| Perilipin deficiency and autosomal dominant partial lipodystrophy S Gandotra, C Le Dour, W Bottomley, P Cervera, P Giral, Y Reznik, ... New England Journal of Medicine 364 (8), 740-748, 2011 | 323 | 2011 |
| Molecular mechanisms of human lipodystrophies: from adipocyte lipid droplet to oxidative stress and lipotoxicity C Vigouroux, M Caron-Debarle, C Le Dour, J Magré, J Capeau The international journal of biochemistry & cell biology 43 (6), 862-876, 2011 | 173 | 2011 |
| ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene M Chatzifrangkeskou, C Le Dour, W Wu, JP Morrow, LC Joseph, ... Human Molecular Genetics 25 (11), 2220-2233, 2016 | 95 | 2016 |
| Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene C Le Dour, C Macquart, F Sera, S Homma, G Bonne, JP Morrow, ... Human molecular genetics 26 (2), 333-343, 2017 | 77 | 2017 |
| LMNA mutations induce a non-inflammatory fibrosis and a brown fat-like dystrophy of enlarged cervical adipose tissue V Béréziat, P Cervera, C Le Dour, MC Verpont, S Dumont, MC Vantyghem, ... The American journal of pathology 179 (5), 2443-2453, 2011 | 68 | 2011 |
| A homozygous mutation of prelamin-A preventing its farnesylation and maturation leads to a severe lipodystrophic phenotype: new insights into the pathogenicity of … C Le Dour, S Schneebeli, F Bakiri, F Darcel, ML Jacquemont, MA Maubert, ... The Journal of Clinical Endocrinology & Metabolism 96 (5), E856-E862, 2011 | 47 | 2011 |
| Microtubule cytoskeleton regulates Connexin 43 localization and cardiac conduction in cardiomyopathy caused by mutation in A-type lamins gene C Macquart, R Jüttner, B Morales Rodriguez, C Le Dour, F Lefebvre, ... Human Molecular Genetics 28 (24), 4043-4052, 2019 | 46 | 2019 |
| The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress VLRM Verstraeten, S Caputo, MAM Van Steensel, I Duband‐Goulet, ... Journal of Cellular and Molecular Medicine 13 (5), 959-971, 2009 | 45 | 2009 |
| Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy C Le Dour, W Wu, V Béréziat, J Capeau, C Vigouroux, HJ Worman Journal of Lipid Research 58 (1), 151-163, 2017 | 39 | 2017 |
| Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria S Dominici, V Fiori, M Magnani, E Schena, C Capanni, D Camozzi, ... European journal of histochemistry: EJH 53 (1), 2009 | 35 | 2009 |
| Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives C Vigouroux, AC Guénantin, C Vatier, E Capel, C Le Dour, P Afonso, ... Nucleus 9 (1), 251-264, 2018 | 31 | 2018 |
| Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice JY Shin, C Le Dour, F Sera, S Iwata, S Homma, LC Joseph, JP Morrow, ... Nucleus 5 (3), 260-268, 2014 | 22 | 2014 |
| Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations C Le Dour, M Chatzifrangkeskou, C Macquart, MM Magiera, C Peccate, ... Nature Communications 13 (1), 7886, 2022 | 10 | 2022 |
| The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies N Vignier, M Chatzifrangkeskou, L Pinton, H Wioland, T Marais, ... Cell reports 36 (8), 2021 | 8 | 2021 |
| Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene M Chatzifrangkeskou, C Le Dour, A Muchir American Journal of Physiology-Cell Physiology 324 (6), C1223-C1235, 2023 | 4 | 2023 |
| Les lipodystrophies génétiques C Vatier, G Bidault, C Le Dour, V Béréziat, O Lascols, J Capeau, ... Médecine & Nutrition 47 (2), 29-41, 2011 | 1 | 2011 |
| Les diabètes insulinorésistants familiaux: Endocrinopathies familiales C Vatier, C Le Dour, V Béréziat, M Caron-Debarle, O Lascols, J Magré Correspondances en MHDN 15 (3), 63-74, 2011 | 1 | 2011 |
| Remodeling of adipose tissue from lipodystrophic patients with LMNA mutations: presence of fibrosis and mitochondrial alterations but no inflammation V Béréziat, P Cervera, MC Verpont, C Le Dour, B Antuna-Puente, ... Diabetologia 52, S254-S255, 2009 | 1 | 2009 |
| Adipose tissue of lipodystrophic patients carry mutations of the lamina A/C has fibrotic changes and mitochondrial alterations in the absence of inflammation V Béréziat, P Cervera, MC Verpont, C Le Dour, B Antuna-Puente, ... DIABETES & METABOLISM 35, A27-A27, 2009 | 1 | 2009 |
| Une brève histoire des laminopathies C Vigouroux, O Lascols, V Béréziat, C Le Dour, S Hernandez, M Caron, ... Médecine des maladies Métaboliques 2 (4), 382-387, 2008 | 1 | 2008 |
Muchir AntoineINSERM CRVerified email at institut-myologie.org
