4.7 Article

Aggregation of the 35-kDa fragment of TDP-43 causes formation of cytoplasmic inclusions and alteration of RNA processing

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

Edor Kabashi et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

Characterization of Alternative Isoforms and Inclusion Body of the TAR DNA-binding Protein-43

Yoshinori Nishimoto et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Review Clinical Neurology

The evidence for altered RNA metabolism in amyotrophic lateral sclerosis (ALS)

Michael J. Strong

JOURNAL OF THE NEUROLOGICAL SCIENCES (2010)

Review Biochemistry & Molecular Biology

Rethinking ALS: The FUS about TDP-43

Clotilde Lagier-Tourenne et al.

Article Biochemistry & Molecular Biology

Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43

Takashi Nonaka et al.

HUMAN MOLECULAR GENETICS (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

Expression of TDP-43 C-terminal Fragments in Vitro Recapitulates Pathological Features of TDP-43 Proteinopathies

Lionel M. Igaz et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2009)

Article Biochemistry & Molecular Biology

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)

Article Biochemistry & Molecular Biology

TDP-43 is recruited to stress granules in conditions of oxidative insult

Claudia Colombrita et al.

JOURNAL OF NEUROCHEMISTRY (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 Multidisciplinary Sciences

Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity

Yong-Jie Zhang et al.

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

Article Genetics & Heredity

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

H. Daoud et al.

JOURNAL OF MEDICAL GENETICS (2009)

Review Clinical Neurology

ALS and FTLD: two faces of TDP-43 proteinopathy

R. M. Liscic et al.

EUROPEAN JOURNAL OF NEUROLOGY (2008)

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 Biochemistry & Molecular Biology

TDP-43 Overexpression Enhances Exon 7 Inclusion during the Survival of Motor Neuron Pre-mRNA Splicing

Jayarama Krishnan Bose et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Cell Biology

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

Youhna M. Ayala et al.

JOURNAL OF CELL SCIENCE (2008)

Article Genetics & Heredity

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi et al.

NATURE GENETICS (2008)

Article Multidisciplinary Sciences

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Jemeen Sreedharan et al.

SCIENCE (2008)

Review Biochemistry & Molecular Biology

TDP-43: an emerging new player in neurodegenerative diseases

I-Fan Wang et al.

TRENDS IN MOLECULAR MEDICINE (2008)

Article Genetics & Heredity

Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

Nicola J. Rutherford et al.

PLOS GENETICS (2008)

Article Neurosciences

Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43

Yong-Jie Zhang et al.

JOURNAL OF NEUROSCIENCE (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

A double reporter assay for detecting changes in the ratio of spliced and unspliced mRNA in mammalian cells

MT Nasim et al.

NUCLEIC ACIDS RESEARCH (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)