Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mansour S. Aljabry"'
Autor:
Ghaleb Elyamany, Hassan Rizwan, Ariz Akhter, Mansour S. Aljabry, Sultan Alotaibi, Mohammad A. Hameed Albalawi, Meer-Taher Shabani-Rad, Tariq Mahmood Roshan, Adnan Mansoor
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 1, Pp 604-613 (2023)
Dysregulated Wnt/β-catenin signal transduction is implicated in initiation, propagation, and poor prognosis in AML. Epigenetic inactivation is central to Wnt/β-catenin hyperactivity, and Wnt/β-catenin inhibitors are being investigated as targeted
Externí odkaz:
https://doaj.org/article/746f41bdca8942769698ebe1e6722423
Autor:
Nawaf Alkhayat, Mohammad Alshahrani, Ghaleb Elyamany, Qanita Sedick, Walid Ibrahim, Hasna Hamzi, Amal Binhassan, Mohamed Othman, Saeed Alshieban, Mansour S. Aljabry, Shuaa Asiri, Muneerah Alzouman, Omar Alsuhaibani, Fahad Alabbas, Omar Alsharif, Yasser Elborai
Publikováno v:
Journal of the Egyptian National Cancer Institute, Vol 33, Iss 1, Pp 1-9 (2021)
Abstract Background Hodgkin lymphoma (HL) is lymphoid neoplasm usually affecting lymphatic system; it accounts 3.6% of cancers in Saudi Arabia. Modern treatment protocols had shown particular success rates in overall-survival (OS) and event-free-surv
Externí odkaz:
https://doaj.org/article/4be7a1fa2d86480c9736eca49e7c675a
Autor:
Nawaf Alkhayat, Ghaleb Elyamany, Yasser Elborai, Qanita Sedick, Mohammad Alshahrani, Omar Al Sharif, Abdulmalik Alenezy, Amjad Hammdan, Hatem Elghezal, Omar Alsuhaibani, Mansour S. Aljabry, May AlMoshary, Eman Al Mussaed
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract Background Childhood Acute Leukemia (AL) is characterized by recurrent genetic aberrations in 60% of AML cases and 90% of ALL cases. Insufficient data exists of rare cytogenetic abnormalities in AL. Therefore, we tested rare cytogenetic abno
Externí odkaz:
https://doaj.org/article/b55d7fca52f44ddebb9ef81726568a3e
Publikováno v:
Hematology Reports, Vol 10, Iss 2 (2018)
Extramedullary hematopoiesis (EMH) is a presence of hematopoietic activity in the extramedullary sites. EMH can occur in both benign and malignant hematologic diseases. The liver and spleen are the most common sites, but may also occur infrequently a
Externí odkaz:
https://doaj.org/article/ceedf02dafc644679a74eea9bbf2d995
Autor:
Mansour S. Aljabry
Publikováno v:
Journal of Hematopathology. 16:27-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c98afeac4c05c5c8895c2c29edcb0aa6
https://doi.org/10.1007/s12308-022-00528-1
https://doi.org/10.1007/s12308-022-00528-1
Autor:
Mansour S Aljabry
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 2, Pp 39-44 (2018)
Primary familial and congenital polycythemia (PFCP) is a rare autosomal dominant disorder caused by hypersensitivity of erythropoietin receptor of erythroid progenitors leading to increased rate of erythropoiesis at any given serum erythropoietin lev
Externí odkaz:
https://doaj.org/article/61a5a42563fa4eefaee9fbfc12c40e17
Autor:
Mansour S. Aljabry
Publikováno v:
Journal of Hematopathology. 12:27-30
Anaplastic plasma cell myeloma (PCM) is an aggressive morphological variant of myeloma characterized by involvement of extramedullary sites and extremely poor prognosis. Moreover, anaplastic PCM is frequently associated with high frequency of 17p(p53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3b95530f73d19fcdd831441ccbca44e
https://doi.org/10.1007/s12308-018-0338-y
https://doi.org/10.1007/s12308-018-0338-y
Autor:
Abdullah Alhowidi, Saad Alrubaia, Abdulaziz Alhoshan, Mansour S. Aljabry, Abdullah Alsahli, Adnan Alkhayat, Mohammed Khalid Alabdulaali, Fahad Alrawaf, Abdulmajeed Alshaikh
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 84-87 (2019)
BACKGROUND: Sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency (G6PD) are the most common causes of inherited hemolytic anemia in Saudi Arabia. Due to high prevalence, some blood transfusion services perform routine blood donor scree
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bea12a1c9e63a94a74f14e209d8a5c19
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127
Autor:
Mohamed S. Othman, Raniah Alqawahmed, Mansour S. Aljabry, Omar Alsuhaibani, Nawaf Alkhayat, Yasir Alrusayni, Mohammad Alshahrani, Ghaleb Elyamany, Amal Binhassan, Omar Alsharif, Walid Ibrahim, Yasser Elborai, Khadijah Abdulhaleem, Hasna Hamzi
Publikováno v:
Rare Tumors
Rare Tumors, Vol 13 (2021)
Rare Tumors, Vol 13 (2021)
Rare pediatric tumors are heterogeneous group containing a variety of histopathological diseases, they represent approximately 10% of all childhood cancers. These rare tumors had a diversity of histology and clinical behaviors that pose different cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dceca5b4ddf404c0de2acac22a140ae9
http://europepmc.org/articles/PMC7907711
http://europepmc.org/articles/PMC7907711
Autor:
Muneerah Alzouman, Saeed Alshieban, Fahad Alabbas, Mohammad Alshahrani, Omar Alsuhaibani, Nawaf Alkhayat, Mohamed S. Othman, Mansour S. Aljabry, Omar Alsharif, Walid Ibrahim, Hasna Hamzi, Shuaa Asiri, Amal Binhassan, Yasser Elborai, Qanita Sedick, Ghaleb Elyamany
Publikováno v:
Journal of the Egyptian National Cancer Institute, Vol 33, Iss 1, Pp 1-9 (2021)
BackgroundHodgkin lymphoma (HL) is lymphoid neoplasm usually affecting lymphatic system; it accounts 3.6% of cancers in Saudi Arabia. Modern treatment protocols had shown particular success rates in overall-survival (OS) and event-free-survival (EFS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a44204ecd90e3520a27fb2129af2fef
https://pubmed.ncbi.nlm.nih.gov/34396456
https://pubmed.ncbi.nlm.nih.gov/34396456