A citation-based method for searching scientific literature

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.
Harrison W Gabel, Benyam Kinde, Hume Stroud, Caitlin S Gilbert, David A Harmin, Nathaniel R Kastan, Martin Hemberg, Daniel H Ebert, Michael E Greenberg. Nature 2015
Times Cited: 319



Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.
R Z Chen, S Akbarian, M Tudor, R Jaenisch. Nat Genet 2001
Times Cited: 937




List of shared articles



Times cited

The Role of MeCP2 in Regulating Synaptic Plasticity in the Context of Stress and Depression.
Carla L Sánchez-Lafuente, Lisa E Kalynchuk, Hector J Caruncho, Juan Ausió. Cells 2022
0

Recent advances in gene therapy for neurodevelopmental disorders with epilepsy.
Thomas J Turner, Clara Zourray, Stephanie Schorge, Gabriele Lignani. J Neurochem 2021
11

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics.
Katrina V Good, John B Vincent, Juan Ausió. Front Genet 2021
13

MECP2 and the biology of MECP2 duplication syndrome.
Santosh R D'Mello. J Neurochem 2021
4

The Molecular Functions of MeCP2 in Rett Syndrome Pathology.
Osman Sharifi, Dag H Yasui. Front Genet 2021
2

Transcriptomic and Epigenomic Landscape in Rett Syndrome.
Domenico Marano, Salvatore Fioriniello, Maurizio D'Esposito, Floriana Della Ragione. Biomolecules 2021
1

MeCP2 is a microsatellite binding protein that protects CA repeats from nucleosome invasion.
Abdulkhaleg Ibrahim, Christophe Papin, Kareem Mohideen-Abdul, Stéphanie Le Gras, Isabelle Stoll, Christian Bronner, Stefan Dimitrov, Bruno P Klaholz, Ali Hamiche. Science 2021
4

Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models.
Yan Jiang, Xing Fu, Yuhan Zhang, Shen-Fei Wang, Hong Zhu, Wei-Kang Wang, Lin Zhang, Ping Wu, Catherine C L Wong, Jinsong Li,[...]. Nat Commun 2021
0

Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular Dysfunctions.
Snow Bach, Stephen Shovlin, Michael Moriarty, Barbara Bardoni, Daniela Tropea. Front Cell Neurosci 2021
0

Accelerated Hyper-Maturation of Parvalbumin Circuits in the Absence of MeCP2.
Annarita Patrizi, Patricia N Awad, Bidisha Chattopadhyaya, Chloe Li, Graziella Di Cristo, Michela Fagiolini. Cereb Cortex 2020
21

Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development.
Mayara C Ribeiro, Jessica L MacDonald. Brain Res 2020
14

Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome.
Laura A Lavery, Kerstin Ure, Ying-Wooi Wan, Chongyuan Luo, Alexander J Trostle, Wei Wang, Haijing Jin, Joanna Lopez, Jacinta Lucero, Mark A Durham,[...]. Elife 2020
15

Dosage-sensitive genes in autism spectrum disorders: From neurobiology to therapy.
Sehrish Javed, Tharushan Selliah, Yu-Ju Lee, Wei-Hsiang Huang. Neurosci Biobehav Rev 2020
4

MeCP2 Levels Regulate the 3D Structure of Heterochromatic Foci in Mouse Neurons.
Aya Ito-Ishida, Steven A Baker, Roy V Sillitoe, Yaling Sun, Jian Zhou, Yukiteru Ono, Junichi Iwakiri, Michisuke Yuzaki, Huda Y Zoghbi. J Neurosci 2020
7


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