Citation Impact
Citing Papers
α-Synuclein Promotes SNARE-Complex Assembly in Vivo and in Vitro
2010 StandoutScienceNobel
Water Channel Properties of Major Intrinsic Protein of Lens
1995 StandoutNobel
The small heat shock protein Hsp27 binds α-synuclein fibrils, preventing elongation and cytotoxicity
2018
The synaptic pathology of α-synuclein aggregation in dementia with Lewy bodies, Parkinson’s disease and Parkinson’s disease dementia
2010
Astrocytes: biology and pathology
2009 Standout
Human prion diseases with variant prion protein
1994
Molecular profile of reactive astrocytes—Implications for their role in neurologic disease
1993
Creutzfeldt-Jakob disease with codon 129 polymorphism (Valine): a comparative study of patients with codon 102 point mutation or without mutations
1992
Molecular dissection of reactive astrogliosis and glial scar formation
2009 Standout
Detecting prion protein gene mutations by denaturing gradient gel electrophoresis
1994 StandoutNobel
First experimental transmission of fatal familial insomnia
1995 NatureNobel
Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies
1994
Presynaptic α-Synuclein Aggregates, Not Lewy Bodies, Cause Neurodegeneration in Dementia with Lewy Bodies
2007
A new inherited prion disease (PrP‐P105L mutation) showing spastic paraparesis
1993
Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
2004 Standout
A quantitative NMR spectroscopic examination of the flexibility of the C-terminal extensions of the molecular chaperones, αA- and αB-crystallin
2010
Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains
1992
Rapidly progressive aphasic dementia and motor neuron disease
1993
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
1996
Molecular properties of complexes formed between the prion protein and synthetic peptides
1997 StandoutNobel
The Heat Shock Response: Life on the Verge of Death
2010 Standout
αB-Crystallin is present in reactive glia in Creutzfeldt-Jakob disease
1992
Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)
1995
The small heat-shock protein αB-crystallin as candidate autoantigen in multiple sclerosis
1995 Nature
A Phospho-Switch Controls the Dynamic Association of Synapsins with Synaptic Vesicles
1999 StandoutNobel
The function of alpha-crystallin in vision
2000
Parkinson's disease
2015 Standout
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
1997
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
Human prion diseases
1994 StandoutNobel
Inherited Prion Diseases and Transmission to Rodents
1995
Ubiquitin in Neurodegenerative Diseases
1993
αA‐crystallin confers cellular thermoresistance
1994
A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform 1 1Edited by M. Yaniv
1997 StandoutNobel
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
Prion Diseases: From Protein to Cell Pathology
2008
Multiple Sclerosis
2000 Standout
Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities
2008 Standout
Reactive Astrocytes: Production, Function, and Therapeutic Potential
2017 Standout
Visualization of Prion Infection in Transgenic Mice Expressing Green Fluorescent Protein-Tagged Prion Protein
2005
Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent
1995
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
Interaction of the Molecular Chaperone αB-Crystallin with α-Synuclein: Effects on Amyloid Fibril Formation and Chaperone Activity
2004
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Synaptic Vulnerability in Neurodegenerative Disease
2006
O-GlcNAc modification of small heat shock proteins enhances their anti-amyloid chaperone activity
2021 StandoutNobel
Prion (PrPSc)-specific epitope defined by a monoclonal antibody
1997 StandoutNatureNobel
Inflammation in obesity, diabetes, and related disorders
2022 Standout
CSPα knockout causes neurodegeneration by impairing SNAP‐25 function
2011 StandoutNobel
Alpha-crystallin
2003
Time-tagged ticker tapes for intracellular recordings
2023 StandoutNobel
Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice
1997 StandoutNobel
Physiological Implications of Hydrogen Sulfide: A Whiff Exploration That Blossomed
2012 Standout
Molecular evolution of the eye lens
1994
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
GENETICS OF PRIONS
1997 StandoutNobel
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Practice parameter: Management of dementia (an evidence-based review) [RETIRED]
2001 Standout
Small heat shock proteins are molecular chaperones.
1993 Standout
Prion protein immunocytochemistry – UK five centre consensus report
1997
IMMUNOLOGY OF MULTIPLE SCLEROSIS
2005 Standout
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
1999
Cystathionine β‐synthase, a key enzyme for homocysteine metabolism, is preferentially expressed in the radial glia/astrocyte lineage of developing mouse CNS
2005
Classification of Intrinsically Disordered Regions and Proteins
2014 Standout
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Frontotemporal lobar degeneration
1998 Standout
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Propagation of prion strains through specific conformers of the prion protein
1997 StandoutNobel
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
2001 Standout
Prions
1998 StandoutNobel
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family
1997
Alpha-crystallin can function as a molecular chaperone.
1992 Standout
Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible
1997 StandoutNobel
Evidence of Presynaptic Location and Function of the Prion Protein
1999
Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy
1994
Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.
1994 StandoutNobel
Heat shock protein 27 and alpha B-crystallin can form a complex, which dissociates by heat shock.
1992
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
Overexpression and abnormal modification of the stress proteins alpha B-crystallin and HSP27 in Alexander disease.
1993
Oxidative stress‐related increase in ubiquitination in early coronary atherogenesis
2003 StandoutNobel
HEAT-SHOCK PROTEINS, MOLECULAR CHAPERONES, AND THE STRESS RESPONSE: Evolutionary and Ecological Physiology
1999 Standout
Role of Inflammation in Diabetic Retinopathy
2018
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996 StandoutNobel
Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging
2008 Standout
Ultrastructural localization of prion proteins: Physiological and pathological implications
2000
LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia
2006 Standout
Works of N. Tomokane being referenced
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.
1992
Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold.
1991
Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions.
1992