教員情報 - 青山　友佳

アオヤマ　ユカ AOYAMA Yuka
青山　友佳

所属生命健康科学部臨床工学科

大学院生命健康科学研究科生命医科学専攻

臨地実習推進部臨床工学実習センター

教務部

人間力創成教育院専門職教育プログラム

職名准教授

著書・論文歴
著書	引いて調べる先天代謝異常症 INHERITED METABOLIC DISEASES (共著) 2014/07
論文	University students' living conditions during the COVID-19 pandemic and predictors of their subjective health views: A cross-sectional survey. Drug discoveries & therapeutics 2023/04/29
論文	Nicotine Dependence among College Students Uninterested in Smoking Cessation during the COVID-19 Pandemic: A Cross-Sectional Survey International Journal of Environmental Research and Public Health 20 (6),5135-5135頁 2023/03/14
論文	Factors affecting health-related quality of life among firefighters during the COVID-19 pandemic: A single-center study Drug Discoveries & Therapeutics 2023
論文	Effects of Heat-Not-Burn Cigarette Smoking on the Secretion of Saliva and Its Innate Immune System Components Healthcare 11 (1),132-132頁 2022/12/31
論文	A Survey of Living Conditions and Psychological Distress in Japanese University Freshmen during the COVID-19 Pandemic Healthcare 11 (1),94-94頁 2022/12/28
論文	Willingness and Predictors of Bystander CPR Intervention in the COVID-19 Pandemic: A Survey of Freshmen Enrolled in a Japanese University International Journal of Environmental Research and Public Health 19 (23),15770-15770頁 2022/11/27
論文	繁田正子賞セッション喫煙がCOVID-19ハイリスク要因と認知している大学生のKTSND・FTNDの評価日本禁煙学会学術総会プログラム・抄録集 16回,93-93頁 2022/10
論文	Evaluation of Japanese university students' perception of smoking, interest in quitting, and smoking behavior: An examination and public health challenges during the COVID-19 pandemic. Drug discoveries & therapeutics 16 (3),118-123頁 2022/07/20
論文	Antibody response of smokers to the COVID-19 vaccination: Evaluation based on cigarette dependence. Drug discoveries & therapeutics 16 (2),78-84頁 2022/05/17
論文	Prevalence of SARS-CoV-2 antibodies among university athletic club members: A cross-sectional survey Drug Discoveries & Therapeutics 2022
論文	A大学における加熱式たばこを含む喫煙者のCOVID-19に関する不安の実態調査日本禁煙学会学術総会プログラム・抄録集 15回,74-74頁 2021/10
論文	A大学における喫煙者と非喫煙者のCOVID-19に関する認識と感染予防行動の比較日本禁煙学会学術総会プログラム・抄録集 15回,105-105頁 2021/10
論文	Japanese patients with mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: In vitro functional analysis of five novel HMGCS2 mutations. Experimental and therapeutic medicine 20 (5),39-39頁 2020/11
論文	Deficiency of 3-hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting. Journal of inherited metabolic disease 43 (5),960-968頁 2020/04
論文	Recent advances in understanding beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency. Journal of human genetics 64 (2),99-111頁 2018/11
論文	BCL2 inhibitor ABT-199 and JNK inhibitor SP600125 exhibit synergistic cytotoxicity against imatinib-resistant Ph+ ALL cells. Biochemistry and biophysics reports 15,69-75頁 2018/09
論文	Intronic antisense Alu elements have a negative splicing effect on the inclusion of adjacent downstream exons Gene 664,84-89頁 2018/07/20
論文	絶食負荷による3ヒドロキシ酪酸脱水素酵素(Bdh1)KOマウスの病態解析日本小児科学会雑誌 122 (2),240-240頁 2018/02
論文	BCL2とJNK経路はPh1陽性ALLの良い治療標的となる生命科学系学会合同年次大会 2017年度,[1P-1022]頁 2017/12
論文	Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis JOURNAL OF INHERITED METABOLIC DISEASE 40 (6),845-852頁 2017/11
論文	絶食負荷試験において3ヒドロキシ酪酸脱水素酵素(Bdh1)KOマウスではケトン体産生が障害される日本先天代謝異常学会雑誌 33,164-164頁 2017/09
論文	A novel mutation (c.121-13T > A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene MOLECULAR MEDICINE REPORTS 15 (6),3879-3884頁 2017/06
論文	Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years' experience of a medical center in northern Vietnam JOURNAL OF INHERITED METABOLIC DISEASE 40 (3),395-401頁 2017/05
論文	Two Libyan siblings with beta-ketothiolase deficiency: A case report and review of literature Egyptian Journal of Medical Human Genetics 18 (2),199-203頁 2017/04/01
論文	Modulation of the sphingolipid rheostat is involved in paclitaxel resistance of the human prostate cancer cell line PC3-PR BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 486 (2),551-557頁 2017/04
論文	Single-nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene MOLECULAR GENETICS & GENOMIC MEDICINE 5 (2),177-184頁 2017/03
論文	Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency. JIMD reports 35,59-65頁 2017
論文	Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) Without Neurological Regression. JIMD reports 32,81-85頁 2017
論文	Exon 10 skipping in ACAT1 caused by a novel c.949G > A mutation located at an exonic splice enhancer site MOLECULAR MEDICINE REPORTS 14 (5),4906-4910頁 2016/11
論文	Mechanism of paclitaxel resistance in a human prostate cancer cell line, PC3-PR, and its sensitization by cabazitaxel BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 479 (4),808-813頁 2016/10
論文	3-hydroxy-3-methylglutaryl CoA（HMGCL）lyase欠損症における新たな遺伝子診断中部大学生命健康科学研究所紀要 12,87-91頁 2016/03
論文	Beta-ketothiolase deficiency: resolving challenges in diagnosis Journal of Inborn Errors of Metabolism and Screening 4,1-9頁 2016/03
論文	OXCT1ヘテロキャリアーでもケトアシドーシス発作を起こしうる日本先天代謝異常学会雑誌 31,144-144頁 2015/10
論文	ミトコンドリアHMG-CoA合成酵素欠損症の2例における臨床的、生化学的共通点日本先天代謝異常学会雑誌 31,146-146頁 2015/10
論文	3-hydroxy-3-methylglutaryl CoA lyase（HMGCL）遺伝子におけるMLPA法を用いた新たな遺伝子診断法の確立岐阜大学連合創薬医療情報研究科,1-43頁 2015/09
論文	Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response BRAIN & DEVELOPMENT 37 (7),698-703頁 2015/08
論文	Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 35 (6),1554-1560頁 2015/06
論文	The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation JOURNAL OF HUMAN GENETICS 59 (11),609-614頁 2014/11
論文	Ketone body metabolism and its defects JOURNAL OF INHERITED METABOLIC DISEASE 37 (4),541-551頁 2014/07
論文	Metabolic encephalopathy in beta-ketothiolase deficiency: The first report from India BRAIN & DEVELOPMENT 36 (6),537-540頁 2014/06
論文	Development of MLPA for human ACAT1 gene and identification of a heterozygous Alu-mediated deletion of exons 3 and 4 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency MOLECULAR GENETICS AND METABOLISM 110 (1-2),184-187頁 2013/09