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Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2011, v. 27, n. 5, p. 499, doi. 10.1002/dmrr.1194
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- Publication type:
- Article
A mutation in the c-Fos gene associated with congenital generalized lipodystrophy.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-119
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- Publication type:
- Article
A mutation in the c-fos gene associated with congenital generalized lipodystrophy.
- Published in:
- 2013
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- Publication type:
- journal article
Germline Mutations of the TMEM127 Gene in Patients with Paraganglioma of Head and Neck and Extraadrenal Abdominal Sites.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 8, p. E1279, doi. 10.1210/jc.2011-0114
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- Publication type:
- Article
Dysregulation of the Mitochondrial Proteome Occurs in Mice Lacking Adiponectin Receptor 1.
- Published in:
- Frontiers in Endocrinology, 2019, v. 10, p. 1, doi. 10.3389/fendo.2019.00872
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- Publication type:
- Article
Myocardial Mitochondrial and Contractile Function Are Preserved in Mice Lacking Adiponectin.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119416
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- Publication type:
- Article
Single Nucleotide Variants in the Protein C Pathway and Mortality in Dialysis Patients.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0097251
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- Publication type:
- Article
Diversification and Molecular Evolution of ATOH8, a Gene Encoding a bHLH Transcription Factor.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023005
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- Publication type:
- Article
Inverse association between apolipoprotein C-II and cardiovascular mortality: role of lipoprotein lipase activity modulation.
- Published in:
- European Heart Journal, 2023, v. 44, n. 25, p. 2335, doi. 10.1093/eurheartj/ehad261
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- Publication type:
- Article
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
- Published in:
- 2010
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- Publication type:
- journal article
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.
- Published in:
- 2008
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- Publication type:
- journal article
Germline NF1 Mutational Spectra and Loss-of Heterozygosity Analyses in Patients with Pheochromocytoma and Neurofibromatosis Type 1.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2784, doi. 10.1210/jc.2006-2833
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- Publication type:
- Article
Alanine to Serine Polymorphism at Position 986 of the Calcium-Sensing Receptor Associated with Coronary Heart Disease, Myocardial Infarction, All-Cause, and Cardiovascular Mortality.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2363, doi. 10.1210/jc.2006-0071
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- Publication type:
- Article
Comprehensive Mutation Scanning of NF1 in Apparently Sporadic Cases of Pheochromocytoma.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3478, doi. 10.1210/jc.2006-0780
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- Publication type:
- Article
Triglyceride-Rich Lipoproteins Are Associated with Hypertension in Preeclampsia.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 3, p. 1162, doi. 10.1210/jc.2002-021160
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- Publication type:
- Article
Effect of Fluvastatin Slow-Release on Low Density Lipoprotein (LDL) Subfractions in Patients with Type 2 Diabetes Mellitus: Baseline LDL Profile Determines Specific Mode of Action.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 12, p. 5485, doi. 10.1210/jc.2002-020370
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- Publication type:
- Article
Type I Hyperlipoproteinemia Due to a Novel Loss of Function Mutation of Lipoprotein Lipase, Cys<sup>239</sup>→Trp, Associated with Recurrent Severe Pancreatitis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4795, doi. 10.1210/jcem.85.12.7069
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- Publication type:
- Article
Low Density Lipoprotein (LDL) Subfractions during Pregnancy: Accumulation of Buoyant LDL with Advancing Gestation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4543, doi. 10.1210/jcem.85.12.7027
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- Publication type:
- Article
Cytochrome P450 2C19*2 polymorphism in patients with stable coronary heart disease and risk for secondary cardiovascular disease events: results of a long-term follow-up study in routine clinical care.
- Published in:
- BMC Cardiovascular Disorders, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2261-13-61
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- Publication type:
- Article
Cytochrome P450 2C19*2 polymorphism in patients with stable coronary heart disease and risk for secondary cardiovascular disease events: results of a long-term follow-up study in routine clinical care.
- Published in:
- 2013
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- Publication type:
- journal article
Prognostic value of interleukin-1 receptor antagonist gene polymorphism and cytomegalovirus seroprevalence in patients with coronary artery disease.
- Published in:
- BMC Cardiovascular Disorders, 2005, v. 5, p. 10, doi. 10.1186/1471-2261-5-10
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- Publication type:
- Article
Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 3, p. 235, doi. 10.1007/s00109-004-0618-0
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- Publication type:
- Article
The variable number of tandem repeat polymorphism in the P-selectin glycoprotein ligand-1 gene is not associated with coronary heart disease.
- Published in:
- Journal of Molecular Medicine, 2003, v. 81, n. 8, p. 495, doi. 10.1007/s00109-003-0459-2
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- Publication type:
- Article
The interleukin-6 G(–174)C promoter polymorphism in the LURIC cohort: no association with plasma interleukin-6, coronary artery disease, and myocardial infarction.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 8, p. 507, doi. 10.1007/s00109-002-0354-2
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- Publication type:
- Article
Hidden population substructures in an apparently homogeneous population bias association studies.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 236, doi. 10.1038/sj.ejhg.5201546
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- Publication type:
- Article
The apolipoprotein E polymorphism is associated with circulating C-reactive protein (the Ludwigshafen risk and cardiovascular health study).
- Published in:
- European Heart Journal, 2004, v. 25, n. 23, p. 2109, doi. 10.1016/j.ehj.2004.08.024
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- Publication type:
- Article
Association of RANTES G-403A gene polymorphism with increased risk of coronary arteriosclerosis.
- Published in:
- European Heart Journal, 2004, v. 25, n. 16, p. 1438, doi. 10.1016/j.ehj.2004.05.005
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- Publication type:
- Article
A mathematical model to estimate cholesterylester transfer protein (CETP) triglycerides flux in human plasma.
- Published in:
- BMC Systems Biology, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s12918-019-0679-x
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- Publication type:
- Article
Association of secreted frizzled-related protein 4 (SFRP4) with type 2 diabetes in patients with stable coronary artery disease
- Published in:
- Cardiovascular Diabetology, 2014, v. 13, n. 1, p. 155, doi. 10.1186/s12933-014-0155-2
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- Publication type:
- Article
Predictors and Prevalence of Paraganglioma Syndrome Associated With Mutations of the SDHC Gene.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 294, n. 16, p. 2057, doi. 10.1001/jama.294.16.2057
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- Publication type:
- Article
Identification of an apolipoprotein(e) variant associated with type III hyperlipoproteinaemia in an indigenous Australian.
- Published in:
- Annals of Clinical Biochemistry, 2001, v. 38, n. 1, p. 46, doi. 10.1258/0004563011900272
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- Publication type:
- Article
Age-Related Penetrance of Hereditary Atypical Hemolytic Uremic Syndrome.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 6, p. 639, doi. 10.1111/j.1469-1809.2011.00671.x
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- Publication type:
- Article
Epidemiological Approach to Identifying Genetic Predispositions for Atypical Hemolytic Uremic Syndrome.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 1, p. 17, doi. 10.1111/j.1469-1809.2009.00554.x
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- Publication type:
- Article
Towards a More Personalized Treatment of Dyslipidemias to Prevent Cardiovascular Disease.
- Published in:
- Current Cardiology Reports, 2018, v. 20, n. 7, p. 1, doi. 10.1007/s11886-018-0996-5
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- Publication type:
- Article
Vitamin D and Mortality: A Mendelian Randomization Study.
- Published in:
- Clinical Chemistry, 2013, v. 59, n. 5, p. 793, doi. 10.1373/clinchem.2012.193185
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- Publication type:
- Article
J-shaped association between circulating apoC-III and cardiovascular mortality.
- Published in:
- European Journal of Preventive Cardiology, 2022, v. 29, n. 2, p. e68, doi. 10.1093/eurjpc/zwaa169
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- Publication type:
- Article
Lipoprotein-associated phospholipase A2 and outcome in patients with type 2 diabetes on haemodialysis.
- Published in:
- European Journal of Clinical Investigation, 2012, v. 42, n. 7, p. 693, doi. 10.1111/j.1365-2362.2011.02634.x
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- Publication type:
- Article
Research update for articles published in EJCI in 2009.
- Published in:
- European Journal of Clinical Investigation, 2011, v. 41, n. 11, p. 1149, doi. 10.1111/j.1365-2362.2011.02588.x
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- Publication type:
- Article
Association of theCYP3A5 A6986G (CYP3A5*3) polymorphism with saquinavir pharmacokinetics.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Endothelial venodilator response in carriers of genetic polymorphisms involved in NO synthesis and degradation.
- Published in:
- British Journal of Clinical Pharmacology, 2004, v. 58, n. 2, p. 169, doi. 10.1111/j.1365-2125.2004.02130.x
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- Publication type:
- Article
Subclinical inflammation, telomere shortening, homocysteine, vitamin B6, and mortality: the Ludwigshafen Risk and Cardiovascular Health Study.
- Published in:
- European Journal of Nutrition, 2020, v. 59, n. 4, p. 1399, doi. 10.1007/s00394-019-01993-8
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- Publication type:
- Article
Preserved recovery of cardiac function following ischemia-reperfusion in mice lacking SIRT3.
- Published in:
- Canadian Journal of Physiology & Pharmacology, 2016, v. 94, n. 1, p. 72, doi. 10.1139/cjpp-2015-0152
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- Publication type:
- Article
Lipoprotein Lipase Deficiency.
- Published in:
- Indian Journal of Pediatrics, 2021, v. 88, n. 2, p. 147, doi. 10.1007/s12098-020-03305-z
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- Publication type:
- Article
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002292
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- Publication type:
- Article
Alu- Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients.
- Published in:
- Human Mutation, 2009, v. 30, n. 5, p. 776, doi. 10.1002/humu.20948
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- Publication type:
- Article
Epidemiology of autosomal-dominant polycystic kidney disease: an in-depth clinical study for south-western Germany.
- Published in:
- Nephrology Dialysis Transplantation, 2013, v. 28, n. 6, p. 1472
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- Publication type:
- Article
Smoking, apolipoprotein E genotypes, and mortality (the Ludwigshafen RIsk and Cardiovascular Health study).
- Published in:
- European Heart Journal, 2013, v. 34, n. 17, p. 1298, doi. 10.1093/eurheartj/eht001
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- Publication type:
- Article
Molecular basis of type III hyperlipoproteinemia in Germany.
- Published in:
- Human Mutation, 1998, v. 11, n. 6, p. 417, doi. 10.1002/(SICI)1098-1004(1998)11:6<417::AID-HUMU1>3.0.CO;2-5
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- Publication type:
- Article
Gene expression analysis to identify mechanisms underlying heart failure susceptibility in mice and humans.
- Published in:
- Basic Research in Cardiology, 2018, v. 113, n. 1, p. 1, doi. 10.1007/s00395-017-0666-6
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- Publication type:
- Article
SIRT3 deficiency impairs mitochondrial and contractile function in the heart.
- Published in:
- Basic Research in Cardiology, 2015, v. 110, n. 4, p. 1, doi. 10.1007/s00395-015-0493-6
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- Publication type:
- Article