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Cytoskeletal proteins in cortical development and disease: actin associated proteins in periventricular heterotopia

Frontiers in cellular neuroscience, 2015-04, Vol.9, p.99-99

2015

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Cytoskeletal proteins in cortical development and disease: actin associated proteins in periventricular heterotopia

Frontiers in cellular neuroscience, 2015-04, Vol.9, p.99

2015

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Filamin B regulates chondrocyte proliferation and differentiation through Cdk1 signaling

PloS one, 2014-02, Vol.9 (2), p.e89352-e89352

2014

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Filamin A- and formin 2-dependent endocytosis regulates proliferation via the canonical Wnt pathway

Development (Cambridge), 2016-12, Vol.143 (23), p.4509-4520

2016

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FilaminA and Formin2 regulate skeletal, muscular, and intestinal formation through mesenchymal progenitor proliferation

PloS one, 2017-12, Vol.12 (12), p.e0189285-e0189285

2017

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Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreading

Human molecular genetics, 2017-04, Vol.26 (7), p.1294-1304

2017

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Global hypermethylation in fetal cortex of Down syndrome due to DNMT3L overexpression

Human molecular genetics, 2016-05, Vol.25 (9), p.1714-1727

2016

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Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation

The Journal of neuroscience, 2012-05, Vol.32 (22), p.7672-7684

2012

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Filamin A regulates neuronal migration through brefeldin A-inhibited guanine exchange factor 2-dependent Arf1 activation

The Journal of neuroscience, 2013-10, Vol.33 (40), p.15735-15746

2013

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Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

Human molecular genetics, 2009-02, Vol.18 (3), p.497-516

2009

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Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

Nature genetics, 2004-01, Vol.36 (1), p.69-76

2004

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Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate

Human molecular genetics, 2014-09, Vol.23 (17), p.4663-4673

2014

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Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration

The Journal of neuroscience, 2012-09, Vol.32 (36), p.12619-12629

2012

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Filamin A mediated Big2 dependent endocytosis: From apical abscission to periventricular heterotopia

Tissue barriers, 2014-01, Vol.2 (1), p.e29431-e29431

Sheen, Volney L

2014

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BranchAnalysis2D/3D automates morphometry analyses of branching structures

Journal of neuroscience methods, 2018-01, Vol.294, p.1-6

2018

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OLIG2 over-expression impairs proliferation of human Down syndrome neural progenitors

Human molecular genetics, 2012-05, Vol.21 (10), p.2330-2340

2012

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S100B and APP promote a gliocentric shift and impaired neurogenesis in Down syndrome neural progenitors

PloS one, 2011-07, Vol.6 (7), p.e22126-e22126

2011

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Seizure or syncope: Lessons over time

Journal of clinical neuroscience, 2012-03, Vol.19 (3), p.481-483

Sheen, Volney L

2012

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Insights into the gyrification of developing ferret brain by magnetic resonance imaging

Journal of anatomy, 2007-01, Vol.210 (1), p.66-77

2007

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Genomic and functional profiling of human Down syndrome neural progenitors implicates S100B and aquaporin 4 in cell injury

Human molecular genetics, 2008-02, Vol.17 (3), p.440-457

2008

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Methylphenidate and Continuous Spike and Wave During Sleep in a Child With Attention Deficit Hyperactivity Disorder

Pediatric neurology, 2013-07, Vol.49 (1), p.54-57

2013

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Periventricular Heterotopia : Shuttling of Proteins through Vesicles and Actin in Cortical Development and Disease

Scientifica (Cairo), 2012-01, Vol.2012 (2012), p.1-13

2012

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Disruption of neurogenesis and cortical development in transgenic mice misexpressing Olig2, a gene in the Down syndrome critical region

Neurobiology of disease, 2015-05, Vol.77, p.106-116

2015

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Filamin A and Big2: A shared endocytic pathway

Bioarchitecture, 2014-03, Vol.4 (2), p.53-57

Sheen, Volney L.

2014

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Filamin B mutations cause chondrocyte defects in skeletal development

Human molecular genetics, 2007-07, Vol.16 (14), p.1661-1675

2007

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Cytoskeletal proteins in cortical development and disease: actin associated proteins in periventricular heterotopia

Cytoskeletal proteins in cortical development and disease: actin associated proteins in periventricular heterotopia

Filamin B regulates chondrocyte proliferation and differentiation through Cdk1 signaling

Filamin A- and formin 2-dependent endocytosis regulates proliferation via the canonical Wnt pathway

FilaminA and Formin2 regulate skeletal, muscular, and intestinal formation through mesenchymal progenitor proliferation

Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreading

Global hypermethylation in fetal cortex of Down syndrome due to DNMT3L overexpression

Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation

Filamin A regulates neuronal migration through brefeldin A-inhibited guanine exchange factor 2-dependent Arf1 activation

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate

Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration

Filamin A mediated Big2 dependent endocytosis: From apical abscission to periventricular heterotopia

BranchAnalysis2D/3D automates morphometry analyses of branching structures

OLIG2 over-expression impairs proliferation of human Down syndrome neural progenitors

S100B and APP promote a gliocentric shift and impaired neurogenesis in Down syndrome neural progenitors

Seizure or syncope: Lessons over time

Insights into the gyrification of developing ferret brain by magnetic resonance imaging

Genomic and functional profiling of human Down syndrome neural progenitors implicates S100B and aquaporin 4 in cell injury

Methylphenidate and Continuous Spike and Wave During Sleep in a Child With Attention Deficit Hyperactivity Disorder

Periventricular Heterotopia : Shuttling of Proteins through Vesicles and Actin in Cortical Development and Disease

Disruption of neurogenesis and cortical development in transgenic mice misexpressing Olig2, a gene in the Down syndrome critical region

Filamin A and Big2: A shared endocytic pathway

Filamin B mutations cause chondrocyte defects in skeletal development

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