Cargando…

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 environmental components are believed to be the main cause of these diseases. Recently, many variants in interleukin...

Descripción completa

Detalles Bibliográficos
Autores principales:	Serbati, Nadia, Senhaji, Nezha, Diakite, Brehima, Badre, Wafaa, Nadifi, Sellama
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162942/ https://www.ncbi.nlm.nih.gov/pubmed/25159710 http://dx.doi.org/10.1186/1756-0500-7-570

Ejemplares similares

Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis
por: Senhaji, Nezha, et al.
Publicado: (2014)

Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease among Moroccan Patients
por: Senhaji, Nezha, et al.
Publicado: (2015)

Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease
por: Senhaji, Nezha, et al.
Publicado: (2017)

The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease
por: Zaid, Younes, et al.
Publicado: (2018)

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population
por: Marouf, Chaymaa, et al.
Publicado: (2015)

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients
por: El Khachibi, Meryam, et al.
Publicado: (2015)

Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis
por: Tazzite, Amal, et al.
Publicado: (2016)

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals
por: Hamzi, Khalil, et al.
Publicado: (2013)

Impact of I/D polymorphism of angiotensin-converting enzyme (ACE) gene on myocardial infarction susceptibility among young Moroccan patients
por: Hmimech, Wiam, et al.
Publicado: (2017)

Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
por: Kindil, Zineb, et al.
Publicado: (2017)

Genetics of Glioblastoma in Moroccan population: Review of literature
por: Idrissi, Hossam Hilal El, et al.
Publicado: (2018)

Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco
por: Hassani Idrissi, Hind, et al.
Publicado: (2016)

Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations
por: Tazzite, Amal, et al.
Publicado: (2013)

Relationship Between Family History of Breast Cancer and Clinicopathological Features in Moroccan Patients
por: Tazzite, Amal, et al.
Publicado: (2013)

MTHFR C677T polymorphism and risk of nonsyndromic cleft lip with or without cleft palate in the Moroccan population
por: Rafik, Amine, et al.
Publicado: (2019)

Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population
por: Marouf, Chaymaa, et al.
Publicado: (2016)

G894T endothelial nitric oxide synthase polymorphism and ischemic stroke in Morocco
por: Diakite, Brehima, et al.
Publicado: (2014)

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients
por: Jouhadi, Hassan, et al.
Publicado: (2016)

Association of Multidrug Resistance Gene-1 (MDR1 C1236T) Polymorphism with the Risk of Acute Myeloid Leukemia in a Moroccan Population
por: Boujmia, Oum Kaltoum Ait, et al.
Publicado: (2020)

Does i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients?
por: Hassani Idrissi, Hind, et al.
Publicado: (2017)

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
por: Karkar, Adnane, et al.
Publicado: (2015)

The Contribution of CD40/CD40L Axis in Inflammatory Bowel Disease: An Update
por: Senhaji, Nezha, et al.
Publicado: (2015)

Association of PIN3 16-bp duplication polymorphism of TP53 with breast cancer risk in Mali and a meta-analysis
por: Diakite, Brehima, et al.
Publicado: (2020)

A synergic effect between CYP2C19*2, CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Syndromes patients
por: Hassani Idrissi, Hind, et al.
Publicado: (2018)

Distribution of alleles, genotypes and haplotypes of the CYP2B6 (rs3745274; rs2279343) and CYP3A4 (rs2740574) genes in the Malian population: Implication for pharmacogenetics
por: Kassogue, Yaya, et al.
Publicado: (2021)

Association between variants of the autophagy related gene ATG16L1 in inflammatory bowel diseases and clinical statues
por: Baradaran Ghavami, Shaghayegh, et al.
Publicado: (2019)

EWSR1 Rearrangement and CD99 Expression as Diagnostic Biomarkers for Ewing/PNET Sarcomas in a Moroccan Population
por: Louati, Sara, et al.
Publicado: (2018)

Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians
por: Pugazhendhi, Srinivasan, et al.
Publicado: (2017)

Psychological distress in a sample of Moroccan prisoners with drug-dependence
por: Sfendla, Anis, et al.
Publicado: (2021)

Retention of an endoscopic videocapsule on inflammatory polyposis of the small bowel
por: El abbassi, Taoufik, et al.
Publicado: (2021)

p.Arg72Pro polymorphism of P53 and breast cancer risk: a meta-analysis of case-control studies
por: Diakite, Brehima, et al.
Publicado: (2020)

Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
por: Hamzi, Khalil, et al.
Publicado: (2011)

The phenotypes of ATG9, ATG16 and ATG9/16 knock-out mutants imply autophagy-dependent and -independent functions
por: Xiong, Qiuhong, et al.
Publicado: (2015)

Association of the Interleukin-10-592C/A Polymorphism and Cervical Cancer Risk: A Meta-Analysis
por: Diakite, Brehima, et al.
Publicado: (2022)

Genetic polymorphism in ATG16L1 gene is associated with adalimumab use in inflammatory bowel disease
por: Nuij, V. J. A. A., et al.
Publicado: (2017)

Evolution of IL-23 Blockade in Inflammatory Bowel Disease
por: Danese, Silvio, et al.
Publicado: (2022)

Somatic health and its association with negative psychosocial factors in a sample of Moroccan adolescents
por: Zouini, Btissame, et al.
Publicado: (2019)

Gene Polymorphisms of NOD2, IL23R, PTPN2 and ATG16L1 in Patients with Crohn’s Disease: On the Way to Personalized Medicine?
por: Hoffmann, Peter, et al.
Publicado: (2021)

Crystallization of the Atg12–Atg5 conjugate bound to Atg16 by the free-interface diffusion method
por: Noda, Nobuo N., et al.
Publicado: (2008)

Risk and protective factors for drug dependence in two Moroccan high-risk male populations
por: Sfendla, Anis, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_tp3f230jgflo2dqhrikbuon5uq