(Q41702537)

7 October 2017

1 reference

title

Differences and similarities between various tandem repeat sequences: minisatellites and microsatellites (English)

1 reference

7 October 2017

1 reference

Debrauwere H

1

1 reference

7 October 2017

Gendrel CG

series ordinal

2

1 reference

7 October 2017

Lechat S

series ordinal

3

1 reference

7 October 2017

Dutreix M

series ordinal

4

1 reference

7 October 2017

publication date

1 October 1997

1 reference

7 October 2017

1 reference

7 October 2017

volume

79

1 reference

7 October 2017

issue

9-10

1 reference

7 October 2017

page(s)

577-586

1 reference

Simple sequences are ubiquitous repetitive components of eukaryotic genomes.

7 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

1 reference

7 January 2021

Hypervariable 'minisatellite' regions in human DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mouse DNA 'fingerprints': analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Genomic simple repetitive DNAs are targets for differential binding of nuclear proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

A highly polymorphic region 3' to the human type II collagen gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

On the use of DNA fingerprints for linkage studies in cattle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

The M13 repeat probe detects RFLPs between two strains of the protozoan malaria parasite Plasmodium falciparum.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

A fungal minisatellite

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Genetic control of microsatellite stability

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mutation of human short tandem repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Complex gene conversion events in germline mutation at human minisatellites

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Analysis of somatic mutations at human minisatellite loci in tumors and cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Somatic mutation processes at a human minisatellite

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Triplet repeat mutations in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Microsatellite instability in primary neoplasms from HIV+ patients

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Simple repeat DNA is not replicated simply

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Enzymatic amplification of synthetic oligodeoxyribonucleotides: implications for triplet repeat expansions in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

DNA damage tolerance, mismatch repair and genome instability

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Big, bad minisatellites

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mismatch repair in replication fidelity, genetic recombination, and cancer biology

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Minisatellite repeat coding as a digital approach to DNA typing

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Mutation processes at human minisatellites.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Double-strand breaks at an initiation site for meiotic gene conversion

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110).

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

CTG triplet repeats from the myotonic dystrophy gene are expanded in Escherichia coli distal to the replication origin as a single large event.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Regulation of insulin gene expression by the IDDM associated, insulin locus haplotype

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Members of therel/NF-χB family of transcriptional regulatory proteins bind theHRAS1minisatellite DNA sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Allelic variation of reporter gene activation by the HRAS1 minisatellite

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2897%2982006-8

7 January 2021

10.1016/S0300-9084(97)82006-8

Identifiers

DOI

1 reference

7 October 2017

1 reference