(Q38070839)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

review article

1 reference

title

Optineurin and amyotrophic lateral sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

21 February 2020

main subject

0 references

author

Hirofumi Maruyama

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Hideshi Kawakami

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Hideshi Kawakami

series ordinal

2

1 reference

28 August 2017

publication date

26 December 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

Geriatrics and Gerontology International

21 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

page(s)

528-532

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

Amyotrophic lateral sclerosis.

21 February 2020

cites work

1 reference

Protein aggregation in motor neurone disorders.

21 January 2018

1 reference

Familial aggregation of amyotrophic lateral sclerosis

21 January 2018

1 reference

An estimate of amyotrophic lateral sclerosis heritability using twin data.

21 January 2018

1 reference

A high-density genome-wide association screen of sporadic ALS in US veterans

21 January 2018

1 reference

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

21 January 2018

1 reference

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

Interaction of an adenovirus E3 14.7-kilodalton protein with a novel tumor necrosis factor alpha-inducible cellular protein containing leucine zipper domains

21 January 2018

1 reference

Optineurin negatively regulates TNFalpha- induced NF-kappaB activation by competing with NEMO for ubiquitinated RIP

21 January 2018

1 reference

Ubiquitin binding mediates the NF-kappaB inhibitory potential of ABIN proteins

21 January 2018

1 reference

Phosphorylation of the autophagy receptor optineurin restricts Salmonella growth

21 January 2018

1 reference

Optineurin mediates a negative regulation of Rab8 by the GTPase-activating protein TBC1D17

21 January 2018

1 reference

Adult-onset primary open-angle glaucoma caused by mutations in optineurin

21 January 2018

1 reference

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

21 January 2018

1 reference

Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of bone

21 January 2018

1 reference

Mutations in the SLC34A2 gene are associated with pulmonary alveolar microlithiasis

21 January 2018

1 reference

Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.

21 January 2018

1 reference

Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese

21 January 2018

1 reference

Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case series.

21 January 2018

1 reference

Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders

21 January 2018

1 reference

Optineurin with amyotrophic lateral sclerosis-related mutations abrogates inhibition of interferon regulatory factor-3 activation

21 January 2018

1 reference

Mechanisms underlying inflammation in neurodegeneration

21 January 2018

1 reference

Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis

21 January 2018

1 reference

FUS pathology in basophilic inclusion body disease

21 January 2018

1 reference

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

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

21 January 2018

1 reference

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

Evidence for an oligogenic basis of amyotrophic lateral sclerosis

21 January 2018

1 reference

Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/GGI.12022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279185%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference