ライフサイエンスコーパス: orthograde

1 Orthograde activation of the preganglionic nerve trunk,

2 nctional coupling with RyRs, preserving both orthograde and retrograde Ca(2+) signaling between LCCs

3 In summary, FKBP12 deficiency alters both orthograde and retrograde coupling between the L-type Ca

4 endritic depolarizations, thereby regulating orthograde and retrograde propagation of dendritic poten

5 TCS potently impairs orthograde and retrograde signaling between L-type Ca(2+

6 By using both immunohistochemical as well as orthograde and retrograde tracer methods, we have identi

7 Orthograde and retrograde tracers were used to examine s

8 ased on APP-A4 IHC that demonstrated similar orthograde axonal transport block in the LC in children

9 es) share multiple features (for example, an orthograde body plan facilitating upright positional beh

10 Orthograde coupling was previously shown to be ablated b

11 ctive retinal ganglion cells (DSGCs) utilize orthograde dendritic spikes during physiological activit

12 We conclude from these data that this orthograde DHPR-to-RyR1 signal inhibits the transition o

13 ational changes induced by DP4 regulate both orthograde E-C coupling and retrograde RyR1-DHPR signali

14 Here we explore the effects of DP4 on orthograde excitation-contraction coupling and retrograd

15 This genetic knockout eliminated orthograde high jitter synaptic events and EPSCs evoked

16 cortex in the cat to produce retrograde and orthograde labeling in the thalamus, chiefly in the late

17 Orthograde LH perfusion of L-arginine (10[-3] M) reduced

18 ll in proximal stopflow pressure produced by orthograde LH perfusion of L-arginine in LS rats.

19 rom proximal stop flow pressure (PSF) during orthograde loop perfusion from the proximal tubule with

20 combined sensory stimulation, whether in the orthograde or pronograde posture.

21 rupedal patterns of most monkeys than to the orthograde patterns of apes.

22 h the glomerulus from the end of the Af-Art (orthograde perfusion [OP]) to maintain the influence of

23 nk rotation about the C1-C2 axis while in an orthograde posture and (2) lateral side-to-side flexion

24 ngated colon; (2) larger faecal pellets; (3) orthograde propulsion followed by retropulsion (not obse

25 caffeine-induced Ca2+ release, suggesting an orthograde regulation of the TT membrane on the SR Ca2+

26 These findings suggest that the orthograde signal and DHPR tetrad formation require the

27 oupling is bidirectional; in addition to the orthograde signal from CaV1.1 to RyR1 that triggers Ca(2

28 lease during the short-term stage acts as an orthograde signal to recruit postsynaptic mechanisms of

29 lease from the presynaptic neuron acts as an orthograde signal to recruit the postsynaptic mechanisms

30 receptor (DHPR) is the primary source of the orthograde signal.

31 l-type excitation-contraction (EC) coupling (orthograde signaling) but failed to enhance DHPR Ca(2+)

32 sarcoplasmic reticulum Ca(2)(+) release via orthograde signaling.

33 dently of changes at the target tissues when orthograde signals acting by means of neuronal alpha7 ni

34 Injection of the orthograde tracer Phaseolus vulgaris-leucoagglutinin int

35 In general, orthograde translocations are longer than retrograde tra

36 system, and NO appears to be released as an orthograde transmitter from descending inputs to the STG

37 rmer by BNOS/ChAT labeling and the latter by orthograde transport of biocytin injected into cortical

38 We identified corticogeniculate terminals by orthograde transport of biocytin injected into the visua

39 Notably, its skeleton indicates that an orthograde (upright) body plan preceded suspensory adapt

40 a combination of pronograde (horizontal) and orthograde (vertical) body postures, used both above bra