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

Riedhammer, K. M., Nguyen, T.-M. T., Koşukcu, C., Calzada-Wack, J., Li, Y., Assia Batzir, N., Saygılı, S., Wimmers, V., Kim, G.-J., Chrysanthou, M., Bakey, Z., Sofrin-Drucker, E., Kraiger, M., Sanz-Moreno, A., Amarie, O. V., Rathkolb, B., Klein-Rodewald, T., Garrett, L., Hölter, S. M., … Hoefele, J. (2024). Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney International, 105(4), 844–864. https://doi.org/10.1016/j.kint.2023.11.032
Authors:
Korbinian M Riedhammer
Thanh-Minh T Nguyen
Can Koşukcu
Julia Calzada-Wack
Yong Li
Nurit Assia Batzir
Seha Saygılı
Vera Wimmers
Gwang-Jin Kim
Marialena Chrysanthou
Zeineb Bakey
Efrat Sofrin-Drucker
Markus Kraiger
Adrián Sanz-Moreno
Oana V Amarie
Birgit Rathkolb
Tanja Klein-Rodewald
Lillian Garrett
Sabine M Hölter
Claudia Seisenberger
Stefan Haug
Pascal Schlosser
Susan Marschall
Wolfgang Wurst
Helmut Fuchs
Valerie Gailus-Durner
Matthias Wuttke
Martin Hrabe de Angelis
Jasmina Ćomić
Özlem Akgün Doğan
Yasemin Özlük
Mehmet Taşdemir
Ayşe Ağbaş
Nur Canpolat
Naama Orenstein
Salim Çalışkan
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 Köttgen
Sebastian J Arnold
Fatih Ozaltin
Miriam Schmidts
Julia Hoefele
Affiliated Authors:
Tze Y Lim
Author Keywords:
cakut
chronic kidney disease
foxd2
pax2
renal hypoplasia
wnt4
urinary albumin-to-creatinine ratio (uacr)
Publication Type:
Article
Unique ID:
10.1016/j.kint.2023.11.032
PMID:
Publication Date:
Data Source:
PubMed

Record Created: