(Q72345863)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

author name string

Lalande M

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 April 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

page(s)

386-394

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

Completion of mouse embryogenesis requires both the maternal and paternal genomes

26 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Allele-specific replication timing of imprinted gene regions

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Analysis of replication timing properties of human X-chromosomal loci by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Allelic inactivation regulates olfactory receptor gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Transvection: allelic cross talk

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Transvection and long-distance gene regulation

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Igf2r and Igf2 gene expression in androgenetic, gynogenetic, and parthenogenetic preimplantation mouse embryos: absence of regulation by genomic imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Imprinting: a gamete's point of view

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Early signaling defects in human T cells anergized by T cell presentation of autoantigen

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Analysis and sorting of living cells according to deoxyribonucleic acid content

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Use of DiO-C5-3 to improve Hoechst 33342 uptake, resolution of DNA content, and survival of CHO cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-386

7 January 2021

Identifiers

DOI

10.1038/NG0495-386

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795644%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference