| 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 | 236 | 2014 |
| Spectrin-and ankyrin-based membrane domains and the evolution of vertebrates V Bennett, DN Lorenzo Current topics in membranes 72, 1-37, 2013 | 161 | 2013 |
| 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 | 93 | 2014 |
| 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 | 88 | 2016 |
| 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 | 85 | 2019 |
| 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 | 83 | 2010 |
| 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 | 73 | 2002 |
| 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 | 51 | 2019 |
| 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 | 43 | 2021 |
| 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 | 34 | 2016 |
| 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 | 33 | 2018 |
| 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 | 30 | 2017 |
| 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 | 23 | 2015 |
| 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 | 21 | 2000 |
| Cargo hold and delivery: Ankyrins, spectrins, and their functional patterning of neurons DN Lorenzo Cytoskeleton 77 (3-4), 129-148, 2020 | 20 | 2020 |
| 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 | 14 | 2021 |
| 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 | 14 | 2006 |
| Spectrins: molecular organizers and targets of neurological disorders DN Lorenzo, RJ Edwards, AL Slavutsky Nature Reviews Neuroscience 24 (4), 195-212, 2023 | 11 | 2023 |
| 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 | 10 | 2009 |
| 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 | 4 | 2020 |
Alexandra BadeaDuke UniversityПотвърден имейл адрес: duke.edu
