相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Are the UK genetic testing criteria for dementia too exclusive?
Annita Christodoulidou et al.
JOURNAL OF NEUROLOGY (2021)
Sustained Expression of TDP-43 and FUS in Motor Neurons in Rodent's Lifetime
Cao Huang et al.
International Journal of Biological Sciences (2012)
Distinct pathological subtypes of FTLD-FUS
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease
Richard A. Armstrong et al.
ACTA NEUROPATHOLOGICA (2011)
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
Hazel Urwin et al.
ACTA NEUROPATHOLOGICA (2010)
Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology
Clement T. Loy et al.
BRAIN (2010)
TDP-43 Redistribution is an Early Event in Sporadic Amyotrophic Lateral Sclerosis
Maria Teresa Giordana et al.
BRAIN PATHOLOGY (2010)
Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein
Shu Yang et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2010)
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
FUS pathology in basophilic inclusion body disease
David G. Munoz et al.
ACTA NEUROPATHOLOGICA (2009)
A new subtype of frontotemporal lobar degeneration with FUS pathology
Manuela Neumann et al.
BRAIN (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)
TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
Sigrun Roeber et al.
ACTA NEUROPATHOLOGICA (2008)
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
Fumiaki Mori et al.
ACTA NEUROPATHOLOGICA (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)
Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
Emanuele Buratti et al.
FRONTIERS IN BIOSCIENCE-LANDMARK (2008)
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)
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
Yvonne Davidson et al.
ACTA NEUROPATHOLOGICA (2007)
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Tetsuaki Arai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker et al.
NATURE (2006)
Delocalization of the multifunctional RNA splicing factor TLS/FUS in hippocampal neurones: exclusion from the nucleus and accumulation in dendritic granules and spine heads
A Belly et al.
NEUROSCIENCE LETTERS (2005)
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
KA Josephs et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)
Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy
DC Paviour et al.
BRAIN (2004)
α-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease
NJ Cairns et al.
AMERICAN JOURNAL OF PATHOLOGY (2004)
Neurofilament inclusion body disease: a new proteinopathy?
KA Josephs et al.
BRAIN (2003)
Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia
JL Holton et al.
AMERICAN JOURNAL OF PATHOLOGY (2001)