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1 the most probable ancestral range of Fijian iguanas.
2 we show unidirectional airflow in the green iguana, a lizard with a strikingly different natural his
3 he spill to show that a population of marine iguanas (Amblyrhychus cristatus) on Sante Fe island suff
4 radiocarbon dates on individual bones of the iguana, an extinct megapode (Megapodius alimentum), and
5 entified four mutants (neckless, motionless, iguana and doc) that lacked mbp expression in parts of t
6 Fijian iguanas is the North American desert iguana and that the two taxa likely diverged during the
7 t, and densities of rodents, howler monkeys, iguanas, and leaf-cutter ants are 10 to 100 times greate
11 Lapita-style pottery and bones of an extinct iguana (Brachylophus undescribed sp.) and numerous speci
14 Conservation breeding of West Indian rock iguanas (Cyclura) has met with limited success historica
16 sduction proteins Cos2/Kif27/Kif7, Fused, or Iguana do not result in detectable Hh signaling defects;
19 ers can accurately identify and count marine iguanas from drone images, though there is a tendency fo
24 genetic analysis, we show that the zebrafish iguana gene product acts downstream of the Smoothened pr
27 urons in the lizards Anolis carolinensis and Iguana iguana were immunolabeled with antisera generated
30 to study but a new review of work on marine iguanas in the Galapagos islands suggests an answer may
33 critical and broadly conserved function for Iguana is in ciliogenesis and that this function has com
34 the closest living relative of extant Fijian iguanas is the North American desert iguana and that the
36 identified at least six distinct Cuban Rock Iguana MUs, encompassing demographically isolated and ge
37 's vesicle promotes left-right asymmetry and iguana mutant embryos had left-right asymmetry defects.
41 Our analyses support the hypothesis that iguanas reached Fiji via an extraordinary oceanic disper