(Q24312925)

DNA methylation involved in embryo development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Carlo L Acerini

5

0 references

Sian Ellard

Sian Ellard

16

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Andrew Tym Hattersley

17

Andrew T Hattersley

0 references

Helen V. Firth

8

Helen V Firth

0 references

Judith A Goodship

9

Judith A Goodship

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author name string

Deborah J G Mackay

1

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Jonathan L A Callaway

2

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Sophie M Marks

3

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Helen E White

4

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Susanne E Boonen

6

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Pinar Dayanikli

7

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Andreas P Haemers

10

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Johanne M D Hahnemann

11

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Olga Kordonouri

12

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Ahmed F Masoud

13

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Elsebet Oestergaard

14

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John Storr

15

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David O Robinson

18

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I Karen Temple

Identification and characterization of ZFP-57, a novel zinc finger transcription factor in the mammalian peripheral nervous system

19

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language of work or name

English

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publication date

August 2008

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published in

Nature Genetics

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volume

40

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issue

8

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page(s)

949-51

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG.187

Genomic imprinting: parental influence on the genome

20 April 2017

1 reference

"Stemness": transcriptional profiling of embryonic and adult stem cells

20 April 2017

1 reference

Epigenetics and the germline

20 April 2017

1 reference

Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib

21 January 2018

1 reference

Allele-specific demethylation at an imprinted mammalian promoter

21 January 2018

1 reference

Transient neonatal diabetes, a disorder of imprinting.

21 January 2018

1 reference

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

21 January 2018

1 reference

Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings

21 January 2018

1 reference

A stem cell molecular signature

21 January 2018

1 reference

Identification of Zfp-57 as a downstream molecule of STAT3 and Oct-3/4 in embryonic stem cells.

21 January 2018

1 reference

Bisulphite sequencing of the transient neonatal diabetes mellitus DMR facilitates a novel diagnostic test but reveals no methylation anomalies in patients of unknown aetiology

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Central precocious puberty in a girl with triple X syndrome and neonatal diabetes mellitus associated with paternal isodisomy of chromosome 6

1 reference