Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maria Saif"'
Autor:
Rubén Blay-Roger, Maria Saif, Luis F. Bobadilla, Tomas Ramirez-Reina, Muhammad Asif Nawaz, José Antonio Odriozola
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
The urgent need for mitigating climate change necessitates a transformative shift in energy production and consumption paradigms. Amidst this challenge, bioenergy emerges as a pivotal contributor to the global energy transition, offering a diverse ar
Externí odkaz:
https://doaj.org/article/10133a79b6114e9dbfb373dc912bea92
Autor:
Maria Saif, Muhammad Asif Nawaz, Minzhe Li, Guiyao Song, Zihao Wang, Chonghao Chen, Dianhua Liu
Publikováno v:
Energy & Fuels. 36:4510-4523
Publikováno v:
ChemCatChem. 13:1966-1980
Publikováno v:
Catalysis Science & Technology. 11:7992-8006
A one-step process for the conversion of syngas to aromatics (STA) has become an alternative key technology for non-petroleum carbon resources in the growing demand of the modern petrochemical sector. In the current study, the influence of various co
Autor:
Muhammad Asif Nawaz, Maria Saif, Minzhe Li, Guiyao Song, Wang Zihao, Chonghao Chen, Dianhua Liu
Publikováno v:
Fuel. 324:124390
Autor:
Maria Saif, Muhammad Latif, Musharraf Jelani, Hafiz Muhammad Jafar Hussain, Atta Ullah Khan, Hilal Ahmad, Muhammad Ismail Khan, Muhammad Imran Naseer
Publikováno v:
The journal of gene medicineREFERENCES. 23(1)
Background Joubert syndrome (JBTS) is a heterogenous disorder characterized by intellectual disability, developmental delays, molar tooth sign in brain imaging, hypotonia, ocular motor apraxia and overlapping features of ciliopathies. There are 36 cl
Autor:
Koutsokera, Alexandra Kiagia, Maria Saif, Muhammad W. and Souliotis, Kyriakos Syrigos, Kostas N.
Lung cancer is the leading cause of cancer death worldwide. Because of high incidence rates and low survival rates, it is important to study the risk factors that may help prevent the disease from developing. It has been well established that cigaret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::1ed28ac6d4649974d8a3436157daec07
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3157995
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3157995
Wiskott-Aldrich syndrome is a rare X-linked immunodeficiency disorder that is characterized by a variable clinical phenotype. Matched donor bone marrow transplantation is currently the only curative therapeutic option. We present the case of a 24-yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::235c83063db17bf353a0b5998fab65ce
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3150747
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3150747