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English
Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution
scientific article published on 01 April 1995
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Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
title
Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
author
Janine M. LaSalle
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
author name string
Lalande M
series ordinal
2
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Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
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26 October 2019
publication date
1 April 1995
1 reference
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Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
published in
Nature Genetics
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Europe PubMed Central
PubMed ID
7795644
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
volume
9
1 reference
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Europe PubMed Central
PubMed ID
7795644
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
page(s)
386-394
1 reference
stated in
Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
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26 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0495-386
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Completion of mouse embryogenesis requires both the maternal and paternal genomes
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Crossref
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7 January 2021
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Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
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Parental imprinting of the mouse H19 gene
1 reference
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Crossref
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7 January 2021
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Parental imprinting of the mouse insulin-like growth factor II gene.
1 reference
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7 January 2021
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Relaxation of imprinted genes in human cancer.
1 reference
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Crossref
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7 January 2021
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IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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Monoallelic expression of the human H19 gene
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0495-386
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7 January 2021
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Parental origin of chromosome 15 deletion in Prader-Willi syndrome
1 reference
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Crossref
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7 January 2021
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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
1 reference
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reference URL
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7 January 2021
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Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
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Uniparental paternal disomy in Angelman's syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
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Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
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Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allele-specific replication timing of imprinted gene regions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-386
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of replication timing properties of human X-chromosomal loci by fluorescence in situ hybridization
1 reference
stated in
Crossref
reference URL
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Allelic inactivation regulates olfactory receptor gene expression
1 reference
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Transvection: allelic cross talk
1 reference
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Transvection and long-distance gene regulation
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Crossref
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Igf2r and Igf2 gene expression in androgenetic, gynogenetic, and parthenogenetic preimplantation mouse embryos: absence of regulation by genomic imprinting
1 reference
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Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development
1 reference
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Crossref
reference URL
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7 January 2021
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Imprinting: a gamete's point of view
1 reference
stated in
Crossref
reference URL
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7 January 2021
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Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?
1 reference
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Analysis and sorting of living cells according to deoxyribonucleic acid content
1 reference
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Crossref
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Use of DiO-C5-3 to improve Hoechst 33342 uptake, resolution of DNA content, and survival of CHO cells
1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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Identifiers
DOI
10.1038/NG0495-386
1 reference
stated in
Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
PubMed ID
7795644
1 reference
stated in
Europe PubMed Central
PubMed ID
7795644
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
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