Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Asem Alkhateeb"'
Publikováno v:
Arabian Journal for Science and Engineering. 46:5421-5427
Multiple sclerosis (MS) is a chronic inflammatory autoimmune disease, which leads to neurodegenerative processes that cause neuron demyelination. MS is multifactorial with uncertain etiology, where interactions between genetic makeup of an individual
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 6, p e0252616 (2021)
PLoS ONE, Vol 16, Iss 6, p e0252616 (2021)
BackgroundThe neuropeptide substance P is a potential biomarker and therapeutic target in cancer. The main objectives of this study were to investigate the expression level of substance P in different breast cancer molecular subtypes and identify its
Publikováno v:
Meta Gene. 13:57-62
Intellectual disability (ID) is a common heterogeneous disease. Many genes have been implicated in the etiology of ID, yet gene discovery continues at a fast pace. In this study, we investigated the genetic cause of ID in a consanguineous Arab family
Autor:
Aya Abu-sheikha, Asem Alkhateeb, Ziad W. Jaradat, Yazan Haddad, Mohammed A. Al-Ghazo, Yousef Jarun, Khaldon Bodoor, Abdulhameed Al-Ghabkari, Sara Abu Jalboush, Saied A. Jaradat, Ismail Matalka
Publikováno v:
Meta Gene. 12:33-42
Bladder cancer is the most common cancer of the urinary tract with an estimate of 401,000 new cases diagnosed annually worldwide. In Jordan, bladder cancer accounts for 4.3% of all newly diagnosed cancer cases. Several studies have linked p53 molecul
Autor:
Wafa Alazaizeh, Asem Alkhateeb
Intellectual disability is a common condition with multiple etiologies. The number of monogenic causes has increased steadily in recent years due to the implementation of next generation sequencing. Here, we describe a 2-year-old boy with global deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07025190c0bb36ffa69d26093dfc3532
https://europepmc.org/articles/PMC6375718/
https://europepmc.org/articles/PMC6375718/
Autor:
Abdulhameed Ghabkari, Ahmad Magableh, Asem Alkhateeb, Yazan Haddad, Khaldon Bodoor, Nazzal Bsoul, Mohammad Dowairi, Abdullah Al-Abbadi
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 15:75-84
Aberrant DNA methylation of tumor suppressor genes has been reported in all major types of leukemia with potential involvement in the inactivation of regulatory cell cycle and apoptosis genes. However, most of the previous reports did not show the ex
Publikováno v:
Oral Diseases. 20:693-699
Objectives Recurrent aphthous stomatitis (RAS) is a common oral inflammatory disease induced by genetic and environmental factors. Gelatinases (MMP-2 and MMP-9) and their natural inhibitor TIMP-1 are active players in the inflammatory process. We aim
Autor:
Karem H. Alzoubi, Mera A. Ababneh, Asem Alkhateeb, Sayer I Al-Azzam, Omar F. Khabour, Raya N. Alzayadeen
Publikováno v:
Experimental and Therapeutic Medicine
The aim of this study was to examine the effect of atorvastatin treatment on levels of leptin, adiponectin and insulin resistance, and their correlation with clinical parameters, in patients with type II diabetes. Patients with diabetes (n=394) were
Publikováno v:
Journal of Oral Pathology & Medicine. 42:741-746
Background Recurrent aphthous stomatitis (RAS) is a common oral ulcerative condition. At ulcer sites vascular adhesion molecule-1 (VCAM-1), E-selectin and intercellular adhesion molecule-1 (ICAM-1) are strongly expressed on blood vessels, and ICAM-1
Autor:
William B. Dobyns, Katherine C. Nickels, Berkley R. Powell, Barbara K. Burton, Art Grix, Asem Alkhateeb, Elizabeth Berry-Kravis, Soma Das, Eric D. Marsh, Wendy K. Chung, Alex R. Paciorkowski, Livija Medne, Ghayda M. Mirzaa, Andrea Paras, Elaine C. Wirrell, Katherine H. Kim
Publikováno v:
Pediatric Neurology. 48:367-377
Mutations in CDKL5 and ARX are known causes of early-onset epilepsy and severe developmental delay in males and females. Although numerous males with ARX mutations associated with various phenotypes have been reported in the literature, the majority