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Localization of mariner DNA transposons in the human genome by PRINS
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Localization of mariner DNA transposons in the human genome by PRINS
(English)
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author
Lawrence T Reiter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
T Liehr
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
B Rautenstrauss
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
H M Robertson
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
J R Lupski
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 September 1999
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Genome Research
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
9
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
839-843
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
9
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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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=310809
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8 July 2018
The impact of L1 retrotransposons on the human genome
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PubMed Central
reference URL
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The mechanisms involved in formation of deletions and duplications of 15q11-q13.
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8 July 2018
Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients
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stated in
PubMed Central
reference URL
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8 July 2018
A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK
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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=310809
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8 July 2018
Molecular evolution of the second ancient human mariner transposon, Hsmar2, illustrates patterns of neutral evolution in the human genome lineage
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=310809
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8 July 2018
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome
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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=310809
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8 July 2018
The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs.
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=310809
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8 July 2018
Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.
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PubMed Central
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8 July 2018
Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot
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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=310809
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8 July 2018
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients
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stated in
PubMed Central
reference URL
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8 July 2018
7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossover.
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=310809
retrieved
25 October 2018
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.
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=310809
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25 October 2018
Mariner transposons in humans.
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=310809
retrieved
25 October 2018
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10508842
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10508842
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Modes of DAPI banding and simultaneous in situ hybridization
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10508842
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10508842
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1101/GR.9.9.839
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PMCID
310809
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed ID
10508842
1 reference
stated in
Europe PubMed Central
PMCID
310809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508842%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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