Screening for CCNF Mutations in a Chinese Amyotrophic Lateral Sclerosis Cohort. (Q55634425)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30008669%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

title

Screening for CCNF Mutations in a Chinese Amyotrophic Lateral Sclerosis Cohort (English)

1 reference

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amyotrophic lateral sclerosis

12 April 2020

main subject

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author name string

Danyang Tian

1

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12 April 2020

Jiao Li

2

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12 April 2020

Lu Tang

3

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12 April 2020

Nan Zhang

4

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12 April 2020

Dongsheng Fan

5

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12 April 2020

publication date

29 June 2018

1 reference

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Frontiers in Aging Neuroscience

12 April 2020

published in

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12 April 2020

volume

10

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12 April 2020

page(s)

185

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Creative Commons Attribution 4.0 International

12 April 2020

copyright license

start time

29 June 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

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TUBA4A may not be a significant genetic factor in Chinese ALS patients

27 July 2018

1 reference

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Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China

27 July 2018

1 reference

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

27 July 2018

1 reference

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Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype.

12 August 2018

1 reference

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Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China

12 August 2018

1 reference

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Optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in China

12 August 2018

1 reference

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C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.

12 August 2018

1 reference

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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

12 August 2018

1 reference

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Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort

12 August 2018

1 reference

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

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

12 August 2018

1 reference

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The ALSFRSr predicts survival time in an ALS clinic population

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

Amyotrophic lateral sclerosis

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

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

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

Proposed criteria for familial amyotrophic lateral sclerosis

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6034086

Casein kinase II phosphorylation of cyclin F at serine 621 regulates the Lys48-ubiquitylation E3 ligase activity of the SCF(cyclin F) complex.

30 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/30008669

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3389/FNAGI.2018.00185

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30008669%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30008669%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

PubMed publication ID

30008669

1 reference