Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Salem Bashanfer"'
Publikováno v:
Anemia, Vol 2018 (2018)
Background. Iron deficiency anemia (IDA) is one of the most common types of nutritional anemia in the worldwide and considered a major public health problem in developing countries especially in Yemen. Therefore, this cross-sectional study was conduc
Externí odkaz:
https://doaj.org/article/68f277a39a294bdea36d8bd4ea32d01e
Autor:
Ahmed M. E. Elkhalifa, Abozer Y. Elderdery, Ibrahim Ali Al Bataj, Abdelhakam G. Tamomh, Masaud M. Alyami, Hussein A. Almakrami, Mubarak A. Alofair, Mohammed A. Almorish, Salem Bashanfer, Mohammed I. Tabash, Hadeil M. E. Idris, Dania Z. Ahmed, Abdulaziz H. Alhamidi, Pooi Ling Mok
Publikováno v:
BioMed Research International.
COVID-19 is a global pandemic viral infection that has affected millions worldwide. Limited data is available on the effect of COVID-19 on hematological parameters in Saudi Arabia. This study is aimed at examining the role of hematological parameters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f345d8f0d54304bb774c0de8b9ca5933
Autor:
Richard A. Anderson, Katrin Ottersbach, Hélène Jakobczyk, Foteini Fotopoulou, Rishi S. Kotecha, Camille Malouf, Andrew J. Finch, Vasiliki Symeonidou, Salem Bashanfer
Publikováno v:
Cell Reports
Symeonidou, V, Jakobczyk, H, Bashanfer, S, Malouf, C, Fotopoulou, F, Kotecha, R S, Anderson, R A, Finch, A J & Ottersbach, K 2021, ' Defining the fetal origin of MLL-AF4 infant leukemia highlights specific fatty acid requirements. ', Cell Reports, vol. 37, no. 4 . https://doi.org/10.1016/j.celrep.2021.109900
Symeonidou, V, Jakobczyk, H, Bashanfer, S, Malouf, C, Fotopoulou, F, Kotecha, R S, Anderson, R A, Finch, A J & Ottersbach, K 2021, ' Defining the fetal origin of MLL-AF4 infant leukemia highlights specific fatty acid requirements. ', Cell Reports, vol. 37, no. 4 . https://doi.org/10.1016/j.celrep.2021.109900
Summary Infant MLL-AF4-driven acute lymphoblastic leukemia (ALL) is a devastating disease with dismal prognosis. A lack of understanding of the unique biology of this disease, particularly its prenatal origin, has hindered improvement of survival. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::025f38cdcc64cc9ffaaa0290715a11e7
http://europepmc.org/articles/PMC8567312
http://europepmc.org/articles/PMC8567312
Publikováno v:
British Journal of Medicine and Medical Research. 19:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f460d3a7180d34b8ce964cb05e7a5c8
https://doi.org/10.9734/bjmmr/2017/27623
https://doi.org/10.9734/bjmmr/2017/27623
Publikováno v:
British Microbiology Research Journal. 13:1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::153c0cc5788c16f956d37418f92895b6
https://doi.org/10.9734/bmrj/2016/23629
https://doi.org/10.9734/bmrj/2016/23629
Autor:
Salem Ali Al‑Salem Bashanfer, Narazah Mohd Yusoff, Olaf Heidenreich, Mohamed Saleem, Emmanuel Jairaj Moses
Publikováno v:
Oncology Reports.
The t(8;21) translocation is one of the most frequent chromosome abnormalities associated with acute myeloid leukaemia (AML). This abberation deregulates numerous molecular pathways including the ERK signalling pathway among others. Therefore, the ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a14ab6bc28213c30d8cccb4ea6d0a1
https://doi.org/10.3892/or.2018.6926
https://doi.org/10.3892/or.2018.6926
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mohamed Saifulaman Mohamed Said, Faisal Mutee Al-Hassan, Rosline Hassan, Olaf Heidenreich, Narazah Mohd Yusoff, Salem Ali Al‑Salem Bashanfer
Publikováno v:
BMC Proceedings
BMC Proceedings, Vol 6, Iss Suppl 6, p P29 (2012)
BMC Proceedings, Vol 6, Iss Suppl 6, p P29 (2012)
Background The t(8;21) translocation is one of the most frequent chromosome abnormalities associated with acute myeloid leukemia (AML). This translocation generates the (AML1/ MTG8) fusion protein causing blockage of the differentiation process. More
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83e0fab1a13e59b74fcc27af40bce1a4