Genetic, environmental, and epigenetic factors involved in CAKUT
Nicolaou, Nayia, Renkema, Kirsten Y., Bongers, Ernie M. H. F., Giles, Rachel H., Knoers, Nine V. A. M.·2015·Nature Reviews Nephrology
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Items 301–346 of 346
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- Clinical, laboratory, imaging features and prognosis in pediatric patients with Congenital anomalies of the kidney and the urinary tract (CAKUT): a referral center experienceMasoumeh Mohkam, Soodeh Ghadimi, Mohammadreza Shafiei, Leily Mohajerzadeh, Mitra Khalili, Arefeh Zahmatkesh, Monireh Sadat Motaharifard, Raziyeh Alipour Aftabi, Mohammadreza Jafari, Farnaz Kamali et al. · 2025 · African Journal of Urology
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- Additional file 3 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Chen, Jing et al. · 2024 · Figshare
- Additional file 4 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Chen, Jing et al. · 2024 · Figshare
- Additional file 1 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Chen, Jing et al. · 2024 · Figshare
- Additional file 1 of Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)Stefan Kohl, Sandra Habbig, Weber, Lutz T., Max C. Liebau · 2021 · Figshare
- Additional file 1 of Clinical outcomes and temporal trends of immunological and non-immunological rare diseases in adult kidney transplantEster Gallo, Silvia Mingozzi, Alberto Mella, Fabrizio Fop, Roberto Presta, Manuel Burdese, Elena Boaglio, Maria Cristina Torazza, Roberta Giraudi, Gianluca Leonardi et al. · 2021 · Figshare
- Additional file 6 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Jing Chen et al. · 2024 · Figshare
- Additional file 1 of A preliminary study of the miRNA restitution effect on CNV-induced miRNA downregulation in CAKUTKristina Mitrovic, Ivan Životić, Ivana Kolić, Jelena J. Žakula, Zivkovic, Maja, Stankovic, Aleksandra, Ivan B. Jovanović · 2024 · Figshare
- Additional file 2 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Chen, Jing et al. · 2024 · Figshare
- Additional file 5 of GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, C N Wang, Liu, Jialu, Yu, Minghui, Haixin Ju, Shanshan Xue, Li, Yaxin, Liu, Jiaojiao, Rufeng Dai, Chen, Jing et al. · 2024 · Figshare
- Loss of minichromosome maintenance 4 leads to early renal dysplasia and cystogenesis outcomesJing Huang, Hui-Ling Xiang, Qian Yuan, Chun Zhang, Xian-Fang Meng · 2025 · Genes & Diseases
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- Bilateral ovarian fibromas with duplex collecting system and ectopic ureter in an 11-year-old girl: a case report with genetic analysisLei Zhang, Chunhua Dong, Cuihua Yang, Meng Gui · 2026 · Frontiers in Pediatrics
- Exome Reanalysis Identifies Novel Candidate Genes Associated with Congenital Anomalies of the Kidney and Urinary Tract in ChinaHuaping Sun, C N Wang, Wentao Zhang, Mingji Deng, Qian Shen, Jianhua Mao, Qing Sun, Huimin Luo, Huijun Shen, Jingjing Wang et al. · 2026 · medRxiv
- Maternal and fetal determinants influencing the occurrence of congenital abnormalities of the kidney and urinary tract: a nested case–control studyWeizhen Bu, xiaohua LI, yan Xuan, xiaojing Hu, Zhenli Zhao · 2026 · Research Square
- Temporal trends and projections in the global burden of congenital genitourinary anomalies from 1990 to 2021: A cross-sectional studySiyang Xu, Hua Zhu, Bing Zheng, Bing Zheng, Wen Zhang · 2026 · Journal of International Medical Research
- Dose-Dependent and Non-Autonomous Signaling in CAKUT: A Lineage-Specific Framework from Conditional Knockout StudiesNela Kelam, Petar Todorović, Patricija Bajt, Nikola Pavlović, Tomislav Rakić, Katarina Vukojević, Anita Racetin · 2026 · Biomolecules
- Étude fonctionnelle de gènes candidats impliqués dans les ciliopathiesMarie Alice Dupont · 2019 · theses.fr (ABES)
- Identification and characterisation of loss of function mutations in KIF14 leading to syndromic renal hypodysplasiaMadeline Louise Reilly · 2018 · theses.fr (ABES)
- Role of Tshz3 in the development and function of the kidneyIrene Sanchez-Martin · 2018
- Regulatory interactions involved in pronephros development and patterningLaura Goea · 2018
- Application de la biologie des systèmes pour l'identification de marqueurs moléculaires des maladies rénales dans les fluides biologiquesFranck Boizard · 2019
- Identification and implication of novel genes in the pathogenesis of congenital abnormalities of the kidney and urinary tractLara De Tomasi · 2018
- Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tracton behalf of the ArtDECO consortium, Genetica Groep Van Tintelen, Genetica, Child Health, Genetica Sectie Research, Genetica Klinische Genetica, Cancer, Nefrologie, MS Verloskunde, Circulatory Health et al. · 2025 · Utrecht University Repository (Utrecht University)
- L'analyse protéomique du liquide amniotique : une clé pour améliorer la compréhension des mécanismes du développement rénal et des maladies associéesCamille Fédou · 2020 · theses.fr (ABES)
- Le séquençage haut débit de l’ADN pour l’identification des bases moléculaires des pathologies mendéliennes : opportunités et défisAlban C. Ziegler · 2022
- Genotipo ir fenotipo įvertinimas sergančiųjų cistinėmis inkstų ligomis grupėjeDeimante Brazdziunaite · 2026
- Congenital Abnormalities and Cystic and Hereditary Tubular Diseases2026 · American Registry of PathologyArlington, Virginia eBooks
- A review of congenital anomalies of the kidney and urinary tract (CAKUT) in AfricaSiyanda Mazaleni, Terisha Ghazi, Anil Amichund Chuturgoon, Rajendra Bhimma · 2026 · Annals of Medicine and Surgery
- Clinical and Molecular characteristics of kidney and urinary tract congenital anomalies in a cohort of Egyptian patients using whole-exome sequencingTamer H. A. Ammar, Heba Mostafa Ahmed, Eman E.A. Mohammed, Hazem Mohamed El‐Hariri, Alice AbdelAleem, M J Thomas · 2026 · Molecular Biology Reports
- Whole Exome Sequencing Reveals Promising Genes Associated with Congenital Renal Parenchymal Anomalies in Greek ChildrenAnna Zisi, Charilaos Kostoulas, Athanasia Sesse, Chrysoula Kosmeri, Anastasios Serbis, Hane Lee, Ioannis A. Georgiou, Ekaterini C. Siomou · 2026 · Children
- Prenatal body fluid analysis in the evaluation of CAKUTThomas Simon, Bénédicte Buffin‐Meyer, Julie Klein, Stéphane Decramer, Joost Peter Schanstra · 2026 · Pediatric Nephrology
- Excessive maternal methionine intake increases the incidence of congenital anomalies of the kidney and urinary tract in offspring miceNingli Ye, Minghui Yu, Haixin Ju, Yuanyan Jiang, Yumeng Zhang, Lei Sun, Xiaohui Wu, Jing Chen, Hong Xu, Qian Shen · 2026 · Nutrition Research
- Silymarin mitigates tartrazine-induced fetal nephrotoxicity and oxidative stress following gestational exposure in ratsMona M. Abdalraheem, Omayma Mahfouz Mahmoud, Eman N. Draz, Eman Mohamed Kamel · 2026 · Tissue and Cell
- Swimming Upstream to Understand Congenital Anomalies of the Kidney and Urinary Tract: Zebrafish Models for Developmental Biology, Disease Mechanisms, and Functional Interpretation of Genetic VariationZachary W. Nurcombe, Lina Mougharbel, Thomas M. Kitzler · 2026 · Genes
- Transcript- and Protein-Level Preservation and Spatial Reorganization of EMT and Vascular–Mesenchymal Gene Programs (SNAI1, TGFB1, PECAM1, VIM) in Human Fetal Kidneys with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)Lucija Bavčević, Anita Racetin, Petar Todorović, Sandra Kostić, Sandra Zekić Tomaš, Katarina Vukojević, Nela Kelam · 2026 · Genes
- Environmental risk factors across the phenotypic spectrum of CAKUTBenthe H König, Sander Groen in ’t Woud, Iris Lekkerkerker, Lisanne M. Vendrig, M.D.PhD Wout F J Feitz, Albertien M. van Eerde, Jaap Mulder, Rik Westland, Michiel F. Schreuder, Loes van der Zanden et al. · 2026 · Kidney International Reports
- BindingDB Entry 50017641: Discovery of indol-6-yl-pyrrolo[2,3-c]pyridin-7-one derivatives as bromodomain-containing protein 4 (BRD4) inhibitors for the treatment of kidney fibrosis.BindingDB · 2023 · UC San Diego