Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ahmad M. Almatrafi"'
Publikováno v:
Heliyon, Vol 10, Iss 14, Pp e34506- (2024)
Melanoma antigen gene (MAGE) families are cancer-testis genes that normally show expression in the testes. However, their expressions have been linked with various types of human cancers, including BC. Therefore, the primary purposes of the present r
Externí odkaz:
https://doaj.org/article/0ff674920faf46b981d82030b33f5da6
Publikováno v:
Biomedicines, Vol 11, Iss 11, p 2983 (2023)
Background and objectives: Congenital myasthenic syndromes (CMSs) are rare inherited diseases characterized by muscle weakness and fatigability on exertion resulting from defects in the neuromuscular junctions. Mutations in 32 genes have been reporte
Externí odkaz:
https://doaj.org/article/d016e87e1f5043e8877b3d15029e3dcd
Autor:
Nahed N. Mahrous, Yahya F. Jamous, Ahmad M. Almatrafi, Deema I. Fallatah, Abdulrahman Theyab, Bayan H. Alanati, Suliman A. Alsagaby, Munifa K. Alenazi, Mohammed I. Khan, Yousef M. Hawsawi
Publikováno v:
Biomedicines, Vol 11, Iss 10, p 2762 (2023)
Alport syndrome (AS) is a rare genetic disorder categorized by the progressive loss of kidney function, sensorineural hearing loss and eye abnormalities. It occurs due to mutations in three genes that encode for the alpha chains of type IV collagen.
Externí odkaz:
https://doaj.org/article/67569b7fa2af4048b4c9c6fe610191e6
Autor:
Maan Abdullah Albarry, Muhammad Latif, Ahdab Qasem Alreheli, Mohammed A Awadh, Ahmad M Almatrafi, Alia M Albalawi, Sulman Basit
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0246607 (2021)
Waardenburg syndrome (WS) is a hereditary disorder affecting the auditory system and pigmentation of hair, eyes, and skin. Different variants of the disease exist with the involvement of mutation in six genes. The aim of the study is to identify the
Externí odkaz:
https://doaj.org/article/9e57bb30209b442dac9ec16c7338094d
Autor:
Asmat Ullah, Abid Ali Shah, Majed Alluqmani, Nighat Haider, Hasan Aman, Fatima Alfadhli, Ahmad M. Almatrafi, Alia M. Albalawi, Jai Krishin, Fati Ullah Khan, Bilal Ali Anjam, null Abdullah, Elionora Peña Lozano, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit
Publikováno v:
International Journal of Developmental Neuroscience. 82:788-804
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::468db3c4a9b3f58d13f207f601ae2a05
https://doi.org/10.1002/jdn.10231
https://doi.org/10.1002/jdn.10231