Histone chaperone activity of Fanconi anemia proteins, FANCD2 and FANCI, is required for DNA crosslink repair

Fanconi anaemia (FA) is a rare hereditary disorder characterized by genomic instability and cancer susceptibility. A key FA protein, FANCD2, is targeted to chromatin with its partner, FANCI, and plays a critical role in DNA crosslink repair. However, the molecular function of chromatin-bound FANCD2-...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Sato, Koichi, Ishiai, Masamichi, Toda, Kazue, Furukoshi, Satoshi, Osakabe, Akihisa, Tachiwana, Hiroaki, Takizawa, Yoshimasa, Kagawa, Wataru, Kitao, Hiroyuki, Dohmae, Naoshi, Obuse, Chikashi, Kimura, Hiroshi, Takata, Minoru, Kurumizaka, Hitoshi
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Nature Publishing Group 2012
Θέματα:
Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3433790/
https://ncbi.nlm.nih.gov/pubmed/22828868
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/emboj.2012.197
Ετικέτες: Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!

Παρόμοια τεκμήρια