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1.
PLoS One ; 18(5): e0284556, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37163468

RESUMO

Based on the longitudinal data of 30 Major League Baseball (MLB) teams over seasons from 2017 to 2020, we used random effect (RE) models to conduct regression analyses on the detailed data of pitchers and fielders. Cultural distance (CD) was measured in terms of Hofstede's cultural indicators and Global Preference Survey (GPS) data. The results showed that salary premiums for foreign MLB players existed and CD was significantly positively correlated with salaries. Further, the risk preference (/altruism) difference between foreign pitchers and American pitchers was significantly positively (/negatively) correlated with the salaries of foreign pitchers. Salary estimation data showed that the salary premium was nearly 20% for players from South Korea and Panama, the lowest (only 0.11%) for players from Australia, and only 6.13% for players from Dominican Republic (accounting for the largest proportion of foreign MLB players), indicating that the MLB's foreign player recruitment policy is correct.


Assuntos
Beisebol , Altruísmo , Salários e Benefícios , Austrália , República Dominicana
2.
Fish Shellfish Immunol ; 124: 462-471, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-35483595

RESUMO

Exocyst complex component 3 Sec6 of mammals, one of the components of the exocyst complex, participates in numerous cellular functions, such as promoting cell migration and inhibiting apoptosis. In this study, the Sec6 was obtained from Epinephelus coioides, an economically important cultured fish. The full length of E. coioides Sec6 was 2655 bp including a 245 bp 5' UTR, a 154 bp 3' UTR, and a 2256 bp open reading frame (ORF) encoding 751 amino acids, with a molecular mass of 86.76 kDa and a theoretical pI of 5.57. Sec6 mRNA was detected in all the tissues examined, but the expression level is different in these tissues. Using fluorescence microscopy, Sec6 were distributed in both the nucleus and the cytoplasm. After SGIV infection, the expression of E. coioides Sec6 was significantly up-regulated in both trunk kidney and spleen response to Singapore grouper iridovirus (SGIV), an important pathogens of E. coioides. Sec6 could increase the SGIV-induced cytopathic effects (CPE), the expression of the SGIV genes VP19, LITAF, MCP, ICP18 and MCP, and the viral titers. Besides, E. coioides Sec6 significantly downregulated the promoter of NF-κB and AP-1, and inhibited the SGIV-induced apoptosis. The results demonstrated that E. coioides Sec6 might play important roles in SGIV infection.


Assuntos
Bass , Infecções por Vírus de DNA , Doenças dos Peixes , Iridovirus , Ranavirus , Animais , Bass/genética , Bass/metabolismo , Clonagem Molecular , Infecções por Vírus de DNA/veterinária , Proteínas de Peixes/genética , Proteínas de Peixes/metabolismo , Mamíferos/genética , Mamíferos/metabolismo , Filogenia
3.
Nurs Open ; 8(4): 1892-1908, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-33745219

RESUMO

AIM: The threats of novel coronavirus disease 2019 (COVID-19) have caused fears worldwide. The Fear of COVID-19 Scale (FCV-19S) was recently developed to assess the fear of COVID-19. Although many studies found that the FCV-19S is psychometrically sound, it is unclear whether the FCV-19S is invariant across countries. The present study aimed to examine the measurement invariance of the FCV-19S across eleven countries. DESIGN: Cross-sectional study. METHODS: Using data collected from prior research on Bangladesh (N = 8,550), United Kingdom (N = 344), Brazil (N = 1,843), Taiwan (N = 539), Italy (N = 249), New Zealand (N = 317), Iran (N = 717), Cuba (N = 772), Pakistan (N = 937), Japan (N = 1,079) and France (N = 316), comprising a total 15,663 participants, the present study used the multigroup confirmatory factor analysis (CFA) and Rasch differential item functioning (DIF) to examine the measurement invariance of the FCV-19S across country, gender and age (children aged below 18 years, young to middle-aged adults aged between 18 and 60 years, and older people aged above 60 years). RESULTS: The unidimensional structure of the FCV-19S was confirmed. Multigroup CFA showed that FCV-19S was partially invariant across country and fully invariant across gender and age. DIF findings were consistent with the findings from multigroup CFA. Many DIF items were displayed for country, few DIF items were displayed for age, and no DIF items were displayed for gender. CONCLUSION: Based on the results of the present study, the FCV-19S is a good psychometric instrument to assess fear of COVID-19 during the pandemic period. Moreover, the use of FCV-19S is supported in at least ten countries with satisfactory psychometric properties.


Assuntos
COVID-19 , Adolescente , Adulto , Idoso , Ansiedade , Bangladesh , Brasil , Criança , Estudos Transversais , Cuba , Medo , França , Humanos , Irã (Geográfico) , Itália , Japão/epidemiologia , Pessoa de Meia-Idade , Nova Zelândia , Paquistão , Reprodutibilidade dos Testes , SARS-CoV-2 , Taiwan , Reino Unido , Adulto Jovem
4.
Biol Res ; 48: 23, 2015 May 06.
Artigo em Inglês | MEDLINE | ID: mdl-25943891

RESUMO

BACKGROUND: Hepcidin, encoding by HAMP gene, is the pivotal regulator of iron metabolism, controlling the systemic absorption and transportation of irons from intracellular stores. Abnormal levels of HAMP expression alter plasma iron parameters and lead to iron metabolism disorders. Therefore, it is an important goal to understand the mechanisms controlling HAMP gene expression. RESULTS: Overexpression of Sox2 decrease basal expression of HAMP or induced by IL-6 or BMP-2, whereas, knockdown of Sox2 can increase HAMP expression, furthermore, two potential Sox2-binding sites were identified within the human HAMP promoter. Indeed, luciferase experiments demonstrated that deletion of any Sox2-binding site impaired the negative regulation of Sox2 on HAMP promoter transcriptional activity in basal conditions. ChIP experiments showed that Sox2 could directly bind to these sites. Finally, we verified the role of Sox2 to negatively regulate HAMP expression in human primary hepatocytes. CONCLUSION: We found that Sox2 as a novel factor to bind with HAMP promoter to negatively regulate HAMP expression, which may be further implicated as a therapeutic option for the amelioration of HAMP-overexpression-related diseases, including iron deficiency anemia.


Assuntos
Regulação Neoplásica da Expressão Gênica/genética , Hepatócitos/metabolismo , Hepcidinas/genética , Fatores de Transcrição SOXB1/genética , Anemia/genética , Anemia/metabolismo , Sítios de Ligação , Proteína Morfogenética Óssea 2/metabolismo , Técnicas de Silenciamento de Genes , Vetores Genéticos , Células Hep G2 , Hepcidinas/metabolismo , Humanos , Interleucina-6/metabolismo , Ferro/metabolismo , Luciferases , Plasmídeos/genética , Regiões Promotoras Genéticas/genética , Fatores de Transcrição SOXB1/metabolismo
5.
Biol. Res ; 48: 1-8, 2015. graf
Artigo em Inglês | LILACS | ID: biblio-950787

RESUMO

BACKGROUND: Hepcidin, encoding by HAMP gene, is the pivotal regulator of iron metabolism, controlling the systemic absorption and transportation of irons from intracellular stores. Abnormal levels of HAMP expression alter plasma iron parameters and lead to iron metabolism disorders. Therefore,itis animportant goal to understand the mechanisms controlling HAMP gene expression. RESULTS: Overexpression of Sox2 decrease basal expression of HAMP or induced by IL-6 or BMP-2, whereas, knockdown of Sox2 can increase HAMP expression, furthermore, two potential Sox2-binding sites were identified within the human HAMP promoter. Indeed, luciferase experiments demonstrated that deletion of any Sox2-binding site impaired the negative regulation of Sox2 on HAMP promoter transcriptional activity in basal conditions. ChIP experiments showed that Sox2 could directly bind to these sites. Finally, we verified the role of Sox2 to negatively regulate HAMP expression in human primary hepatocytes. CONCLUSION: We found that Sox2 as a novel factor to bind with HAMP promoter to negatively regulate HAMP expression, which may be further implicated as a therapeutic option for the amelioration of HAMP-overexpression-related diseases, including iron deficiency anemia.


Assuntos
Humanos , Regulação Neoplásica da Expressão Gênica/genética , Hepatócitos/metabolismo , Fatores de Transcrição SOXB1/genética , Hepcidinas/genética , Plasmídeos/genética , Sítios de Ligação , Interleucina-6/metabolismo , Regiões Promotoras Genéticas/genética , Proteína Morfogenética Óssea 2/metabolismo , Fatores de Transcrição SOXB1/metabolismo , Técnicas de Silenciamento de Genes , Células Hep G2 , Hepcidinas/metabolismo , Vetores Genéticos , Anemia/genética , Anemia/metabolismo , Ferro/metabolismo , Luciferases
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