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Artykuły w czasopismach na temat "Codex Washingtonianus I (O.T.)"
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Prior, J. Bruce. "Who Is "Full of Grace and Truth" in the Ws Text of John 1:14?" Bulletin for Biblical Research 11, nr 2 (1.01.2001): 233–38. http://dx.doi.org/10.2307/26422272.
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Abstract Authorities disagree in their readings of "full" in the Codex Washingtonianus text of John 1:14. The Alands, Swanson, and I opt for πληρη, whereas Sanders and Goodspeed read πληρις. If the former reading is correct, then the referent for the accusative masculine-singular adjective πληρη is still the Word, or Jesus Christ. If πληρις is the correct reading, however, then the crucial question is whether πληρις is merely an itacism for πλήρης or whether it is the same word as the plural adjective πλήρεις. If πληρις is plural, then the substitute scribe of Ws as well as the scribe of Codex Seidelianus and others understood that it is we rather than the Word who are "full of grace and truth."
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Prior, J. Bruce. "Who Is "Full of Grace and Truth" in the Ws Text of John 1:14?" Bulletin for Biblical Research 11, nr 2 (1.01.2001): 233–38. http://dx.doi.org/10.2307/26422272.
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Abstract Authorities disagree in their readings of "full" in the Codex Washingtonianus text of John 1:14. The Alands, Swanson, and I opt for πληρη, whereas Sanders and Goodspeed read πληρις. If the former reading is correct, then the referent for the accusative masculine-singular adjective πληρη is still the Word, or Jesus Christ. If πληρις is the correct reading, however, then the crucial question is whether πληρις is merely an itacism for πλήρης or whether it is the same word as the plural adjective πλήρεις. If πληρις is plural, then the substitute scribe of Ws as well as the scribe of Codex Seidelianus and others understood that it is we rather than the Word who are "full of grace and truth."
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Hickey, John, Garry Nolan, Markus Covert, Eran Agmon, Nina Horowitz i John Sunwoo. "180 T cell phenotype drives restructuring of tumor microenvironment to balance T cell longevity and tumor control: insights from multiplexed imaging and multi-scale agent based modeling". Journal for ImmunoTherapy of Cancer 9, Suppl 2 (listopad 2021): A192. http://dx.doi.org/10.1136/jitc-2021-sitc2021.180.
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BackgroundImmune cell therapies continue to have success in treatment of cancers yet face challenges of complexity, cost, toxicity, and low solid-tumor efficacy. Much work has focused on the phenotype characterization and control of ex vivo expanded cells; however, little is known about its relationship to changes in the tumor microenvironment in vivo. Thus, we imaged tumors treated with different phenotype tumor-specific CD8+ T cells with CODEX multiplexed imaging1–4 that is able to visualize 42 antibodies at the same tissue in the tissue (figure 1A). To further probe this data in a systems immunology approach we created a multiscale agent-based model including critical circuits from the T cell-tumor microenvironment interactions (figure 1B).MethodsWe initialized our agent-based models various percentages of either PD1+, PD1-, PDL1+, or PDL1- phenotypes and ran simulations for 72 hours. We also treated PMEL CD8+ T cells with or without 2 hydroxycitrate as a metabolic inhibitor during activation to achieve different input phenotypes of CD8+ T cells for therapeutic adoptive transfer on day 10 following B16-F10 tumors had been established. We performed neighborhood analysis on CODEX multiplexed imaging data by clustering neighboring cell types using a sliding window for neighborhood analysis.ResultsInterestingly, the agent-based modeling indicated that the tumor phenotype switch to decrease proliferation was more effective than direct T cell killing. We observed spatially restricted inflammatory immune fronts when simulating with different initial percentages of PD1+ T cells and also from our CODEX multiplexed imaging. Quantitatively we observe that there is a drastic increase in the PDL1+, MHCI+, Ki67- tumor phenotype that increases with metabolically inhibited T cells. Neighborhood analysis indicated that metabolically treated T cells were able to create distinct immune cell environments that supported productive T cell-tumor interactions and also helped maintain T cell phenotype.ConclusionsThis indicates there is a balance for therapeutic T cell to mitigate chronic tumor exposure while controlling tumor growth through killing and by changing tumor phenotype. We observe T cells create distinct tumor microenvironments that differs significantly based on the starting T cell phenotype. Controlling T cell phenotype to promote productive immune-tumor structures will be critical to maintain T cell functionality and efficacy. In the future we will investigate T cell recruitment of immune structures by similar systems biology technologies.AcknowledgementsJ.W.H. is funded by an ACS Postdoctoral Fellowship (PF-20-032-01-CSM).ReferencesGoltsev Y, Samusik N, Kennedy-Darling J, Bhate S, Hale M, Vazquez G, Black S and Nolan GP, Deep profiling of mouse splenic architecture with CODEX multiplexed imaging. Cell, 174(4):968–981.Schürch CM, Bhate SS, Barlow GL, Phillips DJ, Noti L, Zlobec I, Chu P, Black S, Demeter J, McIlwain DR and Samusik N. Coordinated cellular neighborhoods orchestrate antitumoral immunity at the colorectal cancer invasive front. Cell 182(5):1341–1359.Black S, Phillips D, Hickey JW, Kennedy-Darling J, Venkataraaman VG, Samusik N, Goltsev Y, Schürch CM. and Nolan GP. CODEX multiplexed tissue imaging with DNA-conjugated antibodies. Nature Protocols 1–36.Kennedy-Darling J, Bhate SS, Hickey JW, Black S, Barlow GL, Vazquez G, Venkataraaman VG, Samusik N, Goltsev Y, Schürch CM and Nolan GP. Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction. European Journal of Immunology 51(5):1262–1277.Ethics ApprovalAll studies involving mice were approved under Stanford’s APLAC protocol 33502.
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Argın, Sanem, i Sibel Şimşek Yazıcı. "Türkiye’de Üretilen Mısırlarda Mikotoksin Düzeylerinin ve GDO Varlığının Araştırılması". Turkish Journal of Agriculture - Food Science and Technology 7, nr 1 (14.01.2019): 54. http://dx.doi.org/10.24925/turjaf.v7i1.54-60.2108.
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In Turkey, there is a continuous increase in the annual production of corn. Nevertheless, consumers’ perception of corn becomes more negative each day, since corn is the most genetically modified product worldwide, after soybean. While the potential negative effects of genetically modified corn are being debated, the greatest threat to human health in corn is the presence of mycotoxins. In this study, corn samples were collected from 634 fields in 552 villages of 24 cities in Turkey, and the presence of GMO, aflatoxin B1, total aflatoxins, fumonisin B1, fumonisin B2, T-2 toxin, HT-2 toxin, zearalenone and deoxynivalenol was investigated. No transgenic element was found in any of the corn samples. The total aflatoxin levels of the corn samples were found to be below the Turkish Food Codex limit and, among the total of 634 samples, only one sample exceeded the Turkish Food Codex limit for aflatoxin B1. Moreover, no T-2 toxin, HT-2 toxin, zearalenone and deoxynivalenol were detected in the samples. The total amounts of fumonisins were also found to be below the Turkish Food Codex limit. These results show that domestically produced corn meets the standards for food safety.
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Xu, Mina, Stephanie Halene, Rong Fan i Archibald Enninful. "Spatial Multiomics Profiling of Angioimmunoblastic T-Cell Lymphoma". Blood 142, Supplement 1 (28.11.2023): 6109. http://dx.doi.org/10.1182/blood-2023-190647.
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Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is a subtype of non-Hodgkin lymphoma (NHL) characterized primarily by a T follicular helper cell (TFH) phenotype. AITL presents with a highly complex tumor microenvironment with the tumor cells on a scaffold of highly arborized CD21+ follicular dendritic cells found in proximity to high endothelial venules (HEVs). The organized structure of the lymph node with distinct B cell and T cell zones is disrupted in the lymph node samples from patients with AITL. Lymphoid follicles in most AITL cases tend to be depleted, not hyperplastic as in other lymphomas. AITL tumor cells express CD10, BCL6, PD1, CXCL13, C-X-C motif chemokine receptor 5 (CXCR5), ICOS, and signaling lymphocytic activation molecule-associated protein (SAP) with diagnosis based on the expression of at least 2 of these markers. Our study uses novel spatial omics technology (Deterministic Barcoding in Tissue (DBiT-seq) and multiplexed immunofluorescence staining (CODEX)) to fully characterize the transcriptional and proteomic landscape of AITL. Methods: In this study, initial FFPE biopsy specimens from 22 patients with AITL were collected from archives. 10 µm thick tissue sections on poly-L-lysine coated slides were prepared for the performance of multiplexed immunofluorescence imaging (CODEX) for 12 immune-related markers: Podoplanin, CD20, CD4, CD8, CD68, CD45RO, CD3e, GranzymeB, PD1, Ki67, CD21 and CD34 using the PhenoCycler-Fusion system. We also validated anti-EBV Latent Membrane Protein 1 antibody. Cell segmentation was performed using a Stardist-based model in QuPath and downstream analysis done using the Seurat package. On an adjacent tissue section, we used Spatial CITE-seq to co-map the whole transcriptome and ~160 proteins. Results: From the multiplexed immunofluorescence staining, we observed CD21+ Follicular dendritic cells in close proximity to HEVs as expected from the spatial architecture of AITL. We also found 11 spatially distinct clusters differentially expressing the marker proteins. We observed a lower number of CD8+ cytotoxic T cells relative to CD4+ Helper T cells. We also identified cellular neighborhoods and their composition found a population of FDCs that directly interact with the tumor cells. From spatial CITE-seq, we average of ~670 genes were found in each spot. We also found the expression of CXCL13, TET2, DNMT3A and PDCP1 which are markers associated with AITL. There was a strong correlation between the transcript signals detected in Spatial CITE-seq and the protein expression from CODEX. Conclusions: Our study revealed the spatial organization of the tumor microenvironment of AITL. We envision that combining multiplexed immunofluorescence and Spatial CITE-seq will further our understanding of the AITL tumor environment and could lead to the discovery of novel clinical targets.
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Jung, Wulf-Ingo, Otto Lutz i Markus Pfeffer. "Localized NMR Spectroscopy with a 1.5 T Whole- Body Imager Using CODEX". Zeitschrift für Naturforschung A 46, nr 5 (1.05.1991): 401–4. http://dx.doi.org/10.1515/zna-1991-0504.
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AbstractWith a whole-body NMR imager working at 1.5 T localized 1H and 31P spectra were obtained using the CODEX sequence. Examples are presented: With ethanol 'H spectra the resolution, stability, and sensitivity are documented. Human in vivo investigations of the yellow bone marrow of (13 mm)3 volume elements show well resolved spectra with a good signal-to-noise ratio. An example for 31P spectroscopy is also given
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Jung, W. I., i O. Lutz. "Volume Selective NMR Spectroscopy by Coded Slice Excitation (CODEX)". Zeitschrift für Naturforschung A 43, nr 11 (1.11.1988): 909–13. http://dx.doi.org/10.1515/zna-1988-1101.
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Abstract A method for volume selective nuclear magnetic resonance spectroscopy has been developed and implemented on an 1.5 T whole body imager for in vivo investigations. Four single experiments produce different magnetizations in the same slice, and a special subtract scheme yields the signal of only the volume of interest, which is accurately defined. The resolution of the spectra and the stability of the method have been verified with a water phantom containing acetone, ethanol, methanol, and oil vessels.
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Baertsch, Marc-Andrea, Alexander Brobeil, John Hickey, Maximilian Haist, Alexandra Maria Poos, Guolan Lu, Wilson Kuswanto i in. "Spatial Dissection of the Bone Marrow Microenvironment in Multiple Myeloma By High Dimensional Multiplex Tissue Imaging". Blood 142, Supplement 1 (28.11.2023): 85. http://dx.doi.org/10.1182/blood-2023-189255.
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Introduction Multiple myeloma (MM) is shaped by interactions between immune, stromal and tumor cells in the bone marrow (BM) microenvironment (BMME). Our understanding of these processes is based on high parametric flow cytometry and single cell transcriptomics, which lack spatial resolution. Thus, crucial aspects of the in situ tumor ecosystem, including cell-cell interactions, can only be predicted. Novel high dimensional, multiplex tissue imaging methods are able to capture similar granularity while also preserving spatial organization. By optimizing antibody selection, as well as staining, imaging and data processing protocols we have established a BMME-targeted CODEX workflow based on a 60 marker panel. Here, we conducted the first comprehensive multiplex protein imaging survey of the BMME across the spectrum of MM and precursor stages and leveraged paired FISH and whole genome sequencing (WGS) to elucidate the interplay of tumor intrinsic features and the BMME. Methods We imaged 489 BM trephine biopsies in tissue microarray format on the CODEX (Akoya Biosciences) platform. After quality control (≥750 cells per core, <25% unclassifiable cells) we retained data from 12 non-malignant controls, 13 MGUS, 20 smoldering MM, 349 uniformly treated newly diagnosed MM (NDMM) patients from a phase III clinical trial, as well as 22 relapsed MM samples with a median of 3 (range 1-6) tissue cores per sample, comprising a total of 3.1 million single cells. CODEX data was processed and analyzed using custom scripts. Cellular neighborhoods were computed by clustering the cell type composition of sliding windows (n=10 nearest neighboring cells) across the tissue. WGS (n=212) and FISH (n=309) were performed on CD138-purified BM mononuclear cells and analyzed using in-house pipelines. Results We identified 40 cell types, encompassing the relevant lineages (myeloid, lymphoid, stromal, endothelial, tumor), subtypes (e.g. T, B, NK cells) and functional states (e.g GRZB, Ki67, and PD1) of the BMME. The degree of plasma cell infiltration determined by CODEX correlated with the clinical pathologist's quantification based on classical immunohistology (r=0.77, p<0.0001), and the kappa/lambda status of MM cells matched the reported light chain restriction, supporting the validity of our data. At the compositional level, we observed shifts in relative cell type abundance from precursor to MM stages. Major changes in the BMME included enriched stromal, endothelial and CD8+ T cells as well as depleted polymorphonuclear (PMN), erythropoietic and CD4+ T cells in advanced stages. The highest proportion of monocytoid dendritic cells, monocytes, mast cells and cytotoxic CD8+ T cells was seen in relapsed MM. Leveraging the spatial resolution of the CODEX data, we identified multiple distinct cellular neighborhoods (CNs) defined by recurrent local cell type composition. CNs enriched for plasma cells in combination with different immune cell subsets including exhausted T cells increased towards the MM stage, while CNs dominated by PMNs, erythropoietic cells and CD206 negative macrophages decreased. To investigate links between MM subtypes and BMME patterns, we correlated CODEX data with MM-initiating and driver events. While patients with t(4;14) showed a significant increase in eosinophils, patients with gain1q had higher levels of endothelial and stromal subsets colocalizing in the same CN. Distinct types of stromal cells were also enriched in patients with double hits (≥2 FISH high risk features). RAS mutations and biallelic inactivation of tumor suppressor genes were associated with altered T cell subset composition. Further corroborating the importance of BMME architecture, a CN with colocalization of plasma and exhausted CD8 T cells was associated with unfavorable prognosis in NDMM patients. Conclusions High dimensional, multiplex tissue imaging of the BMME enables interrogation of cellular interactions and tissue architecture in situ in clinical samples at single cell resolution. To our knowledge this is the first highly multiplexed spatial study of the human BMME in a large clinical cohort and the first such study in multiple myeloma. We track characteristic shifts in tissue composition associated with disease progression, reveal genotype-phenotype associations in the BMME as a correlate of tumor-microenvironment co-evolution and detect prognostically relevant tissue architectural features.
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Pinheiro, Paulo José Moraes. "Sobre o manuscrito Alfa da Poética de Aristóteles (Parisinus Gr. 1741)". O que nos faz pensar 27, nr 42 (30.06.2018): 47. http://dx.doi.org/10.32334/oqnfp.2018n42a594.
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Dos manuscritos da Poética de Aristóteles que chegaram aos nossos dias, na condição de fonte primária subsistente (codd.), temos apenas dois textos gregos (o que consta no codex Parisinus Graecus 1741 (=A), proveniente do séc. X/XI, e o que consta no codex Riccardianus 46 (=B), do séc. XII), a tradução latina de G. de Moerbeke (codices Etonensis 129 (=O), de 1300, e Toletanus bibl. Capit. 47.10 (= T), de 1280), e a tradução árabe de Abu-Bishr Matta, feita a partir da tradução siríaca desaparecida. O que pretendo, nesse artigo, é descrever o percurso do assim chamado Manuscrito Alfa da Poética de Aristóteles, ou seja, a que consta no codex Parisinus Graecus 1741 entre as páginas 184 e 199. Pretendo ainda fazer alusão à importância de um estudo sobre as condições em que se dá a apreensão do texto antigo. De fato, a leitura que fazemos hoje da Poética é composta da variação de sentido inerente ao entendimento, o que é óbvio, e da variação, muitas vezes sutil e, via de regra, determinante, do que foi efetivamente escrito, há tantos séculos, com o estilete de um ou outro escriba.
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Delgado-Gonzalez, Antonio, Kenyi Donoso, Maximilian Haist, Veronica D. Gonzalez, Ying-Wen Huang, Brooke E. Howitt, Garry P. Nolan, Katherine Fuh i Wendy J. Fantl. "Abstract B061: Multiparametric single-cell characterization of the immune tumor microenvironment in ovarian carcinomas". Cancer Research 84, nr 5_Supplement_2 (4.03.2024): B061. http://dx.doi.org/10.1158/1538-7445.ovarian23-b061.
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Abstract Tubo-ovarian high-grade serous carcinoma (HGSC) has an overall 5-year survival rate of ~50%. Standard-of-care treatment is surgical debulking followed by platinum-based chemotherapy. Initially, most women respond, but eventually, most (~80%) will relapse within 5 years. Nevertheless, for women with tumors for whom upfront debulking surgery is not possible, neoadjuvant chemotherapy (NACT) with interval debulking surgery followed by chemotherapy is an alternative. Cancer immunotherapy, an alternative treatment modality, drives an anti-tumor immune response. Immunotherapy approaches targeting a patient’s T cells have shown remarkable success for a variety of malignancies. Unfortunately, HGSC is largely unresponsive. In a previous study, we applied mass cytometry to newly diagnosed HGSC tumors to characterize intra-tumoral T and natural killer (NK) cells. We identified intra-tumoral decidual-like (dl)-NK cells that were positively correlated with tumor cell and transitioning epithelial-mesenchymal cell abundance. Decidual NK cells comprise 70% of lymphocytes during the first trimester of pregnancy and have a critical immune tolerant role in preventing a mother-to-be from rejecting her hemi-allogenic fetus. dl-NK cells, like their decidual counterparts, are distinguished from other NK cell phenotypes by the expression of the tetraspanin CD9. In vitro data demonstrated that CD9 endowed NK cells with immune-suppressive functions (attenuated cytotoxicity and reduced anti-tumor cytokine production). This study also revealed that in four out of ten patient-matched HGSC samples pre- and post-NACT, chemotherapy induced a more immune-suppressive immune tumor microenvironment (iTME). These data led to our hypothesis that the spatial architecture of the HGSC iTME, specifically encompassing cellular neighborhoods (CNs) comprising dl-NK and T cells, will predict response to platinum-based chemotherapy. Thus, we have applied CO-Detection by indEXing (CODEX), a highly-multiplex single-cell proteomic imaging technology, to comprehensively characterize the iTME of HGSC tumors. By measuring ~60 markers per tissue section at a resolution of <400 nm, CODEX generates proteomic co-expression information to deeply phenotype individual cells while preserving their spatial coordinates and relationships within the HGSC iTME. We have developed and validated a CODEX antibody panel targeting tumor, stroma and immune cells, NK cells receptors and ligands, and proteins specific for decidual NK cells, for formalin-fixed paraffin-embedded tissues. We developed and validated a panel comprised of 57 CODEX antibodies to image the iTME of 14 HGSC tumors, 7 matched before- and after-NACT. Our continuing data analyses will identify the spatial features of cellular neighborhoods enriched for dl-NK and T-cells to gain insight into their role in disease progression and treatment outcomes. In conclusion, we used CODEX, a highly multiplex single-cell imaging platform to deeply characterize the cellular architecture of the iTME in HGSC tumors before and after NACT. Citation Format: Antonio Delgado-Gonzalez, Kenyi Donoso, Maximilian Haist, Veronica D Gonzalez, Ying-Wen Huang, Brooke E. Howitt, Garry P. Nolan, Katherine Fuh, Wendy J. Fantl. Multiparametric single-cell characterization of the immune tumor microenvironment in ovarian carcinomas [abstract]. In: Proceedings of the AACR Special Conference on Ovarian Cancer; 2023 Oct 5-7; Boston, Massachusetts. Philadelphia (PA): AACR; Cancer Res 2024;84(5 Suppl_2):Abstract nr B061.
Rozprawy doktorskie na temat "Codex Washingtonianus I (O.T.)"
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Paulson, Gregory Scott. "Scribal habits in Codex Sinaiticus, Vaticanus, Ephraemi, Bezae, and Washingtonianus in the Gospel of Matthew". Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/8957.
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This study examines singular readings in the Gospel of Matthew across five of the earliest extant Greek copies of Matthew: Codex Sinaiticus, Vaticanus, Ephraemi, Bezae, and Washingtonianus. In each of the selected MSS, it is determined where a spelling, word, clause, phrase, sentence, or group of sentences is different from other MSS. These “singular readings” are collected in order to shine light on what such idiosyncrasies can tell us about the MS or tendencies of the scribe who copied the MS. One of the more interesting finds is that some of our MSS add text more than they omit it, which is contrary to other studies. Apart from itacistic changes, alternate spellings are not always the most frequent type of singular reading in our MSS. The MSS have similar types of singular readings, but they often go about creating them in different ways. Conclusions are that our MSS either prefer Attic Greek to Koine (Washingtonianus) or vice versa (Sinaiticus), but two MSS (Vaticanus and Bezae) fluctuate between both grammatical standards. Our MSS typically have a high percentage of error due to parablepsis, but one MS seems to skip letters within words more often than entire words (Ephraemi). Ephraemi does not transpose words, but when the other MSS create transpositions, they all record instances where the genitive pronoun is placed prior to the word it modifies and verbs are moved forward in sentences. In addition, transpositions in Sinaiticus could have resulted from corrected leaps. Context often plays a part in the creation of singular readings, but context affects each MS differently. Nearby text seems to prompt changes in all of our MSS, but remote text such as a gospel parallel, does not often influence our scribes: Ephraemi contains the only harmonization seems to be intentional. In Sinaiticus and Washingtonianus, several readings exhibit possible interpretations of the text (but typically these do not appear to be theological changes) and they both contain readings that conflate textual variants. All of the singular readings record either a textual addition, omission, or substitution, but the MSS do not end up with the same amount of text: both Codex Vaticanus and Ephraemi add more words than they omit, whereas Codex Sinaiticus, Bezae, and Washingtonianus end up with more omissions. This final element adds a counterweight to other studies that contend MSS omit text more than they add. The examination yields few singular readings of dramatic theological import. Rather, the singular readings expose grammatical currents of the 4th-5/6th centuries, currents that are more prevalent than scribal attempts to re-present the text of Matthew.
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Stefanidis, Emmanuelle. "Du texte à l’histoire : la question de la chronologie coranique". Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUL003.
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Parole sans contexte évident ni trame narrative, le texte fondateur de l’islam ne dévoile pas aisément ses origines. Cette thèse examine un code de lecture particulier qui a pour effet de contextualiser le texte sacré de l’islam dans ce qu’on imagine avoir été son contexte premier. La lecture chronologique consiste à déterminer l’inscription temporelle de chaque sourate ou énoncé coranique par rapport, d’une part, aux autres énoncés et, d’autre part, à la carrière prophétique de Muḥammad. En (ré-)introduisant une dimension temporelle et narrative, l’interprétation du Coran est facilitée. Ce dernier est ainsi en mesure de raconter, sinon son histoire, du moins une histoire. La chronologie coranique structure à la fois l’exégèse musulmane prémoderne et la recherche universitaire occidentale sur le Coran. Dans cette thèse, nous examinons ces deux domaines de production de savoir, non pas en opposition l’un avec l’autre mais comme deux moments de la réception du texte coranique. Cette approche inclusive permet, à travers l’étude d’une problématique spécifique, d’entamer une réflexion sur les convergences et les divergences entre l’érudition islamique et la recherche occidentale. Notre point de départ et fil conducteur est la liste chronologique des sourates, qui circule dans la Tradition musulmane avant d’être reprise et retravaillée par des universitaires occidentaux. La quête de la séquence originelle du Coran a engendré des débats autant parmi les exégètes que dans la recherche historico-critique. Nous retraçons ces débats et portons une attention particulière à la « textualité » du Coran, qui en fait un texte particulièrement difficile à ancrer dans un contexteDevoid of a clear context and a narrative frame, the founding text of Islam does not easily reveal its origins. This thesis examines a particular reading code that contextualises the Muslim scripture in what is imagined to have been its original context. A chronological reading aims at determining the temporal position of each sura or qur'ānic passage in relation to, on the one hand, the rest of the text and, on the other hand, the prophetic career of Muḥammad. By (re-)introducing a temporal and narrative frame, the interpretation of the Qur’ān is facilitated. The text is thus allowed to tell its own story or – in any case – a story. The issue of qur’ānic chronology structures both pre-modern Muslim exegesis and Western academic research on the Qur’ān. In this thesis, we examine these two fields of knowledge, not in opposition to one another but as representing two moments in the Qur’ān’s reception. This inclusive approach enables a reflection on the continuities and discontinuities between the Muslim scholarly tradition and Western research. The chronological list of suras, transmitted by Muslim tradition and examined by Western academics, provides the starting point and the connecting thread of the thesis. The search for the original sequence of the Qur’ān has generated debates, both in exegetical circles and in historical-critical research. We explore what is at stake in these debates and pay specific attention to the textuality of the Qur’ān, which, we argue, does not easily allow us to inscribe the Muslim Scripture in a clear context
Książki na temat "Codex Washingtonianus I (O.T.)"
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Olley, John W. Ezekiel: A commentary based on Iezekiēl in Codex Vaticanus. Leiden: Brill, 2009.
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1943-, Littman Robert J., red. Tobit: The Book of Tobit in Codex Sinaiticus. Leiden: Brill, 2008.
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Walser, Georg. Jeremiah: A commentary based on Ieremias in Codex Vaticanus. Leiden: Brill, 2012.
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D, De Conick April, red. Codex Judas papers: Proceedings of the International Congress on the Tchacos Codex held at Rice University, Houston, Texas, March 13-16, 2008. Leiden: Brill, 2009.
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International Congress on the Tchacos Codex (2008 Houston, Tex.). Codex Judas papers: Proceedings of the International Congress on the Tchacos Codex held at Rice University, Houston, Texas, March 13-16, 2008. Leiden: Brill, 2009.
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Rodolphe, Kasser, Meyer Marvin i Wurst Gregor, red. The Gospel of Judas: From Codex Tchacos. Washington, D.C: National Geographic, 2006.
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Bird, Michael F. 1 Esdras: Introduction and commentary on the Greek text in Codex Vaticanus. Leiden: Brill, 2012.
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Epp, Eldon Jay. The theological tendency of Codex Bezae Cantabrigiensis in Acts. Cambridge: Cambridge University Press, 2005.
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Charles, Horton, i Aland Barbara, red. The earliest gospels: The origins and transmission of the earliest Christian gospels - the contribution of the Chester Beatty Gospel Codex P[45 superscript]. London: T.& T.Clark, 2004.
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Ben-Asher, Aaron ben Moses, 10th cent i Dotan Aron 1928-, red. [Torah Neviʾim u-Khetuvim] =: Biblia Hebraica Leningradensia : prepared according to the vocalization, accents, and masora of Aaron ben Moses ben Asher in the Leningrad Codex. Peabody: Hendrickson Publishers, 2001.
Znajdź pełny tekst źródłaCzęści książek na temat "Codex Washingtonianus I (O.T.)"
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Tobias, Michael Charles. "May 8, 2011, 12:25 pm, inside DS&T, McLean, VA". W Codex Orféo, 5–8. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30622-3_2.
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"Acknowledgements". W Codex Washingtonianus, ix—x. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-001.
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"Frontmatter". W Codex Washingtonianus, i—vi. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-fm.
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"TABLE OF CONTENTS". W Codex Washingtonianus, vii—viii. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-toc.
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"Chapter Five. An Analysis of Segmentation and Punctuation". W Codex Washingtonianus, 119–30. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-008.
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"Chapter Four. Pre-genealogical Analysis: Text und Textwert". W Codex Washingtonianus, 113–18. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-007.
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"Chapter Two. Methodology of the Quantitative Analysis". W Codex Washingtonianus, 47–58. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-005.
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"Chapter One. Mining Codex W: Description, Observations, Transcriptions". W Codex Washingtonianus, 23–46. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-004.
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"Chapter Eight. An Analysis of Singular Readings and Corrections in W". W Codex Washingtonianus, 151–64. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-011.
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"Introduction". W Codex Washingtonianus, 1–22. Gorgias Press, 2022. http://dx.doi.org/10.31826/9781463244521-003.
Pełny tekst źródłaStreszczenia konferencji na temat "Codex Washingtonianus I (O.T.)"
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García-Pulido, Luis José. "Dos fortalezas fronterizas entre los reinos de Castilla y Granada en las Cantigas de Santa María de Alfonso X El Sabio (último tercio del siglo XIII)". W FORTMED2024 - Defensive Architecture of the Mediterranean. Valencia: Universitat Politàcnica de València, 2024. http://dx.doi.org/10.4995/fortmed2024.2024.18064.
Pełny tekst źródłaStreszczenie:
Cantigas de Santa Maria (‘Canticles of Holy Mary’) consists of 420 poems with musical notation written during the reign of Alfonso X of Castile (r. 1251-1284). Two of the codices preserved are richly illuminated with medieval narrative vignettes.Canticle number 185 depicts a ploy of war between the Castilian and Nasrid commanders of two mythical fortresses in the valley of the river Jandulilla, next to Sierra Mágina in south-eastern Spain, in the present-day province of Jaén. The location of the first of them, Chincoya, has generated a debate in the last decades given its early destruction and abandonment. At the second one, Bélmez, many structures have survived, since an imposing keep was built on top of its fortress when it first fell into Castilian hands in the first half of the 14th century.Over the centuries, this valley has been an important pass connecting the upper valley of the river Guadalquivir with the northern highlands of Granada. In the 13th century, this natural route was reinforced with fortifications that would later become key elements in the control of the border between the Christian kingdom of Castile and the Muslim state of Granada.This area formed part of the land that Ferdinand III of Castile had promised to deliver to Baeza in 1243 when it was conquered. The Treaty of Jaén in 1246 between the Christian king and the first ruler of the Nasrid dynasty, Muḥammad I, left some of these castles on Muslim territory, converting them into border posts in the face of the southern expansion of the Castilian kingdom after the Battle of Navas de Tolosa (1212).This paper analyses the configuration of the fortresses of Chincoya and Bélmez on the basis of the preserved remains, contrasting it with the iconography that illuminated the Códice Rico de las Cantigas de Alfonso X El Sabio (codex T, Library of El Escorial, MS T.I.1).