Wang X, Yin G, Yang Y, Tian X
Int J Mol Sci. 2025; 26(5).
PMID: 40076734
PMC: 11901018.
DOI: 10.3390/ijms26052110.
Romero A, Walker B, Krneta-Stankic V, Gerner-Mauro K, Youmans L, Miller R
Development. 2025; 152(3).
PMID: 39959988
PMC: 11883272.
DOI: 10.1242/dev.202820.
Moye A, Robichaux M, Agosto M, Rivolta C, Moulin A, Wensel T
bioRxiv. 2025; .
PMID: 39896654
PMC: 11785020.
DOI: 10.1101/2025.01.20.633784.
Kleene S
Pflugers Arch. 2024; 477(3):479-494.
PMID: 39688695
DOI: 10.1007/s00424-024-03050-8.
Van Sciver R, Caspary T
Dis Model Mech. 2024; 17(10).
PMID: 39263856
PMC: 11512102.
DOI: 10.1242/dmm.052000.
Disease-associated missense mutations in the pore loop of polycystin-2 alter its ion channel function in a heterologous expression system.
Staudner T, Geiges L, Khamseekaew J, Sure F, Korbmacher C, Ilyaskin A
J Biol Chem. 2024; 300(8):107574.
PMID: 39009345
PMC: 11630642.
DOI: 10.1016/j.jbc.2024.107574.
Molecular and structural perspectives on protein trafficking to the primary cilium membrane.
Palicharla V, Mukhopadhyay S
Biochem Soc Trans. 2024; 52(3):1473-1487.
PMID: 38864436
PMC: 11346432.
DOI: 10.1042/BST20231403.
DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2.
Rezi C, Aslanyan M, Diwan G, Cheng T, Chamlali M, Junger K
EMBO Rep. 2024; 25(7):3040-3063.
PMID: 38849673
PMC: 11239879.
DOI: 10.1038/s44319-024-00170-1.
Mechanistic complement of autosomal dominant polycystic kidney disease: the role of aquaporins.
Lan Q, Li J, Zhang H, Zhou Z, Fang Y, Yang B
J Mol Med (Berl). 2024; 102(6):773-785.
PMID: 38668786
DOI: 10.1007/s00109-024-02446-4.
Polycystin-2 Mediated Calcium Signalling in the Model for Autosomal Dominant Polycystic Kidney Disease.
Allan C, Sanislav O, Fisher P
Cells. 2024; 13(7.
PMID: 38607049
PMC: 11012017.
DOI: 10.3390/cells13070610.
Emerging mechanistic understanding of cilia function in cellular signalling.
Hilgendorf K, Myers B, Reiter J
Nat Rev Mol Cell Biol. 2024; 25(7):555-573.
PMID: 38366037
PMC: 11199107.
DOI: 10.1038/s41580-023-00698-5.
Role of the microtubules in the electrical activity of the primary cilium of renal epithelial cells.
Scarinci N, Gutierrez B, Albarracin V, Cantero M, Cantiello H
Front Mol Biosci. 2023; 10:1214532.
PMID: 38074099
PMC: 10702962.
DOI: 10.3389/fmolb.2023.1214532.
DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2.
Rezi C, Aslanyan M, Diwan G, Cheng T, Chamlali M, Junger K
bioRxiv. 2023; .
PMID: 37987012
PMC: 10659422.
DOI: 10.1101/2023.11.10.566524.
Primary cilia: a novel research approach to overcome anticancer drug resistance.
Lee K
Front Mol Biosci. 2023; 10:1270639.
PMID: 37900915
PMC: 10602908.
DOI: 10.3389/fmolb.2023.1270639.
Transport and barrier mechanisms that regulate ciliary compartmentalization and ciliopathies.
Moran A, Louzao-Martinez L, Norris D, Peters D, Blacque O
Nat Rev Nephrol. 2023; 20(2):83-100.
PMID: 37872350
DOI: 10.1038/s41581-023-00773-2.
Emerging principles of primary cilia dynamics in controlling tissue organization and function.
Gopalakrishnan J, Feistel K, Friedrich B, Grapin-Botton A, Jurisch-Yaksi N, Mass E
EMBO J. 2023; 42(21):e113891.
PMID: 37743763
PMC: 10620770.
DOI: 10.15252/embj.2023113891.
Polycystin-2-dependent transcriptome reveals early response of autosomal dominant polycystic kidney disease.
Jung H, Dixon E, Coleman R, Watnick T, Reiter J, Outeda P
Physiol Genomics. 2023; 55(11):565-577.
PMID: 37720991
PMC: 11178268.
DOI: 10.1152/physiolgenomics.00040.2023.
Seriously cilia: A tiny organelle illuminates evolution, disease, and intercellular communication.
Derderian C, Canales G, Reiter J
Dev Cell. 2023; 58(15):1333-1349.
PMID: 37490910
PMC: 10880727.
DOI: 10.1016/j.devcel.2023.06.013.
Convergence of Calcium Channel Regulation and Mechanotransduction in Skeletal Regenerative Biomaterial Design.
LaGuardia J, Shariati K, Bedar M, Ren X, Moghadam S, Huang K
Adv Healthc Mater. 2023; 12(27):e2301081.
PMID: 37380172
PMC: 10615747.
DOI: 10.1002/adhm.202301081.
Cardiovascular perspectives of the TRP channel polycystin 2.
Marquez-Nogueras K, Kuo I
J Physiol. 2023; 602(8):1565-1577.
PMID: 37312633
PMC: 10716366.
DOI: 10.1113/JP283835.
