Researchers craft a new approach for mining genomic data for rare genetic variations that may play a role in disease risk.
Screening for all children newly diagnosed with the high-risk leukemia AMKL to check for genetic alterations that can help guide treatment.
DNA sequencing of bacteria leads to discovery of mutation that helps VRE tolerate antibiotics
Mystery sensor protein NLRC3 revealed as a central player in preventing colon cells from becoming cancerous
Research reveals principal tumor suppressor function of ARID1A and suggests that loss of the protein contributes to colon cancer
A possible targeted therapy is found for a high-risk form of acute lymphoblastic leukemia, the most common childhood cancer.
To improve patient safety, hospital leaders should provide feedback that demonstrates to staff the value of reporting safety events and errors.
Research from the Pediatric Cancer Genome Project identifies genomic landscape that contributes to the diversity of core-binding factor acute myeloid leukemia.
Research from the Pediatric Cancer Genome Project identifies the mechanism of action for two transcription factors underlying a type of B-precursor acute lymphoblastic leukemia.
New findings help increase understanding of molecular mechanisms for common forms of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).
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Browse all scientific publications by St. Jude investigators in 2015.