Found: 20
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Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.
- Published in:
- Movement Disorders, 2011, v. 26, n. 3, p. 516, doi. 10.1002/mds.23459
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- Article
Scoring the correlation of genes by their shared properties using OScal, an improved overlap quantification model.
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- Scientific Reports, 2015, p. 10583, doi. 10.1038/srep10583
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- Publication type:
- Article
Angiotensin II increases angiogenesis by NF-κB-mediated transcriptional activation of angiogenic factor AGGF1.
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- FASEB Journal, 2018, v. 32, n. 9, p. 5051, doi. 10.1096/fj.201701543RR
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- Article
Identification of a new adtrp1-tfpi regulatory axis for the specification of primitive myelopoiesis and definitive hematopoiesis.
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- FASEB Journal, 2018, v. 32, p. 183, doi. 10.1096/fj.201700166RR
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- Publication type:
- Article
Identification of a new adtrp1-tfpi regulatory axis for the specification of primitive myelopoiesis and definitive hematopoiesis.
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- FASEB Journal, 2018, v. 32, n. 1, p. 183, doi. 10.1096/fj.201700166RR
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- Publication type:
- Article
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 660, doi. 10.1038/jhg.2009.92
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- Publication type:
- Article
Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery disease.
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- Human Molecular Genetics, 2012, v. 21, n. 6, p. 1364, doi. 10.1093/hmg/ddr574
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- Publication type:
- Article
Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm.
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- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0310-6
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- Publication type:
- Article
Ubiquitination-activating enzymes UBE1 and UBA6 regulate ubiquitination and expression of cardiac sodium channel Na<sup>v</sup>1.5.
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- Biochemical Journal, 2020, v. 477, n. 9, p. 1683, doi. 10.1042/BCJ20200138
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- Publication type:
- Article
A novel mutation in the ATP2C1 gene is associated with Hailey–Hailey disease in a Chinese family.
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- International Journal of Dermatology, 2009, v. 48, n. 1, p. 47, doi. 10.1111/j.1365-4632.2009.03878.x
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- Publication type:
- Article
Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population.
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- Annals of Human Genetics, 2011, v. 75, n. 4, p. 475, doi. 10.1111/j.1469-1809.2011.00646.x
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- Publication type:
- Article
CADgene: a comprehensive database for coronary artery disease genes.
- Published in:
- Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D991, doi. 10.1093/nar/gkq1106
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- Publication type:
- Article
Additive effect of LRP8/APOER2 R952Q variant to APOE ε2/ε3/ε4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study.
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- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-41
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- Publication type:
- Article
Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-24
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- Publication type:
- Article
Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation.
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- Human Mutation, 2019, v. 40, n. 3, p. 310, doi. 10.1002/humu.23691
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- Publication type:
- Article
Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies.
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- 2020
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- Publication type:
- journal article
De Novo (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia.
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- 2017
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- Publication type:
- journal article
Haploinsufficiency of Klippel-Trenaunay syndrome gene Aggf1 inhibits developmental and pathological angiogenesis by inactivating PI3K and AKT and disrupts vascular integrity by activating VE-cadherin.
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- Human Molecular Genetics, 2016, v. 25, n. 23, p. 5094, doi. 10.1093/hmg/ddw273
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- Publication type:
- Article
Angiogenic Factor AGGF1 Activates Autophagy with an Essential Role in Therapeutic Angiogenesis for Heart Disease.
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- PLoS Biology, 2016, v. 14, n. 8, p. 1, doi. 10.1371/journal.pbio.1002529
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- Publication type:
- Article
Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
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- Journal of Clinical Periodontology, 2009, v. 36, n. 8, p. 627, doi. 10.1111/j.1600-051X.2009.01438.x
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- Publication type:
- Article