401 results on '"Copp, Andrew J."'
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2. A topographical analysis of encephalocele locations: generation of a standardised atlas and cluster analysis
3. Folate deficiency increases the incidence of dolutegravir-associated foetal defects in a mouse pregnancy model
4. Metabolic implications and safety of dolutegravir use in pregnancy
5. The surface ectoderm exhibits spatially heterogenous tension that correlates with YAP localisation during spinal neural tube closure in mouse embryos
6. Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryos
7. Maternal Inositol Status and Neural Tube Defects: A Role for the Human Yolk Sac in Embryonic Inositol Delivery?
8. Association of embryonic inositol status with susceptibility to neural tube defects, metabolite profile, and maternal inositol intake.
9. International Consensus Statement on the Radiologic Evaluation of Dysraphic Malformations of the Spine and Spinal Cord.
10. Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice
11. Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in mice
12. Impaired folate 1-carbon metabolism causes formate-preventable hydrocephalus in glycine decarboxylase-deficient mice
13. Infectious causes of microcephaly: epidemiology, pathogenesis, diagnosis, and management
14. Biomechanical coupling facilitates spinal neural tube closure in mouse embryos
15. Spinal neural tube closure depends on regulation of surface ectoderm identity and biomechanics by Grhl2
16. Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in mice.
17. A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele.
18. Embryonic Folate Metabolism and Mouse Neural Tube Defects
19. Neural tube defects: recent advances, unsolved questions, and controversies
20. Use of high‐frequency ultrasound to study the prenatal development of cranial neural tube defects and hydrocephalus in Gldc‐deficient mice
21. 169 - Pathophysiology of NeuralTube Defects
22. Apoptosis Is Not Required for Mammalian Neural Tube Closure
23. Quantitative analysis of myo-inositol in urine, blood and nutritional supplements by high-performance liquid chromatography tandem mass spectrometry
24. Investigating Genetic Determinants of Plasma Inositol Status in Adult Humans.
25. Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain
26. The importance of myo-inositol and D-chiro-inositol to support fertility and reproduction
27. Planar cell polarity and the kidney
28. Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice
29. Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young mice
30. The genetic basis of mammalian neurulation
31. Homocysteine is embryotoxic but does not cause neural tube defects in mouse embryos
32. Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse
33. Cordon-bleu is a conserved gene involved in neural tube formation
34. Curly tail: a 50-year history of the mouse spina bifida model
35. Quantitative analysis of s-adenosylmethionine and s-adenosylhomocysteine in neurulation-stage mouse embryos by liquid chromatography tandem mass spectrometry
36. Neural tube defects : Prevention by folic acid and other vitamins
37. Could microRNAs be biomarkers for neural tube defects?
38. Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans
39. Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis
40. Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse
41. Genetics of human neural tube defects
42. Inositol, neural tube closure and the prevention of neural tube defects
43. Development of the vertebrate central nervous system: formation of the neural tube
44. Genetic interaction of Pax3 mutation and canonical Wnt signaling modulates neural tube defects and neural crest abnormalities.
45. Gene–environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function
46. Regional differences in morphogenesis of the neuroepithelium suggest multiple mechanisms of spinal neurulation in the mouse
47. Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos
48. Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model
49. Abnormal folate metabolism in foetuses affected by neural tube defects
50. The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
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