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1 infection in immunocompetent leopard frogs (Rana pipiens).
2 sed mesenteric microvessels in pithed frogs (Rana pipiens).
3 the inner ear of frogs (Rana catesbeiana and 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.
16 MHC diversity in the Northern leopard frog, Rana pipiens, a species found throughout North America t
17 the optic nerve, chiasm, and optic tracts of Rana pipiens after the anterograde and retrograde transp
18 njections, including sperm heads of the frog Rana pipiens and the zebrafish Danio rerio in Xenopus GV
19 hA and ephrin-A expression in leopard frogs (Rana pipiens and utricularia), species capable of regene
21 n and midbrain in the northern leopard frog (Rana pipiens) and common American toad (Bufo americanus)
22 nd tonic) were initially identified in adult Rana pipiens anterior tibialis muscle based on myosin AT
23 expression patterns in the tectum of larval Rana pipiens, as studied by means of in situ affinity an
24 axonomically problematic group of frogs (the Rana pipiens complex, or leopard frogs) that are widely
25 riant, oocytes of the Northern Leopard frog (Rana pipiens) contain another homologue of ribonuclease
26 meter, we demonstrate that (i) aggregates of Rana pipiens deep germ layers do possess liquid-like sur
27 work of 41 populations of the amphibian host Rana pipiens in Ontario, Canada, we present the spatial
28 optic nerve into the telencephalon in adult Rana pipiens induces a projection to olfactory cortex.
29 ggests that trigeminal motoneurons (Vmns) in Rana pipiens innervate distinct myofiber populations in
32 ween enhancement and depression at the frog (Rana pipiens) neuromuscular synapse, data obtained over
34 NO synthase (NOS) activity is present in the Rana pipiens optic tectum throughout development in a di
35 dorsal nucleus of the Northern leopard frog (Rana pipiens pipiens), which is a homolog of the cochlea
44 of four MHC isoforms from skeletal muscle in Rana pipiens that are specifically expressed in four mec
45 ised cilium preparation from the grass frog (Rana pipiens) to measure the cAMP diffusion coefficient.
46 e isolated epithelium of frog skin (northern Rana pipiens) was carried out in the frequency range bet
47 n of OCT for imaging developing structure in Rana pipiens, Xenopus laevis, and Brachydanio rerio.