340 results on '"Sohara, Eisei"'
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2. Impact of COVID-19 versus other pneumonia on in-hospital mortality and functional decline among Japanese dialysis patients: a retrospective cohort study
3. A case of unexpected diagnosis of fibronectin glomerulopathy with histological features of membranoproliferative glomerulonephritis
4. Importance of IFT140 in Patients with Polycystic Kidney Disease Without a Family History
5. Sex disparities in the risk of urgent dialysis following acute aortic dissections in Japan
6. ZNF185 prevents stress fiber formation through the inhibition of RhoA in endothelial cells
7. Rapidly progressive IgA nephropathy with membranoproliferative glomerulonephritis-like lesions in an elderly man following the third dose of an mRNA COVID-19 vaccine: a case report
8. Genetic Diagnosis of Adult Hemodialysis Patients With Unknown Etiology
9. Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus
10. A novel SLC5A2 heterozygous variant in a family with familial renal glucosuria
11. LMX1B-associated nephropathy that showed myelin figures on electron microscopy
12. Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis
13. A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatment
14. Osteomalacia caused by atypical renal tubular acidosis with vitamin D deficiency: a case report
15. Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiency
16. HPRT-related hyperuricemia with a novel p.V35M mutation in HPRT1 presenting familial juvenile gout
17. Congenital nephrogenic diabetes insipidus presenting as osmotic demyelination syndrome in infancy: A case report
18. Chronic kidney disease causes blood-brain barrier breakdown via urea-activated matrix metalloproteinase-2 and insolubility of tau protein
19. Disease-Causing Mutant WNK4 Increases Paracellular Chloride Permeability and Phosphorylates Claudins
20. Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report
21. Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report
22. Inherited, not acquired, Gitelman syndrome in a patient with Sjögren’s syndrome: importance of genetic testing to distinguish the two forms
23. Tolvaptan activates the Nrf2/HO-1 antioxidant pathway through PERK phosphorylation
24. Circulating Extracellular Vesicle-Propagated microRNA Signature as a Vascular Calcification Factor in Chronic Kidney Disease
25. NCC regulation by WNK signal cascade
26. Different Clinical Courses of Nephronophthisis in Dizygotic Twins
27. Case of hereditary kidney disease presenting thin basement membrane with a single heterozygous variant of Intersectin 2
28. Absence of ULK1 decreases AMPK activity in the kidney, leading to chronic kidney disease progression
29. WNK3 kinase maintains neuronal excitability by reducing inwardly rectifying K+ conductance in layer V pyramidal neurons of mouse medial prefrontal cortex
30. Primary Cilia Elongation in Early-Onset Polycystic Kidney Disease with 2 Hypomorphic PKD1 Alleles: A Case Report
31. WNK1 regulates skeletal muscle cell hypertrophy by modulating the nuclear localization and transcriptional activity of FOXO4
32. LRBA is essential for urinary concentration and body water homeostasis
33. Impaired phosphorylation of Na⁺ -K⁺ -2CI⁻ cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome
34. Once-daily low-dose cyclosporine A treatment for steroid-resistant nephrotic syndrome in a patient with Galloway-Mowat syndrome: A case report
35. Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
36. Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease
37. Burden of kidney disease on the discrepancy between reasons for hospital admission and death: An observational cohort study
38. Absence of ULK1 decreases AMPK activity in the kidney, leading to chronic kidney disease progression.
39. Development of minimal-change glomerular disease and Hashimoto’s thyroiditis during the treatment of sarcoidosis
40. Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus
41. Dietary Magnesium Insufficiency Induces Salt-Sensitive Hypertension in Mice Associated With Reduced Kidney Catechol-O-Methyl Transferase Activity
42. Vasopressin Induces Urinary Uromodulin Secretion By Activating PKA (Protein Kinase A)
43. Impaired degradation of WNK1 and WNK4 kinases causes PHAII in mutant KLHL3 knock-in mice
44. Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease.
45. Molecular Pathogenesis of Pseudohypoaldosteronism Type II: Generation and Analysis of a Wnk4 D561A/+ Knockin Mouse Model
46. Morphologic and functional analysis of sperm and testes in Aquaporin 7 knockout mice
47. A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype
48. A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatment
49. Sodium–calcium exchanger 1 is the key molecule for urinary potassium excretion against acute hyperkalemia
50. Copy Number Variation: A New Genetic Form of Polycystic Kidney and Liver Disease
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