Search Results - "Connaughton, M"
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Mechanisms of obesity-induced inflammation and insulin resistance: insights into the emerging role of nutritional strategies
Published in Frontiers in endocrinology (Lausanne) (2013)“…Obesity and associated chronic inflammation initiate a state of insulin resistance (IR). The secretion of chemoattractants such as MCP-1 and MIF and of…”
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2
Spatial and Temporal Clustering of Anti-Glomerular Basement Membrane Disease
Published in Clinical journal of the American Society of Nephrology (08-08-2016)“…An environmental trigger has been proposed as an inciting factor in the development of anti-GBM disease. This multicenter, observational study sought to define…”
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Reclassification of Genetic Testing Results: A Case Report Demonstrating the Need for Structured Re-Evaluation of Genetic Findings
Published in Canadian journal of kidney health and disease (01-01-2024)“…Alport Syndrome (AS) is a progressive genetic condition characterized by chronic kidney disease (CKD), hearing loss, and eye abnormalities. It is caused by…”
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Karyomegalic Interstitial Nephritis: Cancer Risk Following Transplantation
Published in Nephron (2015) (2020)“…A brother and sister presented individually in their forties with progressive renal failure, bronchiectasis and mild derangements of their liver function…”
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Tacrolimus trough-level variability predicts long-term allograft survival following kidney transplantation
Published in Journal of nephrology (01-04-2016)“…Aims The purpose of this study is to investigate tacrolimus trough-level variability from 3 to 12 months following transplantation and its association with…”
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Weighted Gene Co‐Expression Network Analysis Identifies Gender Specific Modules and Hub Genes Related to Metabolism and Inflammation in Response to an Acute Lipid Challenge
Published in Molecular nutrition & food research (01-01-2018)“…Scope Inflammation is characteristic of diet‐related diseases including obesity and type 2 diabetes (T2D). However, biomarkers of inflammation that reflect the…”
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An Exome Sequencing Study of 10 Families with IgA Nephropathy
Published in Nephron (2015) (01-01-2020)“…Immunoglobulin A nephropathy (IgAN) is a heterogeneous disorder with a strong genetic component. The advent of whole exome sequencing (WES) has accelerated the…”
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COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
Published in Human genetics (01-10-2019)“…Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease (~ 45%) that manifests before 30 years of age…”
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Utility of Genomic Testing after Renal Biopsy
Published in American journal of nephrology (01-01-2020)“…Renal biopsy is the mainstay of renal pathological diagnosis. Despite sophisticated diagnostic techniques, it is not always possible to make a precise…”
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Personalized medicine in chronic kidney disease by detection of monogenic mutations
Published in Nephrology, dialysis, transplantation (01-03-2020)“…Abstract A large fraction of early-onset chronic kidney disease (CKD) is known to be monogenic in origin. To date, ∼450 monogenic (synonymous with single-gene…”
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Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland
Published in Renal failure (01-01-2019)“…Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic cause of renal impairment resulting from mutations in the MUC1,…”
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Non-adherence to statin therapy: a major challenge for preventive cardiology
Published in Expert opinion on pharmacotherapy (01-12-2009)“…Hypercholesterolemia is a major risk factor for atherosclerosis and cardiovascular disease, the leading cause of death worldwide. In the last twenty years,…”
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13
Effects of fish size and temperature on weakfish disturbance calls: implications for the mechanism of sound generation
Published in Journal of experimental biology (01-05-2000)“…To categorize variation in disturbance calls of the weakfish Cynoscion regalis and to understand their generation, we recorded sounds produced by…”
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Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01-09-2022)“…Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) is a developmental disorder of the kidney and/or genito‐urinary tract that results in end stage…”
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Weakfish sonic muscle: influence of size, temperature and season
Published in Journal of experimental biology (01-08-2002)“…The influence of temperature, size and season on the sounds produced by the sonic muscles of the weakfish Cynoscion regalis are categorized and used to…”
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Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01-09-2022)“…Abstract Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) is a developmental disorder of the kidney and/or genito‐urinary tract that results in end…”
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Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Published in Journal of molecular medicine (Berlin, Germany) (01-08-2023)“…Atypical hemolytic uremic syndrome (aHUS) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Complement and…”
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Fatty acids and chronic low grade inflammation associated with obesity and the metabolic syndrome
Published in European journal of pharmacology (15-08-2016)“…The metabolic syndrome is a group of obesity associated metabolic conditions that result in increased risk of cardiovascular disease and type 2 diabetes…”
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Teaching NeuroImage: Extensive Brainstem and Striatal Involvement in Neuropsychiatric Systemic Lupus Erythematosus
Published in Neurology (27-02-2024)Get full text
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Proteomic analysis identifies ZMYM2 as endogenous binding partner of TBX18 protein in 293 and A549 cells
Published in Biochemical journal (14-01-2022)“…The TBX18 transcription factor regulates patterning and differentiation programs in the primordia of many organs yet the molecular complexes in which TBX18…”
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