Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Olfa, Messaoud"'
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, CRYSTEL Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/d1f20ca9f1e041b5805610de30e16616
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to com
Externí odkaz:
https://doaj.org/article/d53f3da42b5b4e8f9503ec02796dd375
Autor:
Asma Hammami, Afrah Bardaoui, Shimaa Eissa, Walid A. M. Elgaher, Radhouane Chtourou, Olfa Messaoud
Publikováno v:
Molecules, Vol 29, Iss 12, p 2837 (2024)
The current study focused on the design of an extremely sensitive electrochemical sensor of ascorbic acid based on a mixture of NiAl2O4-NiO nanoparticles that, produced in a single step using the sol–gel method, on an ITO electrode. This new sensin
Externí odkaz:
https://doaj.org/article/a45163581b6e40a382a2a6a634c521f9
Autor:
Hamza Dallali, Wided Boukhalfa, Nadia Kheriji, Meriem Fassatoui, Haifa Jmel, Meriem Hechmi, Ismail Gouiza, Mariem Gharbi, Wafa Kammoun, Mehdi Mrad, Marouen Taoueb, Asma Krir, Hajer Trabelsi, Afef Bahlous, Henda Jamoussi, Olfa Messaoud, Abdelmajid Abid, Rym Kefi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionType 2 diabetes (T2D) is a multifactorial disease involving genetic and environmental components. Several genome-wide association studies (GWAS) have been conducted to decipher potential genetic aberrations promoting the onset of this met
Externí odkaz:
https://doaj.org/article/ec2f2977e6d94ae5b458346728bffc4e
Autor:
Najlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, Mariem Chargui, Mohamed Zghal, Bashir Zendah, Najat Saqer, Mourad Mokni, Sonia Abdelhak, Othman A. Mohamed
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background Xeroderma pigmentosum is an autosomal recessive disease characterized by a high sensitivity to UV radiations. The disease is clinically and genetically heterogeneous, thus making accurate early clinical diagnosis difficult. Althou
Externí odkaz:
https://doaj.org/article/38ec3159672749948c32a81fc0e52b3f
Autor:
Afrah Bardaoui, Asma Hammami, Rabiaa Elkarous, Mohamed Ali Aloui, Rania Oueslati, Olfa Messaoud, Diogo M. F. Santos, Radhouane Chtourou
Publikováno v:
Inorganics, Vol 11, Iss 4, p 173 (2023)
Understanding and regulating DNA interactions with solvents and redox-active centers opens up new possibilities for improving electrochemical signals and developing adequate biosensors. This work reports the development of a modified indium tin oxide
Externí odkaz:
https://doaj.org/article/16727b3ba96f4dc7993a9a84ffbb4147
Autor:
Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud, Jingxuan Shan, Khalid A. Fakhro, Rym Kefi, Lotfi Chouchane, Sonia Abdelhak
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-18 (2021)
Abstract Copy number variation (CNV) is considered as the most frequent type of structural variation in the human genome. Some CNVs can act on human phenotype diversity, encompassing rare Mendelian diseases and genomic disorders. The North African po
Externí odkaz:
https://doaj.org/article/399d7564503448b8a9d14b264646b319
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/baa98890da3341e5a04116fdfed8e2c3
Autor:
Rahma Mkaouar, Lamia Cherif Ben Abdallah, Chokri Naouali, Saida Lahbib, Zinet Turki, Sahar Elouej, Yosra Bouyacoub, Maali Somai, Kenneth Mcelreavey, Anu Bashamboo, Sonia Abdelhak, Olfa Messaoud
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
The role of the prokineticin 2 pathway in human reproduction, olfactory bulb morphogenesis, and gonadotropin-releasing hormone secretion is well established. Recent studies have highlighted the implication of di/oligogenic inheritance in this disorde
Externí odkaz:
https://doaj.org/article/6da776bdce8e458aa2276521a5264d82
Autor:
Yosr Hamdi, Najah Mighri, Maroua Boujemaa, Nesrine Mejri, Sonia Ben Nasr, Mariem Ben Rekaya, Olfa Messaoud, Hanen Bouaziz, Yosra Berrazega, Haifa Rachdi, Olfa Jaidane, Nouha Daoud, Aref Zribi, Jihene Ayari, Houda El Benna, Soumaya Labidi, Jamel Ben Hassouna, Abderazzek Haddaoui, Khaled Rahal, Farouk Benna, Ridha Mrad, Slim Ben Ahmed, Hamouda Boussen, Samir Boubaker, Sonia Abdelhak
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundBreast cancer is the world’s most common cancer among women. It is becoming an increasingly urgent problem in low- and middle-income countries (LMICs) where a large fraction of women is diagnosed with advanced-stage disease and have no ac
Externí odkaz:
https://doaj.org/article/225f32cd0a4b4ec88e0e601d86e0c31b