hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations (Q44742682)

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scientific article published on 5 February 2013

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English	hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations	scientific article published on 5 February 2013

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scholarly article

1 reference

Europe PubMed Central

5 December 2017

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations (English)

1 reference

Europe PubMed Central

5 December 2017

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Christian Haass

15

object named as

Christian Haass

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object named as

Kohji Mori

1

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7

object named as

Dieter Edbauer

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Europe PubMed Central

5 December 2017

Christine Van Broeckhoven

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object named as

Christine Van Broeckhoven

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Europe PubMed Central

5 December 2017

Manuela Neumann

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Manuela Neumann

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Europe PubMed Central

5 December 2017

Gernot Kleinberger

9

object named as

Gernot Kleinberger

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Europe PubMed Central

5 December 2017

11

object named as

Jochen Herms

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Europe PubMed Central

5 December 2017

Thomas Arzberger

14

object named as

Thomas Arzberger

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Europe PubMed Central

5 December 2017

2

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Sven Lammich

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Europe PubMed Central

5 December 2017

Hans Kretzschmar

6

object named as

Hans Kretzschmar

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Europe PubMed Central

5 December 2017

Jonathan Laflamme Janssen

8

object named as

Jonathan Janssens

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Europe PubMed Central

5 December 2017

10

object named as

Marc Cruts

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Europe PubMed Central

5 December 2017

author name string

Ian R A Mackenzie

3

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5 December 2017

Ignasi Forné

4

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5 December 2017

Sonja Zilow

5

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5 December 2017

publication date

5 February 2013

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Europe PubMed Central

5 December 2017

number of pages

11

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Acta Neuropathologica

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5 December 2017

125

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413-423

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5 December 2017

3

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5 December 2017

https://scigraph.springernature.com/pub.10.1007/s00401-013-1088-7

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TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

1 reference

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Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion

1 reference

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The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

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21 January 2018

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

1 reference

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Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.

1 reference

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Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes

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https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Milestones in PD genetics

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21 January 2018

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

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https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid beta-peptide

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https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Nuclear functions of heterogeneous nuclear ribonucleoproteins A/B.

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https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Cytoplasmic degradation of splice-defective pre-mRNAs and intermediates.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Heterogeneous nuclear ribonucleoprotein A3, a novel RNA trafficking response element-binding protein

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

A harmonized classification system for FTLD-TDP pathology

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Mutations of optineurin in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Expression profile and interactions of hnRNP A3 within hnRNP/mRNP complexes in mammals

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

RNA-mediated neuromuscular disorders

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

The genetics and neuropathology of frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Cytoplasmic decay of intergenic transcripts in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

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Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

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Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

1 reference

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Non-ATG-initiated translation directed by microsatellite expansions

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p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

1 reference

https://api.crossref.org/works/10.1007%2FS00401-013-1088-7

21 January 2018

Identifiers

10.1007/S00401-013-1088-7

1 reference

Europe PubMed Central

5 December 2017

1 reference

Europe PubMed Central

5 December 2017

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