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Alterations of presynaptic proteins in autism spectrum disorder.
Yeo, Xin Yi; Lim, Yi Tang; Chae, Woo Ri; Park, Chungwon; Park, Hyokeun; Jung, Sangyong.
Afiliação
  • Yeo XY; Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
  • Lim YT; Department of Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Chae WR; Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
  • Park C; Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
  • Park H; Department of BioNano Technology, Gachon University, Seongnam, South Korea.
  • Jung S; Division of Life Science, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.
Front Mol Neurosci ; 15: 1062878, 2022.
Article em En | MEDLINE | ID: mdl-36466804
ABSTRACT
The expanded use of hypothesis-free gene analysis methods in autism research has significantly increased the number of genetic risk factors associated with the pathogenesis of autism. A further examination of the implicated genes directly revealed the involvement in processes pertinent to neuronal differentiation, development, and function, with a predominant contribution from the regulators of synaptic function. Despite the importance of presynaptic function in synaptic transmission, the regulation of neuronal network activity, and the final behavioral output, there is a relative lack of understanding of the presynaptic contribution to the pathology of autism. Here, we will review the close association among autism-related mutations, autism spectrum disorders (ASD) phenotypes, and the altered presynaptic protein functions through a systematic examination of the presynaptic risk genes relating to the critical stages of synaptogenesis and neurotransmission.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article