Articles tagged with Stem Cell Research
Researchers at Cedars-Sinai Medical Center have developed a new gene-editing technique involving low-dose irradiation, which is 10 times more effective than existing methods. This breakthrough could enable scientists to model human diseases more accurately and accelerate the discovery process.
Researchers at Yale School of Medicine have developed a stem cell study that could help predict autism spectrum disorder and identify new drug targets. The study used skin cells to generate simulated brain organoids, revealing gene expression and developmental abnormalities in autism.
Scientists have developed a new method to generate healthy stem cells from patient cells with mitochondrial mutations, which can then be converted into various cell types. This breakthrough has the potential to treat debilitating mitochondrial diseases that affect the brain and muscles, offering new hope for patients worldwide.
Scientists at UC Berkeley and Gladstone Institutes develop a system to grow beating cardiac tissue from stem cells, allowing for the screening of drugs that may cause cardiac birth defects. The model uses patient-derived human pluripotent stem cells to mimic early heart development.
Researchers at USC's Stem Cell labs have discovered new genes affecting blood stem cell development and function. The study found that certain genetic regulators, such as Hopx, play a crucial role in the formation of red and white blood cells in adults.
A team of researchers has identified netrin-1 as a molecule that can favour the production of induced pluripotent stem cells, which have huge potential applications in regenerative medicine. The discovery may ultimately enable the creation of new organs from patient cells, eliminating rejection risks and ethical concerns.
Researchers found that dental pulp stem cells can regenerate myelinated axons in laboratory rats with sciatic nerve defects, outperforming autologous nerve grafts. The study suggests that MDPSCs contribute to peripheral nerve regeneration through the secretion of neurotrophic and angiogenic factors.
A study published in Cell Reports reveals how Sox9 regulates cartilage production and its essential role in skeletal development. Researchers discovered that Sox9 binding to DNA controls gene expression, leading to the formation of chondrocytes and cartilage production.
Researchers used new methods to compare two stem cell types and found one superior at producing retinal cells. The study demonstrates a standardized method for quantifying effectiveness, which could advance treatments for age-related macular degeneration and other vision loss disorders.
A new method has been discovered to culture stem cells, allowing them to grow twice as fast and be more efficient in regulating the immune response. This breakthrough could lead to more effective treatments for transplant patients by reducing side effects of current immunosuppressant drugs.
Scientists at University of Michigan and University of Texas Southwestern Medical Center discovered microscopic nanotubes facilitating cell-to-cell communication in stem cells. The findings suggest that these structures may play a crucial role in retaining stem cell identities during division.
Researchers identified microtubule-based nanotubes in stem cells that tap into the niche, enabling specific signaling for self-renewal. This discovery sheds light on how stem cells reproduce and miscommunication can lead to diseases like cancer.
Researchers have evaluated the best potential sources for adult stem cells to be used for treating diabetic retinopathy. They found that cells taken from donors without diabetes are more effective than those from patients' own bodies. This discovery provides a crucial framework for evaluating stem cells for future treatments.
A new study reveals that Mycobacterium tuberculosis hijack protective hypoxic zones in bone marrow stem cells to hide and survive. The research found that these stem cells exhibit strong binding to pimonidazole, indicating hypoxia localization, and express a key gene involved in regulating oxygen levels.
A team of Temple researchers led by Dr. Raj Kishore used stem cell exosomes to induce the repair of damaged mouse hearts, improving heart function and reducing scar tissue. The study's findings suggest a unique way to regenerate the heart without using stem cells.
Researchers find nucleoporins, proteins that guard the nucleus, also regulate gene expression and control stem cell differentiation into neurons. The discovery sheds new light on genetic diseases caused by mutations in these proteins.
Researchers discovered that high doses of antioxidants can disrupt intracellular signaling in neural stem cells, leading to a decrease in their stemness properties. However, treatment with antioxidants improved stem cell function, but only up to a point.
Researchers at the University of York have identified individual stem cells that can regenerate tissue, cartilage and bone, opening the way for improved treatment options for osteoarthritis. The discovery has the potential to develop targeted therapies for arthritis patients, making cell-based treatments less of a lottery.
Depletion of naïve T cells from stem cell grafts limits chronic graft-versus host disease by reducing its occurrence and severity. This approach also results in generally responsive acute GVHD to corticosteroid therapy, supporting it as a potential treatment option.
Massey researchers have identified three patterns of lymphocyte recovery following stem cell transplantation that are significantly associated with clinical outcomes. The study found Group B patients experienced the best clinical outcomes, while Groups A and C had poorer survival rates. The discovery builds on previous research into th...
Researchers at Uppsala University have made significant progress in using stem cells to treat spinal cord injuries. Human stem cells transplanted into injured mice restored damaged sensory nerve connections, enabling long-term recovery of sensory functions.
Researchers found that autologous bone marrow stem cells significantly reduced cranial pressure and therapeutic intensity in TBI patients, decreasing neurointensive care time by nearly 60%.
A special issue of Cell Stem Cell highlights the biology of aging and sex differences in stem cell behavior. Research suggests that estrogen may play a role in increasing lifespan in females, while testosterone may have different effects on males. Scientists are also exploring ways to model late-onset conditions using stem cells.
The Azrieli Foundation donated $10 million to fund groundbreaking stem cell and genetic research at the Hebrew University of Jerusalem's newly inaugurated center. Researchers will focus on developing therapies for Down syndrome, Prader-Willi syndrome, and Fragile X syndrome, among other conditions.
The study provides a starting point to understand the role of methyl groups in influencing gene expression and development. Researchers detected unusual methylation patterns in various tissues, suggesting potential stem cell populations and new avenues for exploration.
Researchers developed an algorithm called KeyGenes that uses gene expression to predict the future identity of human fetal stem cells. The platform integrates data from both human fetal and adult tissue, allowing for more accurate differentiation protocols.
Researchers at the Buck Institute discovered that macrophage-like hemocytes play a crucial role in regulating stem cell activity in the fly gut. This complex signaling interaction helps control intestinal regeneration after damage, but goes awry with age, potentially contributing to human diseases like IBS and colorectal cancer.
Researchers have found that epilepsy reduces the generation of new neurons in the hippocampus, a brain region crucial for learning and stress response. The study's findings suggest that preserving neural stem cells could prevent or mitigate epilepsy symptoms.
Scientists at University of Toronto have made breakthroughs in cell transplantation using hydrogel biomaterials, showing potential for partially restoring vision and aiding brain recovery from stroke. The new gel-like material boosts cell survival and integration in the eye and brain, paving the way for stem-cell-based therapies.
The journal Regenerative Medicine has published a special focus issue on methods to avoid immune rejection in regenerative medicine. The field is immature, but research continues to address the importance of immunity in progress and development.
Researchers find single protein, nuclear Fibroblast Growth Factor Receptor 1 (nFGFR1), orchestrates gene expression in embryo development. This discovery has potential to enhance understanding and treatment of cancers and congenital diseases.
Researchers at the Salk Institute have discovered a novel type of pluripotent stem cell capable of developing into any type of tissue. The new cells, dubbed region-selective pluripotent stem cells (rsPSCs), were easier to grow in the laboratory and offered advantages for large-scale production and gene editing.
Researchers from Mount Sinai presented a first successful 3D printed trachea, as well as studies on increased mortality in black patients after esophageal cancer surgery and the potential benefits of surgical resection for myasthenia gravis. These findings highlight the importance of personalized medicine and access to specialized care.
The study, which followed four individuals for a year after they were treated with embryonic stem cell-derived retinal pigment epithelial cells, observed no serious side effects related to the therapy. The researchers reported positive results in visual acuity improvements among patients.
Researchers analyzed 3,550 North American rodent fossils to show how fundamental evolutionary mechanisms drive the emergence of novel mammalian stem cells. The study found that most extinct species can acquire continuously growing molars through evolution, and the final developmental step is surprisingly simple.
Researchers at the University of Cambridge have identified a pathway linking proteins amyloid precursor protein and tau, which may be targeted for treatment. This discovery using human stem cells suggests that manipulating this pathway could halt disease progression.
Researchers have identified a key role for Gli1+ stem cells in skull development and facial bone repair. Transplanting these stem cells into injured areas may help restore normal anatomy and facilitate brain growth, offering potential treatment options for infants with craniosynostosis and patients with facial disfigurement.
Scientists have isolated dental stem cell lines and identified a natural mechanism for repairing tooth lesions. The study reveals that dopamine and serotonin play a crucial role in recruiting stem cells, which then repair the tooth. This breakthrough discovery opens up new therapeutic strategies to mobilize resident dental stem cells.
Researchers have developed a new technique for islet transplantation under the skin, which shows promise in reversing diabetes in preclinical models. This approach harnesses the body's natural ability to respond to a foreign body by growing new blood vessels, offering a safer and more reliable treatment option.
Scientists at Case Western Reserve University found that two topical medicines can activate mouse and human brain stem cells, reversing paralysis and repairing damage caused by multiple sclerosis. The approach offers a potential new way to reverse disability in MS patients.
Researchers at the University of Missouri have identified a new form of human embryonic stem cell that can help advance research on pre-eclampsia and other reproductive problems. These 'BMP-primed' stem cells are more robust and easily manipulated than traditional stem cells, making them ideal for future studies.
A new study suggests that injecting stem cells into the eye may preserve vision in people with early-stage age-related macular degeneration. The treatment, which uses adult-derived human cells, has shown promise in laboratory rats and could potentially be used to slow or reverse the effects of the disease.
A molecular pathway permits stem cells to grow rapidly and aggressively in pediatric bone cancers, according to researchers at NYU Langone Health. The transcription factor Sox2 releases the floodgates in the Hippo pathway, allowing for the growth of highly aggressive tumor-forming stem cells.
Scientists have discovered that the chromosomes in laboratory stem cells open slowly over time, allowing them to respond to growth factors and differentiate into specific cell types. This understanding could lead to advancements in stem cell research and the development of new therapies for diseases such as type 1 diabetes.
Researchers have created a disease signature for alpha-1 antitrypsin deficiency using induced pluripotent stem cells (iPSCs), which may lead to new treatments. The study found that liver cells derived from AAT deficient iPSCs are more sensitive to drugs that cause liver toxicity than normal cells.
Researchers at the Buck Institute have confirmed that Parkinson's disease mutations alter mitochondrial function in human cells for the first time. The study provides a tool for testing potential therapeutics and promises to address concerns about genetic differences between patients.
Researchers from Johns Hopkins Medicine discovered that premature aging of stem cell telomeres drives emphysema, not inflammation. This finding redirects research efforts to fix the underlying problem rather than treating symptoms.
Dr. Ayman Al-Hendy has received two top honors from the Society for Reproductive Investigation for his outstanding record of scientific investigation and promising research career. He is being recognized for his work on fibroids, uterine growths affecting up to 75% of women, which can complicate pregnancy and cause excessive bleeding.
A UCI team led by Leslie Thompson will establish an HD therapy employing human embryonic stem cells that can be evaluated in clinical trials. The researchers have identified a highly promising neural stem cell line showing disease-modifying activity in HD mice, and will conduct preclinical efficacy and safety studies.
The American Association of Anatomists has awarded Young Investigators to R.R. Bensley Award winner Bungo Akiyoshi for his discovery of unconventional kinetochores in Kinetoplastids, and Feng Zhang for his contributions to comparative neuroanatomy through genome manipulations using CRISPR-Cas9.
A stem cell-based approach using human embryonic stem cells proved effective in improving insulin sensitivity and glucose metabolism in mice. The combination of stem cell transplantation and antidiabetic drugs resulted in rapid weight loss and significant improvements in glucose control compared to individual treatments.
Researchers have identified a critical molecular pathway in blood stem cells that can be manipulated to enhance their regenerative capacity and reduce the signs of aging. By slowing down mitochondrial activity, they found that levels of SIRT7 can help cope with stress caused by misfolded proteins.
Researchers at Rockefeller University identified Sox9 as a key molecule controlling stem cell plasticity in hair follicles. Sox9 enables hair follicle stem cells to regain their ability to produce new tissue and heal wounds by amplifying genes associated with stemness.
Researchers at University of British Columbia found a new approach to treating Type 2 diabetes using stem cell transplants and conventional drugs. The study showed mice became glucose tolerant after receiving the transplants, while those without received only drugs, resulting in unexpected weight loss.
Researchers used super-resolution microscopy to visualize genome packaging and found that nucleosomes are assembled in irregular groups across the chromatin. This study reveals a link between genome packaging and cell pluripotency, with more pluripotent stem cells having less dense nucleosome clutches.
A new study by University of Alberta researchers found that media coverage of stem cell therapies often presents unrealistic timelines and overhypes the field. The study examined 307 news reports between 2010 and 2013, revealing that 69% predicted therapies would be available within 5-10 years or sooner.
A team of scientists has successfully repaired the damaged cerebral cortex of adult mice using cortical neurons derived from embryonic stem cells. The study suggests that only neurons of the same type as the damaged area can restore damaged circuits, providing new hope for treating brain injuries and diseases.
Scientists have made a breakthrough in treating patients with sickle cell disease by engineering custom blood cells that can evade the immune system. Lab-grown stem cells were reprogrammed and edited using CRISPR to replace the defective gene, resulting in healthy red blood cells that function just as well as those from unaffected donors.
The New York Stem Cell Foundation (NYSCF) has proposed seven strategies to advance women in science, engineering, and medicine, including flexible family care spending and recruiting gender-balanced review committees. The initiatives aim to promote gender equality and break down barriers to advancement in these fields.
A new study finds that Republicans generally defer to science on most issues, with only four exceptions: global warming, evolution, gay adoption, and mandatory health insurance. The study reveals that Republicans are more likely to trust science than independents and Democrats across a range of policy areas.