TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function von Reiser, Jochen, Pollak, Martin R, Polu, Krishna R, Möller, Clemens C, Kenlan, Peter, Altintas, Mehmet M, Wei, Changli, Faul, Christian, Herbert, Stephanie, Villegas, Ivan, Avila-Casado, Carmen, McGee, Mary, Sugimoto, Hikaru, Brown, Dennis, Kalluri, Raghu, Mundel, Peter, Smith, Paula L, Clapham, David E

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Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor von Scadden, David T, Adams, Gregor B, Chabner, Karissa T, Alley, Ian R, Olson, Douglas P, Szczepiorkowski, Zbigniew M, Poznansky, Mark C, Kos, Claudine H, Pollak, Martin R, Brown, Edward M

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Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation von Berrigan, Margaret, Austrie, Jasmine, Fleishman, Aaron, Tercyak, Kenneth P., Pollak, Martin R., Pavlakis, Martha, Rohan, Vinayak, Baliga, Prabhakar K., Kayler, Liise K., Feeley, Thomas H., Rodrigue, James R.

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Mutations in ACTN4 , encoding α-actinin-4, cause familial focal segmental glomerulosclerosis von Kaplan, Joshua M, Rennke, Helmut, North, Kathryn N, A Correia, Lori, Rodríguez-Pérez, José-Carlos, Pollak, Martin R, Beggs, Alan H, Tong, Hui-Qi, Allen, Philip G, H Kim, Sung, Mathis, Beverly J

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Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint von POLLAK, Martin R

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Mutational and biological analysis of α-actinin-4 in focal segmental glomerulosclerosis von WEINS, Astrid, KENLAN, Peter, HERBERT, Stephanie, LE, Tu C, VILLEGAS, Ivan, KAPLAN, Bernard S, APPEL, Gerald B, POLLAK, Martin R

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Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein von Yao, June, Le, Tu Cam, Kos, Claudine H, Henderson, Joel M, Allen, Phillip G, Denker, Bradley M, Pollak, Martin R

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Mice deficient in alpha -actinin-4 have severe glomerular disease von Kos, CH, Le, T C, Sinha, S, Henderson, J M, Kim, SH, Sugimoto, H, Kalluri, R, Gerszten, R E, Pollak, M R

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The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone von Kos, CH, Karaplis, A C, Peng, Ji-Bin, Hediger, MA, Goltzman, D, Mohammad, K S, Guise, T A, Pollak, M R

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NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele von Tsukaguchi, H, Sudhakar, A, Le, T C, Nguyen, T, Yao, J, Schwimmer, JA, Schachter, AD, Poch, E, Abreu, P F, Appel, G B, Pereira, AB, Kalluri, R, Pollak, M R

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A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism von Ho, Chrystal, Conner, David A, Pollak, Martin R, Ladd, Daniel J, Kifor, Olga, Warren, Henry B, Brown, Edward M, Seidman, J.G, Seidman, Christine E

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The genetic basis of FSGS and steroid-resistant nephrosis von Pollak, Martin R.

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NPHS2 R229Q functional variant is associated with microalbuminuria in the general population von Pereira, Alexandre C., Pereira, Aparecido B., Mota, Glória F., Cunha, Roberto S., Herkenhoff, Fernando L., Pollak, Martin R., Mill, José G., Krieger, José E.

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Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism von POLLAK, M. R, BROWN, E. M, YAH-HUEI WU CHOU, HEBERT, S. C, MARX, S. J, STEINMANN, B, LEVI, T, SEIDMAN, C. E, SEIDMAN, J. G

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Extracellular calcium elicits a chemokinetic response from monocytes in vitro and in vivo von Olszak, I. T., Poznansky, M. C., Evans, R. H., Olson, D., Kos, C., Pollak, M. R., Brown, E. M., Scadden, D. T., O'Malley, B. W.

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Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction f... von HUNT, Jennifer L, POLLAK, Martin R, DENKER, Bradley M

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Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation von Ellinor, P T, Moore, R K, Patton, K K, Ruskin, J N, Pollak, M R, MacRae, C A

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Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism : effects of mutant gene dosage on phenotype von POLLAK, M. R, YAH-HUEI CHOU, SEIDMAN, C. E, SEIDMAN, J. G, MARX, S. J, STEINMANN, B, COLE, D. E. C, BRANDI, M. L, PAPAPOULOS, S. E, MENKO, F. H, HENDY, G. N, BROWN, E. M

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A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13 von Mathis, Beverly J., Kim, Sung H., Calabrese, Kenneth, Haas, Mark, Seidman, J.G., Seidman, Christine E., Pollak, Martin R.

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A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31 von TSUKAGUCHI, Hiroyasu, YAGER, Henry, DAWBORN, John, JOST, Luis, COHLMIA, Jerry, ABREU, Patricia F, PEREIRA, Aparecido B, POLLAK, Martin R

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