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1 c nerves) to maintain continence or initiate micturition.
2 projecting to spinal cord nuclei controlling micturition.
3 lgesia, blood pressure, mating behavior, and micturition.
4 chanisms that control urinary continence and micturition.
5 whose activity modulates hierarchy-dependent micturition.
6 to maintain continence and achieve efficient micturition.
7 erized by incomplete bladder emptying during micturition.
8 ivation became synchronized 20-30 s prior to micturition.
9 dal ventrolateral PAG is essential to permit micturition.
10 orsal caudal PAG is not essential for reflex micturition.
11 pical for the rat, with phasic firing during micturition.
12 s predicts suppression of withdrawals during micturition.
13 M neurons was recorded during continence and micturition.
14  and management of neurological disorders of micturition.
15 e cells may also play a preparatory role for micturition.
16 that either advanced or delayed the onset of micturition.
17 ce of two spinal reflex pathways involved in micturition: a pathway limited to a reflex arc in the pe
18 h muscle and striated muscle reflexes during micturition and colorectal distention (CRD) in urethane-
19  could lead to improved voluntary control of micturition and defecation for patients with neurogenic
20 , the internal layer, which provides primary micturition and defecation regulation, and the transvers
21 isengage from ongoing behaviors unrelated to micturition and initiate specific voiding behaviors so t
22  prevents the bacteria from being removed by micturition and it triggers bacterial invasion as well a
23 eurons and their synaptic afferents to study micturition and other pelvic functions.
24 g swimming, walking, scratching, swallowing, micturition and sexual climax, are episodic: even in the
25 rd, which are associated with the control of micturition and sexual reflexes.
26                                  During both micturition and sleep, OFF cells discharge and sensory r
27 siological and pathophysiological control of micturition and suggest that urothelial pannexin may be
28 %) were associated with rarer causes such as micturition and swallowing.
29 maintain continence and to achieve efficient micturition and when compromised by disease or injury ca
30 in in this region may contribute to impaired micturition and/or constipation in Parkinson disease and
31 rized by severe pain, increased frequency of micturition, and chronic inflammation.
32  of the pudendal nerve can elicit or inhibit micturition, and low frequency stimulation of the compou
33 luding hunger for air, thirst, hunger, pain, micturition, and sleep, is discussed with particular ref
34 transition between continence (guarding) and micturition (augmenting) reflexes.
35 plays a physiological role in the control of micturition because intravesical perfusion of apyrase or
36 the integration center for context-dependent micturition behavior.
37 adder contraction, and when silenced impairs micturition behavior.
38 l by 98% and pressure threshold for inducing micturition by 115%, but did not change bladder contract
39 ropin-releasing hormone (Crh) in the pontine micturition center (PMC) is electrophysiologically disti
40      Previous work has revealed that pontine micturition center (PMC) neurons send projections to the
41 ortical micturition circuit from the pontine micturition center (PMC), locus coeruleus (LC) and media
42  bladder neurons were located in the pontine micturition center and external urethral sphincter neuro
43 le-labeled neurons were found in the pontine micturition center and the locus coeruleus or subcoerule
44 ht to determine whether the putative pontine micturition center in the human dorsal pons contains cor
45 etion of CRF neurons in the putative pontine micturition center may contribute to the severe bladder
46 n of the descending pathway from the pontine micturition center to the sacral spinal cord in the late
47 Neurons of Barrington's nucleus (the pontine micturition center) have been identified which project t
48 Barrington's nucleus, considered the pontine micturition center, in regulation of colonic function.
49 nd the brainstem, in particular, the pontine micturition center.
50 voiding and thereby function as the "pontine micturition center." Lacking detailed information on thi
51 sconnected by spinal injury from the pontine micturition centre, vanilloid-sensitive fibres assume a
52    These results suggest that the changes in micturition characteristics observed in aged rats may in
53 termine the effects of ageing on the in vivo micturition characteristics of male Wistar rats and to a
54 were made within a putative pontine-cortical micturition circuit from the pontine micturition center
55 iding dysfunction characterized by a loss of micturition contractions with overflow incontinence.
56 ed with Barrington's nucleus neurons such as micturition control and pelvic visceral function.
57 ult male mice, confirming the existence of a micturition control center that integrates pro- and anti
58 d reversibly manipulate switching within the micturition control circuitry, to defer voiding and main
59 nd the complex nature of bladder storage and micturition control.
60 control center that integrates pro- and anti-micturition cues.
61 fy spinal neurons that are active during the micturition cycle, and demonstrate that a behaviorally r
62 uscle active during the filling phase of the micturition cycle.
63  both the storage and emptying phases of the micturition cycle.
64 rally associated with distinct phases of the micturition cycle.
65 ractile activity in the filling phase of the micturition cycle.
66 rk that controls pelvic functions, including micturition, defecation, and penile erection, as well as
67 ne encephalomyelitis (EAE), a MS model, have micturition dysfunction and altered expression of genes
68 yed similar neurological deficits but lesser micturition dysfunction compared to Panx1(+/+) EAE.
69 face of innate defense mechanisms, including micturition, epithelial exfoliation, and the influx of p
70 onist PPADS suggests that bradykinin-induced micturition facilitation may be due in part to increased
71 rate bother, and a bladder diary documenting micturition frequency (>or=8 micturitions per 24 hours)
72 nt bladder hyperactivity with an increase in micturition frequency and a decrease in bladder capacity
73 P/GRP combined with NBQX promote recovery of micturition function following spinal cord injury, likel
74 l layer, which supplements both erectile and micturition function, the internal layer, which provides
75  a behaviorally relevant stimulus (isometric micturition) generated more widespread and greater inten
76 y cells within the spinal cord that regulate micturition in male cats.
77 fects female sexual behavior, analgesia, and micturition in mammals.
78 hincter EMG also showed phasic firing during micturition in synchrony with EUS activity but, in addit
79 of the pudendal nerve, a period of isometric micturition (induced by ligating the proximal urethra an
80 olorectal distension, a stimulus that delays micturition, inhibited M-inh cells and excited M-exc cel
81                              During this pre-micturition interval, a theta oscillation developed in t
82 trates that PN stimulation also can elicit a micturition-like response and that the response to PN st
83 e response, PN stimulation can also elicit a micturition-like response, and this response is dependen
84 mid-frequency (33 Hz) stimulation produced a micturition-like response, including excitation of the b
85 en the shift in LC-mPFC network activity and micturition may allow time to disengage from ongoing beh
86                                     However, micturition may be initiated from this region via projec
87 ween noxious stimulus-evoked withdrawals and micturition, movements that are necessary for survival b
88 arrington's nucleus plays a critical role in micturition, MPO projections to Barrington's nucleus may
89  initiate specific voiding behaviors so that micturition occurs in environmentally and socially appro
90 c cells inhibit bladder afferents, advancing micturition onset when M-inh cells are activated and del
91              In animals undergoing isometric micturition or stimulation of Barrington's nucleus, neur
92 d the effects of acute colonic irritation on micturition parameters were assessed.
93 cal instillation of bradykinin activated the micturition pathway.
94             Changes in galanin expression in micturition pathways after SCI may be mediated by changi
95 or TrkB may be involved in reorganization of micturition pathways after SCI.
96      There was a loss of a diurnal rhythm in micturition patterns and a large increase in voided volu
97  effect of olfaction and social hierarchy on micturition patterns in adult male mice, confirming the
98                DSP-4 lesions neither altered micturition patterns nor water intake in the young adult
99           Significant age-related changes in micturition patterns were observed.
100 ithout incontinence (-3.33 vs -2.54, P=.03), micturitions per 24 hours (-2.54 vs -1.41, P<.001), and
101 ary documenting micturition frequency (>or=8 micturitions per 24 hours) and urgency (>or=3 episodes p
102 s per 24 hours (-2.54 vs -1.41, P<.001), and micturitions per night (-0.59 vs -0.39, P.02).
103 ited an accelerated recovery, with decreased micturition pressure and fewer episodes of detrusor hype
104 tric parameters in both operated groups, and micturition pressure in NRP/GRP rats recovered to normal
105  threshold pressure or bladder capacity, but micturition pressure was elevated compared to control mi
106 urinary bladder and in the inhibition of the micturition reflex by pudendal nerve stimulation (PNS).
107 a human subject with C5 SCI, stimulating the micturition reflex caused AD with exaggerated catecholam
108 e central nervous mechanisms controlling the micturition reflex have also recently attracted attentio
109 eral, spinal and supraspinal segments of the micturition reflex in diseases such as cystitis, bladder
110 he role for this afferent stimulation on the micturition reflex is gradually gaining importance in th
111                     The afferent limb of the micturition reflex is often compromised following bladde
112  a consequence of abnormal expression of the micturition reflex or changes in the properties of the s
113  mechanisms controlling the spinobulbospinal micturition reflex pathway.
114 ory modulation of the descending limb of the micturition reflex pathway.
115 of the neuropeptide galanin were examined in micturition reflex pathways 6 weeks after complete spina
116 te cyclase-activating polypeptide (PACAP) in micturition reflex pathways after chronic cystitis induc
117 actors in Trk-mediated signaling cascades in micturition reflex pathways after SCI but may play a rol
118 GAP-43) were examined in lower urinary tract micturition reflex pathways in a chronic model of cyclop
119 and was not due to activation of supraspinal micturition reflex pathways.
120 al cutaneous nerve (PFCN) could modulate the micturition reflex recorded under isovolumetric conditio
121 t high bladder volumes, excites the bladder (micturition reflex) and relaxes the EUS (augmenting refl
122 er afferents which are known to modulate the micturition reflex.
123 of bladder afferent pathways controlling the micturition reflex.
124 dies demonstrate that p75(NTR) expression in micturition reflexes is present constitutively and modif
125 ional significance of p75(NTR) expression in micturition reflexes remains to be determined.
126 ation of tyrosine kinase receptors (Trks) in micturition reflexes with urinary bladder inflammation.
127 f the urinary tract and return of functional micturition reflexes, suggesting that this surgical repa
128 nts and DRG (L1, L2, L6, and S1) involved in micturition reflexes.
129                                       Normal micturition requires coordinated activation of smooth mu
130  treatment (NBQX&NRP/GRP) had voided volumes/micturition resembling that of normal animals and showed
131                               Urine release (micturition) serves an essential physiological function
132 re capable of carrying diverse pro- and anti-micturition signals, and whose activity modulates hierar
133 ition, whereas most M-inh cells fired before micturition, suggesting that these cells may also play a
134 ed by a suppression of afferent input to the micturition switching circuitry in the pons, whereas the
135 om scale scores, APR patients reported worse micturition symptoms than the SSS group at 1 year (26.9
136 eurons support withdrawal suppression during micturition, the discharge of VMM neurons was recorded d
137 terine contractions (amplitude and rate) and micturition thresholds (MT) assessed by cystometry.
138  Mice lacking the TRPV1 channel have altered micturition thresholds suggesting that TRPV1 channels ma
139 st frequently reported drug-related AEs were micturition urgency (n = 16; 40%), dysuria (n = 16; 40%)
140 ased the bladder capacity while reducing the micturition volume thus resulting in a marked increase i
141  increase in the ratio of residual volume to micturition volume.
142                In lightly anesthetized rats, micturition was favored, because noxious stimulation nev
143  inhibited (M-inh) or excited (M-exc) during micturition were observed.
144 ing lower urinary tract functions, including micturition, were studied using immunohistochemistry for
145    Although muscimol failed to change reflex micturition when microinjected into the dorsal caudal PA
146     M-exc cells were typically silent before micturition, whereas most M-inh cells fired before mictu
147 ecause noxious stimulation never interrupted micturition, whereas withdrawals were suppressed during
148 ic stimulation and noxious paw heat advanced micturition while exciting M-inh cells and inhibiting M-
149 , VMM cells appear to modulate the timing of micturition, with ON cells promoting the initiation of v

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