984 resultados para super-resolution microscopy
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Catalogus codicum manuscriptorum Bibliothecae regiae. Pars tertia. Tomus tertius (-quartus), Parisiis : ex typographia regia, 1744 : "1.° Anonymi grammatica, in qua de verborum conjugatione. — 2.° Bedae, Presbyteri, de arte metrica liber ad Gutbertum. — 3.° Ejusdem de schematibus et tropis liber ad eundem. — 4.° Claudii Marii Victoris Massiliensis, de Genesi libri tres : carmine heroïco ; porro hi libri iidem prorsus cum illis qui commentariorum in Genesim in editis titulum prae se ferunt : praemittitur Victoris precatio ad Deum, oratione soluta. — 5.° Sancti Paulini carmina ad Ausonium. — 6.° Ausonii, qui in hoc codice sanctus appellatur, carmina ad Paulinum. — 7.° Anonymi carmen in laudem sancti Joannis Baptistae. — 8.° Anonymi carmen cujus is est titulus : laudes Domini cum miraculo quod accidit in Aedrico. — 9.° Anonymi carmen in laudem Christi Domini ; incipit : Jam mihi polliceor. — 10.° Bebiani carmen de uxore sua morti proxima, è variis versuum generibus contextum ; incipit : ô vir beatus cui remissa iniquitas. — 11.° Drepanii Flori Diaconi Lugdunensis, carmen de cereo paschali. — 12.° Hymnus in solemnitate S. Michaëlis, Archangeli. — 13.° Drepanii Flori, Diaconi Lugdunensis, epistola ad Modoinum, Episcopum Augustodunensem. — 14.° Servii Honorati de ultimarum syllabarum natura liber ad Aquilinum. — 15.° Anonymi grammatica. — 16.° Epigrammata quorumdam psalmorum, sive potiùs, psalmi XXII. XXVI. XXVII. versibus haeroïcis expositi ; authore Drepanio Floro. — 17.° Canticum trium puerorum, versibus heroïcis : eodem authore. — 18.° Anonymi cohortatio ad Wlfinum, Aurelianensem Grammaticum. — 19.° Sedulii carmen elegiacum de incarnatione Christi. Saeculo nono videtur exaratus."
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Colbertinus
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Colbertinus
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En tête, formule de confession écrite en 1389.
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Donné le 14 juillet 1848 par M. Guyot; cf. B.n.F., département des Manuscrits, registre des dons 1848-1895, n° 4661
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Intracellular mature vaccinia virus, also called intracellular naked virus, and its core envelope have been observed in their native, unfixed, unstained, hydrated states by cryoelectron microscopy of vitrified samples. The virion appears as a smooth rounded rectangle of ca. 350 by 270 nm. The core seems homogeneous and is surrounded by a 30-nm-thick surface domain delimited by membranes. We show that surface tubules and most likely also the characteristic dumbbell-shaped core with the lateral bodies which are generally observed in negatively stained or conventionally embedded samples are preparation artifacts.
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The atomic force microscope is a convenient tool to probe living samples at the nanometric scale. Among its numerous capabilities, the instrument can be operated as a nano-indenter to gather information about the mechanical properties of the sample. In this operating mode, the deformation of the cantilever is displayed as a function of the indentation depth of the tip into the sample. Fitting this curve with different theoretical models permits us to estimate the Young's modulus of the sample at the indentation spot. We describe what to our knowledge is a new technique to process these curves to distinguish structures of different stiffness buried into the bulk of the sample. The working principle of this new imaging technique has been verified by finite element models and successfully applied to living cells.
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The Caulobacter DNA methyltransferase CcrM is one of five master cell-cycle regulators. CcrM is transiently present near the end of DNA replication when it rapidly methylates the adenine in hemimethylated GANTC sequences. The timing of transcription of two master regulator genes and two cell division genes is controlled by the methylation state of GANTC sites in their promoters. To explore the global extent of this regulatory mechanism, we determined the methylation state of the entire chromosome at every base pair at five time points in the cell cycle using single-molecule, real-time sequencing. The methylation state of 4,515 GANTC sites, preferentially positioned in intergenic regions, changed progressively from full to hemimethylation as the replication forks advanced. However, 27 GANTC sites remained unmethylated throughout the cell cycle, suggesting that these protected sites could participate in epigenetic regulatory functions. An analysis of the time of activation of every cell-cycle regulatory transcription start site, coupled to both the position of a GANTC site in their promoter regions and the time in the cell cycle when the GANTC site transitions from full to hemimethylation, allowed the identification of 59 genes as candidates for epigenetic regulation. In addition, we identified two previously unidentified N(6)-methyladenine motifs and showed that they maintained a constant methylation state throughout the cell cycle. The cognate methyltransferase was identified for one of these motifs as well as for one of two 5-methylcytosine motifs.
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Collection : Italian books before 1601 ; 440.1