研究者総覧
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キヨタ キョウコ
清田 今日子
所属
大分大学 医学部附属病院 診療科・小児科
職種
助教
論文
論文
Analysis of the mechanism of SLE onset by a novel PIK3CD mutation The Asia Pacific League of Associations for Rheumatology(APLAR)2025 2025/09
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A gain-of-function PIK3CD variant, R512W, impairs T cell function through polyamine-dependent metabolic dysregulation. Biochemical and biophysical research communications 778,152378-152378頁 2025/07/17
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新規PIK3CD変異による細胞機能解析 日本小児腎臓病学会雑誌 38 (Suppl.),125-125頁 2025/05
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Effect of nonsense-mediated mRNA decay factor SMG9 deficiency on premature aging in zebrafish. Communications biology 7 (1),654-654頁 2024/05/28
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A pH imbalance is linked to autophagic dysregulation of inner ear hair cells in Atp6v1ba-deficient zebrafish. Biochemical and biophysical research communications 699,149551-149551頁 2024/01/19
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Rituximab induced serum sickness in a girl with frequently relapsing The 18th Congress of the Asian Society for Pediatric Research 2023/11
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Elucidation of the mechanism of hearing loss associated with distal tubular acidosis Asian Conference on Fish Models for Diseases 2023/02
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Rituximab-induced serum sickness in a girl with nephrotic syndrome. CEN case reports 11 (4),506-510頁 2022/05/20
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Renal lesions mimicking acute focal bacterial nephritis in pediatric leukemia. Pediatrics international : official journal of the Japan Pediatric Society 64 (1),e14838 2022/01
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Metabolome Characteristics of Liver Autophagy Deficiency under Starvation Conditions in Infancy Nutrients 13 (9),3026-3026頁 2021/08/29
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Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafish. Scientific reports 11 (1),8392-8392頁 2021/04/16
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A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess CEN CASE REPORTS 10 (2),241-243頁 2020/11
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Auto-immune disorders in a child with PIK3CD variant and 22q13 deletion. European journal of medical genetics 61 (10),631-633頁 2018/10
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単純ヘルペス脳炎に急性散在性脳脊髄炎を合併した1例 日本小児科学会雑誌 122 (8),1375-1375頁 2018/08
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周期性片側性てんかん性放電を認めたコクサッキーウイルスA6による限局性脳炎の1例 日本小児科学会雑誌 122 (2),428-428頁 2018/02
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A transient myelodysplastic/myeloproliferative neoplasm in a patient with cardio-facio-cutaneous syndrome and a germline BRAF mutation. American journal of medical genetics. Part A 161A (10),2600-3頁 2013/10
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