about
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmoninAnti-inflammatory potential of Capparis spinosa L. in vivo in mice through inhibition of cell infiltration and cytokine gene expressionPopulation genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework.Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis.IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel diseasec.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population.Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patientsA novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report.Association of methylenetetrahydrofolate reductase gene (C677T) with the risk of hypertension in MoroccoAnalysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients.Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis.Allium sativum L. regulates in vitro IL-17 gene expression in human peripheral blood mononuclear cellsPeroxiredoxin-2 up-regulation in inflammatory bowel disease: Friend or foe?Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levelsAssociation of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in MoroccoRelationship between family history of breast cancer and clinicopathological features in Moroccan patients.Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations.Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.Association of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarctionDoes i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients?Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals.Biomarkers for Alzheimer disease: Classical and novel candidates' review.Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.Genetic polymorphisms of T-1131C APOA5 and ALOX5AP SG13S114 with the susceptibility of ischaemic stroke in Morocco.First study of C2491T FV mutation with ischaemic stroke risk in Morocco.The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease.Influence of mutation of the HFE gene on the progression of chronic viral hepatitis B and C in Moroccan patients.Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.Assessment of GAPDH expression by quantitative real time PCR in blood of Moroccan AD cases.Prenatal diagnosis of BMD in Morocco: evolution and limits.A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1).Food hygiene assessment in catering establishments in Hay Hassani district-Casablanca.Functional polymorphism of CYP2B6 G15631T is associated with hematologic and cytogenetic response in chronic myeloid leukemia patients treated with imatinib.Genotype variability and haplotype frequency of MDR1 (ABCB1) gene polymorphism in Morocco.Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan population.Association of TP53 PIN3 polymorphism with breast cancer in Moroccan population.
P50
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