Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Basma Al-Abdulaziz"'
Autor:
Abeer A. Alabdullah, Basma Al-Abdulaziz, Hanan Alsalem, Amna Magrashi, Subramanian M. Pulicat, Amer A. Almzroua, Falah Almohanna, Abdullah Mohamed Assiri, Nada A. Al Tassan, Bashayer R. Al-Mubarak
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-7 (2019)
Abstract Objective Delivery of constructs for silencing or over-expressing genes or their modified versions is a crucial step for studying neuronal cell biology. Therefore, efficient transfection is important for the success of these experimental tec
Externí odkaz:
https://doaj.org/article/eead3479070b41148e82426a27eddf8e
Autor:
Batoul Baz, Dorota Monies, Thamer A Alamoudi, Ahmed Tarawah, Nouf S Al-Numair, Mahasen Saleh, Nada Al Tassan, Hala AbaAlkhail, M. Abouelhoda, Randa AlNounou, Hazza Alzahrani, Abdulrahman Al-Musa, Rahaf Altahan, Amjad Jabaan, Basma Al Abdulaziz, Tarek Owaidah
Publikováno v:
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-7 (2019)
NPJ Genomic Medicine
NPJ Genomic Medicine
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder. Around 490 mutations in ITGA2B and ITGB3 genes were reported. We aimed to use targeted next-generation sequencing (NGS) to identify variants in patients with GT. We screen
Autor:
Mohamed Abouelhoda, John A. Sayer, Maha Alnemer, Dorota Monies, Maha Tulbah, Nada Al-Tassan, Salma Majid, Haya Al-Jurayb, Ahmed Alahmed, Mamdouh Albaqumi, Brian F. Meyer, Nada Alsahan, Dania S. Khalil, Mohamed H Al-Hamed, Basma Al Abdulaziz, Faisal S. BinHumaid, Rania Abudraz, Wesam Kurdi, Mohamed El-Kalioby, Noel Edwards, Asma I. Tahir, Zainab Alabdullah, Rubina Khan, Tariq Faquih
Publikováno v:
Journal of Medical Genetics
Background Inherited cystic kidney disorders are a common cause of end-stage renal disease. Over 50 ciliopathy genes, which encode proteins that influence the structure and function of the primary cilia, are implicated in cystic kidney disease. Metho