Events
Seminars, meetings, defenses and public events connected to the laboratory.
Abstract Splicing is a well-known process that consists in the removal from pre-messenger RNAs of intronic sequences recognized thanks to […]
Abstract Centronuclear and myotubular myopathies (CNM) are severe congenital myopathies linked to muscle weakness and often respiratory distress. A main […]
Abstract Chromatin within the cell nucleus acquires a complex structure fundamental for genome function. The tridimensional organization of the genome […]
Abstract Sensory neurons have the capacity to grow long distances and high morphological plasticity during development. Upon injury this plasticity […]
INMG-PGNM students, engineers, researchers and teacher-researchers organized cake and drink sales and other actions for AFM-Telethon. In 2023, these actions […]
Abstract Duchenne muscular dystrophy (DMD) is a rare genetic disease due to the absence of dystrophin from striated muscles. Affected […]
Abstract Maintenance of optimal mitochondrial function plays a crucial role in the regulation of muscle stem cell (MuSC) behavior, but […]
Abstract The second messenger Ca2+ regulates a broad repertoire of cellular processes. Upon physiological stimuli, skeletal muscle mitochondria rapidly and […]
Abstract Ultrastructure expansion microscopy can be useful for structural cell biology, placing specific emphasis on centrioles and their inner scaffold […]
Abstract The function of many organs, including skeletal muscle, depends on its three-dimensional structure. Muscle regeneration therefore requires not only […]
Abstract Functional selectivity, a phenomenon where a ligand favors activation of specific signaling pathways over others, emerges as an innovative […]
Les Cellules Déambulent co-organized an afternoon Science Festival event at the Woman-Mother-Child Hospital.
Abstract Poly-ADP-Ribose Polymerases (PARPs) are a family of proteins that consume nicotinamide adenine dinucleotide (NAD+; a form of Vitamin B3) […]
Abstract The identification of a point mutation (p.Ser59Leu) in the CHCHD10 gene was the first genetic evidence that mitochondrial dysfunction […]
Abstract Spinocerebellar ataxia type 1 (SCA1) is a fatal neurodegenerative disease caused by a polyglutamine (PolyQ) expansion in the Ataxin-1 […]
Abstract Second messengers, including cAMP, cGMP and Ca2+ are often placed in an integrating position to combine the extracellular cues […]
Abstract Ludo research focuses on the cause, mechanism and treatment options for neurodegenerative diseases. In particular, he studies amyotrophic lateral […]
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