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Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss

Human molecular genetics, 2008-07, Vol.17 (14), p.2150-2159

2008

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Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model

Human molecular genetics, 2007-11, Vol.16 (21), p.2640-2646

2007

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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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Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse model

Magnetic resonance in medicine, 2015-02, Vol.73 (2), p.731-739

2015

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Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain

Molecular and cellular biochemistry, 2013-06, Vol.378 (1-2), p.229-236

2013

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Lactococcus lactis carrying a DNA vaccine coding for the ESAT‐6 antigen increases IL‐17 cytokine secretion and boosts the BCG vaccine immune response

Journal of applied microbiology, 2017-06, Vol.122 (6), p.1657-1662

2017

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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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The arms race between heliconiine butterflies and Passiflora plants – new insights on an ancient subject

Biological reviews of the Cambridge Philosophical Society, 2018-02, Vol.93 (1), p.555-573

2018

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Phenotypic plasticity in chemical defence of butterflies allows usage of diverse host plants

Biology letters (2005), 2021-03, Vol.17 (3), p.20200863-20200863, Article 20200863

2021

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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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AAV-mediated expression of mouse or human GLDC normalises metabolic biomarkers in a GLDC-deficient mouse model of Non-Ketotic Hyperglycinemia

Molecular genetics and metabolism, 2024-07, Vol.142 (3), p.108496, Article 108496

2024

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Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities

American journal of human genetics, 2009-02, Vol.84 (2), p.197-209

2009

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The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low Abundance

Molecular & cellular proteomics, 2024-03, Vol.23 (3), p.100718-100718, Article 100718

2024

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Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues

Developmental biology, 2018-03, Vol.435 (2), p.130-137

2018

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Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice

Human molecular genetics, 2018-12, Vol.27 (24), p.4218-4230

2018

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Variation of chemical compounds in wild Heliconiini reveals ecological factors involved in the evolution of chemical defenses in mimetic butterflies

Ecology and evolution, 2020-03, Vol.10 (5), p.2677-2694

2020

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Glycine Cleavage System H Protein Is Essential for Embryonic Viability, Implying Additional Function Beyond the Glycine Cleavage System

Frontiers in genetics, 2021-01, Vol.12, p.625120-625120

2021

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SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development

The journal of clinical endocrinology and metabolism, 2008-05, Vol.93 (5), p.1865-1873

2008

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Regulation of glycine metabolism by the glycine cleavage system and conjugation pathway in mouse models of non‐ketotic hyperglycinemia

Journal of inherited metabolic disease, 2020-11, Vol.43 (6), p.1186-1198

2020

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Formate supplementation enhances folate-dependent nucleotide biosynthesis and prevents spina bifida in a mouse model of folic acid-resistant neural tube defects

Biochimie, 2016-07, Vol.126, p.63-70

2016

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Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse

Brain (London, England : 1878), 2013-09, Vol.136 (Pt 9), p.2836-2841

2013

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Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse

Human molecular genetics, 2011-04, Vol.20 (8), p.1536-1546

2011

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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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Is LMNB1 a susceptibility gene for neural tube defects in humans?

Birth defects research. A Clinical and molecular teratology, 2013-06, Vol.97 (6), p.398-402

2013

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Transient expression of the conserved zinc finger gene INSM1 in progenitors and nascent neurons throughout embryonic and adult neurogenesis

Journal of comparative neurology (1911), 2008-04, Vol.507 (4), p.1497-1520

2008

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Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss

Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model

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

Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse model

Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain

Lactococcus lactis carrying a DNA vaccine coding for the ESAT‐6 antigen increases IL‐17 cytokine secretion and boosts the BCG vaccine immune response

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

The arms race between heliconiine butterflies and Passiflora plants – new insights on an ancient subject

Phenotypic plasticity in chemical defence of butterflies allows usage of diverse host plants

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

AAV-mediated expression of mouse or human GLDC normalises metabolic biomarkers in a GLDC-deficient mouse model of Non-Ketotic Hyperglycinemia

Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities

The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low Abundance

Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues

Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice

Variation of chemical compounds in wild Heliconiini reveals ecological factors involved in the evolution of chemical defenses in mimetic butterflies

Glycine Cleavage System H Protein Is Essential for Embryonic Viability, Implying Additional Function Beyond the Glycine Cleavage System

SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development

Regulation of glycine metabolism by the glycine cleavage system and conjugation pathway in mouse models of non‐ketotic hyperglycinemia

Formate supplementation enhances folate-dependent nucleotide biosynthesis and prevents spina bifida in a mouse model of folic acid-resistant neural tube defects

Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse

Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse

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

Is LMNB1 a susceptibility gene for neural tube defects in humans?

Transient expression of the conserved zinc finger gene INSM1 in progenitors and nascent neurons throughout embryonic and adult neurogenesis

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