The Fanconi Anemia Ortholog FANCM Ensures Ordered Homologous Recombination in Both Somatic and Meiotic Cells in Arabidopsis([W])

The human hereditary disease Fanconi anemia leads to severe symptoms, including developmental defects and breakdown of the hematopoietic system. It is caused by single mutations in the FANC genes, one of which encodes the DNA translocase FANCM (for Fanconi anemia complementation group M), which is r...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Knoll, Alexander, Higgins, James D., Seeliger, Katharina, Reha, Sarah J., Dangel, Natalie J., Bauknecht, Markus, Schröpfer, Susan, Franklin, F. Christopher H., Puchta, Holger
Format: Artigo
Idioma:Inglês
Publicat: American Society of Plant Biologists 2012
Matèries:
Research Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3398556/
https://ncbi.nlm.nih.gov/pubmed/22547783
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1105/tpc.112.096644
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars