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Sign in to add traineeBrook DeRosa | grad student | University of Miami | |
Sara Linker | grad student | 2014 | University of Miami |
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Publications
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Song E, Lee SK, Dykxhoorn DM, et al. (2023) Correction for Song et al., "Sustained Small Interfering RNA-Mediated Human Immunodeficiency Virus Type 1 Inhibition in Primary Macrophages". Journal of Virology. e0093623 |
Cukier HN, Duarte CL, Laverde-Paz MJ, et al. (2023) An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons. Neurobiology of Aging. 131: 182-195 |
Cukier HN, Duarte CL, Laverde-Paz MJ, et al. (2023) An Alzheimer's disease risk variant in modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons. Biorxiv : the Preprint Server For Biology |
Edwards JS, Delabat SA, Badilla AD, et al. (2022) Downregulation of SOCS1 increases interferon-induced ISGylation during differentiation of induced-pluripotent stem cells to hepatocytes. Jhep Reports : Innovation in Hepatology. 4: 100592 |
Brandenburg C, Griswold AJ, Van Booven DJ, et al. (2022) Transcriptomic analysis of isolated and pooled human postmortem cerebellar Purkinje cells in autism spectrum disorders. Frontiers in Genetics. 13: 944837 |
Tang PC, V Roche M, Young Um S, et al. (2022) Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43. Stem Cell Research. 61: 102758 |
Frei JA, Niescier RF, Bridi MS, et al. (2021) Regulation of Neural Circuit Development by Cadherin-11 Provides Implications for Autism. Eneuro |
Frei JA, Brandenburg CJ, Nestor JE, et al. (2021) Postnatal expression profiles of atypical cadherin FAT1 suggest its role in autism. Biology Open. 10 |
Frei JA, Brandenburg C, Nestor JE, et al. (2021) Postnatal expression profiles of atypical cadherin FAT1 suggest its role in autism. Biology Open |
Hatzistergos KE, Williams AR, Dykxhoorn DM, et al. (2019) Tumor Suppressors RB1 and CDKN2a Cooperatively Regulate Cell-Cycle Progression and Differentiation During Cardiomyocyte Development and Repair: Implications for Stimulating Neomyogenesis with Cell-Based Therapy. Circulation Research |