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

Chromosome breakage has most frequently been described ... of whom 12 had the Fanconi type of anemia. A variety of structural aberrations and a specific type of polyploidy were observed in the ...

Cephalopods may have the oldest sex chromosomes of any animal, according to a new discovery in the octopus genome. That's a big deal given that scientists didn't know until now if these oddball ...

Autozygome double-strand DNA breaks Fanconi anaemia genetics RAD51 Fanconi anaemia (FA) is a group of disorders characterised by progressive bone marrow failure and a characteristic but variable ...

Last week, Founders Fund partner Delian Asparouhov realized he hadn’t checked on his genetics in a while. He clicked open a dashboard created by Nucleus Genomics, a Founders Fund-backed startup ...

Fanconi anemia (FA) is the most common inherited bone marrow failure syndrome, characterized by cellular DNA repair deficiency, developmental defects, and a 700-fold increased risk of developing ...

The Fanconi anemia (FA) pathway is a major mechanism of homologous recombination DNA repair. The functional readout of the pathway is activation through mono-ubiquitination of FANCD2 leading to ...