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Nature Communications
|
April 29, 2023
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia, et al.
Journal of the American Society of Nephrology : JASN
|
August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
Science (New York, N.Y.)
|
May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle McNulty, et al.
Nature Genetics
|
October 13, 2014
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Krzysztof Kiryluk, Yifu Li, Francesco Scolari, et al.
Journal of the American Society of Nephrology : JASN
|
February 18, 2021
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, et al.
Journal of the American Society of Nephrology : JASN
|
March 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis
Dina F Ahram, Tze Y Lim, Juntao Ke, et al.
Nature Communications
|
November 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle T McNulty, et al.
The New England Journal of Medicine
|
January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
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Search research articles
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Showing results (131-140 of 149) with videos related to
Sort By:
Page
of 15
Nature Communications
|
April 29, 2023
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia, et al.
Journal of the American Society of Nephrology : JASN
|
August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
Science (New York, N.Y.)
|
May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle McNulty, et al.
Nature Genetics
|
October 13, 2014
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Krzysztof Kiryluk, Yifu Li, Francesco Scolari, et al.
Journal of the American Society of Nephrology : JASN
|
February 18, 2021
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, et al.
Journal of the American Society of Nephrology : JASN
|
March 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis
Dina F Ahram, Tze Y Lim, Juntao Ke, et al.
Nature Communications
|
November 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle T McNulty, et al.
The New England Journal of Medicine
|
January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
Page
of 15