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Hypermutable minisatellites, a human affair?
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scholarly article
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Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
review article
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Europe PubMed Central
title
Hypermutable minisatellites, a human affair?
(English)
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Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
author name string
Philippe R J Bois
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
publication date
1 April 2003
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Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
published in
Genomics
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stated in
Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
volume
81
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stated in
Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
issue
4
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Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
page(s)
349-355
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Europe PubMed Central
PubMed ID
12676558
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6 August 2017
cites work
A highly polymorphic locus in human DNA
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Hypervariable 'minisatellite' regions in human DNA.
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Individual-specific ‘fingerprints’ of human DNA
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Variable number of tandem repeat (VNTR) markers for human gene mapping
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Minisatellite diversity supports a recent African origin for modern humans
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Minisatellite instability and germline mutation
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Fragile sites still breaking
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Proceedings of the 4th International DNA Fingerprinting Conference. Melbourne, Australia, December 2-7, 1996
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Human minisatellites, repeat DNA instability and meiotic recombination
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Minisatellites: mutability and genome architecture.
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Minisatellite repeat coding as a digital approach to DNA typing
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Complex gene conversion events in germline mutation at human minisatellites
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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7 January 2021
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Somatic mutation processes at a human minisatellite
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice.
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Repeat instability at human minisatellites arising from meiotic recombination
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90).
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Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles
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Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism
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Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot.
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Clustering of hypervariable minisatellites in the proterminal regions of human autosomes
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Isolation and characterization of mouse minisatellites.
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Analysis of distribution in the human, pig, and rat genomes points toward a general subtelomeric origin of minisatellite structures.
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Minisatellites show rare and simple intra-allelic instability in the mouse germ line
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Allele diversity and germline mutation at the insulin minisatellite
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Human minisatellite MS32 (D1S8) displays somatic but not germline instability in transgenic mice
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Hotspots of homologous recombination in mouse meiosis.
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An initiation site for meiotic crossing-over and gene conversion in the mouse
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High-resolution sperm typing of meiotic recombination in the mouse MHC Ebeta gene.
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High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot
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Single-strand interruptions in replicating chromosomes cause double-strand breaks
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Replication and recombination intersect
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The importance of repairing stalled replication forks
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Initiation of genetic recombination and recombination-dependent replication
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Mini- and microsatellite expansions: the recombination connection
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Instability of the human minisatellite CEB1 in rad27Delta and dna2-1 replication-deficient yeast cells.
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Influences of array size and homogeneity on minisatellite mutation.
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RAD1 controls the meiotic expansion of the human HRAS1 minisatellite in Saccharomyces cerevisiae
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Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks
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Human minisatellite mutation rate after the Chernobyl accident
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Nuclear weapons tests and human germline mutation rate.
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Elevated minisatellite mutation rate in the post-chernobyl families from ukraine
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Mouse minisatellite mutations induced by ionizing radiation
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Stage specificity, dose response, and doubling dose for mouse minisatellite germ-line mutation induced by acute radiation
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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Wheat mutation rate after Chernobyl
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7 January 2021
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Fitness loss and germline mutations in barn swallows breeding in Chernobyl
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Multilocus DNA fingerprinting reveals high rate of heritable genetic mutation in herring gulls nesting in an industrialized urban site
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Minisatellite mutation frequency in human sperm following radiotherapy
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Children of chernobyl cleanup workers do not show elevated rates of mutations in minisatellite alleles
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Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events
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A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development.
1 reference
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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A novel unstable mouse VNTR family expanded from SINE B1 elements.
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Length of uninterrupted repeats determines instability at the unstable mouse expanded simple tandem repeat family MMS10 derived from independent SINE B1 elements.
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A novel single molecule analysis of spontaneous and radiation-induced mutation at a mouse tandem repeat locus.
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Transgenerational mutation by radiation
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Elevated mutation rates in the germ line of first- and second-generation offspring of irradiated male mice
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Ionising radiation and mutation induction at mouse minisatellite loci. The story of the two generations
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Untargeted mutation of the maternally derived mouse hypervariable minisatellite allele in F1 mice born to irradiated spermatozoa
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Taming of transposable elements by homology-dependent gene silencing.
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Induction, repair and biological relevance of radiation-induced DNA lesions in eukaryotic cells
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No correlation between germline mutation at repeat DNA and meiotic crossover in male mice exposed to X-rays or cisplatin
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A domain that assumes a Z-conformation includes a specific deletion in some cloned variants of a complex satellite
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Ionizing radiation damage repair: a role for topoisomerases?
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Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX
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High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
1 reference
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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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7 January 2021
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Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900021-1
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7 January 2021
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Identifiers
DOI
10.1016/S0888-7543(03)00021-1
1 reference
stated in
Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
PubMed ID
12676558
1 reference
stated in
Europe PubMed Central
PubMed ID
12676558
retrieved
6 August 2017
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