SHANK3 Protein - SH3 and Multiple Ankyrin Repeat Domains 3
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SHANK3 Protein - SH3 and Multiple Ankyrin Repeat Domains 3
Introduction
Shank3 Protein Sh3 And Multiple Ankyrin Repeat Domains 3 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
Overview
SHANK3 (SH3 and Multiple Ankyrin Repeat Domains 3) is a critical scaffolding protein located at the postsynaptic density (PSD) of excitatory synapses[@sheng2000]. It plays a fundamental role in synapse formation, dendritic spine morphology, and synaptic signaling. Mutations in SHANK3 are causative for Phelan-McDermid syndrome (22q13.3 deletion syndrome) and have been implicated in autism spectrum disorder (ASD), intellectual disability, and neurodegenerative diseases including Alzheimer's disease and Parkinson's disease[@durand2007].
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SHANK3 Protein - SH3 and Multiple Ankyrin Repeat Domains 3
Introduction
Shank3 Protein Sh3 And Multiple Ankyrin Repeat Domains 3 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
Overview
SHANK3 (SH3 and Multiple Ankyrin Repeat Domains 3) is a critical scaffolding protein located at the postsynaptic density (PSD) of excitatory synapses[@sheng2000]. It plays a fundamental role in synapse formation, dendritic spine morphology, and synaptic signaling. Mutations in SHANK3 are causative for Phelan-McDermid syndrome (22q13.3 deletion syndrome) and have been implicated in autism spectrum disorder (ASD), intellectual disability, and neurodegenerative diseases including Alzheimer's disease and Parkinson's disease[@durand2007].
[SHANK3 in autism - Nature Reviews](https://pubmed.ncbi.nlm.nih.gov/23554086/)
Background
The study of Shank3 Protein Sh3 And Multiple Ankyrin Repeat Domains 3 has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.
References
[Sheng M, Kim E, (2000) (2000)](https://pubmed.ncbi.nlm.nih.gov/10769202/)
[Durand CM, et al, (2007) (2007)](https://pubmed.ncbi.nlm.nih.gov/17376978/)
[Svitkina T, et al, (1996) (1996)](https://pubmed.ncbi.nlm.nih.gov/8707845/)
[Sheng M, Kim E, (2011) (2011)](https://pubmed.ncbi.nlm.nih.gov/22003169/)
[Phelan MC, et al, (2001) (2001)](https://pubmed.ncbi.nlm.nih.gov/11343340/)
[Boccuto L, et al, (2013) (2013)](https://pubmed.ncbi.nlm.nih.gov/23365780/)
[Gong Y, et al, (2009) (2009)](https://pubmed.ncbi.nlm.nih.gov/19726658/)