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Artykuły w czasopismach na temat "Orthoparamyxovirinae"
Roy, Ada, Emeric Chan Mine, Lorenzo Gaifas, Cédric Leyrat, Valentina A. Volchkova, Florence Baudin, Luis Martinez-Gil i in. "Orthoparamyxovirinae C Proteins Have a Common Origin and a Common Structural Organization". Biomolecules 13, nr 3 (1.03.2023): 455. http://dx.doi.org/10.3390/biom13030455.
Pełny tekst źródłaDe Francesco, Maria Antonia. "Measles Resurgence in Europe: An Open Breakthrough in the Field of Vaccine-Preventable Diseases". Pathogens 12, nr 10 (25.09.2023): 1192. http://dx.doi.org/10.3390/pathogens12101192.
Pełny tekst źródłaWeber, Matheus Nunes, i Mariana Soares da Silva. "Corona- and Paramyxoviruses in Bats from Brazil: A Matter of Concern?" Animals 14, nr 1 (26.12.2023): 88. http://dx.doi.org/10.3390/ani14010088.
Pełny tekst źródłaMuzeniek, Therese, Thejanee Perera, Sahan Siriwardana, Fatimanur Bayram, Dilara Bas, Mizgin Öruc, Beate Becker-Ziaja i in. "Paramyxovirus Diversity within One Population of Miniopterus fuliginosus Bats in Sri Lanka". Pathogens 11, nr 4 (2.04.2022): 434. http://dx.doi.org/10.3390/pathogens11040434.
Pełny tekst źródłaMartins, Nathana B., Julio C. Neves de Almeida, Marianne S. S. Gonçalves, Lana I. Gila, Débora R. Yogui, Mario H. Alves, Arnaud L. J. Desbiez, Paulo E. Brandão i Aline S. da Hora. "Occurrence of Typical Domestic Animal Viruses in Wild Carnivorans: An Emerging Threat to the Conservation of Endangered Species". Transboundary and Emerging Diseases 2024 (7.02.2024): 1–13. http://dx.doi.org/10.1155/2024/3931047.
Pełny tekst źródłaVanmechelen, Bert, Sien Meurs, Marie Horemans, Arne Loosen, Tibe Joly Maes, Lies Laenen, Valentijn Vergote i in. "The Characterization of Multiple Novel Paramyxoviruses Highlights the Diverse Nature of the Subfamily Orthoparamyxovirinae". Virus Evolution, 30.06.2022. http://dx.doi.org/10.1093/ve/veac061.
Pełny tekst źródłaAshida, Shoichi, Shohei Kojima, Takashi Okura, Fumihiro Kato, Wakako Furuyama, Shuzo Urata i Yusuke Matsumoto. "Phylogenetic analysis of the promoter element 2 of paramyxo- and filoviruses". Microbiology Spectrum, 12.04.2024. http://dx.doi.org/10.1128/spectrum.00417-24.
Pełny tekst źródłaWells, Heather L., Elizabeth Loh, Alessandra Nava, Mónica Romero Solorio, Mei Ho Lee, Jimmy Lee, Jum R. A. Sukor i in. "Classification of new morbillivirus and jeilongvirus sequences from bats sampled in Brazil and Malaysia". Archives of Virology, 4.07.2022. http://dx.doi.org/10.1007/s00705-022-05500-z.
Pełny tekst źródłaRozprawy doktorskie na temat "Orthoparamyxovirinae"
Chan, Mine Emeric. "La protéine C du virus Nipah : mécanismes d'expression et implications virales". Electronic Thesis or Diss., Lyon, École normale supérieure, 2024. http://www.theses.fr/2024ENSL0002.
Pełny tekst źródłaThe Nipah virus (NiV) is a non-segmented negative-sense RNA virus belonging to the Paramyxoviridae family. The NiV genome contains only 6 genes but codes for 9 different proteins. Several proteins are expressed from the P gene, including the phosphoprotein P and the C protein. The C protein, expressed from an alternative open reading frame through a ribosomal leaky scanning mechanism, plays a yet poorly understood role in viral replication. To study its function, numerous studies have been conducted on a recombinant NiV deficient in C expression (rNiV CKO), where the initiator codons of C have been removed, without altering other reading frames of the proteins derived from the P gene. We hypothesized that the absence of the C translation initiation site does not prevent the ribosomal leaky scanning mechanism but that these mutations lead to a disorganization of the expression of proteins derived from the P gene. We confirmed this hypothesis by demonstrating that rNiV CKO expresses truncated forms of the C and P proteins, named respectively C’ and P’. Furthermore, our comparative evaluation of rNiV CKO and wild-type NiV (WT) revealed that rNiV CKO produces less infectious viral particles, which directed our research towards the impact of C, C', and P' proteins on viral replication. We developed a NiV minigenome system and studied the effect of these proteins on the viral polymerase activity in this system. C and C' showed negative regulation of polymerase activity, with a more pronounced regulation by C'. Additionally, we observed differences in cellular localization between C and C', with the latter localizing in inclusion bodies in the presence of viral proteins involved in RNA synthesis. Regarding the P' protein, although it lost its primary function of binding to monomeric nucleoproteins, no dominant negative effect was observed on NiV polymerase activity. Moreover, a mixture of P’ and P lacking their C-terminal Px domain can effectively substitute for wild-type P in the minigenome system, providing new insights into the NiV replication mechanism. In conclusion, our results collectively suggest that the organization of P gene expression is complex, likely due to two interdependent requirements: the synthesis of C depends on weak initiation of P translation, and the translation initiation of C protein is necessary to prevent potentially aberrant expression of truncated forms of C and P