Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Mashael Alharbi"'
Autor:
Mashael Alharbi
Publikováno v:
International Journal of Educational Innovation and Research, Vol 3, Iss 2, Pp 145-154 (2024)
Developing teacher training programs is one of the essential objectives of Saudi Arabia’s Vision 2030. This research highlighted one of the Ministry of Education's initiatives, the Optimum Utilization of Teaching Staff Project (OUTSP), to enhance t
Externí odkaz:
https://doaj.org/article/96fb6663ee534f33adcfe575fb9e3d2d
Autor:
Majedah Almokhalafi, Mashael Alhilabi, Ayed alrashdi, Mansour Alharbi, Amal Surrati, Mashael Alharbi
Publikováno v:
F1000Research, Vol 12 (2024)
Background There is a huge burden of nutrition-related non-communicable diseases, and diabetes is one of the leading chronic nutrition-related diseases affecting more than 500 million people globally. Collecting information regarding the awareness of
Externí odkaz:
https://doaj.org/article/ef205cc3107b4245a3ce437bd6d3ff54
Autor:
Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad AlEidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 4, Pp n/a-n/a (2023)
Abstract Background Congenital disorders of glycosylation (CDG) are a group of heterogeneous disorders caused by abnormal lipid or protein glycosylation. Variants in the FCSK gene have been reported to cause CDG. Defective FCSK‐induced CDG (FCSK–
Externí odkaz:
https://doaj.org/article/749d1d3869cd49fbb491ca3b51a3fe3b
Autor:
Yusra Alyafee, Abeer Al Tuwaijri, Muhammad Umair, Mashael Alharbi, Shahad Haddad, Maryam Ballow, Latifah Alayyar, Qamre Alam, Saleh Althenayyan, Nadia Al Ghilan, Aziza Al Khaldi, Majid S. Faden, Hamad Al Sufyan, Majid Alfadhel
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: In pregnant women at risk of autosomal recessive (AR) disorders, prenatal diagnosis of AR disorders primarily involves invasive procedures, such as chorionic villus sampling and amniocentesis.Methods: We collected blood samples from four
Externí odkaz:
https://doaj.org/article/6349c6a25dd14c8d86f5e7a5721f6c04
Autor:
Abeer Al Tuwaijri, Yusra Alyafee, Mashael Alharbi, Maryam Ballow, Mohammed Aldrees, Qamre Alam, Rola A. Sleiman, Muhammad Umair, Majid Alfadhel
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Dilated cardiomyopathy with ataxia syndrome (DCMA) or 3‐methylglutaconic aciduria type V is a rare global autosomal recessive mitochondrial syndrome that is clinically and genetically heterogeneous. It is characterized by early
Externí odkaz:
https://doaj.org/article/24ff3b1c93b5491089cb4bf443c751b5
Autor:
Yusra Alyafee, Abeer Al Tuwaijri, Qamre Alam, Muhammad Umair, Shahad Haddad, Mashael Alharbi, Maryam Ballow, Mohammed Al Drees, Abdulkareem AlAbdulrahman, Aziza Al Khaldi, Majid Alfadhel
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Non-invasive prenatal testing (NIPT) for aneuploidy in pregnant women screening has been recently established in Saudi Arabia. We aim from this study to report our experience in the implementation of this new technology in clinical practi
Externí odkaz:
https://doaj.org/article/9782d8417dd84d6cab88830843dd6000
Autor:
Zeyad Alehaideb PhD, Saleh AlGhamdi PhD, Wesam Bin Yahya BSc, Hamad Al-Eidi BSc, Mashael Alharbi MSc, Monira Alaujan MSc, Abeer Albaz MSc, Muruj Tukruni BSc, Atef Nehdi PhD, Maha-Hamadien Abdulla PhD, Sabine Matou-Nasri PhD
Publikováno v:
Journal of Evidence-Based Integrative Medicine, Vol 25 (2020)
Triple-negative breast cancer (TNBC), the most aggressive subtype, does not respond to targeted therapy due to the lack of hormone receptors. There is an urgent need for alternative therapies, including natural product-based anti-cancer drugs, at low
Externí odkaz:
https://doaj.org/article/95af4562276b4d5eb2cf8f330a35466d
Autor:
Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad AlEidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel
Publikováno v:
Molecular Genetics & Genomic Medicine. 11
Congenital disorders of glycosylation (CDG) are a group of heterogeneous disorders caused by abnormal lipid or protein glycosylation. Variants in the FCSK gene have been reported to cause CDG. Defective FCSK-induced CDG (FCSK-CDG) has only been repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b7925762c554bfa7957a20a5b7aa78
https://doi.org/10.1002/mgg3.2117
https://doi.org/10.1002/mgg3.2117
Autor:
Mashael Alharbi, Mansour Alharbi, Amal Surrati, Mashael Alhilabi, Ayed alrashdi, Majedah Almokhalafi
Publikováno v:
F1000Research. 12:416
Background: There is a huge burden of nutrition-related non-communicable diseases, and diabetes is one of the leading chronic nutrition-related diseases affecting more than 500 million people globally. Collecting information regarding the awareness o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db485ea59fe8163cb92b0a8661fbb119
https://doi.org/10.12688/f1000research.131518.1
https://doi.org/10.12688/f1000research.131518.1
Publikováno v:
Teaching in Higher Education. 28:532-549
This case examined five students’ experiences of participating in a film-mediated community-based discourse about local Asian Canadian communities, where students viewed and created documentary fil...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc399180af85777e7ffedb80a7623964
https://doi.org/10.1080/13562517.2020.1830366
https://doi.org/10.1080/13562517.2020.1830366