Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1 (Q24683661)

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Paul D Chastain

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Stephanie M Cohen

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Marila Cordeiro-Stone

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David G Kaufman

Experimental and Molecular Pathology

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language of work or name

English

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publication date

April 2007

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published in

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volume

82

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issue

2

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page(s)

190-6

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cites work

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

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Size bias of fragile X premutation alleles in late-onset movement disorders.

7 April 2017

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Premature ovarian failure (POF) syndrome: towards the molecular clinical analysis of its genetic complexity

28 September 2017

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The genetic basis of premature ovarian failure.

28 September 2017

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A late origin of DNA replication in the trinucleotide repeat region of the human FMR2 gene

28 September 2017

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A question of timing: emerging links between transcription and replication

28 September 2017

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Principal genetic syndromes and autism: from phenotypes, proteins to genes.

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Repeat instability: mechanisms of dynamic mutations

28 September 2017

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Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability

28 September 2017

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Recent advances in X-chromosome inactivation

28 September 2017

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An ATR- and Chk1-dependent S checkpoint inhibits replicon initiation following UVC-induced DNA damage

28 September 2017

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Trinucleotide repeats: mechanisms and pathophysiology

28 September 2017

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Construction of a cosmid library of DNA replicated early in the S phase of normal human fibroblasts

28 September 2017

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FRAXA and FRAXE: the results of a five year survey

28 September 2017

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The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes

28 September 2017

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Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

28 September 2017

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Effects of temperature, Mg2+ concentration and mismatches on triplet-repeat expansion during DNA replication in vitro

28 September 2017

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DNA secondary structure: a common and causative factor for expansion in human disease

28 September 2017

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Structural analysis of slipped-strand DNA (S-DNA) formed in (CTG)n. (CAG)n repeats from the myotonic dystrophy locus

28 September 2017

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A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication

28 September 2017

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Fine mapping of a replication origin of human DNA.

28 September 2017

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Replication program of active and inactive multigene families in mammalian cells

28 September 2017

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Characterization of human DNA sequences synthesized at the onset of S-phase

28 September 2017

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Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

28 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Biological implications of the DNA structures associated with disease-causing triplet repeats

28 September 2017

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CTG repeats associated with human genetic disease are inherently flexible

30 May 2018

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Mapping replication origins by quantifying relative abundance of nascent DNA strands using competitive polymerase chain reaction

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

30 May 2018

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Effect of benzo[a]pyrene-diol-epoxide-I on growth of nascent DNA in synchronized human fibroblasts

30 May 2018

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

30 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

30 May 2018

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Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

28 November 2018

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An investigation of FRAXA intermediate allele phenotype in a longitudinal sample

28 November 2018

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Autism in fragile X syndrome

28 November 2018

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Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

28 November 2018

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Protein composition of the intranuclear inclusions of FXTAS.

28 November 2018

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Same origins of DNA replication function on the active and inactive human X chromosomes

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation†

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Molecular-neurobehavioral associations in females with the fragile X full mutation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934615

Mapping of an origin of DNA replication near the transcriptional promoter of the human HPRT gene

28 November 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

Association of fragile X syndrome with delayed replication of the FMR1 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

Premature ovarian failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2006.10.004

Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17196195

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Role of postreplication repair in transformation of human fibroblasts to anchorage independence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17196195

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Expansion of trinucleotide repeats]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17196195