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2. A torpor-like state (TLS) in mice slows blood epigenetic aging and prolongs healthspan

8. Neurons that regulate mouse torpor

9. Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease

10. Utility of Genomic Testing after Renal Biopsy

11. Atrasentan and renal events in patients with type 2 diabetes and chronic kidney disease (SONAR): a double-blind, randomised, placebo-controlled trial

12. Monogenic causes of chronic kidney disease in adults

14. Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease

16. Unusual cause of loin pain

17. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

18. The Irish Kidney Gene Project - Prevalence of Family History in Patients with Kidney Disease in Ireland

19. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS

20. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity

22. C3 glomerulopathy: consensus report

23. TNXB Mutations Can Cause Vesicoureteral Reflux

25. A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy

26. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

28. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

32. TRPC6 Enhances Angiotensin II-induced Albuminuria

33. A New Locus for Familial FSGS on Chromosome 2P

39. Reviews

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