ライフサイエンスコーパス: seahorse

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

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

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

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

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

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

7 We provide evidence that Seahorse associates with Dishevelled.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

22 Yet seahorse is dispensable for cilia assembly or motility a

23 seahorse is expressed in zebrafish tissues known to cont

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 ondrial regulation which was confirmed using Seahorse technology.

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

47 Seahorses use their tails as flexible grasping appendage

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

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

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

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

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

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

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