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11. Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations

13. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

15. Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis

17. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

22. TRPC6 Enhances Angiotensin II-induced Albuminuria

25. SP001A Novel Heterozygous Missense Mutation of Wilms’ Tumor 1 May Cause FSGS Through Dysregulated Expression of ARHGAP24

26. FO068The LMX1βR246Q Mutation Induces Podocyte Injury Through Dysregulation of Cholesterol Transport Gene Expression

27. Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population

30. The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes

34. Study on the pharmacokinetics of enrofloxacin in the Chinese mitten-handed crab,Eriocheir sinensis, after different administration regimes

41. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

42. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

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

44. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

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

46. Microwave laboratory using PUFF

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

49. TNXB Mutations Can Cause Vesicoureteral Reflux

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