TY  - JOUR
AU  - Peña-Gómez, María José
AU  - Moreno-Gordillo, Paula
AU  - Narmontė, Milda
AU  - García-Calderón, Clara B
AU  - Rukšėnaitė, Audronė
AU  - Klimašauskas, Saulius
AU  - Rosado, Iván V
PY  - 2022
DO  - 10.1038/s41419-022-04952-0
UR  - http://hdl.handle.net/10668/19528
T2  - Cell death & disease
AB  - Fanconi anemia (FA) is a rare hereditary disorder caused by mutations in any one of the FANC genes. FA cells are mainly characterized by extreme hypersensitivity to interstrand crosslink (ICL) agents. Additionally, the FA proteins play a crucial role...
LA  - en
KW  - DNA Demethylation
KW  - DNA Replication
KW  - Deoxycytidine
KW  - Fanconi Anemia
KW  - Fanconi Anemia Complementation Group D2 Protein
KW  - Humans
KW  - Thymidine
TI  - FANCD2 maintains replication fork stability during misincorporation of the DNA demethylation products 5-hydroxymethyl-2'-deoxycytidine and 5-hydroxymethyl-2'-deoxyuridine.
TY  - research article
VL  - 13
ER  -