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2. Precision nephrology identified tumor necrosis factor activation variability in minimal change disease and focal segmental glomerulosclerosis

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

5. APOL1 genetic variants are not associated with longitudinal blood pressure in young black adults

6. Apolipoprotein-1 risk variants and associated kidney phenotypes in an adult HIV cohort in Nigeria

22. Screening, diagnosis, and management of patients with Fabry disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

24. Sequencing rare and common APOL1 coding variants to determine kidney disease risk

26. Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1

27. Increased mitochondrial activity in renal proximal tubule cells from young spontaneously hypertensive rats

28. APOL1nephropathy risk variants do not associate with subclinical atherosclerosis or left ventricular mass in middle-aged black adults

29. APOL1genetic variants are not associated with longitudinal blood pressure in young black adults

31. Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach

32. Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

33. HIV-associated nephropathy patients with and without apolipoprotein L1 gene variants have similar clinical and pathological characteristics

35. Angiotensin II overcomes strain-dependent resistance of rapid CKD progression in a new remnant kidney mouse model

39. Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

40. Urinary exosomal transcription factors, a new class of biomarkers for renal disease

48. Tubular-specific expression of HIV protein Vpr leads to severe tubulointerstitial damage accompanied by progressive fibrosis and cystic development

50. Urinary exosomal transcription factors, a new class of biomarkers for renal disease.

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