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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 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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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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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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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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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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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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Gabapentin-induced exacerbation of myasthenia gravis

Muscle & nerve, 2010-07, Vol.42 (1), p.149-149

2010

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Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

Human molecular genetics, 2002-11, Vol.11 (23), p.2845-2854

2002

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Hyperostosis cranii ex vacuo from ventricular shunting

Journal of pediatric neurology, 2011-12, Vol.9 (4), p.509-511

Sheen, Volney

2011

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Generation of neural stem cells from discarded human fetal cortical tissue

Journal of visualized experiments, 2011-05 (51)

2011

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Periventricular nodular heterotopia and Williams syndrome

American journal of medical genetics. Part A, 2006-06, Vol.140A (12), p.1305-1311

2006

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Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

American journal of medical genetics. Part A, 2006-08, Vol.140A (15), p.1692-1695

2006

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Formin 2 Regulates Lysosomal Degradation of Wnt-Associated β-Catenin in Neural Progenitors

Cerebral cortex (New York, N.Y. 1991), 2019-05, Vol.29 (5), p.1938-1952

2019

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

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

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

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

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

Filamin A and Big2: A shared endocytic pathway

Filamin B mutations cause chondrocyte defects in skeletal development

Gabapentin-induced exacerbation of myasthenia gravis

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

Hyperostosis cranii ex vacuo from ventricular shunting

Generation of neural stem cells from discarded human fetal cortical tissue

Periventricular nodular heterotopia and Williams syndrome

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

Formin 2 Regulates Lysosomal Degradation of Wnt-Associated β-Catenin in Neural Progenitors

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