The genetic basis of Fanconi anemia (FA) is mysterious and complex, as none of the five genes previously associated with the disorder have homology to genes encoding proteins of known function.

Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...

"This information will help parents of children with Fanconi anemia understand that the poor growth and weight gain is not ...

In the area of growth control, our recent work is focused on the mTOR pathway that controls multiple aspects of cell growth and homeostasis. Our work on genomic integrity ranges from the Fanconi ...

Fanconi syndrome is a hereditary or acquired disease of the renal proximal tubules, without primary involvement of kidney glomeruli, and is characterized by the tubular wasting of nutrients and ...

Fanconi anemia has no known cure and can cause bone marrow failure and cancer. So Jimbo and his ex-wife, Candi Fisher, established the Kidz 1st Fund in 2011 to help spread awareness and raise ...

Rocket’s lentiviral (LV) vector-based hematology portfolio consists of late-stage programs for Fanconi Anemia (FA), a difficult-to-treat genetic disease that leads to bone marrow failure (BMF ...

Its clinical program is an LVV-based gene therapy for the treatment of Fanconi Anemia (FA), a difficult to treat genetic disease that leads to bone marrow failure and potentially cancer.