Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Reza K. Arta"'
Autor:
Di Ja Lasham, Reza K. Arta, Abdul Fuad Hadi, Jun Egawa, Vance P. Lemmon, Toshiyuki Takasugi, Michihiro Igarashi, Toshiyuki Someya
Publikováno v:
Molecular Brain, Vol 16, Iss 1, Pp 1-7 (2023)
Abstract Protein kinases are responsible for protein phosphorylation and are involved in important intracellular signal transduction pathways in various cells, including neurons; however, a considerable number of poorly characterized kinases may be i
Externí odkaz:
https://doaj.org/article/54b74222724944afb38e497231ab2e84
Autor:
Jun Egawa, Reza K. Arta, Vance P. Lemmon, Melissa Muños-Barrero, Yan Shi, Michihiro Igarashi, Toshiyuki Someya
Publikováno v:
Molecular Brain, Vol 15, Iss 1, Pp 1-5 (2022)
Abstract Protein kinases are responsible for protein phosphorylation and are involved in important signal transduction pathways; however, a considerable number of poorly characterized kinases may be involved in neuronal development. Here, we consider
Externí odkaz:
https://doaj.org/article/7a5657b35acb4c48aad0a7a846d298cd
Autor:
Ryo Morikawa, Yuichiro Watanabe, Hirofumi Igeta, Reza K. Arta, Masashi Ikeda, Satoshi Okazaki, Satoshi Hoya, Takeo Saito, Ikuo Otsuka, Jun Egawa, Takaki Tanifuji, Nakao Iwata, Toshiyuki Someya
Publikováno v:
Psychiatry research. 310
SETD1A has been identified as a substantial risk gene for schizophrenia. To further investigate the role of SETD1A in the genetic etiology of schizophrenia in the Japanese population, we performed resequencing and association analyses. First, we rese
Autor:
Satoshi Hoya, Itaru Kushima, Norio Ozaki, Yoshihiro Nawa, Reza K. Arta, Jun Egawa, Toshiyuki Someya, Yuichiro Watanabe, Ryo Morikawa, Atsunori Sugimoto, Hirofumi Igeta, Andi J. Tanra, Emiko Inoue
Publikováno v:
Research in Autism Spectrum Disorders. 82:101729
Background Growth-associated protein 43 (GAP43), a synaptic protein involved in axonal growth and synaptic plasticity, is implicated in the pathophysiology of autism spectrum disorder (ASD) and schizophrenia. To examine the role of rare GAP43 variant