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genetic renal disease

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    The Search for Monogenic Causes of Kidney Stones
    David S. Goldfarb
    JASN March 2015, 26 (3) 507-510; DOI: https://doi.org/10.1681/ASN.2014090847
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    Exonic Mutations in the SLC12A3 Gene Cause Exon Skipping and Premature Termination in Gitelman Syndrome
    Yoichi Takeuchi, Eikan Mishima, Hisato Shima, Yasutoshi Akiyama, Chitose Suzuki, Takehiro Suzuki, Takayasu Kobayashi, Yoichi Suzuki, Tomohiro Nakayama, Yasuhiro Takeshima, Norma Vazquez, Sadayoshi Ito, Gerardo Gamba and Takaaki Abe
    JASN February 2015, 26 (2) 271-279; DOI: https://doi.org/10.1681/ASN.2013091013
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    A Novel Atypical Hemolytic Uremic Syndrome–Associated Hybrid CFHR1/CFH Gene Encoding a Fusion Protein That Antagonizes Factor H–Dependent Complement Regulation
    Elisabetta Valoti, Marta Alberti, Agustin Tortajada, Jesus Garcia-Fernandez, Sara Gastoldi, Luca Besso, Elena Bresin, Giuseppe Remuzzi, Santiago Rodriguez de Cordoba and Marina Noris
    JASN January 2015, 26 (1) 209-219; DOI: https://doi.org/10.1681/ASN.2013121339
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    Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing
    Vincent Morinière, Karin Dahan, Pascale Hilbert, Marieline Lison, Said Lebbah, Alexandra Topa, Christine Bole-Feysot, Solenn Pruvost, Patrick Nitschke, Emmanuelle Plaisier, Bertrand Knebelmann, Marie-Alice Macher, Laure-Hélène Noel, Marie-Claire Gubler, Corinne Antignac and Laurence Heidet
    JASN December 2014, 25 (12) 2740-2751; DOI: https://doi.org/10.1681/ASN.2013080912
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    Lupus Nephritis Susceptibility Loci in Women with Systemic Lupus Erythematosus
    Sharon A. Chung, Elizabeth E. Brown, Adrienne H. Williams, Paula S. Ramos, Celine C. Berthier, Tushar Bhangale, Marta E. Alarcon-Riquelme, Timothy W. Behrens, Lindsey A. Criswell, Deborah Cunninghame Graham, F. Yesim Demirci, Jeffrey C. Edberg, Patrick M. Gaffney, John B. Harley, Chaim O. Jacob, M. Ilyas Kamboh, Jennifer A. Kelly, Susan Manzi, Kathy L. Moser-Sivils, Laurie P. Russell, Michelle Petri, Betty P. Tsao, Tim J. Vyse, Raphael Zidovetzki, Matthias Kretzler, Robert P. Kimberly, Barry I. Freedman, Robert R. Graham and Carl D. Langefeld
    JASN December 2014, 25 (12) 2859-2870; DOI: https://doi.org/10.1681/ASN.2013050446
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    A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS
    Evelyne Huynh Cong, Albane A. Bizet, Olivia Boyer, Stéphanie Woerner, Olivier Gribouval, Emilie Filhol, Christelle Arrondel, Sophie Thomas, Flora Silbermann, Guillaume Canaud, Jamil Hachicha, Nasr Ben Dhia, Marie-Noëlle Peraldi, Kais Harzallah, Daouia Iftene, Laurent Daniel, Marjolaine Willems, Laure-Hélène Noel, Christine Bole-Feysot, Patrick Nitschké, Marie-Claire Gubler, Géraldine Mollet, Sophie Saunier and Corinne Antignac
    JASN November 2014, 25 (11) 2435-2443; DOI: https://doi.org/10.1681/ASN.2013101126
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    Race, Class, and AKI
    Sevag Demirjian
    JASN August 2014, 25 (8) 1615-1617; DOI: https://doi.org/10.1681/ASN.2014030275
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    Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
    Ekim Z. Taskiran, Emine Korkmaz, Safak Gucer, Can Kosukcu, Figen Kaymaz, Cansu Koyunlar, Elizabeth C. Bryda, Moumita Chaki, Dongmei Lu, Komal Vadnagara, Cengiz Candan, Rezan Topaloglu, Franz Schaefer, Massimo Attanasio, Carsten Bergmann and Fatih Ozaltin
    JASN August 2014, 25 (8) 1653-1661; DOI: https://doi.org/10.1681/ASN.2013060646
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    MicroRNA-17~92 Is Required for Nephrogenesis and Renal Function
    April K. Marrone, Donna B. Stolz, Sheldon I. Bastacky, Dennis Kostka, Andrew J. Bodnar and Jacqueline Ho
    JASN July 2014, 25 (7) 1440-1452; DOI: https://doi.org/10.1681/ASN.2013040390
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    Inflammasome Activation by Cystine Crystals: Implications for the Pathogenesis of Cystinosis
    Giusi Prencipe, Ivan Caiello, Stephanie Cherqui, Thomas Whisenant, Stefania Petrini, Francesco Emma and Fabrizio De Benedetti
    JASN June 2014, 25 (6) 1163-1169; DOI: https://doi.org/10.1681/ASN.2013060653
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