Zobrazeno 1 - 10
of 714
pro vyhledávání: '"Omar, A. E."'
Autor:
Jamil Alenbawi, Yasser A. Al-Sarraj, Umm-Kulthum I. Umlai, Ayat Kadhi, Nagham N. Hendi, Georges Nemer, Omar M. E. Albagha
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-12 (2024)
Abstract Sitosterolemia is a rare inherited disorder caused by mutations in the ABCG5/ABCG8 genes. These genes encode proteins involved in the transport of plant sterols. Mutations in these genes lead to decreased excretion of phytosterols, which can
Externí odkaz:
https://doaj.org/article/4b41350d245544dabc97274275caff03
Publikováno v:
Zagazig Journal of Agricultural Research. Sep/Oct2024, Vol. 51 Issue 5, p963-970. 8p.
Autor:
Asma A Elashi, Salman M Toor, Umm-Kulthum Ismail Umlai, Yasser A Al-Sarraj, Shahrad Taheri, Karsten Suhre, Abdul Badi Abou-Samra, Omar M E Albagha
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-12 (2024)
Abstract Background The genetic basis of type 2 diabetes (T2D) is under-investigated in the Middle East, despite the rapidly growing disease prevalence. We aimed to define the genetic determinants of T2D in Qatar. Methods Using whole genome sequencin
Externí odkaz:
https://doaj.org/article/c774abd0646240a2b405daad8348f9b2
Autor:
Usama Aliyu, Umm-Kulthum Ismail Umlai, Salman M. Toor, Asma A. Elashi, Yasser A. Al-Sarraj, Abdul Badi Abou−Samra, Karsten Suhre, Omar M. E. Albagha
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Insulin resistance (IR) and beta cell dysfunction are the major drivers of type 2 diabetes (T2D). Genome-Wide Association Studies (GWAS) on IR have been predominantly conducted in European populations, while Middle Eastern populations remain largely
Externí odkaz:
https://doaj.org/article/bc21fd641a684049950681181649ca07
Autor:
Schoeman, Judy, Kellerman, Ilde-Marié, Ladas, Elena J., Ndlovu, Sandile, Rogers, Paul C., du Plessis, Jan, Herholdt, Mariechen, Reynders, David T., Naidu, Gita, Rowe, Biance, Thomas, Karla, Vanemmenes, Barry, Mathews, Rema, Büchner, Ané, Omar, Fareed E., Ronelle, Uys, Kruger, Mariana
Publikováno v:
In Clinical Nutrition ESPEN October 2024 63:870-877
Autor:
Abdel-Raheem, Sherief M. *, El-Hamid, Marwa I. Abd, Khamis, Tarek, Baz, Heba A., Omar, Anaam E., Gad, Wafaa M., El-Azzouny, Mona M., Habaka, Manal A.M., Mohamed, Rania I., Elkenawy, Mona E., Dawod, Rehab E., Elalfy, Eman. A., Ibrahim, Doaa
Publikováno v:
In Poultry Science December 2024 103(12)
Autor:
Yasser Al-Sarraj, Rowaida Z. Taha, Eman Al-Dous, Dina Ahram, Somayyeh Abbasi, Eman Abuazab, Hibah Shaath, Wesal Habbab, Khaoula Errafii, Yosra Bejaoui, Maryam AlMotawa, Namat Khattab, Yasmin Abu Aqel, Karim E. Shalaby, Amina Al-Ansari, Marios Kambouris, Adel Abouzohri, Iman Ghazal, Mohammed Tolfat, Fouad Alshaban, Hatem El-Shanti, Omar M. E. Albagha
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Autism spectrum disorder (ASD) is characterized by aberrations in social interaction and communication associated with repetitive behaviors and interests, with strong clinical heterogeneity. Genetic factors play an important role in ASD
Externí odkaz:
https://doaj.org/article/1cb66fb1f0d64cfb9ab254e423381745
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-20 (2023)
Abstract Background T2D is of high prevalence in the middle east and thus studying its mechanisms is of a significant importance. Using 1026 Qatar BioBank samples, epigenetics, whole genome sequencing and metabolomics were combined to further elucida
Externí odkaz:
https://doaj.org/article/dd40fe7719a44abc9ffe5f560a43e254
Autor:
Abdelmoneem, Shimaa, Omar, Rasha E., Hassan Ahmed, Nabila, Mohamed, Sara Refaee Abdo, Walaa, Mohammad, Abbas, Ahmad, Abdel-Sattar, Eman M., Abdel-hameed, Abdullah Mohammad, El-Korashi, Lobna A., Youssef Mohamed, Salem, Chen, Tse-Wei, Aljowaie, Reem M., Almutairi, Saeedah Musaed, Embaby, Ahmed
Publikováno v:
In Journal of King Saud University - Science May 2024 36(5)
Publikováno v:
In International Journal of Biological Macromolecules March 2024 261 Part 2