[HTML][HTML] Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease …
N Senhaji, Y Kassogue, M Fahimi, N Serbati… - Mediators of …, 2015 - hindawi.com
Inflammatory bowel diseases (IBD) are multifactorial disorders resulting from environmental
and genetic factors. Polymorphisms in MDR1 and GSTs genes might explain individual …
and genetic factors. Polymorphisms in MDR1 and GSTs genes might explain individual …
[HTML][HTML] Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: new data and a meta-analysis
Background The pathogenesis of inflammatory bowel disease (IBD) involves interactions
between the host genetic susceptibility, intestinal microflora and mucosal immune responses …
between the host genetic susceptibility, intestinal microflora and mucosal immune responses …
[HTML][HTML] IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease
Background Inflammatory bowel diseases (IBD) are chronic diseases of the gastrointestinal
tract. Although their pathogenesis is unclear, the combination of genetic predisposition and …
tract. Although their pathogenesis is unclear, the combination of genetic predisposition and …
[PDF][PDF] NOD2/CARD15 gene influences disease behaviour but not IBD susceptibility in a Moroccan population
N Serbati, W Badre, B Diakite, S Nadifi - Turk J Gastroenterol, 2014 - researchgate.net
Background/Aims: IBD (Crohn’s disease and Ulcerative Colitis) is chronic and multifactorial
disease of the gastrointestinal tract. Till now, his pathogenesis remains unclear. It involves …
disease of the gastrointestinal tract. Till now, his pathogenesis remains unclear. It involves …
Methylenetetrahydrofolate reductase C677T variant in Moroccan patients with inflammatory bowel disease
BACKGROUND: The association of genetic polymorphisms related to metabolism of
homocysteine and folate with inflammatory bowel disease has been evidenced. Several studies …
homocysteine and folate with inflammatory bowel disease has been evidenced. Several studies …
[HTML][HTML] Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease
…, A Serrano, DAL Rodriguez, N Serbati… - World Journal of …, 2017 - ncbi.nlm.nih.gov
AIM To investigate whether common variants in the oxidative pathway genes influence
inflammatory bowel disease (IBD) risk among Moroccan patients. METHODS The distribution of (…
inflammatory bowel disease (IBD) risk among Moroccan patients. METHODS The distribution of (…
Trisomy 18 or postnatal Edward´ s syndrome: descriptive study conducted at the University Hospital Center of Casablanca and literature review
…, R Errahli, N Imelloul, G Jabrane, N Serbati… - The Pan African …, 2020 - europepmc.org
La trisomie 18 est une maladie chromosomique, dû à la présence d'un chromosome 18
surnuméraire. Les nourrissons atteints de trisomie 18 ont un taux de mortalité élevé, secondaire …
surnuméraire. Les nourrissons atteints de trisomie 18 ont un taux de mortalité élevé, secondaire …
[HTML][HTML] The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease
…, N Senhaji, FZ Bakhtaoui, A Serrano, N Serbati… - BMC Research …, 2018 - Springer
Objective In view of the discrepant data regarding the association between the protein tyrosine
phosphatase non-receptor 22 (PTPN22) rs2476601 (R620W, 1858C→T) polymorphism …
phosphatase non-receptor 22 (PTPN22) rs2476601 (R620W, 1858C→T) polymorphism …
La trisomie 18 ou syndrome d'Edwards en post-natal: étude descriptive au Centre Hospitalier Universitaire de Casablanca et revue de littérature
…, R Errahli, N Imelloul, G Jabrane, N Serbati… - Pan African Medical …, 2020 - ajol.info
La trisomie 18 est une maladie chromosomique, dû à la présence d'un chromosome 18
surnuméraire. Les nourrissons atteints de trisomie 18 ont un taux de mortalité élevé, secondaire …
surnuméraire. Les nourrissons atteints de trisomie 18 ont un taux de mortalité élevé, secondaire …
Trisomy 18 or postnatal Edward's syndrome: descriptive study conducted at the University Hospital Center IBN Rochd of Casablanca and literature review.
FZ Outtaleb, G Jabrane, R Errahli, N Imelloul, N Serbati… - 2020 - cabidigitallibrary.org
Trisomy 18 is a chromosomal disease, caused by the presence of a supernumerary chromosome
18. Mortality among infants with trisomy 18 is high, secondary to lethal malformations …
18. Mortality among infants with trisomy 18 is high, secondary to lethal malformations …