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1 ir species, the American robin and the house sparrow.
2  field sparrow from the more aggressive song sparrow.
3  to some degree pre-encoded in white-crowned sparrows.
4 that controls song behavior in white-crowned sparrows.
5 tion typically removes circulating T in tree sparrows.
6 a pedigreed insular population of wild house sparrows.
7 dial amygdala of field sparrows but not song sparrows.
8  the song system in adult male white-crowned sparrows.
9 d cerebrosides in the SC compared with mesic sparrows.
10 ty in RA was not altered by deafening in the sparrows.
11 ain in breeding-condition male white-crowned sparrows 2 days prior to T withdrawal and shifting them
12 ying neural representations of song in swamp sparrows, a species in which juveniles learn and practic
13 nd for communication between neighbors (song sparrows address or reply to a neighbor with a song they
14 ons for a threatened songbird, the saltmarsh sparrow (Ammodramus caudacutus), in a region where sea l
15 rea, dorsal arcopallium, and optic tectum in sparrow and was essentially undetectable in zebra finch.
16 erborne transmission of A/duck/Laos/25/06 in sparrows and chickens.
17 g T, we captured 18 adult male white-crowned sparrows and kept them on short days for 12 weeks.
18 issue, we castrated adult male white-crowned sparrows and rapidly shifted them to short-day photoperi
19                                        House sparrows and rock doves are potential free-ranging senti
20 phrase types characteristic of white-crowned sparrows and, thus, could contribute to innate song reco
21 was detected in samples examined from geese, sparrows, and starlings.
22                     To elucidate the role of sparrows as intermediate hosts of highly pathogenic avia
23 he suppression of winter aggression in field sparrows, because similar winter differences were found
24 ely to threaten the persistence of saltmarsh sparrows beyond 2060 and could cause extinction as soon
25 ral septum (LS) and medial amygdala of field sparrows but not song sparrows.
26  We here confirm earlier findings that swamp sparrows categorically perceive the notes that constitut
27 lts from a 20-year study of free-living song sparrows confirm that attractive males contribute more o
28 easonal changes in the song nuclei, the song sparrows continued to sing the same number of different
29 er quality data analysis, the application of SPARROW controls for confounding factors such as hydrolo
30 d susceptibility to infection we observed in sparrows, coupled with their presence in poultry houses,
31  Zanobetti A, Bind MC, Kloog I, Koutrakis P, Sparrow D, Vokonas PS, Schwartz JD.
32                Dai L, Koutrakis P, Coull BA, Sparrow D, Vokonas PS, Schwartz JD.
33 t common mammal species captured while house sparrows, European starlings, rock pigeons, swallows, an
34                        Free-living male song sparrows experience three annually repeating life histor
35 ensorimotor neurons in freely behaving swamp sparrows expressed categorical auditory responses to cha
36  analyses further identify groups (New World sparrows, finches, and vireos) disproportionally affecte
37 A in photosensitive adult male white-crowned sparrows for one month.
38 st recognized, or more subordinate levels - 'sparrow', for example - which require additional percept
39 , M. Hashimoto, K. Nakanishi, J. Dillon & J. Sparrow, for the biosynthesis of A2E: (i) condensation o
40 that a certain class of neurons in the swamp sparrow forebrain displays a precise auditory-vocal corr
41 that differentiate the less aggressive field sparrow from the more aggressive song sparrow.
42 examined the population genetics of 576 song sparrows from 23 populations using seven microsatellite
43                We showed that nestling house sparrows from both localities had higher CWL than adults
44 d lipid composition of the SC of adult house sparrows from two populations, one living in the deserts
45 e a northward shift in current White-crowned sparrow habitat range and a 20-60% increase in their pre
46                           Adult desert house sparrows had a lower CWL, a lower proportion of free fat
47                          A new study of song sparrows has revealed a parent-offspring resemblance for
48  In a field study, we show that a young song sparrow (i) selects his songs from three or four older b
49 d to acute myeloid leukemia expression data, SPARROW identifies an apoptotic biomarker (PYCARD) for a
50  We showed previously that in white-throated sparrows, immediate early gene responses in the auditory
51          For example, in adult white-crowned sparrows, increased Spring photoperiod raises circulatin
52                    Our results indicate that SPARROW is a powerful complementary approach to identify
53 were investigated in fledgling white-crowned sparrows lacking song experience.
54 s to social signals in female white-throated sparrows listening to recordings of male song.
55                            Juvenile chipping sparrow males develop five to seven potential precursor
56                                  As chipping sparrow males return from migration to start their first
57      Our results suggest that white-throated sparrows may fall back to a simple constant-vector orien
58  We fitted animal models to 38 years of song sparrow (Melospiza melodia) phenology and pedigree data
59  the rate of nest failure in an insular song sparrow (Melospiza melodia) population.
60  learns new songs in adulthood, and the song sparrow (Melospiza melodia) that does not.
61 e examine song type representations in swamp sparrows (Melospiza georgiana), a multiple song type spe
62 attributes of Area X in wild adult male song sparrows (Melospiza melodia) captured during the spring
63 d juvenile survival for a population of Song Sparrows (Melospiza melodia) in California.
64                                         Song sparrows (Melospiza melodia) in western North America pr
65 c paternity and pedigree data from wild song sparrows (Melospiza melodia) to partition variance in ea
66 illa), which seasonally flock, and male song sparrows (Melospiza melodia), which are territorial year
67 nuclei, and song behavior in adult male song sparrows (Melospiza melodia).
68 nogamous but genetically polygynandrous song sparrows (Melospiza melodia).
69 of wild-caught, hand-reared songbirds (swamp sparrows, Melospiza georgiana).
70                A recent study has found that sparrows moved gradually east above the Arctic Circle co
71 does not exceed 20 cm, whereas White-crowned sparrows nested only under shrubs between 20 cm and 1 m
72                       In adult white-crowned sparrows, new neurons are added continually to the song
73 veral aspects of song structure in wild song sparrows of a nonmigratory population.
74 ncreases observed in the abundances of house sparrow (Passer domesticus) and spotted dove (Streptopel
75 s France, screening populations of the house sparrow (Passer domesticus) for malaria (Plasmodium reli
76 marked females in eight populations of house sparrows (Passer domesticus) from North America and Euro
77 tion: songs composed of single white-crowned sparrow phrases and songs played in reverse elicited voc
78 undary measured in field studies of the same sparrow population.
79                                        House-sparrow populations have declined sharply in Western Eur
80  widespread local extinctions of rural house-sparrow populations in southern England.
81                           Furthermore, swamp sparrow populations that learned different song dialects
82 f differentiation among Pacific coastal song sparrow populations.
83 enile, long-distance migrating white-crowned sparrows rapidly recognize and correct for a continent-w
84 of the SC in desert and mesic nestling house sparrows reared in low and high humidity and compared ou
85 se inhibitors in vivo in adult white-crowned sparrows rescued neurons within the hormone-sensitive so
86                           SERs identified by SPARROW reveal known driver mutations in multiple human
87 g circuitry was incompletely developed, male sparrows sang less stereotyped songs than males at day 2
88                                    Male song sparrows sang songs that were more variable in structure
89 as capable of detecting anti-WN IgM in house sparrow serum samples from laboratory-infected birds but
90 able when wild, adult, free-ranging chipping sparrows sing at dawn than when they sing during the day
91  expression data with a novel method, namely SPARROW ( SPAR: se selected exp R: essi O: n regulators
92  show how a migratory songbird, the chipping sparrow (Spizella passerina), achieves prompt and precis
93  brains in spring and winter from male field sparrows (Spizella pusilla), which seasonally flock, and
94 were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from sentinel duck
95                            In white-throated sparrows, the selectivity of the zenk response requires
96 seasonally breeding adult male white-crowned sparrows, the song system nucleus HVC loses approximatel
97 l U.S. Geological Survey water-quality model SPARROW to investigate whether spatial differences in co
98  in form from the simple notes of a Chipping Sparrow to the rich performance of the nightingale.
99                    We exposed juvenile swamp sparrows to a suite of tutor songs and confirmed that, a
100 the sensorimotor nucleus HVC in anesthetized sparrows to assess neuronal responsiveness to songs in t
101 posed estrogen-primed, female white-throated sparrows to conspecific male song and looked for evidenc
102      Waterborne transmission from inoculated sparrows to contact chickens was absent, while 25% of sp
103 We exposed adult male Gambel's white-crowned sparrows to either short-day photoperiod or long-day pho
104         In female nonbreeding white-throated sparrows treated with E2, the density of fibers immunore
105 ree model species: humans (type I survival), sparrow (type II), and barnacle (type III).
106                                              SPARROW uncovers a previously unknown connection between
107 strildidae and a limited number of emberizid sparrows) using antibodies against 10 neuropeptides and
108                          Across warblers and sparrows, we found little support linking timing of flig
109                           Male American tree sparrows were exposed to one of three photoperiodic cond
110                 Photosensitive white-crowned sparrows were exposed to one of three treatments.
111                (3) HVc was lesioned, and the sparrows were housed on short-day (SD) photoperiods in t
112 to contact chickens was absent, while 25% of sparrows were infected via waterborne transmission from
113            Adult male Gambel's white-crowned sparrows were surgically deafened, which eliminates audi
114                     We tutored white-crowned sparrows with syntax information ranging from acoustic i
115 o model songbird species, the white-throated sparrow (Zonotrichia albicollis) and zebra finch (Taenio
116 l behavior and plumage in the white-throated sparrow (Zonotrichia albicollis) is linked to an inversi
117 polymorphism (ZAL2(m)) in the white-throated sparrow (Zonotrichia albicollis) is linked to variation
118                        In the white-throated sparrow (Zonotrichia albicollis), a chromosomal polymorp
119 l (Conirostrum cinereum) and Rufous-collared Sparrow (Zonotrichia capensis) respectively.
120 dressed this issue in Gambel's white-crowned sparrow (Zonotrichia leucophrys gambelii), a songbird th
121 rder--is such a feature in the white-crowned sparrow (Zonotrichia leucophrys), the authors tutored ma
122 ensory systems in experienced white-throated sparrows (Zonotrichia albicollis) captured in southern O
123 ort-term flocks for wintering golden-crowned sparrows (Zonotrichia atricapilla) across three years an
124 e studied two populations of rufous-collared sparrows (Zonotrichia capensis) that breed, only 25 km a
125 rols song behavior in Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) and examined
126 aught wild adult male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) during spring
127 r injected in RA of adult male white-crowned sparrows (Zonotrichia leucophrys gambelii) in breeding o
128                        We used white-crowned sparrows (Zonotrichia leucophrys gambelii) to test the h
129 arius lapponicus) and Gambel's White-crowned sparrows (Zonotrichia leucophrys gambelii) with modeled
130 in wild-caught female Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii).
131 rs of the HVC in male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii): Nissl staini
132                                White-crowned sparrows (Zonotrichia leucophrys), whose song typically
133 ary history of a supergene in white-throated sparrows, Zonotrichia albicollis.
134 ays to show that male mountain white-crowned sparrows, Zonotrichia leucophrys oriantha, must learn to

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