R. Magnoni

发表

Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.

E. Rugarli, G. Casari, A. Quattrini, 2009, Human molecular genetics.

Molecular Chaperone Disorders: Defective Hsp60 in Neurodegeneration

P. Bross, A. Bie, R. Magnoni, 2013 .

Activation of the p38MAPK cascade is associated with upregulation of TNF alpha receptors in the spinal motor neurons of mouse models of familial ALS

J. Julien, C. Bendotti, D. Coco, 2006, Molecular and Cellular Neuroscience.

The heat shock protein amplifier arimoclomol improves refolding, maturation and lysosomal activity of glucocerebrosidase

B. Bembi, T. Kirkegaard, Arnela Mehmedbasic, 2018, EBioMedicine.

Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice

P. Bross, M. West, J. Christensen, 2013, Neurobiology of Disease.

Haploinsufficiency of AFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration

G. Casari, A. Quattrini, G. Cox, 2009, The Journal of Neuroscience.

Arimoclomol as a potential therapy for neuronopathic Gaucher Disease

B. Bembi, T. Kirkegaard, A. Dardis, 2018, bioRxiv.

Arimoclomol increases the transcription of lysosomal genes, including and , to facilitate lysosomal function

M. T. Pedersen, T. Kirkegaard, C. Valacca, 2022, Molecular Genetics and Metabolism.

The Hsp60 folding machinery is crucial for manganese superoxide dismutase folding and function

P. Bross, J. Christensen, T. Corydon, 2014, Free radical research.

Intermolecular disulfide-bond formation in human FICD modulates the activity of the hyperactive E234G mutant

J. Enghild, C. Scavenius, L. Ellgaard, 2017, bioRxiv.

Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.

E. Rugarli, G. Casari, A. Quattrini, 2009, Human Molecular Genetics.