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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Knoll, Alexander, Higgins, James D., Seeliger, Katharina, Reha, Sarah J., Dangel, Natalie J., Bauknecht, Markus, Schröpfer, Susan, Franklin, F. Christopher H., Puchta, Holger
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society of Plant Biologists 2012
Gaiak:
Research Articles
Sarrera elektronikoa: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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