Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR. (Q51688227)

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12 January 2020

title

Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR (English)

1 reference

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12 January 2020

main subject

Silver-Russell syndrome

1 reference

2

1 reference

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12 January 2020

Tsutomu Ogata

series ordinal

5

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12 January 2020

4

Keiko Matsubara

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12 January 2020

3

Maki Fukami

1 reference

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12 January 2020

1

Kazuki Yamazawa

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12 January 2020

publication date

16 August 2008

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Journal of Human Genetics

12 January 2020

published in

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12 January 2020

volume

53

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12 January 2020

issue

10

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12 January 2020

page(s)

950-955

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https://scigraph.springernature.com/pub.10.1007/s10038-008-0329-4

12 January 2020

exact match

0 references

cites work

An enhancer deletion affects both H19 and Igf2 expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

12 December 2020

Female carriers of Xp22.3 deletion including MRX locus

1 reference

12 December 2020

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations

1 reference

12 December 2020

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

1 reference

12 December 2020

Monozygotic twins discordant for the Russell-Silver syndrome

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

Tumour-suppressor activity of H19 RNA

1 reference

12 December 2020

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

1 reference

12 December 2020

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

12 December 2020

Monozygotic twins discordant for the Russell-Silver syndrome

1 reference

12 December 2020

Evidence for evolutionarily conserved secondary structure in the H19 tumor suppressor RNA.

1 reference

12 December 2020

The DNA methyltransferases of mammals

1 reference

12 December 2020

Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development

1 reference

12 December 2020

Russell-Silver syndrome: an explanation for discordant growth in monozygotic twins

1 reference

12 December 2020