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1 g at an adaptation mechanism controlling the flagellar beat.
2 ructures play a critical role in shaping the flagellar beat.
3 c1b-3 cells displayed altered phototaxis and flagellar beat.
4 mechanical force to generate the ciliary and flagellar beat.
5 tive flagellum, but are unable to coordinate flagellar beat.
6 dynamics that is not observed for symmetric flagellar beats.
7 ynein is a critical regulator of ciliary and flagellar beating.
8 witches between synchronous and asynchronous flagellar beating.
9 T-shape radial spokes regulate flagellar beating.
10 flagellar axoneme generate forces needed for flagellar beating.
11 llar waves and, usually, highly asymmetrical flagellar beating.
12 the RIIa/AKAP module to regulate ciliary and flagellar beating; absence of the spoke RIIa protein exp
13 (2) is required for bicarbonate to speed the flagellar beat and facilitate Ca(2+) entry channels.
15 tally confirmed the two-way coupling between flagellar beating and cell-body rocking predicted by our
17 ation rapidly elevates cAMP, accelerates the flagellar beat, and, thereby, changes swimming behavior
19 es to the mechanism that produces asymmetric flagellar beating, and pose a new challenge for the func
21 ins produce the motive force for ciliary and flagellar beating by inducing sliding between adjacent m
22 dyneins generating the force for ciliary and flagellar beating essential to movement of extracellular
25 mouse epididymal sperm in vitro, the resting flagellar beat frequency is 2-3 Hz at 22-25 degrees C.
27 as a "high-load environment," we reduced the flagellar beat frequency of wild-type cells through enha
28 ck only LC2 and LC10, this strain exhibits a flagellar beat frequency that is consistently less than
29 nt early step in capacitation, by increasing flagellar beat frequency through a pathway that requires
30 micro M cAMP acetoxylmethyl ester increases flagellar beat frequency to nearly 7 Hz and increases th
31 esulted in absent outer dynein arms, reduced flagellar beat frequency, and decreased cell velocity.
32 ed with central pair microtubules and reduce flagellar beat frequency, but do not prevent changes in
33 d in sAC(-/-) sperm, cAMP-AM ester increases flagellar beat frequency, progressive motility, and alte
38 nce between the ATP consumption rate and the flagellar beating frequency, with approximately 2.3 x 10
39 y increased flagellar Ca(2+), which switches flagellar beating from a symmetrical to an asymmetrical
40 on the doublets near the switch point of the flagellar beat is sufficiently strong that it could term
41 c surface-interactions, and chirality of the flagellar beat leads to stable upstream spiralling motio
42 plicated in critical processes as diverse as flagellar beating, membrane trafficking, histone methyla
43 n, but in cells generating oscillations, the flagellar beat mode alternated in synchrony with the osc
44 CO(3)(-) is unable to rapidly accelerate the flagellar beat or facilitate evoked Ca(2+) entry into sA
45 with surface swimming, are sensitive to the flagellar beat pattern wavenumber and even to the asympt
46 sweeps varying the sperm head morphology and flagellar beat pattern wavenumber are conducted and reve
47 3D reconstruction algorithm to identify the flagellar beat patterns causing left or right turning, w
48 BAPTA-AM in wild-type sperm, they exhibited flagellar beat patterns more closely resembling those of
50 xperiments with mathematical modeling and 3D flagellar beat reconstruction to quantify the response o
52 y more common model systems, and the complex flagellar beating shapes that power it make its quantita
54 (repetitive store mobilization) which modify flagellar beating, whereas bolus application of micromol
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