Inducible Podocyte Injury and Proteinuria in Transgenic Zebrafish von WEIBIN ZHOU, HILDEBRANDT, Friedhelm

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Nephronophthisis-associated ciliopathies von HILDEBRANDT, Friedhelm, WEIBIN ZHOU

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Convolutional Neural Network Approach Based on Multimodal Biometric System with Fusion of Face and Finger Vein Features von Wang, Yang, Shi, Dekai, Zhou, Weibin

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Thyroid Function Abnormalities in COVID-19 Patients von Wang, Weibin, Su, Xingyun, Ding, Yongfeng, Fan, Weina, Zhou, Weibin, Su, Junwei, Chen, Zhendong, Zhao, Hong, Xu, Kaijin, Ni, Qin, Xu, Xiaowei, Qiu, Yunqing, Teng, Lisong

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Oncogenic Role of THOR, a Conserved Cancer/Testis Long Non-coding RNA von Hosono, Yasuyuki, Niknafs, Yashar S., Prensner, John R., Iyer, Matthew K., Dhanasekaran, Saravana M., Mehra, Rohit, Pitchiaya, Sethuramasundaram, Tien, Jean, Escara-Wilke, June, Poliakov, Anton, Chu, Shih-Chun, Saleh, Sahal, Sankar, Keerthana, Su, Fengyun, Guo, Shuling, Qiao, Yuanyuan, Freier, Susan M., Bui, Huynh-Hoa, Cao, Xuhong, Malik, Rohit, Johnson, Timothy M., Beer, David G., Feng, Felix Y., Zhou, Weibin, Chinnaiyan, Arul M.

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A latent code based multi-variable modulation network for susceptibility mapping von Zhou, Weibin, Xi, Jiaxiu, Bao, Lijun

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Giant cystic parathyroid adenoma: two case reports and a literature review von Weng, Junwei, Zhou, Weibin, Feng, Yunfei

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Optimization of an electrical impedance flow cytometry system and analysis of submicron particles and bacteria von Xie, Xinwu, Gong, Meiling, Zhang, Zhiwei, Dou, Xuechen, Zhou, Weibin, Li, Jisheng, Zhu, Mengfu, Du, Yaohua, Xu, Xinxi

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ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption von Ashraf, Shazia, Gee, Heon Yung, Woerner, Stephanie, Xie, Letian X, Vega-Warner, Virginia, Lovric, Svjetlana, Fang, Humphrey, Song, Xuewen, Cattran, Daniel C, Avila-Casado, Carmen, Paterson, Andrew D, Nitschké, Patrick, Bole-Feysot, Christine, Cochat, Pierre, Esteve-Rudd, Julian, Haberberger, Birgit, Allen, Susan J, Zhou, Weibin, Airik, Rannar, Otto, Edgar A, Barua, Moumita, Al-Hamed, Mohamed H, Kari, Jameela A, Evans, Jonathan, Bierzynska, Agnieszka, Saleem, Moin A, Böckenhauer, Detlef, Kleta, Robert, El Desoky, Sherif, Hacihamdioglu, Duygu O, Gok, Faysal, Washburn, Joseph, Wiggins, Roger C, Choi, Murim, Lifton, Richard P, Levy, Shawn, Han, Zhe, Salviati, Leonardo, Prokisch, Holger, Williams, David S, Pollak, Martin, Clarke, Catherine F, Pei, York, Antignac, Corinne, Hildebrandt, Friedhelm

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A zebrafish model of diabetic nephropathy shows hyperglycemia, proteinuria and activation of the PI3K/Akt pathway von Zang, Liqing, Saitoh, Sei, Katayama, Kan, Zhou, Weibin, Nishimura, Norihiro, Shimada, Yasuhito

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Particle Self-Aligning, Focusing, and Electric Impedance Microcytometer Device for Label-Free Single Cell Morphology Discrimination and Yeast Budding Analysis von Xie, Xinwu, Zhang, Zhiwei, Ge, Xiang, Zhao, Xiaohao, Hao, Limei, Cheng, Zhen, Zhou, Weibin, Du, Yaohua, Wang, Lei, Tian, Feng, Xu, Xinxi

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Characterization of mesonephric development and regeneration using transgenic zebrafish von Zhou, Weibin, Boucher, Rudrick C, Bollig, Frank, Englert, Christoph, Hildebrandt, Friedhelm

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Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling von Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Yasunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O’Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Omran, Heymut, Lee, Eva Y.-H.P., Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm

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Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy von Horstick, Eric J., Linsley, Jeremy W., Dowling, James J., Hauser, Michael A., McDonald, Kristin K., Ashley-Koch, Allison, Saint-Amant, Louis, Satish, Akhila, Cui, Wilson W., Zhou, Weibin, Sprague, Shawn M., Stamm, Demetra S., Powell, Cynthia M., Speer, Marcy C., Franzini-Armstrong, Clara, Hirata, Hiromi, Kuwada, John Y.

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Characterization of polymethyl methacrylate/polyethylene glycol/aluminum nitride composite as form-stable phase change material prepared by in situ polymerization method von Zhang, Lei, Zhu, Jiaoqun, Zhou, Weibin, Wang, Jun, Wang, Yan

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FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair von Zhou, Weibin, Otto, Edgar A, Cluckey, Andrew, Airik, Rannar, Hurd, Toby W, Chaki, Moumita, Diaz, Katrina, Lach, Francis P, Bennett, Geoffrey R, Gee, Heon Yung, Ghosh, Amiya K, Natarajan, Sivakumar, Thongthip, Supawat, Veturi, Uma, Allen, Susan J, Janssen, Sabine, Ramaswami, Gokul, Dixon, Joanne, Burkhalter, Felix, Spoendlin, Martin, Moch, Holger, Mihatsch, Michael J, Verine, Jerome, Reade, Richard, Soliman, Hany, Godin, Michel, Kiss, Denes, Monga, Guido, Mazzucco, Gianna, Amann, Kerstin, Artunc, Ferruh, Newland, Ronald C, Wiech, Thorsten, Zschiedrich, Stefan, Huber, Tobias B, Friedl, Andreas, Slaats, Gisela G, Joles, Jaap A, Goldschmeding, Roel, Washburn, Joseph, Giles, Rachel H, Levy, Shawn, Smogorzewska, Agata, Hildebrandt, Friedhelm

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Acute adrenal insufficiency caused by antiphospholipid syndrome von Feng, Yunfei, Zhou, Weibin, Fang, Daiqiong

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Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure von Reichold, Markus, Klootwijk, Enriko D, Reinders, Joerg, Otto, Edgar A, Milani, Mario, Broeker, Carsten, Laing, Chris, Wiesner, Julia, Devi, Sulochana, Zhou, Weibin, Schmitt, Roland, Tegtmeier, Ines, Sterner, Christina, Doellerer, Hannes, Renner, Kathrin, Oefner, Peter J, Dettmer, Katja, Simbuerger, Johann M, Witzgall, Ralph, Stanescu, Horia C, Dumitriu, Simona, Iancu, Daniela, Patel, Vaksha, Mozere, Monika, Tekman, Mehmet, Jaureguiberry, Graciana, Issler, Naomi, Kesselheim, Anne, Walsh, Stephen B, Gale, Daniel P, Howie, Alexander J, Martins, Joana R, Hall, Andrew M, Kasgharian, Michael, O'Brien, Kevin, Ferreira, Carlos R, Atwal, Paldeep S, Jain, Mahim, Hammers, Alexander, Charles-Edwards, Geoffrey, Choe, Chi-Un, Isbrandt, Dirk, Cebrian-Serrano, Alberto, Davies, Ben, Sandford, Richard N, Pugh, Christopher, Konecki, David S, Povey, Sue, Bockenhauer, Detlef, Lichter-Konecki, Uta, Gahl, William A, Unwin, Robert J, Warth, Richard, Kleta, Robert

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A rare case of coexistence of autoimmune polyglandular syndrome type 3 with growth hormone deficiency and hyperthyroidism in a patient with pseudo-Turner’s syndrome von Zhou, Weibin, Lin, Haiyang, Chen, Min, Ning, Jianwen

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Assaying autophagic activity in transgenic GFP-Lc3 and GFP-Gabarap zebrafish embryos von He, Congcong, Bartholomew, Clinton R., Zhou, Weibin, Klionsky, Daniel J.

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