Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Marwa Ammar"'
Publikováno v:
Energy Reports, Vol 10, Iss , Pp 4064-4077 (2023)
The purpose of this research is the evaluation of heat transfer by natural convection in an innovative flat plate solar collector operating in natural convection mode. The design consists of inclined, perforated slats of transparent insulation materi
Externí odkaz:
https://doaj.org/article/52428ece4619402c92bc30537e502bb0
Publikováno v:
Energy Reports, Vol 10, Iss , Pp 2448-2466 (2023)
This paper aims to investigate the energy performance of several techniques integrated into the fenestration system of an office building. The first step was to compare the simulated and real energy consumption of a case study of an office building l
Externí odkaz:
https://doaj.org/article/469f848bf2654eb5809866a88b7f66f0
Publikováno v:
Energy Reports, Vol 6, Iss , Pp 3412-3424 (2020)
The most promising collector must achieve the best thermal efficiency and fill out high requirements of low weight, low power consumption, ease of manufacturing, and low cost. In this study; a novel efficiently optimized flat plate solar air collecto
Externí odkaz:
https://doaj.org/article/a9817c913805433cb28beb3958898e97
Autor:
Amin Mahmood Thawabteh, Zain Swaileh, Marwa Ammar, Weam Jaghama, Mai Yousef, Rafik Karaman, Sabino A. Bufo, Laura Scrano
Publikováno v:
Toxins, Vol 15, Iss 2, p 93 (2023)
To combat the ineffectiveness of currently available pharmaceutical medications, caused by the emergence of increasingly resistant bacterial and fungal strains, novel antibacterial and antifungal medications are urgently needed. Novel natural compoun
Externí odkaz:
https://doaj.org/article/3c4d821943494aa7b88474ed3494163f
Autor:
Marwa Ammar, Walid Oueslati
Publikováno v:
Advances in Civil Engineering, Vol 2018 (2018)
This work reports characterization of the possible effects that might distress the hydration properties of Mg-exchanged low-charge montmorillonite (SWy-2) when it undergoes external environmental solicitation. This perturbation was created by an alte
Externí odkaz:
https://doaj.org/article/86787ff5378246e484627bec59034667
Publikováno v:
Minerals, Vol 5, Iss 3, Pp 507-526 (2015)
The structural changes along the c axis, of the Ba-exchanged montmorillonite (Swy-2-Ba), under variable relative humidity (% RH), is investigated. In this regard, the arrangement, amount and position of both exchangeable cation and the water molecule
Externí odkaz:
https://doaj.org/article/d162753ade88413fa499d68602c51146
Autor:
Marwa Ammar, Wajdi Safi, Abdelaziz Tlili, Olfa Alila‐Fersi, Fakher Frikha, Jihen Chouchen, Fatma Mnif, Marwa Kharrat, Marwa Maalej, Rahma Felhi, Mohamed Abid, Mouna Mnif‐Feki, Faten Hadj Kacem, Faiza Fakhfakh, Emna Mkaouar‐Rebai
Publikováno v:
International Journal of Developmental Neuroscience. 82:626-638
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE; OMIM 603041) is a rare inherited metabolic disorder mostly caused by mutations in TYMP gene encoding thymidine phosphorylase (TP) protein that affects the mitochondrial nucleotide metaboli
Autor:
Marwa Maalej, Lamia Sfaihi, Marwa Ammar, Fakher Frikha, Marwa Kharrat, Olfa Alila-Fersi, Emna Mkaouar-Rebai, Abdelaziz Tlili, Thouraya Kammoun, Faiza Fakhfakh
Publikováno v:
neurogenetics. 23:257-270
Progressive encephalopathy with brain edema and/or leukoencephalopathy, PEBEL1, is a severe neurometabolic disorder characterized by rapidly progressive neurologic deterioration associated with a febrile illness. PEBEL1 is a lethal encephalopathy cau
Autor:
Rahma Felhi, Kamel Monastiri, Hayet Ben Hamida, Marwa Ammar, Fatma Zohra Chioukh, Brahim Tabarki, Jihene Chouchen, Faiza Fakhfakh, Abdelaziz Tlili, Emna Mkaouar‐Rebai
Publikováno v:
International journal of developmental neuroscience : the official journal of the International Society for Developmental NeuroscienceREFERENCES. 82(8)
MEGDEL syndrome is a rare recessive disorder, with about 100 cases reported worldwide, which is defined by 3-methylglutaconic aciduria (MEG), deafness (D), encephalopathy (E) and Leigh-like syndrome (L). When these manifestations were added to hepato
Autor:
Marwa Kharrat, Chahnez Charfi Triki, Olfa Alila-Fersi, Olfa Jallouli, Bassem khemakham, Salma Mallouli, Marwa Maalej, Marwa Ammar, Fakher frikha, Fatma Kamoun, Faiza Fakhfakh
Publikováno v:
Journal of molecular neuroscience : MN. 72(8)
FoxG1 encoded by FOXG1 gene is a transcriptional factor interacting with the DNA of targeted genes as well as with several proteins to regulate the forebrain development. Mutations in the FOXG1 gene have been shown to cause a wide spectrum of brain d