Repeat instability at human minisatellites arising from meiotic recombination (Q33889147)

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English	Repeat instability at human minisatellites arising from meiotic recombination	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

title

Repeat instability at human minisatellites arising from meiotic recombination (English)

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Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

author name string

A J Jeffreys

series ordinal

1

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Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

D L Neil

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

R Neumann

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

language of work or name

English

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publication date

1 July 1998

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stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

published in

The EMBO Journal

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stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

volume

17

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

issue

14

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stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

page(s)

4147-4157

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stated in

Europe PubMed Central

PubMed publication ID

9670029

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29 July 2017

cites work

Allele-specific MVR-PCR analysis at minisatellite D1S8.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

Effective amplification of long targets from cloned inserts and human genomic DNA

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

Allele-dependent recombination frequency: homology requirement in meiotic recombination at the hot spot in the mouse major histocompatibility complex

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

The 1993-94 Généthon human genetic linkage map

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

The double-strand-break repair model for recombination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

Exchanges at the bobbed locus of Drosophila melanogaster

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

Hypervariable 'minisatellite' regions in human DNA.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

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

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

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5 July 2018

The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

Mismatch repair-induced meiotic recombination requires the pms1 gene product

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

Minisatellite repeat coding as a digital approach to DNA typing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

'Touchdown' PCR to circumvent spurious priming during gene amplification

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

A second-generation linkage map of the human genome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170747

retrieved

5 July 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unequal meiotic recombination within tandem arrays of yeast ribosomal DNA genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic gene conversion mediates gene amplification in yeast

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic recombination in yeast: alteration by multiple heterozygosities

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a panel of highly variable minisatellites cloned from human DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA-minisatellite mutations: recent investigations concerning distribution and impact on parentage testing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex gene conversion events in germline mutation at human minisatellites

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of allelic structures at the D7S21 (MS31A) locus in the Japanese, using minisatellite variant repeat mapping by PCR (MVR-PCR)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutation processes at a human minisatellite

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Big, bad minisatellites

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of Repeated DNA Sequences by Unequal Crossover

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9670029

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/EMBOJ/17.14.4147

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

PMC publication ID

1170747

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

PubMed publication ID

9670029

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9670029

retrieved

29 July 2017

ResearchGate publication ID

13615001

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