(Q28593334)

31 January 2017

title

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression (English)

1 reference

Methyl CpG binding protein 2

31 January 2017

0 references

1 reference

GOA release 2020-03-11

author name string

Kirill Makedonski

1

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31 January 2017

Liron Abuhatzira

2

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31 January 2017

Yotam Kaufman

3

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31 January 2017

Aharon Razin

4

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31 January 2017

Ruth Shemer

5

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31 January 2017

publication date

15 April 2005

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31 January 2017

published in

Human Molecular Genetics

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31 January 2017

volume

14

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31 January 2017

issue

8

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31 January 2017

page(s)

1049–1058

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A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

31 January 2017

cites work

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30 December 2023

https://opencitations.net/index/api/v1/citations/10.1016/S1097-2765(03)00276-4

Identifiers

1 reference

31 January 2017

1 reference