41 results on '"Hall, Gentzon"'
Search Results
2. Interleukin-15 in kidney disease and therapeutics
3. β-Arrestin pathway activation by selective ATR1 agonism promotes calcium influx in podocytes, leading to glomerular damage
4. List of Contributors
5. Genetic Causes of Chronic Kidney Disease
6. Tobacco exposure in adults and children with proteinuric glomerulopathies: a NEPTUNE cohort study
7. JAK inhibitor blocks COVID-19 cytokine–induced JAK/STAT/APOL1 signaling in glomerular cells and podocytopathy in human kidney organoids
8. IL-1 receptor signaling in podocytes limits susceptibility to glomerular damage
9. Outscoring Current Classification Systems for Nephrotic Syndrome
10. Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis
11. Mechanisms of Proteinuria in HIV
12. Twist1 in podocytes ameliorates podocyte injury and proteinuria by limiting CCL2-dependent macrophage infiltration
13. TRPC Channels in Proteinuric Kidney Diseases
14. SP001A Novel Heterozygous Missense Mutation of Wilms’ Tumor 1 May Cause FSGS Through Dysregulated Expression of ARHGAP24
15. FO068The LMX1βR246Q Mutation Induces Podocyte Injury Through Dysregulation of Cholesterol Transport Gene Expression
16. Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population
17. The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes
18. Losing their footing: Rac1 signaling causes podocyte detachment and FSGS
19. Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype
20. Dysregulation of WTI (−KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation
21. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux
22. Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation
23. Translating genetic findings in hereditary nephrotic syndrome: the missing loops
24. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
25. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
26. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis
27. Abstract 601: A Biased AT1 Receptor Agonist Stimulates COX2 Expression In Intercalated Cells
28. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
29. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity
30. TNXB Mutations Can Cause Vesicoureteral Reflux
31. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis
32. Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector
33. 112 Ang II Induces FAK Activation and Podocyte Migration Via a TRPC6-Dependent Mechanism
34. TRPC6 Enhances Angiotensin II-induced Albuminuria
35. Mesenchymal stem cells stimulate protective genetic reprogramming of injured cardiac ventricular myocytes
36. Regulating the regulator: NF-κB signaling in heart
37. Human mesenchymal stem cells exert potent antitumorigenic effects in a model of Kaposi's sarcoma
38. Human mesenchymal stem cells exert potent antitumorigenic effects in a model of Kaposi's sarcoma
39. Inhibitor-κB kinase-β regulates LPS-induced TNF-α production in cardiac myocytes through modulation of NF-κB p65 subunit phosphorylation
40. Endotoxin stress-response in cardiomyocytes: NF-κB activation and tumor necrosis factor-α expression
41. Pregnancy and estradiol decrease GTPase activity in the guinea pig uterine artery
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