(Q40431790)

20 September 2017

1 reference

title

Mechanisms of DNA expansion (English)

1 reference

20 September 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7587591

26 May 2024

author name string

C. T. McMurray

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7587591

26 May 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7587591

26 May 2024

publication date

1 October 1995

1 reference

full work available at URL

20 September 2017

http://link.springer.com/content/pdf/10.1007/BF00352220.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00352220/fulltext.html

26 May 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF00352220

26 May 2024

1 reference

26 May 2024

1 reference

20 September 2017

volume

104

1 reference

20 September 2017

issue

1

1 reference

20 September 2017

page(s)

2-13

1 reference

https://scigraph.springernature.com/pub.10.1007/s004120050086

20 September 2017

exact match

0 references

cites work

Unstable genes--unstable mind?

1 reference

12 December 2020

Origins of DNA replication that function in eukaryotic cells

1 reference

12 December 2020

Mismatch repair, genetic stability, and cancer

1 reference

12 December 2020

Greater susceptibility to mutations in lagging strand of DNA replication in Escherichia coli than in leading strand.

1 reference

12 December 2020

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

1 reference

12 December 2020

Coordination of leading and lagging strand DNA synthesis at the replication fork of bacteriophage T7

1 reference

12 December 2020

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype

1 reference

12 December 2020

Chemical self-replication of palindromic duplex DNA.

1 reference

12 December 2020

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

1 reference

12 December 2020

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

12 December 2020

Trinucleotide repeat expansions in neurological disease

1 reference

12 December 2020

Identification of a chromosome 18q gene that is altered in colorectal cancers

1 reference

12 December 2020

Characterization of a highly unstable mouse minisatellite locus: evidence for somatic mutation during early development.

1 reference

12 December 2020

The effect of the T7 and Escherichia coli DNA-binding proteins at the replication fork of bacteriophage T7

1 reference

12 December 2020

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

12 December 2020

Microdeletions in the factor IX gene: three recurrences associated with a quasipalindromic sequence

1 reference

12 December 2020

Predicting DNA duplex stability from the base sequence

1 reference

12 December 2020

Slippery DNA and diseases

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

The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure

1 reference

12 December 2020

Apparent regression of the CGG repeat in FMR1 to an allele of normal size

1 reference

12 December 2020

Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals

1 reference

12 December 2020

Mechanisms of insertional mutagenesis in human genes causing genetic disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

1 reference

12 December 2020

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

1 reference

12 December 2020

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

1 reference

12 December 2020

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

1 reference

12 December 2020

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

1 reference

12 December 2020

Clues to the pathogenesis of familial colorectal cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes

1 reference

12 December 2020

Mutations of GTBP in genetically unstable cells

1 reference

12 December 2020

Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

1 reference

12 December 2020

Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins

1 reference

12 December 2020

Frequency and stability of the fragile X premutation.

1 reference

12 December 2020

Dynamic mutations hit double figures

1 reference

12 December 2020

Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli

1 reference

12 December 2020

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

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

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

1 reference

12 December 2020

Microsatellite instability in cancer of the proximal colon

1 reference

12 December 2020

Precursor arrays for triplet repeat expansion at the fragile X locus

1 reference

12 December 2020

Slipped-strand mispairing: a major mechanism for DNA sequence evolution

1 reference

12 December 2020

Allelic instability in mitosis: a unified model for dominant disorders

1 reference

12 December 2020

Trinucleotide diseases on the rise

1 reference

12 December 2020

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

1 reference

12 December 2020

The influence of primary and secondary DNA structure in deletion and duplication between direct repeats in Escherichia coli

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

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

1 reference

12 December 2020

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

1 reference

12 December 2020

DNA loop repair by human cell extracts

1 reference

12 December 2020

A single trinucleotide, 5'AGC3'/5'GCT3', of the triplet-repeat disease genes confers metal ion-induced non-B DNA structure

1 reference

12 December 2020

Genes with triplet repeats: a new class of mutations causing neurological diseases

1 reference

12 December 2020

Dynamic mutations: a new class of mutations causing human disease

1 reference

12 December 2020

New colon cancer gene discovered

1 reference

12 December 2020

Intramolecular DNA triplexes: unusual sequence requirements and influence on DNA polymerization

1 reference

12 December 2020

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

1 reference

12 December 2020

Potential DNA slippage structures acquired during evolutionary divergence of Acinetobacter calcoaceticus chromosomal benABC and Pseudomonas putida TOL pWW0 plasmid xylXYZ, genes encoding benzoate dioxygenases

1 reference

12 December 2020

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

12 December 2020

Mechanisms and biological effects of mismatch repair

1 reference

12 December 2020

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

1 reference

12 December 2020

Requirements for primer synthesis by bacteriophage T7 63-kDa gene 4 protein. Roles of template sequence and T7 56-kDa gene 4 protein

1 reference

12 December 2020

Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications

1 reference

12 December 2020

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population

1 reference

12 December 2020

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

1 reference

12 December 2020

Rapid evolution of a heteroplasmic repetitive sequence in the mitochondrial DNA control region of carnivores.

1 reference

12 December 2020

Specific sequences in native DNA that arrest synthesis by DNA polymerase alpha

1 reference

12 December 2020

Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.

1 reference

12 December 2020

The role of DNA repeats and associated secondary structures in genomic instability and neoplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Direct detection of novel expanded trinucleotide repeats in the human genome

1 reference

12 December 2020

DNA repair. DNA surveillance defect in cancer cells

1 reference

12 December 2020

Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

1 reference

12 December 2020

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

1 reference

12 December 2020

Gametic but not somatic instability of CAG repeat length in Huntington's disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

12 December 2020

Triad-DNA: a model for trinucleotide repeats

1 reference

12 December 2020

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number

1 reference

12 December 2020

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

1 reference

12 December 2020

Pauses at positions of secondary structure during in vitro replication of single-stranded fd Bacteriophage DNA by T4 DNA polymerase

1 reference

12 December 2020

Characterization of the helicase and primase activities of the 63-kDa component of the bacteriophage T7 gene 4 protein.

1 reference

12 December 2020

Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene.

1 reference

12 December 2020

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

1 reference

12 December 2020

Protein‐protein interactions at a DNA replication fork: bacteriophage T4 as a model

1 reference

12 December 2020

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

1 reference

12 December 2020

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

1 reference

12 December 2020

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

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

Triplet repeat genes raise questions

1 reference

12 December 2020

Studies on the mechanism of enzymatic DNA elongation by Escherichia coli DNA polymerase II.

1 reference

12 December 2020

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

1 reference

12 December 2020

Unusual structures of the tandem repetitive DNA sequences located at human centromeres

1 reference

12 December 2020

Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells

1 reference

12 December 2020

Trinucleotide repeat expansion in neurological disease

1 reference

12 December 2020

The effect of template secondary structure on vaccinia DNA polymerase

1 reference

12 December 2020

Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats

1 reference

12 December 2020

Trinucleotide repeat expansions and human genetic disease

1 reference

12 December 2020

Evidence for Ritscher‐Schinzel syndrome in Canadian native Indians

series ordinal

36

1 reference

Molecular Biology and Evolution

26 May 2024

51

4

203

G Levinson

1987

1 reference

Genotype mosaicism in fragile X fetal tissues

26 May 2024

series ordinal

99

1 reference

26 May 2024

Identifiers

DOI

10.1007/S004120050086

1 reference

National Center for Biotechnology Information

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7587591

release_byv53wzf3va6lnlv345fxrjhii

26 May 2024

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/byv53wzf3va6lnlv345fxrjhii

24 November 2022

mapped directly with Wikidata item

1 reference