Proteomic analysis of a eukaryotic cilium von Pazour, Gregory J, Agrin, Nathan, Leszyk, John, Witman, George B

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Intraflagellar transport and cilia-dependent renal disease: The ciliary hypothesis of polycystic kidney disease von PAZOUR, Gregory J

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The vertebrate primary cilium is a sensory organelle von Pazour, Gregory J, Witman, George B

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A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney von Sun, Zhaoxia, Amsterdam, Adam, Pazour, Gregory J, Cole, Douglas G, Miller, Mark S, Hopkins, Nancy

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Intraflagellar transport and cilia-dependent diseases von Pazour, Gregory J, Rosenbaum, Joel L

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Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease von Pazour, Gregory J, San Agustin, Jovenal T, Follit, John A, Rosenbaum, Joel L, Witman, George B

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Chlamydomonas IFT88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg737, Are Required for Assembly of Cilia and Flagella von Pazour, Gregory J., Dickert, Bethany L., Vucica, Yvonne, Seeley, E. Scott, Rosenbaum, Joel L., Witman, George B., Cole, Douglas G.

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The Intraflagellar Transport Protein, IFT88, Is Essential for Vertebrate Photoreceptor Assembly and Maintenance von Pazour, Gregory J., Baker, Sheila A., Deane, James A., Cole, Douglas G., Dickert, Bethany L., Rosenbaum, Joel L., Witman, George B., Besharse, Joseph C.

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Radial spoke proteins of Chlamydomonas flagella von Yang, Pinfen, Diener, Dennis R, Yang, Chun, Kohno, Takahiro, Pazour, Gregory J, Dienes, Jennifer M, Agrin, Nathan S, King, Stephen M, Sale, Winfield S, Kamiya, Ritsu, Rosenbaum, Joel L, Witman, George B

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DHC1b (DHC2) isoform of cytoplasmic dynein is required for flagellar assembly von Pazour, G.J, Dickert, B.L, Witman, G.B

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orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization von Cano, David A, Murcia, Noel S, Pazour, Gregory J, Hebrok, Matthias

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Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes von Pazour, G J, Agrin, N, Walker, B L, Witman, G B

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Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia von Thevenon, J., Duplomb, L., Phadke, S., Eguether, T., Saunier, A., Avila, M., Carmignac, V., Bruel, A.-L., St-Onge, J., Duffourd, Y., Pazour, G.J., Franco, B., Attie-Bitach, T., Masurel-Paulet, A., Rivière, J.-B., Cormier-Daire, V., Philippe, C., Faivre, L., Thauvin-Robinet, C.

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Pericentrin Forms a Complex with Intraflagellar Transport Proteins and Polycystin-2 and Is Required for Primary Cilia Assembly von Jurczyk, Agata, Gromley, Adam, Redick, Sambra, San Agustin, Jovenal, Witman, George, Pazour, Gregory J., Dorien J. M. Peters, Doxsey, Stephen

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A dynein light chain is essential for the retrograde particle movement of intraflagellar transport (IFT) von Pazour, G.J. (University of Massachusetts Medical Center, Shrewberry, MA.), Wilkerson, C.G, Witman, G.B

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A dynein light intermediate chain, D1bLIC, is required for retrograde intraflagellar transport von Hou, Yuqing, Pazour, Gregory J, Witman, George B

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IFT20 Links Kinesin II with a Mammalian Intraflagellar Transport Complex That Is Conserved in Motile Flagella and Sensory Cilia von Baker, Sheila A., Freeman, Katie, Luby-Phelps, Katherine, Pazour, Gregory J., Besharse, Joseph C.

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The role of intraflagellar transport proteins in ciliary assembly and function von Pazour, GJ

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Comparative Genomics: Prediction of the Ciliary and Basal Body Proteome von Pazour, Gregory J

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Localization of transient receptor potential ion channels in primary and motile cilia of the female murine reproductive organs von Teilmann, Stefan C., Byskov, Anne Grete, Pedersen, Per A., Wheatley, Denys N., Pazour, Gregory J., Christensen, Søren T.

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