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Implication of Transcription Factor FOXD2 Dysfunction in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).

Korbinian M. Riedhammer,Thanh-Minh T. Nguyen,Can Kosukcu,Julia Calzada-Wack,Yong Li,Nurit Assia Batzir,Seha Saygili, Vera Wimmers,Gwang-Jin Kim, Marialena Chrysanthou,Zeineb Bakey,Efrat Sofrin-Drucker,Markus Kraiger,Adrian Sanz-Moreno,Oana V. Amarie,Birgit Rathkolb,Tanja Klein-Rodewald,Lillian Garrett,Sabine M. Hoelter,Claudia Seisenberger,Stefan Haug,Pascal Schlosser,Susan Marschall,Wolfgang Wurst,Helmut Fuchs,Valerie Gailus-Durner,Matthias Wuttke,Martin Hrabe de Angelis,Jasmina Comic,Ozlem Akgun Dogan,Yasemin Ozluk,Mehmet Tasdemir,Ayse Agbas,Nur Canpolat,Naama Orenstein,Salim Caliskan,Ruthild G. Weber,Carsten Bergmann,Cecile Jeanpierre,Sophie Saunier,Tze Y. Lim,Friedhelm Hildebrandt,Bader Alhaddad,Lina Basel-Salmon,Yael Borovitz,Kaman Wu,Dinu Antony,Julia Matschkal, Christian W. Schaaf,Lutz Renders,Christoph Schmaderer,Manuel Rogg,Christoph Schell,Thomas Meitinger,Uwe Heemann,Anna Koettgen,Sebastian J. Arnold,Fatih Ozaltin,Miriam Schmidts,Julia Hoefele

Kidney International（2023）

Cited 0|Views86
Key words
CAKUT,chronic kidney disease,FOXD2,PAX2,renal hypoplasia,WNT4,urinary albumin-to-creatinine ratio (UACR)
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