Cargando…

L1 retrotransposition in neurons is modulated by MeCP2

Detalles Bibliográficos
Autores principales:	Muotri, Alysson R., Marchetto, Maria C. N., Coufal, Nicole G., Oefner, Ruth, Yeo, Gene, Nakashima, Kinichi, Gage, Fred H.
Formato:	Texto
Lenguaje:	English
Publicado:	2010
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059197/ https://www.ncbi.nlm.nih.gov/pubmed/21085180 http://dx.doi.org/10.1038/nature09544

Ejemplares similares

Interchromosomal translocation in neural progenitor cells exposed to L1 retrotransposition
por: Muotri, Alysson R.
Publicado: (2023)

Alternative Splicing Events Identified in Human Embryonic Stem Cells and Neural Progenitors
por: Yeo, Gene W, et al.
Publicado: (2007)

MeCP2 and Chromatin Compartmentalization
por: Schmidt, Annika, et al.
Publicado: (2020)

Transcriptional Signature and Memory Retention of Human-Induced Pluripotent Stem Cells
por: Marchetto, Maria C. N., et al.
Publicado: (2009)

MeCP2 modulates gene expression pathways in astrocytes
por: Yasui, Dag H, et al.
Publicado: (2013)

Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
por: Wu, Tao, et al.
Publicado: (2016)

The Crucial Role of DNA Methylation and MeCP2 in Neuronal Function
por: Fasolino, Maria, et al.
Publicado: (2017)

Novel MeCP2 Isoform-Specific Antibody Reveals the Endogenous MeCP2E1 Expression in Murine Brain, Primary Neurons and Astrocytes
por: Zachariah, Robby M., et al.
Publicado: (2012)

The role of MeCP2 in learning and memory
por: Robinson, Holly A., et al.
Publicado: (2019)

Neuronal non-CG methylation is an essential target for MeCP2 function
por: Tillotson, Rebekah, et al.
Publicado: (2021)

Structural investigation of Rett-inducing MeCP2 mutations()
por: Spiga, Ottavia, et al.
Publicado: (2018)

Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders
por: Meng, Xiangling, et al.
Publicado: (2016)

Rett Syndrome and MECP2 Duplication Syndrome: Disorders of MeCP2 Dosage
por: Collins, Bridget E, et al.
Publicado: (2022)

Genetic Modifiers of MeCP2 Function in Drosophila
por: Cukier, Holly N., et al.
Publicado: (2008)

MeCP2-Related Diseases and Animal Models
por: Ezeonwuka, Chinelo D., et al.
Publicado: (2014)

MeCP2 mediated dysfunction in senescent EPCs
por: Wang, Chunli, et al.
Publicado: (2017)

MeCP2 as a genome-wide modulator: the renewal of an old story
por: Ragione, Floriana Della, et al.
Publicado: (2012)

MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation
por: Schmidt, Annika, et al.
Publicado: (2022)

Engineered LINE-1 retrotransposition in nondividing human neurons
por: Macia, Angela, et al.
Publicado: (2017)

MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome
por: Takeguchi, Ryo, et al.
Publicado: (2019)

A critique of the hypothesis that CA repeats are primary targets of neuronal MeCP2
por: Chhatbar, Kashyap, et al.
Publicado: (2022)

MeCP2 mutations: progress towards understanding and treating Rett syndrome
por: Shah, Ruth R., et al.
Publicado: (2017)

MeCP2 Promotes Colorectal Cancer Metastasis by Modulating ZEB1 Transcription
por: Luo, Dan, et al.
Publicado: (2020)

The Role of MeCP2 in Brain Development and Neurodevelopmental Disorders
por: Gonzales, Michael L., et al.
Publicado: (2010)

Rett mutations attenuate phase separation of MeCP2
por: Fan, Chunyan, et al.
Publicado: (2020)

MeCP2 mediates transgenerational transmission of chronic pain
por: Tao, Wenjuan, et al.
Publicado: (2020)

The Molecular Functions of MeCP2 in Rett Syndrome Pathology
por: Sharifi, Osman, et al.
Publicado: (2021)

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics
por: Good, Katrina V., et al.
Publicado: (2021)

Epigenetic Dysfunction of Neurodegenerative Diseases, MeCP2 and More
por: Im, Heh-In
Publicado: (2022)

High Levels of MeCP2 Depress MHC Class I Expression in Neuronal Cells
por: Miralvès, Julie, et al.
Publicado: (2007)

Loss of MeCP2 disrupts cell autonomous and autocrine BDNF signaling in mouse glutamatergic neurons
por: Sampathkumar, Charanya, et al.
Publicado: (2016)

The methyl-CpG-binding domain (MBD) is crucial for MeCP2’s dysfunction-induced defects in adult newborn neurons
por: Zhao, Na, et al.
Publicado: (2015)

Direct Homo- and Hetero-Interactions of MeCP2 and MBD2
por: Becker, Annette, et al.
Publicado: (2013)

Circadian Cycle-Dependent MeCP2 and Brain Chromatin Changes
por: Martínez de Paz, Alexia, et al.
Publicado: (2015)

Sequence‐specific DNA binding by AT‐hook motifs in MeCP2
por: Lyst, Matthew J., et al.
Publicado: (2016)

Toxicity of overexpressed MeCP2 is independent of HDAC3 activity
por: Koerner, Martha V., et al.
Publicado: (2018)

Sex-Based Mhrt Methylation Chromatinizes MeCP2 in the Heart
por: K.N., Harikrishnan, et al.
Publicado: (2019)

Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants
por: Beribisky, Alexander V., et al.
Publicado: (2022)

A Comprehensive and Integrative Approach to MeCP2 Disease Transcriptomics
por: Trostle, Alexander J., et al.
Publicado: (2023)

Quantitative analysis questions the role of MeCP2 as a global regulator of alternative splicing
por: Chhatbar, Kashyap, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_5plkjgjka4h4i7bl1mnjm4i90d