Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Nahla O. Mousa"'
Autor:
Nabila El-Sheikh, Nahla O. Mousa, Ahmed Osman, Amany M. Tawfeik, Bothiana A. Taha, Hazem Mahran, Alaa M. Saleh, Iman El-shiekh, Wagdy Amin, Mohamed Elrefaei
Publikováno v:
International Journal of Infectious Diseases, Vol 109, Iss , Pp 223-229 (2021)
Objectives: Current diagnostic tests for tuberculosis (TB) in children living in low-endemic countries are limited by low specificity and the inability of the current tests to differentiate between active TB and latent TB infection (LTBI). This study
Externí odkaz:
https://doaj.org/article/87834dfb45094c8fb23911d62bbb6e8c
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 1 (2021)
Abstract Investigating the etiological causes of acute myeloid leukemia (AML) at the molecular level should help in identifying targets and strategies that would increase the efficacy of the current management regimens. Some genes may act as molecula
Externí odkaz:
https://doaj.org/article/51407ac2dd004298838092515a60a0c8
Autor:
Wagdy Amin, Iman El-shiekh, Mohamed Elrefaei, Ahmed M. Osman, Nabila El-Sheikh, Hazem Mahran, Amany M. Tawfeik, Bothiana A. Taha, Alaa M. Saleh, Nahla O. Mousa
Publikováno v:
International Journal of Infectious Diseases, Vol 109, Iss, Pp 223-229 (2021)
Objectives: Current diagnostic tests for tuberculosis (TB) in children living in low-endemic countries are limited by low specificity and the inability of the current tests to differentiate between active TB and latent TB infection (LTBI). This study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50d42365198bfb303d83cea841dd6d54
https://doi.org/10.1016/j.ijid.2021.07.024
https://doi.org/10.1016/j.ijid.2021.07.024
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Background: Acute myeloid leukemia (AML) is a set of Myeloproliferative neoplasms that are identified by excessive growth of myeloid blasts and production of abnormal blood cells. AML is the most common type of acute leukemia that occurs in adults. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15017625a2a07ce12899ca159482b05
https://doi.org/10.31557/apjcp.2019.20.12.3625
https://doi.org/10.31557/apjcp.2019.20.12.3625
Autor:
Ahmed A. H. Abdellatif, Nahla O. Mousa, Ahmed M. Osman, Usama Bakry, Nagia Fahmy, Ahmed A. Sayed, Waheed K. Zahra, Mariam G Elzayat
Publikováno v:
Bioscience Reports
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disorder that occurs due to inactivating mutations in DMD gene, leading to muscular dystrophy. Prediction of pathological complications of DMD and the identification of female carriers are im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1eb3b68cc3b07de6ec08dd63ba1b7ad
https://pubmed.ncbi.nlm.nih.gov/34472584
https://pubmed.ncbi.nlm.nih.gov/34472584
Autor:
Nahla O. Mousa, Radwa K. Soliman, Ahmad Gamal El Din Osman, Nagia Fahmy, Ramez Reda Moustafa, Hebatallah R. Rashed, Nabila Hamdi
Publikováno v:
Clinical neurology and neurosurgery. 208
Objective Numerous studies have been carried out to identify the role of microRNA (miRNA) as potential biomarkers for many diseases including amyotrophic lateral sclerosis (ALS). The aim of this study was to explore the circulating levels of some miR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9c02efc63d75878adf60975610a49a
https://pubmed.ncbi.nlm.nih.gov/34454204
https://pubmed.ncbi.nlm.nih.gov/34454204
Publikováno v:
Genetics and Molecular Biology
Genetics and Molecular Biology v.44 n.1 2021
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 44, Iss 1 (2021)
Genetics and Molecular Biology v.44 n.1 2021
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 44, Iss 1 (2021)
Investigating the etiological causes of acute myeloid leukemia (AML) at the molecular level should help in identifying targets and strategies that would increase the efficacy of the current management regimens. Some genes may act as molecular diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::512943c10b6f6d5b982363f37f03c817
https://doi.org/10.1590/1678-4685-gmb-2019-0268
https://doi.org/10.1590/1678-4685-gmb-2019-0268
Duchenne muscular dystrophy (DMD) is one of the fatal X-linked disorders that are characterized by progressive muscle weakness and occur due to mutation in the largest human gene known as the DMD gene which encodes dystrophin protein that is mandator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b8b7b4267add3637f6e2652d36187e2
https://doi.org/10.5772/intechopen.92765
https://doi.org/10.5772/intechopen.92765
Autor:
Ahmed A. H. Abdellatif, Nahla O. Mousa, Suher Zada, Ahmed M. Osman, Hassan A N El-Fawal, Nagia Fahmy
Publikováno v:
Clinical neurology and neurosurgery. 189
Objective The diagnosis of Duchenne Muscular Dystrophy (DMD) currently depends on non-specific measures such as Creatine kinase (CK) levels. MicroRNAs (miRNAs) are a class of small, endogenous RNAs of 21–25 nucleotides, that are important regulator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ba8d670d90456165155cd287e8229c
https://pubmed.ncbi.nlm.nih.gov/31838454
https://pubmed.ncbi.nlm.nih.gov/31838454