Bridging the gap between knowledge and barriers: evaluating healthcare professionals' perspectives on hematopoietic stem cell transplantation
Haitham M.H. Qutob, Raed F. Alserihi
sa (code pays fourni par la source)
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Haitham M.H. Qutob, Raed F. Alserihi
sa (code pays fourni par la source)
Haitham M.H. Qutob, Raed F. Alserihi
sa (code pays fourni par la source)
Abdullah Hamadi, Rashid Mir, Osama M. Al‐Amer, Mohammed Alasseiri et autres
Background Variants linked to the risk of ischemic stroke have been discovered through genome-wide association studies (GWASs). These variations frequently have little consequences that lack apparent biological significance. Hence, these findings demonstrate that exome sequencing can be highly relevant to stroke, even …
sa (code pays fourni par la source)
Hadeel Al Sadoun, Fatimah Alamoudi, Noha Alamoudi, Hossam H. Tayeb et autres
Background: All-trans retinoic acid (ATRA) has revolutionized the management of acute promyelocytic leukemia (APL) and has generated interest in differentiation therapy as means to reduce reliance on conventional chemotherapy in other subtypes of acute myeloid leukemia (AML). However, the precise relationship between …
sa, ie (code pays fourni par la source)
Mashaer Taha Edris, Maye M. Merghani, Shaza Salih Gafar, Ahmed Mohamed Asmeli et autres
Reduced Folate Carrier1 (RFC1) gene's metabolism is crucial for DNA synthesis, epigenetic mechanisms, and cellular methylation events. Nonetheless, RFC1 polymorphisms have drawn a lot of interest in current medical genetics studies. The objectives of the study were to ascertain the relationship between …
Soudan, sa, gb (code pays fourni par la source)
Elrashed B. Yasin, Haitham M.H. Qutob, Raed F. Alserihi
Background: Methionine synthase reductase, which is encoded by the methionine synthase reductase (MTRR) gene, plays a crucial role in the methylation reactions and the production of DNA and its epigenetic processes. There was a correlation between the MTRR (A66G) polymorphism and the …
sa (code pays fourni par la source)
Raed F. Alserihi, Sarah Alswat, Heba Ahmed Alkhatabi, Haitham M.H. Qutob et autres
α-thalassemia (α-thal) is a genetic disorder characterized by a decreased synthesis of α-globin chains. A deletion mutation most often causes it in one or more α-globin chains. No comprehensive characterization studies have been conducted on α-thal patients in the Saudi population. Therefore, …
sa (code pays fourni par la source)
Heba Alkhatabi, S Aldahlawi, Mohannad S. Hazzazi, Reem Alsolami et autres
OBJECTIVE: The use of tyrosine kinase inhibitors (TKIs) and other targeted therapeutics plays a pivotal role in treatment management for individuals diagnosed with chronic myeloid leukemia (CML). However, some patients may experience fewer favorable outcomes and treatment resistance. Our work aims to …
sa (code pays fourni par la source)
Mashaer Taha Edris, Maye M. Merghani, Shaza Salih Gafar, Ahmed Mohamed Asmali et autres
Background and Objectives. The enzyme methionine synthase reductase is involved in cellular methylation reactions, DNA synthesis, and epigenetic processes. It is encoded by the MTRR gene, which garnered a lot of attention in current medical genetics research. This study was conducted to …
Soudan, sa (code pays fourni par la source)
Saeed M. Kabrah, Samer Abuzerr, Ruba Omar Mohammed Almaghrabi, Raed F. Alserihi et autres
The current cross-sectional study was conducted to determine the quality of blood donation services and its association with blood donors’ trust and loyalty at Makkah blood donation centers in Saudi Arabia. A total of 373 healthy blood donors aged ≥18 years who …
sa, ca, ps (code pays fourni par la source)
Raed F. Alserihi, Hameeda Ahmad Hameeda Ahmad, Heba Alkhatabi Heba Alkhatabi, Talal Qadah et autres
Background: The outcome of acute myeloid leukemia (AML) is influenced by ethnicity, geographic variations, and the patient’s molecular profile. We aimed to explore the mutation frequencies of the nucleophosmin 1 (NPM1) and the FMS-like tyrosine kinase 3 (FLT3) internal tandem duplication (ITD) …
sa, Égypte (code pays fourni par la source)
Hesham Abdulla, Raed F. Alserihi, Christoffer Flensburg, Waruni Abeysekera et autres
Cell competition has recently emerged as an important tumor suppressor mechanism in the thymus that inhibits autonomous thymic maintenance. Here, we show that the oncogenic transcription factor Lmo2 causes autonomous thymic maintenance in transgenic mice by inhibiting early T cell differentiation. This …
au, cn (code pays fourni par la source)
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