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Environmental risk factors for respiratory infection and wheeze in young children: A multicentre birth cohort study.
- Published in:
- Pediatric Pulmonology, 2024, v. 59, n. 1, p. 19, doi. 10.1002/ppul.26664
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- Publication type:
- Article
Mannose‐binding lectin genotype is associated with respiratory disease in young children: A multicenter cohort study.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 11, p. 2824, doi. 10.1002/ppul.26109
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- Publication type:
- Article
Identification of ROBO2 as a Potential Locus Associated with Inhaled Corticosteroid Response in Childhood Asthma.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 8, p. 733, doi. 10.3390/jpm11080733
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- Publication type:
- Article
The cholesterol-lowering effect of statins is modified by LILRB5 intolerance genotype: Results from a recruit-by-genotype clinical trial.
- Published in:
- Frontiers in Pharmacology, 2023, v. 14, p. 1, doi. 10.3389/fphar.2023.1090010
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- Publication type:
- Article
Common Statin Intolerance Variants in ABCB1 and LILRB5 Show Synergistic Effects on Statin Response: An Observational Study Using Electronic Health Records.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.713181
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- Publication type:
- Article
Polymorphism in INSR Locus Modifies Risk of Atrial Fibrillation in Patients on Thyroid Hormone Replacement Therapy.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.652878
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- Publication type:
- Article
Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 12, p. 3302, doi. 10.1210/clinem/dgac527
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- Publication type:
- Article
Biomarkers of rapid chronic kidney disease progression in type 2 diabetes.
- Published in:
- 2015
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- Publication type:
- journal article
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.
- Published in:
- Nature Genetics, 2008, v. 40, n. 4, p. 437, doi. 10.1038/ng.106
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- Publication type:
- Article
Common variants in WFS1 confer risk of type 2 diabetes.
- Published in:
- Nature Genetics, 2007, v. 39, n. 8, p. 951, doi. 10.1038/ng2067
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- Publication type:
- Article
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.
- Published in:
- Nature Genetics, 2006, v. 38, n. 4, p. 441, doi. 10.1038/ng1767
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- Publication type:
- Article
Correction to: Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.
- Published in:
- Diabetologia, 2022, v. 65, n. 6, p. 973, doi. 10.1007/s00125-022-05671-z
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- Publication type:
- Article
Diabetes status modifies the long-term effect of lipoprotein-associated phospholipase A2 on major coronary events.
- Published in:
- Diabetologia, 2022, v. 65, n. 1, p. 101, doi. 10.1007/s00125-021-05574-5
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- Publication type:
- Article
Serum kidney injury molecule 1 and β<sub>2</sub>-microglobulin perform as well as larger biomarker panels for prediction of rapid decline in renal function in type 2 diabetes.
- Published in:
- Diabetologia, 2019, v. 62, n. 1, p. 156, doi. 10.1007/s00125-018-4741-9
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- Publication type:
- Article
Lp-PLA<sub>2</sub> activity is associated with increased risk of diabetic retinopathy: a longitudinal disease progression study.
- Published in:
- Diabetologia, 2018, v. 61, n. 6, p. 1344, doi. 10.1007/s00125-018-4601-7
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- Publication type:
- Article
Interaction between variants in the CYP2C9 and POR genes and the risk of sulfonylurea-induced hypoglycaemia: A GoDARTS Study.
- Published in:
- Diabetes, Obesity & Metabolism, 2018, v. 20, n. 1, p. 211, doi. 10.1111/dom.13046
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- Publication type:
- Article
Paradoxical Lower Serum Triglyceride Levels and Higher Type 2 Diabetes Mellitus Susceptibility in Obese Individuals with the PNPLA3 148M Variant.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039362
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- Publication type:
- Article
Activation of PPARβ/δ Causes a Psoriasis-Like Skin Disease In Vivo.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009701
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- Publication type:
- Article
Ligand Modulated Antagonism of PPARγ by Genomic and Non-Genomic Actions of PPARδ.
- Published in:
- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007046
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- Publication type:
- Article
Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort.
- Published in:
- PLoS ONE, 2009, v. 4, n. 6, p. 1, doi. 10.1371/journal.pone.0005784
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- Publication type:
- Article
Peroxisome Proliferator-Activated Receptor-δ Genotype Influences Metabolic Phenotype and May Influence Lipid Response to Statin Therapy in Humans: A Genetics of Diabetes Audit and Research Tayside Study.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 4, p. 1830, doi. 10.1210/jc.2009-1201
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- Publication type:
- Article
A Single Nucleotide Polymorphism on Exon-4 of the Gene Encoding PPARδ Is Associated with Reduced Height in Adults and Children.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 7, p. 2587, doi. 10.1210/jc.2009-0392
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- Publication type:
- Article
The Peroxisome Proliferator-Activated Receptor: Transcriptional Activation of the CYP4A6 Gene<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1996, v. 804, n. 1, p. 373, doi. 10.1111/j.1749-6632.1996.tb18629.x
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- Publication type:
- Article
Association of Genetic Variant at Chromosome 12q23.1 With Neuropathic Pain Susceptibility.
- Published in:
- JAMA Network Open, 2021, v. 4, n. 12, p. e2136560, doi. 10.1001/jamanetworkopen.2021.36560
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- Publication type:
- Article
Both PPARγ and PPARδ influence sulindac sulfide-mediated p21<sup>WAF1/CIP1</sup> upregulation in a human prostate epithelial cell line.
- Published in:
- Oncogene, 2005, v. 24, n. 55, p. 8211, doi. 10.1038/sj.onc.1208983
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- Publication type:
- Article
LTA4H rs2660845 association with montelukast response in early and late-onset asthma.
- Published in:
- PLoS ONE, 2021, v. 16, n. 9, p. 1, doi. 10.1371/journal.pone.0257396
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- Publication type:
- Article
Tailored second-line therapy in asthmatic children with the Arg<sup>16</sup> genotype.
- Published in:
- Clinical Science, 2013, v. 124, n. 8, p. 521, doi. 10.1042/CS20120528
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- Publication type:
- Article
Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis.
- Published in:
- Cardiovascular Diabetology, 2013, v. 12, n. 1, p. 1, doi. 10.1186/1475-2840-12-109
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- Publication type:
- Article
Competing risks analysis for neutrophil to lymphocyte ratio as a predictor of diabetic retinopathy incidence in the Scottish population.
- Published in:
- BMC Medicine, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12916-023-02976-7
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- Publication type:
- Article
Author Correction: Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
The impact of phenotype, ethnicity and genotype on progression of type 2 diabetes mellitus.
- Published in:
- Endocrinology, Diabetes & Metabolism, 2020, v. 3, n. 2, p. 1, doi. 10.1002/edm2.108
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- Publication type:
- Article
FGFR2 protein expression in breast cancer: nuclear localisation and correlation with patient genotype.
- Published in:
- BMC Research Notes, 2011, v. 4, n. 1, p. 72, doi. 10.1186/1756-0500-4-72
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- Publication type:
- Article
Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine.
- Published in:
- PLoS ONE, 2019, v. 14, n. 12, p. N.PAG, doi. 10.1371/journal.pone.0226564
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- Publication type:
- Article
Persistent C-peptide secretion in Type 1 diabetes and its relationship to the genetic architecture of diabetes.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Male preponderance in early diagnosed type 2 diabetes is associated with the ARE insertion/deletion polymorphism in the PPP1R3A locus.
- Published in:
- BMC Genetics, 2003, v. 4, p. 1
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- Publication type:
- Article
Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight.
- Published in:
- BMC Genetics, 2002, v. 3, p. 21, doi. 10.1186/1471-2156-3-21
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- Publication type:
- Article
Elevated circulating amyloid concentrations in obesity and diabetes promote vascular dysfunction.
- Published in:
- 2020
- By:
- Publication type:
- journal article
A Qualitative Study on Perceptions and Practices of Diabetes Prevention and Management in Rural South India.
- Published in:
- Journal of Diabetology: Official Journal of Diabetes in Asia Study Group, 2023, v. 14, n. 4, p. 239, doi. 10.4103/jod.jod_77_23
- By:
- Publication type:
- Article
A Study on the Health and Socioeconomic Impact of COVID-19 Pandemic and Barriers to Self-management of Diabetes during the Lockdown among Rural Residents of South India.
- Published in:
- Journal of Diabetology: Official Journal of Diabetes in Asia Study Group, 2022, v. 13, n. 3, p. 255, doi. 10.4103/jod.jod_68_22
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- Publication type:
- Article
Secular trends in the prevalence of diabetes and prediabetes among the rural population of South India.
- Published in:
- International Journal of Diabetes in Developing Countries, 2023, v. 43, n. 6, p. 883, doi. 10.1007/s13410-023-01204-5
- By:
- Publication type:
- Article
Prevalent and Rare Mutations in the Gene Encoding Filaggrin in Japanese Patients with Ichthyosis Vulgaris and Atopic Dermatitis.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Specific Filaggrin Mutations Cause Ichthyosis Vulgaris and Are Significantly Associated with Atopic Dermatitis in Japan.
- Published in:
- Journal of Investigative Dermatology, 2008, v. 128, n. 6, p. 1436, doi. 10.1038/sj.jid.5701205
- By:
- Publication type:
- Article
Filaggrin Null Alleles Are Not Associated with Psoriasis.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 8, p. 1878, doi. 10.1038/sj.jid.5700817
- By:
- Publication type:
- Article
Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 3, p. 564, doi. 10.1038/sj.jid.5700587
- By:
- Publication type:
- Article
PPARα Is Required for PPARδ Action in Regulation of Body Weight and Hepatic Steatosis in Mice.
- Published in:
- PPAR Research, 2015, p. 1, doi. 10.1155/2015/927057
- By:
- Publication type:
- Article
Conditional Expression of Human PPARδ and a Dominant Negative Variant of hPPARδ In Vivo.
- Published in:
- PPAR Research, 2012, p. 1, doi. 10.1155/2012/216817
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- Publication type:
- Article
Genetic Risk of Diverticular Disease Predicts Early Stoppage of Nicorandil.
- Published in:
- Clinical Pharmacology & Therapeutics, 2020, v. 108, n. 6, p. 1171, doi. 10.1002/cpt.1941
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- Publication type:
- Article
Response to “Influence of Diabetes on Antiplatelet Drug Efficacy”.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor