(Q72296658)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7774561%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

The use of restriction landmark genomic scanning to scan the mouse genome for endogenous loci with imprinted patterns of methylation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7774561%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author

Yoshihide Hayashizaki

6

object named as

Hayashizaki Y

1 reference

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25 October 2019

author name string

Shibata H

1

1 reference

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25 October 2019

Yoshino K

2

1 reference

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25 October 2019

Muramatsu M

3

1 reference

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25 October 2019

Plass C

4

1 reference

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25 October 2019

Chapman VM

5

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25 October 2019

publication date

1 February 1995

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25 October 2019

1 reference

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25 October 2019

volume

16

1 reference

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25 October 2019

issue

2

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25 October 2019

page(s)

210-217

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7774561%20AND%20SRC:MED&resulttype=core&format=json

Chromosome imprinting and the mammalian X chromosome

25 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Parental source of chromosome imprinting and its relevance for X chromosome inactivation.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

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/10.1002%2FELPS.1150160136

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/10.1002%2FELPS.1150160136

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/10.1002%2FELPS.1150160136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Mosaic and polymorphic imprinting of the WT1 gene in humans.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Mouse homologues of human hereditary disease.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Evidence that random and imprinted Xist expression is controlled by preemptive methylation.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

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/10.1002%2FELPS.1150160136

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Differential imprinting and expression of maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Enzymatic amplification of a Y chromosome repeat in a single blastomere allows identification of the sex of preimplantation mouse embryos

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Restriction landmark genomic scanning method and its various applications

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Molecular cloning of polymorphic markers on RLGS gel using the spot target cloning method

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

RI manager, a microcomputer program for analysis of data from recombinant inbred strains

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Use of restriction enzymes to detect potential gene sequences in mammalian DNA.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Number of CpG islands and genes in human and mouse

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Direct determination of NotI cleavage sites in the genomic DNA of adult mouse kidney and human trophoblast using whole-range restriction landmark genomic scanning

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Comparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and human chromosome 5

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150160136

7 January 2021

Identifiers

DOI

10.1002/ELPS.1150160136

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7774561%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference