Subramanian, B., Ko, W.C., Yadav, V., Desrochers, T.M., Perrone, R.D., Zhou, J., and Kaplan, D.L. The regulation of cystogenesis in a tissue engineered kidney disease system by abnormal matrix interactions. Biomaterials. 2012, 1-13.
Zhou, J., Chang, M., Signoretti, S., & Kaelin, W. Genetic and Functional Studies Implicate HIF1a as a 14q Kidney Cancer Suppressor Gene. Cancer Discovery. 2011
Zhou X, Bao H, Takakura A, Zhou J, Albert M, Sun Y. Polycystic kidney disease evaluation by magnetic resonance imaging in ischemia-reperfusion injured PKD1 knockout mouse model: comparison of T2-weighted FSE and true-FISP. Invest Radiol, 2010 vol. 45 (1) pp. 24-8
Zhang J, Wu M, Wang S, Shah J, Wilson PD, Zhou, J. Polycystic kidney disease protein fibrocystin localizes to the mitotic spindle and regulates spindle bipolarity. Hum Mol Genet, Sep 1;19(17):3306-19. Epub 2010 Jun 16.
Qin S, Taglienti M, Nauli SM, Contrino L, Takakura A, Zhou J, Kreidberg JA. Failure to ubiquitinate c-Met leads to hyperactivation of mTOR signaling in a mouse model of autosomal dominant polycystic kidney disease. J Clin Invest. 2010 Oct 1;120(10):3617-28. doi: 10.1172/JCI41531. Epub 2010 Sep 13.
G. V. Z. Dedoussis, Y. Luo, P. Starremans, S. Rossetti, A. J. Ramos, H. F. Cantiello, E. Katsareli,
P. Ziroyannis, K. Lamnissou, P. C. Harris and J. Zhou. Co-inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney disease. Eur J Clin Invest 38 (3): 180?90,2008
Surya M. Nauli, Yoshifumi Kawanabe, John J. Kaminski, William J. Pearce, Donald, E. Ingber and Jing Zhou. Endothelial Cilia Are Fluid Shear Sensors That Regulate Calcium Signaling and Nitric Oxide Production Through Polycystin-1. Circulation 117;1161-1171, 2008
PG Starremans, X Li, PE Finnerty, L Guo, A Takakura, EG Neilson and J Zhou. A mouse model for polycystic kidney disease through a somatic in-frame deletion in the 50 end of Pkd1. Kidney International 73, 1394?405, 2008
Yu Tian, Robert Kolb, Jeong-Ho Hong, John Carroll, Dawei Li, John You, Roderick Bronson,
Michael B. Yaffe, Jing Zhou, and Thomas Benjamin1. TAZ Promotes PC2 Degradation through a SCFb-Trcp E3 Ligase Complex. J Am Soc Nephrol 19: 469–476, 2008.
Wang SX, Zhang JJ, Nauli SM, Li X, Starremans P, Luo Y, Roberts KA, Zhou J. Fibrocystin is associated with polycystin-2 and regulates intracellular calcium concentration. Mol Cell Biol. 27(8):3241-52, 2007.
Nauli SM, Rossetti S, Kolb RJ, Alenghat AJ, Harris PC, Ingber DE, Loghman-Adham M, Zhou J, Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction. J Am Soc Nephrol, 2006, Apr;17(4):1015-25
Li XG, Luo Y, Starremans P, McNamara CA, Pei Y, and Zhou J. Polycystin-1 and polycystin-2 regulate the cell cycle through the helix-loop-helix inhibitor Id2. Nat Cell Biol, 2005 Dec;7(12):1102-12. Epub 2005 Nov 27.
Delmas P, Nauli SM, Li X, Lakkis M, Luo Y, Elia A, Williams E, Frischauf AM, Crest M, Brown DA and Zhou J. Gating of the polycystin channel complex by conformational change of polycystin-1. FASEB, 2004 Apr;18(6):740-2.
Herzog C, Zhuang LY, Gorgan, L, Segal Y, and Zhou J. Identification of cis-regulatory elements that contribute to tissue- and site-specific a5(IV) and a6(IV) collagen expression in vivo. Biochem Biophys Res Commun 2003, Nov 14;311(2):553-60.
Nauli SM, Alenghat FJ, Luo Y, Williams E, Vassilev P, Li X, Elia AEH, Lu W, Brown EM, Quinn SJ, Ingber DE, and Zhou J. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nature Genetics (Article), 2003 Feb;33(2):129-37.
Yuasa T, Venugopal B, Weremowicz S, Morton CC, Guo L, and Zhou J. A Novel Polycystic Kidney Disease 1 Like Gene, PKD1L1, in Human: Sequence, Expression, and Chromosomal Localization. Genomics, 2002 Mar;79(3):376-86.
Delmas P, Nomura H, Li X, Lakkis M, Luo Y, Segal Y, Fern?dez-Fern?dez J, Harris P, Frischauf AM, Brown DA and Zhou J. Constitutive activation of G-proteins by polycystin-1 is antagonized by polycystin-2. J. Biol. Chem, 2002, Mar 29;277(13):11276-83.
Basora N, Nomura H, Berger U, Stayner C, Guo L, Shen XH, and Zhou J. Tissue and cellular localization of a novel polycystic kidney disease-like gene product, polycystin-L. J Am Soc Nephrol 2002 Feb;13(2):293-301.
Lu WN, Shen X, Pavlova A, Lakkis M, Ward C, Pritchard L, Harris P, Genest D, Perez-Atayde A, and Zhou J. Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects. Hum Mol Genetics. 2001, Oct 2;10(21):2385-2396.
Vassilev P, Guo L, Chen XZ, Segal Y, Peng JB, Basora N, Babakhanlou H, Cruger G, Kanazirska M, Ye CP, Brown EM, Hediger MA, and Zhou J. Polycystic kidney disease 2 gene encodes a novel high conductance channel implicated in defective intracellular Ca2+ homeostasis. Biochem Biophys Res Commun 2001, Mar 23;282(1):341-350.
Chen XZ, Segal Y, Basora N, Guo L, Peng JB, Babakhanlou H, Vassilev P, Brown EM, Hediger MA, and Zhou J. The transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X. Biochem Biophys Res Commun 2001 Apr 20;282(5):1251-6.
Guo L, Schreiber TH, Weremowicz S, Morton CC, and Zhou J. Molecular cloning and characterization of a novel polycystin family member, polycystin-l2, in mouse and man. Genomics. 2000, Mar:64,241-251.
Guo, L, Chen, MH, Basora, N, and Zhou, J. The human polycystic kidney disease 2-like (PKDL) gene: exon/intron structure and evidence for a novel splicing mechanism. Mammalian Genome, 2000 Jan;11(1):46-50.
Chen, XZ, Vassilev, PM, Basora, N, Peng, JP, Nomura, N, Segal, Y, Brown, EB, Reeders, ST, Hediger, MA, and Zhou, J. Polycystin-L, a member of the polycystin family of proteins, is a calcium-permeable cation channel. Nature, 1999, 401, 383-386.
Lu WN, Fan XH, Basora N, Babakhanlou H, Law T, Rifai N, Harris PC, Perez-Atayde AR, Rennke HG and Zhou J. Late onset of renal and hepatic cysts in mice heterozygous for a Pkd1 mutation. Nature Genetics 1999, 21(2):160-161.
Segal Y, Peissel B, Renieri A, de Marchi M, Ballabio A, Pei Y, and Zhou J: Line-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis, Am J Hum Genet 1999 Jan;64(1):62-9.
Nomura H, Turco AE, Pei Y, Kalaydjieva L, Weremowicz S, Ji W, Morton C, Meisler M, Reeders, ST, and Zhou J. Identification of PKDL, a novel polycystic kidney disease 2-like gene, whose murine homologue is deleted in mice with kidney and retinal defects. J. Biol. Chem, 1998, 273(40):25967-25973.
Geng L, Segal Y, Pavlova A, Barros EJG.; L?ning C, Lu W, Nigam S.K, Frischauf AM, Reeders ST and Zhou J. Distribution and developmentally regulated expression of murine polycystin. Am J Physiol, F451-F459, 1997.
Lu WN, Peissel B, Babakhanlou H, Fan XH, Pavlova A, Geng L, Larson C, Brent G, and Zhou J. Perinatal lethality and defects with kidneys and pancreas defects in mice with targeted Pkd1 mutations. Nature Genetics, 1997; 17:179-181.
Geng L, Segal Y, Peissel B, Deng N, Pei Y, Carone F, Rennke HG, Glucksmann-Kuis S, Schneider MC, Ericsson M, Reeders ST and Zhou J. Identification and Localization of Polycystin, the PKD1 Gene Product. J Clin Invest. 1996; 98:2674-2682.
Peissel, B, Geng L, Kalluri R, Kashtan K, Rennke HG, Gallo GR, Sun MJ, Hudson BG, Neilson EG and Zhou J. Comparative distribution of the a1(IV), a5(IV) and a6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients. J Clin Invest. 1995; 96: 1948-1957.
Zhou J, Gregory MC, Hertz JM, Barker DF, Atkin C, Spencer E, Tryggvason K. Mutations in the codon for a conserved arginine-1563 in three unrelated families with Alport syndrome. Kidney Int 1993; 43:722-9.
Barker D, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC, Gregory MC, Skolnick MH, Atkin CL, Tryggvason K. Identification of mutations in the COL4A5 collagen gene in Alport syndrome. Science 1990; 248:1224-7.