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1 nd life stage on gut microbiota of red-crown cranes.
2 icrobiota from captive and artificially bred cranes.
3       These effects are likely not unique to cranes.
4    Lastly, bobbing of the head as the animal cranes and explores is phase-locked to sniffing and to m
5 s with pigeons, mesites, and sandgrouse; (3) cranes and their relatives; (4) a comprehensive waterbir
6 ices in avian prion proteins (chicken, duck, crane) are better accommodated in a helical state, which
7  represent a form of disturbance to foraging cranes but is habitat dependent.
8 serves primarily as a visual obstruction for cranes, causing them to increase the frequency of vigila
9                           Writing in Nature, Crane et al. (2015) show that a specialized condensin co
10 ounding zone sediment system at the front of Crane Fjord.
11                   X and Y sex chromosomes in crane fly (Nephrotoma suturalis) spermatocytes exhibit a
12 eiotic chromosomes in spermatocytes from the crane fly Nephrotoma suturalis.
13  forces on chromosome arms during meiosis in crane fly spermatocytes and strongly suggest that the me
14 Cold arrest induced a fraction of meiosis II crane fly spermatocytes to form (n + 1) and (n - 1) daug
15 hat act on chromosome arms during meiosis in crane fly spermatocytes.
16 o stop chromosome movements in Mesostoma and crane-fly spermatocytes and inward movements of spindle
17 ome movements in Mesostoma spermatocytes and crane-fly spermatocytes as 2-3 and 6-10 pN, respectively
18                                           In crane-fly spermatocytes trap powers of 56-85 mW stopped
19  of single kinetochore (K-) fibers in living crane-fly spermatocytes, from their origins as nascent K
20 must be involved in metaphase positioning in crane-fly spermatocytes.
21                      In time-lapse movies of crane-fly spermtocytes, fluorescent speckles generated w
22 ourists influence the vigilance behaviour of cranes foraging in Suaeda salsa salt marshes and S. sals
23 ologic mapping of the fjord suggest that the Crane Glacier grounding zone was well within the fjord b
24 ve model for juvenile (<1 year old) sandhill crane Grus canadensis recruitment of the Rocky Mountain
25 ty and energy expenditure of birds, Eurasian cranes Grus grus, during the winter of 2013-14, which sa
26                   The Endangered Red-crowned Crane (Grus japonensis) is one of the most culturally ic
27                             The black-necked crane (Grus nigricollis) is the only alpine crane specie
28                             Especially, wild cranes had distinct compositions of gut microbiota from
29 sity was found in captive cranes, while wild cranes had the least.
30 Reintroduction of the threatened red-crowned crane has been unsuccessful.
31 of INDOLE-3-ACETIC ACID INDUCIBLE28 (IAA28), CRANE (IAA18), WOODEN LEG, and ARABIDOPSIS RESPONSE REGU
32 nce triggering a high degree of vigilance by cranes identified at 300 m.
33 ting factor on population growth of sandhill cranes in the RMP, which could become more limiting with
34 velopment of China to secure this endangered crane lineage and other wildlife on the Tibetan Plateau.
35 he conservation of the migratory red-crowned crane population that winters in the Yellow River Delta
36   Additionally, our model suggested that the crane prefers to breed in alpine meadows at an elevation
37 ial feeding areas decreased dramatically and cranes restricted their activity to a small partially un
38 tion model (SDM) to analyze the black-necked crane's breeding habitats.
39  crane (Grus nigricollis) is the only alpine crane species and is endemic to the Tibetan Plateau.
40 e is little information on gut microbiota of cranes under different conservation strategies.
41                                              Crane vigilance declined with increasing distance from w
42                       Increased frequency in crane vigilance only occurred in the much taller S. sals
43 ound that both the frequency and duration of crane vigilance significantly increased in the presence
44  Using 8 years of data on migrating whooping cranes, we were able to partition genetic and socially l
45  bred adolescent and artificially bred adult cranes were characterized by next-generation sequencing
46 reatest alpha diversity was found in captive cranes, while wild cranes had the least.
47                                 We fitted 23 cranes with telemetry devices and used remote sensing da

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