Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kriaa A"'
Autor:
Aicha Kriaa, Vincent Mariaule, Amin Jablaoui, Soufien Rhimi, Hela Mkaouar, Juan Hernandez, Brice Korkmaz, Adam Lesner, Emmanuelle Maguin, Ali Aghdassi, Moez Rhimi
Publikováno v:
cells
Cells
Cells, 2022, 11 (5), pp.1-10. ⟨10.3390/cells11050901⟩
Cells
Cells, 2022, 11 (5), pp.1-10. ⟨10.3390/cells11050901⟩
International audience; Inflammatory bowel diseases (IBDs) have emerged as a public health problem worldwide with a limited number of efficient therapeutic options despite advances in medical therapy. Although changes in the gut microbiota compositio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33168d3296d9372367679a49e9912f95
https://zenodo.org/record/6998099
https://zenodo.org/record/6998099
Autor:
Soufien Rhimi, Houda Boudaya, Vincent Mariaule, Souha Soussou, Juan Hernandez, Moez Rhimi, Emmanuelle Maguin, Aicha Kriaa, Adam Lesner
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, MDPI, 2021, 22 (6), pp.2817. ⟨10.3390/ijms22062817⟩
International Journal of Molecular Sciences, 2021, 22 (6), pp.2817. ⟨10.3390/ijms22062817⟩
International Journal of Molecular Sciences, Vol 22, Iss 2817, p 2817 (2021)
International Journal of Molecular Sciences, MDPI, 2021, 22 (6), pp.2817. ⟨10.3390/ijms22062817⟩
International Journal of Molecular Sciences, 2021, 22 (6), pp.2817. ⟨10.3390/ijms22062817⟩
International Journal of Molecular Sciences, Vol 22, Iss 2817, p 2817 (2021)
International audience; Dysregulation of the proteolytic balance is often associated with diseases. Serine proteases and matrix metalloproteases are involved in a multitude of biological processes and notably in the inflammatory response. Within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc274ddd184282586435df428c880c0
https://hal.inrae.fr/hal-03371106
https://hal.inrae.fr/hal-03371106
Autor:
Rania Ghorbel, Neila Belguith, Aida Rouissi, Faiza Fakhfakh, Emna Mkaouar-Rebai, Nourhene Fendri-Kriaa, Naziha Gouider-Khouja
Publikováno v:
Gene. 502:163-167
Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively girls. Rett patients present an apparently normal psychomotor development during the first 6–18 months of life. Thereafter, they show a short period of develop
Autor:
Fakhri Kallabi, Hammadi Ayadi, Ghada Ben Salah, Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Hassen Kamoun, Amine Fourati, Faiza Fakhfakh
Publikováno v:
Molecular Biology Reports. 39:9639-9647
Genetic polymorphisms in DNA repair genes might influence the repair activities of the enzymes predisposing individuals to cancer risk. Owing to the presence of these genetic variants, interethnic differences in DNA repair capacity have been observed
Autor:
Nourhene Fendri-Kriaa, Fatma Kamoun, Zaineb Abdelkafi, Imen Ben Rebeh, Faiza Fakhfakh, Chahnez Triki
Publikováno v:
Genetic Testing and Molecular Biomarkers. 13:109-113
Patients with classical Rett show an apparently normal psychomotor development during the first 6-18 months of life. Thereafter, they enter a short period of developmental stagnation followed by a rapid regression in language and motor development. P
Autor:
Faiza Fakhfakh, Amine Fourati, Hassen Kamoun, Hammadi Ayadi, Emna Mkaouar-Rebai, Ghada Ben Salah, Nourhene Fendri-Kriaa, Imen Ayadi, Fakhri Kallabi
Publikováno v:
Genetic testing and molecular biomarkers. 16(10)
The genetic polymorphisms in DNA repair genes might affect the repair activities of the enzymes, predisposing individuals to cancer risk. Due to these genetic variants, interethnic differences in DNA repair capacity were observed in various populatio
Autor:
Bruno Hurault de Ligny, Willy M. J. M. Bogers, Jacques Dantal, Angelo Testa, Patrick Niaudet, Edith Bigot, Bernard Charpentier, Jean P. Soulillou, Faical Kriaa, Yannick Jacques
Publikováno v:
New England Journal of Medicine. 330:7-14
Among patients with the idiopathic nephrotic syndrome who have focal and segmental glomerulosclerosis and undergo renal transplantation, 15 to 55 percent have recurrent nephrotic syndrome. The recurrence may be caused by a plasma factor or factors th
Autor:
Lilia Kriaa, Olfa El Amine El Hadj, Taher Khalfallah, Arfaoui A, Sadaa Bouraoui, Myriam Khiari, Lasaad Gharbi, Sabeh Mzabi, Majid A. Ben Hmida
Publikováno v:
Virchows Archiv : an international journal of pathology. 457(3)
We examined the association of one linked GC/AT polymorphism at p73 with the risk of colorectal cancer. In the present study, we investigated whether this polymorphism was related to the risk of colorectal cancer, and whether there were relationships
Autor:
Firas Yaïch, Moez Medhaffar, Nourhene Fendri-Kriaa, Ikhlass Hadjsalem, Tawfik Souissi, Faiza Fakhfakh, Emna Mkaouar-Rebai, Moez Elloumi, Houda Kanoun, Nacim Louhichi
Publikováno v:
Annals of hematology. 89(5)
Inherited factor XIII (FXIII) deficiency is a rare bleeding disorder characterized by an umbilical bleeding during the neonatal period, delayed soft tissue bruising, mucosal bleeding spontaneous intracranial hemorrhage, and soft tissue hemorrhages. C
Autor:
Faiza Fakhfakh, Ines Hsairi, Leila Ammar-Keskes, Marwa Kharrat, Nourhene Fendri-Kriaa, Chahnez Triki, H. Kammoun, Hajer Doukali
Publikováno v:
Acta Neurologica Belgica
Rett syndrome (RTT) whose major cause is the mutations in the X-linked MECP2 gene is a genetic disease that affects females. We screened two RTT patients using cytogenetic studies and in silico analysis as well as molecular analysis by the direct seq