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1. Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

2. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

5. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

6. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

7. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

9. Circulating testican-2 is a podocyte-derived marker of kidney health

10. List of contributors

13. A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis

14. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

16. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

23. Cross-link governed dynamics of biopolymer networks

24. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

26. UBD modifies APOL1 -induced kidney disease risk

29. Using population admixture to help complete maps of the human genome

30. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

32. Strong protective effect of theAPOL1p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

33. Apolipoprotein L1 (APOL1) cation current in HEK-293 cells and in human podocytes

38. Inaxaplin for Proteinuric Kidney Disease in Persons with Two APOL1 Variants

45. Nephrotic Syndrome Gene TBC1D8B Is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila

50. Evolution of the primate trypanolytic factor APOL1

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