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1 356) to process visual information as does a tarsier (87).
2             This new specimen indicates that tarsiers already possessed greatly enlarged orbits and a
3                        The placements of the tarsier and the tree shrew within and in relation to pri
4 rom the last common ancestor of haplorhines (tarsiers and anthropoids) to that of anthropoids (New Wo
5 tical to the corresponding anatomy in living tarsiers and differs substantially from that of early an
6                                              Tarsiers and extinct tarsier-like primates have played a
7  lemur species and only minor defects in two tarsiers and two nocturnal lemurs.
8                                              Tarsiers are phylogenetically located between the most b
9 ng been regarded as the nearest relatives of tarsiers, but a sister group relationship between anthro
10                                              Tarsier central cones had 2-microm-wide outer (OS) and i
11 d L/M cone systems are yet to be determined, tarsier cone proteins and distribution have some similar
12 ptive shift that occurred at the base of the tarsier-eosimiid-anthropoid clade.
13 r group relationship between anthropoids and tarsiers has also been proposed.
14 anatomy, but until now, the fossil record of tarsiers has been limited to a single jaw and several is
15                 Because of the importance of tarsiers in so many primatological problems, there has b
16                         Tarsiers and extinct tarsier-like primates have played a central role in view
17                 The phylogenetic position of tarsiers relative to anthropoids and Paleogene omomyids
18                              Only Macaca and tarsier retina contained cones labeled by antiserum to s
19                                           In tarsier retinal whole-mounts, peak cone density ranged f
20                                              Tarsier rod cell bodies were 6-12 deep, depending on ret
21 though the functional characteristics of the tarsier S and L/M cone systems are yet to be determined,
22 ar interest in questions about the origin of tarsier specializations and the biogeography of early ta
23 rtion within the nuclear genome, then reveal tarsier-specific, positive gene selection and posit popu
24 here a new genome assembly of the Philippine tarsier (Tarsius syrichta), and provide extended analyse
25                 The evolutionary position of tarsiers with respect to primates is still debated.

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