スポンサーリンク
Department of Pediatrics, Faculty of Medicine, Saga University | 論文
- Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
- In Vitro Cleavage of the MLL Gene by Topoisomerase II Inhibitor (Etoposide) in Normal Cord and Peripheral Blood Mononuclear Cells
- Classic Rett syndrome in a boy with R133C mutation of MECP2
- Frequent association of autism spectrum disorder in patients with childhood onset epilepsy
- Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure
- OE-141 C-reactive Protein Produced by U937 Monocyte-like Cells Give Proinflammatory Effects on U937cells(Infection/Inflammation/Immunity-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Structure-Activity Relationship of a Transmembrane Peptide Derived form Formyl Peptide Receptor 1