Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

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

doi:10.1016/j.kint.2023.11.032

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Date

2024

Authors

Riedhammer, Korbinian M.

Nguyen, Thanh\\-Minh T.

Kosukcu, Can

Calzada\\-Wack, Julia

Chrysanthou, Marialena

dc.identifier.doi

10.1016/j.kint.2023.11.032

dc.identifier.other

WOS:001230175600001

Publisher

ELSEVIER SCIENCE INC

DOI

10.1016/j.kint.2023.11.032

Keywords

CAKUT , chronic kidney disease , FOXD2 , PAX2 , renal hypoplasia , WNT4 , urinary albumin\\-to\\-creatinine ratio \\(UACR\\)

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https://openaccess.acibadem.edu.tr/handle/11443/5881

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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

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