Zobrazeno 1 - 10 of 188 pro vyhledávání: '"MESH: Tunisia"'
1
Whole genome sequencing and phylogenetic analysis of six SARS-CoV-2 strains isolated during COVID-19 pandemic in Tunisia, North Africa
Autor: Aurélia Kwasiborski, Dorra Rezig, Zina Meddeb, Nissaf Ben Alaya, Wasfi Fares, Henda Touzi, Meriam Gdoura, Véronique Hourdel, Anissa Chouikha, Amel Sadraoui, Walid Hammami, S. Boubaker, Nahed Hogga, Guillain Mikaty, Imen Ben Dhifallah, Jean Claude Manuguerra, Kais Ghedira, Imen Abouda, Henda Triki, Valérie Caro
Publikováno v: BMC Genomics, Vol 22, Iss 1, Pp 1-6 (2021)
BMC Genomics
BMC Genomics, 2021, 22 (1), pp.540. ⟨10.1186/s12864-021-07870-1⟩
Background In Tunisia a first SARS-CoV-2 confirmed case was reported in March 03, 2020. Since then, an increase of cases number was observed from either imported or local cases. The aim of this preliminary study was to better understand the molecular
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::283352e568b9ed424378c3b9bed12b76
https://doaj.org/article/10b69379018d4c99943122d59f3d5118
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2
Comparison of conventional molecular and whole-genome sequencing methods for subtyping Salmonella enterica serovar Enteritidis strains from Tunisia
Autor: Mohamed Salah Abbassi, Boutheina Ksibi, Faouzia Rhimi, Kais Ghedira, Simon Le Hello, Adnene Hammami, Houcemeddine Othman, Basma Mnif, Sonia Ktari, Laetitia Fabre, Sonda Maalej
Publikováno v: European Journal of Clinical Microbiology and Infectious Diseases
European Journal of Clinical Microbiology and Infectious Diseases, 2020, 40 (3), pp.597-606. ⟨10.1007/s10096-020-04055-8⟩
International audience; We sought to determine the relative value of conventional molecular methods and whole-genome sequencing (WGS) for subtyping Salmonella enterica serovar Enteritidis recovered from 2000 to 2015 in Tunisia and to investigate the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb1dc12cfdc86871948f8334795bf39a
https://doi.org/10.1007/s10096-020-04055-8
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3
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Autor: Soumeya Bekri, Olfa Messaoud, Cherine Charfeddine, Hela Boudabbous, Amel Tounsi, Meriem Hechmi, Lotfi Zekri, Rahma Mkaouar, Ghazi Besbes, Ahlem Ben Hmid, Christine Petit, R. M’rad, Neji Tebib, Sami Bouchoucha, Fabrice Giraudet, Rym Kefi, J. Marrakchi, Crystel Bonnet, Imen Chelly, Ichraf Kraoua, Hamza Dallali, Ilhem Turki Ben Youssef, Sonia Abdelhak, Nadia Zitouna, Zied Riahi, Sonia Maalej, Mediha Trabelsi
Publikováno v: PLoS ONE
PLoS ONE, 2021, 16 (10), pp.e0258202. ⟨10.1371/journal.pone.0258202⟩
PLoS ONE, Vol 16, Iss 10, p e0258202 (2021)
Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical presentation of AM includes mental retardation, recurrent infections, hearing loss, dysmorphic featur
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10eed9fa8dee83d1c67ef18ba710098
https://hal-pasteur.archives-ouvertes.fr/pasteur-04072687
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4
Pertussis epidemiology in Tunisian infants and children and characterization of Bordetella pertussis isolates: results of a 9-year surveillance study, 2007 to 2016
Autor: Sylvain Brisse, Ikram Ben Fraj, Amel Kechrid, Nicole Guiso, Hanen Smaoui, Sophie Guillot, Valérie Bouchez
Publikováno v: Journal of Medical Microbiology
Journal of Medical Microbiology, Society for General Microbiology, 2018, 68 (2), pp.241-247. ⟨10.1099/jmm.0.000892⟩
Journal of Medical Microbiology, 2018, 68 (2), pp.241-247. ⟨10.1099/jmm.0.000892⟩
International audience; Purpose. Pertussis remains a public health concern in most countries. Our study aimed to prospectively explore the epidemiology of pertussis in the Tunis area of Tunisia between 2007 and 2016, and to characterize the virulence
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e483eb4fad83f404c85ff6c3a89c3922
https://doi.org/10.1099/jmm.0.000892
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5
Tunisian population of Mycosphaerella graminicola is still sensitive to strobilurin fungicides
Autor: M, Naouari, A, Siah, M, Elgazzah, Ph, Reignault, P, Halama
Publikováno v: Communications in Agricultural and Applied Biological Sciences
Communications in Agricultural and Applied Biological Sciences, University Gent, 2020, 78 (3), pp.559-61
International audience; Septoria tritici blotch caused by the fungal pathogen Mycosphaerella graminicola (anamorph: Zymoseptoria tritici) is one of the most frequently occurring diseases on both bread and durum wheat crops worldwide. One hundred and
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https://hal.archives-ouvertes.fr/hal-02945822
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6
A four-year survey (2011–2014) of West Nile virus infection in humans, mosquitoes and birds, including the 2012 meningoencephalitis outbreak in Tunisia
Autor: Meriadeg Ar Gouilh, Chawki Loussaief, Najet Dimassi, Jordi Serra-Cobo, Lamjed Boughzala, Maha Mastouri, Badereddine Mechri, Mohamed Chakroun, Abir Monastiri, Ana Vázquez-González, Mahjoub Aouni
Publikováno v: Emerging microbes & infections
Emerging microbes & infections, Earliest : Springer-Nature ; Latest : Taylor & Francis, 2019, 7, pp.28. ⟨10.1038/s41426-018-0028-y⟩
Emerging Microbes & Infections
Repisalud
Instituto de Salud Carlos III (ISCIII)
Dipòsit Digital de la UB
Universidad de Barcelona
Emerging microbes & infections, 2019, 7, pp.28. ⟨10.1038/s41426-018-0028-y⟩
A West Nile virus (WNV) outbreak occurred in Tunisia between mid-July and December 2012. To assess the epidemiological features of the WNV transmission cycle, human cerebrospinal fluid samples from patients with suspected cases (n = 79), Culex pipien
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dfb5598d9f28035dc7dd67d59489b9a
https://doi.org/10.1038/s41426-018-0028-y
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7
Polymorphism study of Cryptosporidium hominis gp60 subtypes circulating in Tunisia
Autor: Jean Menotti, Hanen Chelbi, Ines Bensghair, Rym Essid, Aïda Bouratbine, E. Siala
Publikováno v: Microbial Pathogenesis
Microbial Pathogenesis, Elsevier, 2017, 110, pp.298--303. ⟨10.1016/j.micpath.2017.06.011⟩
International audience; Cryptosporidium spp. are a major cause of gastrointestinal diseases in humans worldwide. While a single subtype of Cryptosporidium hominis has been shown to be responsible for several large outbreaks related to water contamina
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https://doi.org/10.1016/j.micpath.2017.06.011
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8
Phytochemical composition and antioxidant activity of medicinal plants collected from the Tunisian flora
Autor: Ikram Guizani, Z Aloui, N Neffati, M Boussaid, Y Zaouali, H. Karoui
Publikováno v: Natural Product Research
Natural Product Research, Taylor & Francis, 2017, 31 (13), pp.1583-1588. ⟨10.1080/14786419.2017.1280490⟩
International audience; Polyphenols, flavonoids and condensed tannins contents, as well as the antioxidant activity of the ethanolic and aqueous extracts obtained from aerial parts of 10 wild Tunisian plants, have been determined. Extracts showed app
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291b4f6644911ba18507d8aca796c366
https://doi.org/10.1080/14786419.2017.1280490
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9
Genome characteristics of Bordetella pertussis isolates from Tunisia
Autor: Sylvain Brisse, Ikram Ben Fraj, Hanen Smaoui, Valérie Bouchez, Amel Kechrid
Publikováno v: Journal of Medical Microbiology
Journal of Medical Microbiology, Society for General Microbiology, 2019, 68 (9), pp.1320-1323. ⟨10.1099/jmm.0.001042⟩
Journal of Medical Microbiology, 2019, 68 (9), pp.1320-1323. ⟨10.1099/jmm.0.001042⟩
The genomic sequence data generated in this work were submitted to the European Nucleotide Archive and are available from the International Nucleotide Sequence Database Collaboration (NCBI/ENA/DDBJ) databases under project accession number PRJEB27412
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb32749026ad16339692a16ed3c3621
http://hdl.handle.net/20.500.12278/28986
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10
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
Autor: M Mahmoudi, Samir Boubaker, Amira Jaballah-Gabteni, Haifa Tounsi, Mousaddak Azzouz, Hamza Dallali, Hamza Yaiche, Sahar Elouej, Maria Kabbage, Ines Ben Ayed, Lamine Hamzaoui, Mouna Medhioub, Sonia Abdelhak, Afifa Maaloul, Yosr Hamdi, Nadia Ben Jemii, Najla Mezghani
Publikováno v: Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩
Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have been iden
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3714aec0aaa66ec377220ed5bbeb7de9
https://doi.org/10.1186/s12967-019-1961-9
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