| Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B D Yang, N Rismanchi, B Renvoisé, J Lippincott-Schwartz, C Blackstone, ... Nature structural & molecular biology 15 (12), 1278-1286, 2008 | 273 | 2008 |
| Lysosomal abnormalities in hereditary spastic paraplegia types SPG 15 and SPG 11 B Renvoisé, J Chang, R Singh, S Yonekawa, EJ FitzGibbon, A Mankodi, ... Annals of clinical and translational neurology 1 (6), 379-389, 2014 | 113 | 2014 |
| SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis B Renvoisé, RL Parker, D Yang, JC Bakowska, JH Hurley, C Blackstone Molecular biology of the cell 21 (19), 3293-3303, 2010 | 97 | 2010 |
| Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation B Renvoisé, B Malone, M Falgairolle, J Munasinghe, J Stadler, C Sibilla, ... Human molecular genetics 25 (23), 5111-5125, 2016 | 86 | 2016 |
| Mutation in CPT1C associated with pure autosomal dominant spastic paraplegia C Rinaldi, T Schmidt, AJ Situ, JO Johnson, PR Lee, K Chen, LC Bott, ... JAMA neurology 72 (5), 561-570, 2015 | 83 | 2015 |
| Emerging themes of ER organization in the development and maintenance of axons B Renvoisé, C Blackstone Current opinion in neurobiology 20 (5), 531-537, 2010 | 72 | 2010 |
| Spg20−/− mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling B Renvoisé, J Stadler, R Singh, JC Bakowska, C Blackstone Human molecular genetics 21 (16), 3604-3618, 2012 | 65 | 2012 |
| Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells B Renvoisé, K Khoobarry, MC Gendron, C Cibert, L Viollet, S Lefebvre Journal of cell science 119 (4), 680-692, 2006 | 54 | 2006 |
| Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology G Zhao, PP Zhu, B Renvoisé, L Maldonado-Báez, SH Park, C Blackstone Experimental cell research 349 (1), 32-44, 2016 | 45 | 2016 |
| MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis S Lee, J Chang, B Renvoisé, A Tipirneni, S Yang, C Blackstone Molecular biology of the cell 23 (22), 4347-4361, 2012 | 44 | 2012 |
| The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy B Renvoisé, S Colasse, P Burlet, L Viollet, UT Meier, S Lefebvre Human molecular genetics 18 (7), 1181-1189, 2009 | 42 | 2009 |
| A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease W Westbroek, M Nguyen, M Siebert, T Lindstrom, RA Burnett, E Aflaki, ... Disease models & mechanisms 9 (7), 769-778, 2016 | 34 | 2016 |
| Neuronal Cx3cr1 deficiency protects against amyloid β-induced neurotoxicity J Dworzak, B Renvoisé, J Habchi, EV Yates, C Combadière, TP Knowles, ... PloS one 10 (6), e0127730, 2015 | 31 | 2015 |
| A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies B Renvoisé, G Quérol, ER Verrier, P Burlet, S Lefebvre Journal of Cell Science 125 (12), 2862-2874, 2012 | 30 | 2012 |
| Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development U Goyal, B Renvoisé, J Chang, C Blackstone PloS one 9 (11), e112428, 2014 | 26 | 2014 |
| Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons PP Zhu, HF Hung, N Batchenkova, J Nixon-Abell, J Henderson, P Zheng, ... Human Molecular Genetics 31 (16), 2779-2795, 2022 | 18 | 2022 |
| Hereditary spastic paraplegias: Genetics and clinical features B Renvoisé, C Blackstone Movement Disorders, 1063-1071, 2015 | 1 | 2015 |
| Please let us know how this document benefits you. H Fujiwara, R Sidhu, B Renvoise, DS Ory | | 2016 |
| Cellular effects of distinct missense mutations at spastin residue 499 that result in clinically different neurologic syndromes H Boucekkine, B Renvoise, L Maldonado-Baez, NB Cole, CD Blackstone MOLECULAR BIOLOGY OF THE CELL 27, 2016 | | 2016 |
| A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease H Fujiwara, R Sidhu, B Renvoise, DS Ory | | 2016 |
