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1 tgroups, Paleognathae (emus) and Crocodilia (alligators).
2 specific stages of tooth development in the alligator.
3 g and scaffolding the genome of the American alligator.
4 ed LFNG and DLL1 expressions in the American alligator.
5 etiological agent of fatal mycoplasmosis of alligators.
6 l fluid, and cerebrospinal fluid of affected alligators.
7 the gastrointestinal tract from the American alligator, a crown archosaur with shared ancestry to ext
10 ifocal arthritis emerged in captive American alligators (Alligator mississippiensis) in Florida, Unit
12 ugh parabronchi in the lungs of the American alligator, an amphibious ectotherm without air sacs, whi
13 te that the FMRP amino acid sequences in the alligator and chicken are highly similar to human FMRP w
14 t of the mesencephalic trigeminal nucleus in Alligator and other jawed animals but not in jawless ver
15 stages of development, similarities between Alligator and other species suggest that these bundles r
16 teeth in the talpid2 mutant with that in the alligator and show the formation of decidedly archosauri
17 hoots, and the sodium current remains small; alligator and steifftier show similar but weaker effects
20 oustic cues in the bellows of adult American alligators and found that formant spacing provided highl
22 ence scanning of genomic clones of a turtle, alligator, and lizard reveals diverse, mammal-like lands
23 r both African slender-snouted crocodile and alligator, and suggest that the spinosaurs were not obli
25 proximate to the TSD-related temperature in alligators, and using pharmacological exposure, we show
26 nome of Alligator mississippiensis (American alligator) but also present in the genomes of Crocodylus
29 ns: Alligator mississippiensis (the American alligator), Crocodylus porosus (the saltwater crocodile)
31 totic labeling to map putative stem cells in alligator dental laminae, which contain quiescent odonto
34 ders of the diencephalon was investigated in Alligator embryos beginning when this structure was a si
35 form RNA sequencing of tissues from American alligator embryos to find genes that are differentially
39 present an improved assembly of the American alligator genome, scaffolded with in vitro proximity lig
42 conclusive evidence that the poikilothermic alligator has GC-rich isochores, like homeothermic birds
47 for the detection of antibodies produced by alligators in response to M. alligatoris exposure was de
48 and metatherian mammals, but not turtles or alligators, indicating that Fgf8 expression is neither a
49 genetic differences between male and female alligators leaves open the question of how the genes res
50 izards; SALs) and Elgaria coerulea (northern alligator lizards; NALs), in response to a thermal chall
51 ermal niche, Elgaria multicarinata (southern alligator lizards; SALs) and Elgaria coerulea (northern
52 brain development, then the diencephalon of Alligator may be built differently from the hindbrain.
53 amily initially recovered from the genome of Alligator mississippiensis (American alligator) but also
54 nerated draft genomes of three crocodilians: Alligator mississippiensis (the American alligator), Cro
56 itis emerged in captive American alligators (Alligator mississippiensis) in Florida, United States, i
59 e development was investigated in a reptile, Alligator mississippiensis, using a variety of methodolo
67 expression does not cycle in the PSM of the alligator, similar to the chicken but unlike the anole.
69 essed sequence tags (ESTs) from the American alligator to overcome sample size limitations suggested
75 renewal in a crocodilian model, the American alligator, which has well-organized teeth similar to mam
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