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Carsten Bergmann

Showing results (161-170 of 228) with videos related to

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Kidney International|December 20, 2021
Scaffold polarity proteins Par3A and Par3B share redundant functions while Par3B acts independent of atypical protein kinase C/Par6 in podocytes to maintain the kidney filtration barrierSybille Koehler, Johanna Odenthal, Vivian Ludwig, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2011
Mutations in multiple PKD genes may explain early and severe polycystic kidney diseaseCarsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle, et al.
Clinical Genetics|October 11, 2020
Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trialJan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, et al.
Kidney International|February 9, 2024
Ibrutinib-associated focal segmental glomerulosclerosis and the impact of podocin mutations in chronic lymphocytic leukemiaJan Czogalla, Simon Schliffke, Shun Lu, et al.
Virchows Archiv : an International Journal of Pathology|March 12, 2013
Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS)Friedrich Modde, Putri Andina Agustian, Juliane Wittig, et al.
Journal of the American Society of Nephrology : JASN|May 14, 2015
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGSEmine Korkmaz, Beata S Lipska-Ziętkiewicz, Olivia Boyer, et al.
Clinical Kidney Journal|July 2, 2026
Clinical impact of genetic testing in inherited kidney diseasesLea M Merz, Sarah Stopp, Ilona Krey, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 18, 2017
Phenotypic Spectrum of Children with Nephronophthisis and Related CiliopathiesJens König, Birgitta Kranz, Sabine König, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
Pageof 23

Showing results (161-170 of 228) with videos related to

Sort By:
Pageof 23
Kidney International|December 20, 2021
Scaffold polarity proteins Par3A and Par3B share redundant functions while Par3B acts independent of atypical protein kinase C/Par6 in podocytes to maintain the kidney filtration barrierSybille Koehler, Johanna Odenthal, Vivian Ludwig, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2011
Mutations in multiple PKD genes may explain early and severe polycystic kidney diseaseCarsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle, et al.
Clinical Genetics|October 11, 2020
Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trialJan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, et al.
Kidney International|February 9, 2024
Ibrutinib-associated focal segmental glomerulosclerosis and the impact of podocin mutations in chronic lymphocytic leukemiaJan Czogalla, Simon Schliffke, Shun Lu, et al.
Virchows Archiv : an International Journal of Pathology|March 12, 2013
Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS)Friedrich Modde, Putri Andina Agustian, Juliane Wittig, et al.
Journal of the American Society of Nephrology : JASN|May 14, 2015
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGSEmine Korkmaz, Beata S Lipska-Ziętkiewicz, Olivia Boyer, et al.
Clinical Kidney Journal|July 2, 2026
Clinical impact of genetic testing in inherited kidney diseasesLea M Merz, Sarah Stopp, Ilona Krey, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 18, 2017
Phenotypic Spectrum of Children with Nephronophthisis and Related CiliopathiesJens König, Birgitta Kranz, Sabine König, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screeningWybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
Pageof 23