About The Study
CAPRIN1 is a widely expressed protein that plays a vital role in regulating key cellular processes, including cell cycle progression, differentiation, and proliferation. Discovered around two decades ago, extensive research has since uncovered its functions and involvement in various diseases. CAPRIN1 has been associated with human cancers, with recent studies identifying its expression as a universal marker for solid tumors. Furthermore, CAPRIN1 exhibits unique functions within the brain.
The CAPRIN1 research study aims to understand the role of CAPRIN1 in genetic conditions and how it affects individuals who are carriers. This includes obtaining an understanding of the phenotypic effects of the mutation and its variability by comparing individuals who have been identified with the mutation. Further research into CAPRIN1's mechanisms in both physiological and pathological states is crucial for developing potential therapeutic interventions for these neurological disorders.
Participants will be asked to provide genetic samples, which will be analyzed by the research team through laboratory testing and further investigations. These samples will help researchers gain valuable insights into genetic factors related to the condition being studied. By taking part, individuals contribute to advancements in medical science, potentially leading to improved treatments and a better understanding of the disease. All genetic data will be handled with strict confidentiality and used solely for research purposes to ensure privacy and ethical integrity.
About The Study
CAPRIN1 is a widely expressed protein that plays a vital role in regulating key cellular processes, including cell cycle progression, differentiation, and proliferation. Discovered around two decades ago, extensive research has since uncovered its functions and involvement in various diseases. CAPRIN1 has been associated with human cancers, with recent studies identifying its expression as a universal marker for solid tumors. Furthermore, CAPRIN1 exhibits unique functions within the brain.
Commitment to Genetic Discovery
Integrity
At CAPRIN1foundation, we are committed to maintaining the highest standards of honesty and transparency in all our interactions. We believe in conducting our research and awareness initiatives with unwavering ethical principles.
Innovation
We strive to be at the forefront of genetic mutation studies, embracing cutting-edge research and innovative approaches to better understand and communicate the complexities of genetic mutations.
Collaboration
Our success is built on collaboration. We actively partner with researchers, healthcare professionals, and communities to share knowledge and resources, ensuring a comprehensive approach to genetic mutation awareness.
Empowerment
We empower individuals and families affected by genetic mutations through education and support, helping them make informed decisions and advocating for their needs and rights.
Compassion
Understanding the challenges faced by those impacted by genetic mutations, we approach our work with empathy and compassion, providing a supportive environment for all involved.