Fragile X gene instability: anchoring AGGs and linked microsatellites (Q35644624)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668261%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Fragile X gene instability: anchoring AGGs and linked microsatellites (English)

1 reference

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23 October 2019

1 reference

N Zhong

1

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23 October 2019

W Yang

series ordinal

2

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23 October 2019

C Dobkin

series ordinal

3

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23 October 2019

W T Brown

series ordinal

4

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23 October 2019

language of work or name

English

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publication date

1 August 1995

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American Journal of Human Genetics

23 October 2019

published in

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23 October 2019

volume

57

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23 October 2019

issue

2

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23 October 2019

page(s)

351-361

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Origins of the fragile X syndrome mutation

23 October 2019

cites work

1 reference

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

12 July 2018

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

12 July 2018

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Advances in molecular analysis of fragile X syndrome

12 July 2018

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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

12 July 2018

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A complex mutable polymorphism located within the fragile X gene.

12 July 2018

1 reference

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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

12 July 2018

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Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes

12 July 2018

1 reference

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Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

12 July 2018

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Length of uninterrupted CGG repeats determines instability in the FMR1 gene

12 July 2018

1 reference

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Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population

12 July 2018

1 reference

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DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

12 July 2018

1 reference

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CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

12 July 2018

1 reference

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Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes

12 July 2018

1 reference

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Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

12 July 2018

1 reference

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High resolution of human evolutionary trees with polymorphic microsatellites

12 July 2018

1 reference

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Identification of an origin of bidirectional DNA replication in mammalian chromosomes

12 July 2018

1 reference

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Mammalian subtilisins: the long-sought dibasic processing endoproteases

12 July 2018

1 reference

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

12 July 2018

1 reference

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Fragile X genotype characterized by an unstable region of DNA.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

Dynamic mutations: a new class of mutations causing human disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

A second-generation linkage map of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801568

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

12 July 2018

1 reference

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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

12 July 2018

1 reference

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Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test

27 July 2018

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Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat

25 September 2018

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Striking founder effect for the fragile X syndrome in Finland.

25 September 2018

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

25 September 2018

1 reference

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Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population

25 September 2018

1 reference

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Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?

25 September 2018

1 reference

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

25 September 2018

1 reference

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Normal variation at the myotonic dystrophy locus in global human populations

25 September 2018

1 reference

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Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations

25 September 2018

1 reference

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Complex gene conversion events in germline mutation at human minisatellites

23 October 2018

1 reference

12 December 2020

Evidence of founder chromosomes in fragile X syndrome

1 reference

12 December 2020

Origin of the expansion mutation in myotonic dystrophy

1 reference

12 December 2020

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene

1 reference

12 December 2020

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

12 December 2020

Haplotype analysis at the FRAXA locus in the Japanese population

1 reference

12 December 2020

Precursor arrays for triplet repeat expansion at the fragile X locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Founder effect in a Belgian-Dutch fragile X population

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7668261%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

PubMed publication ID

7668261

1 reference