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Association of embryonic inositol status with susceptibility to neural tube defects, metabolite profile, and maternal inositol intake.
- Published in:
- FASEB Journal, 2024, v. 38, n. 11, p. 1, doi. 10.1096/fj.202400206R
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- Publication type:
- Article
International Consensus Statement on the Radiologic Evaluation of Dysraphic Malformations of the Spine and Spinal Cord.
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- American Journal of Neuroradiology, 2024, v. 45, n. 6, p. 673, doi. 10.3174/ajnr.A8117
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- Publication type:
- Article
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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- Human Molecular Genetics, 2023, v. 32, n. 17, p. 2681, doi. 10.1093/hmg/ddad094
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- Article
A topographical analysis of encephalocele locations: generation of a standardised atlas and cluster analysis.
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- Child's Nervous System, 2023, v. 39, n. 7, p. 1911, doi. 10.1007/s00381-023-05883-7
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- Publication type:
- Article
Dolutegravir and rat whole embryo culture.
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- Birth Defects Research, 2022, v. 114, n. 1, p. 23, doi. 10.1002/bdr2.1969
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- Article
Genetic interaction of Pax3 mutation and canonical Wnt signaling modulates neural tube defects and neural crest abnormalities.
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- Genesis: The Journal of Genetics & Development, 2021, v. 59, n. 11, p. 1, doi. 10.1002/dvg.23445
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- Article
Inositols: From Established Knowledge to Novel Approaches.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 19, p. 10575, doi. 10.3390/ijms221910575
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- Article
Maternal ethnicity and the prevalence of British pregnancies affected by neural tube defects.
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- Birth Defects Research, 2021, v. 113, n. 12, p. 968, doi. 10.1002/bdr2.1893
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- Article
Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21372-4
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- Article
Glycine Cleavage System H Protein Is Essential for Embryonic Viability, Implying Additional Function Beyond the Glycine Cleavage System.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.625120
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- Article
Regulation of glycine metabolism by the glycine cleavage system and conjugation pathway in mouse models of non‐ketotic hyperglycinemia.
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- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 6, p. 1186, doi. 10.1002/jimd.12295
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- Publication type:
- Article
Impaired folate 1-carbon metabolism causes formate-preventable hydrocephalus in glycine decarboxylase-deficient mice.
- Published in:
- 2020
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- Publication type:
- journal article
Refinement of inducible gene deletion in embryos of pregnant mice.
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- Birth Defects Research, 2020, v. 112, n. 2, p. 196, doi. 10.1002/bdr2.1628
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- Publication type:
- Article
Dynamic acetylation profile during mammalian neurulation.
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- Birth Defects Research, 2020, v. 112, n. 2, p. 205, doi. 10.1002/bdr2.1618
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- Article
Mouse whole embryo culture: Evaluating the requirement for rat serum as culture medium.
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- Birth Defects Research, 2019, v. 111, n. 16, p. 1165, doi. 10.1002/bdr2.1538
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- Publication type:
- Article
Spinal neural tube closure depends on regulation of surface ectoderm identity and biomechanics by Grhl2.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10164-6
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- Article
Abstracts of papers presented at the 29<sup>th</sup> Genetic Society's Mammalian Genetics and Development Workshop held at the UCL Great Ormond Street Institute of Child Health, University College London on Thursday 29<sup>th</sup> November 2018.
- Published in:
- Genetics Research, 2019, v. 101, p. N.PAG, doi. 10.1017/S0016672319000016
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- Publication type:
- Article
Perturbation of Retinoid Homeostasis Increases Malformation Risk in Embryos Exposed to Pregestational Diabetes.
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- 2017
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- Publication type:
- journal article
Use of high-frequency ultrasound to study the prenatal development of cranial neural tube defects and hydrocephalus in Gldc-deficient mice.
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- 2017
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- Publication type:
- journal article
Inositol, neural tube closure and the prevention of neural tube defects.
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- Birth Defects Research, 2017, v. 109, n. 2, p. 68, doi. 10.1002/bdra.23533
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- Publication type:
- Article
HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development.
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- Frontiers in Neuroanatomy, 2016, v. 10, p. 1, doi. 10.3389/fnana.2016.00086
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- Publication type:
- Article
Microtubules, polarity and vertebrate neural tube morphogenesis.
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- Journal of Anatomy, 2016, v. 229, n. 1, p. 63, doi. 10.1111/joa.12468
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- Article
Regulation of cell protrusions by small GTPases during fusion of the neural folds.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.13273
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- Article
Planar Cell Polarity Aligns Osteoblast Division in Response to Substrate Strain.
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- 2015
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- Publication type:
- Other
Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice.
- Published in:
- Nature Communications, 2015, v. 6, n. 3, p. 6388, doi. 10.1038/ncomms7388
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- Publication type:
- Article
Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse model.
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- Magnetic Resonance in Medicine, 2015, v. 73, n. 2, p. 731, doi. 10.1002/mrm.25145
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- Publication type:
- Article
Abstracts of papers presented at the 25th Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 7th November 2014.
- Published in:
- Genetics Research, 2015, v. 97, p. N.PAG, doi. 10.1017/S0016672314000214
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- Publication type:
- Article
Planar cell polarity and the kidney.
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- Nephrology Dialysis Transplantation, 2014, v. 29, n. 7, p. 1320, doi. 10.1093/ndt/gft484
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- Article
Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse.
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- Brain: A Journal of Neurology, 2013, v. 136, n. 9, p. 2836, doi. 10.1093/brain/awt209
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- Publication type:
- Article
Neural tube defects-disorders of neurulation and related embryonic processes.
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- WIREs: Developmental Biology, 2013, v. 2, n. 2, p. 213, doi. 10.1002/wdev.71
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- Publication type:
- Article
Abstracts of papers presented at the 23rd Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 22nd November 2012.
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- Genetics Research, 2012, v. 94, n. 6, p. 353, doi. 10.1017/S0016672312000572
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- Publication type:
- Article
Laminin and integrin expression in the ventral ectodermal ridge of the mouse embryo: Implications for regulation of BMP signalling.
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- Developmental Dynamics, 2012, v. 241, n. 11, p. 1808, doi. 10.1002/dvdy.23846
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- Publication type:
- Article
Lamin B1 Polymorphism Influences Morphology of the Nuclear Envelope, Cell Cycle Progression, and Risk of Neural Tube Defects in Mice.
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- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1003059
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- Publication type:
- Article
Could microRNAs be biomarkers for neural tube defects?
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- Journal of Neurochemistry, 2012, v. 122, n. 3, p. 485, doi. 10.1111/j.1471-4159.2012.07800.x
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- Article
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.
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- Human Molecular Genetics, 2012, v. 21, n. 7, p. 1496, doi. 10.1093/hmg/ddr585
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- Publication type:
- Article
Abstracts of papers presented at the 22nd Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 17 November 2011.
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- Genetics Research, 2012, v. 94, n. 1, p. 49, doi. 10.1017/S0016672312000055
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- Publication type:
- Article
Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.
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- Human Mutation, 2012, v. 33, n. 2, p. 440, doi. 10.1002/humu.21662
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- Publication type:
- Article
Abstracts of papers presented at the 21st Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 11 November 2010.
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- Genetics Research, 2011, v. 93, n. 6, p. 433, doi. 10.1017/S0016672311000383
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- Publication type:
- Article
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse.
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- Human Molecular Genetics, 2011, v. 20, n. 8, p. 1536, doi. 10.1093/hmg/ddr031
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- Publication type:
- Article
Lack of motor neuron differentiation is an intrinsic property of the mouse secondary neural tube.
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- Developmental Dynamics, 2010, v. 239, n. 12, p. 3192, doi. 10.1002/dvdy.22457
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- Article
Genetics and development of neural tube defects.
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- Journal of Pathology, 2010, v. 220, n. 2, p. 217, doi. 10.1002/path.2643
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- Publication type:
- Article
Genetics of human neural tube defects.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. R2, p. R113, doi. 10.1093/hmg/ddp347
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- Publication type:
- Article
Development of the vertebrate central nervous system: formation of the neural tube.
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- Prenatal Diagnosis, 2009, v. 29, n. 4, p. 303, doi. 10.1002/pd.2206
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- Publication type:
- Article
Gene–environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function.
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- Human Molecular Genetics, 2008, v. 17, n. 23, p. 3675, doi. 10.1093/hmg/ddn262
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- Publication type:
- Article
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model.
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- Human Molecular Genetics, 2007, v. 16, n. 21, p. 2640, doi. 10.1093/hmg/ddm221
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- Publication type:
- Article
Abstracts of papers presented at the seventeenth Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 9 and 10 November 2006.
- Published in:
- Genetics Research, 2007, v. 89, p. 181, doi. 10.1017/S0016672307008804
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- Publication type:
- Article
Abnormal folate metabolism in foetuses affected by neural tube defects.
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- 2007
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- Publication type:
- journal article
Abnormal folate metabolism in foetuses affected by neural tube defects.
- Published in:
- Brain: A Journal of Neurology, 2007, v. 130, n. 4, p. 1043
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- Publication type:
- Article
The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 2, p. 173, doi. 10.1093/hmg/ddl459
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- Publication type:
- Article