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Journal Abstract Search
459 related items for PubMed ID: 23024041
21. Etiology, pathogenesis and prevention of neural tube defects. Padmanabhan R. Congenit Anom (Kyoto); 2006 Jun; 46(2):55-67. PubMed ID: 16732763 [Abstract] [Full Text] [Related]
23. An expanding role of Vangl proteins in embryonic development. Torban E, Iliescu A, Gros P. Curr Top Dev Biol; 2012 Jun; 101():237-61. PubMed ID: 23140632 [Abstract] [Full Text] [Related]
25. Human neural tube defects: genetic causes and prevention. De Marco P, Merello E, Cama A, Kibar Z, Capra V. Biofactors; 2011 Jun; 37(4):261-8. PubMed ID: 21674647 [Abstract] [Full Text] [Related]
26. Role of chromatin remodeling gene Cecr2 in neurulation and inner ear development. Dawe CE, Kooistra MK, Fairbridge NA, Pisio AC, McDermid HE. Dev Dyn; 2011 Feb; 240(2):372-83. PubMed ID: 21246654 [Abstract] [Full Text] [Related]
28. Genetic evidence in planar cell polarity signaling pathway in human neural tube defects. Cai C, Shi O. Front Med; 2014 Mar; 8(1):68-78. PubMed ID: 24307374 [Abstract] [Full Text] [Related]
29. Cdx mediates neural tube closure through transcriptional regulation of the planar cell polarity gene Ptk7. Savory JG, Mansfield M, Rijli FM, Lohnes D. Development; 2011 Apr; 138(7):1361-70. PubMed ID: 21350009 [Abstract] [Full Text] [Related]
31. A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects. Stegmann K, Boecker J, Richter B, Capra V, Finnell RH, Ngo ET, Strehl E, Ermert A, Koch MC. Teratology; 2001 May; 63(5):167-75. PubMed ID: 11320527 [Abstract] [Full Text] [Related]
33. Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants. Harris MJ. Birth Defects Res A Clin Mol Teratol; 2009 Apr; 85(4):331-9. PubMed ID: 19117321 [Abstract] [Full Text] [Related]
34. The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation. Yates LL, Papakrivopoulou J, Long DA, Goggolidou P, Connolly JO, Woolf AS, Dean CH. Hum Mol Genet; 2010 Dec 01; 19(23):4663-76. PubMed ID: 20843830 [Abstract] [Full Text] [Related]
35. Mutations in planar cell polarity gene SCRIB are associated with spina bifida. Lei Y, Zhu H, Duhon C, Yang W, Ross ME, Shaw GM, Finnell RH. PLoS One; 2013 Dec 01; 8(7):e69262. PubMed ID: 23922697 [Abstract] [Full Text] [Related]
36. Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects. Tian T, Lei Y, Chen Y, Karki M, Jin L, Finnell RH, Wang L, Ren A. Hum Genet; 2020 Oct 01; 139(10):1299-1314. PubMed ID: 32356230 [Abstract] [Full Text] [Related]
37. Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway. Allache R, Lachance S, Guyot MC, De Marco P, Merello E, Justice MJ, Capra V, Kibar Z. Hum Mol Genet; 2014 Apr 01; 23(7):1687-99. PubMed ID: 24203697 [Abstract] [Full Text] [Related]
38. Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b. Wansleeben C, Feitsma H, Montcouquiol M, Kroon C, Cuppen E, Meijlink F. Development; 2010 Apr 01; 137(7):1067-73. PubMed ID: 20215345 [Abstract] [Full Text] [Related]
39. Genetic basis of neural tube defects. I. Regulatory genes for the neurulation process. Gos M, Szpecht-Potocka A. J Appl Genet; 2002 Apr 01; 43(3):343-50. PubMed ID: 12177524 [Abstract] [Full Text] [Related]
40. Neural tube defects--disorders of neurulation and related embryonic processes. Copp AJ, Greene ND. Wiley Interdiscip Rev Dev Biol; 2013 Apr 01; 2(2):213-27. PubMed ID: 24009034 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]