OBO ID: DOID:898

Citations

(16 total)

Term: autosomal dominant polycystic kidney disease

Chen, S., Huang, L., Zhou, S., Zhang, Q., Ruan, M., Fu, L., Yang, B., Xu, D., Mei, C., Mao, Z. (2021) NS398 as a potential drug for autosomal-dominant polycystic kidney disease: Analysis using bioinformatics, and zebrafish and mouse models. Journal of Cellular and Molecular Medicine. 25(20):9597-9608

Metzner, A., Griffiths, J.D., Streets, A.J., Markham, E., Philippou, T., Van Eeden, F.J.M., Ong, A.C.M. (2020) A high throughput zebrafish chemical screen reveals ALK5 and non-canonical androgen signalling as modulators of the pkd2^-/- phenotype. Scientific Reports. 10:72

Liu, D., Huo, Y., Chen, S., Xu, D., Yang, B., Xue, C., Fu, L., Bu, L., Song, S., Mei, C. (2019) Identification of Key Genes and Candidated Pathways in Human Autosomal Dominant Polycystic Kidney Disease by Bioinformatics Analysis. Kidney & blood pressure research. 44:533-552

Sun, Y., Liu, Z., Cao, X., Lu, Y., Mi, Z., He, C., Liu, J., Zheng, Z., Li, M.J., Li, T., Xu, D., Wu, M., Cao, Y., Li, Y., Yang, B., Mei, C., Zhang, L., Chen, Y. (2019) Activation of P-TEFb by cAMP-PKA signaling in autosomal dominant polycystic kidney disease. Science advances. 5:eaaw3593

Xu, D., Lv, J., He, L., Fu, L., Hu, R., Cao, Y., Mei, C. (2018) Scribble influences cyst formation in autosomal-dominant polycystic kidney disease by regulating Hippo signaling pathway. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 32(8):4394-4407

Chang, M.Y., Ma, T.L., Hung, C.C., Tian, Y.C., Chen, Y.C., Yang, C.W., Cheng, Y.C. (2017) Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency. Scientific Reports. 7:7161

Zhu, P., Sieben, C.J., Xu, X., Harris, P.C., Lin, X. (2017) Autophagy Activators Suppress Cystogenesis in an Autosomal Dominant Polycystic Kidney Disease Model. Human molecular genetics. 26(1):158-172

Arif Pavel, M., Lv, C., Ng, C., Yang, L., Kashyap, P., Lam, C., Valentino, V., Fung, H.Y., Campbell, T., Møller, S.G., Zenisek, D., Holtzman, N.G., Yu, Y. (2016) Function and regulation of TRPP2 ion channel revealed by a gain-of-function mutant. Proceedings of the National Academy of Sciences of the United States of America. 113(17):E2363-72

Zheng, W., Shen, F., Hu, R., Roy, B., Yang, J., Wang, Q., Zhang, F., King, J.C., Sergi, C., Liu, S.M., Cordat, E., Tang, J., Cao, Y., Ali, D., Chen, X.Z. (2016) Far Upstream Element-Binding Protein 1 Binds the 3' Untranslated Region of PKD2 and Suppresses Its Translation. Journal of the American Society of Nephrology : JASN. 27(9):2645-57

Roxo-Rosa, M., Jacinto, R., Sampaio, P., Lopes, S.S. (2015) The zebrafish Kupffer's vesicle as a model system for the molecular mechanisms by which the lack of Polycystin-2 leads to stimulation of CFTR. Biology Open. 4(11):1356-66

Beck, B.B., Phillips, J.B., Bartram, M.P., Wegner, J., Thoenes, M., Pannes, A., Sampson, J., Heller, R., Göbel, H., Koerber, F., Neugebauer, A., Hedergott, A., Nürnberg, G., Nürnberg, P., Thiele, H., Altmüller, J., Toliat, M.R., Staubach, S., Boycott, K.M., Valente, E.M., Janecke, A.R., Eisenberger, T., Bergmann, C., Tebbe, L., Wang, Y., Wu, Y., Fry, A.M., Westerfield, M., Wolfrum, U., Bolz, H.J. (2014) Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy. Human Mutation. 35(10):1153-62

Le Corre, S., Eyre, D., Drummond, I.A. (2014) Modulation of the Secretory Pathway Rescues Zebrafish Polycystic Kidney Disease Pathology. Journal of the American Society of Nephrology : JASN. 25(8):1749-59

Adams, M., Simms, R.J., Abdelhamed, Z., Dawe, H.R., Szymanska, K., Logan, C.V., Wheway, G., Pitt, E., Gull, K., Knowles, M.A., Blair, E., Cross, S.H., Sayer, J.A., and Johnson, C.A. (2012) A meckelin-filamin A interaction mediates ciliogenesis. Human molecular genetics. 21(6):1272-1286

Bouvrette, D.J., Sittaramane, V., Heidel, J.R., Chandrasekhar, A., and Bryda, E.C. (2010) Knockdown of bicaudal C in zebrafish (Danio rerio) causes cystic kidneys: a nonmammalian model of polycystic kidney disease. Comparative medicine. 60(2):96-106

Sullivan-Brown, J., Schottenfeld, J., Okabe, N., Hostetter, C.L., Serluca, F.C., Thiberge, S.Y., and Burdine, R.D. (2008) Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants. Developmental Biology. 314(2):261-275

van Rooijen, E., Giles, R.H., Voest, E.E., van Rooijen, C., Schulte-Merker, S., and van Eeden, F.J. (2008) LRRC50, a Conserved Ciliary Protein Implicated in Polycystic Kidney Disease. Journal of the American Society of Nephrology : JASN. 19(6):1128-1138