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1 s") can be revealed by proper comparisons of altricial and precocial species.
2 rved in chicken (precocial) and zebra finch (altricial) and discuss the possibility that this evoluti
3                             Survival of many altricial animals critically depends on the sense of sme
4 stimuli are used early in the development of altricial animals.
5 over the course of several postnatal days in altricial animals.
6    This is the first evidence that embryonic altricial birds are capable of acquiring chemosensory kn
7 cumented but so far unexplained pattern that altricial birds have larger brains than precocial ones.
8  This is the first study to demonstrate that altricial birds may use recruitment calls to extend pare
9 lue similar to those observed in present-day altricial birds that need intensive parental care.
10                                      In many altricial birds, fledglings disperse when they are no lo
11 dinosaurs did not attain rates like those of altricial birds.
12 olic genes, reflecting unique adaptations to altricial birth and delayed weaning, a hallmark of marsu
13  this inversion is likely to result from the altricial birth of Mustelidae species.
14 rly infancy is facilitated by their neurally altricial births (relative to other primates) and their
15 owth and social stimuli, it benefits from an altricial brain and a cooperative breeding environment.
16 nd marmosets was afforded by infants with an altricial brain embedded in a vocally rich environment.
17                Human newborns are considered altricial compared with other primates because they are
18                    It has been proposed that altricial development evolved secondarily in humans due
19 nulatus provide similarly lipid-rich milk to altricial hatchlings during parental care.
20  signaling parental attention to secondarily altricial infants.
21 of the homeostatic regulation of sleep in an altricial mammal.
22 s essential for the survival of offspring in altricial mammalian species.
23 dependent learning and memory emerge late in altricial mammals [14-17], appearing around weaning in r
24                                              Altricial mammals are born with immature nervous systems
25 CANCE STATEMENT Cochlear inner hair cells of altricial mammals display spontaneous electrical activit
26           Behavioral evidence indicates that altricial mammals possess olfactory function at early de
27                   Juvenile rodents and other altricial mammals react with calming, immobility, and po
28             We speculate that closed lids in altricial mammals serve to prevent visual experience unt
29                      Before hearing onset in altricial mammals, cochlear inner hair cells (IHCs) exhi
30  birth in primates and before eye opening in altricial mammals, spontaneous activity generated by the
31 the highest evolutionary rate to become more altricial (measured as the proportion of adult brain siz
32 actation is adapted to provisioning a highly altricial neonate to a degree that suggests equivalence
33 n" is to truncate gestation, resulting in an altricial neonate.
34 cally restricted to birthing a small-brained altricial neonate.
35 ion for high intelligence may occur when (i) altricial neonates require intelligent parents, (ii) int
36 ental mammals, ursids give birth to the most altricial neonates with the lowest neonatal:maternal bod
37 ntained in prey are transferred by adults to altricial offspring during provisioning and (3) plastic
38 i) large brains necessitate having even more altricial offspring.
39  reproduction, their more rigidly determined altricial patterns of social behaviour, the roles of pos
40 th the level of development (position on the altricial-precocial spectrum) exhibited at birth.
41                      Experiments done on the altricial rat and precocial guinea pig neonate demonstra
42 macaques, making humans and marmoset monkeys altricial relative to these other primates.
43 f mammals notable for giving birth to highly altricial (relatively less developed) young.
44  obesity lengthens and amplifies the peak in altricial rodent species.
45  intrinsically generated by immature IHCs of altricial rodents and that apical IHCs showed bursting a
46                                   Studies in altricial rodents attribute dramatic changes in perinata
47   Mother-infant attachment is facilitated in altricial rodents through unique neural mechanisms that
48 postnatal day 11 (P11)-P13, hearing onset in altricial rodents, and at P20-P22 when the OHCs are morp
49                                   In various altricial rodents, OHCs become functionally competent fr
50                            Specifically: (i) altricial species are 50% less productive than precocial
51                         In birds, a focus on altricial species from north temperate latitudes has pre
52 forms the caregiver attachment necessary for altricial species survival.
53 resent study shows that, in contrast to more altricial species, many deep layer SC neurons in the rhe
54                                           In altricial species, maternal stimuli have powerful effect
55                Similar to signal ontogeny in altricial species, maturation is nevertheless important
56 atal developmental periods, than in those of altricial species.
57 tegy as characterized along the precocial to altricial spectrum.
58 n mammals whereby young are born at a highly altricial stage of development with the majority of deve
59 ures of parental provisioning (precocial vs. altricial state at hatching, relative egg mass, time spe
60  comparative context, other mammals are more altricial than humans.
61  which include sampling and observer biases, altricial versus precocial juvenile development, and the
62 es in skull shape and size are ubiquitous in altricial vertebrates, but typically unidirectional and
63 not require prolonged external attachment of altricial young.