Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.

Mutations in the human methyl-CpG-binding protein gene MECP2 cause the neurological disorder Rett syndrome and some cases of X-linked mental retardation (XLMR). We report that MeCP2 interacts with ATRX, a SWI2/SNF2 DNA helicase/ATPase that is mutated in ATRX syndrome (alpha-thalassemia/mental retard...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Nan, X, Hou, J, Maclean, A, Nasir, J, Lafuente, M, Shu, X, Kriaucionis, S, Bird, A
التنسيق:	Journal article
اللغة:	English
منشور في:	2007

مواد مشابهة

Mutations in the chromatin-associated protein ATRX.
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منشور في: (2008)

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منشور في: (2007)

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منشور في: (2004)

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منشور في: (2017)

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منشور في: (2014)

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منشور في: (2004)

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منشور في: (2009)

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منشور في: (2018-11-01)

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حسب: Nitish Gulve, وآخرون
منشور في: (2022-08-01)

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حسب: Kejia Yuan, وآخرون
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MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males
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منشور في: (2023-04-01)

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حسب: PLOS ONE Staff
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منشور في: (2021)

The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin
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منشور في: (2022)

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منشور في: (2012)

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