Evolution of the cryptic FMR1 CGG repeat (Q52012799)

19 April 2018

https://api.crossref.org/works/10.1038/NG1195-301

title

Evolution of the cryptic FMR1 CGG repeat (English)

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22 May 2024

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22 May 2024

molecular evolution

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22 May 2024

repetitive DNA

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22 May 2024

author name string

E. E. Eichler

1

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C. B. Kunst

2

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K. A. Lugenbeel

3

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22 May 2024

O. A. Ryder

4

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D. Davison

5

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S. T. Warren

6

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D. L. Nelson

7

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language of work or name

English

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publication date

1 November 1995

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19 April 2018

full work available at URL

http://www.nature.com/articles/ng1195-301

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https://api.crossref.org/works/10.1038/NG1195-301

http://www.nature.com/articles/ng1195-301.pdf

22 May 2024

file format

Portable Document Format

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https://api.crossref.org/works/10.1038/NG1195-301

22 May 2024

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19 April 2018

volume

11

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19 April 2018

issue

3

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19 April 2018

page(s)

301-308

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19 April 2018

https://scigraph.springernature.com/pub.10.1038/ng1195-301

exact match

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cites work

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

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

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

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

21 January 2018

1 reference

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Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

21 January 2018

1 reference

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Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

Human genes containing polymorphic trinucleotide repeats

21 January 2018

1 reference

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Evolution of the primate beta-globin gene region: nucleotide sequence of the delta-beta-globin intergenic region of gorilla and phylogenetic relationships between African apes and man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

Phylogenetic relations of humans and African apes from DNA sequences in the psi eta-globin region

21 January 2018

1 reference

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Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

21 January 2018

1 reference

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Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome

21 January 2018

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Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

21 January 2018

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

21 January 2018

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Geographic origin of the Y chromosomes in "old" inbred strains of mice

21 January 2018

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Evolution of Repeated DNA Sequences by Unequal Crossover

21 January 2018

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Complex gene conversion events in germline mutation at human minisatellites

21 January 2018

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

21 January 2018

1 reference

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7 January 2021

Precursor arrays for triplet repeat expansion at the fragile X locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

7 January 2021

Conservation of CGG region in FMR1 gene in mammals

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

7 January 2021

Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-301

7 January 2021

Identifiers

DOI

10.1038/NG1195-301

1 reference

19 April 2018

1 reference

19 April 2018