(Q51936727)

17 April 2018

title

Subcellular distribution of HP1 proteins is altered in ICF syndrome. (English)

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17 April 2018

author

Danielle Depetris

2

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17 April 2018

Marie-Geneviève Mattéi

8

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17 April 2018

author name string

Judith J Luciani

1

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17 April 2018

Chantal Missirian

3

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17 April 2018

Cécile Mignon-Ravix

4

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17 April 2018

Catherine Metzler-Guillemain

5

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17 April 2018

André Megarbane

6

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17 April 2018

Anne Moncla

7

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17 April 2018

publication date

1 January 2005

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17 April 2018

European Journal of Human Genetics

published in

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17 April 2018

volume

13

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17 April 2018

issue

1

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17 April 2018

page(s)

41-51

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17 April 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201293

exact match

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cites work

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DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients

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21 January 2018

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Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

21 January 2018

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7 January 2021

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

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7 January 2021

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

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Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16

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Fluorodeoxyuridine synchronization of bone marrow cultures

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7 January 2021

HP1beta and HP1gamma, but not HP1alpha, decorate the entire XY body during human male meiosis

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Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts

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7 January 2021

A cloned repeated DNA sequence in human chromosome heteromorphisms

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201293

1 reference

17 April 2018

1 reference

17 April 2018