438 results on '"McManus, Ross"'
Search Results
102. Dietary saturated fat, gender and genetic variation at the TCF7L2 locus predict the development of metabolic syndrome
103. Dietary fat, abdominal obesity and smoking modulate the relationship between plasma complement component 3 concentrations and metabolic syndrome risk
104. Common variation in the vitamin D receptor gene and risk of inflammatory bowel disease in an Irish case–control study
105. Cytokine Gene Expression After Lung Cancer Resection May Be Affected by the Choice of Surgical Access: Response
106. Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci
107. Gene-nutrient interactions and gender may modulate the association between ApoA1 and ApoB gene polymorphisms and metabolic syndrome risk
108. Post-operative infection and sepsis in humans is associated with deficient gene expression of γc cytokines and their apoptosis mediators
109. ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat
110. Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis
111. Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome
112. Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study
113. Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression
114. Additive Effect of Polymorphisms in the IL-6, LTA, and TNF-α Genes and Plasma Fatty Acid Level Modulate Risk for the Metabolic Syndrome and Its Components
115. Association of gastric disease with polymorphisms in the inflammatory-related genes IL-1B, IL-1RN, IL-10, TNF and TLR4
116. S1751 Copy Number Variant and Extended SNP Genome Wide Association Study in Celiac Disease
117. Session 3: Joint Nutrition Society and Irish Nutrition and Dietetic Institute Symposium on ‘Nutrition and autoimmune disease’
118. OR.68. Genetic Risk Model for Celiac Disease Helps Identify High-risk Individuals
119. Natural selection and the molecular basis of electrophoretic variation at the coagulation F13B locus
120. T1726 Association of Pregnane X Receptor (PXR) with Esophageal Disease in An Irish Population
121. Newly identified genetic risk variants for celiac disease related to the immune response
122. Lack of association between NFKBIL1/LTA polymorphisms and hypertension, myocardial infarct, unstable angina and stable angina in a large Irish population sample
123. Filaggrin Null Alleles Are Not Associated with Psoriasis
124. Genetic Polymorphisms and the Risk of Infection Following Esophagectomy. Positive Association with TNF-α Gene −308 Genotype
125. A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
126. Coagulopathy After Cardiac Surgery May Be Influenced by a Functional Plasminogen Activator Inhibitor Polymorphism
127. THE OCCURRENCE OF SEVERE SEPSIS AND SEPTIC SHOCK ARE RELATED TO DISTINCT PATTERNS OF CYTOKINE GENE EXPRESSION
128. Gene Polymorphism and Requirement for Vasopressor Infusion After Cardiac Surgery
129. Tumor necrosis factor-α and interleukin-10 gene expression in peripheral blood mononuclear cells after cardiac surgery
130. Genetic and nutrient determinants of the metabolic syndrome
131. The Pregnane X Receptor Locus Is Associated With Susceptibility to Inflammatory Bowel Disease
132. A genome-wide approach to identify genetic loci with a signature of natural selection in the Irish population
133. The TNF region in celiac disease
134. Il-1b polymophisms are NOT associated with Helicobacter pylori positive intestinal metaplasia
135. Multiple drug resistance gene (MDRI) polymorphisms and steroid resistance in inflammatory bowel disease (IBD)
136. SNP mapping of the HLA class III region confirms existence of an extended haplotype in coeliac disease
137. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci
138. Post-operative serum mutant k-ras- a sensitive marker of disease recurrence in patients with colorectal cancer
139. A polymorphism in p73, a novel p53-homologue, confers protection against the development of esophageal cancer
140. Polymorphism and loss of heterozygosity (LOH) of themethylenetetrahydrofolate (MTHFR) enzyme is associated with the development of colorectal cancer
141. Analysis of single nucleotide polymorphisms (SNPS) in the Tumour Necrosis Factor (TNF) gene in celiac disease
142. Impact of polymorphisms in the TNF alpha promoter region on outcome in esophageal cancer
143. Human Small Intestinal Epithelial Cells Secrete Interleukin-7 and Differentially Express Two Different Interleukin-7 mRNA Transcripts: Implications for Extrathymic T-Cell Differentiation
144. Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
145. Association of celiac disease with microsatellite polymorphisms close to the tumor necrosis factor genes
146. RAG1 and RAG2 expression in human intestinal epithelium: evidence of extrathymic T cell differentiation
147. Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q
148. Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground With Ankylosing Spondylitis.
149. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
150. An Update on Female Sexual Function and Dysfunction in Old Age and Its Relevance to Old Age Psychiatry.
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