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Kidney International Reports
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April 6, 2026
<i>NPHS2</i> Revisited Through 208 Cases and Podocin Complex Modeling
Nils David Mertens, Camille Nicolas Frank, Leah Bolsius, et al.
Kidney International
|
September 25, 2021
Effect of disease progression on the podocyte cell cycle in Alport Syndrome
Camille Nicolas Frank, Xiaogang Hou, Astgik Petrosyan, et al.
Science Translational Medicine
|
October 30, 2024
A kidney-specific fasting-mimicking diet induces podocyte reprogramming and restores renal function in glomerulopathy
Valentina Villani, Camille Nicolas Frank, Paolo Cravedi, et al.
Scientific Reports
|
July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
Katharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
Journal of Nephrology
|
August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology
|
July 14, 2024
Phenotypic quantification of Nphs1-deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Genes & Diseases
|
June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletions
Konstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models
Chunyan Wang, Steve Seltzsam, Bixia Zheng, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome
Bshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Kidney International Reports
|
April 6, 2026
<i>NPHS2</i> Revisited Through 208 Cases and Podocin Complex Modeling
Nils David Mertens, Camille Nicolas Frank, Leah Bolsius, et al.
Kidney International
|
September 25, 2021
Effect of disease progression on the podocyte cell cycle in Alport Syndrome
Camille Nicolas Frank, Xiaogang Hou, Astgik Petrosyan, et al.
Science Translational Medicine
|
October 30, 2024
A kidney-specific fasting-mimicking diet induces podocyte reprogramming and restores renal function in glomerulopathy
Valentina Villani, Camille Nicolas Frank, Paolo Cravedi, et al.
Scientific Reports
|
July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
Katharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
Journal of Nephrology
|
August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology
|
July 14, 2024
Phenotypic quantification of Nphs1-deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Genes & Diseases
|
June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletions
Konstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models
Chunyan Wang, Steve Seltzsam, Bixia Zheng, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome
Bshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Page
of 2