Published in Am J Physiol Gastrointest Liver Physiol on July 03, 2003
Protein kinase D protects against oxidative stress-induced intestinal epithelial cell injury via Rho/ROK/PKC-delta pathway activation. Am J Physiol Cell Physiol (2006) 1.12
Apple peel polyphenols and their beneficial actions on oxidative stress and inflammation. PLoS One (2013) 1.08
Modification in oxidative stress, inflammation, and lipoprotein assembly in response to hepatocyte nuclear factor 4alpha knockdown in intestinal epithelial cells. J Biol Chem (2010) 1.02
Influence of simulated gastrointestinal conditions on particle-induced cytotoxicity and interleukin-8 regulation in differentiated and undifferentiated Caco-2 cells. Nanotoxicology (2012) 0.86
Oxidative stress and mitochondrial functions in the intestinal Caco-2/15 cell line. PLoS One (2010) 0.82
Iron-ascorbate-mediated lipid peroxidation causes epigenetic changes in the antioxidant defense in intestinal epithelial cells: impact on inflammation. PLoS One (2013) 0.81
Dietary Iron Deficiency and Oversupplementation Increase Intestinal Permeability, Ion Transport, and Inflammation in Pigs. J Nutr (2016) 0.77
Diacylglycerol kinase regulation of protein kinase D during oxidative stress-induced intestinal cell injury. Biochem Biophys Res Commun (2008) 0.76
Influence of Fe(II) and Fe(III) on the expression of genes related to cholesterol- and fatty acid metabolism in human vascular smooth muscle cells. J Mater Sci Mater Med (2010) 0.75
A survey of genetic and epigenetic variation affecting human gene expression. Physiol Genomics (2004) 4.99
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis. Nat Genet (2009) 4.72
Phagosomes are competent organelles for antigen cross-presentation. Nature (2003) 3.97
Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. Am J Hum Genet (2009) 2.56
Transgenic expression of fatty acid transport protein 1 in the heart causes lipotoxic cardiomyopathy. Circ Res (2004) 2.50
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk. Nat Genet (2010) 2.47
Novel associations between activating killer-cell immunoglobulin-like receptor genes and childhood leukemia. Blood (2011) 2.29
Distinct cellular and molecular mechanisms underlie functional remodeling of repolarizing K+ currents with left ventricular hypertrophy. Circ Res (2008) 2.29
Short-chain fatty acids: ready for prime time? Nutr Clin Pract (2006) 2.21
Population genomics in a disease targeted primary cell model. Genome Res (2009) 2.20
Impact of procalcitonin on the management of children aged 1 to 36 months presenting with fever without source: a randomized controlled trial. Am J Emerg Med (2010) 2.12
Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. Blood (2003) 2.03
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders. Nat Genet (2003) 1.99
Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia. Blood (2009) 1.80
Direct and indirect induction by 1,25-dihydroxyvitamin D3 of the NOD2/CARD15-defensin beta2 innate immune pathway defective in Crohn disease. J Biol Chem (2009) 1.68
Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia. Genome Biol (2013) 1.57
CLSI-based transference of the CALIPER database of pediatric reference intervals from Abbott to Beckman, Ortho, Roche and Siemens Clinical Chemistry Assays: direct validation using reference samples from the CALIPER cohort. Clin Biochem (2013) 1.52
An appeal to medical journal editors: the need for a full description of laboratory methods and specimen handling in clinical study reports. Clin Chim Acta (2012) 1.51
The three-gene paraoxonase family: physiologic roles, actions and regulation. Atherosclerosis (2010) 1.50
An appeal to medical journal editors: the need for a full description of laboratory methods and specimen handling in clinical study reports. Transfusion (2012) 1.50
Natriuretic peptide as an adjunctive diagnostic test in the acute phase of Kawasaki disease. Pediatr Cardiol (2009) 1.46
Cardiac troponin testing in the acute care setting: ordering, reporting, and high sensitivity assays--an update from the Canadian society of clinical chemists (CSCC). Clin Biochem (2011) 1.41
Combined budesonide and antibiotic therapy for active Crohn's disease: a randomized controlled trial. Gastroenterology (2002) 1.40
Food allergy: a practical update from the gastroenterological viewpoint. J Pediatr (Rio J) (2007) 1.40
Risk of Lymphoma, Colorectal and Skin Cancer in Patients with IBD Treated with Immunomodulators and Biologics: A Quebec Claims Database Study. Inflamm Bowel Dis (2015) 1.40
Regional distribution and metabolic effect of PCSK9 insLEU and R46L gene mutations and apoE genotype. Can J Cardiol (2013) 1.39
Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children. Am J Gastroenterol (2007) 1.35
Localization and role of NPC1L1 in cholesterol absorption in human intestine. J Lipid Res (2006) 1.32
Clinical utility of fecal biomarkers for the diagnosis and management of inflammatory bowel disease. Inflamm Bowel Dis (2014) 1.29
Vitamin D status is modestly associated with glycemia and indicators of lipid metabolism in French-Canadian children and adolescents. J Nutr (2010) 1.28
Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia. Blood (2006) 1.26
Imbalances in dietary consumption of fatty acids, vegetables, and fruits are associated with risk for Crohn's disease in children. Am J Gastroenterol (2007) 1.26
Blood pressure and adiposity in children and adolescents. Circulation (2004) 1.24
C-reactive protein and features of the metabolic syndrome in a population-based sample of children and adolescents. Clin Chem (2004) 1.21
DNA variants in the dihydrofolate reductase gene and outcome in childhood ALL. Blood (2007) 1.20
Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica (2010) 1.20
Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. J Med Genet (2006) 1.17
Adiponectin, adiposity, and insulin resistance in children and adolescents. J Clin Endocrinol Metab (2006) 1.16
Adenoviral-mediated modulation of Sim1 expression in the paraventricular nucleus affects food intake. J Neurosci (2006) 1.14
Pediatric research and the return of individual research results. J Law Med Ethics (2011) 1.14
Intracellular adaptation of Brucella abortus. J Proteome Res (2009) 1.13
Parental genotypes in the risk of a complex disease. Am J Hum Genet (2002) 1.13
Apo A-IV: an update on regulation and physiologic functions. Biochim Biophys Acta (2003) 1.11
Role of DNA mismatch repair genetic polymorphisms in the risk of childhood acute lymphoblastic leukaemia. Br J Haematol (2003) 1.11
Hepatocyte nuclear factor-4alpha promotes gut neoplasia in mice and protects against the production of reactive oxygen species. Cancer Res (2010) 1.09
Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Res (2012) 1.09
Estrogen-related receptor alpha (ERRalpha) is a transcriptional regulator of apolipoprotein A-IV and controls lipid handling in the intestine. J Biol Chem (2004) 1.09
Intestinal cholesterol transport proteins: an update and beyond. Curr Opin Lipidol (2007) 1.09
The Childhood Leukemia International Consortium. Cancer Epidemiol (2013) 1.09
Plasma PCSK9 is associated with age, sex, and multiple metabolic markers in a population-based sample of children and adolescents. Clin Chem (2009) 1.09
Apple peel polyphenols and their beneficial actions on oxidative stress and inflammation. PLoS One (2013) 1.08
Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia. Haematologica (2011) 1.07
Maternal and fetal leptin, adiponectin levels and associations with fetal insulin sensitivity. Obesity (Silver Spring) (2013) 1.07
Maternal glucose tolerance in pregnancy affects fetal insulin sensitivity. Diabetes Care (2010) 1.07
Distribution of LDL particle size in a population-based sample of children and adolescents and relationship with other cardiovascular risk factors. Clin Chem (2005) 1.06
Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. Int J Cancer (2002) 1.05
Gene expression profiles of normal proliferating and differentiating human intestinal epithelial cells: a comparison with the Caco-2 cell model. J Cell Biochem (2006) 1.05
The peptidomimetic CXCR4 antagonist TC14012 recruits beta-arrestin to CXCR7: roles of receptor domains. J Biol Chem (2010) 1.05
Polymorphisms in genes encoding drugs and xenobiotic metabolizing enzymes, DNA repair enzymes, and response to treatment of childhood acute lymphoblastic leukemia. Clin Cancer Res (2002) 1.05
Dietary patterns and risk for Crohn's disease in children. Inflamm Bowel Dis (2008) 1.04
Localization, function and regulation of the two intestinal fatty acid-binding protein types. Histochem Cell Biol (2009) 1.04
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. PLoS Genet (2013) 1.03
Association between cigarette smoking and C-reactive protein in a representative, population-based sample of adolescents. Nicotine Tob Res (2008) 1.02
Modification in oxidative stress, inflammation, and lipoprotein assembly in response to hepatocyte nuclear factor 4alpha knockdown in intestinal epithelial cells. J Biol Chem (2010) 1.02
ATF5 polymorphisms influence ATF function and response to treatment in children with childhood acute lymphoblastic leukemia. Blood (2011) 1.01
Omega-3 fatty acid treatment of children with attention-deficit hyperactivity disorder: A randomized, double-blind, placebo-controlled study. Paediatr Child Health (2009) 1.01
PPARalpha-mediated remodeling of repolarizing voltage-gated K+ (Kv) channels in a mouse model of metabolic cardiomyopathy. J Mol Cell Cardiol (2008) 1.01
Genomic and genealogical investigation of the French Canadian founder population structure. Hum Genet (2011) 1.00
CD133 expression is associated with poor outcome in neuroblastoma via chemoresistance mediated by the AKT pathway. Histopathology (2012) 1.00
Cholesterol content in brains of suicide completers. Int J Neuropsychopharmacol (2006) 1.00
Maternal and fetal IGF-I and IGF-II levels, fetal growth, and gestational diabetes. J Clin Endocrinol Metab (2012) 0.99
Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein. Mol Genet Metab (2007) 0.99
Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia. Cancer Res (2013) 0.99
Prevalence of cardiometabolic risk factors by weight status in a population-based sample of Quebec children and adolescents. Can J Cardiol (2008) 0.99
Cardiomyocytes from AKAP7 knockout mice respond normally to adrenergic stimulation. Proc Natl Acad Sci U S A (2012) 0.98
Localization of microsomal triglyceride transfer protein in the Golgi: possible role in the assembly of chylomicrons. J Biol Chem (2002) 0.98
IL-10 and TNF-alpha promoter haplotypes are associated with childhood Crohn's disease location. World J Gastroenterol (2009) 0.98
Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines. Hum Genet (2012) 0.98
Glutathione S-transferase P1 genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukaemia. Pharmacogenetics (2002) 0.98