MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats

A national survey of Rett syndrome: Age, clinical characteristics, current abilities, and health

(2015) Rina Cianfaglione et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Conditional depletion of methyl-CpG-binding protein 2 in astrocytes depresses the hypercapnic ventilatory response in mice

(2015) Saurabh K. Garg et al.   JOURNAL OF APPLIED PHYSIOLOGY

MECP2 disorders: from the clinic to mice and back

(2015) Laura Marie Lombardi et al.   JOURNAL OF CLINICAL INVESTIGATION

MeCP2 in the Rostral Striatum Maintains Local Dopamine Content Critical for Psychomotor Control

(2015) San-Hua Su et al.   JOURNAL OF NEUROSCIENCE

Rett syndrome: a complex disorder with simple roots

(2015) Matthew J. Lyst et al.   NATURE REVIEWS GENETICS

The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders

(2015) Daniel C. Tarquinio et al.   PEDIATRIC NEUROLOGY

Applying the ethoexperimental approach to neurodevelopmental syndrome research reveals exaggerated defensive behavior in Mecp2 mutant mice

(2015) Brandon L. Pearson et al.   PHYSIOLOGY & BEHAVIOR

MeCP2 Affects Skeletal Muscle Growth and Morphology through Non Cell-Autonomous Mechanisms

(2015) Valentina Conti et al.   PLoS One

Regulation of breathing by CO2 requires the proton-activated receptor GPR4 in retrotrapezoid nucleus neurons

(2015) N. N. Kumar et al.   SCIENCE

Deficient Purposeful Use of Forepaws in Female Mice Modelling Rett Syndrome

(2015) Bianca De Filippis et al.   NEURAL PLASTICITY

Motor and cognitive deficits in aged tau knockout mice in two background strains

(2014) Peng Lei et al.   Molecular Neurodegeneration

Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X

(2014) J.M. Bissonnette et al.   NEUROSCIENCE

Gait Analysis in a Mecp2 Knockout Mouse Model of Rett Syndrome Reveals Early-Onset and Progressive Motor Deficits

(2014) Kamal K. E. Gadalla et al.   PLoS One

Characterization of the MeCP2R168X Knockin Mouse Model for Rett Syndrome

(2014) Eike Wegener et al.   PLoS One

Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures

(2013) Chiranjeevi Bodda et al.   AMERICAN JOURNAL OF PATHOLOGY

MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome

(2013) Fang-Chi Kao et al.   Brain Structure & Function

Rett Syndrome and Epilepsy: An Update for Child Neurologists

(2013) Alison Dolce et al.   PEDIATRIC NEUROLOGY

Breathing challenges in Rett Syndrome: Lessons learned from humans and animal models

(2013) Jan-Marino Ramirez et al.   RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY

Preclinical research in Rett syndrome: setting the foundation for translational success

(2012) D. M. Katz et al.   Disease Models & Mechanisms

Female Mecp2+/− mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies

(2012) Rodney C. Samaco et al.   HUMAN MOLECULAR GENETICS

Growth failure and outcome in Rett syndrome: Specific growth references

(2012) D. C. Tarquinio et al.   NEUROLOGY

Structured cognition and neural systems: From rats to language

(2012) Francesco P. Battaglia et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Acetyl-L-Carnitine Improves Behavior and Dendritic Morphology in a Mouse Model of Rett Syndrome

(2012) Laura R. Schaevitz et al.   PLoS One

A role for glia in the progression of Rett’s syndrome

(2011) Daniel T. Lioy et al.   NATURE

Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses

(2011) Darren Goffin et al.   NATURE NEUROSCIENCE

Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice

(2011) Basil Cardoza et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

Rett syndrome diagnostic criteria: Lessons from the Natural History Study

(2010) Alan K. Percy et al.   ANNALS OF NEUROLOGY

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

(2010) Garilyn M Jentarra et al.   BMC NEUROSCIENCE

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

(2010) Hsiao-Tuan Chao et al.   NATURE

Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice

(2010) Jennifer Anne D'Cruz et al.   NEUROBIOLOGY OF DISEASE

Epilepsy and the natural history of Rett syndrome

(2010) D. G. Glaze et al.   NEUROLOGY

Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome

(2010) M. Santos et al.   NEUROSCIENCE

Profiling Scoliosis in Rett Syndrome

(2010) Alan K Percy et al.   PEDIATRIC RESEARCH

Correction of respiratory disorders in a mouse model of Rett syndrome

(2010) A. P. L. Abdala et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

On the generality and limits of abstraction in rats and humans

(2009) Gonzalo P. Urcelay et al.   ANIMAL COGNITION

Early postnatal behavioral changes in theMecp2-308 truncation mouse model of Rett syndrome

(2009) B. De Filippis et al.   GENES BRAIN AND BEHAVIOR

An investigation of playful behaviour in Rattus norvegicus and Mus musculus (Mammalia)

(2009) Trevor B. Poole et al.   JOURNAL OF ZOOLOGY

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

(2009) R. C. Samaco et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function

(2009) J. Tao et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome

(2009) Nicolas Voituron et al.   RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY

Breathing disorders in Rett syndrome: Progressive neurochemical dysfunction in the respiratory network after birth

(2009) David M. Katz et al.   RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY

Early abnormalities of post-sigh breathing in a mouse model of Rett syndrome

(2009) N. Voituron et al.   RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY

Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp21lox mice

(2008) Nupur Nag et al.   BEHAVIOURAL BRAIN RESEARCH

Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)

(2008) A. Renieri et al.   BRAIN & DEVELOPMENT

Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice

(2008) Bredford Kerr et al.   HUMAN MOLECULAR GENETICS

Comparative study of brain morphology inMecp2mutant mouse models of Rett syndrome

(2008) Nadia P. Belichenko et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline

(2008) B.C. Ward et al.   NEUROBIOLOGY OF DISEASE

Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation

(2008) An-Hsun Chou et al.   NEUROBIOLOGY OF DISEASE

Deletion of Mecp2 in Sim1-Expressing Neurons Reveals a Critical Role for MeCP2 in Feeding Behavior, Aggression, and the Response to Stress

(2008) Sharyl L. Fyffe et al.   NEURON

Autonomic dysregulation in young girls with Rett Syndrome during nighttime in-home recordings

(2008) Debra E. Weese-Mayer et al.   PEDIATRIC PULMONOLOGY

Breathing dysfunction in Rett syndrome: Understanding epigenetic regulation of the respiratory network

(2008) Michael Ogier et al.   RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY