The multifaceted roles of lysosomes in cancer
Lysosomes support cancer cell adaptation by integrating macromolecule degradation and nutrient recycling with nutrient sensing, inter‐organelle communication and immune regulation. These interconnected functions can promote tumour growth, stress tolerance and therapy resistance, while also creating context‐dependent vulnerabilities that may be ...
Jia Li, Kevin M. Ryan
wiley +1 more source
Disease-associated mutations in Niemann-Pick type C1 alter ER calcium signaling and neuronal plasticity [PDF]
Niemann-Pick type C1 (NPC1) protein is essential for the transport of externally derived cholesterol from lysosomes to other organelles. Deficiency of NPC1 underlies the progressive NPC1 neurodegenerative disorder.
Vivas, Oscar +15 more
core +1 more source
Identifizierung und Charakterisierung von pharmakologischen Chaperonen zur Behandlung von Morbus Niemann-Pick Typ C1 unter Verwendung von neuralen und Hepatozyten-ähnlichen Zellen abgeleitet aus patientenspezifischen induzierten pluripotenten Stammzellen [PDF]
Das Ziel der vorliegenden Arbeit war die Identifizierung und Charakterisierung von pharmakologischen Chaperonen zur Behandlung von Morbus Niemann-Pick Typ C1 (NP-C1) unter Verwendung von neuralen und Hepatozyten-ähnlichen Zellen abgeleitet aus ...
Völkner, Christin (gnd: 1275524036)
core +1 more source
Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid
To address the effect of the n-3 fatty acid, docosahexaenoic acid (22:6), on proteins that play a role in cholesterol absorption, CaCo-2 cells were incubated with taurocholate micelles alone or micelles containing 22:6 or oleic acid (18:1). Compared with
Satya N. Mathur +2 more
doaj +1 more source
Altered gene expression in the liver and small intestine of horses with equine neuroaxonal dystrophy
Abstract Background Equine neuroaxonal dystrophy/degenerative myeloencephalopathy (eNAD/EDM) is the second most common diagnosis of spinal ataxia in horses in the United States. The disease develops due to a combination of vitamin E deficiency and an unknown genetic risk factor(s), and there currently is no effective treatment.
Stephanie Ryan +4 more
wiley +1 more source
Funktionelle Charakterisierung von zerebellären Purkinjezellen eines Mausmodells des Morbus Niemann-Pick Typ C1 [PDF]
Morbus Niemann Pick Typ C1 (NPC1) ist durch den Verlust von zerebellären Purkinjezellen gekennzeichnet, der in einer zerebellären Ataxie zum Ausdruck kommt. Hierbei sind die zugrunde liegenden pathophysiologischen Vorgänge nur ungenügend verstanden. Ziel
Rabenstein, Michael Jürgen (gnd: 1203734778)
core +1 more source
Cholesterol auxotrophy and intolerance to ezetimibe in mice with SREBP-2 deficiency in the intestine
SREBP-2 activates transcription of all genes needed for cholesterol biosynthesis. To study SREBP-2 function in the intestine, we generated a mouse model (Vil-BP2−/−) in which Cre recombinase ablates SREBP-2 in intestinal epithelia. Intestines of Vil-BP2−/
Shunxing Rong +2 more
doaj +1 more source
Abstract The aim of this systematic review and meta‐analysis was to evaluate comprehensively the therapeutic potential of Abelmoschus esculentus (okra) supplementation across the diabetes spectrum of key metabolic risk factors. A search was conducted in PubMed, Scopus, Web of Science, EMBASE and the Cochrane Library, up to 23 July 2025, to identify ...
Ali Jafari +7 more
wiley +1 more source
reservedIn questa tesi ho deciso di seguire il percorso che ha portato, a partire dalla scoperta di una grave e rara malattia, quale la malattia di Niemann-Pick di tipo C, allo studio di una proteina specifica che regola l’assorbimento intestinale del ...
POMARI, CARLOTTA
core
A genome-wide association study (GWAS) reported that common variation in the human Niemann-Pick C1 gene
L. John Horwood +27 more
core +2 more sources

