Aldo-Keto Reductase 1C1 (AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema S Michelini, P Chiurazzi, V Marino, D Dell’Orco, E Manara, M Baglivo, ... International journal of molecular sciences 21 (17), 6264, 2020 | 52 | 2020 |
Structural effects of Mg2+ on the regulatory states of three neuronal calcium sensors operating in vertebrate phototransduction V Marino, S Sulmann, KW Koch, D Dell'Orco Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1853 (9), 2055-2065, 2015 | 51 | 2015 |
Biochemical and biophysical characterization of a plant calmodulin: Role of the N-and C-lobes in calcium binding, conformational change, and target interaction A Astegno, V La Verde, V Marino, D Dell'Orco, P Dominici Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1864 (3), 297-307, 2016 | 47 | 2016 |
Allosteric communication pathways routed by Ca2+/Mg2+ exchange in GCAP1 selectively switch target regulation modes V Marino, D Dell’Orco Scientific reports 6 (1), 34277, 2016 | 40 | 2016 |
Nanodevice-induced conformational and functional changes in a prototypical calcium sensor protein V Marino, A Astegno, M Pedroni, F Piccinelli, D Dell'Orco Nanoscale 6 (1), 412-423, 2014 | 36 | 2014 |
Conformational Changes in Calcium‐Sensor Proteins under Molecular Crowding Conditions S Sulmann, D Dell'Orco, V Marino, P Behnen, KW Koch Chemistry–A European Journal 20 (22), 6756-6762, 2014 | 35 | 2014 |
Structural plasticity of calmodulin on the surface of CaF 2 nanoparticles preserves its biological function A Astegno, E Maresi, V Marino, P Dominici, M Pedroni, F Piccinelli, ... Nanoscale 6 (24), 15037-15047, 2014 | 35 | 2014 |
Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1 F Vocke, N Weisschuh, V Marino, S Malfatti, SG Jacobson, CM Reiff, ... Human molecular genetics 26 (1), 133-144, 2017 | 33 | 2017 |
Two retinal dystrophy-associated missense mutations in GUCA1A with distinct molecular properties result in a similar aberrant regulation of the retinal guanylate … V Marino, A Scholten, KW Koch, D Dell'Orco Human Molecular Genetics 24 (23), 6653-6666, 2015 | 33 | 2015 |
A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger … V Marino, G Dal Cortivo, E Oppici, PE Maltese, F D’Esposito, E Manara, ... Human Molecular Genetics 27 (24), 4204-4217, 2018 | 32 | 2018 |
Intermolecular disulfide bond influences unphosphorylated STAT3 dimerization and function E Butturini, G Gotte, D Dell'Orco, G Chiavegato, V Marino, D Canetti, ... Biochemical Journal 473 (19), 3205-3219, 2016 | 30 | 2016 |
Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransduction D Dell’Orco, S Sulmann, P Zägel, V Marino, KW Koch Cellular and molecular life sciences 71, 3829-3840, 2014 | 22 | 2014 |
Evolutionary-conserved allosteric properties of three neuronal calcium sensor proteins V Marino, D Dell'Orco Frontiers in Molecular Neuroscience 12, 50, 2019 | 21 | 2019 |
Modulation of Guanylate Cyclase Activating Protein 1 (GCAP1) Dimeric Assembly by Ca2+ or Mg2+: Hints to Understand Protein Activity F Bonì, V Marino, C Bidoia, E Mastrangelo, A Barbiroli, D Dell’Orco, ... Biomolecules 10 (10), 1408, 2020 | 13 | 2020 |
Effects of membrane and biological target on the structural and allosteric properties of recoverin: a computational approach A Borsatto, V Marino, G Abrusci, G Lattanzi, D Dell’Orco International journal of molecular sciences 20 (20), 5009, 2019 | 13 | 2019 |
CaF 2 nanoparticles as surface carriers of GCAP1, a calcium sensor protein involved in retinal dystrophies V Marino, A Borsatto, F Vocke, KW Koch, D Dell'Orco Nanoscale 9 (32), 11773-11784, 2017 | 13 | 2017 |
Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant U Kellner, N Weisschuh, S Weinitz, G Farmand, S Deutsch, F Kortüm, ... International journal of molecular sciences 22 (4), 2089, 2021 | 12 | 2021 |
Expanding the Clinical and Genetic Spectrum of RAB28-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families G Iarossi, V Marino, PE Maltese, L Colombo, F D’Esposito, E Manara, ... International Journal of Molecular Sciences 22 (1), 381, 2020 | 11 | 2020 |
New age-related hearing loss candidate genes in humans: An ongoing challenge M Di Stazio, A Morgan, M Brumat, S Bassani, D Dell'Orco, V Marino, ... Gene 742, 144561, 2020 | 11 | 2020 |
Neuronal Calcium Sensor GCAP1 Encoded by GUCA1A Exhibits Heterogeneous Functional Properties in Two Cases of Retinitis Pigmentosa S Abbas, V Marino, N Weisschuh, S Kieninger, M Solaki, D Dell’Orco, ... ACS Chemical Neuroscience 11 (10), 1458-1470, 2020 | 10 | 2020 |