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Seyoung Yu

Showing results (21-30 of 26) with videos related to

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Journal of Nephrology|July 14, 2024
Phenotypic quantification of Nphs1-deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of the American Society of Nephrology : JASN|August 9, 2024
Regenerative Role of Lrig1+ Cells in Kidney RepairYura Lee, Kwang H Kim, Jihwan Park, et al.
Kidney International Reports|October 27, 2025
Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center CohortKatharina Lemberg, Mohamed A Shalaby, Elena Zion, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Nature|March 27, 2025
The contribution of de novo coding mutations to meningomyeloceleYoo-Jin Jiny Ha, Ashna Nisal, Isaac Tang, et al.
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Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of Nephrology|July 14, 2024
Phenotypic quantification of Nphs1-deficient miceRonen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of the American Society of Nephrology : JASN|August 9, 2024
Regenerative Role of Lrig1+ Cells in Kidney RepairYura Lee, Kwang H Kim, Jihwan Park, et al.
Kidney International Reports|October 27, 2025
Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center CohortKatharina Lemberg, Mohamed A Shalaby, Elena Zion, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Nature|March 27, 2025
The contribution of de novo coding mutations to meningomyeloceleYoo-Jin Jiny Ha, Ashna Nisal, Isaac Tang, et al.
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