J. Paul Taylor
Affiliations: | St Jude Children's Research Hospital, New York, NY, United States |
Area:
neurodegenerationGoogle:
"J. Taylor"Parents
Sign in to add mentor| Kenneth H. Fischbeck | post-doc | National Institute of Neurological Disorders and Stroke, NIH (Neurotree) | |
| Kyung-Tai Min | post-doc | NINDS (Neurotree) |
Children
Sign in to add trainee| Arvind Bhusnurmath | grad student | 2008 | Penn |
| Brett A. McCray | grad student | 2010 | Penn |
| Natalia B. Nedelsky | grad student | 2010 | Penn |
| Gillian P. Ritson | grad student | 2010 | Penn |
| Maria D. Purice | post-doc | 2017- | St. Jude Children's Research Hospital (Neurotree) |
| Victoria J Dardov | post-doc | 2019- | St. Jude Children’s Research Hospital (Neurotree) |
| Peter Todd | post-doc | 2004-2008 | Penn (Neurotree) |
BETA: Related publications
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Publications
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| Badders NM, Korff A, Miranda HC, et al. (2024) Author Correction: Selective modulation of the androgen receptor AF2 domain rescues degeneration in spinal bulbar muscular atrophy. Nature Medicine |
| Bennett CL, Dastidar S, Arnold FJ, et al. (2023) Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity. Acta Neuropathologica Communications. 11: 164 |
| Branch MR, Hsu CL, Ohnishi K, et al. (2023) MAP4K3 inhibits Sirtuin-1 to repress the LKB1-AMPK pathway to promote amino acid-dependent activation of the mTORC1 complex. Life Science Alliance. 6 |
| Holden SK, Bedenfield N, Taylor AS, et al. (2023) Research Priorities of Individuals and Caregivers With Lewy Body Dementia: A Web-based Survey. Alzheimer Disease and Associated Disorders. 37: 50-58 |
| Kim HJ, Mohassel P, Donkervoort S, et al. (2022) Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy. Nature Communications. 13: 2306 |
| Nedelsky NB, Taylor JP. (2021) Pathological phase transitions in ALS-FTD impair dynamic RNA-protein granules. Rna (New York, N.Y.) |
| Beijer D, Kim HJ, Guo L, et al. (2021) Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation. Jci Insight. 6 |
| Zhang J, Velmeshev D, Hashimoto K, et al. (2020) Neurotoxic microglia promote TDP-43 proteinopathy in progranulin deficiency. Nature |
| Haenig C, Atias N, Taylor AK, et al. (2020) Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains. Cell Reports. 32: 108050 |
| Lee AK, Klein J, Fon Tacer K, et al. (2020) Translational Repression of G3BP in Cancer and Germ Cells Suppresses Stress Granules and Enhances Stress Tolerance. Molecular Cell |