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1 nal nerve and from the lingual branch of the hypoglossal nerve.
2 either the medial or lateral branches of the hypoglossal nerve.
3 ioral data obtained after transection of the hypoglossal nerve.
4  fibers from the third spinal nerve into the hypoglossal nerve.
5 e later emerging HMP, neural crest cells and hypoglossal nerve.
6  transecting either the strap muscles or the hypoglossal nerves.
7 .001) and suppressed serotonin excitation of hypoglossal nerve activity (p < 0.05).
8        The 2C antagonist, SB-242084, dropped hypoglossal nerve activity 17 +/- 6% (p < 0.05) and supp
9 tivation, increased the respiratory rate and hypoglossal nerve activity, induced c-fos expression in
10 analysis of MVBs in the normal postnatal rat hypoglossal nerve and under a variety of experimental co
11  but not exclusively, via stimulation of the hypoglossal nerves and also increases upstream resistanc
12 cular septal defect, abnormal development of hypoglossal nerves, and defective remodeling of the aort
13 nd N-methyl-D-aspartate excitatory output of hypoglossal nerves, and that reduced excitatory responsi
14 insufficiency, as evidenced by a loss of the hypoglossal nerve (cranial nerve XII) in embryos from th
15 o the magnitude of motor output; respiratory hypoglossal nerve discharge decreased and its frequency
16 ats underwent unilateral transections of the hypoglossal nerve, followed by intramedullary grafts of
17                      With stimulation of the hypoglossal nerves, greater increases in area in these r
18 hesize that the presence of afferents in the hypoglossal nerve is a derived characteristic of anurans
19 from stimulation of the medial branch of the hypoglossal nerve is predominantly due to ventral displa
20  suggested that afferents are present in the hypoglossal nerve of the leopard frog, Rana pipiens.
21 f transecting the cervical strap muscles and hypoglossal nerves on airflow dynamics during hypercapni
22 apparent correlation between the size of the hypoglossal nerve, or the number of axons it contains, a
23 2A antagonist, MDL-100907, dropped intrinsic hypoglossal nerve respiratory activity by 61 +/- 6% (p <
24 ersus heteroreceptor effects of 8-OH-DPAT on hypoglossal nerve respiratory output.
25 weeks of intermittent hypoxia showed reduced hypoglossal nerve responsiveness (logEC50) for serotonin
26 at hypoglossal canal size is correlated with hypoglossal nerve size, which in turn is related to tong
27                                              Hypoglossal nerve stimulation is a useful second-line th
28 hodamine 101 uptake after the trigeminal and hypoglossal nerves stimulation labeled the bilateral hyp
29 ral and central endings of the branch of the hypoglossal nerve that supplies the syrinx, the tracheos
30 s via retrograde axonal transport within the hypoglossal nerve to the hypoglossal nucleus.
31                                Lesion of the hypoglossal nerve to the syrinx greatly disrupted vocal
32 rupted vocal behavior, whereas lesion of the hypoglossal nerve to the tongue exerted no obvious disru
33 en the drug was administered after bilateral hypoglossal nerve transection.
34 y neurons from the tongue that ascend in the hypoglossal nerve were identified and described in the l
35 iratory-related rhythmic motor activity from hypoglossal nerve (XIIn) and patch-clamped preBotC inspi
36 iratory-related rhythmic motor output in the hypoglossal nerve (XIIn) to 84 % (without IBMX) and to 7

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