Publications by authors named "T Lukas"

It is widely accepted that mobile ions are responsible for the slow electronic responses observed in metal halide perovskite-based optoelectronic devices, and strongly influence long-term operational stability. Electrical characterisation methods mostly observe complex indirect effects of ions on bulk/interface recombination, struggle to quantify the ion density and mobility, and are typically not able to fully quantify the influence of the ions upon the bulk and interfacial electric fields. We analyse the bias-assisted charge extraction (BACE) method for the case of a screened bulk electric field, and introduce a new characterisation method based on BACE, termed ion drift BACE.

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Background: The number of software products in the field of health and medicine increases excessively. Self-tracking, fitness, dose calculation, and analysis of physiological data - apps are popular and commonly used. For young entrepreneurs, it is difficult to recognize and understand the distinction between software as medical product and health software products.

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Conjugative transfer of bacterial plasmids to recipient cells is often mediated by type IV secretion machinery. Experimental investigations into the minimal gene sets required for efficient conjugative transfer suggest that such gene sets are variable, depending on plasmids. We have been analyzing the conjugative transfer of -derived and IncP-9 plasmids, NAH7 and pWW0, whose conjugation systems belong to the MPF type.

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In the present study, the correlation between surface chemical groups and the electrostatic properties of particulate materials was studied. Glass beads were modified to produce OH-, NH-, CN-, and F-functionalized materials. The materials were charged separately both by friction and by conventional corona charging, and the results were compared.

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Article Synopsis
  • The study aimed to find the genetic cause of adult-onset primary lateral sclerosis (PLS) in a family with five affected individuals.
  • Whole-exome sequencing revealed two specific mutations (L695P and I743T) in the SPG7 gene that are linked to the disease, showing an autosomal recessive inheritance pattern.
  • The findings suggest that these mutations impact mitochondrial function, highlighting the need for genetic testing for SPG7 in familial cases of PLS.
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