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Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells
Earle, Ashley J., Kirby, Tyler J., Fedorchak, Gregory R., Isermann, Philipp, Patel, Jineet, Iruvanti, Sushruta, Moore, Steven A., Bonne, Gisèle, Wallrath, Lori L., Lammerding, Jan
Published in Nature materials (01.04.2020)
Published in Nature materials (01.04.2020)
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Journal Article
The 2022 version of the gene table of neuromuscular disorders (nuclear genome)
Cohen, Enzo, Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.12.2021)
Published in Neuromuscular disorders : NMD (01.12.2021)
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Journal Article
The 2020 version of the gene table of neuromuscular disorders (nuclear genome)
Benarroch, Louise, Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.12.2019)
Published in Neuromuscular disorders : NMD (01.12.2019)
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Journal Article
The 2021 version of the gene table of neuromuscular disorders (nuclear genome)
Benarroch, Louise, Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.12.2020)
Published in Neuromuscular disorders : NMD (01.12.2020)
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Journal Article
Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy
Guénantin, Anne-Claire, Jebeniani, Imen, Leschik, Julia, Watrin, Erwan, Bonne, Gisèle, Vignier, Nicolas, Pucéat, Michel
Published in The Journal of clinical investigation (04.01.2021)
Published in The Journal of clinical investigation (04.01.2021)
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Journal Article
The 13C hyperpolarized pyruvate generated by ParaHydrogen detects the response of the heart to altered metabolism in real time
Cavallari, Eleonora, Carrera, Carla, Sorge, Matteo, Bonne, Gisèle, Muchir, Antoine, Aime, Silvio, Reineri, Francesca
Published in Scientific reports (30.05.2018)
Published in Scientific reports (30.05.2018)
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Journal Article
The 2023 version of the gene table of neuromuscular disorders (nuclear genome)
Benarroch, Louise, Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.01.2023)
Published in Neuromuscular disorders : NMD (01.01.2023)
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Journal Article
The 2024 version of the gene table of neuromuscular disorders (nuclear genome)
Benarroch, Louise, Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.01.2024)
Published in Neuromuscular disorders : NMD (01.01.2024)
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Journal Article
TOR1AIP1-Associated Nuclear Envelopathies
Mackels, Laurane, Liu, Xincheng, Bonne, Gisèle, Servais, Laurent
Published in International journal of molecular sciences (07.04.2023)
Published in International journal of molecular sciences (07.04.2023)
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Journal Article
Web Resource
Lamin and the heart
Captur, Gabriella, Arbustini, Eloisa, Bonne, Gisèle, Syrris, Petros, Mills, Kevin, Wahbi, Karim, Mohiddin, Saidi A, McKenna, William J, Pettit, Stephen, Ho, Carolyn Y, Muchir, Antoine, Gissen, Paul, Elliott, Perry M, Moon, James C
Published in Heart (British Cardiac Society) (01.03.2018)
Published in Heart (British Cardiac Society) (01.03.2018)
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Journal Article
The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome)
Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.12.2017)
Published in Neuromuscular disorders : NMD (01.12.2017)
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Journal Article
The 2025 version of the gene table of neuromuscular disorders (nuclear genome)
Benarroch, Louise, Bonne, Gisèle, Rivier, François, Procaccio, Vincent, Hamroun, Dalil
Published in Neuromuscular disorders : NMD (01.01.2025)
Published in Neuromuscular disorders : NMD (01.01.2025)
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Journal Article
Microtubule cytoskeleton regulates Connexin 43 localization and cardiac conduction in cardiomyopathy caused by mutation in A-type lamins gene
Macquart, Coline, Jüttner, Rene, Morales Rodriguez, Blanca, Le Dour, Caroline, Lefebvre, Florence, Chatzifrangkeskou, Maria, Schmitt, Alain, Gotthardt, Michael, Bonne, Gisèle, Muchir, Antoine
Published in Human molecular genetics (15.12.2019)
Published in Human molecular genetics (15.12.2019)
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Journal Article
Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation
Vignier, Nicolas, Chatzifrangkeskou, Maria, Morales Rodriguez, Blanca, Mericskay, Mathias, Mougenot, Nathalie, Wahbi, Karim, Bonne, Gisèle, Muchir, Antoine
Published in Human molecular genetics (15.11.2018)
Published in Human molecular genetics (15.11.2018)
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Journal Article
253rd ENMC international workshop: Striated muscle laminopathies - natural history and clinical trial readiness. 24–26 June 2022, Hoofddorp, the Netherlands
Maggi, Lorenzo, Quijano-Roy, Susana, Bönnemann, Carsten, Bonne, Gisèle
Published in Neuromuscular disorders : NMD (01.06.2023)
Published in Neuromuscular disorders : NMD (01.06.2023)
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Journal Article
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors
Bertrand, Anne T, Ziaei, Simindokht, Ehret, Camille, Duchemin, Hélène, Mamchaoui, Kamel, Bigot, Anne, Mayer, Michèle, Quijano-Roy, Susana, Desguerre, Isabelle, Lainé, Jeanne, Ben Yaou, Rabah, Bonne, Gisèle, Coirault, Catherine
Published in Journal of cell science (01.07.2014)
Published in Journal of cell science (01.07.2014)
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Journal Article
A lamin A/C variant causing striated muscle disease provides insights into filament organization
Kronenberg-Tenga, Rafael, Tatli, Meltem, Eibauer, Matthias, Wu, Wei, Shin, Ji-Yeon, Bonne, Gisèle, Worman, Howard J., Medalia, Ohad
Published in Journal of cell science (22.03.2021)
Published in Journal of cell science (22.03.2021)
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Journal Article