(Q37068291)

18 August 2017

1 reference

title

Genomic imprinting: developmental significance and molecular mechanism (English)

1 reference

regulation of gene expression

18 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1822272

2 December 2022

1 reference

https://api.crossref.org/works/10.1016/S0959-437X(05)80077-2

2 December 2022

1

1 reference

18 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1822272

2 December 2022

publication date

1 August 1991

1 reference

full work available at URL

18 August 2017

https://api.elsevier.com/content/article/PII:S0959437X05800772?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0959-437X(05)80077-2

https://api.elsevier.com/content/article/PII:S0959437X05800772?httpAccept=text/plain

2 December 2022

1 reference

https://api.crossref.org/works/10.1016/S0959-437X(05)80077-2

Current Opinion in Genetics & Development

2 December 2022

published in

1 reference

18 August 2017

1

1 reference

18 August 2017

241-246

1 reference

18 August 2017

2

1 reference

Differential imprinting and expression of maternal and paternal genomes

18 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Parental imprinting of genes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

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/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Ectopic expression of the H19 gene in mice causes prenatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Genomic imprinting in mammalian development: a parental tug-of-war

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Epigenetic control of transgene expression and imprinting by genotype-specific modifiers

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Imprinting a determined state into the chromatin of Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

A sequence motif found in aDrosophilaheterochromatin protein is conserved in animals and plants

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Genomic imprinting and genetic disorders in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Proposed genetic basis of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980077-2

7 January 2021

Sex chromosomes and speciation

series ordinal

4

1 reference

https://api.crossref.org/works/10.1016/S0959-437X(05)80077-2

Inherited type of allelic methylation variations in a mouse chromosome region where an integrated transgene shows methylation imprinting

2 December 2022

series ordinal

23

1 reference

https://api.crossref.org/works/10.1016/S0959-437X(05)80077-2

2 December 2022

Identifiers

1 reference

18 August 2017

1 reference