Yveline Frobert
Overview
Explore the profile of Yveline Frobert including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
18
Citations
569
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Privat N, Laffont-Proust I, Faucheux B, Sazdovitch V, Frobert Y, Laplanche J, et al.
Mod Pathol
. 2007 Dec;
21(2):140-9.
PMID: 18084251
Demonstration of pathological prion protein accumulation in the central nervous system is required to establish the diagnosis of transmissible subacute encephalopathies. In humans, this is frequently achieved using prion protein...
2.
Kleene R, Loers G, Langer J, Frobert Y, Buck F, Schachner M
J Neurosci
. 2007 Nov;
27(45):12331-40.
PMID: 17989297
Prion-related protein (PrP) is a neural cell adhesion molecule involved in neurite outgrowth, neuronal survival, and synaptic function. In search of novel binding partners for PrP, we identified the alpha2/beta2-Na+/K+-ATPase...
3.
Feraudet C, Morel N, Simon S, Volland H, Frobert Y, Creminon C, et al.
J Biol Chem
. 2004 Dec;
280(12):11247-58.
PMID: 15618225
Prion diseases are transmissible neurodegenerative disorders affecting humans and animals for which no therapeutic or prophylactic regimens exist. During the last three years several studies have shown that anti-PrP monoclonal...
4.
Pinon-Lataillade G, Masson C, Bernardino-Sgherri J, Henriot V, Mauffrey P, Frobert Y, et al.
J Cell Sci
. 2004 Jul;
117(Pt 16):3691-702.
PMID: 15252136
Genotoxic agents deform DNA structure thus eliciting a complex genetic response allowing recovery and cell survival. The Kin17 gene is up-regulated during this response. This gene encodes a conserved nuclear...
5.
Tymciu S, Durieux-Alexandrenne C, Wijkhuisen A, Creminon C, Frobert Y, Grassi J, et al.
DNA Cell Biol
. 2004 Jul;
23(6):395-402.
PMID: 15231073
DNA vaccination appears as a very promising approach to raise protective antibodies against a variety of proteins from pathogens or tumor cells, but is often hindered by the low immunogenicity...
6.
Morel N, Simon S, Frobert Y, Volland H, Mourton-Gilles C, Negro A, et al.
J Biol Chem
. 2004 May;
279(29):30143-9.
PMID: 15140886
Transmissible spongiform encephalopathies are characterized by the accumulation in brain tissues of an abnormal isoform of the prion protein named PrPsc, which is the only direct marker known for transmissible...
7.
Perrier V, Solassol J, Crozet C, Frobert Y, Mourton-Gilles C, Grassi J, et al.
J Neurochem
. 2004 Apr;
89(2):454-63.
PMID: 15056288
The use of anti-PrP antibodies represents one of the most promising strategies for the treatment of prion diseases. In the present study, we screened various anti-PrP antibodies with the aim...
8.
Mange A, Beranger F, Peoch K, Onodera T, Frobert Y, Lehmann S
Biol Cell
. 2004 Mar;
96(2):125-32.
PMID: 15050367
It is commonly assumed that the physiological isoform of prion protein, PrP(C), is cleaved during its normal processing between residues 111/112, whereas the pathogenic isoform, PrP(Sc), is cleaved at an...
9.
Morel E, Fouquet S, Chateau D, Yvernault L, Frobert Y, Pincon-Raymond M, et al.
J Biol Chem
. 2003 Oct;
279(2):1499-505.
PMID: 14576159
The physiological function of PrPc, the cellular isoform of prion protein, still remains unclear, although it has been established, in vitro or by using nerve cells, that it can homodimerize,...
10.
Monnet C, Marthiens V, Enslen H, Frobert Y, Sobel A, Marc Mege R
Eur J Neurosci
. 2003 Aug;
18(3):542-8.
PMID: 12911750
The normal cellular prion protein is a small sialoglycoprotein highly expressed in neurons, the physiological function of which is largely unknown. Due to extensive N-glycosylations with a wide range of...