4.7 Article

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

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。
Letter Clinical Neurology

Are the UK genetic testing criteria for dementia too exclusive?

Annita Christodoulidou et al.

JOURNAL OF NEUROLOGY (2021)

Article Biochemistry & Molecular Biology

Sustained Expression of TDP-43 and FUS in Motor Neurons in Rodent's Lifetime

Cao Huang et al.

International Journal of Biological Sciences (2012)

Article Clinical Neurology

Distinct pathological subtypes of FTLD-FUS

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2011)

Article Clinical Neurology

TDP-43 Redistribution is an Early Event in Sporadic Amyotrophic Lateral Sclerosis

Maria Teresa Giordana et al.

BRAIN PATHOLOGY (2010)

Article Biochemistry & Molecular Biology

Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein

Shu Yang et al.

INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2010)

Article Clinical Neurology

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

Manuela Neumann et al.

ACTA NEUROPATHOLOGICA (2009)

Article Clinical Neurology

FUS pathology in basophilic inclusion body disease

David G. Munoz et al.

ACTA NEUROPATHOLOGICA (2009)

Article Clinical Neurology

A new subtype of frontotemporal lobar degeneration with FUS pathology

Manuela Neumann et al.

Article Multidisciplinary Sciences

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

T. J. Kwiatkowski et al.

SCIENCE (2009)

Article Clinical Neurology

The heritability and genetics of frontotemporal lobar degeneration

J. D. Rohrer et al.

NEUROLOGY (2009)

Article Clinical Neurology

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

Sigrun Roeber et al.

ACTA NEUROPATHOLOGICA (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 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 Clinical Neurology

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

KA Josephs et al.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)

Article Clinical Neurology

Neurofilament inclusion body disease: a new proteinopathy?

KA Josephs et al.