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XB--482292
Papers associated with ep300 (and Disease Ontology)
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referenced by: |
The contribution of de novo coding mutations to meningomyelocele., Ha YJ, Nisal A, Tang I, Lee C, Jhamb I, Wallace C, Howarth R, Schroeder S, Vong KI, Meave N, Jiwani F, Barrows C, Lee S, Jiang N, Patel A, Bagga K, Banka N, Friedman L, Blanco FA, Yu S, Rhee S, Jeong HS, Plutzer I, Major MB, Benoit B, Poüs C, Heffner C, Kibar Z, Bot GM, Northrup H, Au KS, Strain M, Ashley-Koch AE, Finnell RH, Le JT, Meltzer HS, Araujo C, Machado HR, Stevenson RE, Yurrita A, Mumtaz S, Ahmed A, Khara MH, Mutchinick OM, Medina-Bereciartu JR, Hildebrandt F, Melikishvili G, Marwan AI, Capra V, Noureldeen MM, Salem AMS, Issa MY, Zaki MS, Xu L, Lee JE, Shin D, Alkelai A, Shuldiner AR, Kingsmore SF, Murray SA, Gee HY, Miller WT, Tolias KF, Wallingford JB, Spina Bifida Sequencing Consortium, Kim S, Gleeson JG., Nature. May 26, 2025; 641 (8062): 419-426. |
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A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB, Willsey HR, Xu Y, Xu Y, Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK, Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. August 17, 2021; 12 (11): 1094-1107.e6.  |
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More similar than you think: Frog metamorphosis as a model of human perinatal endocrinology., Buchholz DR., Dev Biol. December 15, 2015; 408 (2): 188-95.  |
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A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome., Tanaka K, Kato A, Angelocci C, Watanabe M, Kato Y., Dev Biol. March 1, 2014; 387 (1): 28-36.  |
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