scispace - formally typeset
M

Monica Thelestam

Researcher at Karolinska Institutet

Publications -  99
Citations -  4300

Monica Thelestam is an academic researcher from Karolinska Institutet. The author has contributed to research in topics: Toxin & Clostridium difficile toxin B. The author has an hindex of 38, co-authored 99 publications receiving 4173 citations. Previous affiliations of Monica Thelestam include Karolinska University Hospital.

Papers
More filters
Journal ArticleDOI

Large clostridial cytotoxins — a family of glycosyltransferases modifying small GTP-binding proteins

TL;DR: The group of large clostridial cytotoxins, which have homologous protein sequences, exert glycosyltransferase activity and modify GTP-binding proteins of the Ras-superfamily, are valuable tools for developmental and cell biologists.
Journal ArticleDOI

The Haemophilus ducreyi Cytolethal Distending Toxin Induces Cell Cycle Arrest and Apoptosis via the DNA Damage Checkpoint Pathways

TL;DR: It is demonstrated that the effect of the Haemophilus ducreyiCDT is cell type-specific: B cell lines underwent apoptosis, epithelial cells and keratinocytes arrested exclusively in G2, whereas normal fibroblasts arrested both in G1 and G2.
Journal ArticleDOI

Toxins A and B from Clostridium difficile differ with respect to enzymatic potencies, cellular substrate specificities, and surface binding to cultured cells.

TL;DR: The differing enzymatic activities of Clostridium difficile toxins turned out to be the main determinant of the difference in cytotoxic potency, whereas the different in binding contributes to a lesser degree.
Journal ArticleDOI

The Haemophilus ducreyi cytolethal distending toxin induces DNA double-strand breaks and promotes ATM-dependent activation of RhoA

TL;DR: It is shown that a member of the CDT family causes DNA double‐strand breaks in naturally intoxicated cells, acting as a true genotoxic agent, and the existence of a novel signalling pathway for intracellularly triggered activation of the RhoA GTPase via the ATM kinase in response to DNA damage is disclosed.