(Q43837126)

27 November 2017

title

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

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27 November 2017

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Hai-Yan Zheng

1

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27 November 2017

Yan Tang

2

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27 November 2017

Jing Niu

3

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27 November 2017

Pu Li

4

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27 November 2017

De-Sheng Ye

5

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27 November 2017

Xin Chen

6

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27 November 2017

Xiao-Yun Shi

7

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27 November 2017

Li Li

8

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27 November 2017

Shi-Ling Chen

9

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27 November 2017

language of work or name

English

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publication date

4 October 2012

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27 November 2017

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27 November 2017

volume

28

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27 November 2017

issue

1

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27 November 2017

page(s)

265-273

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

27 November 2017

cites work

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

A survey of assisted reproductive technology births and imprinting disorders.

21 January 2018

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

Miscarriage and its associations

21 January 2018

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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

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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

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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

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27 November 2017

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