(Q38473141)

English

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.

scientific article published on January 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Koob MD

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Benzow KA

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Bird TD

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Day JW

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Moseley ML

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Ranum LP

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

language of work or name

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publication date

1 January 1998

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Nature Genetics

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Europe PubMed Central

PubMed publication ID

3 September 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

72-75

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

https://scigraph.springernature.com/pub.10.1038/ng0198-72

0 references

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

21 January 2018

The expanding world of trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Expanded CAG repeats in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

An expanded CAG repeat sequence in spinocerebellar ataxia type 7

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Direct detection of novel expanded trinucleotide repeats in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Growing triplet repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Construction of small-insert genomic DNA libraries highly enriched for microsatellite repeat sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid and efficient site-specific mutagenesis without phenotypic selection

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Putting the human genome on the map

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-72

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0198-72

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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