Deep learning outperforms kidney organoid experts von Yu, Seyoung, Gee, Heon Yung

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Insulin-activated store-operated Ca2+ entry via Orai1 induces podocyte actin remodeling and causes proteinuria von Kim, Ji-Hee, Hwang, Kyu-Hee, Dang, Bao T. N., Eom, Minseob, Kong, In Deok, Gwack, Yousang, Yu, Seyoung, Gee, Heon Yung, Birnbaumer, Lutz, Park, Kyu-Sang, Cha, Seung-Kuy

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PLCE1 regulates the migration, proliferation, and differentiation of podocytes von Yu, Seyoung, Choi, Won-Il, Choi, Yo Jun, Kim, Hye-Youn, Hildebrandt, Friedhelm, Gee, Heon Yung

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Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type von Lemberg, Katharina, Mertens, Nils D., Yousef, Kirollos, Schneider, Ronen, Merz, Lea M., Mansour, Bshara, Salmanullah, Daanya, Kolvenbach, Caroline M., Saida, Ken, Yu, Seyoung, Hölzel, Selina, Steinsapir, Andrew, Goncalves, Kevin A., Nicolas Frank, Camille, Franken, Gijs A. C., Shril, Shirlee, Buerger, Florian, Hildebrandt, Friedhelm

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ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms von Cho, Kyeong Jee, Noh, Shin Hye, Han, Soo Min, Choi, Won-Il, Kim, Hye-Youn, Yu, Seyoung, Lee, Joon Suk, Rim, John Hoon, Lee, Min Goo, Hildebrandt, Friedhelm, Gee, Heon Yung

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Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population von Jung, Jinsei, Lee, Joon Suk, Cho, Kyeong Jee, Yu, Seyoung, Yoon, Joo-Heon, Yung Gee, Heon, Choi, Jae Young

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Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss von Jung, Jinsei, Choi, Hyun Been, Koh, Young Ik, Rim, John Hoon, Choi, Hye Ji, Kim, Sung Huhn, Lee, Jae Hyun, An, Jieun, Kim, Ami, Lee, Joon Suk, Joo, Sun Young, Yu, Seyoung, Choi, Jae Young, Kang, Tong Mook, Gee, Heon Yung

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Kidney organoids: development and applications von Kim, Hye-Youn, Yu, Seyoung, Choi, Yo Jun, Gee, Heon Yung

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Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment von Jung, Jinsei, Lin, Haiyue, Koh, Young Ik, Ryu, Kunhi, Lee, Joon Suk, Rim, John Hoon, Choi, Hye Ji, Lee, Hak Joon, Kim, Hye-Youn, Yu, Seyoung, Jin, Hyunsoo, Lee, Ji Hyun, Lee, Min Goo, Namkung, Wan, Choi, Jae Young, Gee, Heon Yung

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A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction von Yu, Seyoung, Choi, Hye Ji, Lee, Joon Suk, Lee, Hyun Jae, Rim, John Hoon, Choi, Jae Young, Gee, Heon Yung, Jung, Jinsei

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Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes von Yu, Seyoung, Choi, Yo Jun, Rim, John Hoon, Kim, Hye-Youn, Bekheirnia, Nasim, Swartz, Sarah Jane, Dai, Hongzheng, Gu, Shen Linda, Lee, Soyeon, Nishinakamura, Ryuichi, Hildebrandt, Friedhelm, Bekheirnia, Mir Reza, Gee, Heon Yung

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Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains von Joo, Sun Young, Na, Gina, Kim, Jung Ah, Yoo, Jee Eun, Kim, Da Hye, Kim, Se Jin, Jang, Seung Hyun, Yu, Seyoung, Kim, Hye-Youn, Choi, Jae Young, Gee, Heon Yung, Jung, Jinsei

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Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report von Choi, Hye Ji, Lee, Joon Suk, Yu, Seyoung, Cha, Do Hyeon, Gee, Heon Yung, Choi, Jae Young, Lee, Jong Dae, Jung, Jinsei

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Studying Organoid Phenotypes in CoQ10-Deficient Glomerulopathy: SA-PO994 von Yu, Seyoung, Hildebrandt, Friedhelm, Gee, Heon Yung

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Microbiome analysis reveals that Ralstonia is responsible for decreased renal function in patients with ulcerative colitis von Kim, Jung Min, Rim, John Hoon, Kim, Da Hye, Kim, Hye‐Youn, Choi, Sung Kyoung, Kim, Dong Yun, Choi, Yo Jun, Yu, Seyoung, Cheon, Jae Hee, Gee, Heon Yung

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Phenotypic Quantification of an Hnf1b Knockout Mouse Model: SA-PO816 von Hölzel, Selina, Kolvenbach, Caroline M., Buerger, Florian, Lemberg, Katharina, Saida, Ken, Yu, Seyoung, Salmanullah, Daanya, Mansour, Bshara, Elmubarak, Izzeldin, Mertens, Nils D., Shril, Shirlee, Hildebrandt, Friedhelm

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ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment von Widmeier, Eugen, Yu, Seyoung, Nag, Anish, Chung, Youn Wook, Nakayama, Makiko, Fernández-Del-Río, Lucía, Hugo, Hannah, Schapiro, David, Buerger, Florian, Choi, Won-Il, Helmstädter, Martin, Kim, Jae-Woo, Ryu, Ji-Hwan, Lee, Min Goo, Clarke, Catherine F, Hildebrandt, Friedhelm, Gee, Heon Yung

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Comprehensive Genetic Analysis Reveals Novel Variants in Nephrolithiasis and Nephrocalcinosis: FR-PO599 von Saida, Ken, Buerger, Florian, Ottlewski, Isabel, Salmanullah, Daanya, Yu, Seyoung, Kolvenbach, Caroline M., Lemberg, Katharina, Mansour, Bshara, Mertens, Nils D., Hölzel, Selina, Elmubarak, Izzeldin, Franken, Gijs A., Schneider, Ronen, Majmundar, Amar J., Shril, Shirlee, Hildebrandt, Friedhelm

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OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin von Koh, Young Ik, Oh, Kyung Seok, Kim, Jung Ah, Noh, Byunghwa, Choi, Hye Ji, Joo, Sun Young, Rim, John Hoon, Kim, Hye-Youn, Kim, Dong Yun, Yu, Seyoung, Kim, Da Hye, Lee, Sang-Guk, Jung, Jinsei, Choi, Jae Young, Gee, Heon Yung

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Exome Sequencing in Individuals with CAKUT Identifies De Novo Variants in Novel Candidate Genes in 15.5: SA-PO810 von Kolvenbach, Caroline M., Merz, Lea M., Wang, Chunyan, Mertens, Nils D., Seltzsam, Steve, Mansour, Bshara, Hölzel, Selina, Mann, Nina, Lemberg, Katharina, Saida, Ken, Buerger, Florian, Frank, Camille H. Nicolas, Yousef, Kirollos, Salmanullah, Daanya, Yu, Seyoung, Hilger, Alina, Tasic, Velibor, Shril, Shirlee, Hildebrandt, Friedhelm

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