3 research outputs found
Le savant et son époque à travers sa correspondance Seeger A. Bonebakker (1923-2005) et quelques notes sur Ḫalīl b. Aybak al-Ṣafadī (696-764/1297-1363)
This article proposes a survey of two great scholars’ in Arabic literature correspondences:
a European of the 20th century, Seeger Adrianus Bonebakker, who is of
special interest for us because he bequeathed all of his great library, personal notes and
correspondence to Università Ca’ Foscari, and a subject of study of the former, Ḫalīl b.
Aybak al-Ṣafadī, great littérateur and scholar of the first century of the Mamluk period.
Letters sent and received are preserved in both cases and are primary sources on their
network, but also on their personal life, personality and methodology
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The Emergence of ʿIlm al-Bayān: Classical Arabic Literary Theory in the Arabic East in the 7th/13th Century
This dissertation identifies a turning point in the development of literary theory as a discipline in the classical Arabic-Islamic world, starting in the Arabic East in the thirteenth century under the emerging framework of ʿilm al-bayān ‘the science of good style’. Treating a range of poetic, rhetorical, and literary-critical matters that had been studied under various disciplinary headings since the ninth century, the discipline was now consciously recognized as having an underlying theory and an established canon. I trace this development beginning with Ḍiyāʾ al-Dīn Ibn al-Athīr (d. 1239) and follow its progression throughout Greater Syria and Egypt as late as the end of the fourteenth century, after the standard theory of rhetoric (ʿilm al-balāgha) emerged within the madrasa institution. I then analyze in depth one test case for literary-theoretical thinking in this time and place, namely, majāz ‘figurative language’. Although linguistic theories about majāz, inspired by Islamic legal theory, had become a hallmark of literary studies, I argue that literary scholars implicitly espoused a non-linguistic conception of the notion, akin to kadhib ‘lie’ (a term not used due to its negative theological connotations). My analysis demonstrates that despite tensions between being a science concerned with hermeneutics and one concerned with poetics, ʿilm al-bayān was essentially the latter.Near Eastern Languages and Civilization
ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells
Mixed-phenotype acute leukemia is a rare subtype of leukemia in which both myeloid and lymphoid markers are co-expressed on the same malignant cells. The pathogenesis is largely unknown, and the treatment is challenging. We previously reported the specific association of the recurrent t(8;12)(q13;p13) chromosomal translocation that creates the ETV6-NCOA2 fusion with T/myeloid leukemias. Here we report that ETV6-NCOA2 initiates T/myeloid leukemia in preclinical models; ectopic expression of ETV6-NCOA2 in mouse bone marrow hematopoietic progenitors induced T/myeloid lymphoma accompanied by spontaneous Notch1-activating mutations. Similarly, cotransduction of human cord blood CD34(+) progenitors with ETV6-NCOA2 and a nontransforming NOTCH1 mutant induced T/myeloid leukemia in immunodeficient mice; the immunophenotype and gene expression pattern were similar to those of patient-derived ETV6-NCOA2 leukemias. Mechanistically, we show that ETV6-NCOA2 forms a transcriptional complex with ETV6 and the histone acetyltransferase p300, leading to derepression of ETV6 target genes. The expression of ETV6-NCOA2 in human and mouse nonthymic hematopoietic progenitor cells induces transcriptional dysregulation, which activates a lymphoid program while failing to repress the expression of myeloid genes such as CSF1 and MEF2C. The ETV6-NCOA2 induced arrest at an early immature T-cell developmental stage. The additional acquisition of activating NOTCH1 mutations transforms the early immature ETV6-NCOA2 cells into T/myeloid leukemias. Here, we describe the first preclinical model to depict the initiation of T/myeloid leukemia by a specific somatic genetic aberration