Pennington Biomedical's Dr. Emily Flanagan awarded up to $3.55 million NIH grant to study infant energy balance and early-life growth
Grant and Award Announcement
Updates every hour. Last Updated: 24-Oct-2026 19:16 ET (24-Oct-2026 23:16 GMT/UTC)
Dr. Emily Flanagan, Assistant Professor and Director of the Developmental Physiology Laboratory at LSU’s Pennington Biomedical Research Center, has been awarded a prestigious National Institutes of Health R01 grant totaling up to $3.55 million to investigate how energy intake and expenditure influence infant growth during the first year of life.
The five-year grant from the NIH’s National Institute of Diabetes and Digestive and Kidney Diseases will support Flanagan’s project, “Characterization of Infant Energy Balance to Optimize Early Life Growth.” The study will examine the fundamental drivers of infant growth and could help improve how energy needs are estimated during a critical period of development.
As dogs age, many develop more than one chronic health condition. New research from the Texas A&M College of Veterinary Medicine and Biomedical Sciences (VMBS) shows those conditions can dramatically shorten a dog’s lifespan, highlighting the importance of managing multiple diseases together rather than individually.
In a recent study published in GeroScience, researchers with the Dog Aging Project found that dogs with five or more chronic diseases were more than twice as likely to die as dogs living with only one diagnosed condition, regardless of their age or size. The findings suggest that, as in humans, chronic diseases interact in ways that make their combined effects more harmful than each condition alone.
MUSC Hollings Cancer Center researchers have uncovered a new way to exploit a weakness in triple-negative breast cancer (TNBC), an aggressive form of breast cancer that often develops resistance to chemotherapy. The team discovered a previously unknown role for the protein LOX inside cancer cells, where it helps to support energy production, healthy mitochondria and other processes the cells rely on to survive.
When researchers blocked LOX, the cancer cells became vulnerable but adapted by relying more heavily on a backup survival pathway controlled by a protein called DHODH. The team, led by Hollings researcher Ozgur Sahin, Ph.D., turned that adaptation against the cancer with a “one-two punch”: first blocking LOX to weaken the cells, then blocking DHODH to cut off their escape route. The combination significantly blocked tumor growth across multiple patient-derived models without chemotherapy and showed potential advantages over pairing the LOX-blocking drug with standard chemotherapy.
The findings are still preclinical, but they point toward a potential strategy for treating chemotherapy-resistant TNBC while one day reducing reliance on chemotherapy and its serious side effects. The researchers also found evidence that LOX and DHODH could potentially serve as biomarkers to help identify patients most likely to benefit. The team is now developing a newer LOX-blocking drug and completing studies needed to move the approach toward testing in people.
A previously unknown population of long-lived immune cells helps the lungs build lasting protection against influenza. The findings reveal a new way the innate and adaptive immune systems work together and could inform the design of next-generation nasal vaccines that provide broader, longer-lasting protection against respiratory viruses.