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Jan Halbritter

Showing results (51-60 of 106) with videos related to

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Journal of the American Society of Nephrology : JASN|May 11, 2013
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotypeToby W Hurd, Edgar A Otto, Eikan Mishima, et al.
Plos One|February 12, 2011
Genetic and evolutionary analyses of the human bone morphogenetic protein receptor 2 (BMPR2) in the pathophysiology of obesityDorit Schleinitz, Nora Klöting, Yvonne Böttcher, et al.
Journal of the American Society of Nephrology : JASN|October 10, 2014
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosisJan Halbritter, Michelle Baum, Ann Marie Hynes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 22, 2025
In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney diseaseAntonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, et al.
Journal of the American Society of Nephrology : JASN|July 28, 2018
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease RecognitionKarl X Knaup, Thomas Hackenbeck, Bernt Popp, et al.
Kidney International Reports|August 15, 2025
Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney DiseaseChristin Findeisen, Maria Papazian, Linda Pöschla, et al.
ACS Sensors|June 25, 2026
CRISPR-Based Assay for Point-of-Care Pharmacogenetic CYP2C19 GenotypingAlexander J Schubert, Qiyao Meng, Joshua Hoffmann, et al.
Human Genetics|February 20, 2019
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasisAli Amar, Amar J Majmundar, Ihsan Ullah, et al.
American Journal of Human Genetics|January 5, 2019
Mutations of ADAMTS9 Cause Nephronophthisis-Related CiliopathyYo Jun Choi, Jan Halbritter, Daniela A Braun, et al.
Journal of Lipid Research|September 12, 2013
THOC5: a novel gene involved in HDL-cholesterol metabolismMaria Keller, Dorit Schleinitz, Julia Förster, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
Journal of the American Society of Nephrology : JASN|May 11, 2013
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotypeToby W Hurd, Edgar A Otto, Eikan Mishima, et al.
Plos One|February 12, 2011
Genetic and evolutionary analyses of the human bone morphogenetic protein receptor 2 (BMPR2) in the pathophysiology of obesityDorit Schleinitz, Nora Klöting, Yvonne Böttcher, et al.
Journal of the American Society of Nephrology : JASN|October 10, 2014
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosisJan Halbritter, Michelle Baum, Ann Marie Hynes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 22, 2025
In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney diseaseAntonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, et al.
Journal of the American Society of Nephrology : JASN|July 28, 2018
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease RecognitionKarl X Knaup, Thomas Hackenbeck, Bernt Popp, et al.
Kidney International Reports|August 15, 2025
Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney DiseaseChristin Findeisen, Maria Papazian, Linda Pöschla, et al.
ACS Sensors|June 25, 2026
CRISPR-Based Assay for Point-of-Care Pharmacogenetic CYP2C19 GenotypingAlexander J Schubert, Qiyao Meng, Joshua Hoffmann, et al.
Human Genetics|February 20, 2019
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasisAli Amar, Amar J Majmundar, Ihsan Ullah, et al.
American Journal of Human Genetics|January 5, 2019
Mutations of ADAMTS9 Cause Nephronophthisis-Related CiliopathyYo Jun Choi, Jan Halbritter, Daniela A Braun, et al.
Journal of Lipid Research|September 12, 2013
THOC5: a novel gene involved in HDL-cholesterol metabolismMaria Keller, Dorit Schleinitz, Julia Förster, et al.
Pageof 11