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Sandra Habbig

Showing results (41-50 of 74) with videos related to

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Human Molecular Genetics|October 3, 2012
The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZSandra Habbig, Malte P Bartram, Josef G Sägmüller, et al.
Human Molecular Genetics|January 8, 2016
Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGSMalte P Bartram, Sandra Habbig, Caroline Pahmeyer, et al.
The Lancet. Child & Adolescent Health|March 14, 2026
Survival, kidney function, and complications in the first year of life following intrauterine shunting for first-trimester fetal megacystis (IUS1st): analysis of a prospective observational cohortEva C Weber, Stefan Kohl, Ingo Gottschalk, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 15, 2011
Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndromeMarkus J Kemper, Jutta Gellermann, Sandra Habbig, et al.
Kidney International Reports|May 20, 2021
Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo SignalingFrancesca Fabretti, Nikolai Tschernoster, Florian Erger, et al.
Pediatric Transplantation|March 9, 2022
Prevalence and potential relevance of hyperuricemia in pediatric kidney transplant recipients-a CERTAIN registry analysisRasmus Ehren, Sandra Habbig, Kai Krupka, et al.
The Journal of Molecular Diagnostics : JMD|April 10, 2022
Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted SequencingNikolai Tschernoster, Florian Erger, Patrick R Walsh, et al.
JAMA Pediatrics|November 29, 2017
Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature ReviewsCharlotte Gimpel, Fred E Avni, Carsten Bergmann, et al.
The Journal of Biological Chemistry|March 2, 2011
Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monociliaMax C Liebau, Katja Höpker, Roman U Müller, et al.
Scientific Reports|August 9, 2019
Impaired Systolic and Diastolic Left Ventricular Function in Children with Chronic Kidney Disease - Results from the 4C StudyAnke Doyon, Pascal Haas, Sevcan Erdem, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|October 3, 2012
The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZSandra Habbig, Malte P Bartram, Josef G Sägmüller, et al.
Human Molecular Genetics|January 8, 2016
Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGSMalte P Bartram, Sandra Habbig, Caroline Pahmeyer, et al.
The Lancet. Child & Adolescent Health|March 14, 2026
Survival, kidney function, and complications in the first year of life following intrauterine shunting for first-trimester fetal megacystis (IUS1st): analysis of a prospective observational cohortEva C Weber, Stefan Kohl, Ingo Gottschalk, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 15, 2011
Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndromeMarkus J Kemper, Jutta Gellermann, Sandra Habbig, et al.
Kidney International Reports|May 20, 2021
Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo SignalingFrancesca Fabretti, Nikolai Tschernoster, Florian Erger, et al.
Pediatric Transplantation|March 9, 2022
Prevalence and potential relevance of hyperuricemia in pediatric kidney transplant recipients-a CERTAIN registry analysisRasmus Ehren, Sandra Habbig, Kai Krupka, et al.
The Journal of Molecular Diagnostics : JMD|April 10, 2022
Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted SequencingNikolai Tschernoster, Florian Erger, Patrick R Walsh, et al.
JAMA Pediatrics|November 29, 2017
Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature ReviewsCharlotte Gimpel, Fred E Avni, Carsten Bergmann, et al.
The Journal of Biological Chemistry|March 2, 2011
Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monociliaMax C Liebau, Katja Höpker, Roman U Müller, et al.
Scientific Reports|August 9, 2019
Impaired Systolic and Diastolic Left Ventricular Function in Children with Chronic Kidney Disease - Results from the 4C StudyAnke Doyon, Pascal Haas, Sevcan Erdem, et al.
Pageof 8