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MECP2
Developmental Delay and the Methyl Binding Genes H Turner, F Macdonald, S Warburton, F Latif, T Webb
Methyl-Cpg2-Binding Protein 2 Mediates Overlapping Mechanisms Across Brain Disorders
Soothing Sensory Sensitivity May Ease Social Problems in Mice
Electronic Letter 1Of4 J Med Genet: First Published As 10.1136/Jmg.37.12.E41 on 1 December 2000
MECP2 Disorders: from the Clinic to Mice and Back
Mecp2 Nuclear Dynamics in Live Neurons Results from Low and High
An Overview of the Main Genetic, Epigenetic and Environmental Factors Involved in Autism Spectrum Disorder Focusing on Synaptic Activity
The Role of Mecp2 in Learning and Memory
DNA Binding Selectivity of Mecp2 Due to a Requirement for A/T Sequences Adjacent to Methyl-Cpg
Rett Syndrome – Biological Pathways Leading from MECP2 to Disorder Phenotypes Friederike Ehrhart1,2* , Susan L
Mecp2 Enforces Foxp3 Expression to Promote Regulatory T
Role of DNA Methyl-Cpg-Binding Protein Mecp2 in Rett Syndrome Pathobiology and Mechanism of Disease
Mouse Model Links Epigenetics to Autism
Angelman Syndrome, Rett Syndrome, and Tuberous Sclerosis
The Evolving Role of Mecp2 in Rett Syndrome and Autism
Rett Syndrome Exploring the Autism Link
MECP2 Gene Methyl-Cpg Binding Protein 2
Male-Specific Features Are Reduced in Mecp2-Null Mice: Analyses of Vasopressinergic Innervation, Pheromone Production and Social Behaviour
Top View
Analysis of Protein Domains and Rett Syndrome Mutations Indicate That
Mecp2 and Chromatin Compartmentalization
Epigenetic Control of Vasopressin Expression Is Maintained by Steroid Hormones in the Adult Male Rat Brain
Targeting Peripheral Somatosensory Neurons to Improve Tactile-Related Phenotypes in ASD Models
Mecp2 Antibody
Mecp2 Monoclonal Antibody
Modeling Rett Syndrome with Mecp2 T158A Knockin Mice
MECP2 Mutation in Non-Fatal, Non-Progressive Encephalopathy In
Stressed for Life
Mecp2 Interacts with HP1 and Modulates Its Heterochromatin
Mecp2 and the Enigmatic Organization of Brain Chromatin
Autistic Phenotypes and Genetic Testing: State-Of-The- Art for the Clinical Geneticist C Lintas, a M Persico
Dissecting the Role of Mecp2 in Brain & Implications for Autism Spectrum
MECP2–Related Disorders
Methyl Cpg Binding Proteins: Coupling Chromatin Architecture to Gene Regulation
Genetics Evaluation for the Etiologic Diagnosis of Autism Spectrum Disorders G
A Case Report of Chinese Brothers with Inherited MECP2-Containing Duplication: Autism and Intellectual Disability, but Not Seizu
DNA Methylation and Behavioral Dysfunction in Males with 47,XXY and 49,XXXXY: a Pilot Study Richard S
Mecp2 Phosphorylation in the Brain: from Transcription to Behavior
Active Motif Technical Data Sheet (TDS)
Quantitative Modelling Predicts the Impact of DNA Methylation on RNA Polymerase II Traffic
A Rett Syndrome Patient with a Ring X Chromosome: Further Evidence for Skewing of X Inactivation and Heterogeneity in the Aetiology of the Disease
Identification and Characterization of Novel Sir3/Mecp2-Chromatin Interactions" (2009)
Epigenetic Modulation of Vasopressin Expression in Health and Disease
A Central Role for Mecp2 in the Epigenetic Repression of Mir-200C
Autism Genetics
The Many Faces of Mecp2
Heterochromatin: Stable and Unstable Invasions at Home and Abroad
Is Mecp2 a Gene Suppressor Or Activator?
Biological Pathways Leading from MECP2 to Disorder Phenotypes
Identification of Autism-Related MECP2 Mutations by Whole-Exome
Site-Directed RNA Repair of Endogenous Mecp2 RNA in Neurons
Role of Mecp2 in Heterochromatin Organization During Differentiation and Disease
Phenotypic and Genotypic Variability in Four Males with MECP2 Gene Sequence Aberrations Including a Novel Deletion
Parental Origin of De Novo MECP2 Mutations in Rett Syndrome
Epigenetic Regulation in Autism Spectrum Disorder
Leaving a Lasting Mark
Responsive Nuclear Proteins in Collecting Duct Cells
Rett Syndrome Is Caused by Mutations in X-Linked MECP2, Encoding Methyl-Cpg-Binding Protein 2
Mecp2 POST-TRANSLATIONAL MODIFICATIONS OTHER Mechanisms of Action Through Its Ptms
Mecp2 Function in the Basolateral Amygdala in Rett Syndrome