(Q28245695)

4

Andrew J Lees

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Tammaryn Lashley

2

Tammaryn Lashley

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Rina Bandopadhyay

6

Rina Bandopadhyay

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Janice Holton

3

Janice L Holton

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author name string

Jack Brelstaff

1

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Tamas Revesz

https://scigraph.springernature.com/pub.10.1007/s00401-011-0863-6

7

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language of work or name

English

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publication date

November 2011

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published in

Acta Neuropathologica

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volume

122

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issue

5

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page(s)

591-600

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exact match

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cites work

Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS

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The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response

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Karyopherin beta2 mediates nuclear import of a mRNA binding protein

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Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma

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

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The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

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TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines

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Neurofilament inclusion body disease: a new proteinopathy?

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Translocated in liposarcoma (TLS) is a substrate for fibroblast growth factor receptor-1.

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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

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

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Rules for nuclear localization sequence recognition by karyopherin beta 2

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Aberrant localization of importin alpha1 in hippocampal neurons in Alzheimer disease.

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Transport into and out of the nucleus

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

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Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

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

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FUS pathology in basophilic inclusion body disease

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A new subtype of frontotemporal lobar degeneration with FUS pathology

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Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

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Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode

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Transportins 1 and 2 are redundant nuclear import factors for hnRNP A1 and HuR

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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

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Nucleocytoplasmic shuttling of signal transducers.

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

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