(Q40399666)

20 September 2017

Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome (English)

1 reference

20 September 2017

J Han

1

1 reference

20 September 2017

C Hsu

2

1 reference

20 September 2017

Z Zhu

3

1 reference

20 September 2017

J W Longshore

4

1 reference

20 September 2017

W H Finley

5

1 reference

20 September 2017

1 May 1994

1 reference

20 September 2017

Nucleic Acids Research

1 reference

20 September 2017

22

1 reference

20 September 2017

1735-1740

1 reference

20 September 2017

9

1 reference

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

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Selection of antisense oligonucleotides on the basis of genomic frequency of the target sequence.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

The effect of codon usage on the oligonucleotide composition of the E. coli genome and identification of over- and underrepresented sequences by Markov chain analysis.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Over- and under-representation of short oligonucleotides in DNA sequences

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Markov chain analysis finds a significant influence of neighboring bases on the occurrence of a base in eucaryotic nuclear DNA sequences both protein-coding and noncoding.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Hereditary unstable DNA: a new explanation for some old genetic questions?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=308057

Origin of the expansion mutation in myotonic dystrophy

20 August 2018

1 reference

12 December 2020

Molecular evolution of bacteriophages: evidence of selection against the recognition sites of host restriction enzymes

1 reference

12 December 2020

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

12 December 2020

Heritable unstable DNA sequences

1 reference

12 December 2020

Selection againstdam methylation sites in the genomes of DNA of enterobacteriophages

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/22.9.1735

1 reference

20 September 2017

1 reference

20 September 2017

1 reference