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Bodo B Beck

Showing results (71-80 of 105) with videos related to

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Renal Failure|December 22, 2020
Clinical profile of a Polish cohort of children and young adults with cystinuriaMarcin Tkaczyk, Katarzyna Gadomska-Prokop, Iga Załuska-Leśniewska, et al.
Scientific Reports|March 10, 2018
Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutationsAndrea Wenzel, Janine Altmueller, Arif B Ekici, et al.
Journal of the American Society of Nephrology : JASN|July 28, 2018
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease RecognitionKarl X Knaup, Thomas Hackenbeck, Bernt Popp, et al.
Human Molecular Genetics|February 23, 2010
Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expressionFrank Zaucke, Joana M Boehnlein, Sarah Steffens, et al.
Kidney International Reports|July 11, 2022
Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope RegistryLisa J Deesker, Sander F Garrelfs, Giorgia Mandrile, et al.
American Journal of Human Genetics|January 5, 2019
Mutations of ADAMTS9 Cause Nephronophthisis-Related CiliopathyYo Jun Choi, Jan Halbritter, Daniela A Braun, et al.
Kidney International Reports|February 5, 2024
Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1Cristina Martin-Higueras, Lodovica Borghese, Armando Torres, et al.
Clinical Kidney Journal|July 3, 2026
Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group surveyMalte P Bartram, Giovambattista Capasso, Emilie Cornec-Le Gall, et al.
Kidney International Reports|February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> NephrocytesJohanna Odenthal, Sebastian Dittrich, Vivian Ludwig, et al.
European Journal of Human Genetics : EJHG|July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategiesBodo B Beck, Anne Baasner, Anja Buescher, et al.
Pageof 11

Showing results (71-80 of 105) with videos related to

Sort By:
Pageof 11
Renal Failure|December 22, 2020
Clinical profile of a Polish cohort of children and young adults with cystinuriaMarcin Tkaczyk, Katarzyna Gadomska-Prokop, Iga Załuska-Leśniewska, et al.
Scientific Reports|March 10, 2018
Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutationsAndrea Wenzel, Janine Altmueller, Arif B Ekici, et al.
Journal of the American Society of Nephrology : JASN|July 28, 2018
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease RecognitionKarl X Knaup, Thomas Hackenbeck, Bernt Popp, et al.
Human Molecular Genetics|February 23, 2010
Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expressionFrank Zaucke, Joana M Boehnlein, Sarah Steffens, et al.
Kidney International Reports|July 11, 2022
Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope RegistryLisa J Deesker, Sander F Garrelfs, Giorgia Mandrile, et al.
American Journal of Human Genetics|January 5, 2019
Mutations of ADAMTS9 Cause Nephronophthisis-Related CiliopathyYo Jun Choi, Jan Halbritter, Daniela A Braun, et al.
Kidney International Reports|February 5, 2024
Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1Cristina Martin-Higueras, Lodovica Borghese, Armando Torres, et al.
Clinical Kidney Journal|July 3, 2026
Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group surveyMalte P Bartram, Giovambattista Capasso, Emilie Cornec-Le Gall, et al.
Kidney International Reports|February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> NephrocytesJohanna Odenthal, Sebastian Dittrich, Vivian Ludwig, et al.
European Journal of Human Genetics : EJHG|July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategiesBodo B Beck, Anne Baasner, Anja Buescher, et al.
Pageof 11