| Year |
Citation |
Score |
| 2021 |
Creighton BA, Afriyie S, Ajit D, Casingal CR, Voos KM, Reger J, Burch AM, Dyne E, Bay J, Huang JK, Anton ES, Fu MM, Lorenzo DN. Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A. Elife. 10. PMID 34812142 DOI: 10.7554/eLife.69815 |
0.486 |
|
| 2020 |
Lorenzo DN. Cargo hold and delivery: Ankyrins, spectrins, and their functional patterning of neurons. Cytoskeleton (Hoboken, N.J.). 77: 129-148. PMID 32034889 DOI: 10.1002/Cm.21602 |
0.376 |
|
| 2019 |
Creighton BA, Ruffins TW, Lorenzo DN. Visualizing and Analyzing Intracellular Transport of Organelles and Other Cargos in Astrocytes. Journal of Visualized Experiments : Jove. PMID 31524875 DOI: 10.3791/60230 |
0.351 |
|
| 2019 |
Yang R, Walder-Christensen KK, Kim N, Wu D, Lorenzo DN, Badea A, Jiang YH, Yin HH, Wetsel WC, Bennett V. autism mutation targeting giant ankyrin-B promotes axon branching and ectopic connectivity. Proceedings of the National Academy of Sciences of the United States of America. PMID 31285321 DOI: 10.1073/Pnas.1904348116 |
0.571 |
|
| 2019 |
Lorenzo DN, Badea A, Zhou R, Mohler PJ, Zhuang X, Bennett V. βII-spectrin promotes mouse brain connectivity through stabilizing axonal plasma membranes and enabling axonal organelle transport. Proceedings of the National Academy of Sciences of the United States of America. PMID 31209033 DOI: 10.1073/Pnas.1820649116 |
0.748 |
|
| 2018 |
Snouwaert JN, Church RJ, Jania L, Nguyen M, Wheeler ML, Saintsing A, Mieczkowski P, Manuel de Villena FP, Armao D, Moy SS, Lorenzo DN, Koller BH. A Mutation in the Borcs7 Subunit of the Lysosome Regulatory BORC Complex Results in Motor Deficits and Dystrophic Axonopathy in Mice. Cell Reports. 24: 1254-1265. PMID 30067980 DOI: 10.1016/J.Celrep.2018.06.118 |
0.509 |
|
| 2017 |
Lorenzo DN, Bennett V. Cell-autonomous adiposity through increased cell surface GLUT4 due to ankyrin-B deficiency. Proceedings of the National Academy of Sciences of the United States of America. PMID 29133412 DOI: 10.1073/Pnas.1708865114 |
0.536 |
|
| 2016 |
Qu F, Lorenzo DN, King SJ, Brooks R, Bear JE, Bennett V. Ankyrin-B is a PI3P effector that promotes polarized α5β1-integrin recycling via recruiting RabGAP1L to early endosomes. Elife. 5. PMID 27718357 DOI: 10.7554/Elife.20417 |
0.563 |
|
| 2016 |
Bennett V, Lorenzo DN. An Adaptable Spectrin/Ankyrin-Based Mechanism for Long-Range Organization of Plasma Membranes in Vertebrate Tissues. Current Topics in Membranes. 77: 143-84. PMID 26781832 DOI: 10.1016/bs.ctm.2015.10.001 |
0.577 |
|
| 2016 |
Qu F, Lorenzo DN, King SJ, Brooks R, Bear JE, Bennett V. Author response: Ankyrin-B is a PI3P effector that promotes polarized α5β1-integrin recycling via recruiting RabGAP1L to early endosomes Elife. DOI: 10.7554/Elife.20417.022 |
0.508 |
|
| 2015 |
Lorenzo DN, Healy JA, Hostettler J, Davis J, Yang J, Wang C, Hohmeier HE, Zhang M, Bennett V. Ankyrin-B metabolic syndrome combines age-dependent adiposity with pancreatic β cell insufficiency. The Journal of Clinical Investigation. PMID 26168218 DOI: 10.1172/Jci81317 |
0.669 |
|
| 2014 |
Zhong G, He J, Zhou R, Lorenzo D, Babcock HP, Bennett V, Zhuang X. Developmental mechanism of the periodic membrane skeleton in axons. Elife. 3. PMID 25535840 DOI: 10.7554/Elife.04581 |
0.692 |
|
| 2014 |
Lorenzo DN, Badea A, Davis J, Hostettler J, He J, Zhong G, Zhuang X, Bennett V. A PIK3C3-ankyrin-B-dynactin pathway promotes axonal growth and multiorganelle transport. The Journal of Cell Biology. 207: 735-52. PMID 25533844 DOI: 10.1083/Jcb.201407063 |
0.692 |
|
| 2014 |
Zhong G, He J, Zhou R, Lorenzo D, Babcock HP, Bennett V, Zhuang X. Author response: Developmental mechanism of the periodic membrane skeleton in axons Elife. DOI: 10.7554/Elife.04581.025 |
0.664 |
|
| 2013 |
Bennett V, Lorenzo DN. Spectrin- and ankyrin-based membrane domains and the evolution of vertebrates. Current Topics in Membranes. 72: 1-37. PMID 24210426 DOI: 10.1016/B978-0-12-417027-8.00001-5 |
0.598 |
|
| 2010 |
Lorenzo DN, Li MG, Mische SE, Armbrust KR, Ranum LP, Hays TS. Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila. The Journal of Cell Biology. 189: 143-58. PMID 20368622 DOI: 10.1083/Jcb.200905158 |
0.715 |
|
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