TRPP Cation Channels
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Subject Areas on Research
- Another cystic mystery solved.
- Defining a link with autosomal-dominant polycystic kidney disease in mice with congenitally low expression of Pkd1.
- Inactivation of integrin-β1 prevents the development of polycystic kidney disease after the loss of polycystin-1.
- Mitochondrial DNA-depleted A549 cells are resistant to bleomycin.
- Off-response property of an acid-activated cation channel complex PKD1L3-PKD2L1.
- Sec63 and Xbp1 regulate IRE1α activity and polycystic disease severity.
- TRP channels in disease.
- The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development.
- Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor.
- Tuberin-dependent membrane localization of polycystin-1: a functional link between polycystic kidney disease and the TSC2 tumor suppressor gene.