My, oh, MYO9A! Just how complex can regulation of the podocyte actin cytoskeleton get? von Schlondorff, Johannes S.

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Variant upon variant: kidney-disease risk associated with APOL1 G2 genetic variants is abrogated by the APOL1 p.N264K variant von Madhavan, Sethu M., Schlöndorff, Johannes S.

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Gain-of-function, focal segmental glomerulosclerosis Trpc6 mutation minimally affects susceptibility to renal injury in several mouse models von Brown, Brittney J, Boekell, Kimber L, Stotter, Brian R, Talbot, Brianna E, Schlondorff, Johannes S

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Transmembrane insertases and N-glycosylation critically determine synthesis, trafficking, and activity of the nonselective cation channel TRPC6 von Talbot, Brianna E., Vandorpe, David H., Stotter, Brian R., Alper, Seth L., Schlondorff, Johannes S.

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Trpc6 gain-of-function disease mutation enhances phosphatidylserine exposure in murine platelets von Boekell, Kimber L, Brown, Brittney J, Talbot, Brianna E, Schlondorff, Johannes S

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Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury von Subramanian, Balajikarthick, Sun, Hua, Yan, Paul, Charoonratana, Victoria T., Higgs, Henry N., Wang, Fang, Lai, Ka-Man V., Valenzuela, David M., Brown, Elizabeth J., Schlöndorff, Johannes S., Pollak, Martin R.

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Disease-associated mutant α-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity von Weins, Astrid, Schlondorff, Johannes S, Nakamura, Fumihiko, Denker, Bradley M, Hartwig, John H, Stossel, Thomas P, Pollak, Martin R

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Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2) von Sun, Hua, Schlondorff, Johannes S, Brown, Elizabeth J, Higgs, Henry N, Pollak, Martin R

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Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related Podocytopathy von Sun, Hua, Perez-Gill, Chandra, Schlondorff, Johannes S., Subramanian, Balajikarthick, Pollak, Martin R.

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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis von Pollak, Martin R, Brown, Elizabeth J, Schlöndorff, Johannes S, Becker, Daniel J, Tsukaguchi, Hiroyasu, Tonna, Stephen J, Uscinski, Andrea L, Higgs, Henry N, Henderson, Joel M

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Genetic evaluation of living kidney donor candidates: A review and recommendations for best practices von Thomas, Christie P., Daloul, Reem, Lentine, Krista L., Gohh, Reginald, Anand, Prince M., Rasouly, Hila Milo, Sharfuddin, Asif A., Schlondorff, Johannes S., Rodig, Nancy M., Freese, Margaret E., Garg, Neetika, Lee, Brian K., Caliskan, Yasar

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Cosmc-dependent mucin-type O-linked glycosylation is essential for podocyte function von Stotter, Brian R., Talbot, Brianna E., Capen, Diane E., Artelt, Nadine, Zeng, Junwei, Matsumoto, Yasuyuki, Endlich, Nicole, Cummings, Richard D., Schlondorff, Johannes S.

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FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes von Subramanian, Balajikarthick, Chun, Justin, Perez-Gill, Chandra, Yan, Paul, Stillman, Isaac E., Higgs, Henry N., Alper, Seth L., Schlondorff, Johannes S., Pollak, Martin R.

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APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases von Olabisi, Opeyemi A., Zhang, Jia-Yue, VerPlank, Lynn, Zahler, Nathan, DiBartolo, Salvatore, Heneghan, John F., Schlöndorff, Johannes S., Suh, Jung Hee, Yan, Paul, Alper, Seth L., Friedman, David J., Pollak, Martin R.

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Functional genetic variation in aminopeptidase A (ENPEP): Lack of clear association with focal and segmental glomerulosclerosis (FSGS) von Tonna, Stephen, Dandapani, Savita V., Uscinski, Andrea, Appel, Gerald B., Schlöndorff, Johannes S., Zhang, Kang, Denker, Bradley M., Pollak, Martin R.

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234 von Weins, Astrid, Schlondorff, Johannes S, Nakamura, Fumihiko, Pollak, Martin R

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TRPC6 in glomerular health and disease: What we know and what we believe von Schlöndorff, Johannes S., Pollak, Martin R.

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Gain-of-function, focal segmental glomerulosclerosis Trpc6 mutation minimally affects susceptibility to renal injury in several mouse models von Brittney J Brown, Kimber L Boekell, Brian R Stotter, Brianna E Talbot, Johannes S Schlondorff

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Increased Phosphorylation of ACTN4 Leads to Podocyte Dysfunction and Focal Segmental Glomerulosclerosis Mimicking Disease-Causing Mutations: PO1587 von Feng, Di, Kumar, Mukesh, Muntel, Jan, Gurley, Susan B., Birrane, Gabriel, Stillman, Isaac E., Ding, Lai, Wang, Minxian, Ahmed, Saima, Schlondorff, Johannes S., Alper, Seth L., Ferrante, Thomas, Marquez, Susan, Ng, Carlos F., Novak, Richard, Ingber, Donald E., Steen, Hanno, Pollak, Martin R.

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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

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