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Jan Halbritter

Showing results (71-80 of 106) with videos related to

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Clinical Epigenetics|June 16, 2025
Epigenetic silencing and CRISPR-mediated reactivation of tight junction protein claudin10b (CLDN10B) in renal cancerSarah Arroyo Villora, Yufen Zhao, Paula Castellanos Silva, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 20, 2025
The impact of the new WHO Classification of renal cell carcinoma on the diagnosis of hereditary leiomyomatosis and renal cell carcinomaJan Degenhardt, Yuri Tolkach, Mahul B Amin, et al.
Journal of the American Society of Nephrology : JASN|January 15, 2022
Claudin-10a Deficiency Shifts Proximal Tubular Cl<sup>-</sup> Permeability to Cation Selectivity <i>via</i> Claudin-2 RedistributionTilman Breiderhoff, Nina Himmerkus, Luca Meoli, et al.
The Journal of Cell Biology|April 15, 2015
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zoneElle C Roberson, William E Dowdle, Aysegul Ozanturk, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
American Journal of Human Genetics|June 3, 2014
Mutations of CEP83 cause infantile nephronophthisis and intellectual disabilityMarion Failler, Heon Yung Gee, Pauline Krug, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Journal of Medical Genetics|August 16, 2015
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotypeIsabelle Perrault, Jan Halbritter, Jonathan D Porath, et al.
European Journal of Human Genetics : EJHG|February 22, 2023
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney diseaseFloranne Boulogne, Laura R Claus, Henry Wiersma, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Clinical Epigenetics|June 16, 2025
Epigenetic silencing and CRISPR-mediated reactivation of tight junction protein claudin10b (CLDN10B) in renal cancerSarah Arroyo Villora, Yufen Zhao, Paula Castellanos Silva, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 20, 2025
The impact of the new WHO Classification of renal cell carcinoma on the diagnosis of hereditary leiomyomatosis and renal cell carcinomaJan Degenhardt, Yuri Tolkach, Mahul B Amin, et al.
Journal of the American Society of Nephrology : JASN|January 15, 2022
Claudin-10a Deficiency Shifts Proximal Tubular Cl<sup>-</sup> Permeability to Cation Selectivity <i>via</i> Claudin-2 RedistributionTilman Breiderhoff, Nina Himmerkus, Luca Meoli, et al.
The Journal of Cell Biology|April 15, 2015
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zoneElle C Roberson, William E Dowdle, Aysegul Ozanturk, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
American Journal of Human Genetics|June 3, 2014
Mutations of CEP83 cause infantile nephronophthisis and intellectual disabilityMarion Failler, Heon Yung Gee, Pauline Krug, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Journal of Medical Genetics|August 16, 2015
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotypeIsabelle Perrault, Jan Halbritter, Jonathan D Porath, et al.
European Journal of Human Genetics : EJHG|February 22, 2023
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney diseaseFloranne Boulogne, Laura R Claus, Henry Wiersma, et al.
Pageof 11