Fanconi anemia (FA) is a rare genetic disorder impairing bone marrow's blood cell production, leading to severe health issues ...

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 anemia typically manifests in pediatric age, affects the bone marrow stem cells, and is characterized by the progressive loss of blood cells - resulting in serious infections, asthenia ...

In 2023, Autumn was diagnosed with Fanconi anemia, a rare and incurable genetic disorder. For the past month, 18 local high ...

Patients in the EU with Fanconi anaemia (FA) could soon have the first gene therapy option for the disorder, as the EMA starts a review of Rocket Pharma’s RP-L102 candidate. FA is an inherited ...

On Thursday, the Shrewsbury and Westborough High boys' basketball teams joined up to recognize Autumn Carson, a 9-year-old girl with a Fanconi anemia.

Schlacher K, Wu H, Jasin M. A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2. Cancer Cell 22(1):106-16, 7/2012. PMCID: PMC3954744. Siaud N, ...

I was always interested in cancer aetiology and prevention, and undertook a PhD in the role of Fanconi Anemia genes in haematological malignancies which then led to me completing my specialisation ...