Academic literature on the topic 'Proteine rvsp'

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Journal articles on the topic "Proteine rvsp"

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Kim, Young Soo, Wei Li, Ji Hye Kim, Hwan-Suck Chung, and Jang-Gi Choi. "Anti-Influenza Activity of an Ethyl Acetate Fraction of a Rhus verniciflua Ethanol Extract by Neuraminidase Inhibition." Oxidative Medicine and Cellular Longevity 2020 (October 29, 2020): 1–15. http://dx.doi.org/10.1155/2020/8824934.

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Antigenic mismatch can cause influenza vaccines to be ineffective, and influenza viruses resistant to antiviral drugs are rising. Thus, development of antiviral agents against these viruses is an immediate need. Rhus verniciflua (RVS) has long been used in herbal medicine and as a nutritional supplement. The effect of RVS and its components on influenza virus has not, however, been reported. We found that RVS treatment significantly reduced viral replication when evaluated with green fluorescent protein- (GFP-) tagged virus (influenza A virus, A/PR/8/34-GFP) in Madin–Darby canine kidney (MDCK)
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Tran, Pham-Tue-Hung, Naveed Asghar, Urban Höglund, et al. "Development of a Multivalent Kunjin Virus Reporter Virus-Like Particle System Inducing Seroconversion for Ebola and West Nile Virus Proteins in Mice." Microorganisms 8, no. 12 (2020): 1890. http://dx.doi.org/10.3390/microorganisms8121890.

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Kunjin virus (KUNV) is an attenuated strain of the severe neurotropic West Nile virus (WNV). The virus has a single-strand positive-sense RNA genome that encodes a polyprotein. Following gene expression, the polyprotein is cleaved into structural proteins for viral packaging and nonstructural proteins for viral replication and expression. Removal of the structural genes generate subgenomic replicons that maintain replication capacity. Co-expression of these replicons with the viral structural genes produces reporter virus-like particles (RVPs) which infect cells in a single round. In this stud
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Bohning, Kelly, Stephanie Sonnberg, Hui-Ling Chen, et al. "A high throughput reporter virus particle microneutralization assay for quantitation of Zika virus neutralizing antibodies in multiple species." PLOS ONE 16, no. 4 (2021): e0250516. http://dx.doi.org/10.1371/journal.pone.0250516.

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Zika virus is a Flavivirus, transmitted via Aedes mosquitos, that causes a range of symptoms including Zika congenital syndrome. Zika has posed a challenging situation for health, public and economic sectors of affected countries. To quantitate Zika virus neutralizing antibody titers in serum samples, we developed a high throughput plate based Zika virus reporter virus particle (RVP) assay that uses an infective, non-replicating particle encoding Zika virus surface proteins and capsid (CprME) and a reporter gene (Renilla luciferase). This is the first characterization of a Zika virus RVP assay
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Sun, Cheuk-Kwan, Yen-Yi Zhen, Hung-I. Lu, et al. "Reducing TRPC1 Expression through Liposome-Mediated siRNA Delivery Markedly Attenuates Hypoxia-Induced Pulmonary Arterial Hypertension in a Murine Model." Stem Cells International 2014 (2014): 1–19. http://dx.doi.org/10.1155/2014/316214.

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We tested the hypothesis that Lipofectamine siRNA delivery to deplete transient receptor potential cation channel (TRPC) 1 protein expression can suppress hypoxia-induced pulmonary arterial hypertension (PAH) in mice. Adult male C57BL/6 mice were equally divided into group 1 (normal controls), group 2 (hypoxia), and group 3 (hypoxia + siRNA TRPC1). By day 28, right ventricular systolic pressure (RVSP), number of muscularized arteries, right ventricle (RV), and lung weights were increased in group 2 than in group 1 and reduced in group 3 compared with group 2. Pulmonary crowded score showed sim
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Morawe, Tobias, Mona Honemann-Capito, Walter von Stein, and Andreas Wodarz. "Loss of the extraproteasomal ubiquitin receptor Rings lost impairs ring canal growth in Drosophila oogenesis." Journal of Cell Biology 193, no. 1 (2011): 71–80. http://dx.doi.org/10.1083/jcb.201009142.

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In Drosophila melanogaster oogenesis, there are 16 germline cells that form a cyst and stay connected to each other by ring canals. Ring canals allow the cytoplasmic transport of proteins, messenger ribonucleic acids, and yolk components from the nurse cells into the oocyte. In this paper, we describe the protein Rings lost (Rngo) and show that it is required for ring canal growth in germline cysts. rngo is an essential gene, and germline clones of a rngo-null allele show defects in ovary development, including mislocalization of ring canal proteins and fusion of germline cells. Rngo appears t
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Ju, Jeong-Sun, Rodrigo A. Fuentealba, Sara E. Miller, et al. "Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease." Journal of Cell Biology 187, no. 6 (2009): 875–88. http://dx.doi.org/10.1083/jcb.200908115.

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Mutations in valosin-containing protein (VCP) cause inclusion body myopathy (IBM), Paget's disease of the bone, and frontotemporal dementia (IBMPFD). Patient muscle has degenerating fibers, rimmed vacuoles (RVs), and sarcoplasmic inclusions containing ubiquitin and TDP-43 (TARDNA-binding protein 43). In this study, we find that IBMPFD muscle also accumulates autophagosome-associated proteins, Map1-LC3 (LC3), and p62/sequestosome, which localize to RVs. To test whether VCP participates in autophagy, we silenced VCP or expressed adenosine triphosphatase–inactive VCP. Under basal conditions, loss
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Hanna, Sheri L., Theodore C. Pierson, Melissa D. Sanchez, Asim A. Ahmed, Mariam M. Murtadha, and Robert W. Doms. "N-Linked Glycosylation of West Nile Virus Envelope Proteins Influences Particle Assembly and Infectivity." Journal of Virology 79, no. 21 (2005): 13262–74. http://dx.doi.org/10.1128/jvi.79.21.13262-13274.2005.

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ABSTRACT West Nile virus (WNV) encodes two envelope proteins, premembrane (prM) and envelope (E). While the prM protein of all WNV strains contains a single N-linked glycosylation site, not all strains contain an N-linked site in the E protein. The presence of N-linked glycosylation on flavivirus E proteins has been linked to virus production, pH sensitivity, and neuroinvasiveness. Therefore, we examined the impact of prM and E glycosylation on WNV assembly and infectivity. Similar to other flaviviruses, expression of WNV prM and E resulted in the release of subviral particles (SVPs). Removing
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Yip, Matthew C. J., Nicholas O. Bodnar, and Tom A. Rapoport. "Ddi1 is a ubiquitin-dependent protease." Proceedings of the National Academy of Sciences 117, no. 14 (2020): 7776–81. http://dx.doi.org/10.1073/pnas.1902298117.

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TheSaccharomyces cerevisiaeprotein Ddi1 and its homologs in higher eukaryotes have been proposed to serve as shuttling factors that deliver ubiquitinated substrates to the proteasome. Although Ddi1 contains both ubiquitin-interacting UBA and proteasome-interacting UBL domains, the UBL domain is atypical, as it binds ubiquitin. Furthermore, unlike other shuttling factors, Ddi1 and its homologs contain a conserved helical domain (helical domain of Ddi1, HDD) and a retroviral-like protease (RVP) domain. The RVP domain is probably responsible for cleavage of the precursor of the transcription fact
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Reuter, Jon D., Beatriz E. Vivas-Gonzalez, Daniel Gomez, et al. "Intranasal Vaccination with a Recombinant Vesicular Stomatitis Virus Expressing Cottontail Rabbit Papillomavirus L1 Protein Provides Complete Protection against Papillomavirus-Induced Disease." Journal of Virology 76, no. 17 (2002): 8900–8909. http://dx.doi.org/10.1128/jvi.76.17.8900-8909.2002.

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ABSTRACT Immunizations with live recombinant vesicular stomatitis viruses (rVSV) expressing foreign viral proteins have successfully protected animals from challenges with several heterologous viruses. We developed an rVSV expressing the major capsid protein (L1) of cottontail rabbit papillomavirus (CRPV) and tested the efficacy of protection following CRPV challenge. An rVSV expressing L1 of CRPV (VSV-L1) was characterized for the protective ability afforded by intranasal, intradermal, or intramuscular vaccination in rabbits subsequently challenged with CRPV. Protein expression of L1 in VSV-L
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DeMarco, Vincent G., Javad Habibi, Adam T. Whaley-Connell, et al. "Oxidative stress contributes to pulmonary hypertension in the transgenic (mRen2)27 rat." American Journal of Physiology-Heart and Circulatory Physiology 294, no. 6 (2008): H2659—H2668. http://dx.doi.org/10.1152/ajpheart.00953.2007.

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The transgenic (mRen2)27 (Ren2) rat overexpresses mouse renin in extrarenal tissues, causing increased local synthesis of ANG II, oxidative stress, and hypertension. However, little is known about the role of oxidative stress induced by the tissue renin-angiotensin system (RAS) as a contributing factor in pulmonary hypertension (PH). Using male Ren2 rats, we test the hypothesis that lung tissue RAS overexpression and resultant oxidative stress contribute to PH and pulmonary vascular remodeling. Mean arterial pressure (MAP), right ventricular systolic pressure (RVSP), and wall thickness of smal
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Dissertations / Theses on the topic "Proteine rvsp"

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Recordon-Navarro, Patricia. "Interactions entre les protéines Rvs161p, Rvs167p et leurs partenaires en relation avec le cytosquelette d'actine chez la levure Saccharomyces cerevisiae." Bordeaux 2, 1998. http://www.theses.fr/1998BOR28586.

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Rezende, Alexandre Gonçalves de. "Avaliação da expressão gênica em células de mamíferos utilizando o Semliki Forest vírus." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05122014-134720/.

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O sistema de expressão gênica derivado do Semliki Forest Vírus (SFV) vem sendo muito utilizado nos últimos tempos para expressão em grandes quantidades de inúmeras proteínas, quando comparado com outros sistemas. O objetivo desse estudo foi otimizar a capacidade desse vetor viral de expressar proteínas em diferentes linhagens celulares de mamíferos, utilizando como alvo, a glicoproteína do vírus rábico (RVGP). Foram avaliadas formas de obtenção do vetor SFV recombinante, através de diferentes métodos de transfecção, como eletroporação e lipofecção, utilizando um lipossomo comercial chamado Tra
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Shaan, Lakshmanappa Yashavanth. "Development and Evaluation of Efficacy of Novel Porcine Reproductive and Respiratory Syndrome (PRRS) Virus Vaccine Candidates in Pigs." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1532064253191032.

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Kumar, Sushant. "Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4." Thesis, 2016. http://hdl.handle.net/2005/3018.

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Structuraj investigations on the Ddi1 (DNA-damage inducible protein 1) of Leishmania major and on the rotavirus nonstructural protein NSP4 were carried out. Ddi1 belongs to the ubiquitin receptor family of proteins. One of its domains is similar to the retroviral aspartic proteinases. It has been shown that this domain is the target of HIV-protease inhibitors that were being used in the treatment of AIDS and it was observed that these drugs effectively controlled opportunistic diseases caused by many parasitic protozoa such as Leishmania and Plasmodium species. The retroviral protease-like dom
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