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European Heart Journal, ISSN 0195-668X, 2014, Volume 35, Issue 32, pp. 2146 - 2157
Journal Article
European Heart Journal, ISSN 0195-668X, 2015, Volume 36, Issue 36, pp. 2425 - 2437
Journal Article
Atherosclerosis, ISSN 0021-9150, 2015, Volume 241, Issue 1, pp. e37 - e37
Journal Article
Journal of Internal Medicine, ISSN 0954-6820, 2019
Severe hypertriglyceridemia (serum triglyceride >10 mmol/L) is implicated in ~9% of acute pancreatitis cases. Certain guidelines list severe... 
hypertriglyceridemia | pancreatitis | triglycerides | insulin | plasma exchange | plasmapheresis
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 09/2017, Volume 15, Issue 9, pp. 1834 - 1844
Essentials Elevated lipoproteinp(a) is an independent and causal risk factor for atherothrombotic diseases. rs3798220 (Ile/Met substitution in apo(a)... 
fibrinolysis | fibrin | blood coagulation | lipoprotein(a) | apoprotein(a) | MECHANISM | APO(A) | FIBRIN CLOT STRUCTURE | BINDING DOMAIN | ATHEROSCLEROSIS | GENETIC-VARIANTS | PLASMINOGEN ACTIVATION | RECOMBINANT APOLIPOPROTEIN(A) | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | CORONARY-ARTERY-DISEASE | GLU-PLASMINOGEN | Apoprotein(a) - genetics | Apoprotein(a) - blood | Humans | Middle Aged | Lipoprotein(a) - chemistry | Male | Structure-Activity Relationship | Fibrin - chemistry | Transfection | HEK293 Cells | Adult | Female | Lipoprotein(a) - blood | Thrombosis - blood | Genetic Predisposition to Disease | Oxidation-Reduction | Methionine | Molecular Dynamics Simulation | Recombinant Proteins - blood | Homozygote | Phenotype | Fibrinolysis - genetics | Blood Coagulation - genetics | Protein Conformation | Thrombosis - genetics | Polymorphism, Single Nucleotide | Fibrin - metabolism | Lipoprotein(a) - genetics | Apoprotein(a) - chemistry | Fibrin | Proteases | Analysis | Single nucleotide polymorphisms | Apolipoproteins | Coronary heart disease | Lipoprotein A | Risk factors | Aspirin | Proteinase | Coagulation | Cardiovascular disease | Mass spectroscopy | Population studies | Single-nucleotide polymorphism | Gene polymorphism | Fibrinolysis | Coronary artery disease | Lysis | Oxidation | Cardiovascular diseases | Heart diseases
Journal Article
Atherosclerosis, ISSN 0021-9150, 08/2019, Volume 287, pp. e68 - e68
Journal Article
Lancet Diabetes & Endocrinology, The, ISSN 2213-8587, 2014, Volume 2, Issue 8, pp. 655 - 666
Journal Article
Atherosclerosis, ISSN 0021-9150, 08/2018, Volume 275, pp. e98 - e98
Journal Article
Journal Article
Nature Cell Biology, ISSN 1465-7392, 2015, Volume 17, Issue 8, pp. 1074 - 1087
Defects in primary cilium biogenesis underlie the ciliopathies, a growing group of genetic disorders. We describe a whole-genome siRNA-based reverse genetics... 
JOUBERT-SYNDROME | RPGRIP1 | TRANSPORT | CENTRIOLE BIOGENESIS | PROTEIN | C-ELEGANS | MUTATIONS | PHOTORECEPTOR CELLS | MASTER REGULATOR | PRIMARY CILIA | CELL BIOLOGY | Humans | Pregnancy Proteins - genetics | Databases, Genetic | Suppressor Factors, Immunologic - genetics | Photoreceptor Cells - ultrastructure | Pregnancy Proteins - metabolism | Ellis-Van Creveld Syndrome - genetics | Cerebellum - abnormalities | Genetic Testing - methods | Suppressor Factors, Immunologic - metabolism | Membrane Proteins - deficiency | Transfection | RNA Interference | HEK293 Cells | Kidney Diseases, Cystic - genetics | Genomics - methods | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Caenorhabditis elegans - metabolism | Cilia - pathology | Caenorhabditis elegans - genetics | Membrane Proteins - genetics | Mice, Inbred C57BL | Abnormalities, Multiple | Genetic Markers | Eye Abnormalities - genetics | Cilia - metabolism | Zebrafish - genetics | Cilia - genetics | Mice, Knockout | Proteins - genetics | Caenorhabditis elegans - ultrastructure | Phenotype | Animals | Cerebellar Diseases - genetics | Ciliary Motility Disorders - pathology | Proteins - metabolism | Photoreceptor Cells - metabolism | Zebrafish - metabolism | Retina - abnormalities | High-Throughput Nucleotide Sequencing | Ciliary Motility Disorders - metabolism | Mutation | Ciliary Motility Disorders - genetics | RNA | Cilia and ciliary motion | Genetic research | Biosynthesis | Genetic aspects | Research | Gene expression | Properties | reverse genetics | cilia | ciliopathies | Joubert syndrome | whole-genome siRNA screen | Jeune syndrome
Journal Article