(Q48036449)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9660961%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

title

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis (English)

1 reference

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13 November 2019

4

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13 November 2019

author name string

D R Hewett

1

1 reference

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13 November 2019

O Handt

2

1 reference

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13 November 2019

L Hobson

3

1 reference

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13 November 2019

H J Eyre

5

1 reference

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13 November 2019

E Baker

6

1 reference

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13 November 2019

G R Sutherland

7

1 reference

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13 November 2019

S Schuffenhauer

8

1 reference

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13 November 2019

J I Mao

9

1 reference

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13 November 2019

R I Richards

10

1 reference

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13 November 2019

publication date

1 May 1998

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13 November 2019

1 reference

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13 November 2019

volume

1

1 reference

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13 November 2019

issue

6

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13 November 2019

page(s)

773-781

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Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability

13 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Characterization of the COL2A1 VNTR polymorphism

1 reference

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7 January 2021

Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Big, bad minisatellites

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

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

1 reference

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7 January 2021

Repeat expansion--all in a flap?

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

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7 January 2021

Origin of the expansion mutation in myotonic dystrophy

1 reference

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7 January 2021

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy

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7 January 2021

Complex gene conversion events in germline mutation at human minisatellites

1 reference

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7 January 2021

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

What is expanded in progressive myoclonus epilepsy?

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Growing triplet repeats

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Trinucleotide repeats associated with human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Dynamic mutations: a new class of mutations causing human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Dynamic mutation: possible mechanisms and significance in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Evidence of founder chromosomes in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

The molecular basis of fragile sites in human chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980077-5

7 January 2021

10.1016/S1097-2765(00)80077-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9660961%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference