Related references
Note: Only part of the references are listed.Autophagy in Neurodegenerative Diseases: From Mechanism to Therapeutic Approach
Jihoon Nah et al.
MOLECULES AND CELLS (2015)
Novelmutations support a role for Profilin 1 in the pathogenesis of ALS
Bradley N. Smith et al.
NEUROBIOLOGY OF AGING (2015)
Structural basis for mutation-induced destabilization of profilin 1 in ALS
Sivakumar Boopathy et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Distinct pathways leading to TDP-43-induced cellular dysfunctions
Makiko Yamashita et al.
HUMAN MOLECULAR GENETICS (2014)
Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis
Pietro Fratta et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2014)
Profilin 1 Associates with Stress Granules and ALS-Linked Mutations Alter Stress Granule Dynamics
Matthew D. Figley et al.
JOURNAL OF NEUROSCIENCE (2014)
The ubiquitin-proteasome system in neurodegenerative diseases: precipitating factor, yet part of the solution
Nico P. Dantuma et al.
Frontiers in Molecular Neuroscience (2014)
Spliceosome integrity is defective in the motor neuron diseases ALS and SMA
Hitomi Tsuiji et al.
EMBO MOLECULAR MEDICINE (2013)
Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis
Tomohiko Ishihara et al.
HUMAN MOLECULAR GENETICS (2013)
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia
Cinzia Tiloca et al.
NEUROBIOLOGY OF AGING (2013)
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
Lubina Dillen et al.
NEUROBIOLOGY OF AGING (2013)
Prion-like Properties of Pathological TDP-43 Aggregates from Diseased Brains
Takashi Nonaka et al.
CELL REPORTS (2013)
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia
Marka van Blitterswijk et al.
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)
Co-aggregation of RNA binding proteins in ALS spinal motor neurons: evidence of a common pathogenic mechanism
Brian A. Keller et al.
ACTA NEUROPATHOLOGICA (2012)
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Chi-Hong Wu et al.
NATURE (2012)
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
Edward B. Lee et al.
NATURE REVIEWS NEUROSCIENCE (2012)
Molecular Dissection of TDP-43 Proteinopathies
Masato Hasegawa et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2011)
An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity
Weirui Guo et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biology
Stuart J. Rabin et al.
HUMAN MOLECULAR GENETICS (2010)
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy
Tetsuaki Arai et al.
NEUROPATHOLOGY (2010)
The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation
Emanuele Buratti et al.
RNA BIOLOGY (2010)
A Cellular Model To Monitor Proteasome Dysfunction by α-Synuclein
Takashi Nonaka et al.
BIOCHEMISTRY (2009)
Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells
Takashi Nonaka et al.
FEBS LETTERS (2009)
Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43
Takashi Nonaka et al.
HUMAN MOLECULAR GENETICS (2009)
TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
Brian S. Johnson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Masato Hasegawa et al.
ANNALS OF NEUROLOGY (2008)
Abnormal phosphorylation of ser409/410 of TDP-43 in FTLD-U and ALS
Yuki Inukai et al.
FEBS LETTERS (2008)
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry
Maria Pikkarainen et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (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)
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)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
The role of profilin complexes in cell motility and other cellular processes
W Witke
TRENDS IN CELL BIOLOGY (2004)
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)
Share Paper
