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Carsten Bergmann

Showing results (101-110 of 228) with videos related to

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International Journal of Molecular Sciences|July 28, 2022
Hyperinsulinemic Hypoglycemia Associated with a Ca<sub>V</sub>1.2 Variant with Mixed Gain- and Loss-of-Function EffectsSebastian Kummer, Susanne Rinné, Gunnar Seemann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 14, 2020
Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genesRia Schönauer, Sebastian Baatz, Melanie Nemitz-Kliemchen, et al.
Pediatric Nephrology (Berlin, Germany)|February 25, 2022
Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney diseaseJens Michael Hertz, Per Svenningsen, Henrik Dimke, et al.
Plos One|October 12, 2013
Genetic characteristics of the human hepatic stellate cell line LX-2Ralf Weiskirchen, Jörg Weimer, Steffen K Meurer, et al.
European Journal of Medical Genetics|April 25, 2008
Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the ratPamela J Kaisaki, Carsten Bergmann, Joanna H Brown, et al.
BMC Nephrology|May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathyBernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Molecular Diagnosis & Therapy|June 15, 2006
Diagnosis, pathogenesis, and treatment prospects in cystic kidney diseaseCarsten Bergmann, Valeska Frank, Fabian Küpper, et al.
Kidney International Reports|July 14, 2021
Atypical Hemolytic and Uremic Syndrome Triggered by Infection With SARS-CoV2Jessica Kaufeld, Martin Reinhardt, Christoph Schröder, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 15, 2021
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practiceNine Knoers, Corinne Antignac, Carsten Bergmann, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 8, 2022
A SEC61A1 variant is associated with autosomal dominant polycystic liver diseaseBernhard Schlevogt, Vincent Schlieper, Jana Krader, et al.
Pageof 23

Showing results (101-110 of 228) with videos related to

Sort By:
Pageof 23
International Journal of Molecular Sciences|July 28, 2022
Hyperinsulinemic Hypoglycemia Associated with a Ca<sub>V</sub>1.2 Variant with Mixed Gain- and Loss-of-Function EffectsSebastian Kummer, Susanne Rinné, Gunnar Seemann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 14, 2020
Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genesRia Schönauer, Sebastian Baatz, Melanie Nemitz-Kliemchen, et al.
Pediatric Nephrology (Berlin, Germany)|February 25, 2022
Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney diseaseJens Michael Hertz, Per Svenningsen, Henrik Dimke, et al.
Plos One|October 12, 2013
Genetic characteristics of the human hepatic stellate cell line LX-2Ralf Weiskirchen, Jörg Weimer, Steffen K Meurer, et al.
European Journal of Medical Genetics|April 25, 2008
Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the ratPamela J Kaisaki, Carsten Bergmann, Joanna H Brown, et al.
BMC Nephrology|May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathyBernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Molecular Diagnosis & Therapy|June 15, 2006
Diagnosis, pathogenesis, and treatment prospects in cystic kidney diseaseCarsten Bergmann, Valeska Frank, Fabian Küpper, et al.
Kidney International Reports|July 14, 2021
Atypical Hemolytic and Uremic Syndrome Triggered by Infection With SARS-CoV2Jessica Kaufeld, Martin Reinhardt, Christoph Schröder, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 15, 2021
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practiceNine Knoers, Corinne Antignac, Carsten Bergmann, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 8, 2022
A SEC61A1 variant is associated with autosomal dominant polycystic liver diseaseBernhard Schlevogt, Vincent Schlieper, Jana Krader, et al.
Pageof 23