OBO ID: DOID:0080074

Citations

(15 total)

Term: neural tube defect

Li, X., Wang, R., Luo, W., Gu, H., Huang, T., Wang, Q., Yuan, Z. (2025) PCSK9 Loss-of-Function Disrupts Cellular Microfilament Network via LIN28A/HES5/JMY Axis in Neural Tube Defects. Advanced science (Weinheim, Baden-Wurttemberg, Germany). :e04291

Rajesh, V., Karthi, S., Kumudhavalli, M.V. (2025) Protective Effect of myo-Inositol Against Decitabine-Induced Neural Tube Defects in Embryonic Zebrafish. Neurotoxicity research. 43:14

Head, B., La Du, J., Tanguay, R.L., Kioussi, C., Traber, M.G. (2020) Vitamin E is necessary for zebrafish nervous system development. Scientific Reports. 10:15028

Liu, L., Liu, W., Shi, Y., Li, L., Gao, Y., Lei, Y., Finnell, R., Zhang, T., Zhang, F., Jin, L., Li, H., Tao, W., Wang, H. (2020) DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway. Journal of genetics and genomics = Yi chuan xue bao. 47(6):301-310

Ye, J., Tong, Y., Lv, J., Peng, R., Chen, S., Kuang, L., Su, K., Zheng, Y., Zhang, T., Zhang, F., Jin, L., Yang, X., Wang, H. (2020) Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects. Human Mutation. 41(8):1383-1393

Yin, H., Peng, R., Chen, Z., Wang, H., Zhang, T., Zheng, Y. (2020) WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways. Journal of Human Genetics. 65(11):985-993

Shi, Z., Chen, S., Han, X., Peng, R., Luo, J., Yang, L., Zheng, Y., Wang, H. (2019) The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects. Molecular cytogenetics. 12:8

Tian, T., Wang, L., Shen, Y., Zhang, B., Finnell, R.H., Ren, A. (2018) Hypomethylation of GRHL3 gene is associated with the occurrence of neural tube defects. Epigenomics. 10(7):891-901

Shi, Z., Yang, X., Li, B.B., Chen, S., Yang, L., Cheng, L., Zhang, T., Wang, H., Zheng, Y. (2017) Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects. Birth defects research. 110(1):63-71

Miao, C., Jiang, Q., Li, H., Zhang, Q., Bai, B., Bao, Y., Zhang, T. (2016) Mutations in the Motile Cilia Gene DNAAF1 are Associated with Neural Tube Defects in Humans. G3 (Bethesda). 6(10):3307-3316

Qiao, X., Liu, Y., Li, P., Chen, Z., Li, H., Yang, X., Finnell, R.H., Yang, Z., Zhang, T., Qiao, B., Zheng, Y., Wang, H. (2016) Genetic analysis of rare coding mutations in CELSR1-3 in Chinese Congenital Heart and Neural Tube Defects. Clinical science (London, England : 1979). 130(24):2329-2340

Rochtus, A., Winand, R., Laenen, G., Vangeel, E., Izzi, B., Wittevrongel, C., Moreau, Y., Verpoorten, C., Jansen, K., Van Geet, C., Freson, K. (2016) Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development.. Clinical epigenetics. 8:108

Ma, P., Swartz, M.R., Kindt, L.M., Kangas, A.M., Liang, J.O. (2015) Temperature Sensitivity of Neural Tube Defects in Zoep Mutants. Zebrafish. 12(6):448-56

Rochtus, A., Izzi, B., Vangeel, E., Louwette, S., Wittevrongel, C., Lambrechts, D., Moreau, Y., Winand, R., Verpoorten, C., Jansen, K., Van Geet, C., Freson, K. (2015) DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects. Epigenetics. 10(1):92-101

Kao, T.T., Lee, G.H., Fu, C.C., Chen, B.H., Chen, L.T., and Fu, T.F. (2013) Methotrexate-Induced Decrease in Embryonic 5-Methyl-Tetrahydrofolate Is Irreversible with Leucovorin Supplementation. Zebrafish. 10(3):326-37