Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP46780.RAqZjNF2PMhWJqW3w8T1BYLsASOJbP-JeDo48Ewl8AYDU130_assertion description "[These results are consistent with a gender-specific role of the CHRM2 gene in depression in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46780.RAqZjNF2PMhWJqW3w8T1BYLsASOJbP-JeDo48Ewl8AYDU130_provenance.
- NP46784.RAo-anCZ12tzS0pxDd1ZK24YC7khOj-SSdNRBSONtUVA8130_assertion description "[Our results confirm the positive association between CHL1 gene and schizophrenia and indicate that CHL1 may be involved in the etiology of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46784.RAo-anCZ12tzS0pxDd1ZK24YC7khOj-SSdNRBSONtUVA8130_provenance.
- NP46787.RAorVRRxJf9RkGR-q9VgKH0da6LqPix2gKBPgepd0bkis130_assertion description "[We found an association between Gram-negative bacterial infection and common, functional variants in two genes, IL6 and CHIT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46787.RAorVRRxJf9RkGR-q9VgKH0da6LqPix2gKBPgepd0bkis130_provenance.
- NP46789.RAmsNMK69ERYE4BTx3nnN_35t_FQ4GhXcMotJX6TCqtnA130_assertion description "[Polymorphisms of chromogranin B gene associated with schizophrenia in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46789.RAmsNMK69ERYE4BTx3nnN_35t_FQ4GhXcMotJX6TCqtnA130_provenance.
- NP46790.RAsUtlga2o9qQcSu_r5s-hj-YS6nv0oxC6h22vkIlH5Uc130_assertion description "[We analysed the prevalence of CHEK2*1100delC in 668 breast cancer cases, of which 542 were invasive breast cancers, from a hospital-based cohort of breast cancer patients from Kuala Lumpur, Malaysia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46790.RAsUtlga2o9qQcSu_r5s-hj-YS6nv0oxC6h22vkIlH5Uc130_provenance.
- NP46807.RAowzfiamdiwSNMtbBgUDJkDoSzh2N6H0tA9RDlcBss68130_assertion description "[the I157T mutation increases the risk of colorectal cancer in the population, but that truncating mutations may confer a lower risk or no increase in risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46807.RAowzfiamdiwSNMtbBgUDJkDoSzh2N6H0tA9RDlcBss68130_provenance.
- NP46808.RAjmU3L-2rHB_ep6IveMCBDM4m0Dkbzsd2A-fHb9Ts_QQ130_assertion description "[Analysis of familial male breast cancer for germline mutations in CHEK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46808.RAjmU3L-2rHB_ep6IveMCBDM4m0Dkbzsd2A-fHb9Ts_QQ130_provenance.
- NP46812.RAligMXKk0Tzgz-ox1aXYJXkS5MN6DK8QOrIuyA6xzlN0130_assertion description "[A large deletion of exons 9 and 10 of CHEK2 confers an increased risk of prostate cancer in Polish men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46812.RAligMXKk0Tzgz-ox1aXYJXkS5MN6DK8QOrIuyA6xzlN0130_provenance.
- NP46815.RAgoU_HYg-S124rZBrlbE__KHIk_y-tr9OayFqDTKXtuA130_assertion description "[The CHEK2 1100delC mutation is not a clinically important high-risk gene for hereditary prostate cancer susceptibility in the population of southern Sweden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46815.RAgoU_HYg-S124rZBrlbE__KHIk_y-tr9OayFqDTKXtuA130_provenance.
- NP46821.RAnsH2DeaQs4c1rIYQpXnPJFxlUV6nhVlNRiRN9E5EFXs130_assertion description "[There is considerable effect of the ChAT polymorphisms on AD in Korean population and this effect is dependent on ApoE genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46821.RAnsH2DeaQs4c1rIYQpXnPJFxlUV6nhVlNRiRN9E5EFXs130_provenance.
- NP46824.RAizdMnHr8lmj92BmJhw3MqlK1x5Yv64XbQm-os-xq4Jo130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46824.RAizdMnHr8lmj92BmJhw3MqlK1x5Yv64XbQm-os-xq4Jo130_provenance.
- NP46828.RAjWCxTGnL2hlMyOMWFKUWUKm2QDLX2Tp2oLlemE5m3yI130_assertion description "[Together, these results are compatible with a role of CH25Hchi4 as a putative susceptibility factor for sporadic AD; they may explain part of the linkage of chromosome 10 markers with sporadic AD, and they suggest the possibility that CH25H polymorphisms are associated with different rates of brain A beta deposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46828.RAjWCxTGnL2hlMyOMWFKUWUKm2QDLX2Tp2oLlemE5m3yI130_provenance.
- NP46837.RAv8Ib2u6s6tBVZLTBBtp2fBbj8MGu0FRWe3H-_ZmkPyU130_assertion description "[The association of SPINK1 with CFTR gene mutations in IP patients is statistically significant (3/32 IP cases and 0/100 control individuals carrying mutations in both genes; Fisher's exact test P=0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46837.RAv8Ib2u6s6tBVZLTBBtp2fBbj8MGu0FRWe3H-_ZmkPyU130_provenance.
- NP46850.RAg080mDTUBJuVhl2yMIsSCoxhygzKc-6Y_3pfWhBJ5dU130_assertion description "[Forty-four patients affected by nasal polyps were admitted to the Department of Otolaryngology, Lublin University School of Medicine, Lublin, Poland, and screened for the most-commonly identified CFTR mutations DeltaF508, G542X, N1303 K, 1717-1 (G to A), W1282X, G551D, R553X and DeltaI507 by applying the INNO-LIPA CF2 test strips.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46850.RAg080mDTUBJuVhl2yMIsSCoxhygzKc-6Y_3pfWhBJ5dU130_provenance.
- NP46854.RAiHIMcRR3J-VnpQPDKFenOXuTkvL3IboItUonzzHUgWk130_assertion description "[Cystic fibrosis (CF) is caused by compound heterozygosity or homozygosity of CF transmembrane conductance regulator gene (CFTR) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46854.RAiHIMcRR3J-VnpQPDKFenOXuTkvL3IboItUonzzHUgWk130_provenance.
- NP46855.RAs-UA6nxGp3gU_3jlQtZ0mwefvEpN6nFRqotdUPaA7nI130_assertion description "[Frequency of 8 CFTR gene mutations in cystic fibrosis patients in Minas Gerais, Brazil, diagnosed by neonatal screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46855.RAs-UA6nxGp3gU_3jlQtZ0mwefvEpN6nFRqotdUPaA7nI130_provenance.
- NP46856.RAqUo6pyP6onusPXNiLF_Q-9m9_G0Lnz6rMqyXM-ykWzw130_assertion description "[In a case-control study, the authors compared the rates of 39 common cystic fibrosis-associated CFTR mutations between 949 white patients with pancreatic adenocarcinoma and 13,340 white controls from a clinical laboratory database for prenatal testing for CFTR mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46856.RAqUo6pyP6onusPXNiLF_Q-9m9_G0Lnz6rMqyXM-ykWzw130_provenance.
- NP46862.RAjjjtinu4GjFS_FhWXVj7MIVCKCUmDCJBRNudXmkCI_g130_assertion description "[Homozygous (TG)11 allele in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene has a protective role against bicarbonate decrease in pure pancreatic juice among Japanese male alcoholics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46862.RAjjjtinu4GjFS_FhWXVj7MIVCKCUmDCJBRNudXmkCI_g130_provenance.
- NP46863.RAsAYPX_A6hfp3thdlEa2J9I4QP2Oxz3YqO5-9Oe87270130_assertion description "[These results suggest the involvement of the CFTR gene in bronchiectasis of unknown etiology in adult patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46863.RAsAYPX_A6hfp3thdlEa2J9I4QP2Oxz3YqO5-9Oe87270130_provenance.
- NP46864.RAg6fUJqEUyJBiHixaSD-SF88xeYgudhtnlN0fcL4O_pI130_assertion description "[ Compound heterozygosity of severe/mild mutations accounted for the vast majority of the CBAVD patients with two mutations, and underscores the value of a more extensive CF mutation panel for men with CBAVD. The CF100 panel enables higher carrier detection rates especially for men with CBAVD, their partners, partners of known CF carriers, and those with 'mild' CF with rarer mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46864.RAg6fUJqEUyJBiHixaSD-SF88xeYgudhtnlN0fcL4O_pI130_provenance.
- NP46867.RAv_WUsA-H5UlAwweHag8txmFD9swYvDgblym957SkL8Y130_assertion description "[Molecular diagnosis of the CFTR gene, Y chromosome deletion analysis and genetic counseling are necessary diagnostic elements for patients with male infertility, especially if the are included in an ART program.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46867.RAv_WUsA-H5UlAwweHag8txmFD9swYvDgblym957SkL8Y130_provenance.
- NP46873.RAl12SJICFrTjkubdyTDL0wxPdVV_iK3XNseElc9ineW4130_assertion description "[DeltaF508 heterozygosity in cystic fibrosis and susceptibility to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46873.RAl12SJICFrTjkubdyTDL0wxPdVV_iK3XNseElc9ineW4130_provenance.
- NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion description "[In order to investigate the incidence of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and unclassified variants in chronic pulmonary disease in children and adults, we studied 20 patients with asthma, 19 with disseminated bronchiectasis (DB) of unknown aetiology, and 12 patients with chronic obstructive pulmonary disease (COPD), and compared the results to 52 subjects from the general Greek population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance.
- NP46879.RAq8hyszDQ5wN9vxpBT4s30SWC0Xg0aPV8bIF6j22o9tI130_assertion description "[Lung disease associated with the IVS8 5T allele of the CFTR gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46879.RAq8hyszDQ5wN9vxpBT4s30SWC0Xg0aPV8bIF6j22o9tI130_provenance.
- NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_assertion description "[As it is known that certain CFTR variants have consequences on the function of CFTR protein, the aim of this study was to examine the possible role of F508del, M470V, Tn locus, and R75Q variants in COPD development and modulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_provenance.
- NP46881.RAlXzH9Wwj5vmOyfLQ2rU5NxG2cXMBWYEX840JKYt83rQ130_assertion description "[ We have identified specific allele variants of CFH and CFHR5 associated with the MPGN II/DDD disease phenotype. While our data can be interpreted to further implicate complement in the pathogenesis of MPGN II/DDD, these associations could also be unrelated to disease pathophysiology. Functional studies are required to resolve this question.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46881.RAlXzH9Wwj5vmOyfLQ2rU5NxG2cXMBWYEX840JKYt83rQ130_provenance.
- NP46887.RAmuTR5vLEArT1qVXqpCaH-RCHlrMbaxEQUPkzoHS9l9s130_assertion description "[The aim of this study was investigate the association between complement Factor H polymorphism (Y402H) and age-related macular degeneration (AMD) in Brazilian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46887.RAmuTR5vLEArT1qVXqpCaH-RCHlrMbaxEQUPkzoHS9l9s130_provenance.
- NP46890.RAqb9x3bmVtldEhJqZxLK_euM3dGjHkXmv-OGV0t1Mjkk130_assertion description "[The significant association is retained following multivariate analysis with adjustment for age, smoking status, Complement Factor H (CFH), Age-Related Maculopathy Susceptibility 2 (ARMS2), Complement Component 2 (CC2), and Complement Factor B (CFB; OR=1.45; CI: 1.10-1.91; p=0.009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46890.RAqb9x3bmVtldEhJqZxLK_euM3dGjHkXmv-OGV0t1Mjkk130_provenance.
- NP46893.RAnQeZ2xZsM-1zRLfOw0Df3iUMuEHILCb_7_2QeJQB_8c130_assertion description "[Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46893.RAnQeZ2xZsM-1zRLfOw0Df3iUMuEHILCb_7_2QeJQB_8c130_provenance.
- NP46894.RAi7jtgppJWlhXy-uNREP9IvKvnyGo8TmgNO5asj8WidM130_assertion description "[The aetiology of atypical haemolytic uraemic syndrome (aHUS) is, in contrast to classical, Shiga-like toxin induced HUS in children, largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46894.RAi7jtgppJWlhXy-uNREP9IvKvnyGo8TmgNO5asj8WidM130_provenance.
- NP46897.RAo2Q6FXKZ7LCfJP6FyhYMiY8t7oSspaX7WI-AgMJe85g130_assertion description "[Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46897.RAo2Q6FXKZ7LCfJP6FyhYMiY8t7oSspaX7WI-AgMJe85g130_provenance.
- NP46899.RAl13jWUIkzjUnptz4YdhesCi5I54HFiMgx0Oc9IiMNEs130_assertion description "[Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46899.RAl13jWUIkzjUnptz4YdhesCi5I54HFiMgx0Oc9IiMNEs130_provenance.
- NP46904.RAvCl0f9Lm1bEtPULpaO9O6tUFMp47evU7hn2FpLwMfi4130_assertion description "[Genetic and environmental factors affecting the response to statin therapy in patients with molecularly defined familial hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46904.RAvCl0f9Lm1bEtPULpaO9O6tUFMp47evU7hn2FpLwMfi4130_provenance.
- NP46911.RApM6DsfbFfebcYhngkRCqXintHg-DRoxGlztlX9eSSBs130_assertion description "[Pharmacogenetic study of cholesteryl ester transfer protein gene and simvastatin treatment in hypercholesterolaemic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46911.RApM6DsfbFfebcYhngkRCqXintHg-DRoxGlztlX9eSSBs130_provenance.
- NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_assertion description "[To determine the frequencies of 4 mutations of cholesteryl ester transfer protein (CETP) gene in Chinese population and to investigate the association of the mutations with lipid metabolism and the susceptibility to coronary atherosclerotic heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_provenance.
- NP46918.RAryE4sKhwzr6iir5s0hTOx5DaVyHcH9VnBTgXrf1Mp7I130_assertion description "[Prevalence of genetic risk factors for coronary artery disease in Corsica island (France).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46918.RAryE4sKhwzr6iir5s0hTOx5DaVyHcH9VnBTgXrf1Mp7I130_provenance.
- NP46922.RAn1T6X-zR9soZwKyBeuHpWN7Sm9Sw0BQsEJej0gkoyt8130_assertion description "[Influence of cholesteryl ester transfer protein, peroxisome proliferator-activated receptor alpha, apolipoprotein E, and apolipoprotein A-I polymorphisms on high-density lipoprotein cholesterol, apolipoprotein A-I, lipoprotein A-I, and lipoprotein A-I:A-II concentrations: the Prospective Epidemiological Study of Myocardial Infarction study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46922.RAn1T6X-zR9soZwKyBeuHpWN7Sm9Sw0BQsEJej0gkoyt8130_provenance.
- NP46929.RArNZiDKoPbUqcjytsDoGLa-gdPpQjOC3YKSq_udnriKY130_assertion description "[Results from the current study suggest that interaction effects between alcohol consumption and HDL cholesterol metabolism gene variation influence the risk of incident CHD in black men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46929.RArNZiDKoPbUqcjytsDoGLa-gdPpQjOC3YKSq_udnriKY130_provenance.
- NP46933.RAhbpdEB-WZyJPkElkSI9p3L1UAHIjiEqLAEpcU0DHNJM130_assertion description "[Since the identification of cholesteryl ester transfer protein (CETP), its role in the modulation of HDL levels and cardiovascular disease has been debated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46933.RAhbpdEB-WZyJPkElkSI9p3L1UAHIjiEqLAEpcU0DHNJM130_provenance.
- NP46934.RAtpki3g2Ber96gUgWzTMI-Q_T8VLKtREQSN4slvjpOxQ130_assertion description "[Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46934.RAtpki3g2Ber96gUgWzTMI-Q_T8VLKtREQSN4slvjpOxQ130_provenance.
- NP46935.RAolWE0_4kpFqjWaAzPLpgEaWphADEapN5AKn-3Vv4LIw130_assertion description "[Gene-environment interactions of CETP gene variation in a high cardiovascular risk Mediterranean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46935.RAolWE0_4kpFqjWaAzPLpgEaWphADEapN5AKn-3Vv4LIw130_provenance.
- NP46936.RAvlr4dJ6OUnI7e3zwbzE9BqdDfczihUNgdZhKICztuvs130_assertion description "[Information about common SNPs with high impact on the individual cardiovascular risk, such as CETPrs708272, may help to predict an active, symptomatic course atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46936.RAvlr4dJ6OUnI7e3zwbzE9BqdDfczihUNgdZhKICztuvs130_provenance.
- NP46942.RAinVOVgJuLmDXH6R0Bpa8qGznguyxZPYor8i26HVJZi4130_assertion description "[Polymorphism at cholesteryl ester transfer protein gene loci in patients with gallstone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46942.RAinVOVgJuLmDXH6R0Bpa8qGznguyxZPYor8i26HVJZi4130_provenance.
- NP46944.RAklDUFQ9CtmhhyXgXdtt3q3FQU6Y9rJTNzSTqK9ilgnw130_assertion description "[CETP polymorphisms influence cholesterol metabolism but not Alzheimer's disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46944.RAklDUFQ9CtmhhyXgXdtt3q3FQU6Y9rJTNzSTqK9ilgnw130_provenance.
- NP46947.RAtesX43xqwbNX7_Jra60C074XQlukVdRiykNYFlw-pCo130_assertion description "[Cholesteryl ester transfer protein (CETP) polymorphism modifies the Alzheimer's disease risk associated with APOE epsilon4 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46947.RAtesX43xqwbNX7_Jra60C074XQlukVdRiykNYFlw-pCo130_provenance.
- NP46954.RAl_vDVdd0h5ShAYeLNSkBfDTMglD6YkBM3bAk-aRb5oI130_assertion description "[Relationship between TaqIB cholesteryl ester transfer protein gene polymorphism and macrovascular complications in Japanese patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46954.RAl_vDVdd0h5ShAYeLNSkBfDTMglD6YkBM3bAk-aRb5oI130_provenance.
- NP46962.RAm-hfw4yOc5w7RT-bYQiw2CY8heOv_AXYDa--ChPCokA130_assertion description "[No significant association was found between CETP I405V polymorphism and increased risk of CAD in Azeri population studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46962.RAm-hfw4yOc5w7RT-bYQiw2CY8heOv_AXYDa--ChPCokA130_provenance.
- NP46965.RAk1EAOlaXpqAFMRwwoahz6WAmswUYG4OsiD4wF_gvcN0130_assertion description "[The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46965.RAk1EAOlaXpqAFMRwwoahz6WAmswUYG4OsiD4wF_gvcN0130_provenance.
- NP46977.RAkNRhysbX6h800PH7drBIwjMw4rfo93wcrkufMf1BU50130_assertion description "[Prevalence, clinical profile, and prognosis of NPM mutations in AML with normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46977.RAkNRhysbX6h800PH7drBIwjMw4rfo93wcrkufMf1BU50130_provenance.
- NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_assertion description "[Systematic analysis of CEBPA mutations, in addition to that of alterations in master genes of hematopoiesis, may be useful to assess the prognosis of AML particularly in patients belonging to the 'intermediate' prognostic subgroup.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_provenance.
- NP46989.RAmwcA6O1_xbS1MrrmHcz-nuqJKR6cQIUesLZdyZOqC8c130_assertion description "[We assessed the prognostic significance of single (n=7) and double (n=12) CEBPA mutations among 224 AML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46989.RAmwcA6O1_xbS1MrrmHcz-nuqJKR6cQIUesLZdyZOqC8c130_provenance.
- NP46995.RAinstiycvtOjoNoqk7acb68K9JUaeUmm4pBzPyuWuelE130_assertion description "[Corneodesmosin (CDSN) gene association with psoriasis vulgaris in Caucasian but not in Japanese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46995.RAinstiycvtOjoNoqk7acb68K9JUaeUmm4pBzPyuWuelE130_provenance.
- NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_assertion description "[In a case-control association study of psoriasis in the Sardinian population, we analyzed the allele distribution of eight intragenic SNPs (positions 619, 767, 1215, 1118, 1236, 1243, 1331, 1593) of the CDSN gene and the six haplotypes that are coded by these SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46998.RAouRZsvdvYfuGBGbxOCymyhj_G5DcnQUdMCRz8zH3dW8130_provenance.
- NP47011.RAukCk2eSndNn6SdFzVYHwCSmfX9BE3Gth1ALJF_I8a5Y130_assertion description "[ Our findings suggest that the p27 109GG variant genotype may not play a major role in the etiology of SCCHN but may be associated with an increased risk in at-risk subgroups or subsets of SCCHN, particularly oral cavity cancer and possibly tumor progression. Larger studies with oral squamous cell carcinoma are needed to verify these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47011.RAukCk2eSndNn6SdFzVYHwCSmfX9BE3Gth1ALJF_I8a5Y130_provenance.
- NP47012.RAsHPcuUHQbMthiZN5-zqZuIsvjAQYUEl-yw_-kwEj99o130_assertion description "[ We found that the level of education, the age at first intercourse, and the number of children were independent risk factors in cervix carcinogenesis. The specific combinations of p53, p21, and IRF-1 gene-gene and gene-environmental interactions were significantly noted in the cervix carcinogenesis of Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47012.RAsHPcuUHQbMthiZN5-zqZuIsvjAQYUEl-yw_-kwEj99o130_provenance.
- NP47023.RAlmd3kfpkwKI60WykxfFAnejWdlLc7m6vz8rY2NQoc7M130_assertion description "[We hypothesized that the polymorphisms in the two p53 family genes (p53 Arg72Pro and p73 G4C14-to-A4T14 at exon 2 (G4A)) and p21 Ser31Arg polymorphism might modulate the risk of non-Hodgkin's lymphoma, and conducted a hospital-based prevalent case control study at Aichi Cancer Center Hospital to clarify the association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47023.RAlmd3kfpkwKI60WykxfFAnejWdlLc7m6vz8rY2NQoc7M130_provenance.
- NP47024.RAjDeEb9JUYnFO8qby7J3WrFzAefPni8GSR8sGtSpKsqs130_assertion description "[The polymorphism of p21 codon 31 is associated with bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47024.RAjDeEb9JUYnFO8qby7J3WrFzAefPni8GSR8sGtSpKsqs130_provenance.
- NP47029.RAojU_Gc6mbFwEBE_prFoVG3Uu8v0pmelYO7cZzGt1iuA130_assertion description "[Polymorphisms in the BRCA1 and ABCB1 genes modulate menopausal hormone therapy associated breast cancer risk in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47029.RAojU_Gc6mbFwEBE_prFoVG3Uu8v0pmelYO7cZzGt1iuA130_provenance.
- NP47035.RAp9S-jQ423-mk7gj21At1YqWwrrvc7pNQBvPULLBpdSg130_assertion description "[The novel p21 polymorphism p21G251A is associated with locally advanced breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47035.RAp9S-jQ423-mk7gj21At1YqWwrrvc7pNQBvPULLBpdSg130_provenance.
- NP47039.RAs_XrnuYkfiKHwEPGy6ffb6aIqYpNnHFZn0T6WI-sdKE130_assertion description "[We have studied a consecutive case series of patients with multiple primary melanoma (MPM) for the involvement of the melanoma susceptibility loci CDKN2A and CDK4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47039.RAs_XrnuYkfiKHwEPGy6ffb6aIqYpNnHFZn0T6WI-sdKE130_provenance.
- NP47044.RAogMuZPDQ5DTFvAnIR11ufZbqjHpNJ5MZPwBSfcnKxBU130_assertion description "[Breast cancer risk associated with genotypic polymorphism of the genes involved in the estrogen-receptor-signaling pathway: a multigenic study on cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47044.RAogMuZPDQ5DTFvAnIR11ufZbqjHpNJ5MZPwBSfcnKxBU130_provenance.
- NP47064.RAnFdKsik83stDN6LPO8WwS8Xj7V4D9Ic6aX11VxF93pA130_assertion description "[Our results provide new insights into colorectal tumorigenesis and have potential implications in early detection and target treatment of CRC in non-Western populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47064.RAnFdKsik83stDN6LPO8WwS8Xj7V4D9Ic6aX11VxF93pA130_provenance.
- NP47070.RAu6Zqe2LYbQGKc50WnAyc3NFkJsK6GwLAhEUXsldvz9o130_assertion description "[ The authors' data suggest that individuals with E-cadherin -160 A/A genotype have a decreased risk of GC. Further work is mandatory to clarify the functional relevance of the A allele in vivo and to confirm the inverse association of the A/A genotype with GC in large epidemiologic studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47070.RAu6Zqe2LYbQGKc50WnAyc3NFkJsK6GwLAhEUXsldvz9o130_provenance.
- NP47084.RAj2vVgAU7AdTNvJGaEdC3Dt9XFG_dtTfjgofdkGiVyLY130_assertion description "[Our results suggest that the CTLA-4 +49 alone is not associated with overall susceptibility to MS, but may be important in clinical subsets of patients and/or may interact epistatically with other gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47084.RAj2vVgAU7AdTNvJGaEdC3Dt9XFG_dtTfjgofdkGiVyLY130_provenance.
- NP47088.RAo0XJCr6gxORDWdxLg-nY4VkGiajISgAST3jfgIqwd6Q130_assertion description "[Overall, our data add to the increasing body of evidence of the involvement of host genetic factors in infectious disease and hepatitis C infection in particular. Similar studies should be conducted in other population in order to confirm, or otherwise, these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47088.RAo0XJCr6gxORDWdxLg-nY4VkGiajISgAST3jfgIqwd6Q130_provenance.
- NP47089.RAi5MAGj6JY7vXdONpNpHfKkPxFZrOM-iT2frXZXfZRk8130_assertion description "[Polymorphisms of B7 (CD80 and CD86) genes do not affect disease susceptibility to sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47089.RAi5MAGj6JY7vXdONpNpHfKkPxFZrOM-iT2frXZXfZRk8130_provenance.
- NP47091.RAgwBVCpXw8UoFdYXgg3OhEbgYslhJyejvURUhdm9vq7k130_assertion description "[Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47091.RAgwBVCpXw8UoFdYXgg3OhEbgYslhJyejvURUhdm9vq7k130_provenance.
- NP47102.RAqfYMRVWgeH_npCgp26cyi5nNZYctXKSIxJC0Il_Rpng130_assertion description "[The dinucleotide repeat polymorphism in the 3'UTR of the CD154 gene has a functional role on protein expression and is associated with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47102.RAqfYMRVWgeH_npCgp26cyi5nNZYctXKSIxJC0Il_Rpng130_provenance.
- NP47106.RAmDuzwxnvpz6qMUwzR5G10io6O-sN9hZfhXordp3N8pU130_assertion description "[Graves' disease (GD) is known to be associated with thyroglobulin (TG) and CD40 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47106.RAmDuzwxnvpz6qMUwzR5G10io6O-sN9hZfhXordp3N8pU130_provenance.
- NP47107.RAocpKM9wpB2TpYCnCoMPuAaRSdMM2yD-7gCmQxdHqxbY130_assertion description "[Variants in TNFRSF5 locus and association analysis with Hepatitis B virus (HBV) infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47107.RAocpKM9wpB2TpYCnCoMPuAaRSdMM2yD-7gCmQxdHqxbY130_provenance.
- NP47108.RAlEVcWqSLvdzl2m-O9ld_wF5pLomhueC_NizVfqugSCA130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47108.RAlEVcWqSLvdzl2m-O9ld_wF5pLomhueC_NizVfqugSCA130_provenance.
- NP47110.RAirAuU4gL58-QzDSXvQzBPcLpCzCbCzlP2ePkPhcbsKk130_assertion description "[ Although the present results should be replicated in other study populations for confirmation, the present results suggest that SLC12A1 may contribute to hypertension in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47110.RAirAuU4gL58-QzDSXvQzBPcLpCzCbCzlP2ePkPhcbsKk130_provenance.
- NP47113.RAslvK5NqIcqx57_zDWVwWq2Up5G3D9EzSWNOrz3eRYcU130_assertion description "[ Thus, the -178 A/C SNP promoter mutation in the CD36 gene represents a putative genetic marker for insulin-resistance in the French population, although it does not appear to contribute to the genetic risk for T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47113.RAslvK5NqIcqx57_zDWVwWq2Up5G3D9EzSWNOrz3eRYcU130_provenance.
- NP47118.RAgFeiRAus0FNjrQF10bHy1k7f59Nc8O_8F_5B8kblF5c130_assertion description "[Our findings suggest a significant interaction between alcohol consumption and the CD36 gene A52C polymorphism related to the metabolism of long-chain fatty acids and oxidized LDL in the etiology of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47118.RAgFeiRAus0FNjrQF10bHy1k7f59Nc8O_8F_5B8kblF5c130_provenance.
- NP47121.RAlQK-fvKZ7oc5pu8WQ6eXEiKEwHEGBPV5DcG96xOKKlU130_assertion description "[The data highlights the significance of variations in the ICAM1, PECAM1 and CD36 genes in the manifestation of falciparum malaria in India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47121.RAlQK-fvKZ7oc5pu8WQ6eXEiKEwHEGBPV5DcG96xOKKlU130_provenance.
- NP47124.RAtsY3_1TMyY4fm3ZAYbcebafhoJ6z-C38dT-RqbAaSXw130_assertion description "[Haplotypes in the CTLA4 region are associated with coeliac disease in the Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47124.RAtsY3_1TMyY4fm3ZAYbcebafhoJ6z-C38dT-RqbAaSXw130_provenance.
- NP47125.RAoGaZWWtQrj0uZOD2Y1L9UbaeJmF3m_odVv0VpVcGO78130_assertion description "[Multiple common variants for celiac disease influencing immune gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47125.RAoGaZWWtQrj0uZOD2Y1L9UbaeJmF3m_odVv0VpVcGO78130_provenance.
- NP47131.RAnBuNUvz5iRXknF-RcrO24K4p5t-6CBuHmxfnzB7QvlY130_assertion description "[CD24 Ala/Val polymorphism and multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47131.RAnBuNUvz5iRXknF-RcrO24K4p5t-6CBuHmxfnzB7QvlY130_provenance.
- NP47138.RAiI90wMmTBG7Wey36o_jCVifBvjKytexFGbzvR1rJtnM130_assertion description "[Carrier state of the tested CD14, TLR4, and CARD15 SNPs is not associated with NEC risk in VLBW infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47138.RAiI90wMmTBG7Wey36o_jCVifBvjKytexFGbzvR1rJtnM130_provenance.
- NP47151.RAu3XzwWFQkUBatw0WWWUPMlvrm2QR1RnIE2LpjKCg8Lc130_assertion description "[The -159C/T polymorphism in the CD14 gene and the risk of asthma: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47151.RAu3XzwWFQkUBatw0WWWUPMlvrm2QR1RnIE2LpjKCg8Lc130_provenance.
- NP47153.RAlfgzOC7dhAmKpiuI9DJul7D8alxqsOY6dAAxGg1ucxM130_assertion description "[A significant gene-environment interaction affects airways function in laboratory animal workers. More highly endotoxin-exposed workers with CD14/-1619G alleles have significantly lower FEV(1) and FEF(25-75) percent predicted than those with CD14/-1619AA alleles. Atopic workers are particularly affected by cumulative endotoxin exposures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47153.RAlfgzOC7dhAmKpiuI9DJul7D8alxqsOY6dAAxGg1ucxM130_provenance.
- NP47159.RAvJbxOPIbeuAX-HUqN8C33XYgmGCocmqMx5NY_TiKpNY130_assertion description "[The differences of CD14-159 C/T genotypes of SNPs may be associated with the higher risk of susceptibility and mortality of sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47159.RAvJbxOPIbeuAX-HUqN8C33XYgmGCocmqMx5NY_TiKpNY130_provenance.
- NP47161.RAtX37V6IE2uUMyPqfgp1NEbrsvhGQy-Kk6O8khIuEQ34130_assertion description "[We looked for associations between the severity of appendicitis (uncomplicated vs. perforated or gangrenous), plasma and peritoneal cytokine concentrations, and single nucleotide polymorphisms in genes involved in recognizing bacterial molecules CD14 (-159 C-->T); TLR4 (896 A-->G) and in mounting an inflammatory response IL-6 (-174 G-->C), TNF-alpha (-308 G-->A), IL-1beta (-31 C -->T).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47161.RAtX37V6IE2uUMyPqfgp1NEbrsvhGQy-Kk6O8khIuEQ34130_provenance.
- NP47168.RAiyuSOzUJchU2t58-Sr4QMzBlcJKdmTHcbfj5d4fTLRU130_assertion description "[A gene-by-environment interaction between CD14 C-159T and environmental exposure in childhood may modify the development of atopy. CLINICAL IMPLICATIONS: This polymorphism should be considered in interventions studies that use microbial stimuli to reduce sensitization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47168.RAiyuSOzUJchU2t58-Sr4QMzBlcJKdmTHcbfj5d4fTLRU130_provenance.
- NP47173.RAtqrfoOiAu9gIe2HtlSuxKl7I7sasRPPZK1-BUy9I32s130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47173.RAtqrfoOiAu9gIe2HtlSuxKl7I7sasRPPZK1-BUy9I32s130_provenance.
- NP47176.RAqAxKBs3KaVkIn_FUaKgTLESe2tyE-DNJ3B-grJbrFq8130_assertion description "[These results suggest that in the relatively isolated Finnish population, the T allele confers increased risk of alcoholic liver damage. In particular, TT homozygotes are at a high risk to develop cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47176.RAqAxKBs3KaVkIn_FUaKgTLESe2tyE-DNJ3B-grJbrFq8130_provenance.
- NP47181.RAgczcTLjTJl5i9gQAyBrhQ7pASDSnkX0YD1_mgsRzFfs130_assertion description "[However, no significant association with chronic and or aggressive periodontitis and polymorphisms in CD14 and TLR4 could be proven.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47181.RAgczcTLjTJl5i9gQAyBrhQ7pASDSnkX0YD1_mgsRzFfs130_provenance.
- NP47183.RAuKm7XcNXPfDXMoH8R58dp5TLVaMAgsaf8VBHvA7ocKU130_assertion description "[The C -260T polymorphism of CD14 seems to influence the susceptibility for the development of CHF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47183.RAuKm7XcNXPfDXMoH8R58dp5TLVaMAgsaf8VBHvA7ocKU130_provenance.
- NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion description "[ Our results contradict previous reports that have found a protective effect of the T allele of SNP rs2569190 (C-159T) against atopic disorders. Nevertheless, these results confirm the importance of polymorphisms in CD14 in the development of atopy, and future studies of this gene region will need to account for linkage disequilibrium and environmental exposures unique to the study population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance.
- NP47191.RAm1DxVP3rMce0F0xxF7uDZZ3jQ975mSiOFuBBKOLS5GA130_assertion description "[ This study showed that the T/T genotype with a high level of sCD14 is an independent predictor of in-stent restenosis. The activation of monocytes/macrophages, endothelial cells and smooth muscle cells mediated by CD14 and/or sCD14 may play an important role in the restenosis processes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47191.RAm1DxVP3rMce0F0xxF7uDZZ3jQ975mSiOFuBBKOLS5GA130_provenance.
- NP47202.RAhLG8w-4ekkGMnyLLTwazE_nQHYYADaTd-Ny5bJFBW-k130_assertion description "[In this study, we performed a genetic association study on the single nucleotide polymorphisms (SNPs) present in the genes CD14 (-159 C/T), TNFalpha (-308 G/A), IL-1alpha (-889 C/T), IL-6 (-174 G/C), PSMA6 (-8 C/G), and PDE4D (SNP83 T/C, respectively) in order to discern their possible role in the susceptibility to stroke in a North Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47202.RAhLG8w-4ekkGMnyLLTwazE_nQHYYADaTd-Ny5bJFBW-k130_provenance.
- NP47219.RAsTbo_lBItz4q2FhSySApwUPmCQJ5qaObL7s3iDsNHGo130_assertion description "[The aim of this study was to assess the involvement of inherited variations in CCR2, CCR5, and the ligand RANTES in determining disease outcome in hepatitis C virus (HCV) infected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47219.RAsTbo_lBItz4q2FhSySApwUPmCQJ5qaObL7s3iDsNHGo130_provenance.
- NP47230.RAuDWKo7j4vDPxiQxySeZzbI_vhsEHNsiblOiBc4qPwEI130_assertion description "[The importance of chemokine receptors in the pathophysiology of HIV infection became apparent when it was demonstrated that persons at high risk for HIV-1 infection remain uninfected when they carry a polymorphic variant of CCR5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47230.RAuDWKo7j4vDPxiQxySeZzbI_vhsEHNsiblOiBc4qPwEI130_provenance.
- NP47236.RAupU_r88FkuKrW0xnbkbQHn_kONfD4YyicRJ28XQAfv8130_assertion description "[On the basis of our findings we can exclude the possibility that either the chemokine receptor polymorphisms or the SDF-1 polymorphism explain the beneficial outcome of GBV-C infected patients with HIV infection]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47236.RAupU_r88FkuKrW0xnbkbQHn_kONfD4YyicRJ28XQAfv8130_provenance.
- NP47237.RAh49wS9l2mThiMgfeWOIUmeFgdDI90BYV2TlsQ03Zzak130_assertion description "[Thus, among the major CCR2-CCR5 haplotypes/genotypes in chronically infected and predominantly African-American adolescents, only the E/E genotype appeared to influence early host-virus equilibration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47237.RAh49wS9l2mThiMgfeWOIUmeFgdDI90BYV2TlsQ03Zzak130_provenance.
- NP47247.RAtX6UpJzddyuLchzgfsTzUzbdHB4rCvqHLM2D5WPz2BI130_assertion description "[Polymorphism of CC chemokine receptors CCR2 and CCR5 in Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47247.RAtX6UpJzddyuLchzgfsTzUzbdHB4rCvqHLM2D5WPz2BI130_provenance.
- NP47251.RAhjMLe-KZrt3SwSIfCWRaKobxB0GTDJQJtetifFF77mw130_assertion description "[Association of CCR5 delta32 deletion with early death in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47251.RAhjMLe-KZrt3SwSIfCWRaKobxB0GTDJQJtetifFF77mw130_provenance.
- NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_assertion description "[These results represent an independent validation of MS association with DRB1*15(2) and TNFa9 in Russians and are the first to find the interplay of three loci in conferring susceptibility to MS. They demonstrate the efficacy of our approach for the identification of complex-disease-associated combinations of alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_provenance.
- NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion description "[ In a population with a high allelic frequency for the CCR5Delta32 mutation, a significant protection against childhood asthma is evident which is independent of atopy. This protection is lost in the transition between childhood and early adulthood. The contribution of different genetic candidates to the expression of asthma may change with advancing maturity and confound the interpretation of association and linkage studies unless age is taken into account.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance.
- NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_assertion description "[The chemokine receptor genes on 3p21.3 are significantly plausible candidate genes that can influence the expression of asthma. The previous association of the CCR532 deletion with protection from childhood asthma appears to be explained by linkage disequilibrium with the -G190A mutation in the CCR2 receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_provenance.