Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Natural disease history of the dy^2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy.

Autor: Pasteuning-Vuhman, S., Putker, K., Tanganyika-de Winter, C. L., Boertje-van der Meulen, J. W., van Vliet, L., Overzier, M., Plomp, J. J., Aartsma-Rus, A., van Putten, M.

Publikováno v: PLoS ONE; 5/15/2018, Vol. 13 Issue 5, p1-18, 18p

Change of voltage-gated sodium channel repertoire in skeletal muscle of a MuSK myasthenia gravis mouse model.

Autor: Butenko O; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Jensen SM; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Fillié-Grijpma YE; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Verpalen R; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Verschuuren JJ; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands., van der Maarel SM; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Huijbers MG; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands., Plomp JJ; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.

Publikováno v: The European journal of neuroscience [Eur J Neurosci] 2024 Jun; Vol. 59 (12), pp. 3292-3308. Date of Electronic Publication: 2024 Apr 22.

Gangliosides as Therapeutic Targets for Neurodegenerative Diseases.

Autor: Inci, Orhan Kerim¹ (AUTHOR), Basırlı, Hande¹ (AUTHOR), Can, Melike¹ (AUTHOR), Yanbul, Selman¹ (AUTHOR), Seyrantepe, Volkan^1,2 (AUTHOR)

Publikováno v: Journal of Lipids. 4/8/2024, Vol. 2024, p1-10. 10p.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.