(Q79830083)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

title

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

transient neonatal diabetes mellitus

26 December 2019

main subject

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Karen Temple

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

7

P R Njølstad

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

author name string

S E Boonen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

J Clayton-Smith

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

J Goodship

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

J M D Hahnemann

5

1 reference

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26 December 2019

S G Kant

6

1 reference

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26 December 2019

N H Robin

8

1 reference

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26 December 2019

D O Robinson

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

R Siebert

10

1 reference

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26 December 2019

J P H Shield

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816970%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

H E White

12

1 reference

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26 December 2019

publication date

1 July 2006

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26 December 2019

1 reference

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26 December 2019

volume

120

1 reference

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26 December 2019

page(s)

262-269

1 reference

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26 December 2019

issue

2

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00439-006-0205-2

26 December 2019

exact match

0 references

cites work

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

1 reference

12 December 2020

Transient neonatal diabetes, a disorder of imprinting.

1 reference

12 December 2020

Imprinting errors and developmental asymmetry

1 reference

12 December 2020

DNA methylation and human disease

1 reference

12 December 2020

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.

1 reference

12 December 2020

A global disorder of imprinting in the human female germ line.

1 reference

12 December 2020

Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region

1 reference

12 December 2020

Genomic imprinting: parental influence on the genome

1 reference

12 December 2020

Epigenetics and the germline

1 reference

12 December 2020

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

1 reference

12 December 2020

A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7

1 reference

12 December 2020

Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation

1 reference

12 December 2020

Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

1 reference

12 December 2020

Methylation dynamics of imprinted genes in mouse germ cells.

1 reference

12 December 2020

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

1 reference

12 December 2020

Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus

1 reference

12 December 2020

Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

1 reference

12 December 2020

Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles.

1 reference

12 December 2020

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

1 reference

12 December 2020

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior

1 reference

12 December 2020

A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus

1 reference

12 December 2020

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark

1 reference

12 December 2020

Physiological functions of imprinted genes.

1 reference

12 December 2020

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

1 reference

12 December 2020

Stochastic imprinting in the progeny of Dnmt3L-/- females.

1 reference

12 December 2020

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.

1 reference

12 December 2020

An imprinted locus associated with transient neonatal diabetes mellitus

1 reference

12 December 2020

Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region.

1 reference

12 December 2020

Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

1 reference

12 December 2020