(Q57305142)

4

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Francesc Calafell

object named as

Francesc Calafell

2

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António Amorim

object named as

António Amorim

5

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author name string

Virginia C N Wong

European Journal of Human Genetics

3

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publication date

17 May 2006

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published in

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volume

14

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issue

8

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page(s)

932-940

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201643

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cites work

Dynamics of CAG repeat loci revealed by the analysis of their variability

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

21 January 2018

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Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease

21 January 2018

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Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

21 January 2018

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CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro

21 January 2018

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Recombination-induced CAG trinucleotide repeat expansions in yeast involve the MRE11-RAD50-XRS2 complex

21 January 2018

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Codon repeats in genes associated with human diseases: fewer repeats in the genes of nonhuman primates and nucleotide substitutions concentrated at the sites of reiteration

21 January 2018

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Comparative Genetics of Functional Trinucleotide Tandem Repeats in Humans and Apes

21 January 2018

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Machado-Joseph disease gene products carrying different carboxyl termini

21 January 2018

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Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon

21 January 2018

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Tandem repeats finder: a program to analyze DNA sequences

21 January 2018

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Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study

21 January 2018

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Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations

21 January 2018

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Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

21 January 2018

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Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

21 January 2018

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Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes

21 January 2018

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Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats.

21 January 2018

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Evidence for mutational cis-acting factors affecting mutagenesis in the ornithine transcarbamylase gene

21 January 2018

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Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission

21 January 2018

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Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

21 January 2018

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Patterns of CAG repeat interruptions in SCA1 and SCA2 genes in relation to repeat instability

21 January 2018

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Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract

21 January 2018

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Identification of three novel polymorphisms in the MJD1 gene and study of their frequency in the Portuguese population

21 January 2018

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

21 January 2018

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7 January 2021

Small slipped register genetic instabilities in Escherichia coli in triplet repeat sequences associated with hereditary neurological diseases

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7 January 2021

Gene conversion (recombination) mediates expansions of CTG[middle dot]CAG repeats

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7 January 2021

A high-resolution recombination map of the human genome

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7 January 2021

Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India

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7 January 2021

Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies

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7 January 2021

Brief report: reverse mutation in myotonic dystrophy

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7 January 2021

Origin of the expansion mutation in myotonic dystrophy

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7 January 2021