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The occurrence of ADPKD is primarily attributed to mutations in the Pkd1 gene or Pkd2 gene, which, respectively, encode polycystin 1 (PC1) and polycystin 2 (PC2) (Luo et al., 2023a)

ZweersHvan WegbergAMJJanssenMCHWortmannSB.Ketogenic diet for mitochondrial disease: A systematic review on efficacy and safety

Design and activity of specific hypoxia-inducible factor-2 (HIF-2) inhibitors for the treatment of clear cell renal cell carcinoma: discovery of clinical candidate ( S )-3-((2,2-difluoro-1-hydroxy-7-(methylsulfonyl)-2,3-dihydro-1 H -inden-4-yl)oxy)-5-fluorobenzonitrile (PT2385)

QIL1/MIC13(C19orf70) MICOS13 , also known as C19orf70, MIC13 , or QIL1 (155, 156), is a component of mitochondrial contact site and cristae tissue system (MICOS) complex