Molecular fingerprinting of the podocyte reveals novel gene and protein regulatory networks von Boerries, Melanie, Grahammer, Florian, Eiselein, Sven, Buck, Moritz, Meyer, Charlotte, Goedel, Markus, Bechtel, Wibke, Zschiedrich, Stefan, Pfeifer, Dietmar, Laloë, Denis, Arrondel, Christelle, Gonçalves, Sara, Krüger, Marcus, Harvey, Scott J., Busch, Hauke, Dengjel, Joern, Huber, Tobias B.

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Podocyte-Specific Deletion of Dicer Alters Cytoskeletal Dynamics and Causes Glomerular Disease von HARVEY, Scott J, JARAD, George, CUNNINGHAM, Jeanette, GOLDBERG, Seth, SCHERMER, Bernhard, HARFE, Brian D, MCMANUS, Michael T, BENZING, Thomas, MINER, Jeffrey H

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Glomerular filtration is normal in the absence of both agrin and perlecan–heparan sulfate from the glomerular basement membrane von Goldberg, Seth, Harvey, Scott J., Cunningham, Jeanette, Tryggvason, Karl, Miner, Jeffrey H.

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Models for Studies of Proteoglycans in Kidney Pathophysiology von Harvey, Scott J.

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A hypomorphic mutation in the mouse laminin α5 gene causes polycystic kidney disease von BRENDAN SHANNON, M, PATTON, Bruce L, HARVEY, Scott J, MINER, Jeffrey H

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MicroRNAs and the kidney: coming of age von Saal, Samuel, Harvey, Scott J

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Disruption of Glomerular Basement Membrane Charge through Podocyte-Specific Mutation of Agrin Does Not Alter Glomerular Permselectivity von Harvey, Scott J, Jarad, George, Cunningham, Jeanette, Rops, Angelique L, van der Vlag, Johan, Berden, Jo H, Moeller, Marcus J, Holzman, Lawrence B, Burgess, Robert W, Miner, Jeffrey H

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Revisiting the glomerular charge barrier in the molecular era von Harvey, Scott J, Miner, Jeffrey H

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Discovery of microvascular miRNAs using public gene expression data: miR-145 is expressed in pericytes and is a regulator of Fli1 von Larsson, Erik, Fredlund Fuchs, Peder, Heldin, Johan, Barkefors, Irmeli, Bondjers, Cecilia, Genové, Guillem, Arrondel, Christelle, Gerwins, Pär, Kurschat, Christine, Schermer, Bernhard, Benzing, Thomas, Harvey, Scott J, Kreuger, Johan, Lindahl, Per

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Transfer of the α5(IV) Collagen Chain Gene to Smooth Muscle Restores in Vivo Expression of the α6(IV) Collagen Chain in a Canine Model of Alport Syndrome von Harvey, Scott J., Zheng, Keqin, Jefferson, Barbara, Moak, Peter, Sado, Yoshikazu, Naito, Ichiro, Ninomiya, Yoshifumi, Jacobs, Robert, Thorner, Paul S.

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Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome von Lee, Brendan, Morello, Roy, Zhou, Guang, Dreyer, Sandra D, Harvey, Scott J, Ninomiya, Yoshifumi, Thorner, Paul S, Miner, Jeffrey H, Cole, William, Winterpacht, Andreas, Zabel, Bernhard, Oberg, Kerby C

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DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria von Gross, Oliver, Beirowski, Bogdan, Harvey, Scott J., Mcfadden, Catherine, Chen, Dilys, Tam, Stephanie, Thorner, Paul S., Smyth, Neil, Addicks, Klaus, Bloch, Wilhelm, Ninomiya, Yoshifumi, Sado, Yoshikazu, Weber, Manfred, Vogel, Wolfgang F.

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Cyclosporine A slows the progressive renal disease of Alport syndrome (X-linked hereditary nephritis): Results from a canine model von CHEN, Dilys, JEFFERSON, Barbara, HARVEY, Scott J, ZHENG, Keqin, GARTLEY, Cathy J, JACOBS, Robert M, THORNER, Paul S

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Breaking down the barrier: evidence against a role for heparan sulfate in glomerular permselectivity von Harvey, Scott J, Miner, Jeffrey H

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Sequential Expression of Type IV Collagen Networks: Testis as a Model and Relevance to Spermatogenesis von Harvey, Scott J., Perry, Julie, Zheng, Keqin, Chen, Dilys, Sado, Yoshikazu, Jefferson, Barbara, Ninomiya, Yoshifumi, Jacobs, Robert, Hudson, Billy G., Thorner, Paul S.

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Role of distinct type IV collagen networks in glomerular development and function von Harvey, Scott J., Zheng, Keqin, Sado, Yoshikazu, Naito, Ichiro, Ninomiya, Yoshifumi, Jacobs, Robert M., Hudson, Billy G., Thorner, Paul S.

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The Inner Ear of Dogs with X-Linked Nephritis Provides Clues to the Pathogenesis of Hearing Loss in X-Linked Alport Syndrome von Harvey, Scott J., Mount, Richard, Sado, Yoshikazu, Naito, Ichiro, Ninomiya, Yoshifumi, Harrison, Robert, Jefferson, Barbara, Jacobs, Robert, Thorner, Paul S.

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Regulation of collagen type IV genes is organ-specific: Evidence from a canine model of Alport syndrome von Zheng, Keqin, Perry, Julie, Harvey, Scott J., Sado, Yoshikazu, Ninomiya, Yoshifumi, Jefferson, Barbara, Jacobs, Robert, Hudson, Billy G., Thorner, Paul S.

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A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease von Shannon, M Brendan, Patton, Bruce L, Harvey, Scott J, Miner, Jeffrey H

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Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Commentary. Author's reply von KANWAR, Yashpal S, DANESH, Farhad R, HOLZMAN, Lawrence B, BURGESS, Robert W, MINER, Jeffrey H, CHUGH, Sumant S, HARVEY, Scott J, JARAD, George, CUNNINGHAM, Jeanette, ROPS, Angelique L, VAN DER VLAG, Johan, BERDEN, Jo H, MOELLER, Marcus J

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