Case-inspired exploration of renin mutations in autosomal dominant tubulointerstitial kidney disease: not all paths lead to the endoplasmic reticulum
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00467-024-06350-4.pdf
Reference38 articles.
1. Mabillard H, Sayer JA, Olinger E (2023) Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease. Nephrol Dial Transplant 38:271–282. https://doi.org/10.1093/ndt/gfab268
2. Clausmeyer S, Stürzebecher R, Peters J (1999) An Alternative Transcript of the Rat Renin Gene Can Result in a Truncated Prorenin That Is Transported Into Adrenal Mitochondria. Circ Res 84:337–344. https://doi.org/10.1161/01.RES.84.3.337
3. Clausmeyer S, Reinecke A, Farrenkopf R et al (2000) Tissue-Specific Expression of a Rat Renin Transcript Lacking the Coding Sequence for the Prefragment and Its Stimulation by Myocardial Infarction. Endocrinology 141:2963–2970. https://doi.org/10.1210/endo.141.8.7623
4. Wanka H, Keßler N, Ellmer J et al (2009) Cytosolic renin is targeted to mitochondria and inducesapoptosis in H9c2 rat cardiomyoblasts. J Cell Mol Med 13:2926–2937. https://doi.org/10.1111/j.1582-4934.2008.00448.x
5. Wanka H, Lutze P, Staar D et al (2018) An alternative renin isoform is cardioprotective by modulating mitochondrial metabolism. J Cell Mol Med 22:5991–6001. https://doi.org/10.1111/jcmm.13872
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