Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Murad E. Almak"'
Autor:
Yousuf Bakhit, Ina Schmitt, Ahlam Hamed, Etedal Ahmed A. Ibrahim, Inaam N. Mohamed, Sarah M. El-Sadig, Maha A. Elseed, Mohamed A. Alebeed, Mutaz T. Shaheen, Mohamed O. Ibrahim, Ali A. Elhassan, Khalid Eltom, Hiba A. Ali, Yousuf A. Ibrahim, Murad E. Almak, Rayan Abubaker, Mohamed Anwer Ahmed, Ahmed A. Abugrain, Salma M. Elrasheed, Mawia A. Omar, Mohamed A. Almahal, Abubaker A. MohamedSharif, Mohamed Y. Tahir, Sawazen M. Malik, Hazim S. Eldirdiri, Reem J. Khidir, Malaz T. Mohamed, Abdelmohaymin Abdalla, Farouk Yassen Omer, Liena E.O. Elsayed, Haydar El Hadi Babikir, Elfateh Abd-Allah Bukhari, Osheik Seidi, Ullrich Wüllner
Publikováno v:
Parkinsonism & related disorders 101, 6-8 (2022). doi:10.1016/j.parkreldis.2022.05.009
Several studies suggested a significant role of epigenetic changes, including alterations in miRNA, histone modifications, and DNA methylation of α-synuclein (SNCA) in Parkinson's disease (PD) pathogenicity. As of yet, only very few studies have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfd43c3609105238a4b9adf3563e5945
https://doi.org/10.1016/j.parkreldis.2022.05.009
https://doi.org/10.1016/j.parkreldis.2022.05.009
Autor:
Yousuf Bakhit, Mohamed O. Ibrahim, Christelle Tesson, Ali A. Elhassan, Mohamed Anwer Ahmed, Mohamed A. Alebeed, Salma M. Elrasheed, Mawia A. Omar, Rayan Abubaker, Khalid Eltom, Mutaz T. Shaheen, Yousuf A. Ibrahim, Murad E. Almak, Hiba A. Ali, Ahmed A. Abugrain, Mohamed A. Almahal, Abubaker A. MohamedSharif, Mohamed Y. Tahir, Sawazen M. Malik, Hazim Eldirdiri Abdelrahman, Reem J. Khidir, Malaz T. Mohamed, Abdelmohaymin Abdalla, Liena E.O. Elsayed, Suzanne Lesage, Jean-Christophe Corvol, Osheik Seidi, Ullrich Wüllner
Publikováno v:
Parkinsonism & related disorders 111, 105401 (2023). doi:10.1016/j.parkreldis.2023.105401
PINK1 is the second most predominant gene associated with autosomal recessive Parkinson's disease. Homozygous mutations in this gene are associated with an early onset of symptoms. Bradykinesia, tremors, and rigidity are common features, while dyston
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::698fe6b0a1dd89e05ba7f8c52ebe61e2
https://doi.org/10.1016/j.parkreldis.2023.105401
https://doi.org/10.1016/j.parkreldis.2023.105401