Showing 1 - 17 results of 17 for search 'Daniele Dell’Orco', query time: 0.05s
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Evolutionary-Conserved Allosteric Properties of Three Neuronal Calcium Sensor Proteins by Valerio Marino, Valerio Marino, Daniele Dell'Orco
Published 2019-03-01
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Modeling the time evolution of the nanoparticle-protein corona in a body fluid. by Daniele Dell'Orco, Martin Lundqvist, Cecilia Oslakovic, Tommy Cedervall, Sara Linse
Published 2010-06-01
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Modulation of Guanylate Cyclase Activating Protein 1 (GCAP1) Dimeric Assembly by Ca<sup>2+</sup> or Mg<sup>2+</sup>: Hints to Understand Protein Activity by Francesco Bonì, Valerio Marino, Carlo Bidoia, Eloise Mastrangelo, Alberto Barbiroli, Daniele Dell’Orco, Mario Milani
Published 2020-10-01
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Editorial: Neuronal Calcium Sensors in Health and Disease by Daniele Dell'Orco, Karl-Wilhelm Koch, Michael R. Kreutz, Jose R. Naranjo, Jose R. Naranjo, Beat Schwaller
Published 2019-11-01
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Impaired Ca<sup>2+</sup> Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells by Valerio Marino, Giuditta Dal Cortivo, Paolo Enrico Maltese, Giorgio Placidi, Elisa De Siena, Benedetto Falsini, Matteo Bertelli, Daniele Dell’Orco
Published 2021-04-01
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A Novel <i>GUCA1A</i> Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase by Amedeo Biasi, Valerio Marino, Giuditta Dal Cortivo, Paolo Enrico Maltese, Antonio Mattia Modarelli, Matteo Bertelli, Leonardo Colombo, Daniele Dell’Orco
Published 2021-10-01
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Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa by Anna Avesani, Laura Bielefeld, Nicole Weisschuh, Valerio Marino, Pascale Mazzola, Katarina Stingl, Tobias B. Haack, Karl-Wilhelm Koch, Daniele Dell’Orco
Published 2022-03-01
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Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel <i>C1QTNF5</i> Missense Variant by Ulrich Kellner, Nicole Weisschuh, Silke Weinitz, Ghazaleh Farmand, Sebastian Deutsch, Friederike Kortüm, Pascale Mazzola, Karin Schäferhoff, Valerio Marino, Daniele Dell’Orco
Published 2021-02-01
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Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy by Jan-Philipp Bodenbender, Valerio Marino, Leon Bethge, Katarina Stingl, Tobias B. Haack, Saskia Biskup, Susanne Kohl, Laura Kühlewein, Daniele Dell’Orco, Nicole Weisschuh
Published 2023-01-01
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Pendred Syndrome, or Not Pendred Syndrome? That Is the Question by Paola Tesolin, Sofia Fiorino, Stefania Lenarduzzi, Elisa Rubinato, Elisabetta Cattaruzzi, Lydie Ammar, Veronica Castro, Eva Orzan, Claudio Granata, Daniele Dell’Orco, Anna Morgan, Giorgia Girotto
Published 2021-10-01
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Aldo-Keto Reductase 1C1 (<i>AKR1C1</i>) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema by Sandro Michelini, Pietro Chiurazzi, Valerio Marino, Daniele Dell’Orco, Elena Manara, Mirko Baglivo, Alessandro Fiorentino, Paolo Enrico Maltese, Michele Pinelli, Karen Louise Herbst, Astrit Dautaj, Matteo Bertelli
Published 2020-08-01
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Expanding the Clinical and Genetic Spectrum of <i>RAB28</i>-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families by Giancarlo Iarossi, Valerio Marino, Paolo Enrico Maltese, Leonardo Colombo, Fabiana D’Esposito, Elena Manara, Kristjana Dhuli, Antonio Mattia Modarelli, Gilda Cennamo, Adriano Magli, Daniele Dell’Orco, Matteo Bertelli
Published 2020-12-01
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