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Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT)
Authors:Yasmine Neirijnck  Antoine Reginensi  Kirsten Y. Renkema  Filippo Massa  Vladimir M. Kozlov  Haroun Dhib  Ernie M.H.F. Bongers  Wout F. Feitz  Albertien M. van Eerde  Veronique Lefebvre  Nine V.A.M. Knoers  Mansoureh Tabatabaei  Herbert Schulz  Helen McNeill  Franz Schaefer  Michael Wegner  Elisabeth Sock  Andreas Schedl
Affiliation:1. Université Nice Sophia Antipolis, Inserm, CNRS, iBV, Nice, France;2. Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands;3. Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands;4. Department of Urology, Radboudumc Amalia Children’s Hospital, Radboud University Medical Center, Nijmegen, The Netherlands;5. Department of Cellular and Molecular Medicine, Cleveland Clinic–Lerner Research Institute, Cleveland, Ohio, USA;6. Division of Pediatric Nephrology, Heidelberg University Center for Pediatrics and Adolescent Medicine, Heidelberg, Germany;7. University of Cologne, Cologne Center for Genomics, Cologne, Germany;8. Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada;9. Institute of Biochemistry, Friedrich-Alexander University Erlangen-Nürnberg, Germany
Abstract:
Keywords:CAKUT  duplex kidneys  kidney induction  nephron  Sox11
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