Base de dados : MEDLINE
Pesquisa : B01.050.150.900.493.875 [Categoria DeCS]
Referências encontradas : 549 [refinar]
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  1 / 549 MEDLINE  
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[PMID]:29186711
[Au] Autor:Viana PF; Ezaz T; Marajó L; Ferreira M; Zuanon J; Cioffi MB; Bertollo LAC; Gross MC; Feldberg E
[Ad] Endereço:Instituto Nacional de Pesquisas da Amazônia, Coordenação de Biodiversidade, Universidade Federal do Amazonas, Manaus, Brazil.
[Ti] Título:Genomic Organization of Repetitive DNAs and Differentiation of an XX/XY Sex Chromosome System in the Amazonian Puffer Fish, Colomesus asellus (Tetraodontiformes).
[So] Source:Cytogenet Genome Res;153(2):96-104, 2017.
[Is] ISSN:1424-859X
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:The genus Colomesus is the sole representative of the family Tetraodontidae in the Amazon region. Here, Colomesus asellus was analyzed using conventional and molecular cytogenetic protocols. Its diploid chromosome number is 2n = 46 with 12 meta-, 10 submeta-, 16 subtelo-, and 8 acrocentric chromosomes and a fundamental number of FN = 84. An XX/XY sex chromosome system was identified. Mapping of 18S rDNA correlated with the nucleolus organizer regions (Ag-NORs) in the short arms of the 2 X chromosomes in females and in the Y chromosome in males. C-banding revealed heterochromatin in the centromeric regions of all chromosomes, except for pair 3. Prominent sex chromosome-specific heterochromatin amplification was observed, covering the short arms of the Y chromosome almost entirely. FISH with telomeric and tropomyosin (tpm1) sequences, respectively, revealed terminal signals in all chromosomes. The analysis of extended DNA fibers confirmed the colocalization and the interspersed pattern of the telomeric and tpm1 sequences. Thus, this study highlights the remarkable evolutionary dynamism presented by the Amazonian puffer fish regarding the differentiation of a heteromorphic XY sex chromosome system and a particular sex-specific amplification of rDNA sites. This is the first record of such an association in the Tetraodontidae family.
[Mh] Termos MeSH primário: Cromossomos Sexuais/genética
Processos de Determinação Sexual
Tetraodontiformes/genética
[Mh] Termos MeSH secundário: Animais
Antígenos Nucleares/genética
Brasil
Bandeamento Cromossômico
DNA Ribossômico/genética
Feminino
Amplificação de Genes
Hibridização in Situ Fluorescente
Masculino
RNA Ribossômico 18S/genética
Sequências Repetitivas de Ácido Nucleico
Telômero/genética
Telômero/ultraestrutura
Tropomiosina/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antigens, Nuclear); 0 (DNA, Ribosomal); 0 (RNA, Ribosomal, 18S); 0 (Tropomyosin); 0 (nucleolar organizer region associated proteins)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171130
[St] Status:MEDLINE
[do] DOI:10.1159/000484423


  2 / 549 MEDLINE  
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[PMID]:28587910
[Au] Autor:Rambla-Alegre M; Reverté L; Del Río V; de la Iglesia P; Palacios O; Flores C; Caixach J; Campbell K; Elliott CT; Izquierdo-Muñoz A; Campàs M; Diogène J
[Ad] Endereço:IRTA, Ctra, Poble Nou, km 5.5, 43540 Sant Carles de la Ràpita, Tarragona, Spain. Electronic address: maria.rambla@irta.es.
[Ti] Título:Evaluation of tetrodotoxins in puffer fish caught along the Mediterranean coast of Spain. Toxin profile of Lagocephalus sceleratus.
[So] Source:Environ Res;158:1-6, 2017 10.
[Is] ISSN:1096-0953
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Although consumption of Tetraodontidae species is prohibited in the EU, intoxications are still reported. The evaluation of tetrodotoxins (TTXs) by mass spectrometry (LC-MS/MS and LC-HRMS) and a screening immunoassay (mELISA) in tetraodontid fishes caught along the Western Mediterranean Sea revealed high concentrations of TTXs in Lagocephalus sceleratus while no TTXs were identified in L. lagocephalus and Sphoeroides pachygaster individuals. The high TTXs content found in the L. sceleratus analysed herein demonstrate the occurrence of highly toxic puffer fish in the Western Mediterranean Sea. Being L. sceleratus a recent invasive species in the Mediterranean, surveillance, risk assessment and risk management measures are necessary. The strategy used within this research work could be a valuable tool for future food safety monitoring.
[Mh] Termos MeSH primário: Tetraodontiformes/metabolismo
Tetrodotoxina/análise
[Mh] Termos MeSH secundário: Animais
Cromatografia Líquida
Ensaio de Imunoadsorção Enzimática
Feminino
Espécies Introduzidas
Masculino
Espectrometria de Massas
Mar Mediterrâneo
Espanha
Especificidade da Espécie
Espectrometria de Massas em Tandem
Distribuição Tecidual
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
4368-28-9 (Tetrodotoxin)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:171120
[Lr] Data última revisão:
171120
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170608
[St] Status:MEDLINE


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[PMID]:28500070
[Au] Autor:Lu XJ; Chen Q; Rong YJ; Chen F; Chen J
[Ad] Endereço:Laboratory of Biochemistry and Molecular Biology, Ningbo University, Ningbo 315211, People's Republic of China.
[Ti] Título:CXCR3.1 and CXCR3.2 Differentially Contribute to Macrophage Polarization in Teleost Fish.
[So] Source:J Immunol;198(12):4692-4706, 2017 Jun 15.
[Is] ISSN:1550-6606
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The study of multiple copies of chemokine receptor genes in various teleosts has long appealed to investigators seeking to understand the evolution of the immune system. The CXCR CXCR3 gene has two isoforms, CXCR3.1 and CXCR3.2, which are both expressed in macrophages. The distinct roles of teleost CXCR3s have not been identified previously. In this article, we found that CXCR3.1 and CXCR3.2 differentially contributed to macrophage polarization in the teleosts: ayu ( ), grass carp ( ), and spotted green pufferfish ( ). In ayu macrophages, the CXCR3.1 (PaCXCR3.1) gene was constitutively expressed, whereas the CXCR3.2 (PaCXCR3.2) gene was induced postinfection with Upon infection, PaCXCR3.1 and PaCXCR3.2 macrophages showed an M1 and an M2 phenotype, respectively. CXCL9-11-like proteins mediated M1 and M2 polarization by interacting with the PaCXCR3.1 and PaCXCR3.2 proteins on macrophages, respectively. The transcription factors STAT1 and STAT3 were activated in PaCXCR3.1 and PaCXCR3.2 macrophages, respectively. Furthermore, the prognosis of septic ayu adoptively transferred with PaCXCR3.2 macrophages was improved. Our data reveal a previously unknown mechanism for macrophage polarization, suggesting that redundant genes may regulate crucial functions in the teleost immune system.
[Mh] Termos MeSH primário: Carpas/imunologia
Proteínas de Peixes/genética
Macrófagos/fisiologia
Osmeriformes/imunologia
Receptores CXCR3/genética
Tetraodontiformes/imunologia
[Mh] Termos MeSH secundário: Animais
Carpas/genética
Carpas/metabolismo
Diferenciação Celular
Clonagem Molecular
Proteínas de Peixes/metabolismo
Peixes/classificação
Peixes/imunologia
Regulação da Expressão Gênica
Macrófagos/imunologia
Monócitos/imunologia
Osmeriformes/genética
Osmeriformes/metabolismo
Fagocitose
Filogenia
Isoformas de Proteínas/genética
Isoformas de Proteínas/metabolismo
Receptores CXCR3/metabolismo
Fator de Transcrição STAT1/genética
Fator de Transcrição STAT1/metabolismo
Fator de Transcrição STAT3/genética
Fator de Transcrição STAT3/metabolismo
Tetraodontiformes/genética
Tetraodontiformes/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Fish Proteins); 0 (Protein Isoforms); 0 (Receptors, CXCR3); 0 (STAT1 Transcription Factor); 0 (STAT3 Transcription Factor)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170927
[Lr] Data última revisão:
170927
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170514
[St] Status:MEDLINE
[do] DOI:10.4049/jimmunol.1700101


  4 / 549 MEDLINE  
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[PMID]:28484135
[Au] Autor:Miyazaki H; Onoda A; Terada H; Nakajima M
[Ad] Endereço:Nagoya City Public Health Research Institute.
[Ti] Título:Species Identification of Pufferfish Products Using RAPD Analysis.
[So] Source:Shokuhin Eiseigaku Zasshi;58(2):75-79, 2017.
[Is] ISSN:1882-1006
[Cp] País de publicação:Japan
[La] Idioma:jpn
[Ab] Resumo:A simple and rapid method was developed to identify the source species of pufferfish products. Randomly amplified polymorphic DNA (RAPD) analysis was applied to identify 8 species of pufferfish. Commercial kits were used for DNA extraction and amplification. Simultaneous identification was possible by polyacrylamide gel electrophoresis of PCR products. Two primers were chosen based on the result of pre-examination with 40 primers, and the PCR conditions were optimized. Characteristic RAPD patterns were obtained for each pufferfish species. The developed method was applied to identify the source species of 26 pufferfish products. The results suggest that the developed method would be useful for verification of the labeled species of pufferfish products.
[Mh] Termos MeSH primário: Produtos Pesqueiros/análise
Análise de Alimentos/métodos
Técnica de Amplificação ao Acaso de DNA Polimórfico/métodos
Tetraodontiformes/classificação
Tetraodontiformes/genética
[Mh] Termos MeSH secundário: Animais
Primers do DNA
Eletroforese em Gel de Poliacrilamida
Rotulagem de Alimentos
Especificidade da Espécie
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (DNA Primers)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:171016
[Lr] Data última revisão:
171016
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170510
[St] Status:MEDLINE
[do] DOI:10.3358/shokueishi.58.75


  5 / 549 MEDLINE  
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[PMID]:28389698
[Au] Autor:Venkatachalam AB; Parmar MB; Wright JM
[Ad] Endereço:Department of Biology, Dalhousie University, 1355 Oxford Street, PO BOX 15000, Halifax, NS, B3H 4R2, Canada.
[Ti] Título:Evolution of the duplicated intracellular lipid-binding protein genes of teleost fishes.
[So] Source:Mol Genet Genomics;292(4):699-727, 2017 Aug.
[Is] ISSN:1617-4623
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Increasing organismal complexity during the evolution of life has been attributed to the duplication of genes and entire genomes. More recently, theoretical models have been proposed that postulate the fate of duplicated genes, among them the duplication-degeneration-complementation (DDC) model. In the DDC model, the common fate of a duplicated gene is lost from the genome owing to nonfunctionalization. Duplicated genes are retained in the genome either by subfunctionalization, where the functions of the ancestral gene are sub-divided between the sister duplicate genes, or by neofunctionalization, where one of the duplicate genes acquires a new function. Both processes occur either by loss or gain of regulatory elements in the promoters of duplicated genes. Here, we review the genomic organization, evolution, and transcriptional regulation of the multigene family of intracellular lipid-binding protein (iLBP) genes from teleost fishes. Teleost fishes possess many copies of iLBP genes owing to a whole genome duplication (WGD) early in the teleost fish radiation. Moreover, the retention of duplicated iLBP genes is substantially higher than the retention of all other genes duplicated in the teleost genome. The fatty acid-binding protein genes, a subfamily of the iLBP multigene family in zebrafish, are differentially regulated by peroxisome proliferator-activated receptor (PPAR) isoforms, which may account for the retention of iLBP genes in the zebrafish genome by the process of subfunctionalization of cis-acting regulatory elements in iLBP gene promoters.
[Mh] Termos MeSH primário: Proteínas de Ligação a Ácido Graxo/genética
Oryzias/genética
PPAR alfa/genética
PPAR gama/genética
Proteínas de Ligação ao Retinol/genética
Smegmamorpha/genética
Tetraodontiformes/genética
Peixe-Zebra/genética
[Mh] Termos MeSH secundário: Animais
Evolução Biológica
Clofibrato/farmacologia
Evolução Molecular
Duplicação Gênica/genética
Regulação da Expressão Gênica/genética
Genes Duplicados/genética
Família Multigênica/genética
PPAR alfa/agonistas
PPAR gama/agonistas
Regiões Promotoras Genéticas/genética
Ativação Transcricional/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Fatty Acid-Binding Proteins); 0 (PPAR alpha); 0 (PPAR gamma); 0 (Retinol-Binding Proteins); HPN91K7FU3 (Clofibrate)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170803
[Lr] Data última revisão:
170803
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170409
[St] Status:MEDLINE
[do] DOI:10.1007/s00438-017-1313-5


  6 / 549 MEDLINE  
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[PMID]:28262632
[Au] Autor:Work TM; Moeller PD; Beauchesne KR; Dagenais J; Breeden R; Rameyer R; Walsh WJ; Abecassis M; Kobayashi DR; Conway C; Winton J
[Ad] Endereço:US Geological Survey, National Wildlife Health Center-Honolulu Field Station, Honolulu, HI 96850, USA.
[Ti] Título:Pufferfish mortality associated with novel polar marine toxins in Hawaii.
[So] Source:Dis Aquat Organ;123(2):87-99, 2017 Mar 06.
[Is] ISSN:0177-5103
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Fish die-offs are important signals in tropical marine ecosystems. In 2010, a mass mortality of pufferfish in Hawaii (USA) was dominated by Arothron hispidus showing aberrant neurological behaviors. Using pathology, toxinology, and field surveys, we implicated a series of novel, polar, marine toxins as a likely cause of this mass mortality. Our findings are striking in that (1) a marine toxin was associated with a kill of a fish species that is itself toxic; (2) we provide a plausible mechanism to explain clinical signs of affected fish; and (3) this epizootic likely depleted puffer populations. Whilst our data are compelling, we did not synthesize the toxin de novo, and we were unable to categorically prove that the polar toxins caused mortality or that they were metabolites of an undefined parent compound. However, our approach does provide a template for marine fish kill investigations associated with marine toxins and inherent limitations of existing methods. Our study also highlights the need for more rapid and cost-effective tools to identify new marine toxins, particularly small, highly polar molecules.
[Mh] Termos MeSH primário: Doenças dos Peixes/induzido quimicamente
Toxinas Marinhas/toxicidade
Tetraodontiformes
[Mh] Termos MeSH secundário: Animais
Doenças dos Peixes/epidemiologia
Doenças dos Peixes/mortalidade
Doenças dos Peixes/patologia
Hawaii/epidemiologia
Toxinas Marinhas/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Marine Toxins)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170629
[Lr] Data última revisão:
170629
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170307
[St] Status:MEDLINE
[do] DOI:10.3354/dao03096


  7 / 549 MEDLINE  
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[PMID]:28245608
[Au] Autor:Yamada R; Tsunashima T; Takei M; Sato T; Wajima Y; Kawase M; Oshikiri S; Kajitani Y; Kosoba K; Ueda H; Abe K; Itoi S; Sugita H
[Ad] Endereço:Department of Marine Science and Resources, Nihon University, Fujisawa, Kanagawa 252-0880, Japan. rikopin.0202@gmail.com.
[Ti] Título:Seasonal Changes in the Tetrodotoxin Content of the Flatworm Planocera multitentaculata.
[So] Source:Mar Drugs;15(3), 2017 Feb 25.
[Is] ISSN:1660-3397
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:Tetrodotoxin (TTX) is a potent neurotoxin that acts specifically on voltage-gated sodium channels on excitable membranes of muscle and nerve tissues. The biosynthetic process for TTX is unclear, although marine bacteria are generally thought to be the primary producers. The marine flatworm is a known TTX-bearing organism, and is suspected to be a TTX supplier to pufferfish. In this study, flatworm specimens were collected from an intertidal zone in Hayama, Kanagawa, Japan, the TTX content of the flatworm was measured using liquid chromatography with tandem mass spectrometry (LC-MS/MS), and seasonal changes in TTX content were investigated. No significant difference in TTX concentration of the flatworm body was found between the spawning period and other periods. However, the TTX content in individual flatworms was significantly higher in the spawning period than at other times. The TTX content rose in association with an increase in the body weight of the flatworm.
[Mh] Termos MeSH primário: Platelmintos/metabolismo
Tetrodotoxina/metabolismo
[Mh] Termos MeSH secundário: Animais
Cromatografia Líquida/métodos
Japão
Estações do Ano
Espectrometria de Massas em Tandem/métodos
Tetraodontiformes/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
4368-28-9 (Tetrodotoxin)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170622
[Lr] Data última revisão:
170622
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170302
[St] Status:MEDLINE


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[PMID]:28219939
[Au] Autor:Sun CC; Dong WR; Shao T; Li JY; Zhao J; Nie L; Xiang LX; Zhu G; Shao JZ
[Ad] Endereço:College of Life Sciences, Zhejiang University, and Key Laboratory for Cell and Gene Engineering of Zhejiang Province, Hangzhou 310058, China.
[Ti] Título:Peroxiredoxin 1 (Prx1) is a dual-function enzyme by possessing Cys-independent catalase-like activity.
[So] Source:Biochem J;474(8):1373-1394, 2017 Apr 04.
[Is] ISSN:1470-8728
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Peroxiredoxin (Prx) was previously known as a Cys-dependent thioredoxin. However, we unexpectedly observed that Prx1 from the green spotted puffer fish (TnPrx1) was able to reduce H O in a manner independent of Cys peroxidation and reductants. This study aimed to validate a novel function for Prx1, delineate the biochemical features and explore its antioxidant role in cells. We have confirmed that Prx1 from the puffer fish and humans truly possesses a catalase (CAT)-like activity that is independent of Cys residues and reductants, but dependent on iron. We have identified that the GVL motif was essential to the CAT-like activity of Prx1, but not to the Cys-dependent thioredoxin peroxidase (POX) activity, and generated mutants lacking POX and/or CAT-like activities for individual functional validation. We discovered that the TnPrx1 POX and CAT-like activities possessed different kinetic features in the reduction of H O The overexpression of wild-type TnPrx1 and mutants differentially regulated the intracellular levels of reactive oxygen species (ROS) and the phosphorylation of p38 in HEK-293T cells treated with H O Prx1 is a dual-function enzyme by acting as POX and CAT with varied affinities towards ROS. This study extends our knowledge on Prx1 and provides new opportunities to further study the biological roles of this family of antioxidants.
[Mh] Termos MeSH primário: Proteínas de Peixes/metabolismo
Modelos Moleculares
Peroxirredoxinas/metabolismo
Tetraodontiformes
[Mh] Termos MeSH secundário: Substituição de Aminoácidos
Animais
Sítios de Ligação
Biocatálise
Cisteína/química
Proteínas de Peixes/antagonistas & inibidores
Proteínas de Peixes/química
Proteínas de Peixes/genética
Células HEK293
Seres Humanos
Peróxido de Hidrogênio/metabolismo
Mutagênese Sítio-Dirigida
Mutação
Peroxirredoxinas/antagonistas & inibidores
Peroxirredoxinas/química
Peroxirredoxinas/genética
Fosforilação
Conformação Proteica
Processamento de Proteína Pós-Traducional
Interferência de RNA
Espécies Reativas de Oxigênio/metabolismo
Proteínas Recombinantes de Fusão/química
Proteínas Recombinantes de Fusão/metabolismo
Proteínas Recombinantes/química
Proteínas Recombinantes/metabolismo
Especificidade por Substrato
Proteínas Quinases p38 Ativadas por Mitógeno/metabolismo
[Pt] Tipo de publicação:COMPARATIVE STUDY; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Fish Proteins); 0 (Reactive Oxygen Species); 0 (Recombinant Fusion Proteins); 0 (Recombinant Proteins); BBX060AN9V (Hydrogen Peroxide); EC 1.11.1.15 (PRDX1 protein, human); EC 1.11.1.15 (Peroxiredoxins); EC 2.7.11.24 (p38 Mitogen-Activated Protein Kinases); K848JZ4886 (Cysteine)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170607
[Lr] Data última revisão:
170607
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170222
[St] Status:MEDLINE
[do] DOI:10.1042/BCJ20160851


  9 / 549 MEDLINE  
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[PMID]:28105658
[Au] Autor:Ahuir-Baraja AE; Yamanoue Y; Kubicek L
[Ad] Endereço:Oceanogràfic Foundation of the Valencian Community, Eduardo Primo Yúfera (Científic), 1B, Valencia, Spain.
[Ti] Título:First confirmed record of Mola sp. A in the western Mediterranean Sea: morphological, molecular and parasitological findings.
[So] Source:J Fish Biol;90(3):1133-1141, 2017 Mar.
[Is] ISSN:1095-8649
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Recent molecular and morphological studies suggest the existence of at least three species of Mola (Mola spp. A, B and C). Currently, only Mola mola and Mola ramsayi are formally accepted and species A, B or C have not been assigned to these thus far. In this study, a large ocean sunfish in the western Mediterranean Sea was analysed molecularly and morphologically, identified as Mola sp. A and a detailed account of the specimen's parasite load is reported.
[Mh] Termos MeSH primário: Doenças dos Peixes/parasitologia
Tetraodontiformes/fisiologia
[Mh] Termos MeSH secundário: Animais
Doenças dos Peixes/epidemiologia
Mar Mediterrâneo
Tetraodontiformes/classificação
Tetraodontiformes/parasitologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170627
[Lr] Data última revisão:
170627
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170121
[St] Status:MEDLINE
[do] DOI:10.1111/jfb.13247


  10 / 549 MEDLINE  
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[PMID]:27943286
[Au] Autor:Palsson J; Astthorsson OS
[Ad] Endereço:Marine Research Institute, Skulagata 4, Reykjavik, Iceland, P. O. Box 1390, 121, Reykjavik, Iceland.
[Ti] Título:New and historical records of the ocean sunfish Mola mola in Icelandic waters.
[So] Source:J Fish Biol;90(3):1126-1132, 2017 Mar.
[Is] ISSN:1095-8649
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The ocean sunfish Mola mola is considered to be globally distributed in both temperate and tropical waters, but there are many gaps in the knowledge of this species' distribution. A total of 31 records of M. mola from Icelandic waters, dating from 1845 to 2014, are presented and georeferenced. An increase in the number of records at the beginning of this century and particularly in 2012, is suggested to be a consequence of both an increase in ocean temperature on the Icelandic shelf and changes in large scale temperature variations in the North Atlantic Ocean.
[Mh] Termos MeSH primário: Distribuição Animal
Tetraodontiformes/fisiologia
[Mh] Termos MeSH secundário: Animais
Oceano Atlântico
Islândia
Fatores de Tempo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170627
[Lr] Data última revisão:
170627
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161213
[St] Status:MEDLINE
[do] DOI:10.1111/jfb.13237



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BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde