V. Sheen

发表

Mutation in Filamin A Causes Periventricular Heterotopia, Developmental Regression, and West Syndrome in Males

A. Sakamoto, E. Yacubian, E. Garzon, 2006, Epilepsia.

Filamin A Regulates Neural Progenitor Proliferation and Cortical Size through Wee1-Dependent Cdk1 Phosphorylation

S. Cross, R. J. Ferland, Jianjun Hu, 2012, The Journal of Neuroscience.

Filamin A and Big2: A shared endocytic pathway

V. Sheen, 2014, Bioarchitecture.

Filamin B Regulates Chondrocyte Proliferation and Differentiation through Cdk1 Signaling

Jianjun Hu, J. Hecht, V. Sheen, 2014, PloS one.

Periventricular heterotopia with complete agenesis of the corpus callosum

C. Walsh, V. Sheen, J. Neal, 2006, Journal of Neurology.

Lubricated biodegradable polymer networks for regulating nerve cell behavior and fabricating nerve conduits with a compositional gradient.

Lei Cai, V. Sheen, Shanfeng Wang, 2012, Biomacromolecules.

Filamin A Regulates Neuronal Migration through Brefeldin A-Inhibited Guanine Exchange Factor 2-Dependent Arf1 Activation

Jianjun Hu, V. Sheen, J. Neal, 2013, The Journal of Neuroscience.

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.

N W Wood, F Andermann, S M Sisodiya, 2001, Human molecular genetics.

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

C. Walsh, M. Sahin, V. Sheen, 2006, American journal of medical genetics. Part A.

Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males

P. Brugières, S. Amselem, M. Gerard-Blanluet, 2006, American journal of medical genetics. Part A.

Periventricular heterotopia associated with chromosome 5p anomalies

C. Walsh, S. Packman, O. Glenn, 2003, Neurology.

Brefeldin A-inhibited Guanine Exchange Factor 2 Regulates Filamin A Phosphorylation and Neuronal Migration

R. J. Ferland, V. Sheen, J. Neal, 2012, The Journal of Neuroscience.

Hyperperfusion with vasogenic leakage by fMRI in migraine with prolonged aura.

V. Sheen, D. Cros, Marsha S A Smith, 2002, Neurology.

Adult acute disseminated encephalomyelitis associated with poststreptococcal infection

S. Smirnakis, K. Furie, M. Ning, 2005, Journal of Clinical Neuroscience.

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

V. Sheen, Gewei Lian, Sneha Kanaujia, 2017, PloS one.

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

Hui Zhou, Q. Lu, P. Fuchs, 2015, Neurobiology of Disease.

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

M. Downing, A. Chenn, V. Sheen, 2016, Development.

Cortical Interneurons Upregulate Neurotrophinsin Vivoin Response to Targeted Apoptotic Degeneration of Neighboring Pyramidal Neurons

J. D. Macklis, V. Sheen, Youzhen Wang, 1998, Experimental Neurology.

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

V. Sheen, Gewei Lian, 2015, Front. Cell. Neurosci..

Hemichorea as a presentation of recurrent non-Hodgkin's lymphoma

S. Feske, V. Sheen, E. Heyman, 2002, Journal of Neurology.

Optimal poly(L-lysine) grafting density in hydrogels for promoting neural progenitor cell functions.

Lei Cai, V. Sheen, Shanfeng Wang, 2012, Biomacromolecules.

S100B and APP Promote a Gliocentric Shift and Impaired Neurogenesis in Down Syndrome Neural Progenitors

B. Dickinson, L. Steardo, J. Hecht, 2011, PloS one.

Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus

I. Scheffer, C. Walsh, Y. Shugart, 2004, Brain and Development.

Filamin B mutations cause chondrocyte defects in skeletal development.

A. Boskey, V. Sheen, C. Walsh, 2007, Human molecular genetics.

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

R. Folkerth, L. Steardo, J. Chesnut, 2008, Human molecular genetics.

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

R. J. Ferland, Jianjun Hu, V. Sheen, 2014, Human molecular genetics.

Combinatorial Gene Effects on the Neural Progenitor Pool in Down Syndrome

V. Sheen, Jie Lu, 2011 .

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

Giuseppe Esposito, Q Richard Lu, Hui Zhou, 2012, Human molecular genetics.

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

C. Walsh, R. Folkerth, A. Banham, 2009, Human molecular genetics.

Malformations of Cortical Development

Trudy Pang, V. Sheen, Trudy D Pang, 2008, The neurologist.

Genetic and Epigenetic Mechanisms in Down Syndrome Brain

V. Sheen, Jie Lu, 2013 .

Promoting nerve cell functions on hydrogels grafted with poly(L-lysine).

Lei Cai, V. Sheen, Shanfeng Wang, 2012, Biomacromolecules.

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

Anuj Kumar Goyal, Jianjun Hu, J. Hecht, 2017, Human molecular genetics.

Generation of neural stem cells from discarded human fetal cortical tissue.

R. Folkerth, J. Hecht, V. Sheen, 2011, Journal of visualized experiments : JoVE.

Cytoskeletal Associated Filamin A and RhoA Affect Neural Progenitor Specification During Mitosis

Jianjun Hu, V. Sheen, Gewei Lian, 2019, Cerebral cortex.

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

C. Walsh, P. Grant, Y. Shugart, 2004, Nature Genetics.

Impaired proliferation and migration in human Miller‐Dieker neural precursors

J. Corbo, R. Folkerth, A. Chenn, 2006, Annals of neurology.

Neocortical neuronal arrangement in Miller Dieker syndrome

C. Walsh, J. Corbo, R. Folkerth, 2006, Acta Neuropathologica.

DNMT3L promotes neural differentiation by enhancing STAT1 and STAT3 phosphorylation independent of DNA methylation

Chong Qiao, V. Sheen, Jie Lu, 2021, Progress in Neurobiology.

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

A. Chenn, V. Sheen, Gewei Lian, 2019, Cerebral cortex.

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

J. Hecht, V. Sheen, G. Esposito, 2016, Human molecular genetics.

Hyperostosis cranii ex vacuo from ventricular shunting

V. Sheen, 2011, Journal of Pediatric Neurology.

Progressive mental status changes and seizures with fluid attenuated inversion recovery (FLAIR) hyperintensity on brain MRI

S. Ramkissoon, S. Pittock, V. Sheen, 2012, Journal of Clinical Neuroscience.

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

V. Sheen, 2012, Scientifica.

Clinical Report Periventricular Nodular Heterotopia and Williams Syndrome

C. Walsh, R. J. Ferland, V. Sheen, 2006 .

Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: Insights into the cause of periventricular heterotopia

R. Folkerth, G. Tiao, V. Sheen, 2006, The Journal of comparative neurology.

S100B induces tau protein hyperphosphorylation via Dickopff-1 up-regulation and disrupts the Wnt pathway in human neural stem cells

Giuseppe Esposito, L. Steardo, V. Sheen, 2008, Journal of cellular and molecular medicine.

Periventricular heterotopia: new insights into Ehlers-Danlos syndrome.

C. Walsh, V. Sheen, 2005, Clinical medicine & research.

Calcium‐mediated neuronal degeneration following singlet oxygen production

J. D. Macklis, E. Dreyer, V. Sheen, 1992, Neuroreport.

Methylphenidate and continuous spike and wave during sleep in a child with attention deficit hyperactivity disorder.

A. Torres, I. Marín-Valencia, V. Sheen, 2013, Pediatric neurology.

Autosomal recessive form of periventricular heterotopia

C. Walsh, Y. Shugart, S. Berkovic, 2003, Neurology.

Cerebellar ataxia with progressive improvement.

C. Walsh, J. Tsao, W. Dobyns, 2006, Archives of neurology.

Periventricular heterotopia

V. Sheen, Jie Lu, 2005, Epilepsy & Behavior.

Mutations in ARFGEF 2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

C. Walsh, P. Grant, Y. Shugart, 2022 .

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

Christopher A. Walsh, C. Walsh, S. Shapiro, 2002, Human molecular genetics.

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

C. Walsh, Ming-Hui Chen, S. Robertson, 2005, Neurology.

Herpes Zoster Ophthalmicus Followed by Contralateral Hemiparesis

R. Nogueira, V. Sheen, 2002 .

Treatment of paroxysmal sympathetic storm with labetalol

E. Bromfield, V. Sheen, D. Do, 2000, Journal of neurology, neurosurgery, and psychiatry.

Differentiation of transplanted neural precursors varies regionally in adults striatum.

J. D. Macklis, B. Leavitt, V. Sheen, 1999, Neuroreport.

Filamin A mediated Big2 dependent endocytosis

V. Sheen, 2014, Tissue barriers.

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

V. Sheen, 2014 .

Neural Precursor Differentiation Following Transplantation into Neocortex Is Dependent on Intrinsic Developmental State and Receptor Competence

J. D. Macklis, V. Sheen, Jeffrey D. Macklis, 1999, Experimental Neurology.

Cerebral developmental disorders

V. Sheen, Gewei Lian, 2006, Current opinion in pediatrics.

Apoptotic Mechanisms in Targeted Neuronal Cell Death by Chromophore-Activated Photolysis

J. D. Macklis, V. Sheen, 1994, Experimental Neurology.

Response: Filamin A, Periventricular Nodular Heterotopia, and West Syndrome

C. Walsh, A. Sakamoto, R. Hill, 2006 .

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia

C. Walsh, A. Galaburda, D. Hackney, 2005, Neurology.

Developmental genetic malformations of the cerebral cortex

C. Walsh, V. Sheen, 2003, Current neurology and neuroscience reports.

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

Grace Tiao, Jason Neal, Christopher A Walsh, 2007, Journal of anatomy.

Periventricular nodular heterotopia and Williams syndrome

R. J. Ferland, V. Sheen, C. Walsh, 2006, American journal of medical genetics. Part A.

Mutation in PQBP1 is associated with periventricular heterotopia

V. Kimonis, A. Torres, V. Sheen, 2010, American journal of medical genetics. Part A.

Malformations of Cortical Development

V. Sheen, Trudy D Pang, R. Atefy, 2008, The Neurologist.

Mutation in PQBP1 is associated with periventricular heterotopia

V. Kimonis, A. Torres, V. Sheen, 2010, American journal of medical genetics. Part A.

Methylphenidate and continuous spike and wave during sleep in a child with attention deficit hyperactivity disorder.

A. Torres, I. Marín-Valencia, V. Sheen, 2013, Pediatric neurology.

Cavernous sinus syndrome and headache due to bilateral carotid artery aneurysms.

A. Atri, V. Sheen, 2003, Archives of neurology.

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

Hui Zhou, Q. Lu, P. Fuchs, 2015, Neurobiology of Disease.

BranchAnalysis2D/3D automates morphometry analyses of branching structures

Aditya Srinivasan, Russell J. Ferland, Jesús Muñoz-Estrada, 2017, Journal of Neuroscience Methods.