposed as

104 ase A (PKA)-dependent phosphorylation of the serpentine protein Smoothened (Smo) leads to Ci activati

105 Multiple Serpentine Receptor B (SRB) chemosensory receptors regul

106 but distinct from, the previously described serpentine receptor class a (sra) family and shows a dif

107 have identified a chemosensory gene family, serpentine receptor class ab (srab), which exists in bot

108 at disrupts the adjacent chemoreceptor genes serpentine receptor class g (srg)-36 and -37.

109 ent chemoattractant for cells expressing the serpentine receptor CMKLR1 (chemokine-like receptor 1),

110 , extracellular cAMP through activation of a serpentine receptor family.

111 rity in all three systems is mediated by the serpentine receptor Frizzled and a number of additional

112 We show that the mast cell-expressed orphan serpentine receptor mCCRL2 is not required for expressio

113 that inhibits Hh signaling by targeting the serpentine receptor Smoothened (SMO), has produced promi

114 key elements of a general mechanism for the serpentine receptor switch.

115 C5L2 is an enigmatic serpentine receptor that is co-expressed with the C5a re

116 eceptor that acts together with the Frizzled serpentine receptor to initiate Wnt signal transduction.

117 e findings show that acquired mutations in a serpentine receptor with features of a G protein-coupled

118 rtussis toxin (PTX) is a potent inhibitor of serpentine receptor-associated inhibitory trimeric guani

119 (ER) to prevent maturation of Frizzled (Fz) serpentine receptors and fibroblast growth factor recept

120 nary conservation of the switch mechanism of serpentine receptors and help to constrain models of how

121 The seven transmembrane helices of serpentine receptors comprise a conserved switch that re

122 ommunication that is mediated by a family of serpentine receptors containing seven transmembrane doma

123 riety of other chemoattractants that bind to serpentine receptors coupled to heterotrimeric G protein

124 The Frizzled (Fz) family of serpentine receptors function as Wnt receptors, but how

125 rimeric GTP-binding proteins (G-proteins) to serpentine receptors involves several independent contac

126 Frizzled serpentine receptors mediate distinct signaling pathways

127 ing seven-transmembrane G-protein-coupled or serpentine receptors related to the ODR-10 diacetyl chem

128 pressin, angiotensin II, and endothelin bind serpentine receptors that interact with G(q) and activat

129 Frizzled (Fz) proteins are serpentine receptors that transduce critical cellular si

130 Serpentine receptors usually signal to downstream effect

131 In contrast with other known serpentine receptors, CIRL has two subunits of the 120 a

132 In Drosophila, two closely related serpentine receptors, Frizzled (Fz) and D-Frizzled2 (Fz2

133 lassic components of this system include the serpentine receptors, heterotrimeric G-proteins, adenyly

134 Caveolae harbor different serpentine receptors, intracellular components of signal

135 interaction with receptors, and, in several serpentine receptors, regions similar to those in rhodop

136 asmic ends of these two helices in two other serpentine receptors, the beta2-adrenoreceptor and the p

137 nding pockets within the seven-helix core of serpentine receptors, the topography of these binding po

138 Hormones and sensory stimuli activate serpentine receptors, transmembrane switches that relay

139 e biological responses via G protein-coupled serpentine receptors.

140 ost chemokine receptors and is rare in other serpentine receptors.

141 , and srd families of seven-transmembrane or serpentine receptors.

142 the holoreceptor by the plasma membrane, the serpentine region of the TSHR, or by TSHR dimerization.

143 s well as non-accumulating plants growing on serpentine (S) and non-serpentine (NS) soils, respective

144 As a demonstration, smooth straight, serpentine, self-similar, and bead-on-string structures

145 MS detector or for another pass through the serpentine separation region, allowing theoretically unl

146 es of Parkin have been solved, revealing its serpentine shape and modes of auto-inhibition.

147 hts, small- and large-amplitude sine curves, serpentine shapes, circles, and a variety of spirals.

148 We report Cr speciation (i) in four serpentine soil depth profiles derived from the Californ

149 y to reconstruct selective forces generating serpentine soil endemism, which has four to five indepen

150 though Cr(VI) concentrations are elevated in serpentine soil pore water, few studies have reported fi

151 to soil macronutrients, but not relative to serpentine soil use; and that the number of glucosinolat

152 A Sri Lankan serpentine soil was utilized to provide context with reg

153 her Arabidopsis lyrata is locally adapted to serpentine soil, and to map the polymorphisms responsibl

154 de patterns of genetic admixture between the serpentine-soil specialist leather oak (Quercus durata)

155 lianus occurs across a variety of gray-green serpentine soils and brown nonserpentine soils.

156 Hexavalent chromium (Cr(VI)) is generated in serpentine soils and exported to surface and groundwater

157 Serpentine soils, characterized by high heavy-metal cont

158 ous Thlaspi hyperaccumulators collected from serpentine soils, including Thlaspi goesingense, T. oxyc

159 en populations growing on and off phytotoxic serpentine soils.

160 represent a case of adaptation to growth on serpentine soils.

161 y present as Cr(III) in ultramafic rocks and serpentine soils.

162 o be a major pathway of Cr(VI) production in serpentine soils.

163 of eicosanoids and are likely members of the serpentine superfamily of G protein-linked receptors.

164 pressure (80 Torr) formed a 250-microm-wide serpentine trace with uniform width and microcrystalline

165 n thick bars suppresses buckling behavior in serpentine traces that have thicknesses greater than the

166 of liquids, alloys, ceramics and glasses the serpentine trajectories could cause entry into meta-stab

167 libration; the equilibration process follows serpentine trajectories in composition space.

168 es by an unknown mechanism that requires the serpentine transmembrane protein Smoothened (Smo) and th

169 n intracellular conformational switch in the serpentine transmembrane protein Smoothened appears to u

170 Members of the Frizzled family of serpentine transmembrane receptors are required to trans

171 their molecular makeup, including the famed serpentine transmembrane unit; and ultimately, their thr

172 micro stepper motors, a mixer connected to a serpentine tube, and a high-pressure valve.

173 trix, and lumenal secretion of Vermiform and Serpentine, two putative matrix-modifying proteins.

174 Ion accumulation is conducted in a SLIM serpentine ultralong path with extended routing (SUPER)

175 ctures for lossless ion manipulations (SLIM) serpentine ultralong path with extended routing (SUPER)

176 Pressure-induced amorphization of serpentine was observed at temperatures of 200° to 3