4.5 Article

Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows

Related references

Note: Only part of the references are listed.
Article Multidisciplinary Sciences

Adult Neural Function Requires MeCP2

Christopher M. McGraw et al.

SCIENCE (2011)

Article Clinical Neurology

Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database

Michael Freilinger et al.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)

Article Pediatrics

Longevity in Rett Syndrome: Analysis of the North American Database

Russell S. Kirby et al.

JOURNAL OF PEDIATRICS (2010)

Article Biochemistry & Molecular Biology

Neuronal MeCP2 Is Expressed at Near Histone-Octamer Levels and Globally Alters the Chromatin State

Peter J. Skene et al.

MOLECULAR CELL (2010)

Article Biochemistry & Molecular Biology

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

Micaela Galante et al.

HUMAN MOLECULAR GENETICS (2009)

Article Biochemistry & Molecular Biology

A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

Rodney C. Samaco et al.

HUMAN MOLECULAR GENETICS (2008)

Article Biochemistry & Molecular Biology

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

Bredford Kerr et al.

HUMAN MOLECULAR GENETICS (2008)

Review Neurosciences

The story of Rett syndrome: From clinic to neurobiology

Maria Chahrour et al.

NEURON (2007)

Article Multidisciplinary Sciences

Reversal of neurological defects in a mouse model of Rett syndrome

Jacky Guy et al.

SCIENCE (2007)

Article Neurosciences

An altered neonatal behavioral phenotype in Mecp2 mutant mice

JD Picker et al.

NEUROREPORT (2006)

Review Cell Biology

MeCP2 dysfunction in Rett syndrome and related disorders

Paolo Moretti et al.

CURRENT OPINION IN GENETICS & DEVELOPMENT (2006)

Article Clinical Neurology

Neuropathology of Rett syndrome

DD Armstrong

JOURNAL OF CHILD NEUROLOGY (2005)

Article Genetics & Heredity

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

C Schanen et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)

Article Neurosciences

Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study

S Cassel et al.

NEUROBIOLOGY OF DISEASE (2004)