4.7 Article

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

Related references

Note: Only part of the references are listed.
Article Clinical Neurology

Distinct pathological subtypes of FTLD-FUS

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2011)

Article Genetics & Heredity

Mutational Analysis Reveals the FUS Homolog TAF15 as a Candidate Gene for Familial Amyotrophic Lateral Sclerosis

N. Ticozzi et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2011)

Article Clinical Neurology

Nuclear Transport Impairment of Amyotrophic Lateral Sclerosis-Linked Mutations in FUS/TLS

Daisuke Ito et al.

ANNALS OF NEUROLOGY (2011)

Review Neurosciences

TDP-43 and FUS: a nuclear affair

Dorothee Dormann et al.

TRENDS IN NEUROSCIENCES (2011)

Editorial Material Clinical Neurology

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2010)

Article Clinical Neurology

FUS Mutations in Familial Amyotrophic Lateral Sclerosis in the Netherlands

Ewout J. N. Groen et al.

ARCHIVES OF NEUROLOGY (2010)

Article Clinical Neurology

FUS-Immunoreactive Intranuclear Inclusions in Neurodegenerative Disease

John Woulfe et al.

BRAIN PATHOLOGY (2010)

Article Biochemistry & Molecular Biology

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

Dorothee Dormann et al.

EMBO JOURNAL (2010)

Article Clinical Neurology

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

Ian P. Blair et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)

Review Clinical Neurology

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

Ian R. A. Mackenzie et al.

LANCET NEUROLOGY (2010)

Article Clinical Neurology

FUS GENE MUTATIONS IN FAMILIAL AND SPORADIC AMYOTROPHIC LATERAL SCLEROSIS

Rosa Rademakers et al.

MUSCLE & NERVE (2010)

Editorial Material Clinical Neurology

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2009)

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.

BRAIN (2009)

Article Oncology

PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function

Laure Jobert et al.

EXPERIMENTAL CELL RESEARCH (2009)

Article Multidisciplinary Sciences

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

T. J. Kwiatkowski et al.

SCIENCE (2009)

Review Cell Biology

The TET Family of Proteins: Functions and Roles in Disease

Adelene Y. Tan et al.

JOURNAL OF MOLECULAR CELL BIOLOGY (2009)

Article Biochemistry & Molecular Biology

Identification of proteins interacting with protein arginine methyltransferase 8: The Ewing sarcoma (EWS) protein binds independent of its methylation state

Steffen Pahlich et al.

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2008)

Article Biochemistry & Molecular Biology

Identification and characterization of the nuclear localization/retention signal in the EWS proto-oncoprotein

Rouzanna P. Zakaryan et al.

JOURNAL OF MOLECULAR BIOLOGY (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

Rules for nuclear localization sequence recognition by karyopherinβ2

Brittany J. Lee et al.