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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Detalhes bibliográficos
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
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Plant Biologists 2012
Assuntos:
Research Articles
Acesso em linha: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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