Graduate School of Medical Sciences
A partnership with the Sloan Kettering Institute

Research Matters: How Folate Deficiency May Alter Genes to Promote Cancer

Students Break Down Big Science into Inspiring Stories

Three minutes and one slide were all it took for twelve young scientists to turn cutting-edge research into dramatic stories of hope at Weill Cornell Medicine’s tenth annual Three-Minute Thesis (3MT) competition on Nov. 13 in Uris Auditorium. The night showcased bold ideas about tackling Alzheimer’s disease, cancer, infectious diseases and more with creativity and passion.

Aging Midbrain Neurons Face Energy Crisis Linked to Parkinson’s

Dopamine neurons in a part of the brain called the midbrain may, with aging, be increasingly susceptible to a vicious spiral of decline driven by fuel shortages, according to a study led by Weill Cornell Medicine investigators. The findings offer a potential explanation for the degeneration of this neuron population in Parkinson’s disease.

Improving Lives Through Academic Innovation, Commercialization and Entrepreneurship

Why are innovation and entrepreneurship important in academic research? Since the Bayh-Dole Act was passed in 1980, permitting institutions to retain ownership of their inventions arising from federal funding, more than 200 drug treatments and vaccines have been brought to market through academic-commercial partnerships.

Weill Cornell Medicine’s Ninth Annual Dean’s Symposium on Innovation and Entrepreneurship celebrated and fostered this entrepreneurial spirit on Nov. 17 at Weill Cornell's Griffis Faculty Club.

Research Matters: Personalizing Pancreatic Cancer Treatment

Video of Research Matters: Personalizing Pancreatic Cancer Treatment

It’s not surprising that pancreatic cancer is often referred to as a silent killer. With few early symptoms and an aggressive nature, it has one of the lowest survival rates of all cancers.

New Immune Cell Suspects in Lupus

Detailed mapping of CD4⁺ T cells from children with systemic lupus erythematosus (SLE) has revealed distinct immune cell subsets with likely roles in disease pathogenesis, according to a study led by Weill Cornell Medicine investigators. The findings are poised to redirect lupus research and open the door to more precise therapies that avoid broad immune suppression.

Early Brain Differences May Explain Sex-Specific Risks for Addiction

The roots of addiction risk may lie in how young brains function long before substance use begins, according to a new study from Weill Cornell Medicine. The investigators found that children with a family history of substance use disorder (SUD) already showed distinctive patterns of brain activity that differ between boys and girls, which may reflect separate predispositions for addiction. The research, published Nov.

Scientists Identify a Molecular Switch to a Painful Side Effect of Chemotherapy

Chemotherapy activates a stress sensor in immune cells, triggering inflammation and nerve damage, which may help explain why many cancer patients experience debilitating pain as a side effect, according to a new study by Weill Cornell Medicine and Wake Forest University School of Medicine researchers.

Reviving Exhausted Immune Cells Boosts Tumor Elimination

A new study has discovered a molecular signal that tumors exploit to exhaust the T cells meant to destroy them—and how silencing that signal could revive the body’s immunity. The study led by Weill Cornell Medicine researchers was published Nov. 17 in Nature Immunology and shows that tumors not only evade the immune system but can actively reprogram immune cells to stop fighting.

Hypertension Affects the Brain Much Earlier than Expected

Hypertension impairs blood vessels, neurons and white matter in the brain well before the condition causes a measurable rise in blood pressure, according to a new preclinical study from Weill Cornell Medicine investigators. The changes help explain why hypertension is a major risk factor for developing cognitive disorders, such as vascular cognitive impairment and Alzheimer’s disease.