Related references
Note: Only part of the references are listed.Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2010)
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Dorothee Dormann et al.
EMBO JOURNAL (2010)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier-Tourenne et al.
HUMAN MOLECULAR GENETICS (2010)
Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein
Shu Yang et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2010)
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
Ian R. A. Mackenzie et al.
LANCET NEUROLOGY (2010)
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2009)
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 TET Family of Proteins: Functions and Roles in Disease
Adelene Y. Tan et al.
JOURNAL OF MOLECULAR CELL BIOLOGY (2009)
TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
Sigrun Roeber 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)
TDP-43: an emerging new player in neurodegenerative diseases
I-Fan Wang et al.
TRENDS IN MOLECULAR MEDICINE (2008)
Aberrant localization of importin α1 in hippocampal neurons in Alzheimer disease
Hyoung-gon Lee et al.
BRAIN RESEARCH (2006)
Rules for nuclear localization sequence recognition by karyopherinβ2
Brittany J. Lee et al.
CELL (2006)
TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines
R Fujii et al.
JOURNAL OF CELL SCIENCE (2005)
The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology
R Fujii et al.
CURRENT BIOLOGY (2005)
Transportins 1 and 2 are redundant nuclear import factors for hnRNP A1 and HuR
A Rebane et al.
RNA (2004)
Translocated in liposarcoma (TLS) is a substrate for fibroblast growth factor receptor-1
P Klint et al.
CELLULAR SIGNALLING (2004)
Nucleocytoplasmic shuttling of signal transducers
L Xu et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2004)
Neurofilament inclusion body disease: a new proteinopathy?
KA Josephs et al.
BRAIN (2003)
Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode
J Rappsilber et al.
ANALYTICAL CHEMISTRY (2003)
Regulating access to the genome: Nucleocytoplasmic transport throughout the cell cycle
K Weis
CELL (2003)
Transport into and out of the nucleus
IG Macara
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS (2001)