Technical Note : Determination of alleles of the ovine PRNP gene using PCR-single-strand conformational polymorphism analysisZHOU, H; HICKFORD, J. G. H; FANG, Q et al.Journal of animal science. 2005, Vol 83, Num 4, pp 745-749, issn 0021-8812, 5 p.Article

The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents)NADIFI, S; SLASSI, I; EL HACHIMI, K. M et al.Pathologie et biologie. 2008, Vol 56, Num 3, pp 133-136, issn 0369-8114, 4 p.Article

Somatic cell mapping of the bovine prion protein gene and restriction fragment length polymorphism studies in cattle and sheepRYAN, A. M; WOMACK, J. E.Animal genetics (Print). 1993, Vol 24, Num 1, pp 23-26, issn 0268-9146Article

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pterSPEER, M. C; GOLDGABER, D; GOLDFARB, L. G et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 2, pp 366-368, issn 0888-7543, 3 p.Article

Génétique moléculaire des formes familiales et sporadiques des maladies à prions humaines = Molecular genetics of familial and sporadic human prion diseasesLAPLANCHE, J.-L; LAUNAY, J.-M; DREUX, C et al.Annales pharmaceutiques françaises. 1995, Vol 53, Num 5, pp 193-200, issn 0003-4509Article

Analysis of PRNP gene codon 129 polymorphism in the greek populationSAETTA, Angelica A; M ICHALOPOULOS, Nikolaos V; MALAMIS, George et al.European journal of epidemiology. 2006, Vol 21, Num 3, pp 211-215, issn 0393-2990, 5 p.Article

Normal development and behaviour of mice lacking the neuronal cell-surface PrP proteinBÜELER, H; FISCHER, M; LANG, Y et al.Nature (London). 1992, Vol 356, Num 6370, pp 577-582, issn 0028-0836Article

Intérêt de l'étude génétique du gène PRNP devant un syndrome cérébelleux : à propos d'un nouveau cas d'insomnie fatale familiale = Usefulness of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomniaMARCAUD, V; LAPLANCHE, J.-L; VECCHIERINI, F et al.Revue neurologique (Paris). 2003, Vol 159, Num 2, pp 199-202, issn 0035-3787, 4 p.Article

Fatal insomnia in a case of familial Creutzfedlt-Jakob disease with the codon 200^Lys mutationCHAPMAN, J; ARLAZOROFF, A; GOLDFARB, L. G et al.Neurology. 1996, Vol 46, Num 3, pp 758-761, issn 0028-3878Article

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob diseaseRIPOLL, L; LAPLANCHE, J.-L; SALZMANN, M et al.Neurology. 1993, Vol 43, Num 10, pp 1934-1938, issn 0028-3878Article

A patient with dementia with Lewy bodies and codon 232 mutation of PRNPKOIDE, T; OHTAKE, H; NAKAJIMA, T et al.Neurology. 2002, Vol 59, Num 10, pp 1619-1621, issn 0028-3878, 3 p.Article

A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker diseasePANEGYRES, Peter K; TOUFEXIS, Kathrine; KAKULAS, B. A et al.Archives of neurology (Chicago). 2001, Vol 58, Num 11, pp 1899-1902, issn 0003-9942Article

Creutzfeldt-Jakob disease cosegregats with the codon 178^Asn PRNP mutation in families of European originGOLDBAB, L. G; BROWN, P; ASHER, D. M et al.Annals of neurology. 1992, Vol 31, Num 3, pp 274-281, issn 0364-5134Article

Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies?MASULLO, C; MACCHI, G.Clinical neuropathology. 2001, Vol 20, Num 1, pp 19-25, issn 0722-5091Article

A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP geneLIBERSKI, P. P; BARCIKOWSKA, M; CERVENAKOVA, L et al.Acta neuropathologica. 1998, Vol 96, Num 4, pp 425-430, issn 0001-6322Article

Inherited prion disease caused by the V210I mutation: Transmission to transgenic miceMASTRIANNI, J. A; CAPELLARI, S; TELLING, G. C et al.Neurology. 2001, Vol 57, Num 12, pp 2198-2205, issn 0028-3878Article

Molecular genetics of human prion diseases in GermanyWINDL, O; GIESE, A; SCHULZ-SCHAEFFER, W et al.Human genetics. 1999, Vol 105, Num 3, pp 244-252, issn 0340-6717Article

High incidence of Creutzfeldt-Jakob disease in rural Calabria, ItalyD'ALESSANDRO, M; PETRAROLI, R; LADOGANA, A et al.Lancet (British edition). 1998, Vol 352, Num 9145, pp 1989-1990, issn 0140-6736Article

Quantitative trait loci linked to PRNP gene controlling health and production traits in INRA 401 sheepVITEZICA, Zulma G; MORENO, Carole R; BARILLET, Francis et al.Genetics selection evolution (Print). 2007, Vol 39, Num 4, pp 421-430, issn 0999-193X, 10 p.Article

The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutationCHAPMAN, J; BEN-ISRAEL, J; GOLDHAMMER, Y et al.Neurology. 1994, Vol 44, Num 9, pp 1683-1686, issn 0028-3878Article

Transgenesis applied to transmissible spongiform encephalopathies. CommentaryVILOTTE, Jean-Luc; LAUDE, Hubert; PARKER, Jane E et al.Transgenic research. 2002, Vol 11, Num 6, pp 547-566, issn 0962-8819, 20 p.Article

A mouse prion protein transgene rescues mice deficient for the prion protein gene from Purkinje cell degeneration and demyelinationNISHIDA, N; TREMBLAY, P; TORCHIA, M et al.Laboratory investigation. 1999, Vol 79, Num 6, pp 689-697, issn 0023-6837Article

Prion protein and neuronal differentiation : quantitative analysis of prnp gene expression in a murine inducible neuroectodermal progenitorMOUILLET-RICHARD, S; LAURENDEAU, I; VIDAUD, M et al.Microbes and infection. 1999, Vol 1, Num 12, pp 969-976, issn 1286-4579Article

Regulation of PrP^C expression : Nerve growth factor (NGF) activates the prion gene promoter through the MEK1 pathway in PC12 cellsZAWLIK, Izabela; WITUSIK, Monika; HULAS-BIGOSZEWSKA, Krystyna et al.Neuroscience letters. 2006, Vol 400, Num 1-2, pp 58-62, issn 0304-3940, 5 p.Article

The genetics of prions: a contradiction in terms?AGUZZI, A; BRANDNER, S.Lancet (British edition). 1999, Vol 354, pp SI22-SI25, issn 0140-6736, SUP1Article