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Sandra Habbig

Showing results (51-60 of 74) with videos related to

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Pediatric Transplantation|April 4, 2017
Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimensSandra Habbig, Ruth Volland, Kai Krupka, et al.
Scientific Reports|July 18, 2019
Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney diseaseChristian Freise, Betti Schaefer, Maria Bartosova, 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.
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.
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.
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.
Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Plos One|August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasiaBeata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Pediatric Transplantation|April 4, 2017
Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimensSandra Habbig, Ruth Volland, Kai Krupka, et al.
Scientific Reports|July 18, 2019
Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney diseaseChristian Freise, Betti Schaefer, Maria Bartosova, 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.
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.
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.
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.
Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Plos One|August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasiaBeata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Pageof 8