Johan Reimegård

TL;DR: A molecular approach is presented that reveals the comprehensive transcriptional landscape of cell types populating the embryonic heart at three developmental stages and that maps cell-type-specific gene expression to specific anatomical domains.

TL;DR: It is proposed that MicA, when present at high levels, blocks ribosome binding at the ompA translation start site, which-in line with previous work-secondarily facilitates RNase E cleavage and subsequent mRNA decay.

TL;DR: It is shown here that csgD expression is, in part, controlled post‐transcriptionally by two redundant small RNAs, OmrA and OmrB, which results in curli deficiency, in accordance with the inhibition of chromosomally encoded, FLAG‐tagged CsgD.

TL;DR: In this paper, the authors propose a strategy for generating and analysing high-throughput spatial expressions for complex biological systems, which requires functional characterization of specialized tissue domains, such as tissue domains.

TL;DR: Investigation of RNA silencing processes, characterized by non-coding small RNA molecules (sRNA) of 19–40 nt, identified sRNAs matching numerous RxLR and Crinkler effector protein genes in two isolates differing in pathogenicity, and identified six microRNA (miRNA) candidates that have features characteristic of both plant and metazoan miRNAs.