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...

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Bibliografiske detaljer
Main Authors: 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
Sprog:Inglês
Udgivet: American Society of Plant Biologists 2012
Fag:
Research Articles
Online adgang: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
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