(Q41439642)

30 September 2017

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title

DNA methylation in genomic imprinting (English)

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30 September 2017

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Tycko B

1

1 reference

PubMed ID

9113114

30 September 2017

language of work or name

English

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publication date

1 April 1997

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30 September 2017

1 reference

30 September 2017

386

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30 September 2017

131-140

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30 September 2017

2

1 reference

Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse

30 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Demethylation of CpG islands in embryonic cells

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Role of paternal and maternal genomes in mouse development

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Genomic imprinting determines methylation of parental alleles in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Regulation of genomic imprinting by gametic and embryonic processes.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Neomorphic agouti mutations in obese yellow mice

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

DNA methylation: evolution of a bacterial immune function into a regulator of gene expression and genome structure in higher eukaryotes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Methylation and imprinting: from host defense to gene regulation?

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Characteristics of imprinted genes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Creation of genomic methylation patterns

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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%2FS1383-5742%2896%2900049-X

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Parental-origin-specific epigenetic modification of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Comparative analysis of Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Gamete-specific methylation correlates with imprinting of the murine Xist gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Methylation of the mouse Xist gene in sperm and eggs correlates with imprinted Xist expression and paternal X-inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Visualization of chromosomal domains with boundary element-associated factor BEAF-32.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

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/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

5-Methylcytosine, Gene Regulation, and Cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Brief report: treatment with azacitidine of patients with end-stage beta-thalassemia

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

Sex, maps, and imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

An extended region of biallelic gene expression and rodent-human synteny downstream of the imprinted H19 gene on chromosome 11p15.5.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5742%2896%2900049-X

7 January 2021

10.1016/S1383-5742(96)00049-X

Identifiers

DOI

1 reference

30 September 2017

1 reference

PubMed ID

9113114