(Q34659435)

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Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation (English)

1 reference

Europe PubMed Central

3 August 2017

Olga D Razinskaya

object named as

Olga D Razinskaya

6

0 references

Natalie Connor-Robson

object named as

Natalie Connor-Robson

3

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Johnathan Cooper-Knock

object named as

Johnathan Cooper-Knock

2

0 references

object named as

Janine Kirby

5

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Vladimir Buchman

object named as

Vladimir L Buchman

1

0 references

object named as

Pamela J Shaw

8

0 references

author name string

Adrian Higginbottom

4

1 reference

Europe PubMed Central

3 August 2017

Natalia Ninkina

7

1 reference

Europe PubMed Central

3 August 2017

publication date

8 April 2013

1 reference

Europe PubMed Central

3 August 2017

Molecular Neurodegeneration

1 reference

Europe PubMed Central

3 August 2017

8

1 reference

Europe PubMed Central

3 August 2017

12

1 reference

Europe PubMed Central

3 August 2017

https://scigraph.springernature.com/pub.10.1186/1750-1326-8-12

0 references

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

RNA-mediated neurodegeneration in repeat expansion disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626718

7 July 2018

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1326-8-12

21 January 2018

Technical standards and guidelines for myotonic dystrophy type 1 testing.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1326-8-12

21 January 2018

C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan.

1 reference

https://api.crossref.org/works/10.1186%2F1750-1326-8-12

21 January 2018

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10.1186/1750-1326-8-12

1 reference

Europe PubMed Central

3 August 2017

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1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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