Výsledky vyhledávání - Pennetta, Giuseppa

Insights into ALS pathomechanisms: from flies to humans Autor Chai, Andrea, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

Emerging Links between Lipid Droplets and Motor Neuron Diseases Autor Pennetta, Giuseppa, Welte, Michael A.

Získat plný text Získat plný text Získat plný text

Why Quantification Matters: Characterization of Phenotypes at the Drosophila Larval Neuromuscular Junction Autor Sanhueza, Mario, Kubasik-Thayil, Anisha, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

Gain-of-function mutations in the ALS8 causative gene VAPB have detrimental effects on neurons and muscles Autor Sanhueza, Mario, Zechini, Luigi, Gillespie, Trudy, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular j... Autor Chai, Andrea, Withers, James, Koh, Young Ho, Parry, Katherine, Bao, Hong, Zhang, Bing, Budnik, Vivian, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

Network Analyses Reveal Novel Aspects of ALS Pathogenesis Autor Sanhueza, Mario, Chai, Andrea, Smith, Colin, McCray, Brett A., Simpson, T. Ian, Taylor, J. Paul, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis Autor Chen, Han-Jou, Anagnostou, Georgia, Chai, Andrea, Withers, James, Morris, Alex, Adhikaree, Jason, Pennetta, Giuseppa, de Belleroche, Jackie S.

Získat plný text Získat plný text Získat plný text

Increased levels of phosphoinositides cause neurodegeneration in a Drosophila model of amyotrophic lateral sclerosis Autor Forrest, Stuart, Chai, Andrea, Sanhueza, Mario, Marescotti, Manuela, Parry, Katherine, Georgiev, Atanas, Sahota, Virender, Mendez-Castro, Raquel, Pennetta, Giuseppa

Získat plný text Získat plný text Získat plný text

Comparison of independent screens on differentially vulnerable motor neurons reveals alpha-synuclein as a common modifier in motor neuron diseases Autor Kline, Rachel A., Kaifer, Kevin A., Osman, Erkan Y., Carella, Francesco, Tiberi, Ariana, Ross, Jolill, Pennetta, Giuseppa, Lorson, Christian L., Murray, Lyndsay M.

Získat plný text Získat plný text Získat plný text

Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo Autor Llavero Hurtado, Maica, Fuller, Heidi R., Wong, Andrew M. S., Eaton, Samantha L., Gillingwater, Thomas H., Pennetta, Giuseppa, Cooper, Jonathan D., Wishart, Thomas M.

Získat plný text Získat plný text Získat plný text

Membrane and synaptic defects leading to neurodegeneration in Adar mutant Drosophila are rescued by increased autophagy Autor Khan, Anzer, Paro, Simona, McGurk, Leeanne, Sambrani, Nagraj, Hogg, Marion C., Brindle, James, Pennetta, Giuseppa, Keegan, Liam P., O’Connell, Mary A.

Získat plný text Získat plný text Získat plný text

Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense Autor Morris, Otto, Liu, Xi, Domingues, Celia, Runchel, Christopher, Chai, Andrea, Basith, Shaherin, Tenev, Tencho, Chen, Haiyang, Choi, Sangdun, Pennetta, Giuseppa, Buchon, Nicolas, Meier, Pascal

Získat plný text Získat plný text Získat plný text

Proteomic profiling of neuronal mitochondria reveals modulators of synaptic architecture Autor Graham, Laura C., Eaton, Samantha L., Brunton, Paula J., Atrih, Abdelmadjid, Smith, Colin, Lamont, Douglas J., Gillingwater, Thomas H., Pennetta, Giuseppa, Skehel, Paul, Wishart, Thomas M.

Získat plný text Získat plný text Získat plný text

Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphology Autor Amorim, Inês S., Graham, Laura C., Carter, Roderick N., Morton, Nicholas M., Hammachi, Fella, Kunath, Tilo, Pennetta, Giuseppa, Carpanini, Sarah M., Manson, Jean C., Lamont, Douglas J., Wishart, Thomas M., Gillingwater, Thomas H.

Získat plný text Získat plný text Získat plný text