Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Saïda Abdelkefi"'
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
Autor:
Saïda Abdelkefi, Mahjoub Aouni, Vincent Geenen, Hélène Michaux, Moncef Mokni, Habib Jmii, Aymen Halouani, Firas Elmastour, Hela Jaïdane, Tahar Chakroun, Gwennaëlle Bodart, Famara Sane, Didier Hober
Publikováno v:
Clinical and Experimental Immunology. 187:399-407
Summary Type B coxsackievirus (CV-B) infections are involved frequently in the triggering of several autoimmune diseases such as myocarditis, dilated cardiomyopathy, pericarditis, pancreatitis, type 1 diabetes, encephalitis, thyroiditis or Sjögren's
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5d23d304671b51a6db3d5527b7a0cb
https://doi.org/10.1111/cei.12893
https://doi.org/10.1111/cei.12893
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:
S. Jemni Yacoub, B. Houissa, Mouna Ouchari, S. Hmida, H. Romdhane, Saïda Abdelkefi, Christian Gabriel, Helene Polin, T. Chakroun
Publikováno v:
Transfusion Medicine. 23:245-249
Summary Background and Objectives D is the most immunogenic blood group antigen. About 1% of whites carry an altered RHD allele leading to quantitative or qualitative changes in the antigen D expression. T201R and F223V encoded by 602C>G and 667T>G a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b410a0da6310d361ab25db1378332517
https://doi.org/10.1111/tme.12037
https://doi.org/10.1111/tme.12037
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
Autor:
Narjes, Kacem, Tahar, Chakroun, Hajer, Moussa, Saïda, Abdelkefi, Betoul, Houissa, Jacques, Chiaroni, Yacoub Saloua, Jemni
Publikováno v:
Transfusion Medicine
Transfusion Medicine, Wiley, 2012, pp.362-366
Transfusion Medicine, 2012, pp.362-366
Transfusion Medicine, Wiley, 2012, pp.362-366
Transfusion Medicine, 2012, pp.362-366
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.We proposed to determine the genotype frequencies of the RHD locus using a PCR-SSP met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e4b2e09e79bb640e21bdcf2229e2a81f
https://pubmed.ncbi.nlm.nih.gov/22757646
https://pubmed.ncbi.nlm.nih.gov/22757646
Autor:
Mouna Ouchari, Saloua Jemni-Yaacoub, Taher Chakroun, Saida Abdelkefi, Batoul Houissa, Slama Hmida
Publikováno v:
Asian Journal of Transfusion Science, Vol 7, Iss 2, Pp 119-124 (2013)
Background: A comprehensive survey of RHD alleles in Tunisia population was lacking. The aim of this study was to use a multiplex RHD typing assay for simultaneous detection of partial D especially with RHD/RHCE deoxyribonucleic acid (DNA) sequence e
Externí odkaz:
https://doaj.org/article/28b0e69013284005acfb2dc6416fce19