Microbial fuel cell enables phosphate recovery from digested sewage sludge as struvite von Fischer, Fabian, Bastian, Christèle, Happe, Manuel, Mabillard, Eric, Schmidt, Nicolas

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Microwave barrel reactor use in trimethylolpropane oleate synthesis by Candida antarctica lipase in a biphasic non-solvent process von HAPPE, Manuel, GRAND, Pascal, NUSSBAUM, Samuel, RODUIT, Alain, TIECHE, François, SALEM, Sam, CONSTANTIN, Carole, SCHMITT, Esther, ZAHNO, Silvan, ELLERT, Christoph, HABIB, Ahmed, WYSS, Julien, FARQUET, Sebastien, FISCHER, Fabian, AEBY, Sandrine, HERITIER, Jean-Claude, CORTHAY, François, MABILLARD, Eric, MARTI, Roger, VANOLI, Ennio, GROGG, Alain-François

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Microwave barrel reactor use in trimethylolpropane oleate synthesis by Candida antarctica lipase in a biphasic non-solvent processElectronic supplementary information (ESI) availab... von Happe, Manuel, Grand, Pascal, Farquet, Sébastien, Aeby, Sandrine, Héritier, Jean-Claude, Corthay, François, Mabillard, Eric, Marti, Roger, Vanoli, Ennio, Grogg, Alain-François, Nussbaum, Samuel, Roduit, Alain, Tièche, François, Salem, Sam, Constantin, Carole, Schmitt, Esther, Zahno, Silvan, Ellert, Christoph, Habib, Ahmed, Wyss, Julien, Fischer, Fabian

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Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease von Mabillard, Holly, Sayer, John A, Olinger, Eric

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MO042: Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney disease von Olinger, Eric, Phakdeekitcharoen, Pran, Caliskan, Yasar, Mabillard, Holly, Pickles, Charles, Tse, Yincent, Wood, Katrina, Sayer, John

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Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study von Kidd, Kendrah O, Williams, Adrienne H, Taylor, Abbigail, Martin, Lauren, Robins, Victoria, Sayer, John A, Olinger, Eric, Mabillard, Holly R, Papagregoriou, Gregory, Deltas, Constantinos, Stavrou, Christoforos, Conlon, Peter J, Hogan, Richard Edmund, Elhassan, Elhussein A E, Springer, Drahomíra, Zima, Tomáš, Izzi, Claudia, Vrbacká, Alena, Piherová, Lenka, Pohludka, Michal, Radina, Martin, Vylet'al, Petr, Hodanova, Katerina, Zivna, Martina, Kmoch, Stanislav, Bleyer, Sr, Anthony J

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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease von Claus, Laura R., Chen, Chuan, Stallworth, Jennifer, Turner, Joshua L., Slaats, Gisela G., Mabillard, Holly, Senum, Sarah R., Srikanth, Sujata, Flanagan-Steet, Heather, Louie, Raymond J., Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal, Mighton, Chloe, Sleutels, Frank, van Slegtenhorst, Marjon, van Ham, Tjakko, Brooks, Alice S., Dorresteijn, Eiske M., Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric Jean, Olinger, Eric, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., Maleady-Crowe, Fiona, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Pereira, Mariana Buongermino, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Larsen, Martin, Hertz, Jens Michael, Lilien, Marc R., Obeidová, Lena, Stone, Hillarey K., Kerecuk, Larissa, Gurgu, Mihai, Yousef Yengej, Fjodor A., Ammerlaan, Carola M.E., Rookmaaker, Maarten B., Hanna, Christian, Rogers, R. Curtis, Duran, Karen, Peters, Edith, Sayer, John A., van Haaften, Gijs, Harris, Peter C., Ling, Kun, Mason, Jennifer M., van Eerde, Albertien M., Steet, Richard

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UMOD and you! Explaining a rare disease diagnosis von Mabillard, Holly, Olinger, Eric, Sayer, John A

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An intermediate-effect size variant in UMOD confers risk for chronic kidney disease von Olinger, Eric, Schaeffer, Céline, Kidd, Kendrah, Elhassan, Elhussein A E, Cheng, Yurong, Dufour, Inès, Schiano, Guglielmo, Mabillard, Holly, Pasqualetto, Elena, Hofmann, Patrick, Fuster, Daniel G, Kistler, Andreas D, Wilson, Ian J, Kmoch, Stanislav, Raymond, Laure, Robert, Thomas, Genomics England Research Consortium, Eckardt, Kai-Uwe, Bleyer, Anthony J, Köttgen, Anna, Conlon, Peter J, Wiesener, Michael, Sayer, John A, Rampoldi, Luca, Devuyst, Olivier

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An intermediate-effect size variant in UMOD confers risk for chronic kidney disease von Olinger, Eric, Schaeffer, Céline, Kidd, Kendrah, Elhassan, Elhussein A E, Cheng, Yurong, Dufour, Inès, Schiano, Guglielmo, Mabillard, Holly, Pasqualetto, Elena, Hofmann, Patrick, Fuster, Daniel G, Kistler, Andreas D, Wilson, Ian J, Kmoch, Stanislav, Raymond, Laure, Robert, Thomas, Eckardt, Kai-Uwe, Bleyer, Sr, Anthony J, Köttgen, Anna, Conlon, Peter J, Wiesener, Michael, Sayer, John A, Rampoldi, Luca, Devuyst, Olivier

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Use of whole genome sequencing to determine the genetic basis of visceral myopathies including Prune Belly syndrome von Geraghty, Robert M, Orr, Sarah, Olinger, Eric, Neatu, Ruxandra, Barroso-Gil, Miguel, Mabillard, Holly, Consortium, Genomics England Research, Wilson, Ian, Sayer, John A

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Device for locking the legs of a passenger in a seat von Berra, Eric

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