| scholarly article | Q13442814 |
| P50 | author | Dean R Appling | Q90093466 |
| P2093 | author name string | Minhye Shin | |
| Jessica Momb | |||
| Amanda Vaughn | |||
| P2860 | cites work | Targets and dynamics of promoter DNA methylation during early mouse development | Q51896182 |
| Is programmed cell death required for neural tube closure? | Q52195654 | ||
| Deletion of the neural tube defect-associated gene Mthfd1l disrupts one-carbon and central energy metabolism in mouse embryos. | Q52688876 | ||
| Excess methionine suppresses the methylation cycle and inhibits neural tube closure in mouse embryos | Q57839610 | ||
| Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies | Q58726345 | ||
| Expression of the Notch 3 intracellular domain in mouse central nervous system progenitor cells is lethal and leads to disturbed neural tube development | Q62003158 | ||
| Methionine and neural tube closure in cultured rat embryos: morphological and biochemical analyses | Q68627827 | ||
| Intrinsic and extrinsic factors in the mechanism of neurulation: effect of curvature of the body axis on closure of the posterior neuropore | Q72815409 | ||
| Formate rescues neural tube defects caused by mutations in Slc25a32 | Q88390986 | ||
| Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturned | Q89065677 | ||
| Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene | Q22337236 | ||
| Human mitochondrial C1-tetrahydrofolate synthase: gene structure, tissue distribution of the mRNA, and immunolocalization in Chinese hamster ovary calls | Q24317651 | ||
| How to form and close the brain: insight into the mechanism of cranial neural tube closure in mammals | Q24631607 | ||
| Mitochondrial C1-tetrahydrofolate synthase (MTHFD1L) supports the flow of mitochondrial one-carbon units into the methyl cycle in embryos | Q28506233 | ||
| The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure | Q28506634 | ||
| Apaf-1 deficiency and neural tube closure defects are found in fog mice | Q28512476 | ||
| DNA methyltransferase 3b regulates nerve growth factor-induced differentiation of PC12 cells by recruiting histone deacetylase 2 | Q28584099 | ||
| twist is required in head mesenchyme for cranial neural tube morphogenesis | Q28590860 | ||
| Deletion of Mthfd1l causes embryonic lethality and neural tube and craniofacial defects in mice | Q28594629 | ||
| Maternal folate deficiency causes inhibition of mTOR signaling, down-regulation of placental amino acid transporters and fetal growth restriction in mice | Q33822467 | ||
| Mitochondrial MTHFD2L is a dual redox cofactor-specific methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase expressed in both adult and embryonic tissues | Q34075961 | ||
| Integrity of the methylation cycle is essential for mammalian neural tube closure. | Q34560587 | ||
| Sox9 function in craniofacial development and disease | Q34810766 | ||
| Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice | Q35196989 | ||
| The genetic basis of mammalian neurulation. | Q35298412 | ||
| Effects of methionine on the cytoplasmic distribution of actin and tubulin during neural tube closure in rat embryos | Q35953972 | ||
| Epigenetic silencing of maspin expression occurs early in the conversion of keratocytes to fibroblasts | Q36642513 | ||
| Human mitochondrial C1-tetrahydrofolate synthase: submitochondrial localization of the full-length enzyme and characterization of a short isoform | Q37254831 | ||
| Compartmentalization of Mammalian folate-mediated one-carbon metabolism | Q37774367 | ||
| Neural tube closure: cellular, molecular and biomechanical mechanisms | Q39135434 | ||
| Role of Folbp1 in the regional regulation of apoptosis and cell proliferation in the developing neural tube and craniofacies | Q42476267 | ||
| Dynamic changes in the epigenomic state and nuclear organization of differentiating mouse embryonic stem cells | Q42806644 | ||
| Alx3-deficient mice exhibit folic acid-resistant craniofacial midline and neural tube closure defects | Q43037401 | ||
| Neural crest development is regulated by the transcription factor Sox9. | Q47590677 | ||
| The kinetic behaviour of the cranial neural epithelium during neurulation in the rat. | Q48524653 | ||
| Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression | Q48654359 | ||
| The role of the mesenchyme in mouse neural fold elevation. I. Patterns of mesenchymal cell distribution and proliferation in embryos developing in vitro | Q48954877 | ||
| Tissue-specific distribution of aberrant DNA methylation associated with maternal low-folate status in human neural tube defects. | Q51888352 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 19 | |
| P304 | page(s) | 1520-1534 | |
| P577 | publication date | 2019-09-13 | |
| P1433 | published in | Birth Defects Research | Q53952109 |
| P1476 | title | Deletion of neural tube defect-associated gene Mthfd1l causes reduced cranial mesenchyme density | |
| P478 | volume | 111 |
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