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Searching for a Paradigm Shift in Auger-Electron Cancer Therapy with Tumor-Specific Radiopeptides Targeting the Mitochondria and/or the Cell Nucleus

International journal of molecular sciences, 2022-06, Vol.23 (13), p.7238

2022

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Natural and amyloid self‐assembly of S100 proteins: structural basis of functional diversity

The FEBS journal, 2010-11, Vol.277 (22), p.4578-4590

2010

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Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Genomics (San Diego, Calif.), 2015-11, Vol.106 (5), p.268-277

2015

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Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4524

2020

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S100A6 Amyloid Fibril Formation Is Calcium-modulated and Enhances Superoxide Dismutase-1 (SOD1) Aggregation

The Journal of biological chemistry, 2012-12, Vol.287 (50), p.42233-42242

2012

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Intrinsically disordered and aggregation prone regions underlie β-aggregation in S100 proteins

PloS one, 2013-10, Vol.8 (10), p.e76629-e76629

2013

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Edible Seaweeds Extracts: Characterization and Functional Properties for Health Conditions

Antioxidants, 2023-03, Vol.12 (3), p.684

2023

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A Drug Screening Reveals Minocycline Hydrochloride as a Therapeutic Option to Prevent Breast Cancer Cells Extravasation across the Blood-Brain Barrier

Biomedicines, 2022-08, Vol.10 (8), p.1988

2022

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Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids

Cells (Basel, Switzerland), 2022-07, Vol.11 (15), p.2295

2022

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Sulfur Oxygenase Reductase from the Mesophilic Bacterium Halothiobacillus neapolitanus Is a Highly Active Thermozyme

Journal of Bacteriology, 2012-02, Vol.194 (3), p.677-685

2012

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Folding Status Is Determinant over Traffic-Competence in Defining CFTR Interactors in the Endoplasmic Reticulum

Cells (Basel, Switzerland), 2019-04, Vol.8 (4), p.353

2019

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Metal ions as modulators of protein conformation and misfolding in neurodegeneration

Coordination chemistry reviews, 2012-10, Vol.256 (19-20), p.2253-2270

2012

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Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides

Human mutation, 2016-02, Vol.37 (2), p.209-215

2016

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Systems Approaches to Unravel Molecular Function: High-content siRNA Screen Identifies TMEM16A Traffic Regulators as Potential Drug Targets for Cystic Fibrosis

Journal of molecular biology, 2022-03, Vol.434 (5), p.167436-167436, Article 167436

2022

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CFTR processing, trafficking and interactions

Journal of cystic fibrosis, 2020-03, Vol.19 (S1), p.S33-S36

2020

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An open-source high-content analysis workflow for CFTR function measurements using the forskolin-induced swelling assay

Bioinformatics, 2021-04, Vol.36 (24), p.5686-5694

2021

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A novel microscopy-based assay identifies extended synaptotagmin-1 (ESYT1) as a positive regulator of anoctamin 1 traffic

Biochimica et biophysica acta. Molecular cell research, 2018-02, Vol.1865 (2), p.421-431

2018

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R560S: A class II CFTR mutation that is not rescued by current modulators

Journal of cystic fibrosis, 2019-03, Vol.18 (2), p.182-189

2019

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Protein traffic disorders: an effective high-throughput fluorescence microscopy pipeline for drug discovery

Scientific reports, 2015-03, Vol.5 (1), p.9038-9038, Article 9038

2015

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Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G

Biochimica et biophysica acta. Molecular basis of disease, 2020-11, Vol.1866 (11), p.165905-165905, Article 165905

2020

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Exploring YAP1-centered networks linking dysfunctional CFTR to epithelial-mesenchymal transition

Life science alliance, 2022-09, Vol.5 (9), p.e202101326

2022

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Biochemical and biophysical characterization of recombinant yeast proteasome maturation factor ump1

Computational and structural biotechnology journal, 2013-04, Vol.7 (8), p.e201304006-e201304006, Article e201304006

2013

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Unravelling the antitumoral potential of novel bis(thiosemicarbazonato) Zn(II) complexes: structural and cellular studies

Journal of biological inorganic chemistry, 2019-02, Vol.24 (1), p.71-89

2019

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Investigating Alternative Transport of Integral Plasma Membrane Proteins from the ER to the Golgi: Lessons from the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1459, p.105

2016

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The neuronal S100B protein is a calcium-tuned suppressor of amyloid-β aggregation

Science advances, 2018-06, Vol.4 (6), p.eaaq1702-eaaq1702

2018

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Searching for a Paradigm Shift in Auger-Electron Cancer Therapy with Tumor-Specific Radiopeptides Targeting the Mitochondria and/or the Cell Nucleus

Natural and amyloid self‐assembly of S100 proteins: structural basis of functional diversity

Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

S100A6 Amyloid Fibril Formation Is Calcium-modulated and Enhances Superoxide Dismutase-1 (SOD1) Aggregation

Intrinsically disordered and aggregation prone regions underlie β-aggregation in S100 proteins

Edible Seaweeds Extracts: Characterization and Functional Properties for Health Conditions

A Drug Screening Reveals Minocycline Hydrochloride as a Therapeutic Option to Prevent Breast Cancer Cells Extravasation across the Blood-Brain Barrier

Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids

Sulfur Oxygenase Reductase from the Mesophilic Bacterium Halothiobacillus neapolitanus Is a Highly Active Thermozyme

Folding Status Is Determinant over Traffic-Competence in Defining CFTR Interactors in the Endoplasmic Reticulum

Metal ions as modulators of protein conformation and misfolding in neurodegeneration

Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides

Systems Approaches to Unravel Molecular Function: High-content siRNA Screen Identifies TMEM16A Traffic Regulators as Potential Drug Targets for Cystic Fibrosis

CFTR processing, trafficking and interactions

An open-source high-content analysis workflow for CFTR function measurements using the forskolin-induced swelling assay

A novel microscopy-based assay identifies extended synaptotagmin-1 (ESYT1) as a positive regulator of anoctamin 1 traffic

R560S: A class II CFTR mutation that is not rescued by current modulators

Protein traffic disorders: an effective high-throughput fluorescence microscopy pipeline for drug discovery

Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G

Exploring YAP1-centered networks linking dysfunctional CFTR to epithelial-mesenchymal transition

Biochemical and biophysical characterization of recombinant yeast proteasome maturation factor ump1

Unravelling the antitumoral potential of novel bis(thiosemicarbazonato) Zn(II) complexes: structural and cellular studies

Investigating Alternative Transport of Integral Plasma Membrane Proteins from the ER to the Golgi: Lessons from the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

The neuronal S100B protein is a calcium-tuned suppressor of amyloid-β aggregation

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