Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Abeer E Mustafa"'
Autor:
Mohamed Mohamady Ghobashy, Mohamed A. Amin, Abeer E. Mustafa, Mahmoud A. El-diehy, Basem Kh. El‑Damhougy, Norhan Nady
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-19 (2024)
Abstract Water scarcity poses a significant challenge to agricultural production, prompting the development of sustainable technologies to optimize water resource utilization. This study focuses on the synthesis and application of a multifunctional p
Externí odkaz:
https://doaj.org/article/48981aab9102452ea7add9fbc1ff1a9a
Autor:
Hend A. EL-khawaga, Abeer E. Mustafa, Maie A. El khawaga, Amira Y. Mahfouz, Ghadir E. Daigham
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract Heavy metal accumulation is one of the major agronomic challenges that has seriously threatened food safety. As a result, metal-induced phytotoxicity concerns require quick and urgent action to retain and maintain the physiological activitie
Externí odkaz:
https://doaj.org/article/391fc1be75bf417e8fc10df1ab8cd508
Autor:
Bashayer R Al-Mubarak, Saeed A Bohlega, Thamer S Alkhairallah, Amna I Magrashi, Maha I AlTurki, Dania S Khalil, Basma S AlAbdulaziz, Hussam Abou Al-Shaar, Abeer E Mustafa, Eman A Alyemni, Bashayer A Alsaffar, Asma I Tahir, Nada A Al Tassan
Publikováno v:
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
Externí odkaz:
https://doaj.org/article/f62aea7f0947470ea1bff78fbff8926b
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Citrullus lanatus var. Colocynthoide “Gurum” is an unconventional crop that can be utilized as a new source of edible oil and has the ability to grow in a variety of harsh conditions. To mitigate the adverse effects of salinity on seed g
Externí odkaz:
https://doaj.org/article/e32016c1394e4e1496108a6cafbe29ed
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a0c9ababf99a7aada65657951f292c7
http://europepmc.org/articles/PMC6399448
http://europepmc.org/articles/PMC6399448
Autor:
Abeer E, Mustafa, Tariq, Faquih, Batoul, Baz, Rana, Kattan, Abdulelah, Al-Issa, Asma I, Tahir, Faiqa, Imtiaz, Khushnooda, Ramzan, Moeenaldeen, Al-Sayed, Mohammed, Alowain, Zuhair, Al-Hassnan, Hamad, Al-Zaidan, Mohamed, Abouelhoda, Bashayer R, Al-Mubarak, Nada A, Al Tassan
Publikováno v:
Genes
Quick and accurate molecular testing is necessary for the better management of many inherited diseases. Recent technological advances in various next generation sequencing (NGS) platforms, such as target panel-based sequencing, has enabled comprehens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9c3ecec698ab3c70d0f4ef00ced60e7
https://pubmed.ncbi.nlm.nih.gov/29789446
https://pubmed.ncbi.nlm.nih.gov/29789446
Autor:
Batoul Baz, Hamad Al-Zaidan, Zuhair N. Al-Hassnan, Abdulelah AlIssa, Mohamed Abouelhoda, Bashayer R. Al-Mubarak, Faiqa Imtiaz, Rana Kattan, Nada Al Tassan, Mohammed Al-Owain, Asma I. Tahir, Tariq Faquih, Abeer E. Mustafa, Khushnooda Ramzan, Moeenaldeen Al-Sayed
Publikováno v:
Genes; Volume 9; Issue 5; Pages: 267
Genes, Vol 9, Iss 5, p 267 (2018)
Genes, Vol 9, Iss 5, p 267 (2018)
Quick and accurate molecular testing is necessary for the better management of many inherited diseases. Recent technological advances in various next generation sequencing (NGS) platforms, such as target panel-based sequencing, has enabled comprehens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62800c5836f91eda15c45fa129684cab
https://doi.org/10.3390/genes9050267
https://doi.org/10.3390/genes9050267
Autor:
Mohamed El-Kalioby, Nada Al Tassan, Sara Al Haibi, Tariq Faquih, Dania S. Khalil, Bashayer R. Al-Mubarak, Abeer E. Mustafa, Eman A. Alyemni, Mohamed Abouelhoda, Asma I. Tahir, Saeed Bohlega, Hussam Abou Al-Shaar, Dorota Monies
Publikováno v:
BMC Research Notes
Background Recessive mutations in PLA2G6 have been associated with different neurodegenerative disorders, including infantile neuroaxonal dystrophy, neurodegeneration with brain iron accumulation and more recently, early-onset dystonia parkinsonism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b6f64a99e25bd362941ad8a1b5d9879