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1  the teleost Fundulus heteroclitus (Atlantic killifish).
2 RISPR/Cas9-mediated knock-in approach in the killifish.
3 ive measure of cognitive performance for the killifish.
4 e gene in another killifish species, Arabian killifish.
5 me, and proteome in the brain of short-lived killifish.
6  the naturally short-lived African turquoise killifish.
7 vo-morpholino knock down technique for adult killifish.
8 pothalamic sexual dimorphism is conserved in killifish.
9                                              Killifish AHRR encodes a 680-residue protein with a pred
10 gene under control of AHR response elements, killifish AHRR inhibited the TCDD-dependent transactivat
11 pressed AHRR proteins from human, mouse, and killifish all fail to bind [(3)H]TCDD or [(3)H]beta-naph
12          Unlike zebrafish, African turquoise killifish (an emerging aging model) only showed hair cel
13         Recently, we observed in the gill of killifish, an environmental model organism, that arsenic
14                                  Trinidadian killifish (Anablepsoides hartii) are found in sites that
15 men for growth and fertility for the African killifish and a dietary restriction regimen where both f
16  Two distantly related fish species, bluefin killifish and black bream, express these old paralogs di
17  rates in the upstream reach containing only killifish and crabs.
18 port of the use of vivo-morpholinos in adult killifish and demonstrates that vivo-morpholinos are a v
19    Toxicity reduction, which was dramatic in killifish and duckweed even for low extents of sulfidati
20 ing three natural community types: (1) where killifish and guppies live with predators, (2) where kil
21 h and guppies live with predators, (2) where killifish and guppies live without predators and (3) whe
22  interspecific competition on the fitness of killifish and increase in the interspecific effect on gu
23 on in juvenile rainbow trout, zebrafish, and killifish and on the absorbance of visual pigments in ra
24 s with other communities containing guppies, killifish and predators and ones where killifish live by
25                                        Adult killifish and sediments were collected from seven sites
26                Experimental interrogation in killifish and yeast, combined with machine learning, ind
27 show that this system can be used in medaka, killifish, and mouse embryos.
28  size and fitness (survival and growth) when killifish are found in their native habitats and when fi
29 guppies live without predators and (3) where killifish are the only fish species.
30 ach using isogenic self-fertilising mangrove killifish as a tool for identifying mutants and their mu
31                    Our study establishes the killifish as a translational model for investigating kid
32                        Embryos of the annual killifish Austrofundulus limnaeus are the most anoxia-to
33                               Models such as killifish, bats, and ants have much to teach us about hu
34          Eiders have similar Delta(199)Hg as killifish but much higher delta(202)Hg, suggesting that
35 d that guppies are competitively superior to killifish but were less so in sympatric populations.
36 and associated consequences in PAH-resistant killifish by integrating genomic, physiological, and mod
37 io rerio (zebrafish), Fundulus heteroclitus (killifish), Caenorhabditis elegans (nematode worm), and
38                               The euryhaline killifish CFTR coding sequence is highly homologous to t
39                                 The mangrove killifish clade is composed of the two only known exampl
40                                              Killifish collected from Grande Terre had divergent gene
41                      Therefore, the mangrove killifish could be used as a complementary system alongs
42 dues (Ala127, Thr233, Asn317, and Tyr386) of killifish CYP1A to the corresponding residues of human C
43 0G enabled TCB to dock closer to the heme in killifish CYP1A.
44  in ensembles of rat or human CYP1A1 than of killifish CYP1A.
45 ns are due primarily to Leu387 and Val230 in killifish CYP1A.
46  multiple models of rat, human, scup, and/or killifish CYP1As, based on multiple templates, retaining
47 pine densities in the hypothalamus than male killifish (densities of 0.34+/-0.06 microm-1 and 0.25+/-
48                                    Turquoise killifish display differences in lifespan among wild pop
49 invertebrates and plants, such as zebrafish, killifish, Drosophila or Marchantia, mainly comprise mul
50 nating oil across space and time in resident killifish during the first 4 mo of the spill event.
51                              Indeed, Arabian killifish edaradd crispants showed a potent reduction of
52 stuarine organisms (green crab, blue mussel, killifish, eider) to investigate methylmercury (MMHg) so
53 ntal features of the non-conventional annual killifish embryo to study the principles underlying tiss
54  properties of adjacent tissues in the early killifish embryo.
55                                       Annual killifish embryogenesis, however, challenges prepatterni
56 ne turnover in the EVL cells of post-epiboly killifish embryos is accelerated at cell-cell contacts,
57    Furthermore, laboratory exposures of Gulf killifish embryos to field-collected sediments from Gran
58                                         Gulf killifish embryos were exposed to dissolved Cu and CuO N
59 genome for the short-lived African turquoise killifish, establishing its role as a vertebrate system
60 spite their extremely short lifespans, these killifish exhibit complex and individualized heavy-chain
61 a wider range in laboratory experiments with killifish exposed to MeHg enriched food.
62 tly (18 to 34 generations ago) from Atlantic killifish (F. heteroclitus).
63 h using a natural temperature gradient where killifish fed on natural food sources.
64                             We also examined killifish from communities in which we had introduced gu
65 ites are more sensitive to PAH exposure than killifish from nonremediated sites, suggesting loss of P
66                We also provide evidence that killifish from remediated sites are more sensitive to PA
67 havior data from two populations of Atlantic killifish Fundulus heteroclitus [one reference site (SCO
68                    During embryogenesis, the killifish Fundulus heteroclitus forms a monolayered tigh
69  sequences were identified in a teleost (the killifish Fundulus heteroclitus), two elasmobranch speci
70 of Deepwater Horizon crude oil on fish, Gulf killifish ( Fundulus grandis ) were collected from an oi
71 cles (NPs) and their bioavailability to Gulf killifish (Fundulus grandis) embryos, with the aim of qu
72 icant resistance has rapidly evolved in Gulf killifish (Fundulus grandis) that occupy polluted habita
73                                   Using Gulf killifish (Fundulus grandis), we tested whether adult pr
74 ate CYP3 diversity better, we determined the killifish (Fundulus heteroclitus) CYP3A30 and CYP3A56 an
75 the neuroarchitecture of the male and female killifish (Fundulus heteroclitus) hypothalamus to evalua
76 l variation patterns across the range of the killifish (Fundulus heteroclitus) in 310 loci, including
77  aromatic hydrocarbon (PAH)-adapted Atlantic killifish (Fundulus heteroclitus) in the Republic site (
78  metabolic processes, as evident in Atlantic killifish (Fundulus heteroclitus) in Virginia's Elizabet
79                                     Atlantic killifish (Fundulus heteroclitus) inhabiting the Atlanti
80                                 The Atlantic killifish (Fundulus heteroclitus) is an environmental se
81 as many fish species, including the Atlantic killifish (Fundulus heteroclitus) possess two distinct A
82                         However, in Atlantic killifish (Fundulus heteroclitus), a population genetic
83  eurythermal intertidal minnow, the Atlantic killifish (Fundulus heteroclitus), a species that likely
84 o rerio), medaka (Oryzias latipes), Atlantic killifish (Fundulus heteroclitus), Atlantic cod, and thr
85  under varying temperature regimes using the killifish, Fundulus heteroclitus.
86                Through analysis of 384 whole killifish genome sequences and comparative transcriptomi
87 lease (CRISPR/Cas9) system and the turquoise killifish genome, this platform enables the generation o
88 nities were intermediate between the natural killifish-guppy community and the killifish-guppy-predat
89 ng the transition from a killifish only to a killifish-guppy community.
90 nd late (sympatric) evolutionary stages of a killifish-guppy community.
91 community where competition is most intense (killifish-guppy only).
92 he natural killifish-guppy community and the killifish-guppy-predator community, suggesting contempor
93 h as the use of the very short-lived African killifish (Harel et al.), are bridging the translational
94                        The African turquoise killifish has evolved diapause as a form of suspended de
95 ammalian studies, we found that adult female killifish have 25% greater dendritic spine densities in
96 , but only highly resistant diapause eggs of killifish have been found to survive passage through wat
97                                           In killifish, high nucleotide diversity has likely been a c
98 s to seasonal habitat desiccation in African killifishes, identifying the genetic variants associated
99 g a functional role for diversity changes in killifish immunosenescence.
100                                       Annual killifish inhabit ephemeral ponds, producing drought and
101                        The African turquoise killifish is a powerful vertebrate system to study compl
102                        The African turquoise killifish is an exciting new vertebrate model for aging
103                                         Aged killifish kidneys exhibited hallmark features of kidney
104                                 The mangrove killifish (Kryptolebias marmoratus) is the only vertebra
105                                 The mangrove killifish, Kryptolebias marmoratus, can reproduce with s
106                 From an ENU-mutated mangrove killifish line R228, we have isolated a novel mutant lin
107 pies, killifish and predators and ones where killifish live by themselves revealed that these results
108 n females) and impacts the transcriptomes of killifish livers in a sex-specific manner.
109        We found that, in wild-caught bluefin killifish Lucania goodei (Fundulidae) and wild-caught ze
110 SWS1, SWS2-A, and SWS2-B pigments of bluefin killifish (Lucania goodei) have the wavelengths of maxim
111 at bioenergetic changes in pollution-adapted killifish manifest later in life.
112 e, using the naturally short-lived turquoise killifish (N. furzeri), we describe a high-throughput pl
113                             We show that the killifish northern boundary shifts southwards, while dis
114  the basis of aging, the short-lived African killifish Nothobranchius furzeri has recently been estab
115            Here, using the African turquoise killifish (Nothobranchius furzeri), a naturally short-li
116                            African turquoise killifish (Nothobranchius furzeri), a naturally short-li
117                  Using the African turquoise killifish (Nothobranchius furzeri), we show that diapaus
118  genome engineering in the African turquoise killifish (Nothobranchius furzeri), which is the shortes
119 l of vertebrate aging, the African turquoise killifish (Nothobranchius furzeri).
120  the naturally short-lived African turquoise killifish (Nothobranchius furzeri).
121                                The turquoise killifish, Nothobranchius furzeri, is a promising verteb
122 nity changes following the transition from a killifish only to a killifish-guppy community.
123 ty to precisely control food delivery in the killifish opens new areas to assess lifespan and cogniti
124 dy early development in medaka (the Japanese killifish, Oryzias latipes) at 12 time points before, du
125                                     Atlantic killifish populations have rapidly adapted to normally l
126 nal") genetic architecture characteristic of killifish populations previously studied in Florida, whe
127 forces shaping lifespan among wild turquoise killifish populations.
128  the naturally short-lived African turquoise killifish, providing a unique resource for comparative a
129 cking of TCDD to sets of consensus models of killifish, rat, and human CYP1As showed species differen
130 n other vertebrate species-African turquoise killifish, rat, and humans-indicating common signatures
131               Given the limited migration of killifish, recent adaptive introgression was likely medi
132 uvenile rainbow trout (smolt), zebrafish, or killifish remained unchanged.
133                                   Whole-body killifish repertoires decline rapidly in within-individu
134  Trinidadian guppies Poecilia reticulata and killifish Rivulus hartii.
135  Trinidadian guppies Poecilia reticulata and killifish Rivulus hartii.
136 mmon large consumers-primarily insectivorous killifish (Rivulus hartii), omnivorous guppies (Poecilia
137 ompared life history traits in a Trinidadian killifish, Rivulus hartii, from fish communities that di
138                       Finally, zebrafish and killifish show species-specific strategies for lateral l
139 were translocated into sites containing only killifish showed that the experimental communities were
140  and field mesocosms, MeHg concentrations in killifish significantly increased at elevated temperatur
141 sitive and relaxed purifying selection in 45 killifish species and 231 wild individuals distributed t
142  composition of two closely-related mangrove killifish species with different mating systems (self-fe
143 ere designed to suppress the gene in another killifish species, Arabian killifish.
144 of polymorphic inserts in the genomes of the killifish species, Fundulus heteroclitus.
145  by the signalling pathway of the EDA in the killifish species.
146 , and lipidomics) in the embryos of multiple killifish species.
147 ause of the fast life cycle of the turquoise killifish, stable lines can be generated as rapidly as 2
148 fespan differences between various turquoise killifish strains.
149 y suppression, and contaminant resistance in killifish subpopulations from sites throughout the estua
150 results show that contaminants have affected killifish subpopulations throughout the estuary, even in
151 exhibited by laboratory-spawned embryos from killifish subpopulations throughout the estuary.
152 thesis in several subpopulations of Atlantic killifish that have evolved a gradation of resistance to
153             AHRR mRNA is widely expressed in killifish tissues and is inducible by TCDD or polychlori
154 boratory has shown that rapid acclimation of killifish to seawater is mediated by trafficking of CFTR
155      Here, we leverage the African turquoise killifish to systematically profile protein aggregates i
156              Thus, suggesting that while the killifish undergoes extremely rapid growth and maturity,
157          Using the self-fertilizing mangrove killifish, we characterized two mutants, shorttail (stl)
158                                We found that killifish, which are the weaker competitor, had a much l
159 ed the likelihood that sympatric guppies and killifish will coexist.
160  resistance among subpopulations of Atlantic killifish with differing contamination levels in order t

 
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