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Journal of the American Society of Nephrology : JASN
|
October 27, 2022
Genomic Disorders in CKD across the Lifespan
Miguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Annals of Internal Medicine
|
December 6, 2017
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study
Sneh Lata, Maddalena Marasa, Yifu Li, et al.
The Journal of Clinical Investigation
|
March 28, 2025
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Sindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
The Journal of Clinical Investigation
|
June 15, 2026
Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Sindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 25, 2023
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
Jeremiah Martino, Qingxue Liu, Katarina Vukojevic, et al.
Kidney Medicine
|
April 11, 2025
Clinical Decision-Making About Immunosuppressive Treatment in Focal Segmental Glomerulosclerosis
Brooke Blazius, Jonathan P Troost, Jeffrey B Kopp, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disorders
Mark D Elliott, Natalie Vena, Maddalena Marasa, et al.
European Urology Open Science
|
October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Kidney International
|
February 26, 2026
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome
Tiffany Tu, Alejandro Ochoa, Amika Sood, et al.
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Search research articles
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Showing results (111-120 of 149) with videos related to
Sort By:
Page
of 15
Journal of the American Society of Nephrology : JASN
|
October 27, 2022
Genomic Disorders in CKD across the Lifespan
Miguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Annals of Internal Medicine
|
December 6, 2017
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study
Sneh Lata, Maddalena Marasa, Yifu Li, et al.
The Journal of Clinical Investigation
|
March 28, 2025
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Sindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
The Journal of Clinical Investigation
|
June 15, 2026
Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Sindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 25, 2023
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
Jeremiah Martino, Qingxue Liu, Katarina Vukojevic, et al.
Kidney Medicine
|
April 11, 2025
Clinical Decision-Making About Immunosuppressive Treatment in Focal Segmental Glomerulosclerosis
Brooke Blazius, Jonathan P Troost, Jeffrey B Kopp, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disorders
Mark D Elliott, Natalie Vena, Maddalena Marasa, et al.
European Urology Open Science
|
October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Kidney International
|
February 26, 2026
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome
Tiffany Tu, Alejandro Ochoa, Amika Sood, et al.
Page
of 15