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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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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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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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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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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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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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Association of embryonic inositol status with susceptibility to neural tube defects, metabolite profile, and maternal inositol intake

The FASEB journal, 2024-06, Vol.38 (11), p.e23738-n/a

2024

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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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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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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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The influence of statistical properties of Fourier coefficients on random Gaussian surfaces

Scientific reports, 2017-05, Vol.7 (1), p.1961-8, Article 1961

2017

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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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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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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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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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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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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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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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Dynamic acetylation profile during mammalian neurulation

Birth defects research, 2020-01, Vol.112 (2), p.205-211

2020

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Solitary cysticercus brain lesion: a diagnostic dilemma

Anales de pediatría (Barcelona, Spain : 2003), 2009-06, Vol.70 (6), p.602

2009

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Schramm-Loewner evolution and perimeter of percolation clusters of correlated random landscapes

Scientific reports, 2018-03, Vol.8 (1), p.5286-8, Article 5286

2018

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

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

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

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

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

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

Association of embryonic inositol status with susceptibility to neural tube defects, metabolite profile, and maternal inositol intake

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

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

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

The influence of statistical properties of Fourier coefficients on random Gaussian surfaces

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

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

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

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

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

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

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

Dynamic acetylation profile during mammalian neurulation

Solitary cysticercus brain lesion: a diagnostic dilemma

Schramm-Loewner evolution and perimeter of percolation clusters of correlated random landscapes

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

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

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

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