Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Meriem Dallel"'
Autor:
Sameh Sarray, Meriem Dallel, lamine Laila Ben, Nejla Sellami, Amira Turki, Roland Brock, mohamed Ghorbel
Publikováno v:
Endocrine Abstracts.
Autor:
Mouadh Barbirou, Mouna Stayoussef, Balkiss Bouhaouala, Amel Mezlini, Wassim Y. Almawi, Amina Mokrani, Besma Yacoubi-Loueslati, Sinda A. Bedoui, Meriem Dallel
Publikováno v:
Cancer Gene Therapy. 27:311-318
Polymorphic variants in IL-17A gene were differentially associated with colorectal cancer (CRC) susceptibility but their link with response and toxicity to CRC treatment have not yet been evaluated. We investigated association between seven IL-17A va
Autor:
Zainab H. Malalla, Meriem Dallel, Mohamed Ghorbel, Nejla Sellami, Deeba Shamim Jairajpuri, Sameh Sarray, Touhami Mahjoub, Amira Turki, Roland Brock, Laila Ben Lamine
Publikováno v:
Journal of Diabetes and Its Complications, 35, 6
Journal of Diabetes and Its Complications, 35
Journal of Diabetes and Its Complications, 35
Aims Genetic variations mediating MMP-2 expression may result in individual differences in susceptibility to particular diseases. Our aim was to investigate the possible association of certain MMP-2 gene variants with the susceptibility of type 2 dia
Autor:
Dhafer B. Letaifa, Meriem Dallel, Touhami Mahjoub, Ramzi R. Finan, Wassim Y. Almawi, Feten Hachani, Zeineb Douma
Publikováno v:
Bioscience Reports
Background: The present study examined the contribution of ethnicity to the association of leptin receptor gene (LEPR) gene variants with polycystic ovary syndrome (PCOS) in Tunisian and Bahraini Arabic-speaking women. Methods: Subjects consisted of
Autor:
Touhemi Mahjoub, Assila Ben Salem, Wassim Y. Almawi, Faten Hachani Ben Ali, Florin Grigorescu, Meriem Dallel, Corinne Lautier, Sara Haydar, Weal Bahia, Zeineb Douma
Publikováno v:
Gene
Gene, Elsevier, 2020, 741, pp.144560-. ⟨10.1016/j.gene.2020.144560⟩
Gene, Elsevier, 2020, 741, pp.144560-. ⟨10.1016/j.gene.2020.144560⟩
SNV (single nucleotide variation) in estrogen receptor (ESR1 and ESR2) genes are susceptibility markers for complex diseases, such as cancer, metabolic disorders and women infertility. We explored six widely used SNVs in ESR1 (rs2234693, rs9340799, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef8a3c874b0553664ea750fab9f0dda
https://hal.archives-ouvertes.fr/hal-03489803/document
https://hal.archives-ouvertes.fr/hal-03489803/document
Autor:
Touhami Mahjoub, Meriem Dallel, Feten Hachani, Wassim Y. Almawi, Abrar K. Al-Ansari, Zeineb Douma, Sameh Sarray, Dhafer B. Letaifa
Publikováno v:
Gene. 647:79-84
Background and aim Polycystic ovary syndrome (PCOS) is a common endocrine disorder, and results from interaction between modifiable and non-modifiable factors, including genetic predisposition. Previous genome-wide association studies and meta-analys
Autor:
Wassim Y. Almawi, Meriem Dallel
Publikováno v:
Journal of the Endocrine Society
BACKGROUND. Polycystic ovary syndrome (PCOS) is a common though heterogeneous endocrine and metabolic disorder in women of reproductive age. PCOS is characterized by polycystic ovaries, hyperandrogenism and chronic anovulation, as well as being assoc
Autor:
Amel Mezlini, Wassim Y. Almawi, Meriem Dallel, Besma Yacoubi-Loueslati, Mouadh Barbirou, Balkiss Bouhaouala-Zahar, Lamia Makni, Mouna Stayoussef, Sinda A. Bedoui, Amina Mokrani
Publikováno v:
Gene. 754:144893
A central role for advanced glycation end products (AGE) and their receptor (RAGE) in the pathogenesis of multiple cancer types, including colorectal cancer (CRC) was reported. We investigated the association between CRC and rs2853807, rs77170610, rs
Autor:
Lamia Makni, Besma Yacoubi-Loueslati, Mouadh Barbirou, Mouna Stayoussef, Amel Mezlini, Balkiss Bouhaouala, Wassim Y. Almawi, Sinda A. Bedoui, Meriem Dallel, Amina Mokrani
Publikováno v:
Cytokine
Cytokine, Elsevier, 2018, 110, pp.18-23. ⟨10.1016/j.cyto.2018.04.017⟩
Cytokine, Elsevier, 2018, 110, pp.18-23. ⟨10.1016/j.cyto.2018.04.017⟩
International audience; Background: Interleukin (IL)-17A is proinflammatory cytokine produced by Th17 cells, which play key, but sometimes inconsistent role in autoimmunity and cancer. Polymorphic variants in IL-17A gene were differentially associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5f3b37af1cd5b0f841fedb3b698e92
https://hal-riip.archives-ouvertes.fr/pasteur-02009143
https://hal-riip.archives-ouvertes.fr/pasteur-02009143
Autor:
Meriem Dallel, Feten Hachani, Zeineb Douma, Touhami Mahjoub, Ramzi R. Finan, Ikram Sghaier, Wassim Y. Almawi, Dhafer B. Letaifa
Publikováno v:
Gene. 694
Background and aim Epidemiological studies suggested that ethnic/racial background influences the associations of altered leptin secretion and leptin gene (LEP) polymorphisms with polycystic ovary syndrome (PCOS). We investigated the association betw