Cargando…

ERRATUM: FUS-regulated region- and cell-type-specific transcriptome is associated with cell selectivity in ALS/FTLD

Detalles Bibliográficos
Autores principales:	Fujioka, Yusuke, Ishigaki, Shinsuke, Masuda, Akio, Iguchi, Yohei, Udagawa, Tsuyoshi, Watanabe, Hirohisa, Katsuno, Masahisa, Ohno, Kinji, Sobue, Gen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2013
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3837360/ http://dx.doi.org/10.1038/srep03300

Ejemplares similares

FUS-regulated region- and cell-type-specific transcriptome is associated with cell selectivity in ALS/FTLD
por: Fujioka, Yusuke, et al.
Publicado: (2013)

The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons()
por: Honda, Daiyu, et al.
Publicado: (2013)

Corrigendum to “The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons” [FEBS Open Bio 4 (2014) 1–10]
por: Honda, Daiyu, et al.
Publicado: (2014)

ERRATUM: Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions
por: Ishigaki, Shinsuke, et al.
Publicado: (2013)

Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions
por: Ishigaki, Shinsuke, et al.
Publicado: (2012)

FUS regulates AMPA receptor function and FTLD/ALS-associated behaviour via GluA1 mRNA stabilization
por: Udagawa, Tsuyoshi, et al.
Publicado: (2015)

Importance of Functional Loss of FUS in FTLD/ALS
por: Ishigaki, Shinsuke, et al.
Publicado: (2018)

Position-specific binding of FUS to nascent RNA regulates mRNA length
por: Masuda, Akio, et al.
Publicado: (2015)

RNP2 of RNA Recognition Motif 1 Plays a Central Role in the Aberrant Modification of TDP-43
por: Takagi, Shinnosuke, et al.
Publicado: (2013)

The FUS about SFPQ in FTLD spectrum disorders
por: Patani, Rickie
Publicado: (2020)

Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration
por: Riku, Yuichi, et al.
Publicado: (2021)

Abl kinase-mediated FUS Tyr526 phosphorylation alters nucleocytoplasmic FUS localization in FTLD-FUS
por: Motaln, Helena, et al.
Publicado: (2023)

Disruption of Axonal Transport in Motor Neuron Diseases
por: Ikenaka, Kensuke, et al.
Publicado: (2012)

TDP-43 Proteinopathy and Tauopathy: Do They Have Pathomechanistic Links?
por: Riku, Yuichi, et al.
Publicado: (2022)

The SYNGAP1 3′UTR Variant in ALS Patients Causes Aberrant SYNGAP1 Splicing and Dendritic Spine Loss by Recruiting HNRNPK
por: Yokoi, Satoshi, et al.
Publicado: (2022)

Pathogenesis of Frontotemporal Lobar Degeneration: Insights From Loss of Function Theory and Early Involvement of the Caudate Nucleus
por: Sobue, Gen, et al.
Publicado: (2018)

Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS
por: Gittings, Lauren M., et al.
Publicado: (2019)

FUS/TLS acts as an aggregation-dependent modifier of polyglutamine disease model mice
por: Kino, Yoshihiro, et al.
Publicado: (2016)

Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U
por: Lee, Edward B, et al.
Publicado: (2013)

c-Abl Inhibition Delays Motor Neuron Degeneration in the G93A Mouse, an Animal Model of Amyotrophic Lateral Sclerosis
por: Katsumata, Ryu, et al.
Publicado: (2012)

Erratum to: Endogenous TDP-43, but not FUS, contributes to stress granule assembly via G3BP
por: Aulas, Anaïs, et al.
Publicado: (2015)

R-spondin 2 promotes acetylcholine receptor clustering at the neuromuscular junction via Lgr5
por: Nakashima, Hiroaki, et al.
Publicado: (2016)

A unified mechanism for LLPS of ALS/FTLD-causing FUS as well as its modulation by ATP and oligonucleic acids
por: Kang, Jian, et al.
Publicado: (2019)

The principal PINK1 and Parkin cellular events triggered in response to dissipation of mitochondrial membrane potential occur in primary neurons
por: Koyano, Fumika, et al.
Publicado: (2013)

Visuoperceptual disturbances in Parkinson's disease
por: Kawabata, Kazuya, et al.
Publicado: (2020)

Connectivity impairment of cerebellar and sensorimotor connector hubs in Parkinson’s disease
por: Bagarinao, Epifanio, et al.
Publicado: (2022)

In vitro and in silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5′ splice sites
por: Sahashi, Kentaro, et al.
Publicado: (2007)

NPM-hMLF1 fusion protein suppresses defects of a Drosophila FTLD model expressing the human FUS gene
por: Yamamoto, Itaru, et al.
Publicado: (2018)

Neuropathology and Therapeutic Intervention in Spinal and Bulbar Muscular Atrophy
por: Banno, Haruhiko, et al.
Publicado: (2009)

Monomerization of TDP-43 is a key determinant for inducing TDP-43 pathology in amyotrophic lateral sclerosis
por: Oiwa, Kotaro, et al.
Publicado: (2023)

Preclinical progression of neurodegenerative diseases
por: Katsuno, Masahisa, et al.
Publicado: (2018)

Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment
por: Koike, Haruki, et al.
Publicado: (2021)

Neutrophil extracellular traps: from antimicrobial innate immunity to the development of chemotherapy-induced peripheral neuropathy
por: Koike, Haruki, et al.
Publicado: (2023)

Involvement of the Precuneus/Posterior Cingulate Cortex Is Significant for the Development of Alzheimer’s Disease: A PET (THK5351, PiB) and Resting fMRI Study
por: Yokoi, Takamasa, et al.
Publicado: (2018)

Detecting clinical change with the CDR‐FTLD: differences between FTLD and AD dementia
por: Mioshi, Eneida, et al.
Publicado: (2016)

Acute Unilateral Isolated Oculomotor Nerve Palsy in an Adult Patient with Influenza A
por: Senda, Joe, et al.
Publicado: (2018)

Clinical and Imaging Features of Multiple System Atrophy: Challenges for an Early and Clinically Definitive Diagnosis
por: Watanabe, Hirohisa, et al.
Publicado: (2018)

Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen
por: Hamada, Shinsuke, et al.
Publicado: (2015)

dnc-1/dynactin 1 Knockdown Disrupts Transport of Autophagosomes and Induces Motor Neuron Degeneration
por: Ikenaka, Kensuke, et al.
Publicado: (2013)

A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics
por: Nicolas, Gaël, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_6j91hi97u7i2hvfocij25lnqrt