Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Amna Magrashi"'
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:
Bashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham AlDhalaan, Mohammed Aldosari, Michael Nester, Hussain. A. Alshamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma Tahir, Sultana Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies, Nada Al Tassan
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with genetic and clinical heterogeneity. The interplay of de novo and inherited rare variants has been suspected in the development of ASD. Here, we applied whole exome
Externí odkaz:
https://doaj.org/article/4a24e0c676b241eea3acb7405d21bc23
Autor:
Rasha Aljelaify, Abdullah AlObaid, Nada Al-Tassan, Aysha AlSahlawi, Latifa AlMubarak, Abdulellah Alturkistani, Amna Magrashi, Amal Almutairi, Mohamed Abouelhoda, Malak Abedalthagafi, Fatimah Alqubaishi, Mariam AlSaeed
Publikováno v:
Oncotarget
Background: With a prevalence of 170 000 adults in the US alone, meningiomas are the most common primary intracranial tumors. The management of skull base meningiomas is challenging due to their complexity and proximity to crucial nearby structures.
Autor:
Bashayer R. Al-Mubarak, Amer A. Almzroua, Nada A. Al Tassan, Abdullah Mohamed Assiri, Falah Al-Mohanna, Abeer A. Alabdullah, Hanan Alsalem, Basma S. AlAbdulaziz, Amna Magrashi, Subramanian M. Pulicat
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-7 (2019)
BMC Research Notes
BMC Research Notes
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 techniques e
Autor:
Abeer E. Mustafa, Batoul Baz, Amna Magrashi, Tariq Faquih, Eman A.A. Al Yemni, Jameela Shinwari, Dorota Monies, Shazia Subhani, Nada Al-Tassan, Amjad Jabaan, Basma S. AlAbdulaziz, Wafa Ali, Mohamed Abouelhoda, Ewa Goljan, Bashayer R. Al-Mubarak, Thamer Alkhairallah, Mohamed H Al-Hamed, Renad Albar, Saeed Bohlega
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Genetic studies of the familial forms of Parkinson’s disease (PD) have identified a number of causative genes with an established role in its pathogenesis. These genes only explain a fraction of the diagnosed cases. The emergence of Next Generation
Autor:
Alabdullah, Abeer, Al-Abdulaziz, Basma, Alsalem, Hanan, Amna Magrashi, Pulicat, Subramanian, Almzroua, Amer, Almohanna, Falah, Assiri, Abdullah, Tassan, Nada Al, Bashayer Al-Mubarak
Additional file 1: Fig S1. Effect of Lipofection on cell viability. Fig S2. Cell viability of transfected and control AE culture. Fig S3. Phenotyping of primary cortical cultures. Fig S4. Neuron- or astrocyte-specific transfection in primary mouse co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05b4a779e7d50eb2d30cb06609181353
Autor:
Steve Bobis, Hala Abdalrahman Ahmed, Prashant Bavi, Latifa Al Sharif, Nada Abu Dhaim, Dania S. Khalil, Zainularifeen Abduljaleel, Jameela Shinwari, Amna Magrashi, Nada Al Tassan, Samaher AlAhmed, Saeed Bohlega
Publikováno v:
Human Mutation. 33:351-354
Autosomal recessive ataxias are heterogeneous group of disorders characterized by cerebellar atrophy and peripheral sensorimotor neuropathy. Molecular characterization of this group of disorders identified a number of genes contributing to these over
Autor:
Bashayer A. Alsaffar, Hussam Abou Al-Shaar, Thamer Alkhairallah, Basma S. AlAbdulaziz, Bashayer R. Al-Mubarak, Dania S. Khalil, Abeer E. Mustafa, Amna Magrashi, Nada Al Tassan, Saeed Bohlega, Eman A. Alyemni, Asma I. Tahir, Maha I. AlTurki
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 8, p e0135950 (2015)
PLoS ONE, Vol 10, Iss 8, p e0135950 (2015)
Parkinson's disease (PD) is one of the major causes of parkinsonism syndrome. Its characteristic motor symptoms are attributable to dopaminergic neurons loss in the midbrain. Genetic advances have highlighted underlying molecular mechanisms and provi