Search research articles
Contact Us
Filters
Showing results (551-560 of 574) with videos related to
Page
of 58
Sort By:
Kidney International Reports
|
November 20, 2018
Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study
David T Selewski, Josephine M Ambruzs, Gerald B Appel, 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.
Nature Genetics
|
January 3, 2025
ZIC1 is a context-dependent medulloblastoma driver in the rhombic lip
John J Y Lee, Ran Tao, Zhen You, 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.
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 Communications
|
January 4, 2019
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Andrew P Morris, Thu H Le, Haojia Wu, 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 58
Search research articles
Search
Showing results (551-560 of 574) with videos related to
Sort By:
Page
of 58
Kidney International Reports
|
November 20, 2018
Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study
David T Selewski, Josephine M Ambruzs, Gerald B Appel, 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.
Nature Genetics
|
January 3, 2025
ZIC1 is a context-dependent medulloblastoma driver in the rhombic lip
John J Y Lee, Ran Tao, Zhen You, 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.
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 Communications
|
January 4, 2019
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Andrew P Morris, Thu H Le, Haojia Wu, 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 58