(Q33904840)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

4

1 reference

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3 November 2019

author name string

Ingrid Berg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Rita Neumann

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Håkan Cederberg

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Alec J Jeffreys

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

language of work or name

English

0 references

publication date

12 May 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

3 November 2019

published in

1 reference

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3 November 2019

volume

72

1 reference

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3 November 2019

issue

6

1 reference

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3 November 2019

page(s)

1436-1447

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review

3 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Minisatellite instability and germline mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Repeat instability at human minisatellites arising from meiotic recombination

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Influences of array size and homogeneity on minisatellite mutation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Mutations occurring at the human minisatellite MS1 integrated in haploid yeast are similar to MS1 mutations in humans.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Mutation processes at human minisatellites.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Hypervariable 'minisatellite' regions in human DNA.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Minisatellite repeat coding as a digital approach to DNA typing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

A novel single molecule analysis of spontaneous and radiation-induced mutation at a mouse tandem repeat locus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Trinucleotide expansion in haploid germ cells by gap repair

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Length of uninterrupted repeats determines instability at the unstable mouse expanded simple tandem repeat family MMS10 derived from independent SINE B1 elements.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Increased trinucleotide repeat instability with advanced maternal age.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation†

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180304

Tetrad analysis shows that gene conversion is the major mechanism involved in mutation at the human minisatellite MS1 integrated in Saccharomyces cerevisiae

29 October 2018

1 reference

12 December 2020

Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

12 December 2020

Evolutionary transience of hypervariable minisatellites in man and the primates

1 reference

12 December 2020

Amplification and loss of repeat units of the human minisatellite MS1 integrated in chromosome III of a haploid yeast strain

1 reference

12 December 2020

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

1 reference

12 December 2020

Complex gene conversion events in germline mutation at human minisatellites

1 reference

12 December 2020

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

12 December 2020

Recent observations in human DNA-minisatellite mutations

1 reference

12 December 2020

Somatic mutations in VNTR-locus D1S7 in human colorectal carcinomas are associated with microsatellite instability

1 reference

12 December 2020

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

1 reference

12 December 2020

Somatic mutation processes at a human minisatellite

1 reference

12 December 2020

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

1 reference

12 December 2020

Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident

1 reference

12 December 2020

High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot

1 reference

12 December 2020

Cis-regulation of inter-allelic exchanges in mutation at human minisatellite MS205 in yeast

1 reference

12 December 2020

Identifiers

DOI

10.1086/375629

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748906%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

12748906

1 reference