戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 , Siluriformes (catfish), and Salmoniformes (salmonids).
2 m conservation and management of this iconic salmonid.
3 fects specific to the juvenile life-stage of salmonids.
4 d-driven kidney pathology in wild and farmed salmonids.
5 iamine deficiency in California's anadromous salmonids.
6 onova shasta, which causes lethal disease in salmonids.
7 linked to the sex determining locus (sdY) of salmonids.
8 the global and long history introductions of salmonids.
9 presence of CD4-1(+)CD3epsilon(+) T cells in salmonids.
10 re based on studies of embryo-lethality with salmonids.
11 d the AhRs of sturgeons differ from those of salmonids.
12 e resource for functional genome research in salmonids.
13 ain critical instream habitat for ESA-listed salmonids.
14 of carotenoids (red-pink pigments) in farmed salmonids.
15 tion and treatment of infections in cultured salmonids.
16           Pancreas disease (PD), caused by a salmonid alphavirus (SAV), has a large negative economic
17                                              Salmonid alphavirus infection results in pancreas diseas
18  genotypes for SNPs, identified two eQTL for salmonid alphavirus load.
19 onsisting of ~ 110 offspring challenged with salmonid alphavirus subtype 3.
20     Transcript levels for the fifteen unique salmonid AMPK subunit genes were quantified in skeletal
21           Due to the marked heterochiasmy in salmonids, an efficient two-stage mapping approach was a
22 lder' ohnologues that began diverging in the salmonid ancestor.
23                 Our results demonstrate that salmonid and freshwater resources were more important fo
24 the genetic architecture of recombination in salmonids and contribute to a better understanding of ho
25 is important for development and survival of salmonids and crustaceans and has been shown to reduce c
26 uate downstream passage behavior of juvenile salmonids and dam approach behavior of upstream migratin
27 ines, felines, equids, ovids, suids, bovins, salmonids and murids.
28 ghly fatal hemorrhagic septicemic disease in salmonids and other fishes, leading to epizootics throug
29 e superorder Protacanthopterygii (containing salmonids and pike) and corresponds to the insertion of
30 tially impacting both economically-important salmonids and their associated river food web.
31  the impacts of metal and coal extraction on salmonids and their habitat.
32   Sturgeons are evolutionarily distinct from salmonids, and the AhRs of sturgeons differ from those o
33  Large amounts of antimicrobials are used in salmonid aquaculture in Chile.
34                                           In salmonid aquaculture, a variety of technologies have bee
35 ae virus associated with high mortalities in salmonid aquaculture.
36                                      Not all salmonids are sensitive to acute lethality caused by 6PP
37 ng freshwater bryozoans as primary hosts and salmonids as secondary hosts.
38            6PPD-Q is acutely toxic to select salmonids at environmentally relevant concentrations, wh
39 tes resulting from drought for three Pacific salmonids at their ranges' trailing edge.
40 estigating CRF peptides in a more euryhaline salmonid, Atlantic salmon (Salmo salar).
41  duplicated genes retained from an ancestral salmonid autotetraploidization event than expected.
42  mining operations, describes the ecology of salmonid-bearing watersheds in northwestern North Americ
43 nd inform mitigation, mines continue to harm salmonid-bearing watersheds via pathways such as toxic c
44 L development was documented in a cold-water salmonid (brook trout, Salvelinus fontinalis) reared at
45  the Northern Rocky Mountains for two native salmonids-bull trout (BT) and cutthroat trout (CT).
46 rom vegetable sources in the diets of farmed salmonids, but the consequences for the oxidative stabil
47 e model can be used to support management of salmonids by predicting population responses to predicte
48 e health condition of out-migrating juvenile salmonids can influence migration success.
49                                              Salmonid CCL19-like genes all contain the DCCL-conserved
50            Our results have implications for salmonid conservation and aquaculture, where small natur
51 ), spreads easily throughout farmed and wild salmonids, constituting a significant economic burden.
52     Mating between escaped domestic and wild salmonids could favour admixed over wild or feral crosse
53 e the human Alu sequence, the SINEs found in salmonids could provide useful genetic markers and prime
54 nant contribution of algal-derived energy to salmonid diets in manipulated reaches.
55 countries and notably, this is the first non-salmonid disease that has resulted in major impacts glob
56 is, we studied harbor seals preying on adult salmonids during the 2014-2019 fall runs in Whatcom Cree
57 uld have serious implications for cold-water salmonid ecology and survival.
58 es economically significant losses in farmed salmonids, especially Atlantic salmon (Salmo salar) and
59 , we demonstrate the major impact of LORe on salmonid evolution.
60 sease, causes substantial economic losses in salmonid farms and hatcheries.
61 metry assays in situ and after transplanting salmonid fish among different streams to disentangle the
62  common mechanism of toxic action in the two salmonid fish species.
63 fp, which causes enteric redmouth disease in salmonid fish species.
64 eat to healthy and sustainable production of salmonid fish worldwide.
65                     We find that beta2m of a salmonid fish, the rainbow trout (Oncorhynchus mykiss),
66                                              Salmonid fish, whose ancestor underwent WGD by autotetra
67 alternating between freshwater bryozoans and salmonid fish.
68 g of resistance to this important disease of salmonid fish.
69 c redmouth disease (ERM) that mainly affects salmonid fishes and leads to significant economic losses
70        In the embryos and young juveniles of salmonid fishes and rodents, TH induces switches in opsi
71      Jack Brand and colleagues introduce the salmonid fishes comprising over 200 species.
72 the AMPK-alpha, -beta and -gamma families of salmonid fishes due to a history of genome duplication e
73  responsible for bacterial kidney disease in salmonid fishes world-wide.
74                             Six cyprinid and salmonid fishes, including an asymptomatic carrier, were
75                       The common ancestor of salmonid fishes, including rainbow trout (Oncorhynchus m
76 rently related to the tetraploid ancestry of salmonid fishes, was detected at one simple sequence rep
77 ication of QTL for important traits in other salmonid fishes.
78 MDH-B, duplicated by ancestral polyploidy in salmonid fishes.
79 ed DNA fingerprint patterns in 14 species of salmonid fishes.
80  growth according to immunological status in salmonid fishes.
81 age rates comparing favourably to anadromous salmonid fishes.
82 ned ecological and phenotypic variability of salmonid fishes.
83 cates efforts to detect allelic variation in salmonid fishes.
84 er certain conditions, mortality of juvenile salmonid fishes.
85 n the diversity of life histories within the salmonid fishes.
86 mpact of chemical anti-sea lice treatment on salmonids following application in a commercial farm has
87  a reference sequence for the study of other salmonids for a range of purposes.
88                                  While whole salmonid fry showed a small upregulation of IGF-IR expre
89 and brown trout (Salmo trutta) represent two salmonid genera separated for 15--20 million years.
90  tissue (flesh) is a unique trait in several salmonid genera, including Atlantic salmon.
91 C gene was generated for 11 species in three salmonid genera, Oncorhynchus, Salmo, and Salvelinus.
92  gene were generated for 11 species in three salmonid genera: Oncorhynchus, Salmo, and Salvelinus.
93                          One-quarter of each salmonid genome, harbouring at least 4550 ohnologues, ha
94 ach the immunological function of the ILT in salmonid gills.
95                                           In salmonids, growth and development are important fitness
96 revious evidence for the portfolio effect in salmonids has arisen from examinations of time series of
97                       Wild stocks of Pacific salmonids have experienced sharp declines in abundance o
98  of a recent whole genome-duplication event, salmonids have four: MSTN-1 (-1a and -1b) and MSTN-2 (-2
99                                              Salmonid herpesvirus 1 (SalHV-1) is a pathogen of the ra
100  into the molecular mechanisms implicated in salmonid immune response and resistance to whirling dise
101 e foraging and growth patterns of two stream salmonids in a coastal southeast Alaska drainage.
102 lized by, resources obtained and behavior of salmonids in a mountain lake.
103 e-wide effects of 6PPD-Q on early life stage salmonids, including two sensitive species, rainbow trou
104 enthic algae, most insect taxa, and juvenile salmonids increased in manipulated areas.
105 r histocompatibility class (MHC) IIB gene of salmonids is analyzed for patterns indicative of natural
106 e results demonstrate that the IFN system of salmonids is far more complex than previously realized,
107 oductivity and warming water temperatures on salmonids is important for understanding how climate war
108 nism for evolving new MHC class I alleles in salmonids is recombination in intron II that shuffles al
109 thesis that the expanded AMPK gene system of salmonids is transcriptionally regulated by growth and i
110 ucho taimen), the world's largest freshwater salmonid, is threatened, endangered, or extirpated acros
111  lymphoid tissues in mammals, diversified in salmonids leading to the presence of six CCL19-like gene
112                   The striking difference in salmonid MHC class I and class II evolution contrasts wi
113             The difference may arise because salmonid MHC class I and II genes are not linked, wherea
114 s an opportunity to explore the evolution of salmonid miRNAs following the relatively recent whole ge
115                       Here, we discover that salmonid olfactory epithelium contains magnetite crystal
116 l to data on the passage of juvenile Pacific salmonids (Oncorhynchus spp.) at seven dams in the Colum
117 her cause) mortality of landlocked migratory salmonids over half a century.
118            Altogether, our data confirm that salmonid PKR has conserved molecular functions that VHSV
119 ll line were conducted to assess the role of salmonid PKR in the antiviral response.
120 e (PKD) is a major threat to wild and farmed salmonid populations because of its lethal effect at hig
121 Climatic warming elevates mortality for many salmonid populations during their physically challenging
122  of allele frequencies at duplicated loci in salmonid populations.
123                                              Salmonids possess all four subgroups, whereas other tele
124  prey fishes and linked to cohort failure in salmonid predators that eat prey fish with thiaminase ac
125 he presence and absence of widely introduced salmonids rainbow trout (Oncorhynchus mykiss) and brook
126              As previously observed in other salmonids, recombination rates showed large sex differen
127 needs of Endangered Species Act (ESA)-listed salmonids relative to climate change in the central Colu
128 d phylogenetic approaches, we establish that salmonids retain two IGF-IRa paralogues from ssWGD and a
129                                              Salmonids returned to impacted sites in subsequent years
130   This review will focus primarily on farmed salmonids (salmon and trout) within a comparative contex
131 rming industrial broiler chickens and farmed salmonids (salmon, marine trout, and Arctic char) to ide
132  million years ago of the common ancestor of salmonids (salmonid-specific fourth vertebrate whole-gen
133 robes homologous to two previously described salmonid short interspersed nuclear elements (SINEs) det
134  for the biological limit governing suitable salmonid spawning and egg incubation conditions.
135 velinus namaycush) and among several related salmonid species (lake trout; brook trout, Salvelinus fo
136 ely recent whole genome duplication event in salmonid species and to investigate the role of miRNAs i
137 ction on the class IIB gene in all 11 of the salmonid species for both the ABS and the non-ABS codons
138 mpacted the propagation and survival of many salmonid species over six continents, with particularly
139 cal adaptations that potentially facilitated salmonid species radiation.
140  we used genomic DNA sequence data from nine salmonid species to compare nucleotide identities for or
141 chus mykiss) are two of the most susceptible salmonid species to sea lice infestation.
142                                       Across salmonid species, life-history strategies range from who
143 (IPNVs) exhibit a wide range of virulence in salmonid species.
144 s, homologous sequences are present in other salmonid species.
145 apping approach within and across a range of salmonid species.
146 hogen Myxobolus cerebralis, afflicts several salmonid species.
147 n on ecologically and economically important salmonid species.IMPORTANCE Chinook salmon are a keyston
148 ome duplication events, including five novel salmonid-specific AMPK subunit gene paralogue pairs.
149 ars ago of the common ancestor of salmonids (salmonid-specific fourth vertebrate whole-genome duplica
150 ific HIFA paralogs, and provide evidence for salmonid-specific HIFA duplicates.
151 ing probes homologous to the 5' or 3' end of salmonid-specific small interspersed nuclear elements.
152                             However, while a salmonid-specific whole genome duplication (ssWGD) is kn
153 management approaches for restoring depleted salmonid stocks.
154 onstrates that riparian management targeting salmonids strongly affects river food webs via changes i
155 sensus sequence of a transposase gene of the salmonid subfamily of elements was engineered by elimina
156 es were within the range documented in other salmonids, suggesting moderate diversity despite widespr
157 serve the out-migratory behavior of juvenile salmonids tagged by surgical implantation of acoustic mi
158 ative homeologous regions inherited from the salmonid tetraploid ancestor were identified for 10 pair
159 of the two genes expected from the ancestral salmonid tetraploidy.
160 ytscha), a phenotypically diverse anadromous salmonid that is ecologically and economically important
161 at chronic exposure to warming can attenuate salmonid thermal sensitivity.
162 f the plant Arabidopsis thaliana and of four salmonids to assess the impact of WGD on gene expression
163 rologic conditions are suitable for juvenile salmonids to grow large enough to consume salmon eggs by
164 transposase binds to the inverted repeats of salmonid transposons in a substrate-specific manner, and
165 er maintain watershed processes that benefit salmonids, we highlight key windows during the mining go
166 ury conditions, by mid-21st century juvenile salmonids' weights are expected to be lower in the Colum
167 in duplicated genes (ohnologs) following the salmonid WGD 80-100 million years ago.
168  system to explore how TE activity after the salmonid WGD ~100 MYA shaped CRE evolution.
169 ters of ISGs retained as duplicates from the salmonid WGD.
170 sts California's already stressed anadromous salmonids will continue to be impacted by thiamine defic
171                     This symbiosis may endow salmonids with a direct mechanism to sense and respond t
172  bacterial community in the brain of healthy salmonids with bacterial loads comparable to those of th

 
Page Top