Dr. David Greene, R3 Stem Cell

In order to understand the possibilities of stem cell medicine and stem cell therapies from space, we need to understand the context of the human body. The complications of end-stage conditions--cancer, heart disease, chronic conditions--have led to a greater understanding of the aging process, including how stem cell treatments can slow down. This ultimately creates a positive development in regenerative medicine, vitally essential because humans could live longer, healthier lives with the right interventions. From 1970-to 2018, more than 5 billion people were treated for heart disease and cancer. These individuals and their families left behind genetic mutations. These mutations allow scientists to use stem cell infusions to fight heart disease and cancer in space. What implications could this have for the Earth's current population? Most people are unaware of a collaborative effort to apply stem cell technology to treat osteoarthritis, diabetes, and a host of other ills on the g

A series of hereditary abnormalities are primarily defined by increasing muscular deterioration and loss. Muscle degeneration is caused by faulty genes (mutations) in muscular dystrophies. The majority of forms start in infancy. Muscles that have been damaged get weaker with time. The majority of persons with the illness will eventually use a wheelchair. Other signs and symptoms include difficulty breathing and swallowing. Although medication, rehabilitation, breathing apparatuses, and surgery may help preserve function, life expectancy is generally compromised. Proteins that protect muscle tissue are generated by specific genes. When one of these genes is malfunctioning, muscular dystrophy emerges. A genetic mutation particular to that type of muscular dystrophy causes each manifestation of the illness. The majority of these polymorphisms are passed down via the generations. Stem cells are essential in muscular dystrophy research in two ways: in their role as a model for the disease a

We know that there are numerous treatments for genetic diseases. However, each lasts for only a limited period. So, how can we treat a congenital disease? There’s an answer to stem cell therapy. Stem cells have a complete set of the DNA of one or more parents. They have the ability to change into a particular type of cell and differentiate into any other cell in the body. This means stem cells can create new and effective methods for treating these diseases. As we all should know, researchers are already developing ways to use adult stem cells for patients to treat multiple genetic disorders. In addition, there are such therapies as bone marrow transplants which have an extensive range of potentials in the future. For your consideration, many diseases like immune deficiency disorders, lymphomas, leukemias, etc., have been successfully treated by bone marrow transplant since the ’60s. Now, we are in an era where everything is changing from traditional methods to the new and effective on

The human race has been boosted with the unbelievable speed of the technological revolution. Every day we wake up, there are many discoveries and inventions already done in just a single day, and that’s where we can say that we can win over almost everything now. But like everything else, this advancement brought some cons with it. For example, many diseases and viruses came into the picture 2-3 decades. Some are easily curable, and patients could be within a few months, but some are considered untreatable and destroy hundreds of thousands of lives every year. That’s when we understood the potential and future of stem cell therapies. Stem cells are at the forefront in alternative medicine, as they can regenerate tissue of any type while regenerating to health. With the advancement of stem cell research, scientists continue to demonstrate stem cells' capability to help treat many modern disorders, one of which is fibromyalgia. This therapy is not just limited to stem cells. You can