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Jan Halbritter

Showing results (41-50 of 106) with videos related to

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Physiological Reports|June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutationsAmy Fearn, Benjamin Allison, Sarah J Rice, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
<i>In vivo</i> base editing reduces liver cysts in autosomal dominant polycystic kidney diseaseAntonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 2025
Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)Albertien M van Eerde, Ana Teixeira, Flavia Galletti, et al.
Frontiers in Immunology|February 13, 2023
Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantationClaudia Lehmann, Sarah Pehnke, Antje Weimann, et al.
Plos One|July 12, 2021
Acute kidney injury and its progression in hospitalized patients-Results from a retrospective multicentre cohort study with a digital decision support systemThea Sophie Kister, Johannes Remmler, Maria Schmidt, et al.
Clinical Kidney Journal|December 12, 2024
Kidney transplantation in patients with polycystic kidney disease: increased risk of infection does not compromise graft and patient survivalJohannes Waiser, Jens Klotsche, Petra Glander, et al.
Journal of Medical Genetics|November 29, 2012
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencingJan Halbritter, Katrina Diaz, Moumita Chaki, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 3, 2025
Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERAJan Halbritter, Lucile Figueres, Albertien M Van Eerde, et al.
Kidney International|June 8, 2020
Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitmentRia Schönauer, Wenjun Jin, Anastasia Ertel, et al.
Journal of Medical Genetics|December 18, 2015
Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathiesMarkus Schueler, Jan Halbritter, Ian G Phelps, et al.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Physiological Reports|June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutationsAmy Fearn, Benjamin Allison, Sarah J Rice, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
<i>In vivo</i> base editing reduces liver cysts in autosomal dominant polycystic kidney diseaseAntonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 2025
Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)Albertien M van Eerde, Ana Teixeira, Flavia Galletti, et al.
Frontiers in Immunology|February 13, 2023
Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantationClaudia Lehmann, Sarah Pehnke, Antje Weimann, et al.
Plos One|July 12, 2021
Acute kidney injury and its progression in hospitalized patients-Results from a retrospective multicentre cohort study with a digital decision support systemThea Sophie Kister, Johannes Remmler, Maria Schmidt, et al.
Clinical Kidney Journal|December 12, 2024
Kidney transplantation in patients with polycystic kidney disease: increased risk of infection does not compromise graft and patient survivalJohannes Waiser, Jens Klotsche, Petra Glander, et al.
Journal of Medical Genetics|November 29, 2012
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencingJan Halbritter, Katrina Diaz, Moumita Chaki, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 3, 2025
Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERAJan Halbritter, Lucile Figueres, Albertien M Van Eerde, et al.
Kidney International|June 8, 2020
Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitmentRia Schönauer, Wenjun Jin, Anastasia Ertel, et al.
Journal of Medical Genetics|December 18, 2015
Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathiesMarkus Schueler, Jan Halbritter, Ian G Phelps, et al.
Pageof 11