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Neuropsychopharmacology, ISSN 0893-133X, 05/2013, Volume 38, Issue 6, p. 985
  Depression has been associated with inflammation, and inflammation may both influence and interact with growth factors such as brain-derived neurotrophic... 
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 2008, Volume 40, Issue 2, pp. 217 - 224
Journal Article
Nature Protocols, ISSN 1754-2189, 01/2007, Volume 1, Issue 6, pp. 2701 - 2709
The noninvasive character of NMR spectroscopy, combined with the sensitivity of the chemical shift, makes it ideally suited to investigate the conformation,... 
VIVO | ESCHERICHIA-COLI | BIOCHEMICAL RESEARCH METHODS | OOCYTES | ALPHA-SYNUCLEIN | PROTEINS | EXTRACTS | LIVING CELLS | Isotope Labeling - methods | Animals | Macromolecular Substances - chemistry | Nuclear Magnetic Resonance, Biomolecular - methods | Xenopus laevis | Cells, Cultured | Ovum - chemistry | Escherichia coli - chemistry
Journal Article
Science, ISSN 0036-8075, 2/2000, Volume 287, Issue 5454, pp. 848 - 851
Hereditary paraganglioma (PGL) is characterized by the development of benign, vascularized tumors in the head and neck. The most common tumor site is the... 
Honey bees | Bee dances | Exons | Genes | Genomics | Alleles | Hypoxia | Reports | Genetic mutation | Chromosomes | Tumors | CELLS | HEAD | CHROMOSOME 11Q23 | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | NECK REGION | SUCCINATE-UBIQUINONE OXIDOREDUCTASE | CAROTID-BODY CHEMORECEPTORS | HYPOXIA | HYPERPLASIA | HIGH-ALTITUDES | Haplotypes | Genomic Imprinting | Humans | Molecular Sequence Data | Multienzyme Complexes - metabolism | Carotid Body Tumor - metabolism | Succinate Dehydrogenase - chemistry | Mutation, Missense | Loss of Heterozygosity | Oxidoreductases - chemistry | Carotid Body - metabolism | Cytochrome b Group - metabolism | Electron Transport Complex II | Polymorphism, Single-Stranded Conformational | Germ-Line Mutation | Genetic Linkage | Amino Acid Sequence | Oxidoreductases - metabolism | Oxidoreductases - genetics | Paraganglioma - genetics | Chromosomes, Human, Pair 11 - genetics | Mitochondria - metabolism | Multienzyme Complexes - genetics | Carotid Body Tumor - genetics | Cytochrome b Group - genetics | Multienzyme Complexes - chemistry | Succinate Dehydrogenase - genetics | Paraganglioma - metabolism | Heterozygote | Succinate Dehydrogenase - metabolism | Cytochrome b Group - chemistry | Genetic disorders | Research | Mutation (Biology) | Proteins | Oxygen | Mutation | SBHD gene | carotid body | cybS protein | cytochrome b | paraganglioma
Journal Article
by Helgadottir, Anna, MD, PhD and Gretarsdottir, Solveig, PhD and Thorleifsson, Gudmar, PhD and Holm, Hilma, MD and Patel, Riyaz S., MD and Gudnason, Thorarinn, MD, PhD and Jones, Gregory T., PhD and van Rij, Andre M., MD and Eapen, Danny J., MD and Baas, Annette F., PhD and Tregouet, David-Alexandre, PhD and Morange, Pierre-Emmanuel, MD and Emmerich, Joseph, MD, PhD and Lindblad, Bengt, MD, PhD and Gottsäter, Anders, MD, PhD and Kiemeny, Lambertus A., PhD and Lindholt, Jes S., MD, PhD and Sakalihasan, Natzi, MD, PhD and Ferrell, Robert E., PhD and Carey, David J., PhD and Elmore, James R., MD and Tsao, Philip S., PhD and Grarup, Niels, MD, PhD and Jørgensen, Torben, MD, DMSci and Witte, Daniel R., MD, PhD and Hansen, Torben, MD, PhD and Pedersen, Oluf, MD, DMSci and Pola, Roberto, MD, PhD and Gaetani, Eleonora, MD and Magnadottir, Hulda B., MD and Wijmenga, Cisca, PhD and Tromp, Gerard, PhD and Ronkainen, Antti, MD, PhD and Ruigrok, Ynte M., MD and Blankensteijn, Jan D and Mueller, Thomas, MD and Wells, Philip S., MD and Corral, Javier, PhD and Soria, Jose Manuel, PhD and Souto, Juan Carlos, MD, PhD and Peden, John F., PhD and Jalilzadeh, Shapour, MD, PhD and Mayosi, Bongani M., DPhil and Keavney, Bernard, MD and Strawbridge, Rona J., PhD and Sabater-Lleal, Maria, PhD and Gertow, Karl, PhD and Baldassarre, Damiano, PhD and Nyyssönen, Kristiina, PhD and Rauramaa, Rainer, MD, PhD and Smit, Andries J., MD, PhD and Mannarino, Elmo, MD and Giral, Philippe, MD and Tremoli, Elena, PhD and de Faire, Ulf, MD, PhD and Humphries, Steve E., PhD and Hamsten, Anders, MD, PhD and Haraldsdottir, Vilhelmina, MD and Olafsson, Isleifur, MD, PhD and Magnusson, Magnus K., MD and Samani, Nilesh J., MD and Levey, Allan I., MD, PhD and Markus, Hugh S., MD and Kostulas, Konstantinos, MD, PhD and Dichgans, Martin, MD and Berger, Klaus, MD and Kuhlenbäumer, Gregor, MD and Ringelstein, E. Bernd, MD and Stoll, Monika, PhD and Seedorf, Udo, PhD and Rothwell, Peter M., MD, PhD and Powell, Janet T., MD and Kuivaniemi, Helena, MD, PhD and Onundarson, Pall T., MD and Valdimarsson, Einar, MD and Matthiasson, Stefan E., MD, PhD and Gudbjartsson, Daniel F., PhD and Thorgeirsson, Guðmundur, MD, PhD and Quyyumi, Arshed A., MD and Watkins, Hugh, MD, PhD and Farrall, Martin, MD and Thorsteinsdottir, Unnur, PhD and Stefansson, Kari, MD, PhD and Lund University and Vascular Diseases - Clinical Research and Vaskulära sjukdomar - kliniska studier and Lunds universitet
Journal of the American College of Cardiology, ISSN 0735-1097, 08/2012, Volume 60, Issue 8, pp. 722 - 729
Objectives The purpose of this study is investigate the effects of variants in the apolipoprotein(a) gene ( LPA ) on vascular diseases with different... 
Cardiovascular | Internal Medicine | atherosclerosis | genetic | association | thrombosis | lipoprotein(a) | INTIMA-MEDIA THICKNESS | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK-FACTORS | METAANALYSIS | MYOCARDIAL-INFARCTION | VASCULAR-DISEASE | WOMEN | PERIPHERAL ARTERIAL-DISEASE | ISCHEMIC-STROKE | SEVERITY | Severity of Illness Index | Myocardial Infarction - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Apolipoproteins A - genetics | Angiography | Carotid Intima-Media Thickness | Intracranial Aneurysm - genetics | Atherosclerosis - genetics | Humans | Risk Factors | Brain Ischemia - genetics | African Americans - genetics | Linear Models | Logistic Models | Aortic Aneurysm, Abdominal - genetics | Stroke - genetics | Venous Thromboembolism - genetics | Peripheral Arterial Disease - genetics | Age of Onset | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Medical colleges | Neurosciences | Stock options | Genes | Aneurysms | Coronary heart disease | Biometry | Lipoprotein A | Anopheles | Atherosclerosis | Medical genetics | Genetic research | Genetic aspects | Diabetes | Thromboembolism | Cardiology | Public health | Dementia | Stroke | Medical imaging | Values | Cardiovascular disease | Apolipoproteins | Thrombosis | Studies | Confidence intervals | Coronary vessels | Blood pressure | Drug therapy | Age | Methods | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article