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Journal of the American Society of Nephrology : JASN|February 10, 2019
Treatment with 2,4-Dihydroxybenzoic Acid Prevents FSGS Progression and Renal Fibrosis in Podocyte-Specific <i>Coq6</i> Knockout MiceEugen Widmeier, Merlin Airik, Hannah Hugo, et al.Plos One|January 19, 2018
Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish modelTilman Jobst-Schwan, Johanna Magdalena Schmidt, Ronen Schneider, et al.Gastroenterology|August 2, 2016
Inflammation-Induced Expression and Secretion of MicroRNA 122 Leads to Reduced Blood Levels of Kidney-Derived Erythropoietin and AnemiaMila Rivkin, Alina Simerzin, Elina Zorde-Khvalevsky, 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|July 14, 2024
Phenotypic quantification of Nphs1-deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.Kidney International Reports|February 22, 2021
Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent ApproachesVerena Klämbt, Youying Mao, Ronen Schneider, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 9, 2018
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in childrenDavid Schapiro, Ankana Daga, Jennifer A Lawson, et al.Journal of the American Society of Nephrology : JASN|November 17, 2019
<i>TBC1D8B</i> Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic SyndromeLina L Kampf, Ronen Schneider, Lea Gerstner, et al.Human Genetics|June 24, 2019
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humansThomas M Kitzler, Ronen Schneider, Stefan Kohl, et al.Pageof 5