Correction: Post-ischemic modification of neurogenesis and oligodendrogenesis in rodent models
Yoshihide Sehara, Shinya Mochizuki, Reiji Yamazaki
[This corrects the article DOI: 10.3389/fncir.2026.1803118.].
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Yoshihide Sehara, Shinya Mochizuki, Reiji Yamazaki
[This corrects the article DOI: 10.3389/fncir.2026.1803118.].
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Takahiro Kanai, Yuka Hayashi, Yoshihide Sehara, Mitsuaki Yoshino et autres
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Yoshihide Sehara, Shinya Mochizuki, Reiji Yamazaki
Neurogenesis and oligodendrogenesis occur throughout life under both physiological and pathophysiological conditions. Brain insults such as ischemia, trauma, epilepsy, or Alzheimer disease result in the promotion of neurogenesis and oligodendrogenesis; however, the mechanisms and the roles of this promotion are not well …
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Yuki Endo, Yoshihide Sehara, Masaaki Tamura, Keisuke Okubo
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Takayuki Asayama, Yoshihide Sehara, Jun Mimuro
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Ryota Watano, Kenji Ohba, Yoshihide Sehara, Yasushi Saga et autres
Gene therapy using adeno-associated virus (AAV) vectors is currently expanding to broad clinical applications. As the presence of a neutralizing antibody (NAb) against AAV capsids significantly restrains their efficacy, an accurate evaluation of NAb status is crucial for selecting appropriate candidates for …
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Yoshihide Sehara, Yuki Hashimotodani, Ryota Watano, Kenji Ohba et autres
It is established that neurogenesis of dentate gyrus is increased after ischemic insult, although the regulatory mechanisms have not yet been elucidated. In this study, we focused on Ezh2 which suppresses gene expression through catalyzing trimethylation of lysine 27 of histone 3. …
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Yuka Hayashi, Yoshihide Sehara, Ryota Watano, Kenji Ohba et autres
Fabry disease (FD) is an inherited lysosomal storage disease caused by deficiency of α-galactosidase A (α-Gal A), an enzyme that hydrolyzes glycosphingolipids in lysosome. Accumulation of glycosphingolipids, mainly globotriaosylceramide (Gb3) in tissues, induces cellular dysfunction leading to multi-organ disorder. Gene therapy is …
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Yoshihide Sehara, Ryota Watano, Kenji Ohba, Yuki Takayanagi et autres
The cover image is based on the Research Article Therapeutic strategy for Fabry disease by intravenous administration of adeno-associated virus 2 or 9 in α-galactosidase A-deficient mice by Yuka Hayashi et al., https://doi.org/10.1002/jgm.3560.
Yoshihide Sehara, Ryota Watano, Kenji Ohba, Yuki Takayanagi et autres
Abstract Background Fabry disease (FD) is an inherited lysosomal storage disease caused by deficiency of α‐galactosidase A (α‐Gal A) encoded by the GLA gene. The symptoms of FD occur as a result of the accumulation of globotriaosylceramide (Gb3), comprising a substrate of …
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Kenji Ohba, Yoshihide Sehara, Tatsuji Enoki, Junichi Mineno et autres
Adeno-associated virus (AAV) vectors are promising tools for gene therapy. The current AAV vector system produces an abundance of empty capsids that are eliminated before clinical use, leading to increased costs for gene therapy. In the present study, we established an AAV …
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Yoshihide Sehara, Kyoichiro Tsuchiya, Ichizo Nishino, Hirotake Sato et autres
A 72-year-old woman presented with gradually-worsening myalgia and muscle weakness of the proximal lower limbs as well as elevated serum creatine kinase level. Based on a clinicoseropathological examination including a muscle biopsy, she was diagnosed with anti-signal recognition particle (SRP) myopathy. Although …
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