User profiles for "author:Renvoise B"
 | Benoit Renvois�Verified email at roche.com Cited by 1114 |
Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B
D Yang, N Rismanchi, B Renvois�…�- Nature structural &�…, 2008 - nature.com
The e ndosomal s orting c omplex r equired for t ransport (ESCRT) machinery, including
ESCRT-III, localizes to the midbody and participates in the membrane-abscission step of�…
ESCRT-III, localizes to the midbody and participates in the membrane-abscission step of�…
Emerging themes of ER organization in the development and maintenance of axons
B Renvois�, C Blackstone�- Current opinion in neurobiology, 2010 - Elsevier
The endoplasmic reticulum (ER) is a continuous membrane system comprising the nuclear
envelope, polyribosome-studded peripheral sheets, and a polygonal network of smooth�…
envelope, polyribosome-studded peripheral sheets, and a polygonal network of smooth�…
Lysosomal abnormalities in hereditary spastic paraplegia types SPG 15 and SPG 11
B Renvois�, J Chang, R Singh…�- Annals of clinical�…, 2014 - Wiley Online Library
Objective Hereditary spastic paraplegias (HSP s) are among the most genetically diverse
inherited neurological disorders, with over 70 disease loci identified (SPG 1‐71) to date�…
inherited neurological disorders, with over 70 disease loci identified (SPG 1‐71) to date�…
SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis
B Renvois�, RL Parker, D Yang…�- Molecular biology of�…, 2010 - Am Soc Cell Biol
Hereditary spastic paraplegias (HSPs, SPG1-46) are inherited neurological disorders
characterized by lower extremity spastic weakness. Loss-of-function SPG20 gene mutations�…
characterized by lower extremity spastic weakness. Loss-of-function SPG20 gene mutations�…
Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation
B Renvois�, B Malone, M Falgairolle…�- Human molecular�…, 2016 - academic.oup.com
Hereditary spastic paraplegias (HSPs; SPG1-76 plus others) are length-dependent
disorders affecting long corticospinal axons, and the most common autosomal dominant�…
disorders affecting long corticospinal axons, and the most common autosomal dominant�…
Mutation in CPT1C associated with pure autosomal dominant spastic paraplegia
Importance The family of genes implicated in hereditary spastic paraplegias (HSPs) is
quickly expanding, mostly owing to the widespread availability of next-generation DNA�…
quickly expanding, mostly owing to the widespread availability of next-generation DNA�…
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells
B Renvois�, K Khoobarry, MC Gendron…�- Journal of cell�…, 2006 - journals.biologists.com
Mutations of the survival motor neuron gene SMN1 cause the inherited disease spinal
muscular atrophy (SMA). The ubiquitous SMN protein facilitates the biogenesis of�…
muscular atrophy (SMA). The ubiquitous SMN protein facilitates the biogenesis of�…
The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy
B Renvois�, S Colasse, P Burlet, L Viollet…�- Human molecular�…, 2009 - academic.oup.com
Spinal muscular atrophy (SMA) is a common autosomal recessive neurodegenerative
disease caused by reduced survival motor neuron (SMN) levels. The assembly machinery�…
disease caused by reduced survival motor neuron (SMN) levels. The assembly machinery�…
Spg20−/− mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling
B Renvois�, J Stadler, R Singh…�- Human molecular�…, 2012 - academic.oup.com
Hereditary spastic paraplegias (HSPs; SPG1-48) are inherited neurological disorders
characterized by lower extremity spasticity and weakness. Loss-of-function mutations in the�…
characterized by lower extremity spasticity and weakness. Loss-of-function mutations in the�…
Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons
PP Zhu, HF Hung, N Batchenkova…�- Human Molecular�…, 2022 - academic.oup.com
Hereditary spastic paraplegias (HSPs) comprise a large group of inherited neurologic
disorders affecting the longest corticospinal axons (SPG1–86 plus others), with shared�…
disorders affecting the longest corticospinal axons (SPG1–86 plus others), with shared�…