Regulation of the Fanconi Anemia DNA Repair Pathway by Phosphorylation and Monoubiquitination
The Fanconi anemia (FA) DNA repair pathway coordinates a faithful repair mechanism for stalled DNA replication forks caused by factors such as DNA interstrand crosslinks (ICLs) or replication stress. An important role of FA pathway activation is initiated by monoubiquitination of FANCD2 and its bind...
Enregistré dans:
Auteur principal: | Masamichi Ishiai |
---|---|
Format: | article |
Langue: | EN |
Publié: |
MDPI AG
2021
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/48fb5e63ca36405db9f5bb01e9b0345c |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Anemia constitucional infantil asociada con anomalías somáticas múltiples: Síndrome de Fanconi
par: JIMENEZ DE ASUA,FELIPE, et autres
Publié: (1947) -
Síndrome de Fanconi: Relato de tres casos
par: VILDOSOLA,JORGE, et autres
Publié: (1955) -
Differential Gene Expression in Host Ubiquitination Processes in Childhood Malarial Anemia
par: Samuel B. Anyona, et autres
Publié: (2021) -
Self-perception of periodontal health status among individuals with Fanconi anemia
par: Nicole Nichele Perdoncini, et autres
Publié: (2021) -
Fanconi Anemia Pathway Genes Advance Cervical Cancer via Immune Regulation and Cell Adhesion
par: Shizhi Wang, et autres
Publié: (2021)