Bottinelli, Roberto

Branched-chain amino acid supplementation promotes survival and supports cardiac and skeletal muscle mitochondrial biogenesis in middle-aged mice

D'Antona, G., Ragni, M., Cardile, A., Tedesco, L., Dossena, M., Bruttini, F., Caliaro, F., Corsetti, G., Bottinelli, R., Carruba, M. O., et al. (2010) · Cell Metabolism

Genetics, Aging, and Longevity in Model OrganismsMitochondrial Function and Pathology

Cited by 568

Force‐velocity properties of human skeletal muscle fibres: myosin heavy chain isoform and temperature dependence.

Bottinelli, R., Canepari, M., Pellegrino, M. A., & Reggiani, C. (1996) · The Journal of Physiology

Muscle Physiology and DisordersCardiomyopathy and Myosin Studies

Cited by 565

Autophagy Impairment in Muscle Induces Neuromuscular Junction Degeneration and Precocious Aging

Carnio, S., LoVerso, F., Baraibar, M. A., Longa, E., Khan, M. M., Maffei, M., Reischl, M., Canepari, M., Loefler, S., Kern, H., et al. (2014) · Cell Reports

Autophagy in Disease and TherapyGenetics, Aging, and Longevity in Model Organisms

Cited by 423

Whole-muscle and single-fibre contractile properties and myosin heavy chain isoforms in humans

Harridge, S. D. R., Bottinelli, R., Canepari, M., Pellegrino, M. A., Reggiani, C., Esbjörnsson, M., & Saltin, B. (1996) · Pflügers Archiv - European Journal of Physiology

Muscle Physiology and DisordersCardiovascular and exercise physiology

Cited by 402

Specific contributions of various muscle fibre types to human muscle performance: an in vitro study

Bottinelli, R., Pellegrino, M. A., Canepari, M., Rossi, R., & Reggiani, C. (1999) · Journal of Electromyography and Kinesiology

Muscle Physiology and DisordersCardiovascular and exercise physiology

Cited by 201

The role of alterations in mitochondrial dynamics and PGC‐1α over‐expression in fast muscle atrophy following hindlimb unloading

Cannavino, J., Brocca, L., Sandri, M., Grassi, B., Bottinelli, R., & Pellegrino, M. A. (2015) · The Journal of Physiology

Muscle Physiology and DisordersMitochondrial Function and Pathology

Cited by 166

FoxO‐dependent atrogenes vary among catabolic conditions and play a key role in muscle atrophy induced by hindlimb suspension

Brocca, L., Toniolo, L., Reggiani, C., Bottinelli, R., Sandri, M., & Pellegrino, M. A. (2017) · The Journal of Physiology

Muscle Physiology and DisordersFOXO transcription factor regulation

Cited by 93

The KATP channel is a molecular sensor of atrophy in skeletal muscle

Tricarico, D., Mele, A., Camerino, G. M., Bottinelli, R., Brocca, L., Frigeri, A., Svelto, M., George Jr, A. L., & Camerino, D. C. (2010) · The Journal of Physiology

Muscle Physiology and DisordersIon channel regulation and function

Cited by 49