Andrew P. Lieberman, MD PhD
Affiliations: | Pathology | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Mechanisms of neurodegeneration in Kennedy's Disease.Website:
http://www.pathology.med.umich.edu/faculty/Lieberman,A/index.htmlGoogle:
"Andrew Lieberman"Mean distance: 16.15 (cluster 24) | S | N | B | C | P |
Cross-listing: MichiganTree - Neuropathology Tree
Parents
Sign in to add mentorKenneth H. Fischbeck | grad student | 1998-2001 | NINDS | |
Nicholas K. Gonatas | post-doc | Penn | ||
(Mid 1990's) |
Children
Sign in to add traineeJason P. Chua | grad student | University of Michigan | |
Thaddeus J Kunkel | grad student | University of Michigan | |
Chris D. Pacheco | grad student | 2008 | University of Michigan |
Adrienne M. Wang | grad student | 2012 | University of Michigan |
Matthew J. Elrick | grad student | 2013 | University of Michigan |
Mark L Schultz | post-doc | 2013-2018 | University of Michigan Medical School (Cell & Gene Therapy Tree) |
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Publications
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Azaria RD, Correia AB, Schache KJ, et al. (2024) Mutant induced neurons and humanized mice enable identification of Niemann-Pick C1 proteostatic therapies. Jci Insight |
Yuan T, Kumar S, Skinner ME, et al. (2024) Human SIRT5 variants with reduced stability and activity do not cause neuropathology in mice. Iscience. 27: 109991 |
Javanshad R, Nguyen TTA, Azaria RD, et al. (2024) Endogenous Protein-Protein Interaction Network of the NPC Cholesterol Transporter 1 in the Cerebral Cortex. Journal of Proteome Research |
Yuan T, Kumar S, Skinner M, et al. (2023) variants from patients with mitochondrial disease are associated with reduced SIRT5 stability and activity, but not with neuropathology. Biorxiv : the Preprint Server For Biology |
Halseth TA, Correia AB, Schultz ML, et al. (2023) Apolipoprotein-mimetic nanodiscs reduce lipid accumulation and improve liver function in acid sphingomyelinase deficiency. Nanomedicine : Nanotechnology, Biology, and Medicine. 102705 |
Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
Kunkel TJ, Townsend A, Sullivan KA, et al. (2023) The cholesterol transporter NPC1 is essential for epigenetic regulation and maturation of oligodendrocyte lineage cells. Nature Communications. 14: 3964 |
Scalco R, Hamsafar Y, White CL, et al. (2023) The status of digital pathology and associated infrastructure within Alzheimer's Disease Centers. Journal of Neuropathology and Experimental Neurology |
Schultz ML, Schache KJ, Azaria RD, et al. (2022) Species-specific differences in NPC1 protein trafficking govern therapeutic response in Niemann-Pick type C disease. Jci Insight |
Liu EA, Mori E, Hamasaki F, et al. (2021) TDP-43 proteinopathy occurs independently of autophagic substrate accumulation and underlies nuclear defects in Niemann-Pick C disease. Neuropathology and Applied Neurobiology |