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Showing results (71-80 of 93) with videos related to

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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 3, 2025
Ultrasound Super-Resolution Imaging of Neonatal Cerebral Vascular ReorganizationSimone Schwarz, Louise Denis, Emmanuel Nedoschill, et al.
Kidney International Reports|July 18, 2025
FLNA ROD1 and ROD2 Domains are Implicated in Congenital Lower Urinary Tract ObstructionClara Vidic, Jil Stegmann, Charlotte Bendixen, et al.
Biomolecules|July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease FormationRicarda Köllges, Jil Stegmann, Sophia Schneider, et al.
Journal of Medical Genetics|November 15, 2022
X-linked variations in <i>SHROOM4</i> are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systemsCaroline M Kolvenbach, Tim Felger, Luca Schierbaum, et al.
Journal of Extracellular Biology|October 31, 2025
Two Sides of the Same Coin-Mechanistic Insight, Diagnostic Application and Therapeutic Translation of Bacterial and Host-Derived Extracellular VesiclesPhilipp Arnold, Fanni Annamária Boros, Jochen Mattner, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
American Journal of Medical Genetics. Part A|August 2, 2021
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genesCaroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 3, 2025
Ultrasound Super-Resolution Imaging of Neonatal Cerebral Vascular ReorganizationSimone Schwarz, Louise Denis, Emmanuel Nedoschill, et al.
Kidney International Reports|July 18, 2025
FLNA ROD1 and ROD2 Domains are Implicated in Congenital Lower Urinary Tract ObstructionClara Vidic, Jil Stegmann, Charlotte Bendixen, et al.
Biomolecules|July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease FormationRicarda Köllges, Jil Stegmann, Sophia Schneider, et al.
Journal of Medical Genetics|November 15, 2022
X-linked variations in <i>SHROOM4</i> are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systemsCaroline M Kolvenbach, Tim Felger, Luca Schierbaum, et al.
Journal of Extracellular Biology|October 31, 2025
Two Sides of the Same Coin-Mechanistic Insight, Diagnostic Application and Therapeutic Translation of Bacterial and Host-Derived Extracellular VesiclesPhilipp Arnold, Fanni Annamária Boros, Jochen Mattner, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
American Journal of Medical Genetics. Part A|August 2, 2021
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genesCaroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Pageof 10