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HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Frontiers in neuroanatomy, 2016-10, Vol.10, p.86-86

2016

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Neural tube defects

Annual review of neuroscience, 2014-01, Vol.37 (1), p.221-242

2014

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Neural tube closure: cellular, molecular and biomechanical mechanisms

Development (Cambridge), 2017-02, Vol.144 (4), p.552-566

2017

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Neural tube defects: recent advances, unsolved questions, and controversies

Lancet neurology, 2013-08, Vol.12 (8), p.799-810

2013

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Infectious causes of microcephaly: epidemiology, pathogenesis, diagnosis, and management

The Lancet infectious diseases, 2018-01, Vol.18 (1), p.e1-e13

2018

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Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice

Nature communications, 2021-02, Vol.12 (1), p.1159-17, Article 1159

2021

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Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryos

Proceedings of the National Academy of Sciences - PNAS, 2021-05, Vol.118 (19), p.1-11

2021

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Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice

Nature communications, 2015-03, Vol.6 (1), p.6388-6388, Article 6388

2015

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Partitioning of One-Carbon Units in Folate and Methionine Metabolism Is Essential for Neural Tube Closure

Cell reports (Cambridge), 2017-11, Vol.21 (7), p.1795-1808

2017

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Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure

Journal of cell science, 2015-07, Vol.128 (14), p.2468-2481

2015

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Spinal neural tube closure depends on regulation of surface ectoderm identity and biomechanics by Grhl2

Nature communications, 2019-06, Vol.10 (1), p.2487-2487, Article 2487

2019

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Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure

Development (Cambridge), 2007-02, Vol.134 (4), p.789-799

2007

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Knockout of the PKN Family of Rho Effector Kinases Reveals a Non-redundant Role for PKN2 in Developmental Mesoderm Expansion

Cell reports (Cambridge), 2016-01, Vol.14 (3), p.440-448

2016

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Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice

Nature communications, 2021-05, Vol.12 (1), p.3301-3301, Article 3301

2021

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Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos

Disease models & mechanisms, 2018-03, Vol.11 (3)

2018

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Dual mechanism underlying failure of neural tube closure in the Zic2 mutant mouse

Disease models & mechanisms, 2023-03, Vol.16 (3)

2023

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Novel mouse model of encephalocele: post-neurulation origin and relationship to open neural tube defects

Disease models & mechanisms, 2019-11, Vol.12 (11)

2019

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Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extension

Disease models & mechanisms, 2022-01, Vol.15 (1)

2022

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Cellular mechanisms underlying Pax3- related neural tube defects and their prevention by folic acid

Disease models & mechanisms, 2019-11, Vol.12 (11)

2019

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Morphological phenotyping after mouse whole embryo culture

Frontiers in cell and developmental biology, 2023-08, Vol.11, p.1223849

2023

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Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

Human molecular genetics, 2012-04, Vol.21 (7), p.1496-1503

2012

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Fetal spina bifida in a mouse model: loss of neural function in utero

Journal of neurosurgery, 2007-03, Vol.106 (3 Suppl), p.213-221

2007

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Regulation of cell protrusions by small GTPases during fusion of the neural folds

eLife, 2016-04, Vol.5, p.e13273-e13273

2016

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Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice

Disease models & mechanisms, 2014-10, Vol.7 (10), p.1153-1163

2014

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

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HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Neural tube defects

Neural tube closure: cellular, molecular and biomechanical mechanisms

Neural tube defects: recent advances, unsolved questions, and controversies

Infectious causes of microcephaly: epidemiology, pathogenesis, diagnosis, and management

Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice

Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryos

Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice

Partitioning of One-Carbon Units in Folate and Methionine Metabolism Is Essential for Neural Tube Closure

Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure

Spinal neural tube closure depends on regulation of surface ectoderm identity and biomechanics by Grhl2

Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure

Knockout of the PKN Family of Rho Effector Kinases Reveals a Non-redundant Role for PKN2 in Developmental Mesoderm Expansion

Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice

Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos

Dual mechanism underlying failure of neural tube closure in the Zic2 mutant mouse

Novel mouse model of encephalocele: post-neurulation origin and relationship to open neural tube defects

Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extension

Cellular mechanisms underlying Pax3- related neural tube defects and their prevention by folic acid

Morphological phenotyping after mouse whole embryo culture

Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

Fetal spina bifida in a mouse model: loss of neural function in utero

Regulation of cell protrusions by small GTPases during fusion of the neural folds

Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

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