Thierry Baron

Transmissible spongiform encephalopathy diagnosis using PrPsc immunohistochemistry on fixed but previously frozen brain samples.

Identification of inter-species transmission of prion strains.

Mouse models of prion disease transmission.

Comparison of abnormal prion protein glycoform patterns from transmissible spongiform encephalopathy agent-infected deer, elk, sheep, and cattle.

Detection of bovine spongiform encephalopathy, ovine scrapie prion-related protein (PrPSc) and normal PrPc by monoclonal antibodies raised to copper-refolded prion protein.

How the surveillance system may bias the results of analytical epidemiological studies on BSE: prevalence among dairy versus beef suckler cattle breeds in France.

First case of feline spongiform encephalopathy in a captive cheetah born in France: PrP(sc) analysis in various tissues revealed unexpected targeting of kidney and adrenal gland.

Neuropathological characterisation of French bovine spongiform encephalopathy cases.

Distinct molecular phenotypes in bovine prion diseases.

Comparative molecular analysis of the abnormal prion protein in field scrapie cases and experimental bovine spongiform encephalopathy in sheep by use of Western blotting and immunohistochemical methods.

Molecular analysis of the protease-resistant prion protein in scrapie and bovine spongiform encephalopathy transmitted to ovine transgenic and wild-type mice.

Automatic quantitation of vacuolar lesions in the brain of mice infected with transmissible spongiform encephalopathies.

BSE agent signatures in a goat.

An alternative pretreatment procedure in animal transmissible spongiform encephalopathies diagnosis using PrPsc immunohistochemistry.

A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes.

Origin of bovine spongiform encephalopathy.

Diagnosis of transmissible spongiform encephalopathies in animals: a review.

PET-blot analysis contributes to BSE strain recognition in C57Bl/6 mice.

PrP(d) accumulation in organs of ARQ/ARQ sheep experimentally infected with BSE by peripheral routes.

Transmission of new bovine prion to mice.

BSE inoculation to prion diseases-resistant sheep reveals tricky silent carriers.

Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathy.

Bovine spongiform encephalopathy agent in a prion protein (PrP)ARR/ARR genotype sheep after peripheral challenge: complete immunohistochemical analysis of disease-associated PrP and transmission studies to ovine-transgenic mice.

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

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

Similar biochemical signatures and prion protein genotypes in atypical scrapie and Nor98 cases, France and Norway.

Molecular behaviors of "CH1641-like" sheep scrapie isolates in ovine transgenic mice (TgOvPrP4).

Molecular discrimination of atypical bovine spongiform encephalopathy strains from a geographical region spanning a wide area in Europe.

A bovine prion acquires an epidemic bovine spongiform encephalopathy strain-like phenotype on interspecies transmission.

Biochemical identification of bovine spongiform encephalopathies in cattle.

Classic scrapie in sheep with the ARR/ARR prion genotype in Germany and France.

Bovine spongiform encephalopathy in Sweden: an H-type variant.

Phenotypic similarity of transmissible mink encephalopathy in cattle and L-type bovine spongiform encephalopathy in a mouse model.

Atypical bovine spongiform encephalopathies, France, 2001-2007.

Association of a bovine prion gene haplotype with atypical BSE.

Rapid typing of transmissible spongiform encephalopathy strains with differential ELISA.

A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic mice.

Size effects in mechanical deformation and fracture of cantilevered silicon nanowires.

H-type bovine spongiform encephalopathy: complex molecular features and similarities with human prion diseases.

Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice.

Altered expression of CRMPs in the brain of bovine spongiform encephalopathy-infected mice during disease progression.

Self-assembling study of a cylinder-forming block copolymer via a nucleation-growth mechanism.

Possible case of maternal transmission of feline spongiform encephalopathy in a captive cheetah.

Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype.

Strain-specific proteolytic processing of the prion protein in prion diseases of ruminants transmitted in ovine transgenic mice.

Prions of ruminants show distinct splenotropisms in an ovine transgenic mouse model.

Is the presence of abnormal prion protein in the renal glomeruli of feline species presenting with FSE authentic?

Production of a monoclonal antibody, against human α-synuclein, in a subpopulation of C57BL/6J mice, presenting a deletion of the α-synuclein locus.

Strain-specific barriers against bovine prions in hamsters.

Molecular typing of protease-resistant prion protein in transmissible spongiform encephalopathies of small ruminants, France, 2002-2009.

Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice.

An improved AFM cross-sectional method for piezoelectric nanostructures properties investigation: application to GaN nanowires.

Molecular discrimination of sheep bovine spongiform encephalopathy from scrapie.

Transmission of prion strains in a transgenic mouse model overexpressing human A53T mutated α-synuclein.

Atypical prion diseases in humans and animals.

Growth and characterization of gold catalyzed SiGe nanowires and alternative metal-catalyzed Si nanowires.

Histopathological studies of "CH1641-like" scrapie sources versus classical scrapie and BSE transmitted to ovine transgenic mice (TgOvPrP4).

Prion-like acceleration of a synucleinopathy in a transgenic mouse model.

Classical bovine spongiform encephalopathy by transmission of H-type prion in homologous prion protein context.

Selection of distinct strain phenotypes in mice infected by ovine natural scrapie isolates similar to CH1641 experimental scrapie.

Oral transmission of L-type bovine spongiform encephalopathy in primate model.

Bovine PrP expression levels in transgenic mice influence transmission characteristics of atypical bovine spongiform encephalopathy.

An antibody with high reactivity for disease-associated α-synuclein reveals extensive brain pathology.

Chronic wasting disease and atypical forms of bovine spongiform encephalopathy and scrapie are not transmissible to mice expressing wild-type levels of human prion protein.

All major prion types recognised by a multiplex immunofluorometric assay for disease screening and confirmation in sheep.

Differentiation of prions from L-type BSE versus sporadic Creutzfeldt-Jakob disease.

Unique properties of the classical bovine spongiform encephalopathy strain and its emergence from H-type bovine spongiform encephalopathy substantiated by VM transmission studies.

Control of 10 nm scale cylinder orientation in self-organized sugar-based block copolymer thin films.

Specific pesticide-dependent increases in α-synuclein levels in human neuroblastoma (SH-SY5Y) and melanoma (SK-MEL-2) cell lines.

Sequential growth of bistable copper-molybdenum coordination nanolayers on inorganic surfaces.

Stability properties of PrP(Sc) from cattle with experimental transmissible spongiform encephalopathies: use of a rapid whole homogenate, protease-free assay.

Presence of subclinical infection in gene-targeted human prion protein transgenic mice exposed to atypical bovine spongiform encephalopathy.

L-type bovine spongiform encephalopathy in genetically susceptible and resistant sheep: changes in prion strain or phenotypic plasticity of the disease-associated prion protein?

Alpha-synuclein spreading in M83 mice brain revealed by detection of pathological α-synuclein by enhanced ELISA.

Distinct transmissibility features of TSE sources derived from ruminant prion diseases by the oral route in a transgenic mouse model (TgOvPrP4) overexpressing the ovine prion protein.

Composition-dependent interfacial abruptness in Au-catalyzed Si(1-x)Ge(x)/Si/Si(1-x)Ge(x) nanowire heterostructures.

Molecular modeling of prion transmission to humans.

Multimode silicon nanowire transistors.

A variety of pesticides trigger in vitro α-synuclein accumulation, a key event in Parkinson's disease.

Early and persistent expression of phosphorylated α-synuclein in the enteric nervous system of A53T mutant human α-synuclein transgenic mice.

Binding of the PET radiotracer [¹⁸F]BF227 does not reflect the presence of alpha-synuclein aggregates in transgenic mice.

Adjustable continence therapy (ProACT™) after male sling failure for patients with post-radical prostatectomy urinary incontinence: a prospective study with one-year follow-up.

Percolating silicon nanowire networks with highly reproducible electrical properties.

Sheep prions with molecular properties intermediate between classical scrapie, BSE and CH1641-scrapie.