999 resultados para HD6250.U3 B8


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Invocatio: Q.B.V.

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Mennanderin gratulaatio painettu uudelleen: Das Inland (Dorpat) 1856 pg. 562-563

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Invocatio: Divina adfulgente gratia.

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Invocatio: Q.B.V.

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Numerot 12862-67 ilmestyneet kirjana: Philosophia moralis sive Ethica, ex optimis quibusq[ue] philosophis per praecepta commentaria & quaestiones succint [et] dilucid tradita [et] ventilata in Acad. Aboensi, authore & praeside m. Axelio Kempe Acad. bibliothecario. Addita est ad calcem appedicis loco hexilogia codem authore. Aboae, impressâ â Petro Hansonio Acad. typogr. Anno 1656

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Invocatio: I.N.S.S.I.T.

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Inv.: [kreikkaa] Sun Theo.

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Mutant cell lines B3 and B10, which are unresponsive to both interferon (IFN)-alpha and IFN-gamma, and line B9, which does not respond to IFN-gamma stimulation, are described. The mutants were submitted to fluorescence-activated cell sorting (FACS) from a cellular pool, which was obtained from the parental cell line 2C4 after several rounds of mutagenesis. The unresponsiveness to IFN stimulation was observed both in terms of expression of cell surface markers (CD2, class I and II HLAs) and mRNA expression of IFN-stimulated genes (2'-5' oligoadenylate synthetase (OAS), 9-27, and guanylate binding protein (GBP)). Genetic crossing of B3, B9 and B10 with U3 (STAT1-), gamma2a (JAK2-) and U4 (JAK1-) mutants, respectively, did not restore IFN responsiveness to the hybrid cell lines. However, when these cell lines were crossed with the same mutants, but using the pairwise crosses B3 x U4, B9 x U3 and B10 x U3, the cell hybrids recovered full IFN responsiveness. The present genetic experiments permitted us to assign the mutant cell lines B3, B9 and B10 to the U3, gamma2 and U4 complementation groups, respectively. These conclusions were supported by the analysis of IFN-stimulated genes in the mutants.

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This paper presents the first isolation of bovine respiratory syncytial virus in Brazil and its physicochemical, morphological and molecular characterization. The virus was isolated from 33 samples of nasotracheal secretions, successively inoculated into a Madin-Darby bovine kidney cell culture, which was characterized by physicochemical tests and morphological observation by electron microscopy. The Brazilian sample is an RNA pleomorphic, enveloped, thermolabile and non-hemagglutinating spicular virus. Reverse transcription, followed by nested polymerase chain reaction (nRT-PCR) assay was carried out using oligonucleotides B1, B2A, B3 and B4 for the fusion proteins (F) and B5A, B6A, B7A and B8 for the attachment protein (G). The nRT-PCR-F amplified a fragment of 481 bp corresponding to part of the gene that codes for protein F, whereas nRT-PCR-G amplified a fragment of 371 bp, in agreement with part of the G gene. The virus isolated from Brazilian samples in this study corresponded to the bovine respiratory syncytial virus, and RT-PCR proved to be useful for the diagnosis of bovine clinical samples.

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Variantti A.

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Dedikaatio: Johannes Gezelius nuor., Henricus Florinus, Thomas Florinus, Alexander Kepplerus, Ericus Florinus, Christophorus Florinus, Arvidus Florinus, Andreas Prytz, Johannes Wanaeus, Stephanus Swanstrupe.

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Variantti A.

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Invokaatio: Q.F.F.Q.S.

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Invokaatio: Q.F.F.Q.S.