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Journal Abstract Search

336 related items for PubMed ID: 31856916

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  • 5. Chromatin changes in dicer-deficient mouse embryonic stem cells in response to retinoic acid induced differentiation.
    Tennakoon JB, Wang H, Coarfa C, Cooney AJ, Gunaratne PH.
    PLoS One; 2013; 8(9):e74556. PubMed ID: 24040281
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  • 8. Ectopic cross-talk between thyroid and retinoic acid signaling: A possible etiology for spinal neural tube defects.
    Li H, Bai B, Zhang Q, Bao Y, Guo J, Chen S, Miao C, Liu X, Zhang T.
    Gene; 2015 Dec 01; 573(2):254-60. PubMed ID: 26188161
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  • 9. Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.
    Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H.
    Am J Med Genet; 2002 Jul 01; 110(3):203-7. PubMed ID: 12116226
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  • 10. Abnormal epigenetic regulation of the gene expression levels of Wnt2b and Wnt7b: Implications for neural tube defects.
    Bai B, Chen S, Zhang Q, Jiang Q, Li H.
    Mol Med Rep; 2016 Jan 01; 13(1):99-106. PubMed ID: 26548512
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  • 11. Neural tube defects--disorders of neurulation and related embryonic processes.
    Copp AJ, Greene ND.
    Wiley Interdiscip Rev Dev Biol; 2013 Jan 01; 2(2):213-27. PubMed ID: 24009034
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  • 12. The association and significance of H3K27me3 and a folate metabolic gene ACat2 in neural tube defects.
    Zhai S, Zhao M, Zhou C, Lu F, Zhang H, Na L, Feng S, Qiang X, Du Y.
    Nutr J; 2016 Nov 03; 15(1):95. PubMed ID: 27809850
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  • 13. MTHFD1 is critical for the negative regulation of retinoic acid receptor signalling in anencephaly.
    Xie X, Li C, Yu J, Chang S, Cheng X, Wang F, Bao Y, Zhang T, Wang S.
    Brain; 2023 Aug 01; 146(8):3455-3469. PubMed ID: 36928982
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  • 14. UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development.
    Agger K, Cloos PA, Christensen J, Pasini D, Rose S, Rappsilber J, Issaeva I, Canaani E, Salcini AE, Helin K.
    Nature; 2007 Oct 11; 449(7163):731-4. PubMed ID: 17713478
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  • 15. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
    Harris MJ, Juriloff DM.
    Teratology; 1999 Nov 11; 60(5):292-305. PubMed ID: 10525207
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  • 16. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.
    Harris MJ, Juriloff DM.
    Birth Defects Res A Clin Mol Teratol; 2007 Mar 11; 79(3):187-210. PubMed ID: 17177317
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  • 17. Regulation of the expression of tumor necrosis factor‑related genes by abnormal histone H3K27 acetylation: Implications for neural tube defects.
    Wan C, Liu X, Bai B, Cao H, Li H, Zhang Q.
    Mol Med Rep; 2018 Jun 11; 17(6):8031-8038. PubMed ID: 29693124
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  • 18. Folate deficiency reduced aberrant level of DOT1L-mediated histone H3K79 methylation causes disruptive SHH gene expression involved in neural tube defects.
    Li X, Pei P, Shen J, Yu J, Wang F, Wang L, Liu C, Wang S.
    Epigenetics Chromatin; 2023 Dec 14; 16(1):50. PubMed ID: 38093377
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