The role of lysosomes in metabolic and autoimmune diseases
F Gros, S Muller - Nature Reviews Nephrology, 2023 - nature.com
Lysosomes are catabolic organelles that contribute to the degradation of intracellular
constituents through autophagy and of extracellular components through endocytosis …
constituents through autophagy and of extracellular components through endocytosis …
Drug-induced kidney stones and crystalline nephropathy: pathophysiology, prevention and treatment
M Daudon, V Frochot, D Bazin, P Jungers - Drugs, 2018 - Springer
Abstract Drug-induced calculi represent 1–2% of all renal calculi. The drugs reported to
produce calculi may be divided into two groups. The first one includes poorly soluble drugs …
produce calculi may be divided into two groups. The first one includes poorly soluble drugs …
Rare inherited kidney diseases: challenges, opportunities, and perspectives
At least 10% of adults and nearly all children who receive renal-replacement therapy have
an inherited kidney disease. These patients rarely die when their disease progresses and …
an inherited kidney disease. These patients rarely die when their disease progresses and …
Chloride in vesicular trafficking and function
T Stauber, TJ Jentsch - Annual review of physiology, 2013 - annualreviews.org
Luminal acidification is of pivotal importance for the physiology of the secretory and
endocytic pathways and its diverse trafficking events. Acidification by the proton-pumping V …
endocytic pathways and its diverse trafficking events. Acidification by the proton-pumping V …
Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney
BP Festa, Z Chen, M Berquez, H Debaix… - Nature …, 2018 - nature.com
The endolysosomal system sustains the reabsorptive activity of specialized epithelial cells.
Lysosomal storage diseases such as nephropathic cystinosis cause a major dysfunction of …
Lysosomal storage diseases such as nephropathic cystinosis cause a major dysfunction of …
Mouse models of cystic fibrosis: phenotypic analysis and research applications
M Wilke, RM Buijs-Offerman, J Aarbiou… - Journal of Cystic …, 2011 - Elsevier
Genetically modified mice have been studied for more than fifteen years as models of cystic
fibrosis (CF). The large amount of experimental data generated illuminates the complex …
fibrosis (CF). The large amount of experimental data generated illuminates the complex …
Cystic fibrosis: insight into CFTR pathophysiology and pharmacotherapy
Cystic fibrosis is the most common life-threatening recessively inherited disease in
Caucasians. Due to early provision of care in specialized reference centers and more …
Caucasians. Due to early provision of care in specialized reference centers and more …
[HTML][HTML] Bicarbonate in cystic fibrosis
K Kunzelmann, R Schreiber, HB Hadorn - Journal of Cystic Fibrosis, 2017 - Elsevier
Background Cystic fibrosis (CF, mucoviscidosis) is caused by mutations in the gene
encoding CF transmembrane conductance regulator (CFTR), which is a chloride and …
encoding CF transmembrane conductance regulator (CFTR), which is a chloride and …
Catch me if you can! Novel aspects of cadmium transport in mammalian cells
F Thévenod - Biometals, 2010 - Springer
Abstract Cadmium (Cd 2+) is a nonessential divalent metal ion that causes toxicity in
multiple organs in humans. In order for toxicity to occur Cd 2+ must first enter cells by …
multiple organs in humans. In order for toxicity to occur Cd 2+ must first enter cells by …
Digital image analysis of picrosirius red staining: A robust method for multi-organ fibrosis quantification and characterization
Current understanding of fibrosis remains incomplete despite the increasing burden of
related diseases. Preclinical models are used to dissect the pathogenesis and dynamics of …
related diseases. Preclinical models are used to dissect the pathogenesis and dynamics of …