Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation-Reference-Cited by-同舟云学术

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation

Published:2002-12-19 Issue:1 Volume:81 Page:61-68
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Balmer Damina,Goldstine Jared,Rao Y. Manjula,LaSalle Janine M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00109-002-0396-5.pdf

Reference27 articles.

1. Armstrong DD (1997) Review of Rett syndrome. J Neuropathol Exp Neurol 56:843–849

2. Ellaway C, Christodoulou J (1999) Rett syndrome: clinical update and review of recent genetic advances. J Paediatr Child Health 35:419–426

3. Armstrong D, Dunn JK, Antalffy B, Trivedi R (1995) Selective dendritic alterations in the cortex of Rett syndrome. J Neuropathol Exp Neurol 54:195–201

4. Armstrong DD, Dunn K, Antalffy B (1998) Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21. J Neuropathol Exp Neurol 57:1013–1017

5. Van den Veyver IB, Zoghbi HY (2000) Methyl-CpG-binding protein 2 mutations in rett syndrome. Curr Opin Genet Dev 10:275–279

Cited by 97 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unravelling the Cerebellar Involvement in Autism Spectrum Disorders: Insights into Genetic Mechanisms and Developmental Pathways;Cells;2024-07-10

2. MeCP2 represses the activity of topoisomerase IIβ in long neuronal genes;Cell Reports;2023-12

3. MeCP2 Represses the Activity of Topoisomerase IIβ in Long Neuronal Genes;2023-02-26

4. MeCP2 Is an Epigenetic Factor That Links DNA Methylation with Brain Metabolism;International Journal of Molecular Sciences;2023-02-20

5. A brief history of MECP2 duplication syndrome: 20-years of clinical understanding;Orphanet Journal of Rare Diseases;2022-03-21