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English
An estimated frequency of endogenous insertional mutations in humans
scientific article published on 01 June 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
title
An estimated frequency of endogenous insertional mutations in humans
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
author name string
Kazazian HH Jr
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
publication date
1 June 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
volume
22
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
page(s)
130
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/9638
0 references
cites work
The origin of interspersed repeats in the human genome
1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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The impact of L1 retrotransposons on the human genome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
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inferred from DOI database lookup
Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High frequency retrotransposition in cultured mammalian cells
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exon shuffling by L1 retrotransposition
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
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inferred from DOI database lookup
Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
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Developmental and cell type specificity of LINE-1 expression in mouse testis: implications for transposition
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
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7 January 2021
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Mobile elements and disease
1 reference
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reference URL
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Positional cloning of the gene for X-linked retinitis pigmentosa 2
1 reference
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reference URL
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retrieved
7 January 2021
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inferred from DOI database lookup
Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unusual mutations in Btk: an insertion, a duplication, an inversion, and four large deletions.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The rate with which spontaneous mutation alters the electrophoretic mobility of polypeptides
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High genomic deleterious mutation rates in hominids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F9638
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/9638
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
PubMed ID
10369250
1 reference
stated in
Europe PubMed Central
PubMed ID
10369250
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10369250%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
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