Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Mohcine Bennani Mechita"'
Autor:
Fatima Zahra El Ansari, Farah Jouali, Rim Fekkak, Joaira Bakkach, Naima Ghailani Nourouti, Amina Barakat, Mohcine Bennani Mechita, Jamal Fekkak
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-7 (2022)
Abstract Background While the role of BRCA1/2 genes in familial breast and ovarian cancer is well established, their implication in the sporadic form of both cancers is still controversial. With the development of poly (ADP-ribose) polymerase (PARP)
Externí odkaz:
https://doaj.org/article/e62b1e503988426c9584f9dd749f92ca
Autor:
Yousra Benmakhlouf, Renaud Touraine, Ines Harzallah, Zeineb Zian, Kaoutar Ben Makhlouf, Amina Barakat, Naima Ghailani Nourouti, Mohcine Bennani Mechita
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and
Externí odkaz:
https://doaj.org/article/0ca085e180954c6082b8abcd2187fb98
Autor:
Joaira Bakkach, Mohamed Mansouri, Touria Derkaoui, Ali Loudiyi, ElMostafa El Fahime, Amina Barakat, Naima Ghailani Nourouti, Jaime Martinez De Villarreal, Carlos Cortijo Bringas, Mohcine Bennani Mechita
Publikováno v:
BMC Cancer, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background To date, the contribution of BRCA1/2 mutations in Moroccan early onset breast cancer patients remains unknown. Here we assess these genetic alterations for the first time in a cohort from North of Morocco. Methods Thirty-three pat
Externí odkaz:
https://doaj.org/article/c3e2d4ee43df43cc95458127424e8b7e
Autor:
Ayman Reffai PhD, Mohamed Mesmoudi MD, Touria Derkaoui PhD, Naima Ghailani Nourouti PhD, Amina Barakat PhD, Nabila Sellal MD, Parag Mallick PhD, Mohcine Bennani Mechita PhD
Publikováno v:
Cancer Control, Vol 28 (2021)
Background Nasopharyngeal carcinoma is a multifactorial disease mainly affecting the Asian and North African populations including Morocco. This study aimed to determine the epidemiological profile of nasopharyngeal carcinoma in Northern Morocco as w
Externí odkaz:
https://doaj.org/article/0daf63ff4ded4c089aab2866ab543adf
Publikováno v:
Mediators of Inflammation, Vol 2021 (2021)
Systemic lupus erythematosus (SLE) is a complex autoimmune inflammatory disease characterized by an unknown etiology and a highly variable clinical presentation. This clinical heterogeneity might be explained by dysregulation of tolerance to self and
Externí odkaz:
https://doaj.org/article/cacbb2914dd04f2584562b068acf2891
Autor:
Joaira Bakkach, Mohamed Mansouri, Touria Derkaoui, Ali Loudiyi, Mohamed Fihri, Samia Hassani, Amina Barakat, Naima Ghailani Nourouti, Mohcine Bennani Mechita
Publikováno v:
BMC Women's Health, Vol 17, Iss 1, Pp 1-9 (2017)
Abstract Background Literature data reported a higher frequency of breast cancer in young women (BCYW) in developing countries. BCYW is associated with delayed diagnosis, aggressive biology and poor prognosis. However, our knowledge of biological pro
Externí odkaz:
https://doaj.org/article/ef94d6fcb5bb4dd88bc274238823fb12
Autor:
El Houcine Haijoubi, Fatiha Benyahya, Abdrezzak Bendahou, Faima Zahra Essadqui, Mohammed El Behhari, Ahmed Fouad El Mamoune, Naima Nourouti Ghailani, Mohcine Bennani Mechita, Amina Barakat
Publikováno v:
The Pan African Medical Journal, Vol 26, Iss 13 (2017)
INTRODUCTION: l'eau est utilisée d'une façon primordiale dans tout le processus de la fabrication des produits alimentaires. Les industries agroalimentaires du Nord du Maroc utilisent différentes sources d'eaux mais l'eau de réseau public et l'ea
Externí odkaz:
https://doaj.org/article/995c93fe00a14c20a0fb41c9d45fcf19
Autor:
Naima Ghailani Nourouti, Zeineb Zian, Mohcine Bennani Mechita, Amina Barakat, Yousra Benmakhlouf
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 21:569-576
Intellectual disability (ID), previously called mental retardation, is the most common neurodevelopmental disorder characterized by life-long intellectual and adaptive functioning impairments that have an impact on individuals, families, and society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d166a177846dc1f9d10d7f31d2e08a6
https://doi.org/10.2174/1871530320666200628024944
https://doi.org/10.2174/1871530320666200628024944
Autor:
Mohcine Bennani-Mechita, Achraf Laghmich, Naima Ghailani-Nourouti, Amina Barakat, Fatima-Zahra Alaoui-Ismaili
Publikováno v:
Hemoglobin. 44:190-194
Sickle cell disease is one of the most common severe monogenic disorders in the world. The -158 XmnI polymorphism (C>T) of the Gγ-globin gene promoter is known to be associated with increased expression of the Gγ-globin gene, thus, higher productio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79897edc0cd044d7c981c50d01c803ec
https://doi.org/10.1080/03630269.2020.1772284
https://doi.org/10.1080/03630269.2020.1772284
Autor:
Jaime Martinez De Villarreal, Joaira Bakkach, Carlos Cortijo Bringas, Amina Barakat, Naima Ghailani Nourouti, Touria Derkaoui, Mohammed Mansouri, Ali Loudiyi, Mohcine Bennani Mechita
Publikováno v:
Precision Medical Sciences. 9:43-48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36bc8bfb758dbbad79cf3253279ecfec
https://doi.org/10.1002/prm2.12009
https://doi.org/10.1002/prm2.12009