Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

Enhancing Oligodendrocyte Myelination Rescues Synaptic Loss and Improves Functional Recovery after Chronic Hypoxia

(2018) Fei Wang et al.   NEURON

Clemastine fumarate as a remyelinating therapy for multiple sclerosis (ReBUILD): a randomised, controlled, double-blind, crossover trial

(2017) Ari J Green et al.   LANCET

A Sensitized IGF1 Treatment Restores Corticospinal Axon-Dependent Functions

(2017) Yuanyuan Liu et al.   NEURON

Generation of a mouse model for a conditional inactivation ofGtf2iallele

(2016) Badam Enkhmandakh et al.   GENESIS

Clemastine Enhances Myelination in the Prefrontal Cortex and Rescues Behavioral Changes in Socially Isolated Mice

(2016) J. Liu et al.   JOURNAL OF NEUROSCIENCE

A human neurodevelopmental model for Williams syndrome

(2016) Thanathom Chailangkarn et al.   NATURE

Neurobiology of social behavior abnormalities in autism and Williams syndrome

(2016) Boaz Barak et al.   NATURE NEUROSCIENCE

Remodeling myelination: implications for mechanisms of neural plasticity

(2016) Kae-Jiun Chang et al.   NATURE NEUROSCIENCE

Chromatin Landscape Defined by Repressive Histone Methylation during Oligodendrocyte Differentiation

(2015) J. Liu et al.   JOURNAL OF NEUROSCIENCE

Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams–Beuren Syndrome

(2015) Cristina Borralleras et al.   MOLECULAR THERAPY

Myelination of the Nervous System: Mechanisms and Functions

(2014) Klaus-Armin Nave et al.   Annual Review of Cell and Developmental Biology

Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder

(2014) Maria Segura-Puimedon et al.   HUMAN MOLECULAR GENETICS

Micropillar arrays as a high-throughput screening platform for therapeutics in multiple sclerosis

(2014) Feng Mei et al.   NATURE MEDICINE

Novel inter-hemispheric white matter connectivity in the BTBR mouse model of autism

(2013) V.M. Miller et al.   BRAIN RESEARCH

Neuron-Specific Expression of Tomosyn1 in the Mouse Hippocampal Dentate Gyrus Impairs Spatial Learning and Memory

(2013) Boaz Barak et al.   NEUROMOLECULAR MEDICINE

Regulation of conduction time along axons

(2013) A.H. Seidl   NEUROSCIENCE

Differential Joint-Specific Corticospinal Tract Projections within the Cervical Enlargement

(2013) Curtis O. Asante et al.   PLoS One

Impaired adult myelination in the prefrontal cortex of socially isolated mice

(2012) Jia Liu et al.   NATURE NEUROSCIENCE

Quantitative analysis of gray and white matter in Williams syndrome

(2012) Andreia Vasconcellos Faria et al.   NEUROREPORT

The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function

(2012) M. Jabbi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Critical Period for Social Experience-Dependent Oligodendrocyte Maturation and Myelination

(2012) M. Makinodan et al.   SCIENCE

Biochemistry and biology of the inducible multifunctional transcription factor TFII-I: 10years later

(2011) Ananda L. Roy   GENE

Alterations in diffusion properties of white matter in Williams syndrome

(2011) Lori R. Arlinghaus et al.   MAGNETIC RESONANCE IMAGING

White matter integrity deficits in prefrontal–amygdala pathways in Williams syndrome

(2011) Suzanne N. Avery et al.   NEUROIMAGE

Animal models of Williams syndrome

(2010) Lucy R. Osborne   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions

(2010) Takeshi Sakurai et al.   Autism Research

Essential role of the N-terminal region of TFII-I in viability and behavior

(2010) Jaume Lucena et al.   BMC Medical Genetics

Oestrogen receptor β ligand: a novel treatment to enhance endogenous functional remyelination

(2010) Daniel K. Crawford et al.   BRAIN

Williams–Beuren Syndrome

(2010) Barbara R. Pober   NEW ENGLAND JOURNAL OF MEDICINE

Behavioral and neurobiological changes in C57BL/6 mouse exposed to cuprizone: effects of antipsychotics

(2010) Haiyun Xu   Frontiers in Behavioral Neuroscience

Is it Williams syndrome?GTF2IRD1implicated in visual-spatial construction andGTF2Iin sociability revealed by high resolution arrays

(2009) L. Dai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cuprizone Demyelination of the Corpus Callosum in Mice Correlates with Altered Social Interaction and Impaired Bilateral Sensorimotor Coordination

(2009) Norah Hibbits et al.   ASN Neuro

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

(2009) Hong Hua Li et al.   EMBO Molecular Medicine

Modulating myelination: knowing when to say Wnt

(2009) S. S. Rosenberg et al.   GENES & DEVELOPMENT

Assaying the functional effects of demyelination and remyelination: Revisiting field potential recordings

(2009) Daniel K. Crawford et al.   JOURNAL OF NEUROSCIENCE METHODS

Low sociability is associated with reduced size of the corpus callosum in the BALB/cJ inbred mouse strain

(2008) Andrew H. Fairless et al.   BRAIN RESEARCH

A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function

(2008) J. D. Cahoy et al.   JOURNAL OF NEUROSCIENCE

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

(2008) B. Enkhmandakh et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA