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Bodo B Beck

Showing results (91-100 of 105) with videos related to

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Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2023
Germline <i>C1GALT1C1</i> mutation causes a multisystem chaperonopathyFlorian Erger, Rajindra P Aryal, Björn Reusch, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractMarcin Kołbuc, Mateusz F Kołek, Rafał Motyka, et al.
Kidney International Reports|October 27, 2025
Novel <i>RRAGD</i> Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.
Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
Kidney International Reports|October 18, 2023
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria ConsortiumElisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2018
Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney DiseaseMartina Živná, Kendrah Kidd, Anna Přistoupilová, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Kidney International|May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKathrin Burgmaier, Leonie Brinker, Florian Erger, et al.
Kidney International|June 1, 2022
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseasesFlorian J Wopperer, Karl X Knaup, Kira J Stanzick, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2023
Germline <i>C1GALT1C1</i> mutation causes a multisystem chaperonopathyFlorian Erger, Rajindra P Aryal, Björn Reusch, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractMarcin Kołbuc, Mateusz F Kołek, Rafał Motyka, et al.
Kidney International Reports|October 27, 2025
Novel <i>RRAGD</i> Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.
Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
Kidney International Reports|October 18, 2023
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria ConsortiumElisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2018
Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney DiseaseMartina Živná, Kendrah Kidd, Anna Přistoupilová, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Kidney International|May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKathrin Burgmaier, Leonie Brinker, Florian Erger, et al.
Kidney International|June 1, 2022
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseasesFlorian J Wopperer, Karl X Knaup, Kira J Stanzick, et al.
Pageof 11