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Markus Landthaler

Researcher at Max Delbrück Center for Molecular Medicine

Publications -  150
Citations -  31239

Markus Landthaler is an academic researcher from Max Delbrück Center for Molecular Medicine. The author has contributed to research in topics: RNA & Gene. The author has an hindex of 49, co-authored 127 publications receiving 25891 citations. Previous affiliations of Markus Landthaler include Howard Hughes Medical Institute & University at Albany, SUNY.

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Circular RNAs are a large class of animal RNAs with regulatory potency

TL;DR: It is found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7.
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A mammalian microRNA expression atlas based on small RNA library sequencing.

TL;DR: A relatively small set of miRNAs, many of which are ubiquitously expressed, account for most of the differences in miRNA profiles between cell lineages and tissues.
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Transcriptome-wide Identification of RNA-Binding Protein and MicroRNA Target Sites by PAR-CLIP

TL;DR: This study developed a cell-based crosslinking approach to determine at high resolution and transcriptome-wide the binding sites of cellular RBPs and miRNPs and revealed that these factors bind thousands of sites containing defined sequence motifs and have distinct preferences for exonic versus intronic or coding versus untranslated transcript regions.
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Human Argonaute2 Mediates RNA Cleavage Targeted by miRNAs and siRNAs

TL;DR: In this paper, it was shown that miRNAs are incorporated indiscriminately of their sequence into Ago1 through Ago4 containing microRNPs (miRNPs) and endonuclease activity is exclusively associated with Ago2.
Journal Article

Human argonaute2 mediates RNA cleavage targeted by miRNAs and siRNAs

TL;DR: The authors' results suggest that miRNAs are incorporated indiscriminately of their sequence into Ago1 through Ago4 containing microRNPs (miRNPs), and the specific role of Ago2 in guiding target RNA cleavage was confirmed by siRNA-based depletion of individual Ago members in combination with a sensitive positive-readout reporter assay.