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Πλοήγηση ανά Θέμα "Homeodomain Proteins"

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    • MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease 

      Schormair, B.; Plag, J.; Kaffe, M.; Groß, N.; Czamara, D.; Samtleben, W.; Lichtner, P.; Ströhle, A.; Stefanidis, I.; Vainas, A.; Dardiotis, E.; Sakkas, G. K.; Gieger, C.; Müller-Myhsok, B.; Meitinger, T.; Heemann, U.; Hadjigeorgiou, G. M.; Oexle, K.; Winkelmann, J. (2011)
      Background: Restless legs syndrome (RLS) is a sleep related movement disorder that occurs both in an idiopathic form and in symptomatic varieties. RLS is a frequent and distressing comorbidity in end stage renal disease ...

    • Muscle xenografts reproduce key molecular features of facioscapulohumeral muscular dystrophy 

      Mueller A.L., O'Neill A., Jones T.I., Llach A., Rojas L.A., Sakellariou P., Stadler G., Wright W.E., Eyerman D., Jones P.L., Bloch R.J. (2019)
      Aberrant expression of DUX4, a gene unique to humans and primates, causes Facioscapulohumeral Muscular Dystrophy-1 (FSHD), yet the pathogenic mechanism is unknown. As transgenic overexpression models have largely failed ...