Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hamed Vasei"'
Autor:
Maryam Sotoudeh Anvari, Hamed Vasei, Hossein Najmabadi, Reza Shervin Badv, Akram Golipour, Samira Mohammadi-Yeganeh, Saeede Salehi, Mahmood Mohamadi, Hamidreza Goodarzynejad, Seyed Javad Mowla
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs and can cause a range of neurological disorders. Therefore, miRNAs could
Externí odkaz:
https://doaj.org/article/6e3da80d43c44ec9a30becd6734c8572
Autor:
Hamed Vasei, Maryam Sotoudeh Anvari, Samira Mohammadi-Yeganeh, Hamidreza Goodarzynejad, Akram Gholipour, Hossein Najmabadi, Saeede Salehi, Mahmood Mohamadi, Reza Shervin Badv, Seyed Javad Mowla
Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs, and a change can cause a range of neurological disorders. Therefore, miRNAs could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580defd550c8bd29589cafd1ddcaa658
https://doi.org/10.21203/rs.3.rs-523429/v1
https://doi.org/10.21203/rs.3.rs-523429/v1
Autor:
Maryam Sotoudeh Anvari, Hamed Vasei, Hossein Najmabadi, Reza Shervin Badv, Akram Golipour, Samira Mohammadi-Yeganeh, Saeede Salehi, Mahmood Mohamadi, Hamidreza Goodarzynejad, Seyed Javad Mowla
Publikováno v:
Scientific reports. 12(1)
Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs and can cause a range of neurological disorders. Therefore, miRNAs could act as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51f3a8bd6f4b194c8682733c1e81526
https://pubmed.ncbi.nlm.nih.gov/35322102
https://pubmed.ncbi.nlm.nih.gov/35322102