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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.
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.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Atlas of glomerular disease-specific genetic effects on blood transcriptome
Lili Liu, Chen Wang, Oleksandr Kravets, 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.
Medrxiv : the Preprint Server for Health Sciences
|
September 19, 2025
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.
Nature Genetics
|
March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathy
Ali G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
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Search research articles
Search
Showing results (61-70 of 93) with videos related to
Sort By:
Page
of 10
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.
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.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Atlas of glomerular disease-specific genetic effects on blood transcriptome
Lili Liu, Chen Wang, Oleksandr Kravets, 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.
Medrxiv : the Preprint Server for Health Sciences
|
September 19, 2025
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.
Nature Genetics
|
March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathy
Ali G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
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of 10