Related references
Note: Only part of the references are listed.Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
Heather Stewart et al.
ACTA NEUROPATHOLOGICA (2012)
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
Julie S. Snowden et al.
BRAIN (2012)
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
Javier Simon-Sanchez et al.
BRAIN (2012)
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
Ilse Gijselinck et al.
LANCET NEUROLOGY (2012)
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
Safa Al-Sarraj et al.
ACTA NEUROPATHOLOGICA (2011)
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
Melissa E. Murray et al.
ACTA NEUROPATHOLOGICA (2011)
A harmonized classification system for FTLD-TDP pathology
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Katya Rascovsky et al.
BRAIN (2011)
Ubiquilin-1 Is a Molecular Chaperone for the Amyloid Precursor Protein
Emily S. Stieren et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
Adam L. Boxer et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Amyotrophic lateral sclerosis
Matthew C. Kiernan et al.
LANCET (2011)
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Han-Xiang Deng et al.
NATURE (2011)
Classification of primary progressive aphasia and its variants
M. L. Gorno-Tempini et al.
NEUROLOGY (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)
Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP-43 proteinopathies but are only rarely additionally immunopositive for phosphorylation-dependent TDP-43
Andrew King et al.
NEUROPATHOLOGY (2011)
Alzheimer's Disease-Associated Ubiquilin-1 Regulates Presenilin-1 Accumulation and Aggresome Formation
Jayashree Viswanathan et al.
TRAFFIC (2011)
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2010)
Pathological 43-kDa Transactivation Response DNA-Binding Protein in Older Adults With and Without Severe Mental Illness
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2010)
Ubiquilin at a crossroads in protein degradation pathways
Cara Rothenberg et al.
AUTOPHAGY (2010)
Ubiquilin functions in autophagy and is degraded by chaperone-mediated autophagy
Cara Rothenberg et al.
HUMAN MOLECULAR GENETICS (2010)
Genetic contribution of FUS to frontotemporal lobar degeneration
T. Van Langenhove et al.
NEUROLOGY (2010)
Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: A spectrum of TDP-43 proteinopathies
Felix Geser et al.
NEUROPATHOLOGY (2010)
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
Clinical and Pathological Continuum of Multisystem TDP-43 Proteinopathies
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2009)
PLIC proteins or ubiquilins regulate autophagy-dependent cell survival during nutrient starvation
Elsa-Noah N'Diaye et al.
EMBO REPORTS (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)
Ubiquilin and p97/VCP bind erasin, forming a complex involved in ERAD
Precious J. Lim et al.
JOURNAL OF CELL BIOLOGY (2009)
No Evidence for Cognitive Dysfunction or Depression in Patients with Mild Restless Legs Syndrome
Erika Driver-Dunckley et al.
MOVEMENT DISORDERS (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)
Concomitant TAR-DNA-binding in Alzheimer disease and protein 43 pathology is present corticobasal degeneration but not in other tauopathies
Kunihiro Uryu et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2008)
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi et al.
NATURE GENETICS (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
Nicola J. Rutherford et al.
PLOS GENETICS (2008)
Ubiquilin interacts and enhances the degradation of expanded-polyglutamine proteins
Hongmin Wang et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Ubiquilin overexpression reduces GFP-polyalanine-induced protein aggregates and toxicity
Hongmin Wang et al.
EXPERIMENTAL CELL RESEARCH (2007)
Screening for frontotemporal dementias and Alzheimer's disease with the Philadelphia brief assessment of cognition: A preliminary analysis
David J. Libon et al.
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS (2007)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Suppression of polyglutamine-induced toxicity in cell and animal models of Huntington's disease by ubiquilin
H Wang et al.
HUMAN MOLECULAR GENETICS (2006)
Signaling, polyubiquitination, trafficking, and inclusions: Sequestosome 1/p62's role in neurodegenerative disease
Marie W. Wooten et al.
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY (2006)
Ubiquilin regulates presenilin endoproteolysis and modulates γ-secretase components, Pen-2 and nicastrin
LK Massey et al.
BIOCHEMICAL JOURNAL (2005)
Delivery of ubiquitinated substrates to protein-unfolding machines
S Elsasser et al.
NATURE CELL BIOLOGY (2005)
Family-based association between Alzheimer's disease and variants in UBQLN1
L Bertram et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)
Identification of ubiquitin-interacting proteins in purified polyglutamine aggregates
H Doi et al.
FEBS LETTERS (2004)
Ubiquilin interacts with ubiquitylated proteins and proteasome through its ubiquitin-associated and ubiquitin-like domains
HS Ko et al.
FEBS LETTERS (2004)
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study
SM Rosso et al.
BRAIN (2003)
El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
BR Brooks et al.
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2000)
Identification of ubiquilin, a novel presenilin interactor that increases presenilin protein accumulation
AL Mah et al.
JOURNAL OF CELL BIOLOGY (2000)
The hPLIC proteins may provide a link between the ubiquitination machinery and the proteasome
MF Kleijnen et al.
MOLECULAR CELL (2000)
Molecular cloning, chromosome mapping and characterization of UBQLN3 a testis-specific gene that contains an ubiquitin-like domain
D Conklin et al.
GENE (2000)