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Carsten Bergmann

Showing results (71-80 of 228) with videos related to

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Pediatric Nephrology (Berlin, Germany)|March 15, 2012
Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver diseaseAndrea Zingg-Schenk, Jürg Caduff, Silvia Azzarello-Burri, et al.
BMC Nephrology|January 14, 2018
Treating C3 glomerulopathy with eculizumabThomas Welte, Frederic Arnold, Julia Kappes, et al.
Genes & Diseases|July 25, 2022
Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assemblySebastian Sewerin, Jörg Piontek, Ria Schönauer, et al.
Nature Reviews. Disease Primers|December 8, 2018
Polycystic kidney diseaseCarsten Bergmann, Lisa M Guay-Woodford, Peter C Harris, et al.
Scientific Reports|September 12, 2025
Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesisDaniel Epting, John Devane, Ralf Mertes, et al.
Scientific Reports|January 12, 2026
Correction: Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesisDaniel Epting, John Devane, Ralf Mertes, et al.
Brain : a Journal of Neurology|June 14, 2003
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasiaCarsten Bergmann, Klaus Zerres, Jan Senderek, et al.
Acta Ophthalmologica|June 12, 2012
Extended mutation spectrum of Usher syndrome in FinlandHanna Västinsalo, Reetta Jalkanen, Carsten Bergmann, et al.
Hepatology (Baltimore, Md.)|April 15, 2005
A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)Markus Moser, Sonja Matthiesen, Jutta Kirfel, et al.
Kidney International Reports|May 16, 2022
Interstitial Nephritis: A Change in Diagnosis With Next-Generation SequencingMira Choi, Anne Rübsam, Marten Schulz, et al.
Pageof 23

Showing results (71-80 of 228) with videos related to

Sort By:
Pageof 23
Pediatric Nephrology (Berlin, Germany)|March 15, 2012
Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver diseaseAndrea Zingg-Schenk, Jürg Caduff, Silvia Azzarello-Burri, et al.
BMC Nephrology|January 14, 2018
Treating C3 glomerulopathy with eculizumabThomas Welte, Frederic Arnold, Julia Kappes, et al.
Genes & Diseases|July 25, 2022
Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assemblySebastian Sewerin, Jörg Piontek, Ria Schönauer, et al.
Nature Reviews. Disease Primers|December 8, 2018
Polycystic kidney diseaseCarsten Bergmann, Lisa M Guay-Woodford, Peter C Harris, et al.
Scientific Reports|September 12, 2025
Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesisDaniel Epting, John Devane, Ralf Mertes, et al.
Scientific Reports|January 12, 2026
Correction: Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesisDaniel Epting, John Devane, Ralf Mertes, et al.
Brain : a Journal of Neurology|June 14, 2003
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasiaCarsten Bergmann, Klaus Zerres, Jan Senderek, et al.
Acta Ophthalmologica|June 12, 2012
Extended mutation spectrum of Usher syndrome in FinlandHanna Västinsalo, Reetta Jalkanen, Carsten Bergmann, et al.
Hepatology (Baltimore, Md.)|April 15, 2005
A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)Markus Moser, Sonja Matthiesen, Jutta Kirfel, et al.
Kidney International Reports|May 16, 2022
Interstitial Nephritis: A Change in Diagnosis With Next-Generation SequencingMira Choi, Anne Rübsam, Marten Schulz, et al.
Pageof 23