Citation Impact
Citing Papers
Experimental transmission of an autosomal dominant spongiform encephalopathy: does the infectious agent originate in the human genome?
1985
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
1992 StandoutNatureNobel
Amyotrophy in Prion Diseases
2000
The Relationship Between Quantitative MRI and Neuropsychological Functioning in Temporal Lobe Epilepsy
1998
Do defecs in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases?
1993
Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype
2001
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
2009
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene
1992 StandoutNobel
Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?
1992
Mutation of the Prion Protein in Libyan Jews with Creutzfeldt–Jakob Disease
1991 StandoutNobel
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
1990 StandoutNobel
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome
1989 StandoutNatureNobel
Prion Protein Isoforms, a Convergence of Biological and Structural Investigations
1995 StandoutNobel
Gerstmann‐Sträussler‐Scheinker Disease and the Indiana Kindred
1995
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
1992 StandoutNobel
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders
2004
Functional organization of the hippocampal longitudinal axis
2014 StandoutNobel
The Amyloid State of Proteins in Human Diseases
2012 Standout
Familial Danish Dementia
2005
The Human Hippocampus and Spatial and Episodic Memory
2002 StandoutNobel
The spectrum of hippocampal sclerosis: A quantitative magnetic resonance imaging study
1997
Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders
1994 Standout
Insoluble wild–type and protease–resistant mutant prion protein in brains of patients with inherited prion disease
1996 StandoutNobel
A new variant of Creutzfeldt-Jakob disease in the UK
1996 Standout
Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent
1997 StandoutNature
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Amyotrophic Lateral Sclerosis
2001 Standout
Mice devoid of PrP are resistant to scrapie
1993 Standout
Non-hydrophobic extracytoplasmic determinant of stop transfer in the prion protein
1990 StandoutNatureNobel
Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice
1997 StandoutNobel
Oxidative damage and mitochondrial decay in aging.
1994 Standout
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Noncovalent Functionalization of Graphene and Graphene Oxide for Energy Materials, Biosensing, Catalytic, and Biomedical Applications
2016 Standout
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Str�ussler-Scheinker variant?)
1985
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
2002 StandoutScience
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.
1993 Standout
A Century of Alzheimer's Disease
2006 StandoutScience
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
1997 StandoutScience
Primary structure of prion protein may modify scrapie isolate properties.
1989 StandoutNobel
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
1991 StandoutNobel
Navigation-related structural change in the hippocampi of taxi drivers
2000 Standout
Prion-Protein Immunoreactivity in Human Transmissible Dementias
1986 StandoutNobel
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Prions
1998 StandoutNobel
Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid.
1992 StandoutNobel
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.
1994 StandoutNobel
NMR structure of the bovine prion protein
2000 StandoutNobel
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
Inherited prion diseases.
1994 StandoutNobel
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996 StandoutNobel
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
1992 StandoutNobel
Purified prion proteins and scrapie infectivity copartition into liposomes.
1987 StandoutNobel
Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
1986 Nobel
Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein
1990 StandoutScienceNobel
Works of F Scaravilli being referenced
Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation
1999
Quantitative hippocampal MRI and intractable temporal lobe epilepsy
1995
Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
1990
Creutzfeldt-Jakob disease in a young woman
1996
Familial cerebral amyloidosis and spongiform encephalopathy.
1982