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Evolutionary-Conserved Allosteric Properties of Three Neuronal Calcium Sensor Proteins

Frontiers in molecular neuroscience, 2019-03, Vol.12, p.50-50

2019

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Aldo-Keto Reductase 1C1 ( AKR1C1 ) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema

International journal of molecular sciences, 2020-08, Vol.21 (17), p.6264

2020

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Effects of Membrane and Biological Target on the Structural and Allosteric Properties of Recoverin: A Computational Approach

International journal of molecular sciences, 2019-10, Vol.20 (20), p.5009

2019

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Constitutive Activation of Guanylate Cyclase by the G86R GCAP1 Variant Is Due to "Locking" Cation-π Interactions that Impair the Activator-to-Inhibitor Structural Transition

International journal of molecular sciences, 2020-01, Vol.21 (3), p.752

2020

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Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypes

Scientific reports, 2024-05, Vol.14 (1), p.10551-13, Article 10551

2024

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A Novel GUCA1A Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10809

2021

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Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2709

2023

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Impaired Ca2+ Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells

International journal of molecular sciences, 2021-04, Vol.22 (8), p.4030

2021

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Calmodulin variants associated with congenital arrhythmia impair selectivity for ryanodine receptors

Frontiers in molecular biosciences, 2023-01, Vol.9, p.1100992-1100992

2023

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Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3240

2022

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Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2089

2021

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Expanding the Clinical and Genetic Spectrum of RAB28 -Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families

International journal of molecular sciences, 2020-12, Vol.22 (1), p.381

2020

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Modulation of Guanylate Cyclase Activating Protein 1 (GCAP1) Dimeric Assembly by Ca2+ or Mg2+: Hints to Understand Protein Activity

Biomolecules (Basel, Switzerland), 2020-10, Vol.10 (10), p.1408

2020

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Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransduction

Cellular and molecular life sciences : CMLS, 2014-10, Vol.71 (19), p.3829-3840

2014

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Bringing the Ca2+ sensitivity of myristoylated recoverin into the physiological range

Open biology, 2021-01, Vol.11 (1), p.200346-200346

2021

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Choroidal Thickness Measurements in the Case of Diabetic Macular Edema. Comment on Amjad et al. Choroidal Thickness in Different Patterns of Diabetic Macular Edema. J. Clin. Med. 2022, 11 , 6169

Journal of clinical medicine, 2023-04, Vol.12 (8), p.2874

2023

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Editorial: Interactions of nanoparticles with and within living organisms—What can we learn to improve efficacy of nanomedicine?

Frontiers in molecular biosciences, 2022-10, Vol.9, p.1044063-1044063

2022

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Optic nerve sheath diameter measurement by ultrasound after moderate traumatic brain injury

Clinical and experimental emergency medicine, 2023-06, Vol.10 (2), p.249-250

2023

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Choroidal Thickness and Retinal Vein Occlusions [Letter]

Clinical ophthalmology (Auckland, N.Z.), 2023, Vol.17, p.747-748

2023

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Does Subretinal Fluid Influence Choroidal Thickness (ChT) and Structure in Preeclampsia with Serous Retinal Detachment? Comment on Fukui et al. Changes in Choroidal Thickness and Structure in Preeclampsia with Serous Retinal Detachment. J. Clin. Med. 2023, 12 , 609

Journal of clinical medicine, 2023-05, Vol.12 (9), p.3273

2023

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Ionic displacement of Ca2+ by Pb2+ in calmodulin is affected by arrhythmia-associated mutations

Biochimica et biophysica acta. Molecular cell research, 2023-08, Vol.1870 (6), p.119490-119490, Article 119490

2023

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Outpatient Total Hip Arthroplasty: A Meta-Analysis

Applied sciences, 2021-08, Vol.11 (15), p.6853

2021

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Allosteric communication pathways routed by Ca2+/Mg2+ exchange in GCAP1 selectively switch target regulation modes

Scientific reports, 2016-10, Vol.6 (1), p.34277-34277, Article 34277

2016

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Structural effects of Mg2+ on the regulatory states of three neuronal calcium sensors operating in vertebrate phototransduction

Biochimica et biophysica acta, 2015-09, Vol.1853 (9), p.2055-2065

2015

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Disrupted protein interaction dynamics in a genetic neurodevelopmental disorder revealed by structural bioinformatics and genetic code expansion

Protein science, 2024-04, Vol.33 (4), p.e4953-n/a

2024

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Evolutionary-Conserved Allosteric Properties of Three Neuronal Calcium Sensor Proteins

Aldo-Keto Reductase 1C1 ( AKR1C1 ) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema

Effects of Membrane and Biological Target on the Structural and Allosteric Properties of Recoverin: A Computational Approach

Constitutive Activation of Guanylate Cyclase by the G86R GCAP1 Variant Is Due to "Locking" Cation-π Interactions that Impair the Activator-to-Inhibitor Structural Transition

Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypes

A Novel GUCA1A Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase

Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy

Impaired Ca2+ Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells

Calmodulin variants associated with congenital arrhythmia impair selectivity for ryanodine receptors

Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa

Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant

Expanding the Clinical and Genetic Spectrum of RAB28 -Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families

Modulation of Guanylate Cyclase Activating Protein 1 (GCAP1) Dimeric Assembly by Ca2+ or Mg2+: Hints to Understand Protein Activity

Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransduction

Bringing the Ca2+ sensitivity of myristoylated recoverin into the physiological range

Choroidal Thickness Measurements in the Case of Diabetic Macular Edema. Comment on Amjad et al. Choroidal Thickness in Different Patterns of Diabetic Macular Edema. J. Clin. Med. 2022, 11 , 6169

Editorial: Interactions of nanoparticles with and within living organisms—What can we learn to improve efficacy of nanomedicine?

Optic nerve sheath diameter measurement by ultrasound after moderate traumatic brain injury

Choroidal Thickness and Retinal Vein Occlusions [Letter]

Does Subretinal Fluid Influence Choroidal Thickness (ChT) and Structure in Preeclampsia with Serous Retinal Detachment? Comment on Fukui et al. Changes in Choroidal Thickness and Structure in Preeclampsia with Serous Retinal Detachment. J. Clin. Med. 2023, 12 , 609

Ionic displacement of Ca2+ by Pb2+ in calmodulin is affected by arrhythmia-associated mutations

Outpatient Total Hip Arthroplasty: A Meta-Analysis

Allosteric communication pathways routed by Ca2+/Mg2+ exchange in GCAP1 selectively switch target regulation modes

Structural effects of Mg2+ on the regulatory states of three neuronal calcium sensors operating in vertebrate phototransduction

Disrupted protein interaction dynamics in a genetic neurodevelopmental disorder revealed by structural bioinformatics and genetic code expansion

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