Y. Aoyama

发表

Modulation of the sphingolipid rheostat is involved in paclitaxel resistance of the human prostate cancer cell line PC3-PR.

M. Ichihara, Y. Kawamoto, T. Murate, 2017, Biochemical and biophysical research communications.

Mechanism of paclitaxel resistance in a human prostate cancer cell line, PC3-PR, and its sensitization by cabazitaxel.

M. Ichihara, Y. Kawamoto, Y. Nozawa, 2016, Biochemical and biophysical research communications.

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.

A. Shukla, T. Fukao, Elsayed Abdelkreem, 2017, Molecular medicine reports.

Antibody response of smokers to the COVID-19 vaccination: Evaluation based on cigarette dependence.

M. Tsurudome, Y. Aoyama, Morihiro Ito, 2022, Drug discoveries & therapeutics.

Beta-Ketothiolase Deficiency Resolving Challenges in Diagnosis

T. Fukao, Tomohiro Hori, Elsayed Abdelkreem, 2016 .

Deficiency of 3‐hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting

G. Mitchell, T. Fukao, H. Ohnishi, 2020, Journal of inherited metabolic disease.

Recent advances in understanding beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency

T. Fukao, Yasuhiko Ago, Elsayed Abdelkreem, 2018, Journal of Human Genetics.

Ketone body metabolism and its defects

J. Sass, G. Mitchell, T. Fukao, 2014, Journal of Inherited Metabolic Disease.

BCL2 inhibitor ABT-199 and JNK inhibitor SP600125 exhibit synergistic cytotoxicity against imatinib-resistant Ph+ ALL cells

M. Ichihara, Y. Kawamoto, Y. Nozawa, 2018, Biochemistry and biophysics reports.

Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis

O. Ohara, T. Fukao, H. Ohnishi, 2017, Journal of Inherited Metabolic Disease.

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

Y. Kinosada, T. Fukao, Toshiyuki Yamamoto, 2015, International journal of molecular medicine.

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.

Y. Aoyama, Morihiro Ito, Yukihiro Mori, 2022, Drug discoveries & therapeutics.

Effects of Heat-Not-Burn Cigarette Smoking on the Secretion of Saliva and Its Innate Immune System Components

M. Tsurudome, Y. Aoyama, Morihiro Ito, 2022, Healthcare.

Metabolic encephalopathy in beta-ketothiolase deficiency: The first report from India

L. Lingappa, R. Akella, C. Mori, 2014, Brain and Development.

Carnitine–acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response

T. Fukao, S. Yamaguchi, Kenji Yamada, 2015, Brain and Development.

Intronic antisense Alu elements have a negative splicing effect on the inclusion of adjacent downstream exons.

T. Fukao, Yasuhiko Ago, Elsayed Abdelkreem, 2018, Gene.

Recent advances in understanding beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency

T. Fukao, Yasuhiko Ago, Elsayed Abdelkreem, 2019, Journal of Human Genetics.

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

T. Fukao, H. Ohnishi, L. Turner, 2017, Molecular genetics & genomic medicine.

Exon 10 skipping in ACAT1 caused by a novel c.949G>A mutation located at an exonic splice enhancer site.

J. Sass, T. Fukao, H. Ohnishi, 2016, Molecular medicine reports.

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.

R. Wierenga, T. Fukao, N. Kondo, 2013, Molecular genetics and metabolism.

A Survey of Living Conditions and Psychological Distress in Japanese University Freshmen during the COVID-19 Pandemic

M. Tsurudome, Y. Aoyama, Morihiro Ito, 2022, Healthcare.

Nicotine Dependence among College Students Uninterested in Smoking Cessation during the COVID-19 Pandemic: A Cross-Sectional Survey

Y. Aoyama, Morihiro Ito, Yukihiro Mori, 2023, International journal of environmental research and public health.

University students' living conditions during the COVID-19 pandemic and predictors of their subjective health views: A cross-sectional survey.

Y. Aoyama, Morihiro Ito, Yukihiro Mori, 2023, Drug discoveries & therapeutics.

Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) Without Neurological Regression.

K. Kaneko, T. Fukao, Y. Shigematsu, 2016, JIMD reports.

The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation

R. Wierenga, T. Hashimoto, T. Fukao, 2014, Journal of Human Genetics.

Willingness and Predictors of Bystander CPR Intervention in the COVID-19 Pandemic: A Survey of Freshmen Enrolled in a Japanese University

M. Tsurudome, Y. Aoyama, Morihiro Ito, 2022, International journal of environmental research and public health.

Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years’ experience of a medical center in northern Vietnam

T. Fukao, Y. Hasegawa, S. Yamaguchi, 2017, Journal of Inherited Metabolic Disease.

Two Libyan siblings with beta-ketothiolase deficiency: A case report and review of literature

T. Fukao, Hanna Alobaidy, Elsayed Abdelkreem, 2017 .

Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency.

R. Akella, T. Fukao, H. Ohnishi, 2017, JIMD Reports.