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1 r girdle plesiomorphies of mammaliaforms and monotremes.
2 n platypus chromosome X1, which is unique to monotremes.
3 ns evolved in a mammalian clade exclusive of monotremes.
4 t other marsupials and, to some extent, even monotremes.
5 es from a diverse assortment of mammals (one monotreme, 11 marsupials, 37 placentals), including 11 n
6 hic feature retained in the adult, unlike in monotreme and placental adults.
7 rt herein that M6P/IGF2R is not imprinted in monotremes and does not encode for a receptor that binds
8 those of the associated abdominal muscles of monotremes and marsupial mammals have remained unresolve
9  present in all orders of mammals, including monotremes and marsupials.
10 the first tangible evidence that, along with monotremes and therian mammals, multituberculates were h
11 ependently from the middle ear structures of monotremes and therian mammals.
12 n found in ruminants, marsupials, squamates, monotremes, and African mammals.
13 ll as 37 other taxa representing marsupials, monotremes, and all but two orders of placental mammals.
14  to Gondwanan landmasses, survived by extant monotremes; and a boreosphenidan clade of Laurasian cont
15 mmalian comparative analyses, as well as for monotreme biology and conservation.
16 es identified the first homologs of MAGP1 in monotremes, birds, elasmobranchs and agnathans, and the
17 ammals, related tritylodonts, marsupials and monotremes but not in living eutherian (placental) mamma
18 atures similar to those of mammaliaforms and monotremes, but different compared with those of the ear
19   Here, we examine the small RNA pathways of monotremes by deep sequencing of six platypus and echidn
20 80 Ma, but Teinolophos suggests that the two monotreme clades were already distinct in the Early Cret
21 sent in the duckbill platypus, an egg-laying monotreme, consistent with TCRmu being ancient and prese
22 ontradict the popular view of rapid Cenozoic monotreme diversification.
23  earliest branch of mammalian evolution (the monotremes), does not have the pattern of neuronal activ
24 s similar to the embryonic pattern in modern monotremes (egg-laying mammals) and placental mammals, b
25                                         This monotreme exhibits a fascinating combination of reptilia
26                                  Whereas the monotreme fossil record is still sparse and open to inte
27   We show that the DNA coding the CD loop in monotremes functions as an exon splice enhancer (ESE) an
28                        Analysis of the first monotreme genome aligned these features with genetic inn
29                                              Monotremes have left a poor fossil record, and paleontol
30 ephalan), but we find it also in marsupials, monotremes, lizards, turtles, birds, and fishes.
31  in metatherian (marsupial) or prototherian (monotreme) mammals.
32  marsupial) mammals but not in prototherian (monotreme) mammals.
33 r to the evolution of the common ancestor of monotremes, marsupials, and placentals.
34 at as in a number of other mammals including monotremes, marsupials, carnivores, and primates, the an
35  fugu, the amphibian Xenopus tropicalis, the monotreme platypus and the marsupial opossum, to gain fu
36 ssum, and Australian tammar wallaby) and one monotreme (platypus) genomes.
37 f mammals, including marsupial (opossum) and monotreme (platypus), but not in nonmammalian vertebrate
38 native view of a deep geological history for monotremes suggests that rate heterogeneities may have a
39 cal, and taxonomic diversification rates for monotremes than in their sister taxon, the therian mamma
40 nd artiodactyls and on slow afrotherians and monotremes that strongly support this hypothesis.
41                                           In monotremes, which lack imprinting, IGF2 specifically bou
42                                          The monotremes, with only platypus and four species of echid

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