Methylation imprinting of H19 and SNRPN genes in human benign ovarian teratomas (Q34145942)

31 July 2017

Methylation imprinting of H19 and SNRPN genes in human benign ovarian teratomas (English)

1 reference

31 July 2017

Miura K

1

1 reference

31 July 2017

Obama M

2

1 reference

31 July 2017

Yun K

3

1 reference

31 July 2017

Masuzaki H

4

1 reference

31 July 2017

Ikeda Y

5

1 reference

31 July 2017

Yoshimura S

6

1 reference

31 July 2017

Akashi T

7

1 reference

31 July 2017

Niikawa N

8

1 reference

31 July 2017

Ishimaru T

9

1 reference

31 July 2017

Jinno Y

10

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 November 1999

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

65

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31 July 2017

5

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31 July 2017

1359-1367

1 reference

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Epigenotype switching of imprintable loci in embryonic germ cells.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Genetic regulation of traits essential for spontaneous ovarian teratocarcinogenesis in strain LT/Sv mice: aberrant meiotic cell cycle, oocyte activation, and parthenogenetic development.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

A comprehensive genetic map of the human genome based on 5,264 microsatellites

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Role for DNA methylation in genomic imprinting

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

DNA methylation and genomic imprinting

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Mosaic and polymorphic imprinting of the WT1 gene in humans.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Parthenogenic Origin of Benign Ovarian Teratomas

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288288

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10521301

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Automation of genetic linkage analysis using fluorescent microsatellite markers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10521301

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Benign ovarian teratomas. An analysis of their cellular origin

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10521301

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302615

1 reference

31 July 2017

1 reference

31 July 2017

1 reference