R. J. Russo

Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisis

Laurie A. Smith, L. Meijer, G. Carlson, 2016, Human molecular genetics.

Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease.

Laurie A. Smith, O. Ibraghimov-Beskrovnaya, D. Beier, 2006, Journal of the American Society of Nephrology : JASN.

Impaired formation of desmosomal junctions in ADPKD epithelia

O. Ibraghimov-Beskrovnaya, H. Husson, N. Bukanov, 2005, Histochemistry and Cell Biology.

Correction of cilia structure and function alleviates multi-organ pathology in Bardet–Biedl syndrome mice

Laurie A. Smith, K. Klinger, O. Ibraghimov-Beskrovnaya, 2020, Human molecular genetics.

Canine PKD1 is a single-copy gene: genomic organization and comparative analysis.

K. Klinger, O. Ibraghimov-Beskrovnaya, P. Manavalan, 2002, Genomics.

Inhibition of TGF‐β Increases Bone Volume and Strength in a Mouse Model of Osteogenesis Imperfecta

J. Nyman, O. Ibraghimov-Beskrovnaya, R. J. Russo, 2021, JBMR plus.