Meiotic interallelic conversion at the human minisatellite MS32 in yeast triggers recombination in several chromatids (Q64388736)

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2 November 2019

title

Meiotic interallelic conversion at the human minisatellite MS32 in yeast triggers recombination in several chromatids (English)

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2 November 2019

3

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2 November 2019

author name string

H Appelgren

series ordinal

1

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2 November 2019

H Cederberg

series ordinal

2

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2 November 2019

language of work or name

English

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publication date

1 October 1999

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2 November 2019

number of pages

10

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inferred from page(s)

published in

Gene

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2 November 2019

volume

239

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2 November 2019

issue

1

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2 November 2019

page(s)

29-38

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Mutations at the human minisatellite MS32 integrated in yeast occur with high frequency in meiosis and involve complex recombination events

2 November 2019

cites work

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Trinucleotide repeat expansion and human disease

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Clustering of meiotic double-strand breaks on yeast chromosome III

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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

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7 January 2021

Branch migration through DNA sequence heterology

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Human minisatellite MS32 (D1S8) displays somatic but not germline instability in transgenic mice

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Isolation and characterization of mouse minisatellites.

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

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7 January 2021

Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice.

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7 January 2021

Molecular Mechanism of the t(14;18)—A Model for Lymphoid-Specific Chromosomal Translocations

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Somatic mutation processes at a human minisatellite

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Hypervariable 'minisatellite' regions in human DNA.

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

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Minisatellite repeat coding as a digital approach to DNA typing

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Complex gene conversion events in germline mutation at human minisatellites

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Repeat instability at human minisatellites arising from meiotic recombination

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7 January 2021

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

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7 January 2021

An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

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7 January 2021

The human minisatellite consensus at breakpoints of oncogene translocations

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Gene targeting by linear duplex DNA frequently occurs by assimilation of a single strand that is subject to preferential mismatch correction

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7 January 2021

Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309)

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7 January 2021

Meiotic recombination: a mechanism for tracking and eliminating mutations?

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7 January 2021

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

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7 January 2021

Formation of a single base mismatch impedes spontaneous DNA branch migration.

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7 January 2021

Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA

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7 January 2021

The double-strand-break repair model for recombination

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7 January 2021

Four-state MVR-PCR: increased discrimination of digital DNA typing by simultaneous analysis of two polymorphic sites within minisatellite variant repeats at D1S8.

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7 January 2021

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

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7 January 2021

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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Identifiers

DOI

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2 November 2019

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