PAPERS - RESEARCH FRONT: 11

TITLE 1ST AUTHOR YEAR
PLAYING CLUE WITH PRION DISEASE ROBERTS GW 1991
ATTEMPTS TO CONVERT THE CELLULAR PRION PROTEIN INTO THE SCRAPIE ISOFORM IN CELL-FREE SYSTEMS RAEBER AJ 1992
PRION DISEASE - THE ESSENTIAL FACTS CLINTON J 1992
3 SCRAPIE PRION ISOLATES EXHIBIT DIFFERENT ACCUMULATION PATTERNS OF THE PRION PROTEIN SCRAPIE ISOFORM DEARMOND SJ 1993
ALZHEIMERS-DISEASE AND CREUTZFELDT-JAKOB-DISEASE - OVERLAP OF PATHOGENIC MECHANISMS DEARMOND SJ 1993
VERTICAL TRANSFER OF PRION DISEASE LACEY RW 1994
SPONGIFORM ENCEPHALOPATHIES AND PRIONS - AN OVERVIEW OF PATHOLOGY AND DISEASE MECHANISMS FAIRBAIRN DW 1994
DOUBLE REPLACEMENT GENE TARGETING FOR THE PRODUCTION OF A SERIES OF MOUSE STRAINS WITH DIFFERENT PRION PROTEIN GENE ALTERATIONS MOORE RC 1995
PRION PROPAGATION IN MICE EXPRESSING HUMAN AND CHIMERIC PRP TRANSGENES IMPLICATES THE INTERACTION OF CELLULAR PRP WITH ANOTHER PROTEIN TELLING GC 1995
What went wrong in BSE? From prion disease to public disaster Baker HF 1996
Normal host prion protein necessary for scrapie-induced neurotoxicity Brandner S 1996
Human transmissible subacute spongiform encephalopathies. Dormont D 1996
A new variant of prion disease Collinge J 1996
Interactions between wild-type and mutant prion proteins modulate neurodegeneration transgenic mice Telling GC 1996
To what extent is strain variation evidence for an independent genome in the agent of the transmissible spongiform encephalopathies? Ridley RM 1996
Variation on a theme of Creutzfeldt-Jakob disease: Implications of new cases with a young age at onset Ridley RM 1996
Genetics of prions Prusiner SB 1997
A novel hamster prion protein mRNA contains an extra exon: Increased expression in scrapie Li G 1997
Deadly conformations - Protein misfolding in prion disease Horwich AL 1997
Transgenic analysis of prion diseases Moore RC 1997
Selective neuronal targeting in prion disease DeArmond SJ 1997
A transmembrane form of the prion protein in neurodegenerative disease Hegde RS 1998
The paradoxical dynamics of prion disease latency Payne RJH 1998
Prions and the prion disorders Fisher E 1998
Prion's progress: Patterns and rates of molecular evolution in relation to spongiform disease Krakauer DC 1998
Doxycycline control of prion protein transgene expression modulates prion disease in mice Tremblay P 1998
The spatial dynamics of prion disease Payne RJH 1998
Current status of bovine spongiform encephalopathy - A review Brewer MS 1999
Is the pathogen of prion disease a microbial protein? Fuzi M 1999
Transgenic models for prion disease: Have they outlived their useful purpose? Jenkins ES 1999
The welfare problems associated with using transgenic mice to bioassay for bovine spongiform encephalopathy Jenkins ES 1999
A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy Manson JC 1999
Transmissible and genetic prion diseases share a common pathway of neurodegeneration Hegde RS 1999
A transgenic model of a familial prion disease Harris DA 2000
Transgenic models of prion disease Scott MR 2000
Lack of evidence to support the association of the human prion gene with schizophrenia Tsai MT 2001
Transmissible spongiform encephalopathies or prion diseases. Dormont D 2001
Isolation and functional characterisation of the promoter region of the human prion protein gene Mahal SP 2001
Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody Enari M 2001
Huntington disease phenocopy is a familial prion disease Moore RC 2001
The transmissible spongiform encephalopathies (prion diseases): A review for dental surgeons Gill DS 2001
The animal and human prion diseases: Public health importance and risk assessment Vitale K 2001
Rapid detection of the prion protein M129V polymorphism with the LightCycler Teupser D 2002
PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob Disease McCormack JE 2002
All-trans retinoic acid down-regulates prion protein expression independently of granulocyte maturation Rybner C 2002
Expression pattern of a mini human PrP gene promoter in transgenic mice Asante EA 2002
Mouse models of prion disease transmission Baron T 2002
Human prion diseases Thakur R 2002
Fundamentals of prion biology and diseases DeArmond SJ 2002
PrP knock-out and PrP transgenic mice in prion research Weissmann C 2003
Dental practice implications of prion diseases Bebermeyer RD 2003
Perspectives on prion biology, prion disease pathogenesis, and pharmacologic approaches to treatment DeArmond SJ 2003
A murine model of a familial prion disease Harris DA 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics Mead S 2003
Post-transcriptional suppression of pathogenic prion protein expression in Drosophila neurons Deleault NR 2003
What would T. H. Huxley have made of prion diseases? Ridley RM 2003
Molecular distinction between pathogenic and infectious properties of the prion protein Chiesa R 2003
Mutant PrPSc conformers induced by a synthetic peptide and several prion strains Tremblay P 2004
The role of PrP in health and disease Flechsig E 2004
The public health impact of prion diseases Belay ED 2005
Prion disease: A deadly disease for protein misfolding Chakraborty C 2005
Human and animal spongiform encephalopathies are the result of chronic autolmmune attack in the CNS: A novel medical theory supported by overwhelming experimental evidence Zhu BT 2005