Transportin1: a marker of FTLD-FUS (Q28245695)

object named as

Tammaryn Lashley

0 references

Rina Bandopadhyay

object named as

Rina Bandopadhyay

0 references

Janice Holton

object named as

Janice L Holton

0 references

author name string

Jack Brelstaff

0 references

Tamas Revesz

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

0 references

language of work or name

English

0 references

publication date

November 2011

0 references

published in

Acta Neuropathologica

0 references

volume

122

0 references

issue

0 references

page(s)

591-600

0 references

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Karyopherin beta2 mediates nuclear import of a mRNA binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Neurofilament inclusion body disease: a new proteinopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Rules for nuclear localization sequence recognition by karyopherin beta 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Aberrant localization of importin alpha1 in hippocampal neurons in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Transport into and out of the nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

FUS pathology in basophilic inclusion body disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

A new subtype of frontotemporal lobar degeneration with FUS pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

The TET family of proteins: functions and roles in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

TDP-43: an emerging new player in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Regulating access to the genome: nucleocytoplasmic transport throughout the cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

Nucleocytoplasmic shuttling of signal transducers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0863-6