Anzahl der Einträge: 3.
2022
Mingardo, Enrico,
Beaman, Glenda,
Grote, Philip ,
Nordenskjöld, Agneta,
Newman, William ,
Woolf, Adrian S. ,
Eckstein, Markus ,
Hilger, Alina C.,
Dworschak, Gabriel C. ,
Rösch, Wolfgang,
Ebert, Anne-Karolin,
Stein, Raimund,
Brusco, Alfredo,
Di Grazia, Massimo,
Tamer, Ali,
Torres, Federico M.,
Hernandez, Jose L.,
Erben, Philipp,
Maj, Carlo,
Olmos, Jose M. ,
Riancho, Jose A.,
Valero, Carmen,
Hostettler, Isabel C.,
Houlden, Henry,
Werring, David J. ,
Schumacher, Johannes,
Gehlen, Jan,
Giel, Ann-Sophie,
Buerfent, Benedikt C.,
Arkani, Samara,
Åkesson, Elisabeth ,
Rotstein, Emilia,
Ludwig, Michael,
Holmdahl, Gundela,
Giorgio, Elisa,
Berettini, Alfredo,
Keene, David,
Cervellione, Raimondo M.,
Younsi, Nina,
Ortlieb, Melissa,
Oswald, Josef,
Haid, Bernhard,
Promm, Martin,
Neissner, Claudia,
Hirsch, Karin,
Stehr, Maximilian,
Schäfer, Frank-Mattias,
Schmiedeke, Eberhard,
Boemers, Thomas M.,
van Rooij, Iris A. L. M.,
Feitz, Wouter F. J.,
Marcelis, Carlo L. M.,
Lacher, Martin,
Nelson, Jana,
Ure, Benno,
Fortmann, Caroline,
Gale, Daniel P.,
Chan, Melanie M. Y.,
Ludwig, Kerstin U.,
Nöthen, Markus M.,
Heilmann, Stefanie,
Zwink, Nadine,
Jenetzky, Ekkehart,
Odermatt, Benjamin,
Knapp, Michael und
Reutter, Heiko
(2022)
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Communications Biology 5 (1).
Volltext nicht vorhanden.
2018
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 und
Kleta, Robert
(2018)
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
Journal of the American Society of Nephrology 29 (7), S. 1849-1858.
Volltext nicht vorhanden.
2017
Chatziantoniou, Christos ,
Voskarides, Konstantinos,
Stefanou, Charalambos,
Pieri, Myrtani,
Demosthenous, Panayiota ,
Felekkis, Kyriakos,
Arsali, Maria,
Athanasiou, Yiannis,
Xydakis, Dimitris ,
Stylianou, Kostas,
Daphnis, Eugenios,
Goulielmos, Giorgos,
Loizou, Petros,
Savige, Judith,
Höhne, Martin,
Völker, Linus A.,
Benzing, Thomas ,
Maxwell, Patrick H. ,
Gale, Daniel P.,
Gorski, Mathias,
Böger, Carsten,
Kollerits, Barbara ,
Kronenberg, Florian,
Paulweber, Bernhard,
Zavros, Michalis,
Pierides, Alkis und
Deltas, Constantinos
(2017)
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.
PLOS ONE 12 (3), e0174274.
Volltext nicht vorhanden.
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