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1 eing collaboration to learn more about these sturgeon.
2 preservation for the first time in the white sturgeon.
3 cies of extreme conservation concern such as sturgeon.
4 b modules that support the endangered Pallid Sturgeon.
5 iours were consistent and persistent in lake sturgeon.
6 greater sensitivity in vivo relative to lake sturgeon.
7 cells transfected with AhR1 or AhR2 of white sturgeon.
8 the range-wide marine distribution of green sturgeon.
9 n to sensitive or endangered species such as sturgeons.
10 ations evidenced in its sister lineage, i.e. sturgeons.
11 in other fishes, including other species of sturgeons.
12 ose sturgeon and indicate a restricted Dm in sturgeons.
13 ization of both OC and MGP from the Adriatic sturgeon, a ray-finned fish characterized by a slow evol
14 ormed in vivo lineage tracing in the sterlet sturgeon, a representative of nonteleost ray-finned fish
15 the FA signatures of the tissues, where the sturgeons accumulated particular highly-unsaturated FA (
16 t and diverse tissues of the farmed Siberian sturgeon (Acipenser baerii) were analyzed in detail to a
17 federally endangered population of shortnose sturgeon (Acipenser brevirostrum) that has been quietly
18 (SPM), sediment, and various tissues of lake sturgeon (Acipenser fulvescens) and northern pike (Esox
20 udy investigated the spatial ecology of lake sturgeon (Acipenser fulvescens) within the barrier free
27 perimentally tractable relative, the sterlet sturgeon (Acipenser ruthenus), we found that Bmp5 and fo
28 ve responses of two endangered fishes, white sturgeon (Acipenser transmontanus) and lake sturgeon (Ac
31 study investigated the sensitivity of white sturgeon (Acipenser transmontanus) to DLCs in vitro via
32 rant species or life stages, including white sturgeon (Acipenser transmontanus), chinook salmon (Onco
34 ified squamous integument of green and white sturgeons (Acipenser medirostris and transmontanus, resp
36 spawning periodicity shortened as male lake sturgeon age, and future breeding opportunities decrease
40 no differences in sensitivity between white sturgeon and lake sturgeon based on activation of AhR1.
41 ges, and the commonality of habitats between sturgeon and lamprey ammocoetes, suggests that there may
42 nt contamination profiles were found in lake sturgeon and northern pike, implying that the accumulati
44 Furthermore, a distinct PCB signature in sturgeon and whitefish, collected at Hanford study areas
45 cerebellum, unlike the case in the Siberian sturgeon and zebrafish, whereas the absence of Gly-ir ne
48 those reported for the sea lamprey, Siberian sturgeon, and zebrafish revealed some shared features bu
51 into the ecology of marine-resident Atlantic Sturgeon are crucial for both defining monitoring parame
55 overharvesting, natural populations of white sturgeon are threatened and there is a growing effort to
56 determine the oceanic distribution of green sturgeon are unclear, but broad-scale physical condition
63 s of these datasets suggest that the Russian sturgeon blood serum metabolome and the Siberian sturgeo
68 is the purification of the pigment of black sturgeon caviar and its unambiguous identification as a
71 sed and tracked experimental pulses of white sturgeon eDNA (novel to the system) in five fourth-order
73 geon blood serum metabolome and the Siberian sturgeon epidermal mucous metabolome are notably sex spe
74 hery-reared (juvenile) and wild (adult) Lake Sturgeon exhibit extreme crystallographic texture as evi
75 These data demonstrate that juvenile white sturgeon exhibit substantial resilience to heatwaves, as
80 nces in overall fitness traits, where Pallid Sturgeon fecundity was greater than a tenfold difference
81 s of sex, a critical feature for using white sturgeon for transplantation studies since the species s
82 emonstrates the ability of CCSWA to evaluate sturgeon freshness level according to their storage time
83 We assessed the tolerance of juvenile white sturgeon from an endangered population to heatwave expos
84 ntrations of select DLCs in tissues of white sturgeon from British Columbia, Canada, were used to cal
87 ific rivers or lakes by acoustic-tagged lake sturgeon further subdivided individuals into 14 "conting
88 heritance is established, the paddlefish and sturgeon genomes are thus a mosaic of shared and non-sha
89 e associated with an egg-white binder, while sturgeon glue was identified as adhesive in all sheep le
92 gelatin hydrolysates from the skin of beluga sturgeon (Huso huso) on freshwater crayfish (Astacus lep
93 y the WHO might not adequately protect white sturgeon, illuminating the need for additional investiga
94 n the other river, which confirmed that lake sturgeon in the Detroit and St. Clair represent two semi
95 r 6 years (2011-2016), movements of 268 lake sturgeon in the HEC were continuously monitored across t
97 baseline information on endangered Atlantic Sturgeon in the New York Wind Energy Area (NY WEA), a fu
100 f the unique life history characteristics of sturgeon, including longevity, late maturation and long
103 GD is masked by the fact that paddlefish and sturgeon lineage divergence occurred before rediploidiza
106 of heteroplasmy and length variation in Gulf sturgeon mtDNA, indicates that the molecular mechanisms
108 in a context of a reduced rate of evolution, sturgeon OC has retained structural features of the ance
117 centrations of which were relatively high at Sturgeon Point, and PBEB, the concentrations of which we
118 Michigan, whereas that of HBB was highest at Sturgeon Point, approximately 25 km southwest of Buffalo
120 reasing with doubling times of 5-10 years at Sturgeon Point, Sleeping Bear Dunes, and Eagle Harbor, b
121 orts have been proposed worldwide to restore sturgeon populations through the use of hatcheries to su
126 The elucidation of the cDNA sequence for sturgeon proorphanin provides a unique window for interp
127 en possible Gla residues that would make the sturgeon protein the most gamma-carboxylated among known
128 ochemical study in the brain of the Siberian sturgeon reports the neuronal distribution of three cyto
130 all, the largest contributor to our Atlantic sturgeon sampled from the Restigouche River system was t
132 erentiation was achieved between the 4 group sturgeon samples aged: 2 days; 5, 6 and 7 days; 8 and 9
133 leotide (NADH) and vitamin A were scanned on sturgeon samples kept at 4 degrees C up to 12 days.
134 ferences in life history traits among Pallid Sturgeon (Scaphirhynchus albus) occupying river segments
136 Mi'gmaw fishers have reported an increase in sturgeon sightings over the last decade in the Restigouc
137 tes that determine caviar quality, including sturgeon species and processing methods, is still lackin
138 types of caviar, obtained from six different sturgeon species and produced using either salt or a com
140 ributing to a kokumi taste), while the other sturgeon species were primarily distinguished by lipids
142 NA) were used to identify haplotypes of Gulf sturgeon specimens obtained from eight drainages spannin
144 y a unique behavioral phenotype of shortnose sturgeon that occupies habitats in New York Harbor in la
146 nderstanding of the distribution of Atlantic sturgeon through microsatellite analyses and leveraging
147 were 3- to 30-fold more sensitive than lake sturgeon to exposure to 5 different DLCs based on activa
148 is a lack of knowledge of the sensitivity of sturgeons to DLCs, and it is uncertain whether TEFs deve
150 ected sterlet embryos (Acipenser ruthenus, a sturgeon) to test the function of three such genes.
153 lculated for endangered populations of white sturgeon were approximately 10-fold greater than TEQs an
157 mplications of polyploidization have endowed sturgeon with multiple forms of AHR, in this case 3 pair
159 l mucous metabolomes of Russian and Siberian sturgeon, with extensive endogenous metabolite assignmen
160 d heterocercal tails, like modern sharks and sturgeons, with asymmetric caudal fins and a vertebral c
161 c contaminants for both life stages of white sturgeon within 1 order of magnitude of measured values.