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1 tgroups, Paleognathae (emus) and Crocodilia (alligators).
2  with regrowth in an archosaur, the American alligator.
3  specific stages of tooth development in the alligator.
4 g and scaffolding the genome of the American alligator.
5 ed LFNG and DLL1 expressions in the American alligator.
6  etiological agent of fatal mycoplasmosis of alligators.
7 l fluid, and cerebrospinal fluid of affected alligators.
8 easurement of 17a,20B-dihydroxypregnenone in alligators.
9 the gastrointestinal tract from the American alligator, a crown archosaur with shared ancestry to ext
10 rrelation between percent developed land and alligator abundance across tributaries; instead, salinit
11 se on alligators through surveys of relative alligator abundance in nine tributaries of the lower St.
12                Our findings demonstrate that alligators act as ecosystem engineers and enhance food-w
13                                 The American Alligator Alligator mississippiensis is an abundant pred
14 harial Gavialis gangeticus; and the American alligator Alligator mississippiensis.
15  we assess the relationship between American alligator (Alligator mississippiensis) demography and ti
16                                 The American Alligator (Alligator mississippiensis) facilitates a saf
17                         We assessed American alligator (Alligator mississippiensis) morphological sta
18                              In the American alligator (Alligator mississippiensis), eggs incubated d
19 rk, juveniles and adults for crown birds and alligator (Alligator mississippiensis), we find that adu
20                                     American alligators (Alligator mississippiensis) are apex predato
21                                     American alligators (Alligator mississippiensis) create and maint
22 ifocal arthritis emerged in captive American alligators (Alligator mississippiensis) in Florida, Unit
23                                     American alligators (Alligator mississippiensis) inhabit freshwat
24 ressure recordings were taken from sub-adult alligators (Alligator mississippiensis) locomoting on a
25  Vultures (Cathartes aura, 47%) and American Alligators (Alligator mississippiensis, 29%) being the p
26                                 The American alligator, Alligator mississippiensis, like all crocodil
27       Overall, our results demonstrated that alligators ameliorated dry-season stress by engineering
28 ugh parabronchi in the lungs of the American alligator, an amphibious ectotherm without air sacs, whi
29 te that the FMRP amino acid sequences in the alligator and chicken are highly similar to human FMRP w
30 t of the mesencephalic trigeminal nucleus in Alligator and other jawed animals but not in jawless ver
31  stages of development, similarities between Alligator and other species suggest that these bundles r
32 teeth in the talpid2 mutant with that in the alligator and show the formation of decidedly archosauri
33 hoots, and the sodium current remains small; alligator and steifftier show similar but weaker effects
34 and body sizes in juvenile to adult American alligators and a scaled model of the extinct giant allig
35 lligatoris causes lethal invasive disease of alligators and caimans.
36 model's predictions are validated for living alligators and chickens.
37 istinct developmental trajectory compared to alligators and crown birds; (ii) ornithischian and non-a
38                        We showed that larger alligators and D. riograndensis encounter challenges in
39 oustic cues in the bellows of adult American alligators and found that formant spacing provided highl
40 dded in the wall of the middle ear of birds, alligators and Sphenodon.
41  and "eu-tetrapods" such as mammals, turtle, alligator, and birds.
42               The akinetic skull of opossum, alligator, and leatherback turtle evolved in independent
43 ence scanning of genomic clones of a turtle, alligator, and lizard reveals diverse, mammal-like lands
44 r both African slender-snouted crocodile and alligator, and suggest that the spinosaurs were not obli
45 s and tortoises) and Crocodilia (crocodiles, alligators, and gharials) contain numerous threatened, l
46 ius carpio), and osteoderms from armadillos, alligators, and leatherback turtles.
47  of species, including sharks, frogs, birds, alligators, and platypus, that can use an atypical TCRde
48 te levels and a sex steroid in wild juvenile alligators, and to our knowledge represents the first me
49  proximate to the TSD-related temperature in alligators, and using pharmacological exposure, we show
50 ole in regulating soil carbon stock and that alligators are functional apex predators in carbon dynam
51 ng birds change colony site preferences when alligators are not present to serve as nest protectors.
52  less accessible to mammalian predators when alligators are not present, and that this requirement is
53 t, and that this requirement is relaxed when alligators are present.
54                    For example, dolphins and alligators are similar in size but differ in dangerousne
55 nome of Alligator mississippiensis (American alligator) but also present in the genomes of Crocodylus
56 ntegrating with high efficiency an exogenous alligator cathelicidin gene into a targeted non-coding r
57  low-frequency hearing vertebrates including alligator, chicken, gerbil, and human.
58 formed using a 4F quadripolar catheter or an alligator-clip-connected angioplasty wire.
59 ns: Alligator mississippiensis (the American alligator), Crocodylus porosus (the saltwater crocodile)
60 anatomical data of model archosaurs (Gallus, Alligator), crown birds exhibit a distinct allometric re
61                         Hunting and nuisance alligator data suggests that adults are relatively rare
62                            Further, American alligator demographic variables are positively correlate
63               The authors collected juvenile alligator dental laminae at different developmental stag
64 totic labeling to map putative stem cells in alligator dental laminae, which contain quiescent odonto
65                Within the northern fringe of alligator distribution we compared colony characteristic
66                                     However, alligators do not occur throughout the breeding range of
67 logy, cell proliferation was investigated in Alligator during early diencephalon development.
68 sing plasma obtained from naturally infected alligators during the original epidemic.
69                                              Alligator eggs were reared under normoxia or 10% hypoxia
70                                              Alligators eggs were collected from a contaminated site
71 ders of the diencephalon was investigated in Alligator embryos beginning when this structure was a si
72 form RNA sequencing of tissues from American alligator embryos to find genes that are differentially
73                           We investigated if alligators engineer differences in nutrient availability
74                                              Alligator-engineered habitats are ecologically important
75                                          The alligator ESTs were assembled and aligned with their hum
76                                     American alligators experimentally exposed to developmental hypox
77 diate removal of the implant with a 20-gauge alligator forceps over a 2.75-mm long clear corneal tunn
78                                 We show that alligators form maps of ITD very similar to birds, sugge
79 e increased the scaffold N50 of the American alligator from 508 kbp to 10 Mbp.
80 in ovarian follicle density between juvenile alligators from Lake Apopka and the reference site.
81 pand laterally in a manner similar to modern alligator gars and polypterids.
82           We estimate the copy number in the alligator genome to be approximately 46,000 copies.
83 present an improved assembly of the American alligator genome, scaffolded with in vitro proximity lig
84                                       A core alligator gut microbiome comprised of Fusobacteria, but
85                              As such, modern alligator gut microbiomes advance our understanding of a
86 ation and human activity may further degrade alligator habitats and limit the distribution of breedin
87  conclusive evidence that the poikilothermic alligator has GC-rich isochores, like homeothermic birds
88                                          The alligator has the highest resistances to bending and tor
89                                              Alligators have robust regenerative potential for tooth
90 rect transmyocardial perfusion is present in alligator hearts.
91 of transmyocardial and coronary perfusion in alligator hearts.
92  for the detection of antibodies produced by alligators in response to M. alligatoris exposure was de
93 ically sampled juvenile male and female wild alligators in various salinities each month excluding No
94  and metatherian mammals, but not turtles or alligators, indicating that Fgf8 expression is neither a
95  genetic differences between male and female alligators leaves open the question of how the genes res
96 ieved similar velocities, revealing that the alligator lineage is capable of hitherto unappreciated e
97 are ancestral for Crocodylia and lost in the alligator lineage, or that asymmetrical gaits evolved wi
98 etive, 'hard-to-study' species, the Southern Alligator Lizard (Elgaria multicarinata).
99 izards; SALs) and Elgaria coerulea (northern alligator lizards; NALs), in response to a thermal chall
100 ermal niche, Elgaria multicarinata (southern alligator lizards; SALs) and Elgaria coerulea (northern
101  brain development, then the diencephalon of Alligator may be built differently from the hindbrain.
102 amily initially recovered from the genome of Alligator mississippiensis (American alligator) but also
103 nerated draft genomes of three crocodilians: Alligator mississippiensis (the American alligator), Cro
104                                              Alligator mississippiensis captured in marine/estuarine
105                         American alligators (Alligator mississippiensis) are apex predators that have
106                         American alligators (Alligator mississippiensis) create and maintain 'alligat
107 the relationship between American alligator (Alligator mississippiensis) demography and tidally influ
108                      The American Alligator (Alligator mississippiensis) facilitates a safer nesting
109 itis emerged in captive American alligators (Alligator mississippiensis) in Florida, United States, i
110                         American alligators (Alligator mississippiensis) inhabit freshwater wetlands
111 rdings were taken from sub-adult alligators (Alligator mississippiensis) locomoting on a treadmill.
112              We assessed American alligator (Alligator mississippiensis) morphological static allomet
113                   In the American alligator (Alligator mississippiensis), eggs incubated during the T
114 es and adults for crown birds and alligator (Alligator mississippiensis), we find that adult and juve
115 athartes aura, 47%) and American Alligators (Alligator mississippiensis, 29%) being the primary consu
116                      The American alligator, Alligator mississippiensis, like all crocodilians, has t
117 e development was investigated in a reptile, Alligator mississippiensis, using a variety of methodolo
118 ter and marine systems), by the top-predator Alligator mississippiensis.
119 t of Zellweger syndrome and identical to the Alligator mississippiensis.
120 responses in the NL of anesthetized American alligators of either sex and identified the location of
121 en mouse and human lungs but is not found in alligator or turtle lungs, suggesting it arose during th
122   Ovarian phenotypes observed in Lake Apopka alligators or resulting from estrogen treatment were onl
123                Probability of consumption by alligators or vultures was related to distance from nest
124 anscriptomic and follicular profiles between alligators originating from a historically EDC-contamina
125     A biologically detailed model of NL with alligator parameters discriminated ITDs up to 1 kHz.
126 ct habitats extending outward from 10 active alligator ponds across a hydrological gradient in the Ev
127                     Higher P availability in alligator ponds also resulted in bottom-up trophic trans
128 ta, fish CPUE increased by a factor of 12 in alligator ponds as the marsh dried.
129                    Edge habitats surrounding alligator ponds contained the most diverse communities o
130 to community structure by their creation of 'alligator ponds' compared to the surrounding phosphorus
131 gator mississippiensis) create and maintain 'alligator ponds' that serve as dry-season refuges for ot
132 hout this ecosystem could support 16% of the alligator population and 147 adult Turkey Vultures durin
133                                           In alligators, precisely timed spikes in the first-order nu
134                   However, at the fine scale alligators preferred habitats with more open water and v
135 most wading birds, and it is unclear whether alligator presence affects colony site selection.
136               Results indicate that American alligator presence is positively correlated with soil ca
137 ed colony characteristics in locations where alligator presence was either likely or unlikely while c
138 land and farther from landmasses > 5 ha when alligator presence was unlikely compared to when alligat
139            LFNG expression was absent in the alligator PSM, like the anole but unlike the chicken.
140 particularly the lateral oscillations of the alligator's head.
141                  The ELISA reliably detected alligator seroconversion (P < 0.05) beginning 6 weeks af
142                    Rhombomere development in Alligator shares several features in common with hindbra
143  expression does not cycle in the PSM of the alligator, similar to the chicken but unlike the anole.
144 sippiensis), we find that adult and juvenile alligator skulls are topologically similar, whereas juve
145 he potential effects of urban development on alligator spatial distribution and habitat selection at
146                                Thus, smaller alligators still occupy urban habitats because they are
147         Data recorded from the freely moving alligators suggest that fluid inertia, body cavity press
148 s not activate MRs in humans, amphibians, or alligator, suggesting that during the transition to terr
149                     Furthermore, the regrown alligator tail lacked skeletal muscle and instead consis
150                                  The regrown alligator tails constituted approximately 6-18% of the t
151 this study of wild-caught, juvenile American alligator tails identifies a distinct pattern of wound r
152          After explanation from six American alligators, the left ventricle was instrumented, and cor
153 gated potential effects of urban land use on alligators through surveys of relative alligator abundan
154 essed sequence tags (ESTs) from the American alligator to overcome sample size limitations suggested
155                The authors demonstrated that alligator tooth cycle initiation is related to beta-cate
156 molecular pathways related to the process of alligator tooth development.
157                                         Each alligator tooth is a complex family unit composed of the
158                             Here we show the alligator TRPV4 ortholog (AmTRPV4) to be activated at te
159 gator presence was unlikely compared to when alligators were likely.
160                              After hatching, alligators were raised under controlled laboratory setti
161 ce of the dorsoventral diencephalic tract in Alligator which lacks a pineal gland.
162 renewal in a crocodilian model, the American alligator, which has well-organized teeth similar to mam
163 ints of the Helmeted Guineafowl and American alligator, which represent an extant phylogenetic bracke
164 ration was hypothesized from brown anole and alligator, which unexpectedly more resembles the neognat

 
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