A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain

[1]  M. Kuijpers Keeping synapses in shape: degradation pathways in the healthy and aging brain , 2022, Neuronal signaling.

[2]  E. Takahashi,et al.  Comprehensive Volumetric Analysis of Mecp2-Null Mouse Model for Rett Syndrome by T2-Weighted 3D Magnetic Resonance Imaging , 2022, Frontiers in Neuroscience.

[3]  J. Roux,et al.  Rett syndrome: think outside the (skull) box , 2021, Faculty reviews.

[4]  H. Zoghbi,et al.  Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice , 2021, eLife.

[5]  G. Laviola,et al.  Rett syndrome before regression: A time window of overlooked opportunities for diagnosis and intervention , 2019, Neuroscience & Biobehavioral Reviews.

[6]  E. Takahashi,et al.  Surface- and voxel-based brain morphologic study in Rett and Rett-like syndrome with MECP2 mutation , 2019, International Journal of Developmental Neuroscience.

[7]  Gilda Stefanelli,et al.  A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome , 2018, Molecular Neurobiology.

[8]  Gilda Stefanelli,et al.  A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome , 2018, Molecular Neurobiology.

[9]  Daniela Tropea,et al.  Transcriptome level analysis in Rett syndrome using human samples from different tissues , 2018, Orphanet Journal of Rare Diseases.

[10]  Mriganka Sur,et al.  Rett syndrome: insights into genetic, molecular and circuit mechanisms , 2018, Nature Reviews Neuroscience.

[11]  U. Dirnagl,et al.  Atlas registration for edema-corrected MRI lesion volume in mouse stroke models , 2017, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[12]  M. Justice,et al.  Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes , 2017, Molecular Autism.

[13]  N. Landsberger,et al.  Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms. , 2016, Cerebral cortex.

[14]  D. Parolaro,et al.  MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background , 2016, PloS one.

[15]  H. Zoghbi,et al.  MECP2 disorders: from the clinic to mice and back. , 2015, The Journal of clinical investigation.

[16]  Riccardo L. Rossi,et al.  Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action , 2014, Neuroscience & Biobehavioral Reviews.

[17]  Jeff Sigafoos,et al.  Changing the perspective on early development of Rett syndrome , 2013, Research in developmental disabilities.

[18]  A. Giordano,et al.  Reduced expression of MECP2 affects cell commitment and maintenance in neurons by triggering senescence: new perspective for Rett syndrome , 2012, Molecular biology of the cell.

[19]  M. Giustetto,et al.  Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model. , 2011, Human molecular genetics.

[20]  A. Percy,et al.  Experimental models of Rett syndrome based on Mecp2 dysfunction , 2011, Experimental biology and medicine.

[21]  W. Kaufmann,et al.  Rett syndrome: Revised diagnostic criteria and nomenclature , 2010, Annals of neurology.

[22]  C. Barnes,et al.  Neural Protein Synthesis during Aging: Effects on Plasticity and Memory , 2010, Front. Ag. Neurosci..

[23]  I. Izbudak,et al.  White Matter Impairment in Rett Syndrome: Diffusion Tensor Imaging Study with Clinical Correlations , 2010, American Journal of Neuroradiology.

[24]  E. Masliah,et al.  Widespread changes in dendritic and axonal morphology in Mecp2‐mutant mouse models of rett syndrome: Evidence for disruption of neuronal networks , 2009, The Journal of comparative neurology.

[25]  N. Nag,et al.  Neurochemical changes in a mouse model of Rett syndrome: changes over time and in response to perinatal choline nutritional supplementation , 2009, Journal of neurochemistry.

[26]  Huda Y. Zoghbi,et al.  Deletion of Mecp2 in Sim1-Expressing Neurons Reveals a Critical Role for MeCP2 in Feeding Behavior, Aggression, and the Response to Stress , 2008, Neuron.

[27]  J. Berger-Sweeney,et al.  Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline , 2008, Neurobiology of Disease.

[28]  N. Nag,et al.  Behavioral and anatomical abnormalities in Mecp2 mutant mice: A model for Rett syndrome , 2007, Neuroscience.

[29]  S. Confort-Gouny,et al.  Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism. , 2006, Biochemical and biophysical research communications.

[30]  James H. Eubanks,et al.  Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome , 2006, Neurobiology of Disease.

[31]  Juan I. Young,et al.  Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 , 2002, Neuron.

[32]  D. Armstrong Rett syndrome neuropathology review 2000 , 2001, Brain and Development.

[33]  S. Provencher Automatic quantitation of localized in vivo 1H spectra with LCModel , 2001, NMR in biomedicine.

[34]  N. Landsberger,et al.  Rett Syndrome: From the Involved Gene(s) to Treatment , 2015 .

[35]  A. Bird,et al.  A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome , 2001, Nature Genetics.