Cellular atlases and omics studies, such as genomics, transcriptomics and proteomics, have become key tools for identifying the diversity of all the elements that make up the cardiovascular system.

Rare genetic diseases are challenging for patients and their families—made all the more overwhelming because symptoms tend to ...

The Byers Award recognizes outstanding research by faculty members in the middle of their careers. Martin Kampman’s honorary 2025 lecture is titled “A CRISPR approach to neurodegenerative diseases.” ...

In a nutshell Scientists identified four distinct disease pathways that lead to Alzheimer’s: mental health ...

UCLA Health researchers have identified four distinct pathways that lead to Alzheimer's disease by analyzing electronic ...

This study investigates the effectiveness of integrating augmented reality (AR) and concept mapping method in English vocabulary learning and proposes a design thinking-based development framework for ...

When it comes to cutting-edge health technology, Jecizer Biosciences is quickly becoming the name you’ve probably haven’t ...

Up to half of patients with Crohn's disease, an inflammatory bowel disease, develop a complication called fibrosis, where the ...

New Delhi, June 24 A team of international researchers has uncovered a new genetic cause for a rare developmental disorder that profoundly impacts brain growth and function in children. The team led ...

For his birthday, Jenna hopes to give her son a life-saving gift. “You wouldn’t guess that he’s as sick as he is because he’s just so happy most of the time,” she said. Two months after Rhett was born ...

Hampton Roads infant with rare genetic disorder in critical need of liver donor by: Lauren Martinez Posted: Jun 12, 2025 / 06:10 PM EDT Updated: Jun 12, 2025 / 06:32 PM EDT ...

Medical Milestone: 19-month-old Mannat Singh becomes first baby in Singapore cured of SCID at birth with a successful stem-cell transplant.