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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Elisa Rubino et al.
NEUROLOGY (2012)
Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43
I-Fang Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in mice
H. Z. Yin et al.
CELL DEATH & DISEASE (2012)
Transportin1: a marker of FTLD-FUS
Jack Brelstaff et al.
ACTA NEUROPATHOLOGICA (2011)
Differential Involvement of Optineurin in Amyotrophic Lateral Sclerosis With or Without SOD1 Mutations
Han-Xiang Deng et al.
ARCHIVES OF NEUROLOGY (2011)
SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
Faisal Fecto et al.
ARCHIVES OF NEUROLOGY (2011)
Rapamycin treatment augments motor neuron degeneration in SOD1G93A mouse model of amyotrophic lateral sclerosis
Xiaojie Zhang et al.
AUTOPHAGY (2011)
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations
Manuela Neumann et al.
BRAIN (2011)
FTD and ALS: A Tale of Two Diseases
R. Ferrari et al.
CURRENT ALZHEIMER RESEARCH (2011)
TDP-43 regulates its mRNA levels through a negative feedback loop
Youhna M. Ayala et al.
EMBO JOURNAL (2011)
BAG3 mediates chaperone-based aggresome-targeting and selective autophagy of misfolded proteins
Martin Gamerdinger et al.
EMBO REPORTS (2011)
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
Karli K. McDonald et al.
HUMAN MOLECULAR GENETICS (2011)
Regulation of Autophagy by Neuropathological Protein TDP-43
Jayarama Krishnan Bose et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Regulation of TDP-43 aggregation by phosphorylation andp62/SQSTM1
Owen A. Brady et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Autophagy in Spinal Cord Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis
Shoichi Sasaki
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2011)
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Han-Xiang Deng et al.
NATURE (2011)
Molecular chaperones in protein folding and proteostasis
F. Ulrich Hartl et al.
NATURE (2011)
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
Magdalini Polymenidou et al.
NATURE NEUROSCIENCE (2011)
RNA targets of wild-type and mutant FET family proteins
Jessica I. Hoell et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS
Ching-Paio Tsai et al.
NEUROBIOLOGY OF AGING (2011)
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
Mariely DeJesus-Hernandez et al.
NEURON (2011)
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton et al.
NEURON (2011)
Accumulation of Wildtype and ALS-Linked Mutated VAPB Impairs Activity of the Proteasome
Anice Moumen et al.
PLOS ONE (2011)
Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth
Philipp Wild et al.
SCIENCE (2011)
TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies
Todd J. Cohen et al.
TRENDS IN MOLECULAR MEDICINE (2011)
Molecular Determinants and Genetic Modifiers of Aggregation and Toxicity for the ALS Disease Protein FUS/TLS
Zhihui Sun et al.
PLOS BIOLOGY (2011)
VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD
Emilie Tresse et al.
AUTOPHAGY (2010)
New Insights into Biological Markers of Frontotemporal Lobar Degeneration Spectrum
Barbara Borroni et al.
CURRENT MEDICINAL CHEMISTRY (2010)
Protein disulphide isomerase is required for signal peptide peptidase-mediated protein degradation
Seong-Ok Lee et al.
EMBO JOURNAL (2010)
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Dorothee Dormann et al.
EMBO JOURNAL (2010)
Imbalances in p97 co-factor interactions in human proteinopathy
Vanesa Fernandez-Saiz et al.
EMBO REPORTS (2010)
A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum
Elisa Fasana et al.
FASEB JOURNAL (2010)
Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
Atsushi Manno et al.
GENES TO CELLS (2010)
Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy
Jeong-Sun Ju et al.
HUMAN MOLECULAR GENETICS (2010)
Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
Daryl A. Bosco et al.
HUMAN MOLECULAR GENETICS (2010)
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS)
Valeria Crippa et al.
HUMAN MOLECULAR GENETICS (2010)
Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis
Han-Jou Chen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
Lucia Corrado et al.
JOURNAL OF MEDICAL GENETICS (2010)
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotyp-phenotype correlations
Stephanie Millecamps et al.
JOURNAL OF MEDICAL GENETICS (2010)
AAV-mediated expression of wild-type and ALS-linked mutant VAPB selectively triggers death of motoneurons through a Ca2+-dependent ER-associated pathway
Karine Langou et al.
JOURNAL OF NEUROCHEMISTRY (2010)
FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis
Ian P. Blair et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
Synergistic Effect Between Proteasome and Autophagosome in the Clearance of Polyubiquitinated TDP-43
Makoto Urushitani et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2010)
Autophagy: cellular and molecular mechanisms
Danielle Glick et al.
JOURNAL OF PATHOLOGY (2010)
The Nucleolus under Stress
Severine Boulon et al.
MOLECULAR CELL (2010)
Phosphorylation regulates proteasomal-mediated degradation and solubility of TAR DNA binding protein-43 C-terminal fragments
Yong-Jie Zhang et al.
MOLECULAR NEURODEGENERATION (2010)
Mutations of optineurin in amyotrophic lateral sclerosis
Hirofumi Maruyama et al.
NATURE (2010)
Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
Daryl A. Bosco et al.
NATURE NEUROSCIENCE (2010)
Vesicle associated membrane protein B (VAPB) is decreased in ALS spinal cord
Georgia Anagnostou et al.
NEUROBIOLOGY OF AGING (2010)
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis
Janine Kirby et al.
NEUROGENETICS (2010)
Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations
D. Baeumer et al.
NEUROLOGY (2010)
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
J. Yan et al.
NEUROLOGY (2010)
Capturing VCP: Another Molecular Piece in the ALS Jigsaw Puzzle
Christopher E. Shaw
NEURON (2010)
Acetylation of Tau Inhibits Its Degradation and Contributes to Tauopathy
Sang-Won Min et al.
NEURON (2010)
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
Jane O. Johnson et al.
NEURON (2010)
Degradation of TDP-43 and its pathogenic form by autophagy and the ubiquitin-proteasome system
Xiaoju Wang et al.
NEUROSCIENCE LETTERS (2010)
Novel Antibodies Reveal Inclusions Containing Non-Native SOD1 in Sporadic ALS Patients
Karin Forsberg et al.
PLOS ONE (2010)
Effects of sodium valproate on synaptic transmission and neuronal excitability in rat hippocampus
Wu Yong et al.
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY (2009)
Endoplasmic Reticulum Protein Quality Control in Neurodegenerative Disease: The Good, the Bad and the Therapy
Wiep Scheper et al.
CURRENT MEDICINAL CHEMISTRY (2009)
PLIC proteins or ubiquilins regulate autophagy-dependent cell survival during nutrient starvation
Elsa-Noah N'Diaye et al.
EMBO REPORTS (2009)
Molecular Neuropathology of TDP-43 Proteinopathies
Manuela Neumann
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2009)
Potentiation of Amyotrophic Lateral Sclerosis (ALS)-associated TDP-43 Aggregation by the Proteasome-targeting Factor, Ubiquilin 1
Sang Hwa Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
VCP Mutations Causing Frontotemporal Lobar Degeneration Disrupt Localization of TDP-43 and Induce Cell Death
Michael A. Gitcho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Ubiquilin and p97/VCP bind erasin, forming a complex involved in ERAD
Precious J. Lim et al.
JOURNAL OF CELL BIOLOGY (2009)
Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
Jeong-Sun Ju et al.
JOURNAL OF CELL BIOLOGY (2009)
TDP-43 is recruited to stress granules in conditions of oxidative insult
Claudia Colombrita et al.
JOURNAL OF NEUROCHEMISTRY (2009)
ALS-linked P56S-VAPB, an aggregated loss-of-function mutant of VAPB, predisposes motor neurons to ER stress-related death by inducing aggregation of co-expressed wild-type VAPB
Hiroaki Suzuki et al.
JOURNAL OF NEUROCHEMISTRY (2009)
Hereditary Inclusion Body Myopathy-Linked p97/VCP Mutations in the NH2 Domain and the D1 Ring Modulate p97/VCP ATPase Activity and D2 Ring Conformation
Dalia Halawani et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
AUTOPHAGY, LITHIUM, AND AMYOTROPHIC LATERAL SCLEROSIS
Livia Pasquali et al.
MUSCLE & NERVE (2009)
The TBK1 adaptor and autophagy receptor NDP52 restricts the proliferation of ubiquitin-coated bacteria
Teresa L. M. Thurston et al.
NATURE IMMUNOLOGY (2009)
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N. Ticozzi et al.
NEUROLOGY (2009)
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Caroline Vance et al.
SCIENCE (2009)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
The heritability and genetics of frontotemporal lobar degeneration
J. D. Rohrer et al.
NEUROLOGY (2009)
Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Lionel M. Igaz et al.
AMERICAN JOURNAL OF PATHOLOGY (2008)
Autophagy: Basic principles and relevance to disease
Mondira Kundu et al.
ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE (2008)
Altered macroautophagy in the spinal cord of S0D1 mutant mice
Liang Li et al.
AUTOPHAGY (2008)
VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder
Virginia E. Kimonis et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2008)
Profilin, a multi-modal regulator of neuronal plasticity
Andreas Birbach
BIOESSAYS (2008)
The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response
Mattias K. Andersson et al.
BMC CELL BIOLOGY (2008)
ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1
Hideki Nishitoh et al.
GENES & DEVELOPMENT (2008)
VAPB interacts with and modulates the activity of ATF6
Christos Gkogkas et al.
HUMAN MOLECULAR GENETICS (2008)
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
Odity Mukherjee et al.
HUMAN MUTATION (2008)
Anterior horn cells with abnormal TDP-43 immunoreactivities show fragmentation of the Golgi apparatus in ALS
Yukio Fujita et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
New VAPB deletion variant and exclusion of VAPB mutations in familial ALS
J. E. Landers et al.
NEUROLOGY (2008)
A Drosophila Model of ALS: Human ALS-Associated Mutation in VAP33A Suggests a Dominant Negative Mechanism
Anuradha Ratnaparkhi et al.
PLOS ONE (2008)
Adapting proteostasis for disease intervention
William E. Balch et al.
SCIENCE (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
The VAP protein family: from cellular functions to motor neuron disease
Sima Lev et al.
TRENDS IN CELL BIOLOGY (2008)
Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
Nicola J. Rutherford et al.
PLOS GENETICS (2008)
Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases
Jeanne M. M. Tan et al.
HUMAN MOLECULAR GENETICS (2008)
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
G. D. J. Watts et al.
CLINICAL GENETICS (2007)
Increased autophagy in transgenic mice with a G93A mutant SOD1 gene
Nobutoshi Morimoto et al.
BRAIN RESEARCH (2007)
Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates
Eva Teuling et al.
JOURNAL OF NEUROSCIENCE (2007)
Proteomic analysis of membrane-associated proteins from rat liver autophagosomes
Anders Overbye et al.
AUTOPHAGY (2007)
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Nigel J. Cairns et al.
ACTA NEUROPATHOLOGICA (2007)
Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation
Samer Abou Ezzi et al.
JOURNAL OF NEUROCHEMISTRY (2007)
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
Ian R. A. Mackenzie et al.
ANNALS OF NEUROLOGY (2007)
p62 accumulates and enhances aggregate formation in model systems of familial amyotrophic lateral sclerosis
Jozsef Gal et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Proteasome function and protein biosynthesis
Ramunas M. Vabulas
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE (2007)
Phosphorylation inhibits turnover of the tau protein by the proteasome:: influence of RCAN1 and oxidative stress
Diana Poppek et al.
BIOCHEMICAL JOURNAL (2006)
Studies of optineurin, a glaucoma gene - Golgi fragmentation and cell death from overexpression of wild-type and mutant optineurin in two ocular cell types
Bum-Chan Park et al.
AMERICAN JOURNAL OF PATHOLOGY (2006)
Immunoreactivities of p62, an ubiqutin-binding protein, in the spinal anterior horn cells of patients with amyotrophic lateral sclerosis
Yuji Mizuno et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2006)
被撤回的出版物: Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1 (Retracted article. See vol. 292, pg. 12007, 2017)
Julie D. Atkin et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Distribution of Optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States
Michael A. Hauser et al.
JOURNAL OF GLAUCOMA (2006)
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker et al.
NATURE (2006)
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
CC Weihl et al.
HUMAN MOLECULAR GENETICS (2006)
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
Piera Pasinelli et al.
NATURE REVIEWS NEUROSCIENCE (2006)
Structural properties and neuronal toxicity of amyotrophic lateral sclerosis-associated Cu/Zn superoxide dismutase 1 aggregates
G Matsumoto et al.
JOURNAL OF CELL BIOLOGY (2005)
Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis
DA Sahlender et al.
JOURNAL OF CELL BIOLOGY (2005)
Accumulation of human SOD1 and ubiquitinated deposits in the spinal cord of SOD1G93A mice during motor neuron disease progression correlates with a decrease of proteasome
C Cheroni et al.
NEUROBIOLOGY OF DISEASE (2005)
Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis
BJ Turner et al.
JOURNAL OF NEUROSCIENCE (2005)
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
GDJ Watts et al.
NATURE GENETICS (2004)
Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice
D Kieran et al.
NATURE MEDICINE (2004)
NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1
K Miyazaki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Benefit of valproic acid in suppressing disease progression of ALS model mice
F Sugai et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70
M Urushitani et al.
JOURNAL OF NEUROCHEMISTRY (2004)
A novel role for polyamines in adult neurogenesis in rodent brain
J Malaterre et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
Polyamines increase in sympathetic neurons and now neuronal cells after axotomy and enhance neurite outgrowth in nerve growth factor-primed PC12 cells
RC Schreiber et al.
NEUROSCIENCE (2004)
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
AL Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Domain Architectures and characterization of an RNA-binding protein, TLS
Y Iko et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes
PM Andersen et al.
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2003)
Triggering the interferon antiviral response through an IKK-related pathway
S Sharma et al.
SCIENCE (2003)
Proteasome inhibition by paired helical filament-tau in brains of patients with Alzheimer's disease
S Keck et al.
JOURNAL OF NEUROCHEMISTRY (2003)
Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways
S Allen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Aggregate formation in the spinal cord of mutant SOD1 transgenic mice is reversible and mediated by proteasomes
K Puttaparthi et al.
JOURNAL OF NEUROCHEMISTRY (2003)
Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis
M Urushitani et al.
JOURNAL OF NEUROCHEMISTRY (2002)
Proteasomal degradation of tau protein
DC David et al.
JOURNAL OF NEUROCHEMISTRY (2002)
Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity
J Niwa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Amyotrophic lateral sclerosis: A proposed mechanism
A Okado-Matsumoto et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
The ubiquitin-proteasome proteolytic pathway: Destruction for the sake of construction
MH Glickman et al.
PHYSIOLOGICAL REVIEWS (2002)
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
T Rezaie et al.
SCIENCE (2002)
Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)
DS Howland et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation
E Rabinovich et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Pharmacological and therapeutic properties of valproate - A summary after 35 years of clinical experience
E Perucca
CNS DRUGS (2002)
High molecular weight complexes of mutant superoxide dismutase 1: Age-dependent and tissue-specific accumulation
J Wang et al.
NEUROBIOLOGY OF DISEASE (2002)
Mutations of tau protein in frontotemporal dementia promote aggregation of paired helical filaments by enhancing local β-structure
M von Bergen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol
YH Ye et al.
NATURE (2001)
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
MJ Kovach et al.
MOLECULAR GENETICS AND METABOLISM (2001)
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22
SM Rosso et al.
BRAIN (2001)
Mutant Cu/Zn-superoxide dismutase proteins have altered solubility and interact with heat shock/stress proteins in models of amyotrophic lateral sclerosis
GA Shinder et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Profilin I is essential for cell survival and cell division in early mouse development
W Witke et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Formation of high molecular weight complexes of mutant Cu,Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis
JA Johnston et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Impaired proteasome function in Alzheimer's disease
JN Keller et al.
JOURNAL OF NEUROCHEMISTRY (2000)