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European heart journal, ISSN 0195-668X, 2010, Volume 31, Issue 23, pp. 2844 - 2853
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2008, Volume 105, Issue 35, pp. 13051 - 13056
Idiopathic interstitial pneumonias (IIPs) have a progressive and often fatal course, and their enigmatic etiology has complicated approaches to effective... 
Telomeres | Pulmonary alveoli | Lungs | Interstitial lung diseases | Idiopathic pulmonary fibrosis | Liver | Fibrosis | Dyskeratosis congenita | Genetic mutation | Liver cirrhosis | Liver fibrosis | Interstitial lung disease | Telomerase | Aplastic anemia | RNA | MULTIDISCIPLINARY SCIENCES | DOMINANT DYSKERATOSIS-CONGENITA | REVERSE-TRANSCRIPTASE | LENGTH | IN-SITU HYBRIDIZATION | TERMINAL TRANSFERASE | liver fibrosis | dyskeratosis congenita | telomerase | GENE | interstitial lung disease | FAMILIES | aplastic anemia | MUTATIONS | APLASTIC-ANEMIA | Biomarkers - metabolism | Leukocytes, Mononuclear - metabolism | Epithelium - pathology | Pulmonary Alveoli - pathology | Pulmonary Fibrosis - complications | Fibrosis - complications | Humans | Risk Factors | In Situ Hybridization, Fluorescence | Tomography, X-Ray Computed | Pulmonary Fibrosis - genetics | Pulmonary Fibrosis - pathology | Case-Control Studies | RNA - genetics | Fibrosis - diagnostic imaging | Telomerase - genetics | Pulmonary Fibrosis - diagnostic imaging | Germ-Line Mutation | Family | Heterozygote | Telomere - metabolism | Fibrosis - pathology | Genetic aspects | Pulmonary fibrosis | Properties | Health aspects | Risk factors | Tissue | Leucocytes | Pneumonia | Mutation | Chromosomes | Deoxyribonucleic acid--DNA | Epithelial cells | Lung | Lung diseases | Heredity | Leukocytes | Cirrhosis | Etiology | telomerase reverse transcriptase | Alveoli | Age | Biological Sciences
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2013, Volume 61, Issue 4, pp. 427 - 436
Objectives The aim of this study was to test the hypothesis that elevated nonfasting remnant cholesterol is a causal risk factor for ischemic heart disease... 
Cardiovascular | Internal Medicine | atherosclerosis | cardiovascular disease | lipoproteins | myocardial infarction | CARDIAC & CARDIOVASCULAR SYSTEMS | MYOCARDIAL-INFARCTION | PREDICTIVE-VALUE | MENDELIAN RANDOMIZATION | PARTICLE CHOLESTEROL | DIABETES-MELLITUS | DENSITY-LIPOPROTEIN CHOLESTEROL | NONFASTING TRIGLYCERIDES | CARDIOVASCULAR-DISEASE | HDL CHOLESTEROL | CORONARY-ARTERY-DISEASE | Myocardial Ischemia - genetics | Myocardial Ischemia - metabolism | Lipoproteins, HDL - genetics | Humans | Middle Aged | Risk Factors | Lipoproteins, HDL - metabolism | Genotype | Male | Data Collection | Cholesterol - metabolism | Cholesterol - genetics | Genetic Variation - physiology | Triglycerides - metabolism | Time Factors | Denmark - epidemiology | Female | Aged | Triglycerides - genetics | Causality | Odds Ratio | Myocardial Ischemia - epidemiology | Analysis and chemistry | Blood cholesterol | Low density lipoproteins | Atherosclerosis | Myocardial ischemia | Universities and colleges | Heart attack | Risk factors | Blood | Cholesterol | Heart | Lipoproteins (low density) | Cardiovascular disease | Density | Confidence intervals | Variables | Randomization | Ischemia | Population | Blood pressure | Heart diseases | Lipoproteins (high density) | Age | Deoxyribonucleic acid--DNA | Hypertension | Enzymes | Health risks | Triglycerides | Risk analysis | Apolipoproteins | Low density lipoprotein | Coronary artery disease | Studies | Genetic variance | Lipoproteins | Diabetes | Cardiovascular diseases
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2007, Volume 357, Issue 7, pp. 639 - 647
Journal Article
Journal Article
by Williams Amy, A.L and Jacobs Suzanne, S.B.R and Moreno-Macías, Hortensia and Huerta-Chagoya, Alicia and Churchhouse, Claire and Márquez-Luna, Carla and Gómez-Vázquez, María José and Burtt Noël, N.P and Aguilar-Salinas, Carlos A and González-Villalpando, Clicerio and Florez, Jose C and Orozco, Lorena and Tusié-Luna, Teresa and Altshuler, David and Ripke, Stephan and Manning, Alisa K and García-Ortíz, Humberto and Neale, Benjamin and Reich, David and Stram, Daniel O and Fernández-López, Juan Carlos and Romero-Hidalgo, Sandra and Patterson, Nick and Haiman, Christopher A and Aguilar-Delfín, Irma and Martínez-Hernández, Angélica and Centeno-Cruz, Federico and Mendoza-Caamal, Elvia and Revilla-Monsalve, Cristina and Islas-Andrade, Sergio and Córdova, Emilio and Rodríguez-Arellano, Eunice and Soberón, Xavier and Florez Jose, J.C and González-Villalpando María Elena, M.A and Henderson, Brian E and Monroe, Kristine and Wilkens, Lynne and Kolonel, Laurence N and Le Marchand, Loic and Riba, Laura and Ordóñez-Sánchez María Luisa, M.A and Rodríguez-Guillén, Rosario and Cruz-Bautista, Ivette and Rodríguez-Torres, Maribel and Muñoz-Hernández, Linda Liliana and Sáenz, Tamara and Gómez, Donají and Alvirde, Ulices and Onofrio, Robert C and Brodeur, Wendy M and Gage, Diane and Murphy, Jacquelyn and Franklin, Jennifer and Mahan, Scott and Ardlie, Kristin and Crenshaw, Andrew T and Winckler, Wendy and Prüfer, Kay and Shunkov, Michael V and Sawyer, Susanna and Stenzel, Udo and Kelso, Janet and Lek, Monkol and Sankararaman, Sriram and MacArthur, Daniel G and Derevianko, Anatoli P and Pääbo, Svante and Jacobs, Suzanne B.R and Gopal, Shuba and Grammatikos, James A and Smith, Ian C and Bullock, Kevin H and Deik, Amy A and Souza, Amanda L and Pierce, Kerry A and Clish, Clary B and Fennell, Timothy and Farjoun, Yossi and Gabriel, Stacey and Gross, Myron D and Pereira, Mark A and Seielstad, Mark and Koh, Woon-Puay and Tai, E-Shyong and Flannick, Jason and Fontanillas, Pierre and Morris, Andrew and Teslovich, Tanya M and Atzmon, Gil and Blangero, John and Bowden, Donald W and Chambers, John and Cho, Yoon Shin and Duggirala, Ravindranath and Glaser, Benjamin and Hanis, Craig and Kooner, Jaspal and Laakso, Markku and Lee, Jong-Young and ... and SIGMA Type 2 Diabet Consortium and Broad Genomics Platform and T2D-GENES Consortium and SIGMA Type 2 Diabetes Consortium and The SIGMA Type 2 Diabetes Consortium
Nature, ISSN 0028-0836, 2014, Volume 506, Issue 7486, pp. 97 - 101
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2007, Volume 39, Issue 8, pp. 954 - 956
Variants on chromosome 8q24 contribute risk for prostate cancer; here, we tested whether they also modulate risk for colorectal cancer. We studied 1,807... 
OCT4 |