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Caroline M Kolvenbach

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Nature Reviews. Nephrology|July 31, 2023
The genetics and pathogenesis of CAKUTCaroline M Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Pediatric Nephrology (Berlin, Germany)|June 21, 2024
Recessive variants in MYO1C as a potential novel cause of proteinuric kidney diseaseIzzeldin Elmubarak, Shirlee Shril, Bshara Mansour, et al.
Kidney International|April 24, 2019
Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockoutTilman Jobst-Schwan, Charlotte A Hoogstraten, Caroline M Kolvenbach, et al.
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tractCaroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Scientific Reports|July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish typeKatharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
American Journal of Physiology. Renal Physiology|March 14, 2024
Quantitative phenotyping of <i>Nphs1</i> knockout mice as a prerequisite for gene replacement studiesFlorian Buerger, Lea M Merz, Ken Saida, et al.
Journal of Nephrology|August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology|July 14, 2024
Phenotypic quantification of Nphs1-deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Nature Reviews. Nephrology|July 31, 2023
The genetics and pathogenesis of CAKUTCaroline M Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Pediatric Nephrology (Berlin, Germany)|June 21, 2024
Recessive variants in MYO1C as a potential novel cause of proteinuric kidney diseaseIzzeldin Elmubarak, Shirlee Shril, Bshara Mansour, et al.
Kidney International|April 24, 2019
Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockoutTilman Jobst-Schwan, Charlotte A Hoogstraten, Caroline M Kolvenbach, et al.
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tractCaroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Scientific Reports|July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish typeKatharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
American Journal of Physiology. Renal Physiology|March 14, 2024
Quantitative phenotyping of <i>Nphs1</i> knockout mice as a prerequisite for gene replacement studiesFlorian Buerger, Lea M Merz, Ken Saida, et al.
Journal of Nephrology|August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology|July 14, 2024
Phenotypic quantification of Nphs1-deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Pageof 3