scispace - formally typeset
S

Sandrine Chabas

Researcher at University of Bordeaux

Publications -  15
Citations -  1498

Sandrine Chabas is an academic researcher from University of Bordeaux. The author has contributed to research in topics: Transcription (biology) & RNA. The author has an hindex of 10, co-authored 15 publications receiving 1396 citations. Previous affiliations of Sandrine Chabas include French Institute of Health and Medical Research.

Papers
More filters
Journal ArticleDOI

The primary transcriptome of the major human pathogen Helicobacter pylori

TL;DR: A novel differential approach selective for the 5′ end of primary transcripts is presented, establishing a paradigm for mapping and annotating the primary transcriptomes of many living species and discovering hundreds of transcriptional start sites within operons, and opposite to annotated genes.
Journal ArticleDOI

Antisense oligonucleotides targeted to the domain IIId of the hepatitis C virus IRES compete with 40S ribosomal subunit binding and prevent in vitro translation

TL;DR: The antisense efficiency of the oligonucleotides was nicely correlated to their affinity for the IIId subdomain and to their ability to displace 40S ribosomal subunit, making this process a likely explanation for in vitro inhibition of HCV-IRES-dependent translation.
Journal ArticleDOI

Helicobacter pylori interferes with an embryonic stem cell micro RNA cluster to block cell cycle progression

TL;DR: It is reported that Helicobacter pylori, a human stomach-colonizing bacterium responsible for severe gastric inflammatory diseases and gastric cancers, downregulates an embryonic stem cell microRNA cluster in proliferating gastric epithelial cells to achieve cell cycle arrest.
Journal ArticleDOI

Helicobacter pylori Initiates a Mesenchymal Transition through ZEB1 in Gastric Epithelial Cells

TL;DR: In gastric epithelial cells, cagPAI+ H. pylori activates NF-κB, which transactivates ZEB1, subsequently promoting mesenchymal transition, and the unexpected N-FκB-dependent increase of miR-200 levels likely thwarts the irreversible loss of epithelial identity in that critical situation.
Journal ArticleDOI

A promoter activity is present in the DNA sequence corresponding to the hepatitis C virus 5′ UTR

TL;DR: This work presents results suggesting the existence of a strong promoter activity carried by the DNA sequence corresponding to the HCV 5' UTR, and shows the unambiguous activity of such a promoter sequence in stably transfected cells.