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Martin R Pollak

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Journal of the American Society of Nephrology : JASN|July 12, 2014

Localization of APOL1 protein and mRNA in the human kidney: nondiseased tissue, primary cells, and immortalized cell linesLijun Ma, Gregory S Shelness, James A Snipes, et al.

Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.

Journal of the American Society of Nephrology : JASN|March 29, 2014

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGSRasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, et al.

Kidney International|December 26, 2025

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosisJanewit Wongboonsin, Kristen M Gibson, Juntao Ke, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 22, 2020

Circulating testican-2 is a podocyte-derived marker of kidney healthDebby Ngo, Donghai Wen, Yan Gao, et al.

Nature Reviews. Nephrology|May 21, 2026

Gene-disease relationships for glomerular phenotypes: expert recommendations from ClinGenAlicia B Byrne, Anna S Li, Edmund Y M Chung, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 7, 2008

Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complicationsZongzhong Tong, Zhenglin Yang, Shrena Patel, et al.

Nature Genetics|February 12, 2013

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.

JAMA Network Open|March 11, 2026

Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.

Journal of the American Society of Nephrology : JASN|October 1, 2024

Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.

Pageof 17

Search research articles

Showing results (151-160 of 167) with videos related to

Sort By:

Pageof 17

Journal of the American Society of Nephrology : JASN|July 12, 2014

Localization of APOL1 protein and mRNA in the human kidney: nondiseased tissue, primary cells, and immortalized cell linesLijun Ma, Gregory S Shelness, James A Snipes, et al.

Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.

Journal of the American Society of Nephrology : JASN|March 29, 2014

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGSRasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, et al.

Kidney International|December 26, 2025

Proceedings of the National Academy of Sciences of the United States of America|September 22, 2020

Circulating testican-2 is a podocyte-derived marker of kidney healthDebby Ngo, Donghai Wen, Yan Gao, et al.

Nature Reviews. Nephrology|May 21, 2026

Gene-disease relationships for glomerular phenotypes: expert recommendations from ClinGenAlicia B Byrne, Anna S Li, Edmund Y M Chung, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 7, 2008

Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complicationsZongzhong Tong, Zhenglin Yang, Shrena Patel, et al.

Nature Genetics|February 12, 2013

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.