A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells

Frontotemporal lobar degeneration is a progressive neurodegenerative syndrome that is the second most common cause of early-onset dementia. Mutations in the progranulin gene are a major cause of familial frontotemporal lobar degeneration [Baker M, et al. (2006) Nature 442:916–919 and Cruts M, et al....

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kao, Aimee W., Eisenhut, Robin J., Martens, Lauren Herl, Nakamura, Ayumi, Huang, Anne, Bagley, Josh A., Zhou, Ping, de Luis, Alberto, Neukomm, Lukas J., Cabello, Juan, Farese, Robert V., Kenyon, Cynthia
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 2011
Gaiak:
Biological Sciences
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3060230/
https://ncbi.nlm.nih.gov/pubmed/21368173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1100650108
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