Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort (Q48313563)

10 February 2018

title

Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort (English)

1 reference

10 February 2018

amyotrophic lateral sclerosis

main subject

0 references

author name string

Yi Yang

1

1 reference

10 February 2018

Lu Tang

2

1 reference

10 February 2018

Nan Zhang

3

1 reference

10 February 2018

Lei Pan

4

1 reference

10 February 2018

Shinji Hadano

5

1 reference

10 February 2018

Dongsheng Fan

6

1 reference

10 February 2018

publication date

24 February 2015

1 reference

10 February 2018

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

published in

1 reference

10 February 2018

volume

16

1 reference

10 February 2018

issue

5-6

1 reference

10 February 2018

page(s)

378-384

1 reference

10 February 2018

Clinical diagnosis and management of amyotrophic lateral sclerosis

cites work

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

C9orf72 repeat expansions are not detected in Chinese patients with familial ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Detection of a novel frameshift mutation and regions with homozygosis within ARHGEF28 gene in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Detergent-insoluble aggregates associated with amyotrophic lateral sclerosis in transgenic mice contain primarily full-length, unmodified superoxide dismutase-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

p62 Is a common component of cytoplasmic inclusions in protein aggregation diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

p62 accumulates and enhances aggregate formation in model systems of familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Signal integration and diversification through the p62 scaffold protein

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Interaction domains of p62: a bridge between p62 and selective autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

The ALSFRSr predicts survival time in an ALS clinic population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Oxidative damage to the promoter region of SQSTM1/p62 is common to neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

New insights into the role of sequestosome 1/p62 mutant proteins in the pathogenesis of Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Interaction codes within the family of mammalian Phox and Bem1p domain-containing proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Mining the TRAF6/p62 interactome for a selective ubiquitination motif

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Selective autophagy mediated by autophagic adapter proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

The p62 scaffold regulates nerve growth factor-induced NF-kappaB activation by influencing TRAF6 polyubiquitination

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Proposed criteria for familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Loss of Ubiquitin Binding Is a Unifying Mechanism by Which Mutations of SQSTM1 Cause Paget’s Disease of Bone

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

Hypoxia-activated autophagy accelerates degradation of SQSTM1/p62

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1009466

10.3109/21678421.2015.1009466

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

release_hfw5azi7pvcq5o6mskk7ju5jri

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hfw5azi7pvcq5o6mskk7ju5jri

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

10 February 2018