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The New England Journal of Medicine, ISSN 0028-4793, 04/2009, Volume 360, Issue 17, pp. 1729 - 1739
Journal Article
Stroke, ISSN 0039-2499, 12/2003, Volume 34, Issue 12, pp. 2887 - 2892
Journal Article
Neuropathology and Applied Neurobiology, ISSN 0305-1846, 02/2011, Volume 37, Issue 1, pp. 94 - 113
Y. Yamamoto, L. Craggs, M. Baumann, H. Kalimo and R. N. Kalaria (2011) Neuropathology and Applied Neurobiology37, 94–113
Molecular genetics and pathology of... 
leukoencephalopathy | small vessel disease | white matter | CADASIL | cognitive impairment | stroke | Stroke | Small vessel disease | Leukoencephalopathy | White matter | Cognitive impairment | Leukoencephalopathies - pathology | Leukoencephalopathies - genetics | CADASIL - pathology | Capillaries - pathology | Molecular Biology | Humans | Receptors, Notch - physiology | Receptors, Notch - genetics | Signal Transduction - genetics | Cerebral Infarction - genetics | Mutation - genetics | CADASIL - genetics | Retinal Vessels - pathology | Mutation - physiology | Animals | Cerebral Arterial Diseases - genetics | Brain - pathology | Collagen Type IV - genetics | Receptor, Notch3 | Cerebrovascular Disorders - genetics | Cerebrovascular Disorders - pathology | Cerebral Arterial Diseases - pathology | Cerebral Infarction - pathology | Enzymes | Molecular genetics | Collagen | Thrombin | Genetic aspects | Ophthalmology | Universities and colleges | Brain | Retinopathy | Arterioles | Neuropathology | Central nervous system | Cognitive ability | Nervous system | Retina | Smooth muscle | Transforming growth factor- beta | Hemorrhage | Arteries | Vascular diseases | Neurodegeneration | Extracellular matrix | Collagen (type IV) | Children | Leukodystrophy | exonuclease | Substantia alba | Reviews | Fibrosis | Microvasculature | Serine proteinase | Mutation | Notch3 protein
Journal Article
Journal Article
Journal of Stroke and Cerebrovascular Diseases, ISSN 1052-3057, 2017, Volume 26, Issue 5, pp. 1128 - 1135
Journal Article
European Journal of Clinical Pharmacology, ISSN 0031-6970, 10/2017, Volume 73, Issue 10, pp. 1261 - 1269
DNA methylation typically acts to repress gene transcription. ABCB1 is involved in the intestinal absorption of aspirin. We aimed to investigate the impact of... 
Salicylic acid | Aspirin | Thromboelastography | Biomedicine | ABCB1 | Ischemic events | Pharmacology/Toxicology | Methylation | ACETYLSALICYLIC-ACID | CYP2C19 GENOTYPE | GENETIC POLYMORPHISMS | RANDOMIZED-TRIALS | DNA METHYLATION | TRANSIENT ISCHEMIC ATTACK | ANTIPLATELET THERAPY | IMPLEMENTATION CONSORTIUM GUIDELINES | CLOPIDOGREL THERAPY | PERCUTANEOUS CORONARY INTERVENTION | PHARMACOLOGY & PHARMACY | Intracranial Arterial Diseases - prevention & control | Thrombelastography | Humans | Aspirin - pharmacokinetics | DNA Methylation - genetics | Arterial Occlusive Diseases - genetics | Promoter Regions, Genetic - genetics | Case-Control Studies | Aspirin - therapeutic use | Intracranial Arterial Diseases - genetics | Platelet Aggregation Inhibitors - pharmacokinetics | Arterial Occlusive Diseases - prevention & control | Platelet Aggregation Inhibitors - therapeutic use | ATP Binding Cassette Transporter, Sub-Family B - genetics | Stroke (Disease) | Medical research | Patient outcomes | Stenosis | Medicine, Experimental | Myocardial infarction | Transcription | Arachidonic acid | Clinical outcomes | Absorption | Ischemia | Blood platelets | Mathematical analysis | Intestine | DNA methylation | Intestinal absorption | Deoxyribonucleic acid--DNA | CpG islands | Cerebral infarction | Stroke | Cut-off | Exposure | Patients | Transit | Studies | Acids | Correlation analysis | Alleles | Infarction | Diagnostic systems | Platelets | Veins & arteries
Journal Article