24 results on '"Ihara, K."'
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2. Relationship between sensory perception and frailty in a community-dwelling elderly population
3. Improvement of Mixing Conductance and Spin-Seebeck Effect at Fe Interface Treatment
4. Respiratory syncytial virus infection in children with severe motor and intellectual disabilities
5. Advantages of intra-capsular micro-enucleation of schwannoma arising from extremities
6. Preparation of CuO nanoparticles by metal salt-base reaction in aqueous solution and their metallic bonding property
7. Genetic variation of vascular endothelial growth factor pathway does not correlate with the severity of retinopathy of prematurity
8. Measurement of electric field gradient at 117In on the Cu-site in mavicyanin by perturbed angular correlation of γ-rays
9. Low-grade central osteosarcoma mimicking fibrous dysplasia: a report of two cases
10. A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl-phosphate synthetase-1 activity in liver: A pitfall in enzymatic diagnosis for hyperammonaemia
11. Hypertrophy of Vascularized Bone Isograft in Rats Treated with Cyclosporine A
12. Effects of Cerivastatin on Vascularized Allogenic Bone Transplantation in Rats Treated with Cyclosporine A
13. Polymorphisms of transforming growth factor-β1 and transforming growth factor-β1 type II receptor genes are associated with acute graft-versus-host disease in children with HLA-matched sibling bone marrow transplantation
14. Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese population
15. Factors relating to place of death of Japanese people from a small town in a rural area
16. Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells
17. Congenital multiple pituitary hormone deficiency associated with hyperammonemia: a case report with a short review of the literature
18. High-intensity basal ganglia lesions on T1-weighted images in two toddlers with elevated blood manganese with portosystemic shunts
19. Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib
20. High frequency of fusion transcripts of exon 11 and exon 4/5 in AF-4 gene is observed in cord blood, as well as leukemic cells from infant leukemia patients with t(4;11)(q21;q23)
21. Requirement for two conserved cysteine residues in the Ada protein ofEscherichia coli for transactivation of theada promoter
22. Lack of association between atopic asthma and polymorphisms of the histamine H1 receptor, histamine H2 receptor, and histamine N-methyltransferase genes
23. An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease
24. Acute encephalopathy associated with influenza virus infection in a patient with hyperprolinaemia type II
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