| scholarly article | Q13442814 |
| P356 | DOI | 10.1080/09537104.2016.1203404 |
| P698 | PubMed publication ID | 27533483 |
| P50 | author | Marek Postula | Q60973643 |
| Michał Karlinski | Q82428328 | ||
| Shigekazu Sugino | Q99415638 | ||
| Ceren Eyileten | Q42207116 | ||
| Dagmara Mirowska-Guzel | Q42305532 | ||
| P2093 | author name string | Piotr K Janicki | |
| Lukasz Milanowski | |||
| Yuka Imamura | |||
| Justyna Pordzik | |||
| Anna Czlonkowka | |||
| Iwona Kurkowska-Jastrzebka | |||
| Marta Solarska | |||
| Pawel Wylezol | |||
| P2860 | cites work | Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment | Q22306370 |
| The GAPs, GEFs, and GDIs of heterotrimeric G-protein alpha subunits | Q24810130 | ||
| Stroke genetics: prospects for personalized medicine | Q27006885 | ||
| Association of a functional polymorphism in the clopidogrel target receptor gene, P2Y12, and the risk for ischemic cerebrovascular events in patients with peripheral artery disease | Q28176445 | ||
| Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction | Q28239724 | ||
| Systematic evaluation of apoptotic pathway gene polymorphisms and lung cancer risk | Q28391725 | ||
| Cellular regulation of RGS proteins: modulators and integrators of G protein signaling | Q28646133 | ||
| A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke | Q28943400 | ||
| ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data | Q29547161 | ||
| Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits | Q29614876 | ||
| Genetic association studies in stroke: methodological issues and proposed standard criteria | Q30997149 | ||
| Polymorphisms of protein tyrosine phosphatase CD148 influence FcγRIIA-dependent platelet activation and the risk of heparin-induced thrombocytopenia | Q33401678 | ||
| The Stroke Data Bank: design, methods, and baseline characteristics | Q33459915 | ||
| A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease | Q33596843 | ||
| The PlA1/A2 polymorphism of glycoprotein IIIa as a risk factor for stroke: a systematic review and meta-analysis | Q33836873 | ||
| Polymorphism in Integrin ITGA2 is Associated with Ischemic Stroke and Altered Serum Cholesterol in Chinese Individuals | Q33974267 | ||
| VarScan: variant detection in massively parallel sequencing of individual and pooled samples | Q34018143 | ||
| Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations | Q34304320 | ||
| Thinking outside of the "RGS box": new approaches to therapeutic targeting of regulators of G protein signaling. | Q34310119 | ||
| Stroke genetics: a review and update | Q34357593 | ||
| The first comprehensive and quantitative analysis of human platelet protein composition allows the comparative analysis of structural and functional pathways | Q34368551 | ||
| Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function | Q34374101 | ||
| Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists | Q34674600 | ||
| Genetics of ischemic stroke. | Q35008517 | ||
| Phosphatidylinositol-3-kinase gamma plays a central role in blood-brain barrier dysfunction in acute experimental stroke | Q35086740 | ||
| Infections and ischemic stroke outcome. | Q35101646 | ||
| Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders | Q35105533 | ||
| The genetics of common variation affecting platelet development, function and pharmaceutical targeting | Q35149898 | ||
| Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children. | Q35193732 | ||
| Polymorphism in the protease‐activated receptor‐4 gene region associates with platelet activation and perioperative myocardial injury | Q35212303 | ||
| Genetic variation of platelet function and pharmacology: An update of current knowledge | Q50965674 | ||
| The GNB3 C825T polymorphism influences platelet aggregation in human whole blood. | Q51389072 | ||
| Purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene is associated with cerebral infarction in Japanese subjects | Q51614190 | ||
| Association of the platelet glycoprotein IIb HPA-3 polymorphism with survival after acute ischemic stroke | Q52864845 | ||
| Genetic polymorphism of ITGA2 C807T can increase the risk of ischemic stroke | Q53133652 | ||
| An intronic polymorphism in the PAR-1 gene is associated with platelet receptor density and the response to SFLLRN. | Q53857090 | ||
| Platelet glycoprotein Ia C807T, Ib C3550T, and IIIa Pl(A1/A2) polymorphisms and ischemic stroke in young Taiwanese. | Q54693137 | ||
| New single nucleotide polymorphisms associated with differences in platelets reactivity in patients with type 2 diabetes treated with acetylsalicylic acid: genome-wide association approach and pooled DNA strategy. | Q55056757 | ||
| Predictive role of polymorphisms in interleukin-5 receptor alpha-subunit, lipoprotein lipase, integrin A2 and nitric oxide synthase genes on ischemic stroke in type 2 diabetes—An 8-year prospective cohort analysis of 1327 Chinese patients | Q58209563 | ||
| Genome-wide RNA-seq analysis of human and mouse platelet transcriptomes. | Q35346534 | ||
| Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke | Q35611174 | ||
| A newly identified complex of spinophilin and the tyrosine phosphatase, SHP-1, modulates platelet activation by regulating G protein-dependent signaling. | Q35802247 | ||
| New gene variants associated with venous thrombosis: a replication study in White and Black Americans | Q35939912 | ||
| Modulating platelet reactivity through control of RGS18 availability. | Q36350447 | ||
| Genetics of ischaemic stroke | Q36713912 | ||
| Pharmacogenetics of aspirin resistance: a comprehensive systematic review | Q37145122 | ||
| Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association | Q37251490 | ||
| Endothelial dysfunction, vascular disease and stroke: the ARTICO study. | Q37431225 | ||
| ANKS1B is a smoking-related molecular alteration in clear cell renal cell carcinoma. | Q37621806 | ||
| The genetics of ischaemic stroke | Q37696582 | ||
| The role of platelets in athero-thrombotic events | Q38020856 | ||
| Protein tyrosine phosphatase σ in proteoglycan-mediated neural regeneration regulation | Q38041489 | ||
| Statistical power and significance testing in large-scale genetic studies | Q38205106 | ||
| Common genetic variants in platelet surface receptors and its association with ischemic stroke | Q38857206 | ||
| An intronic polymorphism of IRF4 gene influences gene transcription in vitro and shows a risk association with childhood acute lymphoblastic leukemia in males | Q39777738 | ||
| Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. | Q40469466 | ||
| The intronic prothrombin 19911A>G polymorphism influences splicing efficiency and modulates effects of the 20210G>A polymorphism on mRNA amount and expression in a stable reporter gene assay system | Q40632496 | ||
| Chronic cold exposure increases RGS7 expression and decreases alpha(2)-autoreceptor-mediated inhibition of noradrenergic locus coeruleus neurons | Q40828336 | ||
| wANNOVAR: annotating genetic variants for personal genomes via the web | Q42129589 | ||
| Copy number analysis of the murine platelet proteome spanning the complete abundance range | Q42209721 | ||
| A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke | Q44103563 | ||
| Cooperative effect of GNB3 825C>T and GPIIIa PI(A) polymorphisms in enhanced platelet aggregation. | Q44485366 | ||
| Association between common genetic variants of α2A-, α2B-, and α2C-adrenergic receptors and ischemic stroke | Q44501770 | ||
| Collagen platelet receptor polymorphisms integrin alpha2beta1 C807T and GPVI Q317L and risk of ischemic stroke | Q45863839 | ||
| A functional genomics approach reveals novel quantitative trait loci associated with platelet signaling pathways. | Q46017492 | ||
| Association of polymorphisms in thromboxane A2 receptor and thromboxane A synthase 1 with cerebral infarction in a Korean population. | Q46031916 | ||
| Heritability of platelet function in families with premature coronary artery disease | Q46213168 | ||
| 5-Hydroxytryptamine-2A receptor gene (HTR 2 A) candidate polymorphism (T 102 C): Role for human platelet function under pharmacological challenge ex vivo | Q46717097 | ||
| PAR-1 genotype influences platelet aggregation and procoagulant responses in patients with coronary artery disease prior to and during clopidogrel therapy | Q46728502 | ||
| 807C/T polymorphism in the platelet glycoprotein Ia gene in young patients with ischemic stroke of undetermined etiology | Q46985213 | ||
| A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males | Q47390992 | ||
| Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: a novel finding | Q48196812 | ||
| Association of the 5-HT2A receptor gene polymorphism 102T/C with ischemic stroke | Q48221476 | ||
| Endothelial and platelet activation in acute ischemic stroke and its etiological subtypes | Q48231105 | ||
| The Pl(A1/A2) polymorphism of glycoprotein IIIa and cerebrovascular events in hypertension: increased risk of ischemic stroke in high-risk patients. | Q48284904 | ||
| Determinants of platelet-leukocyte aggregation and platelet activation in stroke | Q48308401 | ||
| Smoking and the platelet fibrinogen receptor glycoprotein IIb/IIIA PlA1/A2 polymorphism interact in the risk of lacunar stroke and midterm survival | Q48351043 | ||
| Integrin, alpha 2 gene C807T polymorphism and risk of ischemic stroke: a meta-analysis | Q48479230 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 66-73 | |
| P577 | publication date | 2016-08-17 | |
| P1433 | published in | Platelets | Q1573582 |
| P1476 | title | Association of frequent genetic variants in platelet activation pathway genes with large-vessel ischemic stroke in Polish population | |
| P478 | volume | 28 |
| Q47342183 | Association of miR-21, miR-126 and miR-605 gene polymorphisms with ischemic stroke risk |
| Q47302148 | Population-Specific Associations of Deleterious Rare Variants in Coding Region of P2RY1-P2RY12 Purinergic Receptor Genes in Large-Vessel Ischemic Stroke Patients. |
| Q99566602 | The Relation of the Brain-Derived Neurotrophic Factor with MicroRNAs in Neurodegenerative Diseases and Ischemic Stroke |
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