(Q38882417)

English

The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation

scientific article published on 26 April 2015

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scholarly article

1 reference

Europe PubMed Central

7 September 2017

The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation (English)

1 reference

Europe PubMed Central

7 September 2017

amyotrophic lateral sclerosis

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author name string

Xinxiu Liu

1

1 reference

Europe PubMed Central

7 September 2017

Jiayu Chen

2

1 reference

Europe PubMed Central

7 September 2017

Wenchao Liu

3

1 reference

Europe PubMed Central

7 September 2017

Xiaogang Li

4

1 reference

Europe PubMed Central

7 September 2017

Qi Chen

5

1 reference

Europe PubMed Central

7 September 2017

Tao Liu

6

1 reference

Europe PubMed Central

7 September 2017

Shaorong Gao

7

1 reference

Europe PubMed Central

7 September 2017

Min Deng

8

1 reference

Europe PubMed Central

7 September 2017

publication date

26 April 2015

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Europe PubMed Central

7 September 2017

1 reference

Europe PubMed Central

7 September 2017

16

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Europe PubMed Central

7 September 2017

3

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Europe PubMed Central

7 September 2017

223-231

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Europe PubMed Central

7 September 2017

https://scigraph.springernature.com/pub.10.1007/s10048-015-0448-y

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Amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Protein aggregation in amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Drug screening for ALS using patient-specific induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

PTEN regulates AMPA receptor-mediated cell viability in iPS-derived motor neurons.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Efficient reprogramming of human cord blood CD34+ cells into induced pluripotent stem cells with OCT4 and SOX2 alone.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Few single nucleotide variations in exomes of human cord blood induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Promoter trapping reveals significant differences in integration site selection between MLV and HIV vectors in primary hematopoietic cells

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Reprogramming of murine and human somatic cells using a single polycistronic vector

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Erythroid promoter confines FGF2 expression to the marrow after hematopoietic stem cell gene therapy and leads to enhanced endosteal bone formation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Generation of integration-free human induced pluripotent stem cells from postnatal blood mononuclear cells by plasmid vector expression

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Replacement of Oct4 by Tet1 during iPSC induction reveals an important role of DNA methylation and hydroxymethylation in reprogramming.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Inhibition of Sirt1 promotes neural progenitors toward motoneuron differentiation from human embryonic stem cells

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

A TALEN genome-editing system for generating human stem cell-based disease models

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

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%2FS10048-015-0448-Y

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%2FS10048-015-0448-Y

21 January 2018

Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvement.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Structural and energetic basis of ALS-causing mutations in the atypical proline–tyrosine nuclear localization signal of the Fused in Sarcoma protein (FUS)

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

FUS is sequestered in nuclear aggregates in ALS patient fibroblasts

1 reference

https://api.crossref.org/works/10.1007%2FS10048-015-0448-Y

21 January 2018

Generation of iPS Cells from Human Peripheral Blood Mononuclear Cells Using Episomal Vectors

1 reference

https://pubmed.ncbi.nlm.nih.gov/25912081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation of induced pluripotent stem cells from human beta-thalassemia fibroblast cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/25912081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25912081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/25912081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Generation of induced pluripotent stem cells from amyotrophic lateral sclerosis patientcarrying SOD1-V14M mutation].

1 reference

https://pubmed.ncbi.nlm.nih.gov/25912081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-015-0448-Y

1 reference

Europe PubMed Central

7 September 2017

1 reference

Europe PubMed Central

7 September 2017

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