LIST OF PUBLICATIONS:
1. Bertelli S, Barbieri R, Pusch M, Gavazzo P (2018) Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA. Cephalalgia : an international journal of headache 39: 477-488
2. Barbieri R, Bertelli S, Pusch M, Gavazzo P (2019) Late sodium current blocker GS967 inhibits persistent currents induced by familial hemiplegic migraine type 3 mutations of the SCN1A gene. The journal of headache and pain 20: 107
3. Bertelli S, Remigante A, Zuccolini P, Barbieri R, Ferrera L, Picco C, Gavazzo P, Pusch M (2021) Mechanisms of Activation of LRRC8 Volume Regulated Anion Channels. Cell Physiol Biochem 55: 41-56
4. Brenes O, Barbieri R, Vasquez M, Vindas-Smith R, Roig J, Romero A, del Valle G, Bermudez-Guzman L, Bertelli S, Pusch M, et al. (2021) Functional and Structural Characterization of ClC-1 and Na(v)1.4 Channels Resulting from CLCN1 and SCN4A Mutations Identified Alone and Coexisting in Myotonic Patients. Cells 10
5. Ferrera L, Barbieri R, Picco C, Zuccolini P, Remigante A, Bertelli S, Fumagalli MR ZG, La Porta CAM, Gavazzo P, M P (2021) Activation of BK and IK potassium channels by oxidation via TRPM2 induced calcium increase in melanoma cells. Cells submitted
6. Zifarelli G, Zuccolini P, Bertelli S, M P (2021) The joy of Markov models – channel gating and transport cycling made easy. The Biophysicist in press
CONVENTIONS AND SEMINARS:
- Biophysical society 64th annual meeting San Diego, California, 15-19 February 2020 Oral communication “Characterization of molecular mechanisms underlying VRAC activation” - Physiology 2019, The Physiological Society
Symposium ‘Milestone achievements in anion transporter research’
Oral presentation as invited speaker ‘The Volume Regulated Anion Channel: from molecular identification to physiological roles and 3D structure’. Aberdeen, 7-10 July 2019
-Participation at the ‘Workshop on Structural Biophysics’ Bordeaux, 21-26 October 2018 - SIBPA 2018, XXII School of Pure and Applied Biophysics on "Intracellular ion channels and transporters in plant and animal cells". Venezia, 15-19 January 2018
- Convegno Monotematico SIF ’Rare Diseases and Orphan Drugs: from genes to personalized medicine’. Bari, 10-12 October 2016
Oral presentation ‘“Ex Vivo” study of a mutation associated with FHM3’ -XXIII Nationa Congress SIBPA
Oral presentation “In vitro” and “ex vivo” study of a mutation associated to Familial Hemiplegic Migraine 3. Cortona, 18-21 September 2016
