(Q52840349)

8 May 2018

title

Identification of the porcine homologous of human disease causing trinucleotide repeat sequences. (English)

1 reference

8 May 2018

author

Merete Fredholm

5

1 reference

8 May 2018

Anders Nielsen

7

1 reference

8 May 2018

Bo Thomsen

object named as

Bo Thomsen

2

0 references

Christian Bendixen

4

object named as

Christian Bendixen

1 reference

8 May 2018

Lone Bruhn Madsen

1

1 reference

8 May 2018

Christina Ane Elisabeth Sølvsten

3

1 reference

8 May 2018

Arne Lund Jørgensen

6

1 reference

8 May 2018

publication date

22 May 2007

1 reference

8 May 2018

published in

Neurogenetics

1 reference

8 May 2018

volume

8

1 reference

8 May 2018

issue

3

1 reference

8 May 2018

page(s)

207-218

1 reference

8 May 2018

Molecular basis of genetic instability of triplet repeats

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0088-Y

A role for selection in regulating the evolutionary emergence of disease-causing and other coding CAG repeats in humans and mice.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-007-0088-Y

CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms

21 January 2018

1 reference

12 December 2020

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

1 reference

12 December 2020

Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

12 December 2020

Identification and characterization of the miniature pig Huntington's disease gene homolog: evidence for conservation and polymorphism in the CAG triplet repeat

1 reference

12 December 2020

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

12 December 2020

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis

1 reference

12 December 2020

Comparative analysis of amino acid repeats in rodents and humans

1 reference

12 December 2020

1 reference

12 December 2020

Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice

1 reference

12 December 2020

Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.

1 reference

12 December 2020

Trinucleotide repeats and neurodegenerative disease.

1 reference

12 December 2020

Repeat instability: mechanisms of dynamic mutations

1 reference

12 December 2020

Evolution of the cryptic FMR1 CGG repeat

1 reference

12 December 2020

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

1 reference

12 December 2020

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Transcription promotes contraction of CAG repeat tracts in human cells

1 reference

12 December 2020

Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome

1 reference

12 December 2020

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene

1 reference

12 December 2020

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

1 reference

12 December 2020

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Positive selection of a pre-expansion CAG repeat of the human SCA2 gene

1 reference

12 December 2020

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.

1 reference

12 December 2020

Comparative Genetics of Functional Trinucleotide Tandem Repeats in Humans and Apes

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing

1 reference

12 December 2020

Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.

1 reference

12 December 2020

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

1 reference

12 December 2020

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

1 reference

12 December 2020

Candidate DNA replication initiation regions at human trinucleotide repeat disease loci

1 reference

12 December 2020

RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila

1 reference

12 December 2020

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

12 December 2020

Expansion of GAA trinucleotide repeats in mammals

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

1 reference

12 December 2020

Trinucleotide repeats (CGG)22TGG(CGG)43TGG(CGG)21 from the fragile X gene remain stable in transgenic mice

1 reference

12 December 2020

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

1 reference

12 December 2020

Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes

1 reference

12 December 2020

Molecular architecture of CAG repeats in human disease related transcripts

1 reference

12 December 2020

10.1007/S10048-007-0088-Y

Identifiers

DOI

1 reference

8 May 2018

1 reference

8 May 2018