3 Dokumente gefunden

Klinische und molekulare Marker einer Leberdysfunktion korrelieren mit metabolischen Veränderungen in Erythrozyten

Die Leber ist als zentrales Stoffwechselorgan des Organismus an multiplen Prozessen beteiligt, wie der Synthese von Plasmaproteinen, der Entgiftung und der Energieversorgung durch Glykogenspeicherung. Bei pathologischen Zuständen wie Sepsis, toxisch bedingtem Leberversagen oder chronischen Lebererkrankungen…

Aβ-Induced Alterations in Membrane Lipids Occur before Synaptic Loss Appears

Loss of active synapses and alterations in membrane lipids are crucial events in physiological aging as well as in neurodegenerative disorders. Both are related to the abnormal aggregation of amyloid-beta (Aβ) species, generally known as amyloidosis. There are two major known human Aβ species: Aβ (1–40)…
Basel: Molecular Diversity Preservation International, 2022-02-19

Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate…

Niemann–Pick type C1 (NPC1) is a lysosomal storage disorder, inherited as an autosomal-recessive trait. Mutations in the Npc1 gene result in malfunction of the NPC1 protein, leading to an accumulation of unesterified cholesterol and glycosphingolipids. Beside visceral symptoms like hepatosplenomegaly,…
Basel: Molecular Diversity Preservation International, 2020-06-24