Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rim Sassi"'
Publikováno v:
Climacteric : the journal of the International Menopause Society. 20(4)
The dynamic nature of the skeleton is achieved by a remodeling process. Receptor activator of nuclear factor kappa B (RANK) ligand (RANKL) stimulates bone resorption by activating RANK signaling. Therefore it is considered as a candidate gene regulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a340c38ae7ac1ef39ae4c2313c1a2901
https://pubmed.ncbi.nlm.nih.gov/28453307
https://pubmed.ncbi.nlm.nih.gov/28453307
Autor:
David Meyre, T. Baroudi, Emanuel Vaillant, Martine Vaxillaire, R. Bouhaha, Vincent Vatin, Philippe Froguel, Rim Sassi, Amel Ben Ammar-El Gaaied, Hafawa Abid, Hajer Ennafaa
Publikováno v:
Clinical Biochemistry. 43:549-552
A bstract Objectives We investigated two genetic markers in pro inflammatory molecules : TNFα -308G/A and IL6 -174G/C in order to assess their effect on type 2 diabetes (T2D) and obesity in the Tunisian population. Design and methods The study sampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e794c7d3312e8a208a14cb2e3b43ed5b
https://doi.org/10.1016/j.clinbiochem.2010.01.008
https://doi.org/10.1016/j.clinbiochem.2010.01.008
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:
Nadia Kourda, Raja Marrakchi, Slah Ouerhani, Florent Soubrier, T. Najjar, Y. Blondeau Lahely, Amel Moussa, S. Ben Jilani, A. Ben Ammar Elgaaied, Karim Bougatef, Rim Sassi
Publikováno v:
Pathologie Biologie. 57:e67-e71
Objectives Sporadic colorectal cancer is influenced by numerous single nucleotide polymorphisms (SNPs), each with minor effects on the cancer risk. This study seeks to determine whether there is any association of the I1307K, E1317Q and D1822V varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f8ca9a2564f677e802a0825d63a6446
https://doi.org/10.1016/j.patbio.2008.01.004
https://doi.org/10.1016/j.patbio.2008.01.004
Publikováno v:
Climacteric : the journal of the International Menopause Society. 18(4)
Osteopenia is characterized by intermediate values of bone mineral density (BMD) as compared to normal and osteoporotic subjects. BMD, a surrogate phenotype for osteoporosis, is influenced in part by genetic factors. Among the genes associated with B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e326a6038171389d4fe8c79685f6533
https://pubmed.ncbi.nlm.nih.gov/25603555
https://pubmed.ncbi.nlm.nih.gov/25603555
Autor:
Bechir Zouari, Hejer El Mahmoudi, H. Sahli, Serge Ferrari, Rim Sassi, Amel Benammar Elgaaied, Slaheddine Sellami, Chiraz Bouchlaka Souissi
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol. 15, No 144 (2014)
BMC Musculoskeletal Disorders, Vol. 15, No 144 (2014)
Background Osteoporosis is a highly heritable trait. Among the genes associated with bone mineral density (BMD), the low-density lipoprotein receptor-related protein 5 gene (LRP5) has been consistently identified in Caucasians. However LRP5 contribut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fb0e1a53a6264dd2152d9cedd69638
https://doi.org/10.1186/1471-2474-15-144
https://doi.org/10.1186/1471-2474-15-144
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