Zobrazeno 1 - 10
of 129
pro vyhledávání: '"Abumansour IS"'
Autor:
Abumansour, Amani S., Zubiaga, Arkaitz
An important component of an automated fact-checking system is the claim check-worthiness detection system, which ranks sentences by prioritising them based on their need to be checked. Despite a body of research tackling the task, previous research
Externí odkaz:
http://arxiv.org/abs/2212.08514
Autor:
Wen Li, Zichao Xiang, Wenjing Yu, Xiaobin Huang, Qian Jiang, Arwa Abumansour, Ying Yang, Chider Chen
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-21 (2024)
Abstract Inflammation is a common and important pathological process occurring in any part of the body and relating to a variety of diseases. Effective tissue repair is critical for the survival of impaired organisms. Considering the side effects of
Externí odkaz:
https://doaj.org/article/018c63a4ff3447e2b6cb5df4a9ef0667
As online false information continues to grow, automated fact-checking has gained an increasing amount of attention in recent years. Researchers in the field of Natural Language Processing (NLP) have contributed to the task by building fact-checking
Externí odkaz:
http://arxiv.org/abs/2109.11427
Autor:
Bogari, Neda M, Naffadi, Hind Mansour, Babalghith, Ahmad O., Azher, Zohor Asaad, Abumansour, Iman Sabri, Melibary, Ehab M., Qattan, Muneera, Alluhaibi, Amaal M., Amin, Amr A, Bogari, Mustafa, Bogari, Dema Neda, Obaid, Rami, Allam, Reem M
Publikováno v:
In Journal of Stroke and Cerebrovascular Diseases August 2024 33(8)
Autor:
Balqis A. Ikhmais, Alaa M. Hammad, Osama H. Abusara, Lama Hamadneh, Hamza Abumansour, Qasem M. Abdallah, Ali I. M. Ibrahim, Lina Elsalem, Mariam Awad, Rahaf Alshehada
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 10, Pp 7996-8012 (2023)
Repurposing existing drugs appears to be a potential solution for addressing the challenges in the treatment of non-small cell lung cancer (NSCLC). β-adrenoceptor antagonist drugs (β-blockers) have tumor-inhibiting effects, making them promising ca
Externí odkaz:
https://doaj.org/article/f02a578270174c07bd343311f514c075
Autor:
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, Zohor A. Azher, Alaa H. Falemban, Wefaq M. Madani, Wafaa Alosaimi, Ghydda Alghamdi, Ikhlas A. Sindi
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-15 (2023)
Abstract This review discusses the discovery, epidemiology, pathophysiology, genetic etiology, molecular diagnosis, and medication-based management of fragile X syndrome (FXS). It also highlights the syndrome’s variable expressivity and common como
Externí odkaz:
https://doaj.org/article/3c0b8312931542ca91a8be99b5e1acde
Autor:
Rawan Shamsheer, Suhair Sunoqrot, Violet Kasabri, Dana Shalabi, Rema Alkhateeb, Yusuf Alhiari, Riad Ababneh, Balqis Ikhmais, Hamza Abumansour
Publikováno v:
Journal of Pharmacy and Bioallied Sciences, Vol 15, Iss 3, Pp 107-125 (2023)
Background/Objective/Methods: Capsaicin micelles were prepared by the direct dissolution using the amphiphilic copolymer Pluronic P123 and advanced for substantially novel submicro-nanocytotoxicity. Results: Superior cytotoxicity of capsaicin loaded
Externí odkaz:
https://doaj.org/article/c41c6382604b4434a6f915fdde82fec9
Autor:
Ammar G. Chaudhary, MBChB, FRCPC, Fadi M. AlReefi, MD, Riad G. Abou Zahr, MD, FSCMR, Hossam A. Elzeftawy, MD, Saleh S. Alghamdi, MD, Areej A. Bushnag, MD, Jaudah A. Al-Maghrabi, MD, MSc, FRCPC, Iman S. Abumansour, MD
Publikováno v:
CJC Open, Vol 4, Iss 12, Pp 1031-1035 (2022)
Left ventricular hypertrophy is a common entity with a broad differential diagnosis. We present a case of a middle-aged woman with left ventricular hypertrophy and neuropathy caused by a rare transthyretin variant in the absence of a family history o
Externí odkaz:
https://doaj.org/article/d833ccfd1f9645eca246cff499ae6000
Akademický článek
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Autor:
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, Ezzeldin N. Elhawary, Nagwa Gaboon, Mohammed Dandini, Abdulelah Madkhali, Wafaa Alosaimi, Abdulmajeed Alzahrani, Fawzia Aljohani, Ehab M. Melibary, Osama A. Kensara
Publikováno v:
Human Genomics, Vol 16, Iss 1, Pp 1-17 (2022)
Abstract This review discusses the epidemiology, pathophysiology, genetic etiology, and management of phenylketonuria (PKU). PKU, an autosomal recessive disease, is an inborn error of phenylalanine (Phe) metabolism caused by pathogenic variants in th
Externí odkaz:
https://doaj.org/article/4583e2e4e7bb46e0adcd2247e7f26fe4