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Maxim V. Frolov

Affiliations: 
Biochemistry and Molecular Genetics University of Illinois at Chicago, Chicago, IL, United States 
Area:
Genetics, Molecular Biology, Biochemistry
Website:
https://bcmg.com.uic.edu/faculty/frolov_maxim.html
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"Maxim Frolov"
Bio:

https://cancer.uillinois.edu/member/maxim-frolov/

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Publications

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Rader AE, Bayarmagnai B, Frolov MV. (2023) Combined inactivation of RB and Hippo converts differentiating Drosophila photoreceptors into eye progenitor cells through derepression of homothorax. Developmental Cell. 58: 2261-2274.e6
Rader AE, Bayarmagnai B, Frolov MV. (2023) Combined inactivation of RB and Hippo pathways converts differentiating photoreceptors into eye progenitor cells through derepression of . Biorxiv : the Preprint Server For Biology
Zappia MP, Kwon YJ, Westacott A, et al. (2023) E2F regulation of the gene is functionally important in development. Proceedings of the National Academy of Sciences of the United States of America. 120: e2220770120
Zappia MP, Guarner A, Kellie-Smith N, et al. (2021) E2F/Dp inactivation in fat body cells triggers systemic metabolic changes. Elife. 10
Chen X, Ariss MM, Ramakrishnan G, et al. (2020) Cell-Autonomous versus Systemic Akt Isoform Deletions Uncovered New Roles for Akt1 and Akt2 in Breast Cancer. Molecular Cell
Ariss MM, Terry AR, Islam ABMMK, et al. (2020) Amalgam regulates the receptor tyrosine kinase pathway through Sprouty in glial cell development. Journal of Cell Science
Zappia MP, de Castro L, Ariss MM, et al. (2020) A cell atlas of adult muscle precursors uncovers early events in fibre-type divergence in Drosophila. Embo Reports. e49555
Zappia MP, Rogers A, Islam ABMMK, et al. (2019) Rbf Activates the Myogenic Transcriptional Program to Promote Skeletal Muscle Differentiation. Cell Reports. 26: 702-719.e6
Ariss MM, Islam ABMMK, Critcher M, et al. (2018) Single cell RNA-sequencing identifies a metabolic aspect of apoptosis in Rbf mutant. Nature Communications. 9: 5024
Guarner A, Morris R, Korenjak M, et al. (2017) E2F/DP Prevents Cell-Cycle Progression in Endocycling Fat Body Cells by Suppressing dATM Expression. Developmental Cell. 43: 689-703.e5
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