Early Jaina epistemology: a study of the philosophical chapters of the Tattvārthādhigama; With an English translation of the Tattvārthādhigamabhāṣya I, II.8 25, and V

This thesis provides an analysis and translation of the philosophical chapters of the Tattvārthādhigama (A Study of the Fundamental Categories). The first part of this study consists of three chapters. The first chapter forms an introduction to this thesis and discusses the research questions, methodology, and the position of the Tattvārthādhigama in the history of philosophy from a global perspective. The second chapter situates the Tattvārthādhigama and the first commentary on this text, the Tattvārthādhigamabhāṣya, in their historical context. This chapter deals with the role of both texts in the development of Jaina philosophy, the history of the Jainas in the Gupta Period, and the authorship of both texts. The third chapter forms the core of this thesis and offers a conceptual analysis of the content of Tattvārthādhigama I, II.8 – 25, and V. The second part of this study contains an English translation from the original Sanskrit text of the Tattvārthādhigama. This part also provides the first English translation of the commentary on these passages from the Tattvārthādhigamabhāṣya. This thesis demonstrates that the Tattvārthādhigama offers a coherent philosophical system that was strongly influenced by the Nyāya tradition.Asian Studie

Rationeel onkruidbeheer op verhardingen

Verslag van een workshop over duurzaam onkruidbeheer op verhardingen. Belangrijkste thema's waren afspoeling van herbiciden en kosten-effectief onkruidbehee

Trajectory Deflection of Spinning Magnetic Microparticles, the Magnus Effect at the Microscale

The deflection due to the Magnus force of magnetic particles with a diameter of 80 micrometer dropping through fluids and rotating in a magnetic field was measured. With Reynolds number for this experiment around 1, we found trajectory deflections of the order of 1 degree, in agreement within measurement error with theory. This method holds promise for the sorting and analysis of the distribution in magnetic moment and particle diameter of suspensions of microparticles, such as applied in catalysis, or objects loaded with magnetic particles.Comment: 12 pages, 3 figures. Appendix with 6 figure

Microstamped petri dishes for scanning electrochemical microscopy analysis of arrays of microtissues

While scanning electrochemical microscopy (SECM) is a powerful technique for non-invasive analysis of cells, SECM-based assays remain scarce and have been mainly limited so far to single cells, which is mostly due to the absence of suitable platform for experimentation on 3D cellular aggregates or microtissues. Here, we report stamping of a Petri dish with a microwell array for large-scale production of microtissues followed by their in situ analysis using SECM. The platform is realized by hot embossing arrays of microwells (200 mum depth; 400 mum diameter) in commercially available Petri dishes, using a PDMS stamp. Microtissues form spontaneously in the microwells, which is demonstrated here using various cell lines (e.g., HeLa, C2C12, HepG2 and MCF-7). Next, the respiratory activity of live HeLa microtissues is assessed by monitoring the oxygen reduction current in constant height mode and at various distances above the platform surface. Typically, at a 40 mum distance from the microtissue, a 30% decrease in the oxygen reduction current is measured, while above 250 mum, no influence of the presence of the microtissues is detected. After exposure to a model drug (50% ethanol), no such changes in oxygen concentration are found at any height in solution, which reflects that microtissues are not viable anymore. This is furthermore confirmed using conventional live/dead fluorescent stains. This live/dead assay demonstrates the capability of the proposed approach combining SECM and microtissue arrays formed in a stamped Petri dish for conducting cellular assays in a non-invasive way on 3D cellular models

Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb

Background and purposeIntrachromosomal amplification of chromosome 21 (iAMP21) is a rare subtype of B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). It is unknown how iAMP21 contributes to leukaemia. The currently known commonly amplified region is 5.1 Mb.MethodsWe aimed to narrow down the common region of amplification by using high resolution techniques. Array comparative genomic hybridization (aCGH) was used to determine copy number aberrations, Affymetrix U133 Plus2 expression arrays were used to determine gene expression. Genome-wide expression correlations were evaluated using Globaltest.ResultsWe narrowed down the common region of amplification by combining copy number data from 12 iAMP21 cases with 52 cases from literature. The combined common region of amplification was 1.57 Mb, located from 36.07 to 37.64 Mb (GRCh38). This region is located telomeric from, but not including, RUNX1, which is the locus commonly used to diagnose iAMP21. This narrow region, which falls inside the Down Syndrome critical region, includes 13 genes of which the expression of eight genes was significantly upregulated compared with 143 non-iAMP21 B-other cases. Among these, transcriptional repressor RIPPLY3 (also known as DSCR6) was the highest overexpressed gene (fold change = 4.2, FDR DiscussionThe more precise definition of the common region of amplification could be beneficial in the diagnosis of iAMP21 based on copy number analysis from DNA sequencing or arrays as well as stimulate functional research into the role of the included genes in iAMP21 biology.</p