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1  infection in immunocompetent leopard frogs (Rana pipiens).
2 the inner ear of frogs (Rana catesbeiana and Rana pipiens).
3 sed mesenteric microvessels in pithed frogs (Rana pipiens).
4  of saccular hair cells of the leopard frog, Rana pipiens.
5 nglion cells (RGCs) were studied in the frog Rana pipiens.
6 ntagonist that has not been characterized in Rana pipiens.
7 ed from the liver of gravid female amphibian Rana pipiens.
8 e site(s) of opioid action in the amphibian, Rana pipiens.
9 dentified and described in the leopard frog, Rana pipiens.
10  anatomically these hypoglossal afferents in Rana pipiens.
11 n the hypoglossal nerve of the leopard frog, Rana pipiens.
12 in neuromuscular junctions of the adult frog Rana pipiens.
13 orms) in the declining northern leopard frog Rana pipiens.
14 creatic ribonuclease (RNase A) from the frog Rana pipiens.
15  for M. marinum disease in the leopard frog (Rana pipiens), a natural host species.
16 the optic nerve, chiasm, and optic tracts of Rana pipiens after the anterograde and retrograde transp
17 njections, including sperm heads of the frog Rana pipiens and the zebrafish Danio rerio in Xenopus GV
18 hA and ephrin-A expression in leopard frogs (Rana pipiens and utricularia), species capable of regene
19 an species, which do not produce foot flags (Rana pipiens and Xenopus laevis).
20 n and midbrain in the northern leopard frog (Rana pipiens) and common American toad (Bufo americanus)
21 nd tonic) were initially identified in adult Rana pipiens anterior tibialis muscle based on myosin AT
22  expression patterns in the tectum of larval Rana pipiens, as studied by means of in situ affinity an
23 riant, oocytes of the Northern Leopard frog (Rana pipiens) contain another homologue of ribonuclease
24 meter, we demonstrate that (i) aggregates of Rana pipiens deep germ layers do possess liquid-like sur
25  optic nerve into the telencephalon in adult Rana pipiens induces a projection to olfactory cortex.
26 ggests that trigeminal motoneurons (Vmns) in Rana pipiens innervate distinct myofiber populations in
27 ween enhancement and depression at the frog (Rana pipiens) neuromuscular synapse, data obtained over
28 na berlandieri (Rio Grande leopard frog) and Rana pipiens (Northern leopard frog).
29 NO synthase (NOS) activity is present in the Rana pipiens optic tectum throughout development in a di
30 dorsal nucleus of the Northern leopard frog (Rana pipiens pipiens), which is a homolog of the cochlea
31 chieve in vivo confocal IOS imaging of frog (Rana pipiens) retinas at cellular resolution.
32  the outer segments of living isolated frog (Rana pipiens) rod photoreceptors.
33                             Using grassfrog (Rana pipiens) saccular hair cells, we show that the repo
34 2+)-activated K(+) (K(Ca)) currents of frog (Rana pipiens) saccular hair cells.
35                                    The frog (Rana pipiens) sacculus, which is used for social communi
36 se unit, have been measured in single, frog (Rana pipiens) skeletal muscle fibres.
37                We orally exposed Lithobates (Rana) pipiens tadpoles to environmentally realistic leve
38 ough effects of NO on synaptic function in a Rana pipiens tectal slice were varied.
39 of four MHC isoforms from skeletal muscle in Rana pipiens that are specifically expressed in four mec
40 ised cilium preparation from the grass frog (Rana pipiens) to measure the cAMP diffusion coefficient.
41 e isolated epithelium of frog skin (northern Rana pipiens) was carried out in the frequency range bet
42 n of OCT for imaging developing structure in Rana pipiens, Xenopus laevis, and Brachydanio rerio.

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