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Journal Article
Ekici, Arif B., Hackenbeck, Thomas, Moriniere, Vincent 
ORCID: 0000-0003-1795-222X, Panness, Andrea, Buettner, Maike, Uebe, Steffen, Janka, Rolf, Wiesener, Antje, Hermann, Ingo, Grupp, Sina, Hornberger, Martin, Huber, Tobias B. ORCID: 0000-0001-7175-5062, Isbel, Nikky, Mangos, George, McGinn, Stella, Soreth-Rieke, Daniela, Beck, Bodo B., Uder, Michael, Amann, Kerstin, Antignac, Corinne, Reis, Andre ORCID: 0000-0002-6301-6363, Eckardt, Kai-Uwe and Wiesener, Michael S.
(2014).
Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin.
Kidney Int., 86 (3).
S. 589 - 600.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1523-1755
Gimm, Tina, Wiese, Melanie, Teschemacher, Barbara, Deggerich, Anke, Schoedel, Johannes, Knaup, Karl X., Hackenbeck, Thomas, Hellerbrand, Claus, Amann, Kerstin, Wiesener, Michael S., Hoening, Stefan, Eckardt, Kai-Uwe and Warnecke, Christina (2010). Hypoxia-inducible protein 2 is a novel lipid droplet protein and a specific target gene of hypoxia-inducible factor-1. Faseb J., 24 (11). S. 4443 - 4459. BETHESDA: FEDERATION AMER SOC EXP BIOL. ISSN 1530-6860
Knaup, Karl X., Hackenbeck, Thomas, Popp, Bernt ORCID: 0000-0002-3679-1081, Stoeckert, Johanna, Wenzel, Andrea, Buettner-Herold, Maike, Pfister, Frederick, Schueler, Markus, Seven, Didem, May, Annette M., Halbritter, Jan, Groene, Hermann-Josef, Reis, Andre ORCID: 0000-0002-6301-6363, Beck, Bodo B., Amann, Kerstin, Ekici, Arif B. and Wiesener, Michael S.
(2018).
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease Recognition.
J. Am. Soc. Nephrol., 29 (9).
S. 2298 - 2310.
WASHINGTON:
AMER SOC NEPHROLOGY.
ISSN 1533-3450