List of works - Carole Crozet

Anti-PrP antibodies block PrPSc replication in prion-infected cell cultures by accelerating PrPC degradation.

scientific article published on April 2004

Cationic phosphorus-containing dendrimers reduce prion replication both in cell culture and in mice infected with scrapie

scientific article published in June 2004

Cell-based therapy against prion diseases

scientific article published on 23 November 2018

Cellular pathogenesis in prion diseases.

scientific article published on 17 April 2008

Comparative proteomic analysis of human mesenchymal and embryonic stem cells: towards the definition of a mesenchymal stem cell proteomic signature.

scientific article

Effective gene therapy in a mouse model of prion diseases

scientific article (publication date: 2008)

Gene and cell therapy for prion diseases.

scientific article published on February 2009

Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene

scientific article published on 03 January 2019

Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene

scientific article published on 15 April 2019

High Dub3 expression in mouse ESCs couples the G1/S checkpoint to pluripotency.

scientific article published in November 2013

Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations.

scientific article published on 19 October 2004

Lithium as a disease-modifying agent for prion diseases

Peripheral circulation of the prion infectious agent in transgenic mice expressing the ovine prion protein gene in neurons only.

scientific article

Prion diseases and adult neurogenesis: how do prions counteract the brain's endogenous repair machinery?

scientific article published on 15 May 2014

Prion propagation in cultured cells.

scientific article published on January 2003

Prion replication occurs in endogenous adult neural stem cells and alters their neuronal fate: involvement of endogenous neural stem cells in prion diseases

scientific article

Scrapie strain transmission studies in ovine PrP transgenic mice reveal dissimilar susceptibility

scientific article published on 15 March 2007

Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin.

scientific article published on May 2004

Systemic delivery of siRNA down regulates brain prion protein and ameliorates neuropathology in prion disorder.

scientific article

The cellular prion protein controls the mesenchymal-like molecular subtype and predicts disease outcome in colorectal cancer

scientific article published on 31 July 2019

Transmission and characterization of bovine spongiform encephalopathy sources in two ovine transgenic mouse lines (TgOvPrP4 and TgOvPrP59).

scientific article published in December 2006

[Prions: where do we stand 20 years after the appearance of bovine spongiform encephalopathy?]

scientific article published on 01 December 2007

List of works by Carole Crozet

Anti-PrP antibodies block PrPSc replication in prion-infected cell cultures by accelerating PrPC degradation.

Cationic phosphorus-containing dendrimers reduce prion replication both in cell culture and in mice infected with scrapie

Cell-based therapy against prion diseases

Cellular pathogenesis in prion diseases.

Comparative proteomic analysis of human mesenchymal and embryonic stem cells: towards the definition of a mesenchymal stem cell proteomic signature.

Effective gene therapy in a mouse model of prion diseases

Gene and cell therapy for prion diseases.

Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene

Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene

High Dub3 expression in mouse ESCs couples the G1/S checkpoint to pluripotency.

Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations.

Lithium as a disease-modifying agent for prion diseases

Peripheral circulation of the prion infectious agent in transgenic mice expressing the ovine prion protein gene in neurons only.

Prion diseases and adult neurogenesis: how do prions counteract the brain's endogenous repair machinery?

Prion propagation in cultured cells.

Prion replication occurs in endogenous adult neural stem cells and alters their neuronal fate: involvement of endogenous neural stem cells in prion diseases

Scrapie strain transmission studies in ovine PrP transgenic mice reveal dissimilar susceptibility

Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin.

Systemic delivery of siRNA down regulates brain prion protein and ameliorates neuropathology in prion disorder.

The cellular prion protein controls the mesenchymal-like molecular subtype and predicts disease outcome in colorectal cancer

Transmission and characterization of bovine spongiform encephalopathy sources in two ovine transgenic mouse lines (TgOvPrP4 and TgOvPrP59).

[Prions: where do we stand 20 years after the appearance of bovine spongiform encephalopathy?]