A comprehensive in silico investigation unravels the structural and functional consequences of non-synonymous single-nucleotide polymorphisms in human OXTR gene
Abstract Background The OXTR gene encodes oxytocin receptor (OXTR), a cell surface protein primarily found in the brain, uterus, and mammary glands. This receptor plays a crucial role in signal transduction by binding with the ligand oxytocin. Various polymorphisms in the OXTR have been linked to ca...
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| Principais autores: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
SpringerOpen
2025-03-01
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| Series: | Egyptian Journal of Medical Human Genetics |
| Assuntos: | |
| Acceso en liña: | https://doi.org/10.1186/s43042-025-00680-0 |
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