Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Umm-Kulthum Ismail Umlai"'
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:
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 1-2 (2024)
Externí odkaz:
https://doaj.org/article/3d7da35c5cfd40b79cb786a33c499a5f
Autor:
Nagham Nafiz Hendi, Yasser Al-Sarraj, Umm-Kulthum Ismail Umlai, Karsten Suhre, Georges Nemer, Omar Albagha
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
IntroductionEpidemiological studies have consistently revealed that Vitamin D deficiency is most prevalent in Middle Eastern countries. However, research on the impact of genetic loci and polygenic models related to Vitamin D has primarily focused on
Externí odkaz:
https://doaj.org/article/7eb0b8d3245a4f279c6fed73df3b3fef
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2022)
We describe a sporadic case of a pure, tandem, interstitial chromosome 4q duplication, arr[hg19] 4q28.1q32.3 (127,008,069-165,250,477) x3 in a boy born at 36 weeks of gestation. He presented with microcephaly (head circumference
Externí odkaz:
https://doaj.org/article/bf30324f0aa2475cbc7bf19b2a065fda
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Publikováno v:
Metabolomics ISBN: 9780323999243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dfb83aa6ee524ba8535aeacd7c9cbf3
https://doi.org/10.1016/b978-0-323-99924-3.00004-2
https://doi.org/10.1016/b978-0-323-99924-3.00004-2
Publikováno v:
Briefings in bioinformatics. 23(1)
Rare diseases occur in a smaller proportion of the general population, which is variedly defined as less than 200 000 individuals (US) or in less than 1 in 2000 individuals (Europe). Although rare, they collectively make up to approximately 7000 diff
Publikováno v:
Qatar Foundation Annual Research Conference Proceedings Volume 2016 Issue 1.
Objective: A shortage of studies regarding the ecology of Qatar led to the sampling sand to determine the composition of microbes within the sand (below a certain size). This sampling began with a sand sample obtained from Al Rayyan, Doha Qatar. The
Publikováno v:
Qatar Foundation Annual Research Conference Proceedings Volume 2016 Issue 1.
Objective: In this era of increasing antibiotic resistance (WHO)[1], we are running out of time as common bacterial infections are progressively rejecting drugs that would be standard for treatment. It is due to these reasons that research regarding