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Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

International journal of molecular sciences, 2023-10, Vol.24 (20), p.15089

2023

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Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

International journal of molecular sciences, 2021-04, Vol.22 (9), p.4700

2021

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A Novel KCNJ2 Mutation Identified in an Autistic Proband Affects the Single Channel Properties of Kir2.1

Frontiers in cellular neuroscience, 2018-03, Vol.12, p.76-76

2018

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Binary Biocompatible CNC–Gelatine Hydrogel as 3D Scaffolds Suitable for Cell Culture Adhesion and Growth

Applied nano, 2021-05, Vol.2 (2), p.118-127

2021

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Badania i rozwój: Zaskoczyć klienta – techniki wykorzystywane przez branżę perfumeryjną

OPAKOWANIE, 2020-07, Vol.1 (7), p.52-56

Binda, Anna

2020

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GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death

EBioMedicine, 2020-07, Vol.57, p.102843, Article 102843

2020

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Innovative Therapies and Nanomedicine Applications for the Treatment of Alzheimer’s Disease: A State-of-the-Art (2017–2020)

International journal of nanomedicine, 2020-08, Vol.15, p.6113-6135

2020

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Cardiac and neuronal HCN channelopathies

Pflügers Archiv, 2020-07, Vol.472 (7), p.931-951

2020

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Badania i rozwój: Manipulacja wielkością opakowania - sztuka downsizingu

OPAKOWANIE, 2018-03, Vol.1 (3), p.66-68

Binda, Anna

2018

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BADANIA I ROZWÓJ: Miejsce opakowania w strategii marketingowej przedsiębiorstw sektora kosmetycznego

OPAKOWANIE, 2017-08, Vol.1 (8), p.72-75

BINDA, ANNA

2017

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Effect of the ketogenic diet in excitable tissues

American Journal of Physiology: Cell Physiology, 2021-04, Vol.320 (4), p.C547-C553

2021

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Flakony perfum na miarę XXI w. - współczesne trendy w projektowaniu "małych dzieł sztuki"

OPAKOWANIE, 2016-06, Vol.1 (6), p.78-81

BINDA, ANNA

2016

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Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons

The Journal of general physiology, 2020-09, Vol.152 (9), p.1

2020

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Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients?

Progress in biophysics and molecular biology, 2021-11, Vol.166, p.147-155

2021

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Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

International journal of molecular sciences, 2023-10, Vol.24 (20)

2023

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A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet

Epilepsia (Copenhagen), 2023-12, Vol.64 (12), p.e222-e228

2023

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SCN4A as modifier gene in patients with myotonic dystrophy type 2

Scientific reports, 2018-07, Vol.8 (1), p.11058-10, Article 11058

2018

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Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy

Pharmacological research, 2020-10, Vol.160, p.105200-105200, Article 105200

2020

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Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for the treatment of Alzheimer's disease

International journal of nanomedicine, 2018-01, Vol.13, p.4059-4071

2018

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Acetylation mediates Cx43 reduction caused by electrical stimulation

Journal of molecular and cellular cardiology, 2015-10, Vol.87, p.54-64

2015

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JMV5656, A Novel Derivative of TLQP-21, Triggers the Activation of a Calcium-Dependent Potassium Outward Current in Microglial Cells

Frontiers in cellular neuroscience, 2017-02, Vol.11, p.41-41

2017

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Plasmid vectors for selecting IS1-promoted deletions in cloned DNA : sequence analysis of the omega interposon

Gene, 1991-07, Vol.103 (1), p.17-23

1991

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Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells

Frontiers in pharmacology, 2017-03, Vol.8, p.167-167

2017

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Plasmid vectors for selecting IS 1-promoted deletions in cloned DNA: sequence analysis of the omega interposon

Gene, 1991, Vol.103 (1), p.17-23

1991

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Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature

Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

A Novel KCNJ2 Mutation Identified in an Autistic Proband Affects the Single Channel Properties of Kir2.1

Binary Biocompatible CNC–Gelatine Hydrogel as 3D Scaffolds Suitable for Cell Culture Adhesion and Growth

Badania i rozwój: Zaskoczyć klienta – techniki wykorzystywane przez branżę perfumeryjną

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death

Innovative Therapies and Nanomedicine Applications for the Treatment of Alzheimer’s Disease: A State-of-the-Art (2017–2020)

Cardiac and neuronal HCN channelopathies

Badania i rozwój: Manipulacja wielkością opakowania - sztuka downsizingu

BADANIA I ROZWÓJ: Miejsce opakowania w strategii marketingowej przedsiębiorstw sektora kosmetycznego

Effect of the ketogenic diet in excitable tissues

Flakony perfum na miarę XXI w. - współczesne trendy w projektowaniu "małych dzieł sztuki"

Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons

Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients?

Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet

SCN4A as modifier gene in patients with myotonic dystrophy type 2

Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy

Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for the treatment of Alzheimer's disease

Acetylation mediates Cx43 reduction caused by electrical stimulation

JMV5656, A Novel Derivative of TLQP-21, Triggers the Activation of a Calcium-Dependent Potassium Outward Current in Microglial Cells

Plasmid vectors for selecting IS1-promoted deletions in cloned DNA : sequence analysis of the omega interposon

Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells

Plasmid vectors for selecting IS 1-promoted deletions in cloned DNA: sequence analysis of the omega interposon

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