Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP131196.RAS0DRS5u4vHH5qOjgafPzgVao2kP7ANLxQ5Ey70Vypp8130_assertion description "[mutations/variants of SPINK1 gene with or without cystic fibrosis transmembrane conductance regulator gene may confer a high risk for recurrent pancreatitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131196.RAS0DRS5u4vHH5qOjgafPzgVao2kP7ANLxQ5Ey70Vypp8130_provenance.
- NP131199.RAdXnoJuwV6cJ6Pl8LqhwFdVFmUCPM-Pf1khEr1GpkqA4130_assertion description "[Decreased arylsulfatase B activity is associated with cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131199.RAdXnoJuwV6cJ6Pl8LqhwFdVFmUCPM-Pf1khEr1GpkqA4130_provenance.
- NP131203.RAa1XE0Ivpi4a8o--kLAggWUOBxOrA4_PO2MwdLJvDNp4130_assertion description "[Serum VDBP can be considered a nutritional marker for lipids in cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131203.RAa1XE0Ivpi4a8o--kLAggWUOBxOrA4_PO2MwdLJvDNp4130_provenance.
- NP131207.RAanEo8Gxx8eshwRDmmswUW3wrPRvqxda4WKTnSRSPb8E130_assertion description "[Gilbert UGT1A1 allele increases the risk of gallstone formation in cystic fibrosis (CF)/and exogenous sources contributing to hyperbilirubinbilia might be lithogenic in CF patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131207.RAanEo8Gxx8eshwRDmmswUW3wrPRvqxda4WKTnSRSPb8E130_provenance.
- NP131213.RAXxg4OfIXMCLvfMm8UvCfHZgXjPhauysczhfETbs5Ul0130_assertion description "[potential mechanism for reduced NOS2 expression in cystic fibrosis is diminished signal transducer and activator of transcription-1 (STAT1) activity, possibly due to an increase in expression of protein inhibitor of activated STAT1 (PIAS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131213.RAXxg4OfIXMCLvfMm8UvCfHZgXjPhauysczhfETbs5Ul0130_provenance.
- NP131229.RASx_PgqDFVHdB9g38TKVudqLOGB9M_Llv7q1zfnwXX60130_assertion description "[The BclI polymorphism may modulate the inflammatory burden in the cystic fibrosis lung and in this way influence progression of lung function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131229.RASx_PgqDFVHdB9g38TKVudqLOGB9M_Llv7q1zfnwXX60130_provenance.
- NP131231.RATuNzd7hciot_mMtb3j8YPXTBUgmqh9LciS95ymIB8gI130_assertion description "[polymorphic in cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131231.RATuNzd7hciot_mMtb3j8YPXTBUgmqh9LciS95ymIB8gI130_provenance.
- NP131236.RAQ8rOb8DfJF1b9qeV3pUVZehvDgkU3dWHqgxLplNu6pU130_assertion description "[prostasin is a major regulator of ENaC-mediated Na+ current in DeltaF508 cystic fibrosis epithelia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131236.RAQ8rOb8DfJF1b9qeV3pUVZehvDgkU3dWHqgxLplNu6pU130_provenance.
- NP131244.RAfqcxfdtZ7MhCqywaGKM7y31XhwasNfpP0_DU9f04wkw130_assertion description "[IL-31 acts on a broad range of immune- & non-immune cells & possesses potential pleiotropic physiological functions, including regulating hematopoiesis & immune response, causing inflammatory bowel disease, airway hypersensitivity & dermatitis [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131244.RAfqcxfdtZ7MhCqywaGKM7y31XhwasNfpP0_DU9f04wkw130_provenance.
- NP131245.RAfYjbUKkK5GSUxxW9QqmROQXV0Q4mg3p7DKm37bOZhOc130_assertion description "[a gain-of-function mutation of JAK may explain the hypersensitivity of polycythemia vera progenitor cells to growth factors and cytokines ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131245.RAfYjbUKkK5GSUxxW9QqmROQXV0Q4mg3p7DKm37bOZhOc130_provenance.
- NP131246.RAfYRkkJdZVZtgK2GTDwQHiOSubG4hGjITdgCYw-FQ3_I130_assertion description "[role in Aspergillus mediated allergies and infections ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131246.RAfYRkkJdZVZtgK2GTDwQHiOSubG4hGjITdgCYw-FQ3_I130_provenance.
- NP131247.RAY1QRafosBeI7E01g_GvDJYW-IAvqbvWiO4FLDMpB6iI130_assertion description "[PAR2 may be an important regulator of skin mast cell function during cutaneous inflammation and hypersensitivity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131247.RAY1QRafosBeI7E01g_GvDJYW-IAvqbvWiO4FLDMpB6iI130_provenance.
- NP131248.RAUXjY00TJWy5_FZ5V8VIT_7vzwGl4UIqcIiCaDg-7iW0130_assertion description "[the excitatory effects of 5-HT in human colon are mediated by 5-HT (2B) receptors/( 2B) receptors contribute to the putative 5-HT-induced colonic smooth muscle hypersensitivity associated with irritable bowel syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131248.RAUXjY00TJWy5_FZ5V8VIT_7vzwGl4UIqcIiCaDg-7iW0130_provenance.
- NP131252.RAVWIeszJv1Pg69wEoh6kk3FwjLWQPJuviSyzuWVmwCEY130_assertion description "[The allele HLA-B*1301 is strongly associated with TCE-induced hypersensitivity dermatitis among exposed workers in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131252.RAVWIeszJv1Pg69wEoh6kk3FwjLWQPJuviSyzuWVmwCEY130_provenance.
- NP131257.RAT_T0S_glufsqKOyzNiKnpfQbr_xTQuzfB9QGsZpMi94130_assertion description "[Ex vivo ELISPOT measurements of granzyme B permit the identification of actively ongoing CD8 (+) cell responses-a notion that is pertinent to the immune diagnostic of infections, transplantation, allergies, autoimmune diseases, tumors, vaccine development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131257.RAT_T0S_glufsqKOyzNiKnpfQbr_xTQuzfB9QGsZpMi94130_provenance.
- NP131265.RASutj6lN7gUTakSrgvDUNDTu4nXouyffAImnJuEtW_HY130_assertion description "[Intraplaque hemorrhage evaluated by MRI identified neurologically unstable patients with increased levels of high-sensitivity C-reactive protein regardless of the degree of carotid stenosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131265.RASutj6lN7gUTakSrgvDUNDTu4nXouyffAImnJuEtW_HY130_provenance.
- NP131266.RAdCzVy2hhiOBJtg_4W3fbpXzoFeai-SPJyy-Xg9SXjp4130_assertion description "[von Willebrand factor has roles in minor bleeding and clotting as well as in hemorrhage or thrombosis [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131266.RAdCzVy2hhiOBJtg_4W3fbpXzoFeai-SPJyy-Xg9SXjp4130_provenance.
- NP131270.RAZYBlSAiDxYStK4IO0qjUYrnNJq2Xj3J1thfTT0vS8nI130_assertion description "[IL-1alpha released by epithelial cells triggers the production of IL-1alpha by stromal cells in a paracrine amplification loop during menstruation and dysfunctional bleeding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131270.RAZYBlSAiDxYStK4IO0qjUYrnNJq2Xj3J1thfTT0vS8nI130_provenance.
- NP131271.RAck9Vm1xKIQWjUudqq5KaoPxdyFMhf0XeQMYcKmGVrJY130_assertion description "[MPL mutations lacked prognostic significance with respect to thrombosis, major hemorrhage, myelofibrotic transformation or survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131271.RAck9Vm1xKIQWjUudqq5KaoPxdyFMhf0XeQMYcKmGVrJY130_provenance.
- NP131279.RAWRVYAZVTdGJY1H4eZOR7YHEMEetK65dKZubhiqiSRc0130_assertion description "[In patients on warfarin CYP2C9 genotype is associated with an increased risk of major hemorrhage, which persists even after stabilization of therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131279.RAWRVYAZVTdGJY1H4eZOR7YHEMEetK65dKZubhiqiSRc0130_provenance.
- NP131283.RARusGDXyq-rzgWUmilx0Ryu2IjhDdlhzSyI2Ppy2Npq8130_assertion description "[MMP and TIMP may be involved in the feto-neonatal development and may contribute to the pathogenesis of bronchopulmonary dysplasia and/or intraventricular hemorrhage in critically ill preterm neonates ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131283.RARusGDXyq-rzgWUmilx0Ryu2IjhDdlhzSyI2Ppy2Npq8130_provenance.
- NP131287.RAeOklts3MV1pYWqKnOZoFhXmorH_q4HcHC0zB9qtAIr8130_assertion description "[relative importance of the factor (F) II G20210A or FV G1691A mutations as risk factors or predictors for fatal/non-fatal recurrent venous thromboembolism in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131287.RAeOklts3MV1pYWqKnOZoFhXmorH_q4HcHC0zB9qtAIr8130_provenance.
- NP131289.RASp6C6YDRu04JU_2PjsXSGM93iTlnFPINgncO3NfZZxY130_assertion description "[In the Spanish population, the prothrombin 20210A (PT20210A) allele is the most prevalent genetic risk factor for venous thromboembolism in hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131289.RASp6C6YDRu04JU_2PjsXSGM93iTlnFPINgncO3NfZZxY130_provenance.
- NP131297.RAW6D6DarIaY66E-OZjcmzeIf18Pt8TGNznQO5i9lWs5k130_assertion description "[study concludes that the FV HR2 haplotype significantly affects the risk of venous thromboembolism in subjects with normal FV ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131297.RAW6D6DarIaY66E-OZjcmzeIf18Pt8TGNznQO5i9lWs5k130_provenance.
- NP131300.RAUcqudz4RFbvJx1jDSDrRhm-HYY2ccwovFqZ40v7TIrE130_assertion description "[EPCR 4600A/G and 4678G/C polymorphisms may be involved in venous thromboembolism in carriers of factor V Leiden ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131300.RAUcqudz4RFbvJx1jDSDrRhm-HYY2ccwovFqZ40v7TIrE130_provenance.
- NP131305.RAa1V9XcwxBxjqKQVXS2_ZAmWTeCzF_cvk7NCRAmbQbxY130_assertion description "[Prevalence of the FV Leiden mutation in polycythemia vera and essential thrombocythemia is comparable with that in the general population/is a risk factor for venous thromboembolism (VTE) before and at time of diagnosis and for VTE recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131305.RAa1V9XcwxBxjqKQVXS2_ZAmWTeCzF_cvk7NCRAmbQbxY130_provenance.
- NP131309.RATSjvWTQYesPf4iIHZFnmjQ9RHw2uGDx4EhMIGIfx3-U130_assertion description "[In this population-based study, a low protein C level has been determined to be associated with an increased incidence of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131309.RATSjvWTQYesPf4iIHZFnmjQ9RHw2uGDx4EhMIGIfx3-U130_provenance.
- NP131310.RARiWxsSIE07MzvfKKayrm2Mt3dGhIQsLMh0SLJtsZT2A130_assertion description "[Failed to validate association of protein S Tokushima gene polymorphisms with venous thromboembolism amoung Californians of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131310.RARiWxsSIE07MzvfKKayrm2Mt3dGhIQsLMh0SLJtsZT2A130_provenance.
- NP131313.RAW393Ocb44RieEz7wh75hKdX-6b6BnOyilHEl61T6H6s130_assertion description "[Failed to validate association of EPCR gene polymorphisms with venous thromboembolism amoung Californians of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131313.RAW393Ocb44RieEz7wh75hKdX-6b6BnOyilHEl61T6H6s130_provenance.
- NP131316.RAW74PKthBqNV854oxtVtUHhVbeC65anj9PWttluL4jk0130_assertion description "[elevated plasma fibronectin levels are associated with venous thromboembolism (VTE) especially in males, and extend the potential association between biomarkers and risk factors for arterial atherothrombosis and VTE ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131316.RAW74PKthBqNV854oxtVtUHhVbeC65anj9PWttluL4jk0130_provenance.
- NP131322.RAXwBSjB31f42NjAv173SSsgge-H0_Hmo7BK8nMj8OOWA130_assertion description "[Patients with a first venous thromboembolism and long GT-repeat alleles in HMOX1 have an increased risk of recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131322.RAXwBSjB31f42NjAv173SSsgge-H0_Hmo7BK8nMj8OOWA130_provenance.
- NP131324.RASLBuPB9grYJXzwuNczfnjJZcTn7hCz4AxsuGxzC-Tf8130_assertion description "[Factor VIIIc may play a role in the development of venous thromboembolism in factor V Leiden carriers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131324.RASLBuPB9grYJXzwuNczfnjJZcTn7hCz4AxsuGxzC-Tf8130_provenance.
- NP131328.RAYDIp1uom6wr0V_li92TKPrngjwaJ2RnN8zrj12OQJ7U130_assertion description "[Doubly heterozygous prothrombotic genetic mutations are commonly present among Eastern Mediterranean patients with venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131328.RAYDIp1uom6wr0V_li92TKPrngjwaJ2RnN8zrj12OQJ7U130_provenance.
- NP131329.RAfWOOhRxSUJZ2bq4zqsaIT1uNxmQz_ixnFK8FBv9VycU130_assertion description "[Postdelivery increase in tissue factor-dependent activation of coagulation is likely to be a natural mechanism to prevent excessive blood loss during and after delivery, and may also increase risk of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131329.RAfWOOhRxSUJZ2bq4zqsaIT1uNxmQz_ixnFK8FBv9VycU130_provenance.
- NP131333.RAedRkY8ins2DCNDmp57oyvLQlbXD96RPAh0GPdUuSq2E130_assertion description "[The Marburg I polymorphism of factor VII-activating protease and the risk of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131333.RAedRkY8ins2DCNDmp57oyvLQlbXD96RPAh0GPdUuSq2E130_provenance.
- NP131334.RAZdHzdVsP6Tp09DYkPIxHSrpySu28ywsQLj76VFWDGh8130_assertion description "[Failed to validate association of PAR-1 gene polymorphisms with venous thromboembolism amoung Californians of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131334.RAZdHzdVsP6Tp09DYkPIxHSrpySu28ywsQLj76VFWDGh8130_provenance.
- NP131342.RAYCN-o6BcklmxiQzBX8YjTmXomadpeWXuf92w4yw6npw130_assertion description "[The TAFI 325Thr/Thr genotype might be a possible risk factor for venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131342.RAYCN-o6BcklmxiQzBX8YjTmXomadpeWXuf92w4yw6npw130_provenance.
- NP131345.RAXHDA8lYn0R-Kgx1tNpkqMSIhE6ARhXMHXuNL6frW7WA130_assertion description "[genotyped 2090 women in Heart and Estrogen/progestin Replacement Study for functional polymorphisms in GP1BA and GP6 and assessed the coronary heart disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131345.RAXHDA8lYn0R-Kgx1tNpkqMSIhE6ARhXMHXuNL6frW7WA130_provenance.
- NP131352.RAQ8AqQSzo9VjZU4h02pMPnvfjTH08YMj7KVFFwQQXqyI130_assertion description "[Determination of high molecular weight adiponectin, especially relative to total serum adiponectin, is useful for evaluating coronary disease in type 2 diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131352.RAQ8AqQSzo9VjZU4h02pMPnvfjTH08YMj7KVFFwQQXqyI130_provenance.
- NP131362.RASzAl8Xke8kFiPgt36Fx_ghjWZi16MUP5M6qET3drhjM130_assertion description "[approximately linear relationship of apoE genotype with LDL-C levels & coronary heart disease risk; compared with individuals with epsilon3/epsilon3 genotype, epsilon2 carriers have lower risk & epsilon4 carriers have a slightly higher risk [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131362.RASzAl8Xke8kFiPgt36Fx_ghjWZi16MUP5M6qET3drhjM130_provenance.
- NP131364.RAUoLZRRu_hKyfzij2P3k4C9yPAsDi00D-gTXDnwZUgR0130_assertion description "[Apolipoprotein E polymorphism in Northern Indian patients with coronary heart disease: phenotype distribution and relation to serum lipids and lipoproteins ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131364.RAUoLZRRu_hKyfzij2P3k4C9yPAsDi00D-gTXDnwZUgR0130_provenance.
- NP131368.RAftnP26QKdAM1xhf9kb6GtRFQwEeuZ4t9Ie45NN6U7vU130_assertion description "[ABCA1 gene sequence in a proband with very low HDL cholesterol and premature coronary heart disease family history revealed 2 mutations: G5947A (R1851Q) and single thymidine deletion in a polypyrimidine tract 33 to 46 bps upstream from start of exon 47 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131368.RAftnP26QKdAM1xhf9kb6GtRFQwEeuZ4t9Ie45NN6U7vU130_provenance.
- NP131370.RAfc-nLtQh80DN3vB3W2jyxxI6hobsTGeU-_NkfVtjjMQ130_assertion description "[analysis of genetic variation in the ATP-binding cassette transporter A1, plasma lipids, and risk of coronary heart disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131370.RAfc-nLtQh80DN3vB3W2jyxxI6hobsTGeU-_NkfVtjjMQ130_provenance.
- NP131372.RAaSdKloHs1wzBJzZGN7WScyTPlPdjLMatc5abMb5QQWU130_assertion description "[The KIF6 719Arg variant has been associated with an increased risk of coronary disease and an increased response to statin therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131372.RAaSdKloHs1wzBJzZGN7WScyTPlPdjLMatc5abMb5QQWU130_provenance.
- NP131373.RAXpWvURvZ9ZGO0CVgO-5bAoUIT8859-5Kg0PSZOh3PPw130_assertion description "[Paraoxonase Gln-Arg (192) and Leu-Met (55) gene polymorphisms and enzyme activity in a population with a low rate of coronary heart disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131373.RAXpWvURvZ9ZGO0CVgO-5bAoUIT8859-5Kg0PSZOh3PPw130_provenance.
- NP131374.RAazI6aIzQBVILdX-IdCfVdthQbpY3omJLTzpCrTBdk4E130_assertion description "[Human paraoxonase gene cluster polymorphisms is a predictor of coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131374.RAazI6aIzQBVILdX-IdCfVdthQbpY3omJLTzpCrTBdk4E130_provenance.
- NP131378.RAbDB0WPg3fyr3MPCeBhTNYpXSF3nY1s3PfJuBXi3Jeh0130_assertion description "[genetic variation in the angiotensinogen gene contributes to coronary heart disease risk in patients with familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131378.RAbDB0WPg3fyr3MPCeBhTNYpXSF3nY1s3PfJuBXi3Jeh0130_provenance.
- NP131379.RARIbGmjbyTSsU2WxZs3NkLwu4YSVkDezTnpm07Hrb-TM130_assertion description "[pooled odds ratio of the present meta-analysis, including our own data, presented evidence that there is an increase in the risk of coronary heart disease conferred by the M235T variant of the AGT gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131379.RARIbGmjbyTSsU2WxZs3NkLwu4YSVkDezTnpm07Hrb-TM130_provenance.
- NP131381.RAZCUMbWqmuJBp-YwxIyP7a0n8VsaI26JTWcrmm44OKWk130_assertion description "[MTHFR polymorphism can be a genetic risk factor developing coronary diseases in the third world countries where folate deficiency is quite common.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131381.RAZCUMbWqmuJBp-YwxIyP7a0n8VsaI26JTWcrmm44OKWk130_provenance.
- NP131387.RAdlANeqVsnKvqeR5Al2lSZ-E8pEinlWmKGWiwvZI8ZhA130_assertion description "[CRP levels were clearly associated with future coronary heart disease events in a general population of Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131387.RAdlANeqVsnKvqeR5Al2lSZ-E8pEinlWmKGWiwvZI8ZhA130_provenance.
- NP131398.RAV9ih-JFAwo3d8_DK8s2A181SFH8jIPRMz5Uaud9Zet0130_assertion description "[Persistent and enhanced inflammatory responsiveness to C-reactive protein increases baseline concentrations of IL-6 and TNF-alpha in blood monocytes and may be involved in the pathogenesis of unstable coronary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131398.RAV9ih-JFAwo3d8_DK8s2A181SFH8jIPRMz5Uaud9Zet0130_provenance.
- NP131401.RASDMMCE26ta9a7udRWFZfLLyJcZm8aHh6J86Nt6gdKNY130_assertion description "[Combined mutations in LDLR and proprotein convertase subtilisin kexin 9 are associated with a severe phenotype for premature coronary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131401.RASDMMCE26ta9a7udRWFZfLLyJcZm8aHh6J86Nt6gdKNY130_provenance.
- NP131402.RAcsIEXf23stFDMGYXuUHhAOiEhiuZQH9d9jDEENZ0sG8130_assertion description "[There is a significant correlation between the CC genotype of the APOA5 and the levels of plasma high density lipoprotein-cholosteal in the coronary heart disease group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131402.RAcsIEXf23stFDMGYXuUHhAOiEhiuZQH9d9jDEENZ0sG8130_provenance.
- NP131404.RAbifA5h4bo6n1lhWW0lEE5VFyJ7kXOBzLt4fqOjRFcdU130_assertion description "[Men with a CETP mutation had the lowest rates of coronary heart disease; whether a CETP mutation offers additional protection against CHD warrants further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131404.RAbifA5h4bo6n1lhWW0lEE5VFyJ7kXOBzLt4fqOjRFcdU130_provenance.
- NP131411.RAQeV7YhUZ6KMkprm29ztYG3AO7E_tTG98qLr8EkW_2Io130_assertion description "[type 2 diabetes mellitus is linked with elevated blood level of MMP-1, and polymorphisms of the promoter region of its gene might be associated with coronary heart disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131411.RAQeV7YhUZ6KMkprm29ztYG3AO7E_tTG98qLr8EkW_2Io130_provenance.
- NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_assertion description "[Although the concentration of bilirubin in the UGT1A1 variant is higher than the wild type for the patients with coronary disease (CAD), there is no significant difference in the polymorphism between the patients and the participants in the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131413.RAZVE59SrwPhwRc5333FATRTXHRU0EIrPNvq43qHOPEz8130_provenance.
- NP131423.RAdwrLvkBjM_7QPAgNxnJWQE_os9C0VSi4Ty1pKxNUGYs130_assertion description "[MMP9 levels were significantly higher in diabetic patients with the acute coronary disease syndrome than in nondiabetics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131423.RAdwrLvkBjM_7QPAgNxnJWQE_os9C0VSi4Ty1pKxNUGYs130_provenance.
- NP131426.RAfrzLERVf8GKEpdWwD0JhnfC2WvA32aLIGYZ1QCRHrt8130_assertion description "[PAI-1 may have a pathogenic role in coronary disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131426.RAfrzLERVf8GKEpdWwD0JhnfC2WvA32aLIGYZ1QCRHrt8130_provenance.
- NP131437.RATIA13oCRnSa3JkzeWFAxY_CMAcmtuHd035FaYILyvsw130_assertion description "[the Thr789Ala vWF gene variant is associated with increased plasma concentrations of vWF, ristocetin co factor levels and collagen binding capacity in patients with type 2 diabetes and coronary heart disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131437.RATIA13oCRnSa3JkzeWFAxY_CMAcmtuHd035FaYILyvsw130_provenance.
- NP131440.RAW27SZMMY1jlLsvlLuBRZ5PmKAbohPaJmzMngXn1FAFk130_assertion description "[study examined the potential association between the functional SNP rs9923231 & early-onset coronary heart disease (CHD) in Northern Germans; no evidence for a significant association was detected between VKORC1 genotype & CHD phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131440.RAW27SZMMY1jlLsvlLuBRZ5PmKAbohPaJmzMngXn1FAFk130_provenance.
- NP131443.RAfHbzB74a3nVHrn-PEJh9-5iOFYveZ9wKuszp1eF2G0g130_assertion description "[cigarette smoking may modify the relationship between the I264M and K399R polymorphisms in CYP2C8 and coronary heart disease risk in Caucasians ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131443.RAfHbzB74a3nVHrn-PEJh9-5iOFYveZ9wKuszp1eF2G0g130_provenance.
- NP131452.RAShVjipS5Cws-6fGNu6VfRDNvAsEKp6RCgOD_5j3qkNE130_assertion description "[genetic variation of 3'flanking region of ApoA-I (PstI), 3'untranslated region of ApoC-III (SstI) and intron 2 of ApoA-IV (XbaI) in 193 angiographically diagnosed coronary heart disease Punjab patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131452.RAShVjipS5Cws-6fGNu6VfRDNvAsEKp6RCgOD_5j3qkNE130_provenance.
- NP131455.RATeoAP0eoxNnoYNc7xyiSc403hmU5e0VdeIWZnd4K9aA130_assertion description "[replacing monounsaturated with polyunsaturated fat can benefit coronary heart disease by reducing the availability of oleoyl-CoA in the substrate pool of hepatic ACAT2 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131455.RATeoAP0eoxNnoYNc7xyiSc403hmU5e0VdeIWZnd4K9aA130_provenance.
- NP131457.RAX8x21dPJZirG2lYE2Pat3DAalRL4eJqfGsBRVZq49wI130_assertion description "[Lower PON1 activity and higher oxLDL levels may be predicting factors that denote diffuse, severe or multivessel disease in coronary heart disease patients with hyperglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131457.RAX8x21dPJZirG2lYE2Pat3DAalRL4eJqfGsBRVZq49wI130_provenance.
- NP131461.RAVFcDQjp4FusQdErjtdjLZBXELao_JRphWsTw7BRUN0E130_assertion description "[Genetic variation in CC-chemokine receptor-2 (CCR2) and -5 (CCR5), and their common haplotypes, acting through inflammatory responses, may affect atherosclerosis and risk of coronary heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131461.RAVFcDQjp4FusQdErjtdjLZBXELao_JRphWsTw7BRUN0E130_provenance.
- NP131466.RAXZey7duKg8HLodNzxatKigpEMMYEzkUcbSqpkzNqrvo130_assertion description "[CD36 mRNA expression is significantly increased in patients with coronary heart disease (CHD) and may serve as an indicator of CHD burden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131466.RAXZey7duKg8HLodNzxatKigpEMMYEzkUcbSqpkzNqrvo130_provenance.
- NP131467.RASwL1JlESg6PgJWP_qVYgIZmpFnQk0hDaAutwC-Awz5w130_assertion description "[CDKN2A CDKN2B and ANRIL is the susceptibility locus for coronary heart disease (CHD) and periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131467.RASwL1JlESg6PgJWP_qVYgIZmpFnQk0hDaAutwC-Awz5w130_provenance.
- NP131474.RAUq3w9H5uQQ6ICmGNCjfGzO_Jqb7k7kt8mTiAqzUKL0w130_assertion description "[Plasma F7a level may be an independent risk factor of coronary heart disease in elderly patients, and it may be influenced by the Msp I polymorphism of F7 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131474.RAUq3w9H5uQQ6ICmGNCjfGzO_Jqb7k7kt8mTiAqzUKL0w130_provenance.
- NP131476.RAfNz8fikEoYBhAYoNJNZ962cEWicHk8FadUyDzfqtqNI130_assertion description "[Association of elevated Lp-PLA (2) activity with coronary disease risk in relation to oxidant stress supports a proatherogenic role of Lp-PLA (2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131476.RAfNz8fikEoYBhAYoNJNZ962cEWicHk8FadUyDzfqtqNI130_provenance.
- NP131479.RAbRGsp-pmxCVBUnXQWVWc2kihHr2s7bvxGW7tJRrPoCU130_assertion description "[This genotype is not major determinant of population genetic risk of coronary heart disease (CHD), but association of this genotype with low levels of Lp-PLA (2) strongly support pro-inflammatory causative, and not consequential, role of Lp-PLA (2) in CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131479.RAbRGsp-pmxCVBUnXQWVWc2kihHr2s7bvxGW7tJRrPoCU130_provenance.
- NP131485.RAXnmAfdNqYTB8NRT-no3I-dYHNvbTLIBt290gxINMnQI130_assertion description "[the presence of the APOA5*2 and APOA5*3 haplotypes in the APOA5 gene is associated with a higher postprandial response that could be involved in the higher risk of coronary heart disease associated with the 56G and -1131C alleles ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131485.RAXnmAfdNqYTB8NRT-no3I-dYHNvbTLIBt290gxINMnQI130_provenance.
- NP131495.RAdijDS5iVmWktSKQICPs7wxc0kTMfLyflLRUKJX-t9XU130_assertion description "[Patients with primary hypertriglyceridemia as compared with control subjects showed significant increases in monocyte CD18 (cell adhesion molecule 18) and Lymphocyte CD18 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131495.RAdijDS5iVmWktSKQICPs7wxc0kTMfLyflLRUKJX-t9XU130_provenance.
- NP131496.RAfQE3l5sfNSLFc-D41aqUCgB-My-8q6tt8nh9QLk69Vc130_assertion description "[APOA1/C3/A5 haplotype represents an important locus for predicting risk of hypertriglyceridemia among Taiwanese ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131496.RAfQE3l5sfNSLFc-D41aqUCgB-My-8q6tt8nh9QLk69Vc130_provenance.
- NP131497.RAdv4F8ZAg4SyKchJvtPEAgcfn_FmSwkEr2IRikqsezA4130_assertion description "[The apoE2 allele was negatively associated with hypertriglyceridemia/hyperapobetalipoproteinemia in the absence of a deleterious LPL gene variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131497.RAdv4F8ZAg4SyKchJvtPEAgcfn_FmSwkEr2IRikqsezA4130_provenance.
- NP131499.RATSq2mTRzfnzuhPDXIg-n5G55N8mz2D1r85SrHUBdDBk130_assertion description "[Variant alleles of APOE and APOC3 contribute to an unfavorable lipid profile in patients with HIV, who are therefore at high risk for severe ritonavir-associated hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131499.RATSq2mTRzfnzuhPDXIg-n5G55N8mz2D1r85SrHUBdDBk130_provenance.
- NP131506.RAQjAunkOnXV8QNi8tWkpvMsn8lR9AHhX9-RY0br5EwHM130_assertion description "[These data indicate that despite their association with hypertriglyceridemia and/or predicted protein dysfunction, the 19W, 185C and 341H apoAV variants are equally effective in reducing plasma TG levels in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131506.RAQjAunkOnXV8QNi8tWkpvMsn8lR9AHhX9-RY0br5EwHM130_provenance.
- NP131507.RATBXyOKCval1z2nIqWvbmTJRLwyK3WZFPUr2AraxzX-0130_assertion description "[in hypertriglyceridemia patients, increased triglyceride levels are accompanied by high plasma levels of apoA-V and apoC-III, apolipoproteins with opposite modes of action ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131507.RATBXyOKCval1z2nIqWvbmTJRLwyK3WZFPUr2AraxzX-0130_provenance.
- NP131511.RAQl8iGOfyZbz42QijLIIlQIWXR1VEpiLwQLa9a5YMRek130_assertion description "[APOA1/C3/A5 haplotype represents an important locus for predicting risk of hypertriglyceridemia among Taiwanese ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131511.RAQl8iGOfyZbz42QijLIIlQIWXR1VEpiLwQLa9a5YMRek130_provenance.
- NP131513.RAe0fvVEVqBd54Y54xztZo1k1oN0tqF44Tj1eLbzQwo9s130_assertion description "[DNA polymorphisms within APOA5 are associated with hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131513.RAe0fvVEVqBd54Y54xztZo1k1oN0tqF44Tj1eLbzQwo9s130_provenance.
- NP131514.RAdL9cziv-Cw4eZe_pTZceYhzYlG6vrsxNT6hfQ0J6pmo130_assertion description "[A novel genetic variant in APOA5 is associated with hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131514.RAdL9cziv-Cw4eZe_pTZceYhzYlG6vrsxNT6hfQ0J6pmo130_provenance.
- NP131518.RAecz5DM0C3XLcEVMttQQl8cOSI3Itc26VKBZG0WyV92E130_assertion description "[a rationale to evaluate the effects of CETP inhibitor treatment on plasma cholesterol ester transfer and on cardiovascular risk in diabetes-associated hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131518.RAecz5DM0C3XLcEVMttQQl8cOSI3Itc26VKBZG0WyV92E130_provenance.
- NP131523.RAXRovzA9Cm97KkdY8pvlkb7sbC896iByJV0ww-9hJoOM130_assertion description "[Novel mutations of the LPL gene contribute to the hypertriglyceridemia observed in members of type 2 diabetic pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131523.RAXRovzA9Cm97KkdY8pvlkb7sbC896iByJV0ww-9hJoOM130_provenance.
- NP131526.RAcHArJZIWF5NJHQ9E-uug0wkJoNvD6c21fF0A41CN3wo130_assertion description "[SREBP-1 not necessary for hepatic Akt-mediated hypoglycemic effect/hypertriglyceridemia and hepatic triglyceride accumulation mediated by Akt-induced SREBP-1 expression and mechanism involving fatty acid synthesis independent of SREBP-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131526.RAcHArJZIWF5NJHQ9E-uug0wkJoNvD6c21fF0A41CN3wo130_provenance.
- NP131528.RAZO9cPpFUmRg4phASOCHHckpvTnPBjyTFQq5RVF6vMOc130_assertion description "[ACE polymorphism was associated with hypertriglyceridemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131528.RAZO9cPpFUmRg4phASOCHHckpvTnPBjyTFQq5RVF6vMOc130_provenance.
- NP131530.RAQOHWWxGgOVHHy0hKN8CdZaquvkZu6RL3LjEYjt020Gk130_assertion description "[TRL-bound LPL activity increases in the postprandial state and is strongly reduced in type 2 diabetes, contributing to postprandial hypertriglyceridemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131530.RAQOHWWxGgOVHHy0hKN8CdZaquvkZu6RL3LjEYjt020Gk130_provenance.
- NP131533.RAY595CdywOubxIExybFvSwfCVFRbRiarfA5OrIJXMxHk130_assertion description "[Cohort study provides evidence that RBP4 may be a mechanism through which obesity influences insulin resistance and hypertriglyceridemia in overweight postpubertal black youth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131533.RAY595CdywOubxIExybFvSwfCVFRbRiarfA5OrIJXMxHk130_provenance.
- NP131534.RAbBoCkRZThC-ljj63KgQkaXoQNrDGqc_JRHiML-bfs54130_assertion description "[Patients with primary hypertriglyceridemia as compared with control subjects showed significantly higher plasma ICAM-1 (intercellular adhesion molecule 1) and increases in monocyte and lymphocyte ICAM1 (CD54) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131534.RAbBoCkRZThC-ljj63KgQkaXoQNrDGqc_JRHiML-bfs54130_provenance.
- NP131535.RAStlGDgZJP6ruzaBA5VEClUl7Ck6CCxL77bYiMy_aEoM130_assertion description "[Patients withprimary hypertriglyceridemia as compared with control subjects showed significantly higher VCAM-1 (vascular cell adhesion molecule 1) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131535.RAStlGDgZJP6ruzaBA5VEClUl7Ck6CCxL77bYiMy_aEoM130_provenance.
- NP131539.RAUrp5alcxavDHBvqstQx3pwdicxtvH4RFMwn3-qLaXDA130_assertion description "[The slightly altered structural properties of apoE4-mut2 are associated with slightly reduced binding of this protein to TG-rich lipoprotein particles and milder hypertriglyceridemia as compared with WT apoE4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131539.RAUrp5alcxavDHBvqstQx3pwdicxtvH4RFMwn3-qLaXDA130_provenance.
- NP131545.RAa1f8vlCSyVP0OOk6zC52C3nwHVU8Bxenqeb3Wb-sEFg130_assertion description "[Both common and rare DNA variants of APOC2 gene were found in 10% patients with severe hypertriglyceridemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131545.RAa1f8vlCSyVP0OOk6zC52C3nwHVU8Bxenqeb3Wb-sEFg130_provenance.
- NP131550.RAew1vioNZJ6l_UytX_t2FJ_R8kRPkjxib7BqfR6OFT2w130_assertion description "[Variant alleles of APOE and APOC3 contribute to an unfavorable lipid profile in patients with HIV, who are therefore at high risk for severe ritonavir-associated hypertriglyceridemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131550.RAew1vioNZJ6l_UytX_t2FJ_R8kRPkjxib7BqfR6OFT2w130_provenance.
- NP131553.RAby6C9MrJJ0fcdgdOlR1j44v41sGRtwFYqipHThq8DIo130_assertion description "[APOA5 gene is involved in hypertriglyceridemia associated with hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131553.RAby6C9MrJJ0fcdgdOlR1j44v41sGRtwFYqipHThq8DIo130_provenance.
- NP131555.RAfy-Ned-CAhg4d5_pI5_t9OIHoMfgyvGxx_sb3oCQuxo130_assertion description "[Partial apoA-V deficiency predisposes to hypertriglyceridemia probably in combination with other genetic factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131555.RAfy-Ned-CAhg4d5_pI5_t9OIHoMfgyvGxx_sb3oCQuxo130_provenance.
- NP131561.RAeFsY2l5OCti4MpOJAm0Dllf0EY2xEY_ED865k7mg5I4130_assertion description "[GFAP levels may be used in Guillain-Barre syndrome as a diagnostic marker of the axonal variant and to predict outcome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131561.RAeFsY2l5OCti4MpOJAm0Dllf0EY2xEY_ED865k7mg5I4130_provenance.
- NP131562.RASk3-HvPpqyZu4cnkiTKYQlvxiwbIr5arIkhvlJHak14130_assertion description "[Complement activation mediated by mannose- binding lectin contributes to the extent of nerve damage in Guillain-Barre syndrome, which is codetermined by the MBL2 haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131562.RASk3-HvPpqyZu4cnkiTKYQlvxiwbIr5arIkhvlJHak14130_provenance.
- NP131564.RAUv_QhiIyKVQnd-y6OUbo56IFRebKwZb-y9G5CC59uss130_assertion description "[Data show that serum from a patient with axonal Guillain-Barre syndrome (GBS) with IgG anti-GalNAc-GD1a antibody yielded positive immunostaining with X1, X2, and X3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131564.RAUv_QhiIyKVQnd-y6OUbo56IFRebKwZb-y9G5CC59uss130_provenance.
- NP131571.RAbv1MklGOaUMMiAXk3xHij65BM7UjmklIScxjtcUg-WI130_assertion description "[possible associations between common serological markers of celiac disease with the -1087 IL10 and -308 TNFA polymorphisms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131571.RAbv1MklGOaUMMiAXk3xHij65BM7UjmklIScxjtcUg-WI130_provenance.
- NP131574.RAXWT0U0HVEy53ixL8FmIyemTu8Mpa5x5pED2wnlgklCI130_assertion description "[Single Nucleotide polymorphism is associated with celiac Disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131574.RAXWT0U0HVEy53ixL8FmIyemTu8Mpa5x5pED2wnlgklCI130_provenance.
- NP131578.RAUIpX3X4uycySxOAfW1YjMDuGvPJRIVUVsM5CZBcKKH0130_assertion description "[results show for the first time that NF-kappa B is activated in the inflamed mucosa of celiac patients and suggest that it may represent a molecular target for the modulation of inflammatory response in celiac disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131578.RAUIpX3X4uycySxOAfW1YjMDuGvPJRIVUVsM5CZBcKKH0130_provenance.
- NP131581.RAQnUEGIIGlTKliwB5NR1cC51IAao5255E8_DjBnCWdkA130_assertion description "[Genotyping of the three SNPs which tagged the associated haplotype was performed in a Celiac disease family dataset in a Swedish/Norwegian cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131581.RAQnUEGIIGlTKliwB5NR1cC51IAao5255E8_DjBnCWdkA130_provenance.