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CEN Case Reports|May 20, 2022
Rituximab-induced serum sickness in a girl with nephrotic syndromeYuka Kimura, Kyoko Kiyota, Mayo Ikeuchi, et al.
European Journal of Medical Genetics|April 21, 2018
Auto-immune disorders in a child with PIK3CD variant and 22q13 deletionKyoko Kiyota, Koh-Ichiro Yoshiura, Ryoko Houbara, et al.
Nutrients|September 28, 2021
Metabolome Characteristics of Liver Autophagy Deficiency under Starvation Conditions in InfancyKazuhito Sekiguchi, Hiroaki Miyahara, Masanori Inoue, et al.
CEN Case Reports|November 7, 2020
A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscessMayo Ikeuchi, Kyoko Kiyota, Tomoyo Itonaga, et al.
Scientific Reports|April 17, 2021
Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafishMasanori Inoue, Hiroaki Miyahara, Hiroshi Shiraishi, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
A transient myelodysplastic/myeloproliferative neoplasm in a patient with cardio-facio-cutaneous syndrome and a germline BRAF mutationKazuhito Sekiguchi, Tomoki Maeda, So-ichi Suenobu, et al.
Biochemical and Biophysical Research Communications|January 26, 2024
A pH imbalance is linked to autophagic dysregulation of inner ear hair cells in Atp6v1ba-deficient zebrafishMayo Ikeuchi, Masanori Inoue, Hiroaki Miyahara, et al.
Communications Biology|May 28, 2024
Effect of nonsense-mediated mRNA decay factor SMG9 deficiency on premature aging in zebrafishShaohong Lai, Hiroshi Shiraishi, Wulan Apridita Sebastian, et al.
Biochemical and Biophysical Research Communications|July 22, 2025
A gain-of-function PIK3CD variant, R512W, impairs T cell function through polyamine-dependent metabolic dysregulationKyoko Kiyota, Hiroshi Shiraishi, Shiho Ohno, et al.
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