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pro vyhledávání: '"Parama Paul"'
Autor:
Parama Paul, Sreekumar Ramachandran, Sheng Xia, Jay R Unruh, Juliana Conkright-Fincham, Rong Li
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216220 (2019)
Autosomal dominant polycystic kidney disease (ADPKD) is caused mostly by mutations in polycystin-1 or polycystin-2. Fluid flow leads to polycystin-dependent calcium influx and nuclear export of histone deacetylase 5 (HDAC5), which facilitates the mai
Externí odkaz:
https://doaj.org/article/e5399717e0b5480f90d8c9fb16d26725
Autor:
Juliana Conkright-Fincham, Parama Paul, Rong Li, Jay R. Unruh, Sheng Xia, Sreekumar Ramachandran
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 5, p e0216220 (2019)
PLoS ONE, Vol 14, Iss 5, p e0216220 (2019)
Autosomal dominant polycystic kidney disease (ADPKD) is caused mostly by mutations in polycystin-1 or polycystin-2. Fluid flow leads to polycystin-dependent calcium influx and nuclear export of histone deacetylase 5 (HDAC5), which facilitates the mai
Publikováno v:
Nature cell biology
During yeast cell division, multidrug resistance (MDR) transporters partition unequally, with the older pool remaining in the mother cell. Mutations in MDR transporter genes reduce replicative lifespan, whereas an extra copy of these genes extends it