Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Saloua Jemni, Yacoub"'
Autor:
Abdelbasset Amara, Ilhem Ben Charfeddine, Houda Ghédir, Ons Mamaï, Saloua Jemni-Yacoub, Larbi Chaieb, Ali Saad, Molka Chadli-Chaieb, Moez Gribaa
Publikováno v:
Iranian Journal of Public Health, Vol 44, Iss 3 (2015)
Background: HNF4A-p.I463Vvariant, reported previously in two distinct families suspected of MODY-1, is assessed in this report to determine whether it is a mutation or a polymorphism (frequency >1%). Methods: 200 Tunisian healthy people were screene
Externí odkaz:
https://doaj.org/article/90d3fc4e8d3848d3aaf8489fcb1ed9d9
Autor:
Najoua Kahloul, Céline Barlier, Viviana Granados, Saloua Jemni-Yacoub, Abderrahim Khelif, Sandrine Laradi, Jocelyne Fagan, Tahar Chakroun, Olivier Garraud, Sabeur Hammami, Chaker Aloui, Fabrice Cognasse, Latifa Chkioua
Publikováno v:
Blood Coagulation & Fibrinolysis. 29:689-696
Glanzmann thrombasthenia is an inherited severe bleeding disease. Mutations associated with Glanzmann thrombasthenia are highly heterogeneous and occur across the two genes coding for the platelet αIIbβ3 integrin. This study was aimed at identifyin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9bace58f90e819f73bd170931ab5d3f
https://doi.org/10.1097/mbc.0000000000000779
https://doi.org/10.1097/mbc.0000000000000779
Autor:
Imen Mokdad Bzeouich, Saloua Jemni-Yacoub, Aicha Sassi, Leila Chekir-Ghedira, Dorra El gueder, Mouna Maatouk, Kamel Ghedira, Saïda Abdelkefi-Ben Hatira
Publikováno v:
Chemico-Biological Interactions. 283:10-19
Chrysin (5,7-dihydroxyflavone) is a natural and biologically active compound which has many biological activities as an anticancer agent. The current report is aimed at finding out whether the antitumor potential of chrysin, evidenced in vitro and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3c241632ee2a30455d193489833010
https://doi.org/10.1016/j.cbi.2017.11.022
https://doi.org/10.1016/j.cbi.2017.11.022
Publikováno v:
Transfusion. 58:306-312
Background With more than 460 RHD alleles, this gene is the most complex and polymorphic among all blood group systems. The Tunisian population has the largest known prevalence of weak D Type 4.0 alleles, occurring in one of 105 RH haplotypes. We aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::926c80342e15be24957fb86b828eb4fa
https://doi.org/10.1111/trf.14411
https://doi.org/10.1111/trf.14411
Autor:
Franz F. Wagner, Andrea Döscher, Saloua Jemni Yacoub, Roland Conradi, Willy A. Flegel, Mouna Ouchari, Kshitij Srivastava
Publikováno v:
Transfusion. 57:2542-2544
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27a1034ddaf2894beefc20e977cfcc4d
https://doi.org/10.1111/trf.14218
https://doi.org/10.1111/trf.14218
Autor:
Mouna Ouchari, Saïda Abdelkefi, B. Houissa, T. Chakroun, Saloua Jemni Yacoub, Awatef Sassi, H. Romdhane
Publikováno v:
Transfusion and Apheresis Science. 51:59-63
Background The limitations of serology can be overcome by molecular typing. In order to evaluate the contribution of RH systematic genotyping and its implication in transfusion practice, a genotyping of D− blood donors was initiated. Methods Blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5117716f04bbfa17fc6c0a6cd74236fa
https://doi.org/10.1016/j.transci.2014.10.019
https://doi.org/10.1016/j.transci.2014.10.019
Autor:
Mouna, Ouchari, Kshitij, Srivastava, Houda, Romdhane, Saloua, Jemni Yacoub, Willy Albert, Flegel
With more than 460 RHD alleles, this gene is the most complex and polymorphic among all blood group systems. The Tunisian population has the largest known prevalence of weak D Type 4.0 alleles, occurring in one of 105 RH haplotypes. We aimed to estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9a0db6e38aef5cd1b79b1eebccda9618
https://europepmc.org/articles/PMC5803429/
https://europepmc.org/articles/PMC5803429/
Autor:
Mouna Ouchari, Saloua Jemni Yacoub, Monique Silvy, Jacques Chiaroni, Pascal Bailly, Saadia Abdelkefi, Thierry Peyrard, Sophie Beley
Publikováno v:
Transfusion. 55:1407-1410
Background The rare amorph Rhnull phenotype is caused by silent alleles at the RH locus and usually arises in consanguineous families. To date, only five molecular backgrounds have been identified in five unrelated families. Subjects with Rhnull red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fb97c4e47c9af184dbc4b40ea4849b5
https://doi.org/10.1111/trf.12937
https://doi.org/10.1111/trf.12937
Autor:
Chaker, Aloui, Tahar, Chakroun, Antoine, Prigent, Saloua, Jemni-Yacoub, Fabrice, Cognasse, Sandrine, Laradi, Olivier, Garraud
Publikováno v:
Blood transfusion = Trasfusione del sangue. 16(1)
Leucoreduction of blood components, including platelet components, is strongly encouraged but not yet universal, especially outside high income countries. As both leucocytes and platelets secrete copious amounts of pro-inflammatory cytokines/chemokin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b273374ae2daf2fe81830d1e42b42ad
https://pubmed.ncbi.nlm.nih.gov/27643752
https://pubmed.ncbi.nlm.nih.gov/27643752
Autor:
Betoul Houissa, Saloua Jemni Yacoub, Tahar Chakroun, Hajer Moussa, Saïda Abdelkefi, Narjes Kacem, Jacques Chiaroni
Publikováno v:
Transfusion Medicine. 22:362-366
SUMMARY Background Determination of the RHD zygosity is important for genetic counselling and risk evaluation of hemolytic disease of the newborn HDN in women with D iso-immunisation. Objectives We proposed to determine the genotype frequencies of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fb85407d859fb290e638b990738960d
https://doi.org/10.1111/j.1365-3148.2012.01172.x
https://doi.org/10.1111/j.1365-3148.2012.01172.x