|
XB--483982
Papers associated with smarca4 (and Disease Ontology)
???pagination.result.count???
???pagination.result.page??? 1
Sort Newest To Oldest | Sort Oldest To Newest |
referenced by: |
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus., Singh AK, Allington G, Viviano S, McGee S, Kiziltug E, Ma S, Zhao S, Mekbib KY, Shohfi JP, Duy PQ, DeSpenza T, Furey CG, Reeves BC, Smith H, Sousa AMM, Cherskov A, Allocco A, Nelson-Williams C, Haider S, Rizvi SRA, Alper SL, Sestan N, Shimelis H, Walsh LK, Lifton RP, Moreno-De-Luca A, Jin SC, Kruszka P, Deniz E, Kahle KT., Brain. December 21, 2023; |
|
HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome., Jenness C, Giunta S, Müller MM, Kimura H, Muir TW, Funabiki H., Proc Natl Acad Sci U S A. January 30, 2018; 115 (5): E876-E885. |
|
CHD7 cooperates with PBAF to control multipotent neural crest formation., Bajpai R, Chen DA, Rada-Iglesias A, Zhang J, Xiong Y, Helms J, Chang CP, Zhao Y, Swigut T, Wysocka J., Nature. February 18, 2010; 463 (7283): 958-62. |
|
Neural and eye-specific defects associated with loss of the imitation switch (ISWI) chromatin remodeler in Xenopus laevis., Dirscherl SS, Henry JJ, Krebs JE., Mech Dev. November 1, 2005; 122 (11): 1157-70. |
|
A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase., Wade PA, Jones PL, Vermaak D, Wolffe AP., Curr Biol. July 2, 1998; 8 (14): 843-6. |
???pagination.result.page??? 1