Paul C. Marcogliese, Ph.D.
Affiliations: | 2022- | Biochemistry & Medical Genetics | University of Manitoba, Winnipeg, Manitoba, Canada |
Area:
Neurodevelopment/NeurodegenerationWebsite:
https://www.marcoglieselab.com/Google:
"Paul Marcogliese"Mean distance: 17.78 (cluster 11) | S | N | B | C | P |
Cross-listing: Neuropathology Tree
Parents
Sign in to add mentor| David S. Park | grad student | 2010-2016 | University of Ottawa |
| Hugo J. Bellen | post-doc | 2016-2022 | Baylor College of Medicine/Jan and Dan Duncan Neurological Research Institute |
Children
Sign in to add trainee| Danielle Pascual | grad student | 2022- | University of Manitoba |
| Yina Her | grad student | 2023- | University of Manitoba |
BETA: Related publications
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Publications
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| Liao JZ, Chung HL, Shih C, et al. (2024) Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila. Nature Communications. 15: 3326 |
| Dutta D, Kanca O, Shridharan RV, et al. (2024) Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proceedings of the National Academy of Sciences of the United States of America. 121: e2322582121 |
| Dutta D, Kanca O, Byeon SK, et al. (2023) A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels. Nature Metabolism |
| Sinha Ray S, Dutta D, Dennys C, et al. (2022) Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategy. Cell Reports. 41: 111751 |
| Snijders Blok L, Verseput J, Rots D, et al. (2022) A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder. Hgg Advances. 4: 100157 |
| Marcogliese PC, Deal SL, Andrews J, et al. (2022) Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Reports. 38: 110517 |
| Lu S, Hernan R, Marcogliese PC, et al. (2022) Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures. American Journal of Human Genetics |
| Chung HL, Rump P, Lu D, et al. (2022) De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in drosophila. Human Molecular Genetics |
| Accogli A, Lu S, Musante I, et al. (2022) Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development. Cerebellum (London, England) |
| Marcogliese PC, Dutta D, Ray SS, et al. (2022) Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. Science Advances. 8: eabl5613 |