Zobrazeno 21 - 30
of 98
pro vyhledávání: '"Osama Alsmadi"'
Autor:
osama Alsmadi
Publikováno v:
An-Najah University Journal for Research - B (Humanities). 36:1825-1854
This study aimed to identify the benefit from the services and facilities provided at Imam Muhammad bin Saud Islamic University, to the students with disabilities, the study was implemented by applying a questionnaire consisting of (44) items distrib
Autor:
OSAMA ALSMADI, Hikmat Abdel-Razeq, Yazan Talab, Hazem Abdulelah, Zeena Shaheen, Abdelghani Tbakhi
Common PIK3CA gene activating mutations can be found in 20–30% of all breast cancer cases, and regarded as predictive markers for therapeutic response to PI3K inhibitors. The therascreen PIK3CA mutation companion assay and the alpha-specific PI3K i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af319934568f8b6df60f7a011b252805
https://doi.org/10.21203/rs.3.rs-2699737/v1
https://doi.org/10.21203/rs.3.rs-2699737/v1
Autor:
Anas Al-okaily, Razan Abu Khashabeh, Osama Alsmadi, Yazan Ahmad, Iyad Sultan, Ion Mandoiu, Abdelghani Tbakhi, Pramod Srivast
Somatic mutations in tumors can generate neoantigens that are presented on the cell surface through MHC molecules. As these mutations are expected to be unique to each tumor and as these generated (and presented) neoantigens play a significant role i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e289037fc65421676523c9df9a70198
https://doi.org/10.21203/rs.3.rs-2426010/v1
https://doi.org/10.21203/rs.3.rs-2426010/v1
Autor:
Amal Jabr, Abbas Hawwari, Moheeb Al-Awwami, Tanziel Elamin, Khawar Siddiqui, Lina El-Baik, Osama Alsmadi, Ali Al Ahmari, Ibrahim Al Fawaz, Safa Alhissi, Bandar K. Al Saud, Mouhab Ayas, Atia Sheereen
Publikováno v:
Blood research
Background Our study was designed to investigate the frequencies and distributions of familial hemophagocytic lymphohistiocytosis (FHL) associated genes in Saudi patients. Methods FHL associated gene screening was performed on 87 Saudi patients who w
Autor:
Iyad Sultan, Abdelghani Tbakhi, Osama Abuatta, Sawsan Mubarak, Osama Alsmadi, Adib Edilbi, Ruba Al-Ani, Manar Makhlouf, Rawan Hajir, Omar Khreisat, Majeda A. Al-Ruzzieh, Hikmat Abdelrazeq, Asem Mansour
BACKGROUNDWe aimed to assess the efficacy of 3 COVID-19 vaccines in a population of health care workers at a tertiary cancer center in Amman, Jordan.METHODSWe evaluated the records of 2855 employees who were fully vaccinated with 1 of 3 different vac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8348de156e9eeea40f12be1682b7c510
https://doi.org/10.1101/2022.01.15.22269356
https://doi.org/10.1101/2022.01.15.22269356
Autor:
Ebaa Al-Ozairi, Motasem Melhem, Rasheeba Nizam, Ashraf Al Madhoun, Muthukrishnan Eaaswarkhanth, Fahd Al-Mulla, Osama Alsmadi, Gyaneshwer Chaubey, Prem Sharma
Publikováno v:
The Application of Clinical Genetics. 12:63-70
Background: The association of mitochondrial DNA (mtDNA) variations with obesity has been investigated in diverse populations across the world. However, such obesity-associated mtDNA examinations are rarely conducted in Arab populations. Materials an
Autor:
Sriraman Devarajan, Daisy Thomas, Jaakko Tuomilehto, Thangavel Alphonse Thanaraj, Sumi Elsa John, Arshad Channanath, Fahd Al-Mulla, Muthukrishnan Eaaswarkhanth, Dinu Antony, Prashantha Hebbar, Osama Alsmadi
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-30 (2018)
Scientific Reports
Scientific Reports, 8
Scientific Reports
Scientific Reports, 8
Consanguineous populations of the Arabian Peninsula have been underrepresented in global efforts that catalogue human exome variability. We sequenced 291 whole exomes of unrelated, healthy native Arab individuals from Kuwait to a median coverage of 4
Autor:
Osama Alsmadi, Thangavel Alphonse Thanaraj, Mohamed Abu-Farha, Robert Sladek, Naser Elkum, Janne Pitkäniemi, Fadi Alkayal, Prashantha Hebbar, Rasheeba Iqbal, Sumi Elsa John, Fahd Al-Mulla, Jaakko Tuomilehto, Jehad Abubaker, Arshad Channanath
Publikováno v:
Human Genetics
While the Arabian population has a high prevalence of metabolic disorders, it has not been included in global studies that identify genetic risk loci for metabolic traits. Determining the transferability of such largely Euro-centric established risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b20447b4c28497fd8d6ae134c620961
http://hdl.handle.net/10138/353204
http://hdl.handle.net/10138/353204
Autor:
Osama Alsmadi, Muthukrishnan Eaaswarkhanth, Ajai Kumar Pathak, Prashantha Hebbar, Thangavel Alphonse Thanaraj, Mait Metspalu, Francesco Montinaro, Fahd Al-Mulla, Linda Ongaro
Publikováno v:
European journal of human genetics : EJHG. 30(3)
Recent studies have showed the diverse genetic architecture of the highly consanguineous populations inhabiting the Arabian Peninsula. Consanguinity coupled with heterogeneity is complex and makes it difficult to understand the bases of population-sp
Autor:
Abdullah Bennakhi, Mohamed Abu-Farha, Jaakko Tuomilehto, Sumi Elsa John, Naser Elkum, Fahd Al-Mulla, Arshad Channanath, Thangavel Alphonse Thanaraj, Ebaa Al-Ozairi, Rasheeba Nizam, Jehad Abubaker, Fadi Alkayal, Prashantha Hebbar, Motasem Melhem, Janne Pitkäniemi, Osama Alsmadi
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-17 (2020)
Scientific Reports
Scientific Reports
Consanguineous populations of the Arabian Peninsula, which has seen an uncontrolled rise in type 2 diabetes incidence, are underrepresented in global studies on diabetes genetics. We performed a genome-wide association study on the quantitative trait
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d598c4dc854c09c264b6a2e048adfaf
http://hdl.handle.net/10138/313231
http://hdl.handle.net/10138/313231