Citation Impact
Citing Papers
Neurotoxic protein expression reveals connections between the circadian clock and mating behavior in Drosophila
2006 StandoutNobel
Augmenting neurotransmitter release by enhancing the apparent Ca 2+ affinity of synaptotagmin 1
2005 StandoutNobel
Increased susceptibility of cytoplasmic over nuclear polyglutamine aggregates to autophagic degradation
2005
Parkinson-like syndrome induced by continuous MPTP infusion: Convergent roles of the ubiquitin-proteasome system and α-synuclein
2005 StandoutNobel
Chaperone Suppression of α-Synuclein Toxicity in a Drosophila Model for Parkinson's Disease
2002 StandoutScience
Neuronal Deficiency of Presenilin 1 Inhibits Amyloid Plaque Formation and Corrects Hippocampal Long-Term Potentiation But Not a Cognitive Defect of Amyloid Precursor Protein [V717I] Transgenic Mice
2002
The DNA-damage response in human biology and disease
2009 StandoutNature
Apoptosis in the nervous system
2000 StandoutNature
The Value of Transgenic Models for the Study of Neurodegenerative Diseases
2000
The Ubiquitin Proteasome System in Neurodegenerative Diseases
2003 StandoutNobel
Are Huntington’s and polyglutamine-based ataxias proteasome storage diseases?
2003
Proteolytic Processing of Amyloid-β Precursor Protein by Secretases Does Not Require Cell Surface Transport
2004 StandoutNobel
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
Myotonic dystrophy, knockouts, warts
1996
Direct Interaction of Alzheimer's Disease-related Presenilin 1 with Armadillo Protein p0071
1999 StandoutNobel
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1
1998
Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease
2000
C-terminal ECFP Fusion Impairs Synaptotagmin 1 Function
2004 StandoutNobel
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease
2007
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.
1993
The role of the ubiquitin-proteasomal pathway in Parkinson's disease and other neurodegenerative disorders
2001
Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability
2000
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
2004 StandoutNature
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
Functional Classification and Experimental Dissection of Long Noncoding RNAs
2018 Standout
Mismatch repair gene Msh2 modifies the timing of early disease in HdhQ111 striatum
2003
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch
1998
Pumilio1 Haploinsufficiency Leads to SCA1-like Neurodegeneration by Increasing Wild-Type Ataxin1 Levels
2015
The complex pathology of trinucleotide repeats
1997
Polyglutamine-Expanded Human Huntingtin Transgenes Induce Degeneration of Drosophila Photoreceptor Neurons
1998
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
2006 StandoutNature
Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
2000
Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice
1996 Standout
Polyglutamine Expansion Induces a Protein-damaging Stress Connecting Heat Shock Protein 70 to the JNK Pathway
2003
Processing of p105 Is Inhibited by Docking of p50 Active Subunits to the Ankyrin Repeat Domain, and Inhibition Is Alleviated by Signaling via the Carboxyl-terminal Phosphorylation/ Ubiquitin-Ligase Binding Domain
2001 StandoutNobel
Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract
1996
Glial and neuronal expression of polyglutamine proteins induce behavioral changes and aggregate formation in Drosophila
2004
Radiation hybrids: irradiation and fusion gene transfer
1993
Microsatellite repeat instability and neurological disease
2009
A Genetic Approach to Visualization of Multisynaptic Neural Pathways Using Plant Lectin Transgene
1999
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice
2001
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
2002
Transgenic models of Huntington's disease
1997
When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases
1995
Expanded polyglutamine in the Machado–Joseph disease protein induces cell death in vitro and in vivo
1996
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8
2006
An Akt/β-Arrestin 2/PP2A Signaling Complex Mediates Dopaminergic Neurotransmission and Behavior
2005 StandoutNobel
Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability
2000
A Novel Multiple PDZ Domain-containing Molecule Interacting withN-Methyl-d-aspartateReceptors and Neuronal Cell Adhesion Proteins
1998 StandoutNobel
Identification of genes that modify ataxin-1-induced neurodegeneration
2000 Nature
MutLα and Proliferating Cell Nuclear Antigen Share Binding Sites on MutSβ
2010 StandoutNobel
Nuclear Targeting of Mutant Huntingtin Increases Toxicity
1999
Features of trinucleotide repeat instability in vivo
2008
A method for constructing radiation hybrid maps of whole genomes
1994
Ataxin-1 Nuclear Localization and Aggregation
1998
DRPLA gene (Atrophin-1) sequence and mRNA expression in human brain
1996
Mechanisms of trinucleotide repeat instability during human development
2010
Evolution and Functions of Long Noncoding RNAs
2009 Standout
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function
1997 StandoutNature
The Molecular Architecture of Odor and Pheromone Sensing in Mammals
2000 StandoutNobel
A potential proteasome-interacting motif within the ubiquitin-like domain of parkin and other proteins
2003
SCRAPPER-Dependent Ubiquitination of Active Zone Protein RIM1 Regulates Synaptic Vesicle Release
2007
The Presynaptic Active Zone Protein RIM1α Is Critical for Normal Learning and Memory
2004 StandoutNobel
New order from neurological disorders
1999 Nature
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
1997
PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair
2010 StandoutNobel
Sustained elevation of extracellular dopamine causes motor dysfunction and selective degeneration of striatal GABAergic neurons
2003
Huntingtin Expression Stimulates Endosomal–Lysosomal Activity, Endosome Tubulation, and Autophagy
2000
MUTANT GENES IN FAMILIAL ALZHEIMER'S DISEASE AND TRANSGENIC MODELS
1998
Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia
2001
Glutamine Repeats and Neurodegeneration
2000
Deletion of CASK in mice is lethal and impairs synaptic function
2007 StandoutNobel
Short-Term Synaptic Plasticity
2002 Standout
Formation of Neuronal Intranuclear Inclusions Underlies the Neurological Dysfunction in Mice Transgenic for the HD Mutation
1997 Standout
The role of the ubiquitin-proteasomal pathway in Parkinson's disease and other neurodegenerative disorders
2001
DNA Mismatch Repair: Functions and Mechanisms
2005 StandoutNobel
Binding of F-spondin to amyloid-β precursor protein: A candidate amyloid-β precursor protein ligand that modulates amyloid-β precursor protein cleavage
2004 StandoutNobel
Molecular Chaperones in the Cytosol: from Nascent Chain to Folded Protein
2002 StandoutScience
Synapsins regulate use-dependent synaptic plasticity in the calyx of Held by a Ca 2+ /calmodulin-dependent pathway
2006 StandoutNobel
Neural Science
2000 StandoutNobel
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
Polyglutamine pathogenesis
1999
Alzheimer's Disease Is a Synaptic Failure
2002 StandoutScience
Bruchpilot Promotes Active Zone Assembly, Ca 2+ Channel Clustering, and Vesicle Release
2006 StandoutScienceNobel
RIM genes differentially contribute to organizing presynaptic release sites
2012 StandoutNobel
Rab3B protein is required for long-term depression of hippocampal inhibitory synapses and for normal reversal learning
2011 StandoutNobel
Fission yeast orb 6, a ser/thr protein kinase related to mammalian rho kinase and myotonic dystrophy kinase, is required for maintenance of cell polarity and coordinates cell morphogenesis with the cell cycle
1998 StandoutNobel
Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene
1996 StandoutScience
Neuroscience: Breaking Down Scientific Barriers to the Study of Brain and Mind
2000 StandoutScienceNobel
Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation
2013 StandoutNobel
Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain
1997 StandoutScience
Polyglutamines, nuclear inclusions and neurodegeneration
1997
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
Glutamine repeats and inherited neurodegenerative diseases: molecular aspects
1996
RIM1α phosphorylation at serine-413 by protein kinase A is not required for presynaptic long-term plasticity or learning
2008 StandoutNobel
Impairment of the Ubiquitin-Proteasome System by Protein Aggregation
2001 StandoutScience
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Long CTG Tracts from the Myotonic Dystrophy Gene Induce Deletions and Rearrangements during Recombination at the APRT Locus in CHO Cells
2003
Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice
1999 StandoutNobel
Autophagy in Health and Disease: A Double-Edged Sword
2004 StandoutScience
Works of Eric N. Burright being referenced
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
1995
Identification and characterization of an ataxin-1-interacting protein: A1Up, a ubiquitin-like nuclear protein
2000
Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel
1992
Increased Trinucleotide Repeat Instability with Advanced Maternal Age
1997
Identification of a self-association region within the SCA1 gene product, ataxin-1
1997
A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints
1992
Purkinje Cell Expression of a Mutant Allele ofSCA1in Transgenic Mice Leads to Disparate Effects on Motor Behaviors, Followed by a Progressive Cerebellar Dysfunction and Histological Alterations
1997
Mice Lacking Ataxin-1 Display Learning Deficits and Decreased Hippocampal Paired-Pulse Facilitation
1998