Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mohamed Ahmed Salih"'
Autor:
Izzat Sidahmed Ali Tahir, Elfadil Mohamed Elyayeb Elbashier, Mohamed Ahmed Salih Ibrahim, Abu Sefyan Ibrahim Saad, Osman Suliman Abdalla
Publikováno v:
International Journal of Agronomy, Vol 2020 (2020)
Improved nitrogen use-efficient cultivars could be the most economically beneficial and environmentally friendly approach to reduce pollution associated with excessive N fertilization. The performance and genetic gain in grain yield and nitrogen use
Externí odkaz:
https://doaj.org/article/4b464583431f422395aa59640786cd37
Autor:
Alsmawal A. Elimam, Mohamed Elmogtba Mouaweia Mohamed Aabdein, Mohamed El-Fatih Moly Eldeen, Hisham N. Altayb, Mohamed Adel Taha, Mohammed N. Nimir, Mohamed D. Dafaalla, Musaab M. Alfaki, Mohamed A. Abdelrahim, Abdelmohaymin A. Abdalla, Musab I. Mohammed, Mona Ellaithi, Muzamil Mahdi Abdel Hamid, Mohamed Ahmed Salih Hassan
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-11 (2017)
Abstract Background Breast cancer (BC) is the most common type of cancer in women. Among many risk factors of BC, mutations in BRCA2 gene were found to be the primary cause in 5–10% of cases. The majority of deleterious mutations are frameshift or
Externí odkaz:
https://doaj.org/article/5714daaab3514d7590daea61216261ab
Autor:
Solima M. A. Sabeel, Mohamed Ahmed Salih, Manasik Ali, Salah-Eldin EL-Zaki, Nadir Abuzeid, Zeinab Abubaker Mohammed Elgadi, Hisham N. Altayb, Asrar M. A. Elegail, Nuha Y. Ibrahim, Bahaeldin K. Elamin
Publikováno v:
Tuberculosis Research and Treatment, Vol 2017 (2017)
Background. Currently, mutations in rpoB, KatG, and rrs genes and inhA promoter were considered to be involved in conferring resistance to rifampicin, isoniazid, and streptomycin in Mycobacterium tuberculosis (MTB). Objective. The aims of this study
Externí odkaz:
https://doaj.org/article/240cebfbd0c24fe8885acbf6be8c0660
Autor:
Solima M. Sabeel, Asrar Elegail, Hisham N. Altayb, Bahaeldin K. Elamin, Zeinab Abubaker Mohammed Elgadi, Mohamed Ahmed Salih, Salah-Eldin El-Zaki, Nuha Yousif Ibrahim, Nadir Abuzeid, Manasik Ali
Publikováno v:
Tuberculosis Research and Treatment
Tuberculosis Research and Treatment, Vol 2017 (2017)
Tuberculosis Research and Treatment, Vol 2017 (2017)
Background.Currently, mutations inrpoB,KatG, andrrsgenes andinhApromoter were considered to be involved in conferring resistance to rifampicin, isoniazid, and streptomycin inMycobacterium tuberculosis(MTB).Objective.The aims of this study were to det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99a50521ba8725f34a8d76a2e0aefdb9
https://doi.org/10.1155/2017/8340746
https://doi.org/10.1155/2017/8340746
Autor:
Hassan, Mohamed Ahmed Salih
Publikováno v:
Универзитет Сингидунум
Veliki deo površine Zemlje čine pustinje koje se u poslednjih nekoliko desetina godina ubrzano šire. Za razliku od prirodnog procesa postupnog širenja ili promene areala pustinja, ubrzana dezertifikacija je rezultat ljudskog nepromišljenog i neo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=nardusnacion::e6b286ef1290079c2b19883753872553
https://nardus.mpn.gov.rs/bitstream/id/60356/bitstream_60356.pdf
https://nardus.mpn.gov.rs/bitstream/id/60356/bitstream_60356.pdf
Autor:
Abbas Mh, Mohamed Ahmed Salih, Mohamed Elamin S, Ali Lb, Ahmed Hamdi Abu-haraz, Khoubieb Ali Abd-elrahman, Mustafa Yy, Mahmoud Sm, Osman Aa, Idris Ab, Adam Me
Publikováno v:
Immunome Research. 13
Sin Nombre virus is a category A pathogen with a reported mortality rate ranging from 30% to 50%. It was responsible for the 2012 Yosemite National Park outbreak. Until now, Specific therapy is not available for the treatment of HCPS caused by SNV. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42067a95b423add6789a5b58d64dfb3
https://doi.org/10.4172/1745-7580.1000141
https://doi.org/10.4172/1745-7580.1000141
Autor:
Khoubieb Ali Abd-elrahman, Mojahid Salah Ibrahim, Mohammed Siddig Mohammed, Waleed Hassan Hussien, Marwan Mustafa Badawi, Ahmed Hamdi Abu-haraz, Mohamed Ahmed Salih
Publikováno v:
Advanced Techniques in Biology & Medicine.
Sudan Ebola virus is single stranded negative sense RNA genome belonging to Filovirus Filoviridae family that causes hemorrhagic fever. There is no treatment or vaccine for it, thus the aim of this study is to design a peptide vaccine using immuoinfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b91e82b7433218ee76546192b0fe6ba
https://doi.org/10.4172/2379-1764.1000203
https://doi.org/10.4172/2379-1764.1000203
Autor:
Mawadda Abd-Elraheem Awad-Elkareem, Soada Ahmed Osman, Khoubieb Ali Abd-elrahman, Hanaa Abdalla Mohamed, Mohamed Ahmed Salih, Ahmed Hamdi Abu-haraz, Hadeel Abd-Elrahman Hassan
Publikováno v:
Immunome Research. 13
Merkel cell Polyomavirus is non-enveloped, dsDNA virus belonging to Polyomaviridae family linked to an uncommon aggressive skin malignancy. The poor prognosis and limited understanding of disease pathogenesis warrants innovative treatment. In this cu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ac3abb690e39adf2ab01429237c2aa7
https://doi.org/10.4172/1745-7580.1000134
https://doi.org/10.4172/1745-7580.1000134
Publikováno v:
American Journal of Microbiological Research. 2:217-223
The presence of ESBLs in many E. coli strains are of serious concern, since these organisms are the most common cause of different human infections. In this study we isolate an E. coli bacterium with high hydrolytic activity against cefotaxime. The E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::196ae64b57d94e5698a96dfd711a02d1
https://doi.org/10.12691/ajmr-2-6-8
https://doi.org/10.12691/ajmr-2-6-8
Autor:
Mahmoud Eltayeb Koko Musa, Mohamed Ahmed Salih, Ashraf Ahmed Mohamed Ahmed Fadul, Asaad Tageldein Idris, Yousuf Bakhit, Ashraf Yahia Osman Mohamed
Publikováno v:
Nova Journal of Medical and Biological Sciences. :1-10
Hereditary deafness comprises a large percentage of all causes of hearing loss. Despite the large number of genetic polymorphisms recognized to cause hereditary deafness, a considerable number of patients do not show any of those. To address the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94872dc8ca6288eb1822ecedeef19262
https://doi.org/10.20286/nova-jmbs-030235
https://doi.org/10.20286/nova-jmbs-030235