Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Awad, Omer"'
Autor:
Moez Mohammed Ibrahim Bashir, Mohmed Ahmed Fadelalla Alrayah, Mohamed Esameldeen Elsayed Mustafa, Mohammed Khalid Abdulla Maroof, Mohamed Awad Omer Hamad, Moaid Mohamedosman Ali Mohamedosman
Publikováno v:
BMC Medical Education, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background The medical profession is one of the most highly respected and desired professions among students worldwide, most likely because it provides opportunities for both a financially and socially rewarding career. However, while it has
Externí odkaz:
https://doaj.org/article/9c1156dbd117493bbec70e716e4b4614
Akademický článek
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Akademický článek
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Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Background: In recent years, a somatic point mutation in the Janus Kinase 2 (JAK2) gene (1849 G→T, V617F) has been reported to occur in over 90% of patients with polycythemia vera (PV). Another JAK2 mutation in exon 12 had been described and shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5faa71474b81301ae67cccee78f54c6d
http://europepmc.org/articles/PMC6485582
http://europepmc.org/articles/PMC6485582
Publikováno v:
Anatomy: International Journal of Experimental & Clinical Anatomy. Aug2017, Vol. 11 Issue 2, p72-78. 7p.
Publikováno v:
Petroleum Science and Technology. 36:62-67
A commercial Fluid Catalytic Cracking (FCC) catalyst is used to reduce naphthenic acids (NAs) in a high Total Acid Number (TAN) crude oil sample. The influence of temperature, oil/catalyst ratio is...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47f74e3856fee9e66a5ee663239bacc1
https://doi.org/10.1080/10916466.2017.1403454
https://doi.org/10.1080/10916466.2017.1403454
Publikováno v:
OALib. :1-8
Background: Deep venous thrombosis (DVT) can lead to a serious fatal pulmonary embolism. Many genetic risk factors may predispose to DVT; one of these is the mutation in the PROCR gene responsible for the production of endothelial protein C receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bd0f97e03b89ce91fc9b70e6b299ff4
https://doi.org/10.4236/oalib.1102310
https://doi.org/10.4236/oalib.1102310
Publikováno v:
OALib. :1-6
Background: Deep vein thrombosis (DVT) may lead to serious complication; the pulmonary embolism; one of the most serious conditions that cause morbidity and mortality worldwide. sEPCR circulates in the plasma and has high affinity to bind protein C a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::354be82ebe388ab9f334ab285a1263df
https://doi.org/10.4236/oalib.1102241
https://doi.org/10.4236/oalib.1102241
Publikováno v:
Petroleum Science & Technology; 2018, Vol. 36 Issue 1, p62-67, 6p
Autor:
Amin Al Mohamadi, A. Alsulaiman, Hazaa Al Zahrani, Mohammad Qari, Awad Omer, Soad K. Al Jaouni, Zaki Nasrullah, Abbas Alabdullatif, Abbdulkareem Al Momen, Salam Al Kindi, Mohamad Al Sayegh, Fahad Al Othman, Maha Hegazi, Hussein Al Saeed, Ahamd Tarawa, Shaker A. Mousa, Faisal Al Sayegh
Publikováno v:
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 16(4)
Sickle-cell disease (SCD) is a wide-spread inherited hemolytic anemia that is due to a point mutation, leading to the substitution of valine for glutamic acid, causing a spectrum of clinical manifestations in addition to hemolysis and anemia. Acute p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bec63ca925f53e216f94f01060dd3170
https://pubmed.ncbi.nlm.nih.gov/20530056
https://pubmed.ncbi.nlm.nih.gov/20530056