Human neural tube defects: developmental biology, epidemiology, and genetics - Wikidata - thesis-toulmin - TriplyDB

Human neural tube defects: developmental biology, epidemiology, and genetics

Human neural tube defects: developmental biology, epidemiology, and genetics

http://www.wikidata.org/entity/Q36153596

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Genetics of human neural tube defects Maternal periconceptional occupational pesticide exposure and neural tube defects Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis Neural tube defects and folate: case far from closed The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure The BMP antagonist Noggin promotes cranial and spinal neurulation by distinct mechanisms Parents' psychological adjustment in families of children with spina bifida: a meta-analysis.Nutrition, One-Carbon Metabolism and Neural Tube Defects: A Review Air toxics and birth defects: a Bayesian hierarchical approach to evaluate multiple pollutants and spina bifida Auditory interhemispheric transfer in relation to patterns of partial agenesis and hypoplasia of the corpus callosum in spina bifida meningomyelocele.N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements.Nodal signaling is required for closure of the anterior neural tube in zebrafish.Association between CFL1 gene polymorphisms and spina bifida risk in a California population.Partial agenesis of the corpus callosum in spina bifida meningomyelocele and potential compensatory mechanisms Embryonic toxicokinetic and dynamic differences underlying strain sensitivity to cadmium during neurulation.Anatomical and diffusion MRI of deep gray matter in pediatric spina bifida.Reduction in mortality and teratogenicity following simultaneous administration of folic acid and vitamin E with antiepileptic, antihypertensive and anti-allergic drugs.Novel mutations in VANGL1 in neural tube defects.Development of head organizer of the mouse embryo depends on a high level of mitochondrial metabolism.Untargeted metabolite profiling of murine embryos to reveal metabolic perturbations associated with neural tube closure defects Genetic variations in the GLUT3 gene associated with myelomeningocele Does dietary folic acid supplementation in mouse NTD models affect neural tube development or gamete preference at fertilization?Associations of ethnicity and SES with IQ and achievement in spina bifida meningomyelocele.Functional interactions between the LRP6 WNT co-receptor and folate supplementation Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).Association between MTHFR gene polymorphism and NTDs in Chinese Han population.Concomitant achondroplasia and Chiari II malformation: A double-hit at the cervicomedullary junction.Schizophrenia and neural tube defects: comparisons from an epidemiological perspective.Geographic and urban-rural disparities in the total prevalence of neural tube defects and their subtypes during 2006-2008 in China: a study using the hospital-based birth defects surveillance system.The cerebellum in children with spina bifida and Chiari II malformation: Quantitative volumetrics by region.Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature.Association of SMO polymorphisms and neural tube defects in the Chinese population from Shanxi Province A 10 bp deletion polymorphism and 2 new variations in the GLUT1 gene associated with meningomyelocele.Folic acid supplementation can adversely affect murine neural tube closure and embryonic survival.Agenesis of the corpus callosum associated with spinal open neural tube defect.Epidemiology, prenatal management, and prevention of neural tube defects.Shroom3 functions downstream of planar cell polarity to regulate myosin II distribution and cellular organization during neural tube closure.Roles of planar cell polarity pathways in the development of neural [correction of neutral] tube defects.Brain mechanisms for reading and language processing in spina bifida meningomyelocele: a combined magnetic source- and structural magnetic resonance imaging study.

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Human neural tube defects: developmental biology, epidemiology, and genetics

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J.NTT.2004.12.007

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Neurotoxicology and Teratology

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Human neural tube defects: developmental biology, epidemiology, and genetics

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P2860

Multivitamin/folic acid supplementation in early pregnancy reduces the prevalence of neural tube defects

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Overexpression of murine Pax3 increases NCAM polysialylation in a human medulloblastoma cell line

Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects

Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature

Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3

Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein.

Do familial neural tube defects breed true?

Upper and lower neural tube defects: an alternate hypothesis.

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