Aberrant DNA methylation of imprinted loci in human spontaneous abortions after assisted reproduction techniques and natural conception (Q43837126)

27 November 2017

title

Aberrant DNA methylation of imprinted loci in human spontaneous abortions after assisted reproduction techniques and natural conception (English)

1 reference

27 November 2017

0 references

Hai-Yan Zheng

1

1 reference

27 November 2017

Yan Tang

2

1 reference

27 November 2017

Jing Niu

3

1 reference

27 November 2017

Pu Li

4

1 reference

27 November 2017

De-Sheng Ye

5

1 reference

27 November 2017

Xin Chen

6

1 reference

27 November 2017

Xiao-Yun Shi

7

1 reference

27 November 2017

Li Li

8

1 reference

27 November 2017

Shi-Ling Chen

9

1 reference

27 November 2017

language of work or name

English

0 references

publication date

4 October 2012

1 reference

27 November 2017

1 reference

27 November 2017

volume

28

1 reference

27 November 2017

issue

1

1 reference

27 November 2017

page(s)

265-273

1 reference

Epigenetic and experimental modifications in early mammalian development: part I. Preface

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

A survey of assisted reproductive technology births and imprinting disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Miscarriage and its associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

21 January 2018

Resourceful imprinting.

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Intracytoplasmic sperm injection may increase the risk of imprinting defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Epigenetic regulation of mammalian genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Assessment of day-3 morphology and euploidy for individual chromosomes in embryos that develop to the blastocyst stage

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Imprinting and the epigenetic asymmetry between parental genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

The importance of imprinting in the human placenta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Beckwith-Wiedemann syndrome and IVF: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Genome-wide identification of new imprinted genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Imprinting diseases and IVF: Danish National IVF cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Imprinting in the germ line

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

The role of imprinted genes in fetal growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Chromosome abnormalities and their relationship to morphology and development of human embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Epigenetic reprogramming in mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Nuclear cloning and epigenetic reprogramming of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Aberrant DNA methylation of imprinted loci in superovulated oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Genetics of pregnancy loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Insufficient maintenance DNA methylation is associated with abnormal embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Dynamics of DNA-demethylation in early mouse and rat embryos developed in vivo and in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Assisted reproductive technologies do not increase risk of abnormal methylation of PEG1/MEST in human early pregnancy loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDES358

21 January 2018

Identifiers

DOI

10.1093/HUMREP/DES358

1 reference

27 November 2017

1 reference