Dogs: More Than Man’s Best Friend
Dogs are not just loyal companions they are powerful models for understanding human diseases. Sharing our environment, humans and dogs often develop the same health conditions, including cancer, epilepsy, cardiovascular disorders, and diabetes. While humans have complex genetics, many canine diseases are genetically simpler, making dogs ideal subjects for studying the genetic roots of illness.
Our mission is to explore the genetic basis of canine diseases to improve dog health and advance human medicine. By understanding these diseases in dogs, we can uncover key mechanisms that underlie human conditions.
Symptoms of Canine Diseases
Recognizing early signs of disease is crucial for diagnosis and treatment. While symptoms vary by condition, some common indicators include:
Diagnostic Approaches in Canine Genetics
Genetic research in dogs relies on advanced diagnostic techniques, including:
Genome Comparison :
Comparing affected dogs to healthy dogs of the same breed to identify mutations.
Molecular Analysis :
DNA sequencing and gene mapping to pinpoint genetic defects.
Phenotype Observation :
Careful monitoring of symptoms and clinical signs to correlate with genetic findings.
Scientific Approach and Impact
Our project uses a structured scientific methodology:
3. Functional Study :
Identified genes are analyzed to understand the biological pathways they affect.
2. Genomic Analysis :
Whole-genome sequencing and bioinformatics are used to detect disease-causing variants.
4. Translation to Human Medicine :
Findings in dogs guide research into human disease mechanisms, drug targets, and potential therapies.
Why Canine Genetics Matters for Humans
The identification of disease-related genes in dogs provides insights into:


