FSGS

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Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach
An S. De Vriese, Sanjeev Sethi, Karl A. Nath, Richard J. Glassock and Fernando C. Fervenza

JASN March 2018, 29 (3) 759-774; DOI: https://doi.org/10.1681/ASN.2017090958

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Podocyte Growing Pains in Adaptive FSGS
Vivette D. D’Agati

JASN October 2017, 28 (10) 2825-2827; DOI: https://doi.org/10.1681/ASN.2017060612

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Glomerulosclerosis Induced by Deficiency of Membrane-Associated Guanylate Kinase Inverted 2 in Kidney Podocytes
Naritoshi Shirata, Kan-ichiro Ihara, Kanae Yamamoto-Nonaka, Takuto Seki, Shin-ichi Makino, Juan Alejandro Oliva Trejo, Takafumi Miyake, Hiroyuki Yamada, Kirk Nicholas Campbell, Takahiko Nakagawa, Kiyoshi Mori, Motoko Yanagita, Peter Mundel, Katsuhiko Nishimori and Katsuhiko Asanuma

JASN September 2017, 28 (9) 2654-2669; DOI: https://doi.org/10.1681/ASN.2016121356

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Synaptopodin Is a Coincidence Detector of Tyrosine versus Serine/Threonine Phosphorylation for the Modulation of Rho Protein Crosstalk in Podocytes
Lisa Buvall, Hanna Wallentin, Jonas Sieber, Svetlana Andreeva, Hoon Young Choi, Peter Mundel and Anna Greka

JASN March 2017, 28 (3) 837-851; DOI: https://doi.org/10.1681/ASN.2016040414

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Murine Double Minute-2 Prevents p53-Overactivation-Related Cell Death (Podoptosis) of Podocytes
Dana Thomasova, Hauke A. Bruns, Victoria Kretschmer, Martrez Ebrahim, Simone Romoli, Helen Liapis, Ahmed M. Kotb, Nicole Endlich and Hans-Joachim Anders

JASN July 2015, 26 (7) 1513-1523; DOI: https://doi.org/10.1681/ASN.2014040345

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Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial
Jeffrey B. Kopp, Cheryl A. Winkler, Xiongce Zhao, Milena K. Radeva, Jennifer J. Gassman, Vivette D. D’Agati, Cynthia C. Nast, Changli Wei, Jochen Reiser, Lisa M. Guay-Woodford, Martin R. Pollak, Friedhelm Hildebrandt, Marva Moxey-Mims, Debbie S. Gipson, Howard Trachtman, Aaron L. Friedman and Frederick J. Kaskel

JASN June 2015, 26 (6) 1443-1448; DOI: https://doi.org/10.1681/ASN.2013111242

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Apolipoprotein L1-Associated Nephropathy and the Future of Renal Diagnostics
Christopher P. Larsen and Barry I. Freedman

JASN June 2015, 26 (6) 1232-1235; DOI: https://doi.org/10.1681/ASN.2014101052

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A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
Carolin E. Sadowski, Svjetlana Lovric, Shazia Ashraf, Werner L. Pabst, Heon Yung Gee, Stefan Kohl, Susanne Engelmann, Virginia Vega-Warner, Humphrey Fang, Jan Halbritter, Michael J. Somers, Weizhen Tan, Shirlee Shril, Inès Fessi, Richard P. Lifton, Detlef Bockenhauer, Sherif El-Desoky, Jameela A. Kari, Martin Zenker, Markus J. Kemper, Dominik Mueller, Hanan M. Fathy, Neveen A. Soliman, the SRNS Study Group and Friedhelm Hildebrandt

JASN June 2015, 26 (6) 1279-1289; DOI: https://doi.org/10.1681/ASN.2014050489

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Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD
Nicholette D. Palmer, Maggie C.Y. Ng, Carl D. Langefeld, Jasmin Divers, Janice P. Lea, Mark D. Okusa, Robert P. Kimberly, Donald W. Bowden and Barry I. Freedman

JASN May 2015, 26 (5) 1021-1025; DOI: https://doi.org/10.1681/ASN.2014050444

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A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
Gentzon Hall, Rasheed A. Gbadegesin, Peter Lavin, Guanghong Wu, Yangfan Liu, Edwin C. Oh, Liming Wang, Robert F. Spurney, Jason Eckel, Thomas Lindsey, Alison Homstad, Andrew F. Malone, Paul J. Phelan, Andrey Shaw, David N. Howell, Peter J. Conlon, Nicholas Katsanis and Michelle P. Winn

JASN April 2015, 26 (4) 831-843; DOI: https://doi.org/10.1681/ASN.2013101053

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