ライフサイエンスコーパス: seahorse

1 pecies and the brood pouch epithelium of the seahorse.

2 impaired mitochondrial function measured by Seahorse.

3 ed in the cytosol and colocalizes with Lrrc6/Seahorse.

4 have cloned and characterized two alleles of seahorse, a zebrafish mutation that results in pronephri

5 Using a Seahorse analyser, metabolic function of human primary E

6 Seahorse analyses and phosphorylated p38 staining in IEC

7 Seahorse analysis confirmed sustained mitochondrial impr

8 Seahorse analysis measured metabolic parameters.

9 Seahorse analysis of a large panel of mouse and human tu

10 Seahorse analysis revealed that PRMT1 increased the extr

11 dulated by changes in RICTOR expression, and Seahorse analysis to evaluate the effects of RICTOR depl

12 d retinal mitochondrial function as shown by Seahorse analysis using retinal biopsy.

13 In obese patients, using RNA sequencing, Seahorse analysis, and a series of in vitro experiments,

14 cs, targeted lipidomics, Oil Red O staining, Seahorse analysis, quantitative PCR, immunohistochemistr

15 etabolomics coupled with FDG-PET imaging and seahorse analysis, we found that CCL5 participates in hi

16 timulates cellular glycolysis as measured by Seahorse analysis.

17 used state-of-the-art approaches, including Seahorse Analyzer of mitochondrial function, electron pa

18 l and comprehensive analyses obtained with a Seahorse Analyzer or mass spectrometer come with monetar

19 the-art systems biology approaches including Seahorse Analyzer to assess mitochondrial respiration an

20 n hair bundles: zebrafish larvae bearing the seahorse and ift 172 mutations display specific kinocili

21 , we studied pactacin enzymes in pot-bellied seahorse and medaka (Oryzias latipes).

22 Seahorse and metabolomics flux assays were used to measu

23 Here, we study the seahorse and pipefish family (syngnathids) that have evo

24 e repertoire in a comprehensive sample of 12 seahorse and pipefish genomes along the "male pregnancy"

25 irectly interacts with the PCD protein Lrrc6/Seahorse and this interaction is critical for the in viv

26 sed reef fishes, bottom-dwelling flatfishes, seahorses and pufferfishes.

27 Seahorses and their relatives (syngnathids) show a uniqu

28 Subsequently, using metabolic (Seahorse) and enzymatic assays, we validated our proteom

29 ssay), disruption of cellular bioenergetics (Seahorse), and cell death (terminal deoxynucleotidyl tra

30 clear magnetic resonance (NMR) metabolomics, Seahorse, and the spatial distribution of metabolic co-e

31 belongs to family Syngnathidae (pipefishes, seahorses, and seadragons).

32 ausible mechanism for the diversification of seahorses, and that assortative mating (in this case as

33 , Western blotting, confocal microscopy, and Seahorse assay analyses by using the IL-7/S6K(weak)-stim

34 ncluding flow cytometry, immunofluorescence, Seahorse assay, and tumor xenograft models, were carried

35 etics and dynamics using spectrofluorimetry, Seahorse assay, electron paramagnetic resonance (EPR) sp

36 Using the Seahorse assay, we evaluated the effects of PGI2 signali

37 Moreover, metabolomics, Seahorse Assay-based metabolic profiling, and radiotrace

38 in Neonatal ventricular myocytes measured by seahorse assay.

39 d oxidative phosphorylation were assessed by seahorse assay.

40 We used plate growth and Seahorse assays and LC-MS/MS analysis to show that COQ11

41 hy controls were assessed by RNA sequencing, Seahorse assays, and LC-MS/MS.

42 Indeed, using live-cell Seahorse assays, we establish that pUL13 alone is suffic

43 We provide evidence that Seahorse associates with Dishevelled.

44 A Seahorse ATP rate assay revealed a significant decrease

45 brates, including Old and New World monkeys, seahorses, axolotls, and Xenopus.

46 ence (AF+) and Alde-red assays for CSCs, and Seahorse-based oxygen consumption rate (OCR), extracellu

47 ence (AF+) and Alde-red assays for CSCs, and Seahorse-based oxygen consumption rate (OCR), extracellu

48 Seahorse bioenergetics analysis was performed on EPC2-hT

49 rates measured in intact myotubes using the Seahorse Bioscience (Billerica, MA) flux analyzer and mi

50 els of differentiated functions and used the Seahorse Bioscience analyzer to measure mitochondrial fu

51 nes in an extracellular flux analyser (XF24, Seahorse Bioscience, Billerica, MA, USA) during specific

52 rformed with an extracellular flux analyser (Seahorse Bioscience, Billerica, MA, USA), and mitochondr

53 e and mitochondrial respiration capacity via Seahorse Cell Mito Stress Test were then detected in Per

54 these results suggest that the Reptin-Lrrc6/Seahorse complex is involved in dynein arm formation.

55 Finally, we show that seahorse constrains the canonical Wnt pathway and promot

56 tical gap by providing modular and automated Seahorse data analysis and visualization.

57 seahorse encodes Lrrc6l, a leucine-rich repeat-containin

58 Seahorses evolved in the late Oligocene and subsequent c

59 ed in vitro testing, this study employed the Seahorse Extracellular Flux Analyzer to study cellular m

60 factors, and glucose and/or hypoxia using a Seahorse extracellular flux analyzer.

61 smooth muscle cell (PASMC) cultures, using a Seahorse extracellular flux analyzer.

62 uclear cells (PBMCs) and platelets using the Seahorse extracellular flux technology.

63 Seahorse flux and unbiased metabolomics analysis showed

64 ly enriched in heavily ciliated tissues; and seahorse genetically interacts with the ciliary gene inv

65 As phage Seahorse genome encodes 48 open reading frames with many

66 Cell glycolysis was analyzed using the Seahorse glycolytic stress test.

67 Seahorses have a circum-global distribution in tropical

68 etracycline treatment, suggesting that phage Seahorse hijacked host biosynthesis pathways through pro

69 we first cloned C6AST genes from pot-bellied seahorse (Hippocampus abdominalis) and analyzed their ph

70 The long-snouted seahorse (Hippocampus guttulatus) is one of two seahorse

71 of several genes of the MHC II pathway while seahorses (Hippocampus) featured a highly divergent inva

72 ts, our alleles suggest that the function of seahorse in cilia motility is separable from its functio

73 s critical for the in vivo function of Lrrc6/Seahorse in zebrafish.

74 e show that the zebrafish cystic kidney gene seahorse is closely associated with ciliary functions: s

75 Yet seahorse is dispensable for cilia assembly or motility a

76 seahorse is expressed in zebrafish tissues known to cont

77 s closely associated with ciliary functions: seahorse is required for establishing left-right asymmet

78 dopts an elongated, all-helical, two-domain, seahorse-like structure with an overall architecture unl

79 eal a flexible approximately 30-nm elongated seahorse-like structure, which can adopt contracted and

80 ntitative polymerase chain reaction, and the Seahorse live-cell metabolic assay.

81 The Agilent Seahorse machine is a common method to measure real-time

82 ite data on genetic parentage that show that seahorses mate size-assortatively in nature.

83 Together, these data suggest that Seahorse may provide a link between ciliary signals and

84 ific activation of KRAS, PI3K, or MEK1 using Seahorse measurements, nuclear magnetic resonance metabo

85 Seahorse metabolic assays demonstrated that cytoplasmic

86 xygen consumption rate was assessed with the Seahorse metabolic flux analyzer, and mitochondrial acti

87 Seahorse metabolic flux assays revealed that rHDGF dose

88 hanged in cilia biogenesis mutants and lrrc6/seahorse mutants, suggesting that increased DNA damage r

89 Intriguingly, although seahorse mutations variably affect fluid flow in Kupffer

90 ative encoding mediated by the hippocampus ("seahorse") offers an interesting perspective for underst

91 respiration was assessed by using either the Seahorse or Oroboros technique, mitochondrial mass and b

92 Syngnathid fish (seahorses, pipefish and sea dragons) are slow swimmers y

93 Male pregnancy in seahorses, pipefishes and sea dragons (family Syngnathid

94 f male pregnancy in the family Syngnathidae (seahorses, pipefishes, and sea dragons) undeniably has s

95 Seahorses, pipefishes, and seadragons are fishes from th

96 d one of which is composed of Syngnathoidei (seahorses, pipefishes, and their relatives) plus several

97 Follow-up analysis utilizing the Seahorse platform showed decreased mitochondrial respira

98 Bioenergic profiling was performed using the Seahorse platform.

99 sable for cilia assembly or motility and the Seahorse protein is cytoplasmic.

100 ta and measured extracellular flux using the Seahorse (R) platform.

101 in seadragons as well as their pipefish and seahorse relatives.

102 ns and a 61-nucleotide crRNA assemble into a seahorse-shaped architecture that binds double-stranded

103 uctures of Cascade capture snapshots of this seahorse-shaped RNA-guided surveillance complex before a

104 s and its complexes with ATP or CTP reveal a seahorse-shaped subunit consisting of four domains: head

105 APN is a cell surface-anchored and seahorse-shaped zinc-aminopeptidase that forms head-to-h

106 Yet, seahorses show many adaptations for a sedentary, cryptic

107 Cell metabolic phenotype analysis using Seahorse showed LECs in co-culture exhibited reduced mit

108 sympatric speciation by asking whether tiny seahorse species are sister taxa to large sympatric rela

109 horse (Hippocampus guttulatus) is one of two seahorse species occurring in the North-East Atlantic.

110 zed skin patches of males that express novel seahorse-specific genes such as pastns and syn-lectins.

111 to interact with Disheveled, both alleles of seahorse strongly affect cilia motility in the zebrafish

112 hypothetical (cylindrical) architecture of a seahorse tail to uncover whether or not the square geome

113 shapes of most animal tails are cylindrical, seahorse tails are square prisms.

114 and oxidative phosphorylation measured with Seahorse technology on day 6 before restimulation.

115 real-time cell metabolic analysis using the Seahorse technology shows an inhibition of oxidative pho

116 Seahorse technology was used to investigate effects of v

117 Using Seahorse technology, pulsed stable isotope-resolved meta

118 ondrial regulation which was confirmed using Seahorse technology.

119 ry and for preventing kidney cyst formation; seahorse transcript is highly enriched in heavily ciliat

120 Seahorses use their tails as flexible grasping appendage

121 Phage Seahorse was able to infect the host in a broad range of

122 The vibriophage, designated Seahorse, was classified in the family Siphoviridae beca

123 Here we investigate seahorses' worldwide dispersal and biogeographic pattern

124 real-time metabolic profiling utilizing the Seahorse XF analyzer.

125 us HID1 variant p.R433W were investigated by Seahorse XF Assay in fibroblasts of two patients.

126 e using qPCR, mitochondrial function using a Seahorse XF bioanalyzer, and ROS production using a ROS-

127 y and glycolytic activities as measured with Seahorse XF24 analyzer in medium containing 10 mm glucos

128 using a custom-designed mitoxosome array and Seahorse XF24 Analyzer.

129 ochondria bioenergetics was examined using a Seahorse XF24 Analyzer.

130 We optimize the algorithm to work with the Seahorse XF24 extracellular flux analyzer.

131 y of cultured striatal neurons measured with Seahorse XF24 flux analyzer revealed unaltered cellular

132 changes in mitochondrial function using the Seahorse XF96 analyzer in AD and Control LCLs after expo

133 The Seahorse XF96 respirometer represents the state-of-the-a

134 The Seahorse XFe(96) Analyzer was used to measure the extrac

135 died by biotinylation assay and the Angilent Seahorse XFe96 Analyzer.

136 itochondrial function was assessed using the Seahorse XFe96 in fresh peripheral blood mononuclear cel

137 xisting techniques, including the eight-well Seahorse XFp.