Electron microscopy image enhanced von Haider, Maximilian, Uhlemann, Stephan, Schwan, Eugen, Rose, Harald, Kabius, Bernd, Urban, Knut

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A spherical-aberration-corrected 200 kV transmission electron microscope von Haider, Max, Rose, Harald, Uhlemann, Stephan, Schwan, Eugen, Kabius, Bernd, Urban, Knut

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A spherical-aberration-corrected 200kV transmission electron microscope von Haider, Max, Rose, Harald, Uhlemann, Stephan, Schwan, Eugen, Kabius, Bernd, Urban, Knut

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ELECTRONIC APPARATUS AND METHOD OF MANUFACTURING ELECTRONIC DEVICE von NJIENDE, Hugues, TIKHONOV, Sergey, SCHWAN, Eugen

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ELECTRONIC APPARATUS AND MANUFACTURING METHOD FOR AN ELECTRONIC DEVICE von NJIENDE, Hugues, TIKHONOV, Sergey, SCHWAN, Eugen

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First application of a spherical‐aberration corrected transmission electron microscope in materials science von Kabius, Bernd, Haider, Max, Uhlemann, Stefan, Schwan, Eugen, Urban, Knut, Rose, Harald

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Mutations in WDR4 as a new cause of Galloway–Mowat syndrome von Braun, Daniela A., Shril, Shirlee, Sinha, Aditi, Schneider, Ronen, Tan, Weizhen, Ashraf, Shazia, Hermle, Tobias, Jobst‐Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J., Daga, Ankana, Warejko, Jillian K., Nakayama, Makiko, Schapiro, David, Chen, Jing, Airik, Merlin, Rao, Jia, Schmidt, Johanna Magdalena, Hoogstraten, Charlotte A., Hugo, Hannah, Meena, Jitendra, Lek, Monkol, Laricchia, Kristen M., Bagga, Arvind, Hildebrandt, Friedhelm

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Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment von Ashraf, Shazia, Kudo, Hiroki, Rao, Jia, Kikuchi, Atsuo, Widmeier, Eugen, Lawson, Jennifer A., Tan, Weizhen, Hermle, Tobias, Warejko, Jillian K., Shril, Shirlee, Airik, Merlin, Jobst-Schwan, Tilman, Lovric, Svjetlana, Braun, Daniela A., Gee, Heon Yung, Schapiro, David, Majmundar, Amar J., Sadowski, Carolin E., Pabst, Werner L., Daga, Ankana, van der Ven, Amelie T., Schmidt, Johanna M., Low, Boon Chuan, Gupta, Anjali Bansal, Tripathi, Brajendra K., Wong, Jenny, Campbell, Kirk, Metcalfe, Kay, Schanze, Denny, Niihori, Tetsuya, Kaito, Hiroshi, Nozu, Kandai, Tsukaguchi, Hiroyasu, Tanaka, Ryojiro, Hamahira, Kiyoshi, Kobayashi, Yasuko, Takizawa, Takumi, Funayama, Ryo, Nakayama, Keiko, Aoki, Yoko, Kumagai, Naonori, Iijima, Kazumoto, Fehrenbach, Henry, Kari, Jameela A., El Desoky, Sherif, Jalalah, Sawsan, Bogdanovic, Radovan, Stajić, Nataša, Zappel, Hildegard, Rakhmetova, Assel, Wassmer, Sharon-Rose, Jungraithmayr, Therese, Strehlau, Juergen, Kumar, Aravind Selvin, Bagga, Arvind, Soliman, Neveen A., Mane, Shrikant M., Kaufman, Lewis, Lowy, Douglas R., Jairajpuri, Mohamad A., Lifton, Richard P., Pei, York, Zenker, Martin, Kure, Shigeo, Hildebrandt, Friedhelm

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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients von Mann, Nina, Braun, Daniela A, Amann, Kassaundra, Tan, Weizhen, Shril, Shirlee, Connaughton, Dervla M, Nakayama, Makiko, Schneider, Ronen, Kitzler, Thomas M, van der Ven, Amelie T, Chen, Jing, Ityel, Hadas, Vivante, Asaf, Majmundar, Amar J, Daga, Ankana, Warejko, Jillian K, Lovric, Svjetlana, Ashraf, Shazia, Jobst-Schwan, Tilman, Widmeier, Eugen, Hugo, Hannah, Mane, Shrikant M, Spaneas, Leslie, Somers, Michael J G, Ferguson, Michael A, Traum, Avram Z, Stein, Deborah R, Baum, Michelle A, Daouk, Ghaleb H, Lifton, Richard P, Manzi, Shannon, Vakili, Khashayar, Kim, Heung Bae, Rodig, Nancy M, Hildebrandt, Friedhelm

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Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome von Braun, Daniela A, Warejko, Jillian K, Ashraf, Shazia, Tan, Weizhen, Daga, Ankana, Schneider, Ronen, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J, Nakayama, Makiko, Schapiro, David, Rao, Jia, Schmidt, Johanna Magdalena, Hoogstraten, Charlotte A, Hugo, Hannah, Bakkaloglu, Sevcan A, Kari, Jameela A, El Desoky, Sherif, Daouk, Ghaleb, Mane, Shrikant, Lifton, Richard P, Shril, Shirlee, Hildebrandt, Friedhelm

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Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis von Daga, Ankana, Majmundar, Amar J., Braun, Daniela A., Gee, Heon Yung, Lawson, Jennifer A., Shril, Shirlee, Jobst-Schwan, Tilman, Vivante, Asaf, Schapiro, David, Tan, Weizhen, Warejko, Jillian K., Widmeier, Eugen, Nelson, Caleb P., Fathy, Hanan M., Gucev, Zoran, Soliman, Neveen A., Hashmi, Seema, Halbritter, Jan, Halty, Margarita, Kari, Jameela A., El-Desoky, Sherif, Ferguson, Michael A., Somers, Michael J.G., Traum, Avram Z., Stein, Deborah R., Daouk, Ghaleb H., Rodig, Nancy M., Katz, Avi, Hanna, Christian, Schwaderer, Andrew L., Sayer, John A., Wassner, Ari J., Mane, Shrikant, Lifton, Richard P., Milosevic, Danko, Tasic, Velibor, Baum, Michelle A., Hildebrandt, Friedhelm

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract von van der Ven, Amelie T, Connaughton, Dervla M, Ityel, Hadas, Mann, Nina, Nakayama, Makiko, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Schulz, Julian, Braun, Daniela A, Schmidt, Johanna Magdalena, Schapiro, David, Schneider, Ronen, Warejko, Jillian K, Daga, Ankana, Majmundar, Amar J, Tan, Weizhen, Jobst-Schwan, Tilman, Hermle, Tobias, Widmeier, Eugen, Ashraf, Shazia, Amar, Ali, Hoogstraaten, Charlotte A, Hugo, Hannah, Kitzler, Thomas M, Kause, Franziska, Kolvenbach, Caroline M, Dai, Rufeng, Spaneas, Leslie, Amann, Kassaundra, Stein, Deborah R, Baum, Michelle A, Somers, Michael J G, Rodig, Nancy M, Ferguson, Michael A, Traum, Avram Z, Daouk, Ghaleb H, Bogdanović, Radovan, Stajić, Natasa, Soliman, Neveen A, Kari, Jameela A, El Desoky, Sherif, Fathy, Hanan M, Milosevic, Danko, Al-Saffar, Muna, Awad, Hazem S, Eid, Loai A, Selvin, Aravind, Senguttuvan, Prabha, Sanna-Cherchi, Simone, Rehm, Heidi L, MacArthur, Daniel G, Lek, Monkol, Laricchia, Kristen M, Wilson, Michael W, Mane, Shrikant M, Lifton, Richard P, Lee, Richard S, Bauer, Stuart B, Lu, Weining, Reutter, Heiko M, Tasic, Velibor, Shril, Shirlee, Hildebrandt, Friedhelm

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OXGR1 Is a Candidate Disease Gene for Human Calcium Oxalate Nephrolithiasis: SA-PO566 von Majmundar, Amar J., Widmeier, Eugen, Heneghan, John F., Daga, Ankana, Hugo, Hannah, Amar, Ali, Jobst-Schwan, Tilman, Nelson, Caleb, Halbritter, Jan, Sayer, John A., Fathy, Hanan, Baum, Michelle A., Shril, Shirlee, Mane, Shrikant M., Alper, Seth L., Hildebrandt, Friedhelm

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Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome von Rao, Jia, Ashraf, Shazia, Tan, Weizhen, van der Ven, Amelie T, Gee, Heon Yung, Braun, Daniela A, Fehér, Krisztina, George, Sudeep P, Esmaeilniakooshkghazi, Amin, Choi, Won-Il, Jobst-Schwan, Tilman, Schneider, Ronen, Schmidt, Johanna Magdalena, Widmeier, Eugen, Warejko, Jillian K, Hermle, Tobias, Schapiro, David, Lovric, Svjetlana, Shril, Shirlee, Daga, Ankana, Nayir, Ahmet, Shenoy, Mohan, Tse, Yincent, Bald, Martin, Helmchen, Udo, Mir, Sevgi, Berdeli, Afig, Kari, Jameela A, El Desoky, Sherif, Soliman, Neveen A, Bagga, Arvind, Mane, Shrikant, Jairajpuri, Mohamad A, Lifton, Richard P, Khurana, Seema, Martins, Jose C, Hildebrandt, Friedhelm

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GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome von Hermle, Tobias, Schneider, Ronen, Schapiro, David, Braun, Daniela A, van der Ven, Amelie T, Warejko, Jillian K, Daga, Ankana, Widmeier, Eugen, Nakayama, Makiko, Jobst-Schwan, Tilman, Majmundar, Amar J, Ashraf, Shazia, Rao, Jia, Finn, Laura S, Tasic, Velibor, Hernandez, Joel D, Bagga, Arvind, Jalalah, Sawsan M, El Desoky, Sherif, Kari, Jameela A, Laricchia, Kristen M, Lek, Monkol, Rehm, Heidi L, MacArthur, Daniel G, Mane, Shrikant, Lifton, Richard P, Shril, Shirlee, Hildebrandt, Friedhelm

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Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockout von Jobst-Schwan, Tilman, Hoogstraten, Charlotte A., Kolvenbach, Caroline M., Schmidt, Johanna Magdalena, Kolb, Amy, Eddy, Kaitlyn, Schneider, Ronen, Ashraf, Shazia, Widmeier, Eugen, Majmundar, Amar J., Hildebrandt, Friedhelm

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Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children von Schapiro, David, Daga, Ankana, Lawson, Jennifer A, Majmundar, Amar J, Lovric, Svjetlana, Tan, Weizhen, Warejko, Jillian K, Fessi, Inés, Rao, Jia, Airik, Merlin, Gee, Heon Yung, Schneider, Ronen, Widmeier, Eugen, Hermle, Tobias, Ashraf, Shazia, Jobst-Schwan, Tilman, van der Ven, Amelie T, Nakayama, Makiko, Shril, Shirlee, Braun, Daniela A, Hildebrandt, Friedhelm

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OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis von Majmundar, Amar J., Widmeier, Eugen, Heneghan, John F., Daga, Ankana, Wu, Chen-Han Wilfred, Buerger, Florian, Hugo, Hannah, Ullah, Ihsan, Amar, Ali, Ottlewski, Isabel, Braun, Daniela A., Jobst-Schwan, Tilman, Lawson, Jennifer A., Zahoor, Muhammad Yasir, Rodig, Nancy M., Tasic, Velibor, Nelson, Caleb P., Khaliq, Shagufta, Schönauer, Ria, Halbritter, Jan, Sayer, John A., Fathy, Hanan M., Baum, Michelle A., Shril, Shirlee, Mane, Shrikant, Alper, Seth L., Hildebrandt, Friedhelm

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Friedel-Crafts Crosslinked Highly Sulfonated Polyether Ether Ketone (SPEEK) Membranes for a Vanadium/Air Redox Flow Battery von Merle, Géraldine, Ioana, Filipoi Carmen, Demco, Dan Eugen, Saakes, Michel, Hosseiny, Seyed Schwan

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Advillin acts upstream of phospholipase C euro1 in steroid-resistant nephrotic syndrome von Rao, Jia, Ashraf, Shazia, Tan, Weizhen, van der Ven, Amelie T, Gee, Heon Yung, Braun, Daniela A, Fehér, Krisztina, George, Sudeep P, Esmaeilniakooshkghazi, Amin, Choi, Won-Il, Jobst-Schwan, Tilman, Schneider, Ronen, Schmidt, Johanna Magdalena, Widmeier, Eugen, Warejko, Jillian K, Hermle, Tobias, Schapiro, David, Lovric, Svjetlana, Shril, Shirlee, Daga, Ankana, Nayir, Ahmet, Shenoy, Mohan, Tse, Yincent, Bald, Martin, Helmchen, Udo, Mir, Sevgi, Berdeli, Afig, Kari, Jameela A, El Desoky, Sherif, Soliman, Neveen A, Bagga, Arvind, Mane, Shrikant, Jairajpuri, Mohamad A, Lifton, Richard P, Khurana, Seema, Martins, Jose C, Hildebrandt, Friedhelm

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