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Parcourir par sujet "guanosine triphosphatase activating protein"

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    • Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients 

      Mitropoulos K., Papadima E.M., Xiromerisiou G., Balasopoulou A., Charalampidou K., Galani V., Zafeiri K.-V., Dardiotis E., Ralli S., Deretzi G., John A., Kydonopoulou K., Papadopoulou E., Di Pardo A., Akcimen F., Loizedda A., Dobriĉić V., Novaković I., Kostic V.S., Mizzi C., Peters B.A., Basak N., Orrù S., Kiskinis E., Cooper D.N., Gerou S., Drmanac R., Bartsakoulia M., Tsermpini E.-E., Hadjigeorgiou G.M., Ali B.R., Katsila T., Patrinos G.P. (2017)
      Background: Amyotrophic lateral sclerosis (ALS) is a devastating disease whose complex pathology has been associated with a strong genetic component in the context of both familial and sporadic disease. Herein, we adopted ...