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TDP-43 stabilises the processing intermediates of mitochondrial transcripts

author

Harunori Yoshikawa

Haruhisa Inoue

Richard Simpson

published in: Scientific Reports

date of publication: 2017-08-09

language: English

Cites articles 42

Date

Title

Authors

2016-09-28

Chtop (Chromatin target of Prmt1) auto-regulates its expression level via intron retention and nonsense-mediated decay of its own mRNA

Harunori Yoshikawa, Richard Simpson
2016-08-04

Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly

Oliver Rackham, Stefan Siira, Ilian Atanassov, Tara Richman, James Bruce Stewart, Arnaud Mourier, Aleksandra Filipovska
2016-06-27

The inhibition of TDP-43 mitochondrial localization blocks its neuronal toxicity

Wenzhang Wang, Junjie Lu, Edroaldo Lummertz da Rocha, Sandra L Siedlak
2016-01-13

Interaction of RNA with a C-terminal fragment of the amyotrophic lateral sclerosis-associated TDP43 reduces cytotoxicity

Akira Kitamura, Masataka Kinjo
2014-06-03

ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43.

Kurt J De Vos, Dennis W. Dickson, Kwok-Fai Lau, Christopher Shaw, Leonard Petrucelli
2014-03-03

Disease causing mutants of TDP-43 nucleic acid binding domains are resistant to aggregation and have increased stability and half-life

James A Austin, Gareth S A Wright, Seiji Watanabe, Svetlana Antonyuk, Koji Yamanaka
2014

Friend of Prmt1, FOP is a Novel Component of the Nuclear SMN Complex Isolated Using Biotin Affinity Purification
2013-12

Molecular basis of UG-rich RNA recognition by the human splicing factor TDP-43

Cristiana Stuani, Frédéric H-T Allain, Fred F. Damberger, Jernej Ule, Emanuele Buratti
2013-10-23

Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models

Jordi Magranè
2013-08-08

ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy

Thomas Meitinger, Thomas J Nicholls, Joanna Rorbach, Enrico Baruffini, Michał Mińczuk, Johannes A Mayr, Holger Prokisch, Robert William Taylor, Tobias B Haack, Katharina Danhauser, Thomas Wieland, Tim M Strom, Peter Freisinger, Robert Kopajtich, Ileana Ferrero, Ralf A. Husain, Jessica Schum
2013-07-04

The ALS disease-associated mutant TDP-43 impairs mitochondrial dynamics and function in motor neurons

Dennis W. Dickson, Wenzhang Wang, Xinglong Wang, Leonard Petrucelli
2013-12-05

Identification of truncated forms of U1 snRNA reveals a novel RNA degradation pathway during snRNP biogenesis

Harunori Yoshikawa, Masato Taoka
2012-10-09

Full-length TDP-43 and its C-terminal fragments activate mitophagy in NSC34 cell line
2012-12-12

Accelerated disease onset with stabilized familial amyotrophic lateral sclerosis (ALS)-linked mutant TDP-43 proteins

Koji Yamanaka
2011-09-01

RNA processing in human mitochondria

Oliver Rackham, John S. Mattick, Aleksandra Filipovska
2011-02-27

Characterizing the RNA targets and position-dependent splicing regulation by TDP-43

Jernej Ule, Tomaž Curk, Boris Rogelj, Matteo Cereda, Julian König, Agnes Lumi Nishimura, Rickie Patani, Blaž Zupan, Christopher Shaw
2011-04-06

Neurotoxic 43-kDa TAR DNA-binding protein (TDP-43) triggers mitochondrion-dependent programmed cell death in yeast

Ralf J. Braun, Didac Carmona-Gutierrez
2010-12-03

TDP-43 regulates its mRNA levels through a negative feedback loop

Ashish Dhir, Maurizio Romano, Jernej Ule, Emanuele Buratti
2010-12-03

TDP-43-based animal models of neurodegeneration: new insights into ALS pathology and pathophysiology

Robert H Baloh
2010-12-01

Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy
2010-08-24

Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice

Po-Min Chiang
2010-08-01

Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

Dennis W. Dickson, Leonard Petrucelli, Rosa Rademakers
2010-07-12

ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS.

Clotilde Lagier-Tourenne, Don W. Cleveland
2010-04-15

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

Clotilde Lagier-Tourenne
2010-03-16

TAR DNA-binding protein 43 in neurodegenerative disease

John Q. Trojanowski
2010-01-26

A Drosophila model for TDP-43 proteinopathy
2010-02-03

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

Samir Kumar-Singh, Christine Van Broeckhoven, Gernot Kleinberger
2009-10-01

Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis

John Q. Trojanowski
2009-03-06

Ariadne: a database search engine for identification and chemical analysis of RNA using tandem mass spectrometry data

Masato Taoka
2009-02-17

Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression

Dennis W. Dickson
2009-11-01

An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes

Masato Taoka
2008-10-28

Structural determinants of the cellular localization and shuttling of TDP-43.

Emanuele Buratti, Leonard Petrucelli

Article - wd:Q41332015

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