Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mohammad Al Shahrani"'
Autor:
GHALEB ELYAMANY, Nawaf ALKHAYAT, Omar AL SHARIF, Yasser ELBORAI, Mohammad AL SHAHRANI, Omar ALSUHAIBANI
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S15-S16 (2022)
Objective: NOTCH1 is now established to play a key role in the prognosis of several hematological malignancies. Notch proteins are multifaceted and involved in several key cellular functions with extensive crosstalk with other critical pathways; ther
Externí odkaz:
https://doaj.org/article/695929ea8a774e3b938e9fa9efc6256d
Autor:
Nawaf Alkhayat, Yasser Elborai, Omer Al Sharif, Mohammad Al Shahrani, Omar Alsuhaibani, Mohammed Awad, Hatem Elghezal, Inesse ben-abdallah Bouhajar, Mona Alfaraj, Eman Al Mussaed, Fahad Alabbas, Ghaleb Elyamany
Publikováno v:
Clinical Medicine Insights: Oncology, Vol 11 (2017)
Background: Childhood acute lymphoblastic leukemia (ALL) is characterized by recurrent genetic aberrations. The identification of those abnormalities is clinically important because they are considered significant risk-stratifying markers. Aims: Ther
Externí odkaz:
https://doaj.org/article/211e9ee9ac7e4d9b9d263231b26114c2
Autor:
Ghaleb Elyamany, Mohamed Awad, Omar Alsuhaibani, Kamal Fadalla, Omer Al Sharif, Mohammad Al Shahrani, Fahad Alabbas, Abdulaziz Al-Abulaaly
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 6, Iss 1, Pp e2014038-e2014038 (2014)
The fms-like tyrosine kinase 3 (FLT3) gene is a member of the class III receptor tyrosine kinase family, mutations of FLT3 were first described in 1997 and account for the most frequent molecular mutations in acute myeloid leukemia. No data currentl
Externí odkaz:
https://doaj.org/article/291f610744c74af5af24616221843f68
Autor:
Ghaleb Elyamany, Mohammad Awad, Kamal Fadalla, Mohamed Albalawi, Mohammad Al Shahrani, Abdulaziz Al Abdulaaly
Publikováno v:
Advances in Hematology, Vol 2014 (2014)
The Fms-like tyrosine kinase-3 (FLT3) is a receptor tyrosine kinase that plays a key role in cell survival, proliferation, and differentiation of hematopoietic stem cells. Mutations of FLT3 were first described in 1997 and account for the most freque
Externí odkaz:
https://doaj.org/article/248a411b80124fddaf3ba256be270c86
Autor:
Khalid Al-Qahtani, Mohammad Al Shahrani, Faisal Al Zahrani, AbdulAziz Al Ghamdi, Fareed Al Alghamdi, Zaid Al Alshaalan, Abdulaziz Al-Saif, Areej Bokhari, Amal A. Al-Abdulkarim, Tahera Islam
Publikováno v:
Indian Journal of Otolaryngology and Head & Neck Surgery.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff3b15e4c6ca6e5596f895c12966c252
https://doi.org/10.1007/s12070-023-03627-2
https://doi.org/10.1007/s12070-023-03627-2
Publikováno v:
OncoTargets and Therapy.
Al-Asmari AK, Riyasdeen A, Al-Shahrani MH, Islam M. Onco Targets Ther. 2016;9:6485-6498. It was bought to the authors attention that the images in Figure 1A, panel V1 and V2 (10 µg/mL) were duplicated. The error was introduced inadvertently at the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06e17d24e3761fb4a1829cea6396bd5c
https://www.dovepress.com/corrigendum-snake-venom-causes-apoptosis-by-increasing-the-reactive-ox-peer-reviewed-fulltext-article-OTT
https://www.dovepress.com/corrigendum-snake-venom-causes-apoptosis-by-increasing-the-reactive-ox-peer-reviewed-fulltext-article-OTT
Publikováno v:
Journal of Positive School Psychology; 2022, Vol. 6 Issue 9, p1141-1153, 13p
Autor:
Mohammad Al Shahrani, Yasser Elborai, Hassan Rizwan, Omar Al Sharif, Nawaf Alkhayat, Hamza Kamran, Ariz Akhter, Ghaleb Elyamany, Meer-Taher Shabani-Rad, Adnan Mansoor
Publikováno v:
Pediatric hematology and oncology. 38(6)
Genetic aberrations in the epigenome are rare in pediatric AML, hence expression data in epigenetic regulation and its downstream effect is lacking in childhood AML. Our pilot study screened epigenetic modifiers and its related oncogenic signal trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf9a050417a84bd38763153b226a988
https://pubmed.ncbi.nlm.nih.gov/33764257
https://pubmed.ncbi.nlm.nih.gov/33764257
Autor:
Cesar M. Rueda, Benjamin Prince, Ajay Gupta, Mohammad Al-Shahrani, Hemalatha G. Rangarajan, Jennifer R. Yonkof, Elizabeth Varga, Timothy P. Cripe, Roshini S. Abraham, Shamlal Mangray
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology
Frontiers in Immunology
CARMIL2 deficiency is a rare combined immunodeficiency (CID) characterized by defective CD28-mediated T cell co-stimulation, altered cytoskeletal dynamics, and susceptibility to Epstein Barr Virus smooth muscle tumors (EBV-SMTs). Case reports associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e414b85fbd688c59320a30840057ab62
https://doi.org/10.3389/fimmu.2020.00884
https://doi.org/10.3389/fimmu.2020.00884
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 69(10)
To assess medical students' perception about their satisfaction regarding the preparatory year.The cross-sectional study was conducted at the University of Bisha College of Medicine, Saudi Arabia, from October 2017 to April 2018, and comprised medica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ef4c7ab23b975933de0f88ec4091e17
https://pubmed.ncbi.nlm.nih.gov/31622310
https://pubmed.ncbi.nlm.nih.gov/31622310