令和4年度 学術論文賞・学術発表賞 |
阪大小児科同窓会新年会にて、大阪小児先進医療研究会の優秀賞の発表が行われました。
世話人会による厳正な選考の結果、令和4年度の学術論文賞に山本賢一先生、学術発表賞に大沼真輔先生が選ばれております。
【学術論文賞】
山本 賢一 先生Genetic footprints of assortative mating in the Japanese population
Yamamoto K, Sonehara K, Namba S, Konuma T, Masuko H, Miyawaki S; BioBank Japan Project; Kamatani Y, Hizawa N, Ozono K, Yengo L, Okada Y.
Nat Hum Behav. 2023 Jan;7(1):65-73.
【学術発表賞】
大沼 真輔 先生腸管生物時計の破綻は、グルコース吸収の低下と飢餓耐性の減弱をもたらす
大沼真輔、木下さおり、大薗恵一、道上敏美、川井正信
第55回日本小児内分泌学会学術集会, 2022/11/1-3
過去の受賞
| 年度 | 優秀学術論文賞 | 優秀学術発表賞 |
| R3年度 （第20回） |
An RNA aptamer restores defective bone growth in FGFR3-related skeletal dysplasia in mice. Science Translational Medicine 木村 武司 |
患者由来線維芽細胞、iPS細胞を用いた骨形成不全症の病態解析と4-フェニル酪酸の効果 第94回日本内分泌学会学術総会 武鑓 真司 |
| R2年度 （第19回） |
4-phenylbutyric acid enhances the mineralization of osteogenesis imperfecta iPSC-derived osteoblasts. The Journal of Biological Chemistry 武鑓 真司 |
応募なし |
| R1年度 （第18回） |
CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B. Human Molecular Genetics 山本 景子 |
Genotype-phenotype characteristics in four families of type Ⅱ collagenopathy in our hospital. The 58th Annual ESPE Meeting 山本 賢一 |
| H30年度 （第17回） |
Atypical auditory language processing in adolescents with autism spectrum disorder. Clinical Neurophysiology 谷河 純平 |
患者由来iPS細胞、線維芽細胞を用いた骨形成不全症新規治療薬の探索 第52回日本小児内分泌学会学術集会 武鑓 真司 |
| H29年度 （第16回） |
Phenotype-genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties. Human Mutation 谷河 純平 |
Establishment of a human growth plate model with iPS cell-derived cartilage. 10th International Meeting of Pediatric Endocrinology 木村 武司 |
| H28年度 （第15回） |
Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms. Human Molecular Genetics 近藤 秀仁 |
CNP/NPRB Signaling Expands the Hypertrophic Zone in the Growth Plate Cartilage by Modulation Cell Cycle. ASBMR Annual Meeting 2016 山本 景子 |
| H27年度 （第14回） |
Acromesomelic Dysplasia，Type Maroteaux Caused by Novel Loss-of-Function Mutations of the NPR2 Gene:Three Case Reports. American Journal of Medical Genetics Wei Wong |
疾患特異的iPS細胞モデルを用いた軟骨形成に対するIGF1の効果の検討 第49回 日本小児内分泌学会学術集会 木村 武司 |
| Defined Sets of Transcription Factors Induce the Expression of Functional Sclerostin in Human Dermal Fibroblasts and Its Expression Responds to Parathyroid Hormone，Hypoxia and Prostaglandin E2. ASBMR Annual Meeting 2015 藤原 誠 |
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| H26年度 （第13回） |
Elevated Fibroblast Growth Factor 23 Exerts Its Effects on Placenta and Regulates Vitamin D Metabolism in Pregnancy of Hyp Mice. Journal of Bone and Mineral Research 大幡 泰久 |
Analysis of Hematopoietic Disorders in Down Syndrome Using Trisomy 21 iPSCs and Gene Targeting Technologies. Pediatric Academic Societies and Asian Society For Pediatric Research JOINT MEETING 坂野 公彦 |
| Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions. The Journal of Cell Biology 大友 孝信 |
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| H25年度 （第12回） |
Drastic shift from positive to negative estrogen effect on bone morphogenetic protein signaling in pulmonary arterial endothelial cells under hypoxia. 市森 裕章 |
Fibroblast growth factor 19 was aberrantly expressed in cholestatic hepatocytes, and its signal pathways were inappropriately down-regulated in biliary atresia children. The 64th Annual Meeting of the American Association for the Study of Liver Diseases 長谷川 泰浩 |
| H24年度 （第11回） |
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene. LOS ONE 三浦 弘司 |
自閉症剖検脳の前頭葉における造血器型プロスタグランジンD合成酵素の発現 ー自閉症の病態における神経炎症の関与ー 第54回日本小児神経学会総会 橘 雅弥 |
| H23年度 （第10回） |
Lysosomal Storage Causes Cellular Dysfunction in Mucolipidosis II Skin Fibroblasts. The Journal of Biological Chemistry 大友 孝信 |
Type B Human Natriuretic Peptide Receptor with a novel gain-of-function mutation provides therapeutic potential in the treatment of pulmonary arterial hypertension. American Heart Association Scientific Sessions 2011 那波 伸敏 |
| H22年度 （第9回） |
A circadian-regulated gene, Nocturnin, promotes adipogenesis by stimulating PPAR-gamma nuclear translocation. Proceedings of the National Academy of Sciences of the United States of America 川井 正信 |
ナトリウム利尿ペプチド受容体Bの機能獲得型変異により高身長、巨大母趾を呈した1家系. 第44回日本小児内分泌学会学術集会 三浦 弘司 |
| H21年度 （第8回） |
Inhibition of autophagosome formation restores mitochondrial function in mucolipidosis II and III skin fibroblasts. Molecular Genetics and Metabolism 大友 孝信 |
Serum Levels of Soluble Klotho and FGF23 in Cord Blood. 91st Annual Meeting 大幡 泰久 |
| H20年度 （第7回） |
Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with Mesd. Journal of Bone and Mineral Research 窪田 拓生 |
Different role of SHP2 mutants in cardiomyocyte hypertrophy in Noonan/Leopard syndromespectrum. American Heart Association 成田 淳 |
| Endocrinological analysis of 122 Japanese childhood cancer survivors in a single hospital. Endocrine Journal 三善 陽子 |
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| H19年度 （第6回） |
Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch. Nature 八代 健太 |
Intravenous administration of pamidronate decreases serum levels of FGF23 rapidly in patients with osteogenesis imperfecta. 29th Annual meeting of the American society for bone and mineral research 北岡 太一 |
| Lipocalin-type prostaglandin D synthase/beta-trace is a major amyloid beta-chaperone in human cerebrospinal fluid. Proceedings of the National Academy of Sciences of the United States of America 兼清 貴久 |
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| H18年度 （第5回） |
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies. Human Molecular Genetics 谷口 真理子 |
Early induction of neuronal lipocalin-type prostaglandin D synthase after hypoxic-ischemic injury in developing brains. 第36回アメリカ神経科学学会 谷口 英俊 |
| H17年度 （第4回） |
Anti-inflammatory therapy by ibudilast, a phosphodiesterase inhibitor, in demyelination of twitcher, a genetic demyelination model. Journal of Neuroinflammation 下野 九理子 |
Skeletal Defects in Ringelschwanz Mutant Mice Reveal that Lrp6 Is Involved in Bone Resorption and Essential for Proper Bone Mass Aquisition. 27th Annual Meeting of the American Society for Bone and Mineral Research. 窪田 拓生 |
| H16年度 （第3回） |
Skeletal defects in ringelschwanzmutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesis. Development and disease 國府 力 |
Hypoxia-induced BMPR reduction is associated with different changes BMPR signal transducers in pulmonary artery endothelial cells. American Heart Association 2004 高橋 邦彦 |
| H15年度 （第2回） |
A congenital mutation of the novel gene LRRC8 causes agammaglobulinemia in humans. Journal of Clinical Investigation 澤田 明久 |
Effect of baclofen on emesis and 24-hour esophageal pH in neurologically impaired children with gastroesophageal reflux disease. Digestive Disease Week 2003 川井 正信 |
| H14年度 （第1回） |
High incidence of human herpesvirus 6 infection with a high viral load in cord blood stem cell transplant recipients. Blood 指原 淳志 |
Double-conditioning regimens consisting of thiotepa, melphalan and busulfan with stem cell rescue for the treatment of pediatric solid tumors. International Society of Pediatric Oncology 時政 定雄 |
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