Related references
Note: Only part of the references are listed.Phosphorylated NF-κB subunit p65 aggregates in granulovacuolar degeneration and neurites in neurodegenerative diseases with tauopathy
Yuko Ydmaguchi et al.
NEUROSCIENCE LETTERS (2019)
Review: Neuropathology of non-tau frontotemporal lobar degeneration
M. Neumann et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2019)
Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations
Takashi Ayaki et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2018)
OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes
Orly Goldstein et al.
NEUROLOGY (2016)
RIPK1 mediates axonal degeneration by promoting inflammation and necroptosis in ALS
Yasushi Ito et al.
SCIENCE (2016)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli et al.
SCIENCE (2015)
Autophagosome Biogenesis in Primary Neurons Follows an Ordered and Spatially Regulated Pathway
Sandra Maday et al.
DEVELOPMENTAL CELL (2014)
Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation
Masaki Kamada et al.
NEUROPATHOLOGY (2014)
Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation
Yvette C. Wong et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Optineurin and amyotrophic lateral sclerosis
Hirofumi Maruyama et al.
GERIATRICS & GERONTOLOGY INTERNATIONAL (2013)
The changing scene of amyotrophic lateral sclerosis
Wim Robberecht et al.
NATURE REVIEWS NEUROSCIENCE (2013)
Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons
Sandra Maday et al.
JOURNAL OF CELL BIOLOGY (2012)
NIH Image to ImageJ: 25 years of image analysis
Caroline A. Schneider et al.
NATURE METHODS (2012)
Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese
Aritoshi Iida et al.
NEUROBIOLOGY OF AGING (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)
Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation
Hidefumi Ito et al.
ACTA NEUROPATHOLOGICA (2011)
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis
R. Del Bo et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (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)
Granulovacuolar Degenerations Appear in Relation to Hippocampal Phosphorylated Tau Accumulation in Various Neurodegenerative Disorders
Yuu Yamazaki et al.
PLOS ONE (2011)
Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth
Philipp Wild et al.
SCIENCE (2011)
Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations
Hazel Urwin et al.
HUMAN MOLECULAR GENETICS (2010)
Mutations of optineurin in amyotrophic lateral sclerosis
Hirofumi Maruyama et al.
NATURE (2010)
Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus
Yuu Yamazaki et al.
NEUROSCIENCE LETTERS (2010)
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)
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)
Optineurin negatively regulates TNFα-induced NF-κB activation by competing with NEMO for ubiquitinated RIP
Guozhi Zhu et al.
CURRENT BIOLOGY (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)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Share Paper
