A new study links FLVCR1 mutations to a spectrum of neurodevelopmental disorders. Researchers found that these gene variants ...

Learn how researchers cracked a genetic mystery, diagnosing undiagnosed diseases by identifying FLVCR1 mutations.

Antibodies show promise as candidates for therapeutics as well as tools for advancing mechanistic studies of the HER family receptors.

With millions of mice and rats in US labs alone, scientists can learn a lot of information from their scurrying test subjects ...

Patients with Huntington's disease have a genetic mutation that triggers proteins to misfold and clump together in the brain. These clumps interfere with cell function and eventually lead to cell ...

An international team of researchers has provided a genetic diagnosis for 30 individuals whose condition was undiagnosed for ...

The Center for Zebrafish Research, led by professor David Hyde, uses zebrafish to study and experiment with genetic mutations ...

Interestingly, although the evidence in mice pointed at FLVCR1 as the gene causing DBA ... On one hand, we had a patient with ...

When tested in mice, the compound—named BBI-2779—shrank gastric tumors and prevented the cancer from developing resistance to ...

A Michigan State University researcher's new model for studying breast cancer could help scientists better understand why and ...