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

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dc.contributor.authorRiedhammer, Korbinian M.
dc.contributor.authorNguyen, Thanh\\-Minh T.
dc.contributor.authorKosukcu, Can
dc.contributor.authorCalzada\\-Wack, Julia
dc.contributor.authorLi, Yong
dc.contributor.authorBatzir, Nurit Assia
dc.contributor.authorSaygili, Seha
dc.contributor.authorWimmers, Vera
dc.contributor.authorKim, Gwang\\-Jin
dc.contributor.authorChrysanthou, Marialena
dc.contributor.authorBakey, Zeineb
dc.contributor.authorSofrin\\-Drucker, Efrat
dc.contributor.authorKraiger, Markus
dc.contributor.authorSanz\\-Moreno, Adrian
dc.contributor.authorAmarie, Oana V.
dc.contributor.authorRathkolb, Birgit
dc.contributor.authorKlein\\-Rodewald, Tanja
dc.contributor.authorGarrett, Lillian
dc.contributor.authorHoelter, Sabine M.
dc.contributor.authorSeisenberger, Claudia
dc.contributor.authorHaug, Stefan
dc.contributor.authorSchlosser, Pascal
dc.contributor.authorMarschall, Susan
dc.contributor.authorWurst, Wolfgang
dc.contributor.authorFuchs, Helmut
dc.contributor.authorGailus\\-Durner, Valerie
dc.contributor.authorWuttke, Matthias
dc.contributor.authorde Angelis, Martin Hrabe
dc.contributor.authorComic, Jasmina
dc.contributor.authorDogan, Ozlem Akgun
dc.contributor.authorOzluk, Yasemin
dc.contributor.authorTasdemir, Mehmet
dc.contributor.authorAgbas, Ayse
dc.contributor.authorCanpolat, Nur
dc.contributor.authorOrenstein, Naama
dc.contributor.authorCaliskan, Salim
dc.contributor.authorWeber, Ruthild G.
dc.contributor.authorBergmann, Carsten
dc.contributor.authorJeanpierre, Cecile
dc.contributor.authorSaunier, Sophie
dc.contributor.authorLim, Tze Y.
dc.contributor.authorHildebrandt, Friedhelm
dc.contributor.authorAlhaddad, Bader
dc.contributor.authorBasel\\-Salmon, Lina
dc.contributor.authorBorovitz, Yael
dc.contributor.authorWu, Kaman
dc.contributor.authorAntony, Dinu
dc.contributor.authorMatschkal, Julia
dc.contributor.authorSchaaf, Christian W.
dc.contributor.authorRenders, Lutz
dc.contributor.authorSchmaderer, Christoph
dc.contributor.authorRogg, Manuel
dc.contributor.authorSchell, Christoph
dc.contributor.authorMeitinger, Thomas
dc.contributor.authorHeemann, Uwe
dc.contributor.authorKoettgen, Anna
dc.contributor.authorArnold, Sebastian J.
dc.contributor.authorOzaltin, Fatih
dc.contributor.authorSchmidts, Miriam
dc.contributor.authorHoefele, Julia
dc.date.accessioned2025-10-16T15:13:36Z
dc.date.issued2024
dc.identifier.doi10.1016/j.kint.2023.11.032
dc.identifier.otherWOS:001230175600001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5881
dc.publisherELSEVIER SCIENCE INC
dc.sourceKIDNEY INTERNATIONAL
dc.subjectCAKUT
dc.subjectchronic kidney disease
dc.subjectFOXD2
dc.subjectPAX2
dc.subjectrenal hypoplasia
dc.subjectWNT4
dc.subjecturinary albumin\\-to\\-creatinine ratio \\(UACR\\)
dc.titleImplication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
dc.typeArticle

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