(Q28270779)

12

Jacqueline de Belleroche

0 references

Caroline Vance

5

Caroline Vance

0 references

Kelly L Williams

Kelly L Williams

9

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Christopher C. Miller

Christopher C Miller

16

0 references

Ammar Al-Chalabi

Ammar Al-Chalabi

15

0 references

Emanuele Buratti

Emanuele Buratti

10

0 references

Jemeen Sreedharan

Jemeen Sreedharan

1

0 references

Ian P Blair

Ian P Blair

2

0 references

Christopher Shaw

Christopher E Shaw

18

0 references

P Nigel Leigh

14

P Nigel Leigh

0 references

Jennifer C Durnall

8

Jennifer C Durnall

0 references

Vineeta B Tripathi

3

Vineeta B Tripathi

0 references

author name string

Xun Hu

4

0 references

Boris Rogelj

6

0 references

Steven Ackerley

7

0 references

Francisco Baralle

11

0 references

J Douglas Mitchell

13

0 references

Garth Nicholson

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

17

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language of work or name

English

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publication date

21 March 2008

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published in

Science

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volume

319

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issue

5870

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page(s)

1668-72

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cites work

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1154584

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1154584

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1154584

TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1154584

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

21 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1154584

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1154584

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

21 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1154584

Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity

21 April 2017

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Progress in the pathogenesis of amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Truncated wild-type SOD1 and FALS-linked mutant SOD1 cause neural cell death in the chick embryo spinal cord

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

TDP-43 gene analysis in frontotemporal lobar degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

TDP-43 is deposited in the Guam parkinsonism-dementia complex brains.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

TDP-43 in amyotrophic lateral sclerosis: pathophysiology or patho-babel?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

A novel CpG-free vertebrate insulator silences the testis-specific SP-10 gene in somatic tissues: role for TDP-43 in insulator function

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18309045

12 December 2020

Identifiers

DOI

10.1126/SCIENCE.1154584

1 reference

Consolidated OpenCitations Corpus – April 2017

ADS bibcode

2008Sci...319.1668S

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

PMC publication ID

7116650

0 references

PubMed publication ID

18309045

1 reference

Consolidated OpenCitations Corpus – April 2017