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Pawing way to better healthcare through molecular genetics and fundamental research

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Personalized medicine

Want to know how are we going to change the world? Stay tuned.

Pawing way to better healthcare through molecular genetics and fundamental research

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Customized gene therapies for autism spectrum disorders caused by monogenic mutations

Want to know how are we going to change the world? Stay tuned.

Pawing way to better healthcare through molecular genetics and fundamental research

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Angelman syndrome

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Pawing way to better healthcare through molecular genetics and fundamental research

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Snijders Blok-Campeau syndrome

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Pawing way to better healthcare through molecular genetics and fundamental research

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Beta-propeller Protein-Associated Neurodegeneration

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Pawing way to better healthcare through molecular genetics and fundamental research

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Cell Engineering: Generation of Stable Cell Lines and Functional Studies

Mission

Our mission is to pioneer innovative gene therapy solutions that transform the landscape of medicine. We strive to advance genetic research to develop safe and effective therapies for genetic disorders and complex diseases, empowering individuals and families through groundbreaking discoveries. We are committed to collaboration, ethical research practices, and the relentless pursuit of scientific excellence to improve the quality of life for patients worldwide.

Vision

Our vision is to shape the future of genomic medicine through pioneering research in molecular genetics, cell biology, genome editing, and biotechnology. We strive to develop innovative scientific platforms that will serve as the foundation for the next generation of personalized medicine, creating new opportunities for the treatment of rare genetic disorders, cancer, and other complex diseases.

Our ambition

We have established GeCure Solutions, a genetics research laboratory in Ukraine that brings together scientists, early-career researchers, and international partners to advance the future of genomic medicine. Our work focuses on developing innovative scientific platforms in molecular genetics, cell biology, genome editing, and biotechnology.

We are ambitious, highly qualified, and driven by a shared mission to develop next-generation personalized approaches for rare genetic disorders, cancer, and other complex diseases.

Fields of interest

Personalized medicine

Personalized medicine, often referred to as precision medicine, marks a transformative approach within healthcare that tailors treatment and prevention strategies to the individual's unique characteristics, lifestyle, and ...

Angelman syndrome

A report describing AS was published in 1965 by a British pediatrician Harry Angelman [1] . AS is a genetic disorder causing neurodevelopmental disease with a conserved and recognizable...

Snijders Blok-Campeau syndrome

SBCS is a recently discovered genetic neurodevelopmental disorder, first described in 2018 by clinical researchers Lot Snijders Blok and Philippe Campeau. Individuals with this syndrome typically present with ...

Beta-propeller Protein-Associated Neurodegeneration

SMA is a genetic disorder characterized by weakness and wasting (atrophy) in muscles used for movement (skeletal muscles). It is caused by a loss of specialized nerve cells, called motor neurons, in the spinal...

Cell Engineering: Generation of Stable Cell Lines and Functional Studies

Generation of genetically modified mammalian cell lines (Knockout/Knock-in) using 4D-Nucleofection technology. From transfection with client-provided constructs to the complete development of custom research cell models for functional and preclinical studies. ...

Customized gene therapies for autism spectrum disorders caused by monogenic mutations

Mutation in multiple genes were already described to be contributing to autism spectrum disorder. Although it is hard to make a defined prognosis, it is plausible that early detection of such mutations might allow to design a gene-therapy, tailored specifically for a given individual, and ...

Collaboration Opportunities

Core Facility Services

Access to Laboratory Infrastructure

Contract Research & Grant Partnerships

Foundation

Donate

The world’s most transformative medical breakthroughs begin with fundamental research. By supporting GeCure Solutions, you are investing not only in a research laboratory, but in scientific discoveries that have the potential to shape the future of medicine. Every donation and philanthropic contribution helps advance innovative genetic research, develop next-generation technologies, and build research platforms that may contribute to future breakthroughs with a lasting global impact on human health.

1) Create gene-therapeutic approaches to treat rare genetic disorders by expressing non-mutated alleles of corresponding genes, as well as by genome-editing using CRISPR-Cas9-mediated techniques.

2) Investigate molecular mechanisms of the etiology of rare neurodevelopmental genetic disorders, using cell and laboratory animal models.

3) Study the population genetics of rare neurodevelopmental disorders.

4) Isolate and characterize new soil bacteria, that belong to phyla Actinomycetota, Bacillota, and Myxococota in order to create a strain library, which would be screened for the production of novel natural compounds, biotechnological enzymes, and Cas-like genes.

5) Create gene-engineered platforms to produce known and modified natural products, including antibacterials, anticancer compounds, etc.

Scientific Importance

Advances in molecular genetics, genome editing, and cell engineering are transforming the way complex diseases are studied and future therapeutic strategies are developed. High-quality research models are essential for understanding disease mechanisms, validating genetic targets, evaluating innovative technologies, and supporting translational and preclinical research.

At GeCure Solutions, we integrate molecular genetics, genome editing, cell engineering, and advanced analytical technologies to create reliable research platforms that accelerate scientific discovery and contribute to the development of next-generation precision medicine.