Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Abdelmajid Abid"'
Autor:
Nadia Kheriji, Thouraya Dakhlaoui, Wafa Kamoun Rebai, Sonia Maatoug, Mohamed Taher Thabet, Thouraya Mellah, Mehdi Mrad, Hajer Trabelsi, Manel Soltani, Maria Kabbage, Hichem Ben Hassine, Afef Hadj Salah Bahlous, Faten Mahjoub, Henda Jamoussi, Abdelmajid Abid, Sonia Abdelhak, Rym Kefi
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Diabetes and hypertension are a serious public health problem worldwide. In the last decades, prevalence of these two metabolic diseases has dramatically increased in the Middle East and North Africa region, especially in Tunisia. This study
Externí odkaz:
https://doaj.org/article/69412dadefa24676af55703531bc28f2
Autor:
Hamza Dallali, Wided Boukhalfa, Nadia Kheriji, Meriem Fassatoui, Haifa Jmel, Meriem Hechmi, Ismail Gouiza, Mariem Gharbi, Wafa Kammoun, Mehdi Mrad, Marouen Taoueb, Asma Krir, Hajer Trabelsi, Afef Bahlous, Henda Jamoussi, Olfa Messaoud, Abdelmajid Abid, Rym Kefi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionType 2 diabetes (T2D) is a multifactorial disease involving genetic and environmental components. Several genome-wide association studies (GWAS) have been conducted to decipher potential genetic aberrations promoting the onset of this met
Externí odkaz:
https://doaj.org/article/ec2f2977e6d94ae5b458346728bffc4e
Autor:
Hamza Dallali, Meriem Hechmi, Imane Morjane, Sahar Elouej, Haifa Jmel, Yosra Ben Halima, Abdelmajid Abid, Afef Bahlous, Abdelhamid Barakat, Henda Jamoussi, Sonia Abdelhak, Rym Kefi
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-11 (2022)
Abstract Background Variants in the Hepatocyte Nuclear Factor 1 Alpha gene (HNF1A) are associated with lipoproteins levels and type 2 diabetes. In this study, we aimed to assess the association of HNF1A gene and haplotypes with the metabolic syndrome
Externí odkaz:
https://doaj.org/article/83976765788742f1a3bf0aa0de69fd51
Autor:
Yosra Ben Halima, Rym Kefi, Marco Sazzini, Cristina Giuliani, Sara De Fanti, Chokri Nouali, Majdi Nagara, Giacomo Mengozzi, Sahar Elouej, Abdelmajid Abid, Henda Jamoussi, Lotfi Chouchane, Giovanni Romeo, Sonia Abdelhak, Donata Luiselli
Publikováno v:
Genes & Nutrition, Vol 12, Iss 1, Pp 1-10 (2017)
Abstract Background The ability to digest lactose after weaning, namely, lactase persistence (LP), is encoded by polymorphisms in the MCM6 gene and varies widely in frequency among different human populations. Although, evolution of LP-related geneti
Externí odkaz:
https://doaj.org/article/b541615b7f054027885f5ea339ee95ec
Autor:
Haifa Jmel, Lilia Romdhane, Yosra Ben Halima, Meriem Hechmi, Chokri Naouali, Hamza Dallali, Yosr Hamdi, Jingxuan Shan, Abdelmajid Abid, Henda Jamoussi, Sameh Trabelsi, Lotfi Chouchane, Donata Luiselli, Sonia Abdelhak, Rym Kefi
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0194842 (2018)
Genetic variation is an important determinant affecting either drug response or susceptibility to adverse drug reactions. Several studies have highlighted the importance of ethnicity in influencing drug response variability that should be considered
Externí odkaz:
https://doaj.org/article/750c463436b44044b9ff16d1f5bbd813
Autor:
Afaf Bahlous, Yossra Ben Halima, Rym Kefi, Abdelhamid Barakat, Haifa Jmel, Meriem Hechmi, Meriem Fassatoui, Hamza Dallali, Sonia Bahri, Henda Jamoussi, Meriem Gharbi, Abdelmajid Abid
Publikováno v:
Bioscience Reports
Apolipoprotein A5 (APOA5) has been linked to metabolic syndrome (MetS) in several populations. In North Africa, only the Tunisian and Moroccan populations were investigated. Our aim is to assess the association between APOA5 gene variant (rs662799) a
Autor:
Sonia Abdelhak, Yosr Hamdi, Haifa Jmel, Lotfi Chouchane, Yosra Ben Halima, Chokri Naouali, Jingxuan Shan, Donata Luiselli, Meriem Hechmi, Hamza Dallali, Rym Kefi, Sameh Trabelsi, Lilia Romdhane, Henda Jamoussi, Abdelmajid Abid
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2018, 13 (4), pp.e0194842. ⟨10.1371/journal.pone.0194842⟩
PLoS ONE, Vol 13, Iss 4, p e0194842 (2018)
PLoS ONE, Public Library of Science, 2018, 13 (4), pp.e0194842. ⟨10.1371/journal.pone.0194842⟩
PLoS ONE, Vol 13, Iss 4, p e0194842 (2018)
International audience; Genetic variation is an important determinant affecting either drug response or susceptibility to adverse drug reactions. Several studies have highlighted the importance of ethnicity in influencing drug response variability th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a34f459107db9a6c4e824a08d30d9961
https://hal-riip.archives-ouvertes.fr/pasteur-01802454/document
https://hal-riip.archives-ouvertes.fr/pasteur-01802454/document
Autor:
Chokri Naouali, Haifa Jmel, Belen Nadal, Ghaith Abdessalem, Diana A. Díaz-Rizzolo, Henda Jamoussi, Meriem Fassatoui, Abdelmajid Abid, Margarita Martinez-Medina, Asma Chikhaoui, Rym Kefi, Sonia Abdelhak, Ramon Gomis, Mireia Lopez-Siles
Publikováno v:
Bioscience Reports
Bioscience Reports, 2019, vol. 39, núm. 6, p. BSR20182348
Articles publicats (D-B)
DUGiDocs – Universitat de Girona
instname
Bioscience Reports, 2019, vol. 39, núm. 6, p. BSR20182348
Articles publicats (D-B)
DUGiDocs – Universitat de Girona
instname
Gut microbiota plays an important role in the regulation of the immune system and host’s metabolism. We aimed to characterize the gut microbiota of Tunisian participants with and without diabetes. We enrolled ten participants with type 1 diabetes m
Autor:
Sonia Abdelhak, Henda Jamoussi, Melika Ben Ahmed, Mariem Gharbi, Haifa Jmel, Abdelmajid Abid, Federica Alberico, Om Kalthoum Sallem, Afaf Bahlous, Hamza Dallali, Rym Kefi, Tommaso Mazza, Serena Pezzilli, Sahar Elouej, Luana Mercuri, Yosra Ben Halima, Mariem Chargui, Sabrina Prudente, Meriem Hechmi, Vincenzo Trischitta
Publikováno v:
Acta Diabetologica
Acta Diabetologica, 2019, 56 (5), pp.515-523. ⟨10.1007/s00592-018-01283-5⟩
Acta Diabetologica, Springer Verlag, 2019, 56 (5), pp.515-523. ⟨10.1007/s00592-018-01283-5⟩
Acta Diabetologica, 2019, 56 (5), pp.515-523. ⟨10.1007/s00592-018-01283-5⟩
Acta Diabetologica, Springer Verlag, 2019, 56 (5), pp.515-523. ⟨10.1007/s00592-018-01283-5⟩
International audience; AIMS: Maturity Onset Diabetes of the Young (MODY) is a monogenic form of diabetes with autosomal dominant inheritance pattern. The diagnosis of MODY and its subtypes is based on genetic testing. Our aim was investigating MODY
Autor:
Ines Kamoun, Mariem Chargui, Florin Grigorescu, Abdelmajid Abid, Khaled Lasram, Hanen Belfki-Benali, Claude Ben Slama, Rym Kefi, Lilia Romdhane, Om Kalthoum Sallem, Habiba Ben Romdhane, Majdi Nagara, Sahar Elouej, Henda Jamoussi, Zinet Turki, Sonia Abdelhak, Sonia Bahri, Redha Attaoua
Publikováno v:
Metabolic Syndrome and Related Disorders
Metabolic Syndrome and Related Disorders, Mary Ann Liebert, 2016, 14 (2), pp.121-128. ⟨10.1089/met.2015.0090⟩
Metabolic Syndrome and Related Disorders, Mary Ann Liebert, 2016, 14 (2), pp.121-128. ⟨10.1089/met.2015.0090⟩
International audience; Background: Variants in the fat mass and obesity-associated (FTO) gene are associated with obesity and type 2 diabetes mellitus.Aim of the study: This study aims to assess the association of the rs9939609 variant and haplotype