Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Asma, Jlizi"'
Autor:
Mehdi Dridi, Asma Jlizi, Ning-Ning Wei, Amel Benammar Elgaaied, Nejla Stambouli, Abderahmen Bouraoui
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 32:866-875
The chemokine receptor 5 (CCR5) belongs to the superfamily of serpentine G protein-coupled receptors (GPCRs). The DRY motif (Asp, Arg, Tyr) of the intracellular loop 2 (ICL2), which is highly conserved in the GPCRs has been shown to be essential for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fd23eafbf5c5ea96166028f93171b6
https://doi.org/10.1080/07391102.2013.794373
https://doi.org/10.1080/07391102.2013.794373
Autor:
Asma Jlizi, Amel Benammar Elgaaied, Mohamed Ben Amor, Emna Gouider, H. E. Abdallah, Balkis Meddeb
Publikováno v:
Haemophilia. 16:801-804
Summary. Combined factor V (FV) and factor VIII (FVIII) deficiency (F5F8D) is a rare autosomal recessive disorder caused by mutations in LMAN1 or MCFD2 genes which encode proteins that form a complex involved in the transport of FV and FVIII from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa57bbf5e163ea18b2a9abb1981d9e5e
https://doi.org/10.1111/j.1365-2516.2010.02268.x
https://doi.org/10.1111/j.1365-2516.2010.02268.x
Autor:
Rim Sassi, Emna Gouider, Hejer Elmahmoudi Abdallah, Houssein Khodjet-El-Khil, Balkis Meddeb, Adel Hamza, Raouf Hafsia, Nejla Stambouli, Asma Jlizi, Amel Benammar Elgaaied, Nejla Belhedi, Mohamed Ben Amor
Publikováno v:
Blood Cells, Molecules, and Diseases. 44:120-123
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::200664fb621515a45eeccbd37921bdcb
https://doi.org/10.1016/j.bcmd.2009.11.004
https://doi.org/10.1016/j.bcmd.2009.11.004
Autor:
I. Bouzayen, S. Ben Rejeb, Asma Jlizi, A. Ben Ammar El. Gaaied, A. Azzouzi, A. Slim, Mounira Garbouj
Publikováno v:
Médecine et Maladies Infectieuses. 39:707-713
Resume Cadre En Tunisie, le profil d’echec therapeutique est detecte chez 42,22 % des patients traites et les malades restent confrontes non seulement aux problemes ethiques et socioeconomiques, mais aussi a des problemes therapeutiques et techniqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6781cb4d6d48efad96d7bd7faa65ec5
https://doi.org/10.1016/j.medmal.2008.10.009
https://doi.org/10.1016/j.medmal.2008.10.009
Autor:
M. Chakroun, T. Ben Chaabane, A. Letaief-Omezzine, Asma Jlizi, A. Slim, S. Ben Rejeb, Mounira Garbouj, A. Ben Ammar El. Gaaied, M. Ben Mamou, Fethi Tebourski
Publikováno v:
Archives of Virology. 153:1103-1108
Three years after the introduction of antiretroviral therapy (ART) in Tunisia (North Africa), we aimed to determine the prevalence of drug resistance mutations in Tunisian HIV-1-infected patients failing ART. Plasma samples of 80 patients were tested
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64477c88421349fbbd6059d6cf4bc54
https://doi.org/10.1007/s00705-008-0104-z
https://doi.org/10.1007/s00705-008-0104-z
Autor:
Martine Garnier, C. Fendri, Christophe Burucoa, Khansa Ben Mansour, Hajer Battikh, Asma Jlizi, M. Zribi
Publikováno v:
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 37
Individuals can be infected by either a single or multiple strains of Helicobacter pylori. Multiple infection with genetically different isolates and particularly mixed infection with both antibiotic-susceptible and resistant isolates are difficult t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3c58f079f5ff042449414c2ec85a950
https://pubmed.ncbi.nlm.nih.gov/26518911
https://pubmed.ncbi.nlm.nih.gov/26518911
Autor:
Adel Hamza, Samah Aissa, Ning-Ning Wei, Ben Aissa Hanen Tiouiri, Nejla Stambouli, Baderredine Kilani, Rim Abdelmalek, Asma Jlizi, Amine Slim, Amel Ben Ammar Elgaied, Mahdi Dridi
Publikováno v:
Journal of biomolecular structuredynamics. 32(8)
We report the identification of a novel CC chemokine receptor 5 (CCR5) variant that seems associated with resistance to HIV-1 infection. The V130I mutation of the CCR5 receptor is located in the intracellular loop ICL2 known as DRY box and described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1eeec350db3db25faf028adb8e44e40
https://pubmed.ncbi.nlm.nih.gov/23869485
https://pubmed.ncbi.nlm.nih.gov/23869485
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 138 (2012)
Diagnostic Pathology
Diagnostic Pathology
In this study we report the prevalence of antiretroviral drug resistant HIV-1 genotypes of virus isolated from Djiboutian patients who failed first-line antiretroviral therapy (ART) and from ART naïve patients. Patients and methods A total of 35 blo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa864ce3b4ff9a819152f0c021484b66
http://www.diagnosticpathology.org/content/7/1/138
http://www.diagnosticpathology.org/content/7/1/138
Autor:
Kaouther Zahra, Amel Ben Ammar Elggaaied, Balkis Meddeb, Hejer Elmahmoudi, Christine Vinciguerra, Emna Gouider, Asma Jlizi, Houssein Khodjet-El-Khil, Edvard Wigren, Dorothé Pellechia
Publikováno v:
Diagnostic Pathology
Diagnostic Pathology, Vol 7, Iss 1, p 93 (2012)
Diagnostic Pathology, Vol 7, Iss 1, p 93 (2012)
Introduction Hemophilia A is an X linked recessive hemorrhagic disorder caused by mutations in the F8 gene that lead to qualitative and/or quantitative deficiencies of coagulation factor VIII (FVIII). Molecular diagnosis of hemophilia A is challengin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeee28e7047aabd34baca95943d9c301
https://doi.org/10.1186/1746-1596-7-93
https://doi.org/10.1186/1746-1596-7-93
Autor:
Amel Elgaaied Ben Ammar, Wijden Elborji, Emna Gouider, Asma Jlizi, Kaouther Zahra, Rim Sassi, Balkis Meddeb, Moez Zorgan, Hejer Elmahmoudi, Fatma Ben-lakhal
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 92 (2012)
Diagnostic Pathology
Diagnostic Pathology
Inherited factor VII (FVII) deficiency is a rare disorder characterized by a bleeding phenotype varying from mild to severe. To date, more than 200 mutations have been described along the F7 gene encoding for FVII. The aim of this study was the ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edec4d60759709377da378fd57a3b728
http://www.diagnosticpathology.org/content/7/1/92
http://www.diagnosticpathology.org/content/7/1/92