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Novel lissencephaly‐associated DCX variants in the C‐terminal DCX domain affect microtubule binding and dynamics

Epilepsia (Copenhagen), 2022-05, Vol.63 (5), p.1253-1265

2022

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Asymmetric centrosome inheritance maintains neural progenitors in the neocortex

Nature (London), 2009-10, Vol.461 (7266), p.947-955

2009

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Inhibitory effects of curcumin and cyclocurcumin in 1-methyl-4-phenylpyridinium (MPP+) induced neurotoxicity in differentiated PC12 cells

Scientific reports, 2017-12, Vol.7 (1), p.16977-9, Article 16977

2017

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Muscle atrophy‐related myotube‐derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs

Aging cell, 2020-05, Vol.19 (5), p.e13107-n/a

2020

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PRRT2 missense mutations cluster near C‐terminus and frequently lead to protein mislocalization

Epilepsia (Copenhagen), 2019-05, Vol.60 (5), p.807-817

2019

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LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages

The Journal of cell biology, 2005-09, Vol.170 (6), p.935-945

2005

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Gli2 Rescues Delays in Brain Development Induced by Kif3a Dysfunction

Cerebral cortex (New York, N.Y. 1991), 2019-02, Vol.29 (2), p.751-764

2019

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Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation

Developmental cell, 2019-01, Vol.48 (2), p.184-199.e5

2019

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Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)

Journal of biomedical science, 2021-09, Vol.28 (1), p.1-65, Article 65

2021

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Thymic macrophages consist of two populations with distinct localization and origin

eLife, 2022-11, Vol.11

2022

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Identification of genes associated with cortical malformation using a transposon-mediated somatic mutagenesis screen in mice

Nature communications, 2018-06, Vol.9 (1), p.2498-15, Article 2498

2018

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Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration

Cellular and molecular life sciences : CMLS, 2020-04, Vol.77 (7), p.1421-1434

2020

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WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury

International journal of molecular sciences, 2020-02, Vol.21 (4), p.1463

2020

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An Emerging Role of PRRT2 in Regulating Growth Cone Morphology

Cells (Basel, Switzerland), 2021-10, Vol.10 (10), p.2666

2021

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A rare human CEP290 variant disrupts the molecular integrity of the primary cilium and impairs Sonic Hedgehog machinery

Scientific reports, 2018-11, Vol.8 (1), p.17335-14, Article 17335

2018

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Contributions of Animal Models to the Mechanisms and Therapies of Transthyretin Amyloidosis

Frontiers in physiology, 2019-04, Vol.10, p.338-338

2019

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PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects

Oncotarget, 2016-06, Vol.7 (26), p.39184-39196

2016

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Efficient In Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.493-500

2020

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Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy

Methods in molecular biology (Clifton, N.J.), 2023, Vol.2623, p.61

2023

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Emerging roles for myosin II and cytoplasmic dynein in migrating neurons and growth cones

Trends in cell biology, 2009-07, Vol.19 (7), p.347-355

2009

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Quantification of the Metabolic State in Cell-Model of Parkinson’s Disease by Fluorescence Lifetime Imaging Microscopy

Scientific reports, 2016-01, Vol.6 (1), p.19145-19145, Article 19145

2016

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A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development

Development (Cambridge), 2024-01, Vol.151 (2)

2024

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Gli2 modulates cell cycle re-entry through autophagy-mediated regulation of the length of primary cilia

Journal of cell science, 2018-12, Vol.131 (24)

2018

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The cellular roles of the lissencephaly gene LIS1, and what they tell us about brain development

Genes & development, 2006-06, Vol.20 (11), p.1384-1393

2006

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Lis1 dysfunction leads to traction force reduction and cytoskeletal disorganization during cell migration

Biochemical and biophysical research communications, 2018-03, Vol.497 (3), p.869-875

2018

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Novel lissencephaly‐associated DCX variants in the C‐terminal DCX domain affect microtubule binding and dynamics

Asymmetric centrosome inheritance maintains neural progenitors in the neocortex

Inhibitory effects of curcumin and cyclocurcumin in 1-methyl-4-phenylpyridinium (MPP+) induced neurotoxicity in differentiated PC12 cells

Muscle atrophy‐related myotube‐derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs

PRRT2 missense mutations cluster near C‐terminus and frequently lead to protein mislocalization

LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages

Gli2 Rescues Delays in Brain Development Induced by Kif3a Dysfunction

Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation

Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)

Thymic macrophages consist of two populations with distinct localization and origin

Identification of genes associated with cortical malformation using a transposon-mediated somatic mutagenesis screen in mice

Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration

WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury

An Emerging Role of PRRT2 in Regulating Growth Cone Morphology

A rare human CEP290 variant disrupts the molecular integrity of the primary cilium and impairs Sonic Hedgehog machinery

Contributions of Animal Models to the Mechanisms and Therapies of Transthyretin Amyloidosis

PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects

Efficient In Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65

Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy

Emerging roles for myosin II and cytoplasmic dynein in migrating neurons and growth cones

Quantification of the Metabolic State in Cell-Model of Parkinson’s Disease by Fluorescence Lifetime Imaging Microscopy

A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development

Gli2 modulates cell cycle re-entry through autophagy-mediated regulation of the length of primary cilia

The cellular roles of the lissencephaly gene LIS1, and what they tell us about brain development

Lis1 dysfunction leads to traction force reduction and cytoskeletal disorganization during cell migration

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