ライフサイエンスコーパス: flagellar beat

1 the chemomechanical energy efficiency of the flagellar beat.

2 g at an adaptation mechanism controlling the flagellar beat.

3 mechanical force to generate the ciliary and flagellar beat.

4 ructures play a critical role in shaping the flagellar beat.

5 c1b-3 cells displayed altered phototaxis and flagellar beat.

6 tive flagellum, but are unable to coordinate flagellar beat.

7 ctories while simultaneously recording their flagellar beat.

8 dynamics that is not observed for symmetric flagellar beats.

9 ynein is a critical regulator of ciliary and flagellar beating.

10 witches between synchronous and asynchronous flagellar beating.

11 T-shape radial spokes regulate flagellar beating.

12 flagellar axoneme generate forces needed for flagellar beating.

13 llar waves and, usually, highly asymmetrical flagellar beating.

14 hanges drive sliding of adjacent DMTs during flagellar beating.

15 on N-DRC assembly and its role in regulating flagellar beating.

16 stigation of the interaction between IFT and flagellar beating.

17 models confirmed the importance of TTC29 for flagellar beating.

18 critical for TTC29 axonemal localization and flagellar beating.

19 the RIIa/AKAP module to regulate ciliary and flagellar beating; absence of the spoke RIIa protein exp

20 The CP coordinates the flagellar beat and defects in CP projections are associa

21 (2) is required for bicarbonate to speed the flagellar beat and facilitate Ca(2+) entry channels.

22 gulatory networks that coordinate to produce flagellar beat and waveform.

23 tally confirmed the two-way coupling between flagellar beating and cell-body rocking predicted by our

24 Furthermore, analysis of both flagellar beating and microtubule sliding in vitro demon

25 in regulating mitochondrial respiration and flagellar beating and thus motility.

26 ble to reproduce the experimentally observed flagellar beats and the characteristic geometric signatu

27 ation rapidly elevates cAMP, accelerates the flagellar beat, and, thereby, changes swimming behavior

28 The metabolism, flagellar beating, and acrosome reaction of spermatozoa

29 es to the mechanism that produces asymmetric flagellar beating, and pose a new challenge for the func

30 nnel proteins and robust acceleration of the flagellar beat by bicarbonate.

31 ins produce the motive force for ciliary and flagellar beating by inducing sliding between adjacent m

32 ins within arrays drives muscle contraction, flagellar beating, chromosome segregation, and other bio

33 dyneins generating the force for ciliary and flagellar beating essential to movement of extracellular

34 ydrodynamic power balance, we infer the mean flagellar beat frequency and conjecture that its diurnal

35 bop5-1 cells display wild-type flagellar beat frequency but swim slower than wild-type

36 male reproductive tract that increases sperm flagellar beat frequency in vitro.

37 mouse epididymal sperm in vitro, the resting flagellar beat frequency is 2-3 Hz at 22-25 degrees C.

38 Previous work has shown that the flagellar beat frequency is reduced in sup-pf-2, but lit

39 as a "high-load environment," we reduced the flagellar beat frequency of wild-type cells through enha

40 ck only LC2 and LC10, this strain exhibits a flagellar beat frequency that is consistently less than

41 nt early step in capacitation, by increasing flagellar beat frequency through a pathway that requires

42 micro M cAMP acetoxylmethyl ester increases flagellar beat frequency to nearly 7 Hz and increases th

43 esulted in absent outer dynein arms, reduced flagellar beat frequency, and decreased cell velocity.

44 ed with central pair microtubules and reduce flagellar beat frequency, but do not prevent changes in

45 d in sAC(-/-) sperm, cAMP-AM ester increases flagellar beat frequency, progressive motility, and alte

46 nd mia2, which display slow swimming and low flagellar beat frequency.

47 although it did produce a modest increase in flagellar beat frequency.

48 uter arms but exhibits significantly reduced flagellar beat frequency.

49 slowly than wild type and exhibit a reduced flagellar beat frequency.

50 nce between the ATP consumption rate and the flagellar beating frequency, with approximately 2.3 x 10

51 y increased flagellar Ca(2+), which switches flagellar beating from a symmetrical to an asymmetrical

52 ation of digitised kinematic descriptions of flagellar beating from videomicroscopy.

53 Additionally, we find that the flagellar beat is regulated by the interactions during t

54 on the doublets near the switch point of the flagellar beat is sufficiently strong that it could term

55 ate (AMP) and adenosine diphosphate (ADP) on flagellar beating is not fully understood.

56 c surface-interactions, and chirality of the flagellar beat leads to stable upstream spiralling motio

57 plicated in critical processes as diverse as flagellar beating, membrane trafficking, histone methyla

58 n, but in cells generating oscillations, the flagellar beat mode alternated in synchrony with the osc

59 The flagellar beat of bull spermatozoa and C.

60 We characterize fluid flow and flagellar beating of human and sea urchin sperm with a z

61 CO(3)(-) is unable to rapidly accelerate the flagellar beat or facilitate evoked Ca(2+) entry into sA

62 MIPs can be found in axonemes to stabilize flagellar beat or within cytoplasmic microtubules.

63 with surface swimming, are sensitive to the flagellar beat pattern wavenumber and even to the asympt

64 sweeps varying the sperm head morphology and flagellar beat pattern wavenumber are conducted and reve

65 rom a nearly symmetrical, low-amplitude, and flagellar beating pattern to an asymmetrical, high-ampli

66 3D reconstruction algorithm to identify the flagellar beat patterns causing left or right turning, w

67 BAPTA-AM in wild-type sperm, they exhibited flagellar beat patterns more closely resembling those of

68 , and hyperactivation (faster swim speed and flagellar beat rate) in response to bourgeonal.

69 xperiments with mathematical modeling and 3D flagellar beat reconstruction to quantify the response o

70 Ciliary and flagellar beating requires the coordinated action of mul

71 y more common model systems, and the complex flagellar beating shapes that power it make its quantita

72 ming is caused by the intrinsic asymmetry in flagellar beating such that the curvature of a sperm's c

73 both ciliary beating and typical eukaryotic flagellar beating using different pairs of flagella.

74 Axonemal dynein ATPases direct ciliary and flagellar beating via adenosine triphosphate (ATP) hydro

75 e that CFAP45 supports mammalian ciliary and flagellar beating via an adenine nucleotide homeostasis

76 (repetitive store mobilization) which modify flagellar beating, whereas bolus application of micromol

77 ractivation is characterized by asymmetrical flagellar beating with high beat amplitude.