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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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Genetics and development of neural tube defects

The Journal of pathology, 2010-01, Vol.220 (2), p.217-230

2010

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The relationship between sonic Hedgehog signaling, cilia, and neural tube defects

Birth defects research. A Clinical and molecular teratology, 2010-08, Vol.88 (8), p.633-652

2010

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Neural tube defects-disorders of neurulation and related embryonic processes

Wiley interdisciplinary reviews. Developmental biology, 2013-03, Vol.2 (2), p.213-227

2013

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Development of the vertebrate central nervous system: formation of the neural tube

Prenatal diagnosis, 2009-04, Vol.29 (4), p.303-311

2009

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Neurulation in the cranial region – normal and abnormal

Journal of anatomy, 2005-11, Vol.207 (5), p.623-635

Copp, Andrew J.

2005

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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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Inositol, neural tube closure and the prevention of neural tube defects

Birth defects research, 2017-01, Vol.109 (2), p.68-80

2017

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Microtubules, polarity and vertebrate neural tube morphogenesis

Journal of anatomy, 2016-07, Vol.229 (1), p.63-74

2016

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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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Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice

PLoS genetics, 2012-11, Vol.8 (11), p.e1003059-e1003059

2012

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Mouse models of neural tube defects: Investigating preventive mechanisms

American journal of medical genetics. Part C, Seminars in medical genetics, 2005-05, Vol.135C (1), p.31-41

2005

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Enabling research with human embryonic and fetal tissue resources

Development (Cambridge), 2015-09, Vol.142 (18), p.3073-3076

2015

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Disruption of Planar Cell Polarity Signaling Results in Congenital Heart Defects and Cardiomyopathy Attributable to Early Cardiomyocyte Disorganization

Circulation research, 2007-07, Vol.101 (2), p.137-145

2007

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Embryonic Folate Metabolism and Mouse Neural Tube Defects

Science (American Association for the Advancement of Science), 1998-06, Vol.280 (5372), p.2107-2109

1998

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Genetics of human neural tube defects

Human molecular genetics, 2009-10, Vol.18 (R2), p.R113-R129

2009

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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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Biomechanical coupling facilitates spinal neural tube closure in mouse embryos

Proceedings of the National Academy of Sciences - PNAS, 2017-06, Vol.114 (26), p.E5177-E5186

2017

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Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in mice

Development (Cambridge), 2023-10, Vol.150 (19)

2023

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Grainyhead genes and mammalian neural tube closure

Birth defects research. A Clinical and molecular teratology, 2008-10, Vol.82 (10), p.728-735

2008

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Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis

Human mutation, 2012-02, Vol.33 (2), p.440-447

2012

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A topographical analysis of encephalocele locations: generation of a standardised atlas and cluster analysis

Child's nervous system, 2023-07, Vol.39 (7), p.1911-1920

2023

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A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele

Human molecular genetics, 2023-08, Vol.32 (17), p.2681-2692

2023

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Neural tube defects

Neural tube closure: cellular, molecular and biomechanical mechanisms

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

Genetics and development of neural tube defects

The relationship between sonic Hedgehog signaling, cilia, and neural tube defects

Neural tube defects-disorders of neurulation and related embryonic processes

Development of the vertebrate central nervous system: formation of the neural tube

Neurulation in the cranial region – normal and abnormal

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

Inositol, neural tube closure and the prevention of neural tube defects

Microtubules, polarity and vertebrate neural tube morphogenesis

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

Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice

Mouse models of neural tube defects: Investigating preventive mechanisms

Enabling research with human embryonic and fetal tissue resources

Disruption of Planar Cell Polarity Signaling Results in Congenital Heart Defects and Cardiomyopathy Attributable to Early Cardiomyocyte Disorganization

Embryonic Folate Metabolism and Mouse Neural Tube Defects

Genetics of human neural tube defects

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

Biomechanical coupling facilitates spinal neural tube closure in mouse embryos

Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in mice

Grainyhead genes and mammalian neural tube closure

Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis

A topographical analysis of encephalocele locations: generation of a standardised atlas and cluster analysis

A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele

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