4.8 Article

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

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Clinical Neurology

Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis

Brian C. Kraemer et al.

ACTA NEUROPATHOLOGICA (2010)

Article Biochemistry & Molecular Biology

Neurotoxic effects of TDP-43 overexpression in C-elegans

Peter E. A. Ash et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

TDP-43 Is a Developmentally Regulated Protein Essential for Early Embryonic Development

Chantelle F. Sephton et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Article Biochemistry & Molecular Biology

SF2/ASF autoregulation involves multiple layers of post-transcriptional and translational control

Shuying Sun et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2010)

Article Multidisciplinary Sciences

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

Shuo-Chien Ling et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Multidisciplinary Sciences

A Drosophila model for TDP-43 proteinopathy

Yan Li et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Multidisciplinary Sciences

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

Hans Wils et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Clinical Neurology

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

Michael A. Gitcho et al.

ACTA NEUROPATHOLOGICA (2009)

Article Biochemistry & Molecular Biology

Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior

Fabian Feiguin et al.

FEBS LETTERS (2009)

Review Biochemistry & Molecular Biology

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

G. Scott Pesiridis et al.

HUMAN MOLECULAR GENETICS (2009)

Article Biochemistry & Molecular Biology

Auto- and Cross-Regulation of the hnRNP L Proteins by Alternative Splicing

Oliver Rossbach et al.

MOLECULAR AND CELLULAR BIOLOGY (2009)

Article Biochemistry & Molecular Biology

An integrated workflow for charting the human interaction proteome: insights into the PP2A system

Timo Glatter et al.

MOLECULAR SYSTEMS BIOLOGY (2009)

Article Biochemistry & Molecular Biology

Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo

Andrea D'Ambrogio et al.

NUCLEIC ACIDS RESEARCH (2009)

Article Biochemistry & Molecular Biology

Structural insights into TDP-43 in nucleic-acid binding and domain interactions

Pan-Hsien Kuo et al.

NUCLEIC ACIDS RESEARCH (2009)

Article Multidisciplinary Sciences

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

Iga Wegorzewska et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Biochemistry & Molecular Biology

Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease

Emanuele Buratti et al.

FRONTIERS IN BIOSCIENCE-LANDMARK (2008)

Article Clinical Neurology

Concomitant TAR-DNA-binding in Alzheimer disease and protein 43 pathology is present corticobasal degeneration but not in other tauopathies

Kunihiro Uryu et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2008)

Article Biochemistry & Molecular Biology

Regulation of multiple core spliceosomal proteins by alternative splicing-coupled nonsense-mediated mRNA decay

Arneet L. Saltzman et al.

MOLECULAR AND CELLULAR BIOLOGY (2008)

Article Genetics & Heredity

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi et al.

NATURE GENETICS (2008)

Article Clinical Neurology

Pathological TDP-43 in parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam

Felix Geser et al.

ACTA NEUROPATHOLOGICA (2008)

Article Clinical Neurology

Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

Hanae Nakashima-Yasuda et al.

ACTA NEUROPATHOLOGICA (2007)

Article Clinical Neurology

TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

Catalina Amador-Ortiz et al.

ANNALS OF NEUROLOGY (2007)

Article Clinical Neurology

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations

Manuela Neumann et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)

Article Biochemistry & Molecular Biology

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)

Article Multidisciplinary Sciences

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Manuela Neumann et al.

SCIENCE (2006)

Article Biochemistry & Molecular Biology

Human, Drosophila, and C-elegans TDP43:: Nucleic acid binding properties and splicing regulatory function

YM Ayala et al.

JOURNAL OF MOLECULAR BIOLOGY (2005)

Article Biochemistry & Molecular Biology

A protein interaction framework for human mRNA degradation

B Lehner et al.

GENOME RESEARCH (2004)

Review Cell Biology

The yin and yang of the exosome

JS Butler

TRENDS IN CELL BIOLOGY (2002)

Article Biochemistry & Molecular Biology

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

E Buratti et al.

EMBO JOURNAL (2001)

Article Biochemistry & Molecular Biology

SC35 autoregulates its expression by promoting splicing events that destabilize its mRNAs

A Sureau et al.

EMBO JOURNAL (2001)