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Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability.
Cell Rep Med. 2022 Feb 15;3(2):100501. doi: 10.1016/j.xcrm.2021.100501. eCollection 2022 Feb 15.
Cell Rep Med. 2022.
PMID: 35243414
Free PMC article.
A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse.
Guzman-Moreno C, Zhang P, Phillips OR, Block M, Glennon BJ, Holbrook M, Weigand L, Lo CW, Lin JI.
Guzman-Moreno C, et al. Among authors: glennon bj.
J Vis Exp. 2022 Dec 16;(190). doi: 10.3791/64582.
J Vis Exp. 2022.
PMID: 36591976
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KCTD1/KCTD15 complexes control ectodermal and neural crest cell functions, and their impairment causes aplasia cutis.
Raymundo JR, Zhang H, Smaldone G, Zhu W, Daly KE, Glennon BJ, Pecoraro G, Salvatore M, Devine WA, Lo CW, Vitagliano L, Marneros AG.
Raymundo JR, et al. Among authors: glennon bj.
J Clin Invest. 2023 Dec 19;134(4):e174138. doi: 10.1172/JCI174138.
J Clin Invest. 2023.
PMID: 38113115
Free PMC article.
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Mitotic Block and Epigenetic Repression Underlie Neurodevelopmental Defects and Neurobehavioral Deficits in Congenital Heart Disease.
Gabriel GC, Yagi H, Tan T, Bais AS, Glennon BJ, Stapleton MC, Huang L, Reynolds WT, Shaffer MG, Ganapathiraju M, Simon D, Panigrahy A, Wu YL, Lo CW.
Gabriel GC, et al. Among authors: glennon bj.
bioRxiv [Preprint]. 2024 Feb 26:2023.11.05.565716. doi: 10.1101/2023.11.05.565716.
bioRxiv. 2024.
PMID: 38464057
Free PMC article.
Preprint.
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