37 results on '"Harris, Peter C."'
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2. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
3. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
4. Primary results of the randomized trial of metformin administration in polycystic kidney disease (TAME PKD)
5. The genetic background significantly impacts the severity of kidney cystic disease in the Pkd1RC/RC mouse model of autosomal dominant polycystic kidney disease
6. Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
7. Detection and characterization of mosaicism in autosomal dominant polycystic kidney disease
8. Long-term trajectory of kidney function in autosomal-dominant polycystic kidney disease
9. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
10. CD8+ T cells modulate autosomal dominant polycystic kidney disease progression
11. Baseline total kidney volume and the rate of kidney growth are associated with chronic kidney disease progression in Autosomal Dominant Polycystic Kidney Disease
12. Utility of new image-derived biomarkers for autosomal dominant polycystic kidney disease prognosis using automated instance cyst segmentation
13. Image texture features predict renal function decline in patients with autosomal dominant polycystic kidney disease
14. Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
15. B-type natriuretic peptide overexpression ameliorates hepatorenal fibrocystic disease in a rat model of polycystic kidney disease
16. A polycystin-centric view of cyst formation and disease: the polycystins revisited
17. Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families
18. Cyclic nucleotide signaling in polycystic kidney disease
19. Autosomal dominant polycystic kidney disease: the last 3 years
20. Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease
21. Establishing a nephrology genetic clinic
22. Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome
23. Molecular pathogenesis of ADPKD: The polycystin complex gets complex
24. Epidermal growth factor receptor tyrosine kinase inhibition is not protective in PCK rats
25. Follow-up of intracranial aneurysms in autosomal-dominant polycystic kidney disease
26. EGF receptor tyrosine kinase inhibition attenuates the development of PKD in Han: SPRD rats
27. A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees
28. The time for next-generation molecular genetic diagnostics in nephrology is now!
29. A complete mutation screen of the ADPKD genes by DHPLC
30. Treatment prospects for autosomal-dominant polycystic kidney disease
31. EGF receptor tyrosine kinase inhibition attenuates the development of PKD in Han:SPRD rats
32. Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue
33. The genetic background significantly impacts the severity of kidney cystic disease in the Pkd1RC/RCmouse model of autosomal dominant polycystic kidney disease
34. Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
35. CD8+T cells modulate autosomal dominant polycystic kidney disease progression
36. Cyclic nucleotide signaling in polycystic kidney disease.
37. GENETIC DISORDERS - DEVELOPMENT Follow-up of intracranial aneurysms in autosomal-dominant polycystic kidney disease.
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