Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Leila Ammar Keskes"'
Autor:
Nour El Houda Mathlouthi, Hamadou Oumarou Hama, Imen Belguith, Slim Charfi, Tahya Boudawara, Jean-Christophe Lagier, Leila Ammar Keskes, Ghiles Grine, Radhouane Gdoura
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 9, Pp 7572-7581 (2023)
Colorectal cancer (CRC) is a serious public health problem known to have a multifactorial etiology. The association between gut microbiota and CRC has been widely studied; however, the link between archaea and CRC has not been sufficiently studied. T
Externí odkaz:
https://doaj.org/article/f7dfab1af8044cb8a95f4b5cd870343d
Autor:
Nour El Houda Mathlouthi, Imen Belguith, Mariem Yengui, Hamadou Oumarou Hama, Jean-Christophe Lagier, Leila Ammar Keskes, Ghiles Grine, Radhouane Gdoura
Publikováno v:
Microorganisms, Vol 11, Iss 11, p 2742 (2023)
Background and Aims: Gut microbial imbalances are linked to colorectal cancer (CRC), but archaea’s role remains underexplored. Here, using previously published metagenomic data from different populations including Austria, Germany, Italy, Japan, Ch
Externí odkaz:
https://doaj.org/article/162fd641e3b3479bb9f596057ce856ac
Publikováno v:
Microorganisms, Vol 10, Iss 12, p 2365 (2022)
Colorectal cancer (CRC) is a growing public health challenge, featuring a multifactorial etiology and complex host–environment interactions. Recently, increasing evidence has pointed to the role of the gut microbiota in CRC development and progress
Externí odkaz:
https://doaj.org/article/1bbdba714faf4d68b39dadb972723f07
Autor:
Mahdi Kamoun, Mouna Feki Mnif, Nadia Charfi, Basma Ben Naceur, Fatma Mnif, Nabila Rekik, Zainab Mnif, Mohamed Habib Sfar, Mohamed Tahar Sfar, Mongia Hachicha, Azza Ben Salem, Leila Ammar Keskes, Mohamed Abid
Publikováno v:
Middle East Fertility Society Journal, Vol 19, Iss 2, Pp 89-95 (2014)
Objective: To investigate fertility in a sample of Tunisian patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Design: Tunisian bicentric prospective study. Setting: Endocrinology department, Hedi Chaker Hospital, Sf
Externí odkaz:
https://doaj.org/article/7ede3c2240314239aea23584d9604d9a
Autor:
Dhoha Dhieb, Imen Belguith, Laura Capelli, Elisa Chiadini, Matteo Canale, Sara Bravaccini, Ilhem Yangui, Ons Boudawara, Rachid Jlidi, Tahya Boudawara, Daniele Calistri, Leila Ammar Keskes, Paola Ulivi
Publikováno v:
Cells, Vol 8, Iss 6, p 514 (2019)
The identification of the mutations that drive lung cancer have furnished new targets for the treatment of non-small cell lung cancer (NSCLC) and led to the development of targeted therapies such as tyrosine kinase inhibitors that are used to combat
Externí odkaz:
https://doaj.org/article/844979113ba4446aac0262e43efd1859
Autor:
Myriam Ghorbel, Siwar Baklouti-Gargouri, Rim Keskes, Afifa Sellami, Ken McElreavy, Leila Ammar-Keskes
Publikováno v:
Human fertility (Cambridge, England).
The aim of the present study was to clarify the implication of Y chromosome genetic variations and haplogroups in Tunisian infertile men. A total of 27 Y-chromosomal binary markers partial microdeletions (gr/gr, b1/b3 and b2/b3) and copy number varia
Publikováno v:
The Pan African Medical Journal, Vol 25, Iss 115 (2016)
INTRODUCTION: l'analyse du sperme est d'une importance majeure dans l'exploration de l'infertilité masculine. Afin de s'assurer de la fiabilité des résultats rendus, l'implantation du management de qualité en spermiologie est devenue une nécessi
Externí odkaz:
https://doaj.org/article/7e21f26f27f8456e9a2c344e9d3029b3
Autor:
Rim Sakka, Fatma Abdelhedi, Hanen Sellami, Bruno Pichon, Yosra Lajmi, Mouna Mnif, Sahbi Kebaili, Rihab Derbel, Hassen Kamoun, Radhouane Gdoura, Anne Delbaere, Julie Desir, Marc Abramowicz, François Vialard, Jean-Michel Dupont, Leila Ammar-Keskes
Publikováno v:
European Journal of Medical Genetics. 65:104613
We report on the results of array-CGH and Whole exome sequencing (WES) studies carried out in a Tunisian family with 46,XX premature ovarian insufficiency (POI). This study has led to the identification of a familial Xp22.12 tandem duplication with a
Autor:
David Goudenège, Pascal Reynier, Majida Charif, Rahma Felhi, Dominique Bonneau, Mongia Hachicha, Lamia Sfaihi, Céline Bris, Leila Ammar-Keskes, Guy Lenaers, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, Vincent Procaccio, Faiza Fakhfakh
Publikováno v:
Clinica Chimica Acta
Clinica Chimica Acta, Elsevier, 2019, 488, pp.104-110. ⟨10.1016/j.cca.2018.11.003⟩
Clinica Chimica Acta, Elsevier, 2019, 488, pp.104-110. ⟨10.1016/j.cca.2018.11.003⟩
Introduction Mitochondrial diseases are a group of disorders caused mainly by the impairment of the mitochondrial oxidative phosphorylation process, due to mutations either in the mitochondrial or nuclear genome. Among them, the mitochondrial neuro-g
Autor:
Radhouane Gdoura, Leila Ammar-Keskes, Rihab Derbel, Ahmed Rebai, Hanen Sellami, Elreavy Mcelreavey
Publikováno v:
AndrologiaREFERENCES. 53(8)
Leukocytospermia was previously reported to affect sperm quality by the production of reactive oxygen species (ROS) leading to oxidative stress (OS). In turn, OS decreases sperm functional integrity, increases sperm DNA damage and ultimately alters f