652 results on '"Sekine, Takashi"'
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2. Development of a 100-J DPSSL as a laser processing platform in the TACMI consortium
3. A revision of the multiple‐path particle dosimetry model focusing on tobacco product aerosol dynamics
4. Effects of ZrC and SiC addition on the microstructures and mechanical properties of binderless WC
5. Nephrotoxins and Pediatric Kidney Injury
6. Effects of Si3N4 addition on the microstructure and mechanical properties of binderless tungsten carbides
7. Investigation by microarray analysis of effects of cigarette design characteristics on gene expression in human lung mucoepidermoid cancer cells NCI-H292 exposed to cigarette smoke
8. 253 J at 0.2 Hz, LD pumped cryogenic helium gas cooled Yb:YAG ceramics laser
9. A pure chloride channel mutant of CLC-5 causes Dent’s disease via insufficient V-ATPase activation
10. Renal function in angiotensinogen gene-mutated renal tubular dysgenesis with glomerular cysts
11. Characteristics of spark plasma sintered nanocarbon materials
12. Defective membrane expression of the Na + -HCO 3 − cotransporter NBCe1 is associated with familial migraine
13. Synthesis and Mechanical Properties of Silicon Nitride–Tungsten Carbide Composite Ceramics
14. A case of adult Dent disease in Japan with advanced chronic kidney disease
15. Nephrotoxins and Pediatric Kidney Injury
16. The first two cases of MYH9 disorders in Thailand: an international collaborative study
17. Open the Door to the Future! Advances in the Small Laser Fusion Experimental System TERU
18. Nephrotoxins and Pediatric Kidney Injury
19. Morphological and functional analyses of two infants with obstructive renal dysplasia
20. Resolution of Henoch-Schönlein purpura nephritis after acquired IgA deficiency
21. Defective membrane expression of the [Na.sup.+]-HC[O.sub.3].sup.-] cotransporter NBCe1 is associated with familial migraine
22. 16q12 microdeletion syndrome in two Japanese boys
23. A Case of a Child with an APC Pathogenic Mutation, Aberrant Expression of Splice Variants and Positive Family History of FAP
24. Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents
25. Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria
26. Salt-losing nephrogenic diabetes insipidus caused by fetal exposure to angiotensin receptor blocker
27. Reevaluation of glomerular charge selective protein-sieving function
28. A case of cerebral salt-wasting syndrome associated with aseptic meningitis in an 8-year-old boy
29. Functional analysis of a novel missense NBC1 mutation and of other mutations causing proximal renal tubular acidosis
30. Podocyte expression of nonmuscle myosin heavy chain-IIA decreases in idiopathic nephrotic syndrome, especially in focal segmental glomerulosclerosis
31. OCRL1 mutations in patients with Dent disease phenotype in Japan
32. Solute Transport, Energy Consumption, and Production in the Kidney
33. Core performance tests for the JOYO MK-III upgrade
34. A familial case of multicystic dysplastic kidney
35. Mutational analysis of idiopathic renal hypouricemia in Korea
36. Molecular physiology of renal organic anion transporters
37. Current Status of Laser Fusion Research at HAMAMATSU PHOTONICS K.K.
38. High Energy Density Plasma Heating with Counter Illuminating Ultra-Intense Laser Pulses
39. Progress on 100-J Class Diode-Pumped Yb:YAG Ceramics Laser for Construction of Material Processing Database
40. Evaluation of Dielectric Permittivity of Barium Titanate Fine Powders
41. Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis
42. The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia
43. List of Contributors
44. The multispecific organic anion transporter family: properties and pharmacological significance
45. Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis
46. Organic Anion and Cation Drug Transporters
47. Early occurrence of nephrotic syndrome associated with cord blood stem cell transplantation
48. The multispecific organic anion transporter (OAT) family
49. SIRPα interacts with nephrin at the podocyte slit diaphragm
50. Molecular biology of multispecific organic anion transporter family (OAT family)
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