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Damaris Lorenzo
Damaris Lorenzo
University of Pennsylvania Perelman School of Medicine
Verified email at pennmedicine.upenn.edu
Title
Cited by
Cited by
Year
Developmental mechanism of the periodic membrane skeleton in axons
G Zhong, J He, R Zhou, D Lorenzo, HP Babcock, V Bennett, X Zhuang
Elife 3, e04581, 2014
2352014
Spectrin-and ankyrin-based membrane domains and the evolution of vertebrates
V Bennett, DN Lorenzo
Current topics in membranes 72, 1-37, 2013
1612013
A PIK3C3–Ankyrin-B–Dynactin pathway promotes axonal growth and multiorganelle transport
DN Lorenzo, A Badea, J Davis, J Hostettler, J He, G Zhong, X Zhuang, ...
Journal of Cell Biology 207 (6), 735-752, 2014
922014
An adaptable spectrin/ankyrin-based mechanism for long-range organization of plasma membranes in vertebrate tissues
V Bennett, DN Lorenzo
Current topics in membranes 77, 143-184, 2016
882016
ANK2 autism mutation targeting giant ankyrin-B promotes axon branching and ectopic connectivity
R Yang, KK Walder-Christensen, N Kim, D Wu, DN Lorenzo, A Badea, ...
Proceedings of the National Academy of Sciences 116 (30), 15262-15271, 2019
842019
Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila
DN Lorenzo, M Li, SE Mische, KR Armbrust, LPW Ranum, TS Hays
Journal of Cell Biology 189 (1), 143-158, 2010
832010
Expression of a single-chain Fv antibody fragment specific for the hepatitis B surface antigen in transgenic tobacco plants
N Ram, M Ayala, D Lorenzo, D Palenzuela, L Herrera, V Doreste, M Pérez, ...
Transgenic Research 11, 61-64, 2002
722002
βII-spectrin promotes mouse brain connectivity through stabilizing axonal plasma membranes and enabling axonal organelle transport
DN Lorenzo, A Badea, R Zhou, PJ Mohler, X Zhuang, V Bennett
Proceedings of the National Academy of Sciences 116 (31), 15686-15695, 2019
502019
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
MA Cousin, BA Creighton, KA Breau, RC Spillmann, E Torti, S Dontu, ...
Nature genetics 53 (7), 1006-1021, 2021
402021
Ankyrin-B is a PI3P effector that promotes polarized α5β1-integrin recycling via recruiting RabGAP1L to early endosomes
F Qu, DN Lorenzo, SJ King, R Brooks, JE Bear, V Bennett
Elife 5, e20417, 2016
342016
A mutation in the Borcs7 subunit of the lysosome regulatory BORC complex results in motor deficits and dystrophic axonopathy in mice
JN Snouwaert, RJ Church, L Jania, MT Nguyen, ML Wheeler, A Saintsing, ...
Cell reports 24 (5), 1254-1265, 2018
322018
Cell-autonomous adiposity through increased cell surface GLUT4 due to ankyrin-B deficiency
DN Lorenzo, V Bennett
Proceedings of the National Academy of Sciences 114 (48), 12743-12748, 2017
302017
Ankyrin-B metabolic syndrome combines age-dependent adiposity with pancreatic β cell insufficiency
DN Lorenzo, JA Healy, J Hostettler, J Davis, J Yang, C Wang, ...
The Journal of clinical investigation 125 (8), 3087-3102, 2015
232015
Single-chain antibody fragments specific to the hepatitis B surface antigen, produced in recombinant tobacco cell cultures
N Ramírez, D Lorenzo, D Palenzuela, L Herrera, M Ayala, A Fuentes, ...
Biotechnology letters 22, 1233-1236, 2000
212000
Cargo hold and delivery: Ankyrins, spectrins, and their functional patterning of neurons
DN Lorenzo
Cytoskeleton 77 (3-4), 129-148, 2020
202020
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5
DN Lorenzo, SM Forrest, Y Ikeda, KA Dick, LPW Ranum, MA Knight
Neurology 67 (11), 2084-2085, 2006
142006
Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
BA Creighton, S Afriyie, D Ajit, CR Casingal, KM Voos, J Reger, AM Burch, ...
eLife 10 (e69815), 1-37, 2021
132021
Conventional mutations are associated with a different phenotype than polyglutamine expansions in spinocerebellar ataxias
A Durr, G Stevanin, S Forlani, C Cazeneuve, C Cagnoli, CP Figueroa, ...
Eur J Hum Genet 17 (suppl 2), 335, 2009
102009
Spectrins: molecular organizers and targets of neurological disorders
DN Lorenzo, RJ Edwards, AL Slavutsky
Nature Reviews Neuroscience 24 (4), 195-212, 2023
92023
Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome
MA Cousin, KA Breau, BA Creighton, RC Spillmann, E Torti, S Dontu, ...
medRxiv, 2020.08. 31.20184481, 2020
42020
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