Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Suad AlFadhli"'
Publikováno v:
PLoS ONE, Vol 17, Iss 6, p e0270714 (2022)
Abnormalities in the mitochondria have been linked to psoriasis, a chronic immune-mediated inflammatory skin disease. The mitochondrial DNA (mtDNA) is present in thousands of copies per cell and altered mtDNA copy number (mtDNA-CN), a common indicato
Externí odkaz:
https://doaj.org/article/2a017c535f3148cd80b0f52970cf37e4
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e77681 (2013)
Present study was aimed to explore the effect of (TA)n UGT1A1 gene promoter polymorphism on bilirubin metabolism, bilirubinaemia, predisposition to cholelithiasis and subsequent cholecystectomy, in Sickle-Cell Anemia (SCA) and beta-Thalasemia major (
Externí odkaz:
https://doaj.org/article/159c8c6ac8c945cf99ebae617cb48641
Autor:
Fériel Bouzid, Imen Gtif, Suad Alfadhli, Salma Charfeddine, Walid Ghorbel, Rania Abdelhédi, Riadh Benmarzoug, Leila Abid, Nouha Bouayed Abdelmoula, Inés Elloumi, Saber Masmoudi, Ahmed Rebai, Najla Kharrat
Publikováno v:
Bioscience reports. 42(7)
The coronary artery disease (CAD) is a chronic inflammatory disease involving genetic as well as environmental factors. Recent evidence suggests that the oral microbiome has a significant role in triggering atherosclerosis. The present study assessed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::574ec862681d9881f56da654a74a7ed6
https://pubmed.ncbi.nlm.nih.gov/35695679
https://pubmed.ncbi.nlm.nih.gov/35695679
Publikováno v:
Biomedical Reports
Recent studies have shown the role of mitochondrial DNA (mtDNA) variants in the pathogenesis of both psoriasis (Ps) and type 2 diabetes (T2D) amongst different ethnicities. However, no studies have investigated the mtDNA variants present in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db3f47e61a7da3378087e3d86a4ae242
https://doi.org/10.3892/br.2021.1417
https://doi.org/10.3892/br.2021.1417
Publikováno v:
Med Princ Pract
Objective: Published data show a clear link between psoriasis (Ps) and the increasing prevalence of comorbid conditions, such as diabetes mellitus type 2 (DM2). The role of the mitochondrial genomic haplogroup in the potential coexistence of Ps and D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed35b9f143b9c092b6e0ac18c7f3269f
https://europepmc.org/articles/PMC7923845/
https://europepmc.org/articles/PMC7923845/
Autor:
John T. Anim, Jemima E. Mellerio, Linda Ozoemena, Arti Nanda, Hejab Al-Ajmi, Lu Liu, Qasem A. Alsaleh, Suad AlFadhli, John A. McGrath
Publikováno v:
International Journal of Dermatology. 57:1058-1067
Background Epidermolysis bullosa (EB) is a clinically and genetically heterogeneous blistering skin disease, but in countries such as Kuwait, there are very limited data on the clinical and molecular pathology of EB. To improve understanding of EB in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1669c6cb04aeff4fc224f25c85419d4c
https://doi.org/10.1111/ijd.14099
https://doi.org/10.1111/ijd.14099
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 33:545-551
In this study, the potential effect of three HFE gene polymorphisms (C282Y, H63D and S65C) and the SLC40A1 A77D polymorphism on iron balance was investigated in 234 subjects (91 Arab beta-thalassemia major (BTM) patients, 34 beta-thalassemia trait (B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b95d4ce10fb9f04d32e67acca12f2bb
https://doi.org/10.1007/s12288-016-0775-7
https://doi.org/10.1007/s12288-016-0775-7
Publikováno v:
Gene. 593:110-116
The purpose of our study was to identify the currently lacking molecular mechanism that accounts for the co-occurrence of two seemingly disparate diseases: psoriasis and type II diabetes. We aimed to investigate a panel of 84 genes related to the dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba56dc3b9e7e6c410d0b6bacd4982530
https://doi.org/10.1016/j.gene.2016.08.024
https://doi.org/10.1016/j.gene.2016.08.024
Publikováno v:
Clinical Rheumatology. 35:623-629
The expression of interferon inducible genes are reported to be heightened in systemic lupus erythematosus (SLE); nevertheless, not much is known regarding the genetic variants underlying these genes and their role in the pathogenesis of disease. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e35303663d101295dc1e38c387efccb3
https://doi.org/10.1007/s10067-016-3179-z
https://doi.org/10.1007/s10067-016-3179-z
Publikováno v:
Journal of Genetics. 94:765-770
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecc80b253888b19344c0c6c2d6a939e7
https://doi.org/10.1007/s12041-015-0581-2
https://doi.org/10.1007/s12041-015-0581-2