(Q74771975)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9660942%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

title

GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases (English)

1 reference

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13 November 2019

1 reference

12

S B Melançon

1 reference

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13 November 2019

13

C T McMurray

1 reference

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13 November 2019

author name string

A M Gacy

1

1 reference

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13 November 2019

G M Goellner

2

1 reference

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13 November 2019

C Spiro

3

1 reference

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13 November 2019

X Chen

4

1 reference

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13 November 2019

G Gupta

5

1 reference

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13 November 2019

E M Bradbury

6

1 reference

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13 November 2019

R B Dyer

7

1 reference

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13 November 2019

M J Mikesell

8

1 reference

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13 November 2019

J Z Yao

9

1 reference

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13 November 2019

A J Johnson

10

1 reference

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13 November 2019

A Richter

11

1 reference

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13 November 2019

publication date

1 March 1998

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13 November 2019

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13 November 2019

volume

1

1 reference

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13 November 2019

issue

4

1 reference

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13 November 2019

page(s)

583-593

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Trinucleotide repeat expansions and human genetic disease

13 November 2019

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

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The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinase

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Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications

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Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome

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Hairpin formation within the human enkephalin enhancer region. 1. Kinetic analysis

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Trinucleotide repeats that expand in human disease form hairpin structures in vitro

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Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

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7 January 2021

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Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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7 January 2021

Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases

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7 January 2021

Complex gene conversion events in germline mutation at human minisatellites

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7 January 2021

Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9660942%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference