Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP87174.RAuerd58ByPmZjo7-n8TVMpsWxWh-YJF8JPDjhKwzXOh0130_assertion description "[Haplotype results indicate that the minor allele of the rs4739217 is a risk factor for TD (permuted allelic p = 0.074). Age was also a risk factor for TD in our sample (p = 0.0001). Taken together, our findings suggest that GFRA2 genetic variants and age may play a role in TD susceptibility, but further work is required to confirm these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87174.RAuerd58ByPmZjo7-n8TVMpsWxWh-YJF8JPDjhKwzXOh0130_provenance.
- NP87176.RAsxdv5Wz6o2k584MnaRecGlS15yS3Z8Lyo6FcFko71RA130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87176.RAsxdv5Wz6o2k584MnaRecGlS15yS3Z8Lyo6FcFko71RA130_provenance.
- NP87177.RAl9TcZd5wGWqH-zLHiUTYkropqpgOzjhsxWzaCtqpjY8130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87177.RAl9TcZd5wGWqH-zLHiUTYkropqpgOzjhsxWzaCtqpjY8130_provenance.
- NP87179.RAqQcBWSX40Pij4pDU_Gw2CqZqKmV9zBZJ2i-uGRvwumQ130_assertion description "[In European Americans, variants within C-reactive protein (CRP) and glial cell line-derived neurotrophic factor (GDNF) were associated with AHI (CRP: = 4.6; SE = 1.1; P = 0.0000402) (GDNF: = 4.3; SE = 1; P = 0.0000201) and with the dichotomous OSA trait (CRP: odds ratio = 2.4; 95% confidence interval, 1.5-3.9; P = 0.000170) (GDNF: odds ratio = 2; 95% confidence interval, 1.4-2.89; P = 0.0000433).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87179.RAqQcBWSX40Pij4pDU_Gw2CqZqKmV9zBZJ2i-uGRvwumQ130_provenance.
- NP87181.RAhelDoFrPixQ-p47D6AnEO2jmpluKHT9ILRzl0cPbZ_A130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87181.RAhelDoFrPixQ-p47D6AnEO2jmpluKHT9ILRzl0cPbZ_A130_provenance.
- NP87182.RAnu3_1bsA5KSk4TBgsCaMzuZQ64mLxwivOUQBFs1wGQg130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87182.RAnu3_1bsA5KSk4TBgsCaMzuZQ64mLxwivOUQBFs1wGQg130_provenance.
- NP87193.RApWl4bQ-AvwuzGlnqLMZv2-iRP_7rsZyU4OKhSLB5ytE130_assertion description "[Variants near genes involved in cholesterol synthesis, hydroxylation, and vitamin D transport affect vitamin D status. Genetic variation at these loci identifies individuals who have substantially raised risk of vitamin D insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87193.RApWl4bQ-AvwuzGlnqLMZv2-iRP_7rsZyU4OKhSLB5ytE130_provenance.
- NP87194.RAoyAW6u8oky2kUfP1HxH3uRncDqIRQeWGfZ6iyF-NUMU130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87194.RAoyAW6u8oky2kUfP1HxH3uRncDqIRQeWGfZ6iyF-NUMU130_provenance.
- NP87197.RAhRYjxaSiHquNfg9mN9yyr8oxN8Y2B25-t8vXdGm4ubo130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87197.RAhRYjxaSiHquNfg9mN9yyr8oxN8Y2B25-t8vXdGm4ubo130_provenance.
- NP87201.RAlZ3xlhLPSiLAjHmd9JjQuMO3bS7i3XSg5EY0pTKQ2VU130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87201.RAlZ3xlhLPSiLAjHmd9JjQuMO3bS7i3XSg5EY0pTKQ2VU130_provenance.
- NP87208.RAnAAtYonNI-bstY8A2qhiOJ1OPDLDU58__JnFoP-p4bY130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87208.RAnAAtYonNI-bstY8A2qhiOJ1OPDLDU58__JnFoP-p4bY130_provenance.
- NP87213.RAuAzuvLyU0aH2JN7bG1-rvru9kZ5RrIRXqZlHuy1Yi2o130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87213.RAuAzuvLyU0aH2JN7bG1-rvru9kZ5RrIRXqZlHuy1Yi2o130_provenance.
- NP87216.RAoQgKgTxLKe_Wc6WPG2SBphSkf-tmoiOcmC3qtCBnCaI130_assertion description "[In a previous ovarian cancer case control study that examined polymorphisms in 26 glycosylation-associated genes, we found strong statistical evidence (P = 0.00017) that women who inherited two copies of a single-nucleotide polymorphism in the UDP-N-acetylgalactosamine:polypeptide N-acetylgalactosaminyltransferase, GALNT1, had decreased ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87216.RAoQgKgTxLKe_Wc6WPG2SBphSkf-tmoiOcmC3qtCBnCaI130_provenance.
- NP87217.RApNlJTeCsM4rw6dpLY1qJa5JlxYxtajkz4vb2I1SBl4Q130_assertion description "[Association of single nucleotide polymorphisms in glycosylation genes with risk of epithelial ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87217.RApNlJTeCsM4rw6dpLY1qJa5JlxYxtajkz4vb2I1SBl4Q130_provenance.
- NP87224.RAkX8c0rjurz_4BG58WjKWRlXe9RNiE2GmSeSNZl-2R5c130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87224.RAkX8c0rjurz_4BG58WjKWRlXe9RNiE2GmSeSNZl-2R5c130_provenance.
- NP87227.RAoXh3_PYvw8fYGFVOdf8YsdkgYWEW4s_RwwF4k0XZ9bQ130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87227.RAoXh3_PYvw8fYGFVOdf8YsdkgYWEW4s_RwwF4k0XZ9bQ130_provenance.
- NP87232.RAlIS1Riw-MiBLXkn_LEmpbDl5R9pWUZeEjqxUIiAYEGA130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87232.RAlIS1Riw-MiBLXkn_LEmpbDl5R9pWUZeEjqxUIiAYEGA130_provenance.
- NP87234.RAoF6DqbEtijjoCaTExzImbjvcrY7r7lmhXNThA37_-JY130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87234.RAoF6DqbEtijjoCaTExzImbjvcrY7r7lmhXNThA37_-JY130_provenance.
- NP87237.RArKwmlYratIt2JfLYiz0x4Aydibelx4dTX3P0RFi57W0130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87237.RArKwmlYratIt2JfLYiz0x4Aydibelx4dTX3P0RFi57W0130_provenance.
- NP87240.RAqEc_aHCQ3-Er8uRGKNMXBfJQgY-9Vr7uqgjyZLeB4VM130_assertion description "[Single nucleotide polymorphism (SNP) mapping was performed on an 865-kb candidate region (D6S1683-D6S265) in 166 Tasmanian MS families, and seven candidate genes ubiquitin D (UBD), olfactory receptor 2H3 (OR2H3), gamma-aminobutyric acid B receptor 1 (GABBR1), myelin oligodendrocyte glycoprotein (MOG), HLA-F, HLA complex group 4 (HCG4) and HLA-G were resequenced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87240.RAqEc_aHCQ3-Er8uRGKNMXBfJQgY-9Vr7uqgjyZLeB4VM130_provenance.
- NP87255.RAkIub8lXw1v8fv0QTMxmViPGYzyWU1vpJUZNDdhRfVcg130_assertion description "[In the replication phase, involving 3052 cases and 6335 controls, 12 SNPs were tested; CAD association was replicated and/or verified for 4 (of 12) SNPs from 3 loci: near BRAP and ALDH2 on 12q24 (P=1.6 10(-34)), HLA-DQB1 on 6p21 (P=4.7 10(-7)), and CDKN2A/B on 9p21 (P=6.1 10(-16)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87255.RAkIub8lXw1v8fv0QTMxmViPGYzyWU1vpJUZNDdhRfVcg130_provenance.
- NP87259.RAlWGFMWX7boCN_i00PpGzdDWHedsdEjJrBzL2dBsc0ZI130_assertion description "[XRCC1, CYP2E1 and ALDH2 genetic polymorphisms and sister chromatid exchange frequency alterations amongst vinyl chloride monomer-exposed polyvinyl chloride workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87259.RAlWGFMWX7boCN_i00PpGzdDWHedsdEjJrBzL2dBsc0ZI130_provenance.
- NP87260.RAp0UAcpqeC0lzeZGq8l_Fcoxnoe-XPe3yQdZG5zWG17M130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87260.RAp0UAcpqeC0lzeZGq8l_Fcoxnoe-XPe3yQdZG5zWG17M130_provenance.
- NP87261.RAic2PEiI2aENDgjFEaN1aQwkN0d9ostSJtVAYyy9961Q130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87261.RAic2PEiI2aENDgjFEaN1aQwkN0d9ostSJtVAYyy9961Q130_provenance.
- NP87265.RAiG09FHSjLvbUD0qLxtlJskhNMQjLUsuBERLAXXA92CI130_assertion description "[, Lewis and Secretor genotyping could be useful to predict respectively breast cancer susceptibility and axillary lymph nodes metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87265.RAiG09FHSjLvbUD0qLxtlJskhNMQjLUsuBERLAXXA92CI130_provenance.
- NP87266.RAkXXTiX_FGB_RK7D8wGtScqPSYAEX0m1LqiF4-GtePQU130_assertion description "[, Lewis and Secretor genotyping could be useful to predict respectively breast cancer susceptibility and axillary lymph nodes metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87266.RAkXXTiX_FGB_RK7D8wGtScqPSYAEX0m1LqiF4-GtePQU130_provenance.
- NP87270.RAvzL6BGfopeRHKMd7ILT_ZcWKlJXjp1dOjcYjGAffXEg130_assertion description "[Mutations in FUS/TLS account for 7% (4 of 58) of FALS in our German cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87270.RAvzL6BGfopeRHKMd7ILT_ZcWKlJXjp1dOjcYjGAffXEg130_provenance.
- NP87275.RAvekDQ8jLWkcuZy-9GvjcNdusRXFb4U3TAfunURCdjvs130_assertion description "[Analysis of genetic predisposition to pulmonary tuberculosis in native Russians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87275.RAvekDQ8jLWkcuZy-9GvjcNdusRXFb4U3TAfunURCdjvs130_provenance.
- NP87293.RAjQTkOVt2s12jf2VejZZ49ncx2K264RucDY-F0duDJOs130_assertion description "[HLA-DRB1*04 was negatively associated with risk of DHF (OR 0.31, 95% CI 0.11-0.85).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87293.RAjQTkOVt2s12jf2VejZZ49ncx2K264RucDY-F0duDJOs130_provenance.
- NP87300.RAsXW8tO6weOGrUdUB5QNa3-QShmG8yP8Zkgv8oKGkfdI130_assertion description "[HLA-DRB genotype and specific IgE responses in patients with allergies to penicillins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87300.RAsXW8tO6weOGrUdUB5QNa3-QShmG8yP8Zkgv8oKGkfdI130_provenance.
- NP87302.RAiRAGfvhWxYWJSY7WYK-BO40oHur6yyzD9QnK9OQK3Ec130_assertion description "[For 155 glioblastoma multiforme patients and 157 control subjects closely matched by ethnicity, age, and gender, PCR-based techniques resolved alleles at HLA-A, -B, -C, and -DRB1 loci along with short tandem repeat polymorphisms of MICA exon 5 and TNFb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87302.RAiRAGfvhWxYWJSY7WYK-BO40oHur6yyzD9QnK9OQK3Ec130_provenance.
- NP87305.RAmGZUDrvs54vG4EzzmIlGC5502bp3CKm3Lt8c-n3i4Cs130_assertion description "[B-cell numbers in the blood of patients with non-HLA*B8 or non-HLA*B44 common variable immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87305.RAmGZUDrvs54vG4EzzmIlGC5502bp3CKm3Lt8c-n3i4Cs130_provenance.
- NP87306.RApme6EqeK5Nuiv6d9TDDaObTZqWufoOjUL9eF82Xf-BQ130_assertion description "[Human leukocyte antigens in undifferentiated spondyloarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87306.RApme6EqeK5Nuiv6d9TDDaObTZqWufoOjUL9eF82Xf-BQ130_provenance.
- NP87307.RApQtDHfk9j_OFZN6b3_j_ZW_A7ZLfkYryPvuJ8VIbK9Q130_assertion description "[HLA-DRB1*0101 is a marker for the development of LP in Mexican Mestizo population, yet another gene or HLA marker within MHC region may be the causatively associated gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87307.RApQtDHfk9j_OFZN6b3_j_ZW_A7ZLfkYryPvuJ8VIbK9Q130_provenance.
- NP87308.RArqWgJ-zzNB93a-CG6XCYoXn5RAYmplM9keLsiWEYAEQ130_assertion description "[The frequency of the HLA-DRB1*07 allele was higher in the CSS patients than in controls (27.1% versus 13.3%; chi(2) = 12.64, P = 0.0003, corrected P P(corr) = 0.0042, odds ratio OR 2.42, 95% confidence interval 95% CI 1.47-3.99).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87308.RArqWgJ-zzNB93a-CG6XCYoXn5RAYmplM9keLsiWEYAEQ130_provenance.
- NP87311.RAvTRMyyFcJdzDBwt4iKLDXUkqkmv22_-F5TFWAXPBHI8130_assertion description "[Ancestral haplotype (AH) 8.1(HLA-A1, Cw7, B8, TNFAB*a2b3, TNFN*S, C2*C, Bf*s, C4A*Q0, C4B*1, DRB1*0301, DRB3*0101, DQA1*0501, DQB1*0201) seems to be associated with susceptibility to autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87311.RAvTRMyyFcJdzDBwt4iKLDXUkqkmv22_-F5TFWAXPBHI8130_provenance.
- NP87314.RAimTsFM9ts81nlCY8aOR4U03XvPTEcLtu3D5JzCR-oaM130_assertion description "[Genetic susceptibility to Andes Hantavirus: Association between severity of disease and HLA aleles in Chilean patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87314.RAimTsFM9ts81nlCY8aOR4U03XvPTEcLtu3D5JzCR-oaM130_provenance.
- NP87317.RAiTnzCtJ8vATVkCo8VFs6hCsXyD_ZGvRj7pMBdb4usY4130_assertion description "[HLA-DQ3 is a probable risk factor for CMV infection in high-risk kidney transplant patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87317.RAiTnzCtJ8vATVkCo8VFs6hCsXyD_ZGvRj7pMBdb4usY4130_provenance.
- NP87319.RAnZjwG9fp8LSn1_jPpm3uGhFGKfUFhDucC7RLmvJV1o0130_assertion description "[HLA class II allele and haplotype frequencies in Iranian patients with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87319.RAnZjwG9fp8LSn1_jPpm3uGhFGKfUFhDucC7RLmvJV1o0130_provenance.
- NP87336.RAkZHXJqIAH4mZXlO_65F4PBhp6c7lURhzXAJMg_hkEu8130_assertion description "[HLA-C(*)03 is a risk factor for cardiomyopathy in Chagas disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87336.RAkZHXJqIAH4mZXlO_65F4PBhp6c7lURhzXAJMg_hkEu8130_provenance.
- NP87338.RAiOIj2tHwSloI63_ILEGX58VFUc8R4_bJP7EYoTzZy38130_assertion description "[Immunogenetics and clinical phenotype of sympathetic ophthalmia in British and Irish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87338.RAiOIj2tHwSloI63_ILEGX58VFUc8R4_bJP7EYoTzZy38130_provenance.
- NP87340.RAuvrzg5Jm8xn5aVtddP85DETRDaYnOSAQ6YdnffEop3E130_assertion description "[Associations of HLA-C alleles with multinodular goiters: study in a population from southeastern Spain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87340.RAuvrzg5Jm8xn5aVtddP85DETRDaYnOSAQ6YdnffEop3E130_provenance.
- NP87341.RAqHkCMmUUZ0NJQ-znfjCNbcMlhB04zn6QqzWYfi8HMgw130_assertion description "[Associations between HLA class I alleles and the prevalence of nasopharyngeal carcinoma (NPC) among Tunisians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87341.RAqHkCMmUUZ0NJQ-znfjCNbcMlhB04zn6QqzWYfi8HMgw130_provenance.
- NP87342.RAoMvaz6sO49UZF8xoBy_q-u_cVvW2zxaj1xnk4tgepnQ130_assertion description "[Human leukocyte antigens in undifferentiated spondyloarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87342.RAoMvaz6sO49UZF8xoBy_q-u_cVvW2zxaj1xnk4tgepnQ130_provenance.
- NP87343.RAmpFOcy5vBYCF6mZN_CQx-FvMWsc1laG-8XMN_wlEXWM130_assertion description "[Analysis of HLA class I-II haplotype frequency and segregation in a cohort of patients with advanced stage ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87343.RAmpFOcy5vBYCF6mZN_CQx-FvMWsc1laG-8XMN_wlEXWM130_provenance.
- NP87347.RAtOsvu_ojqHT4R8x1WM7e3XX3LNR7uOH48NW_sOPdYHI130_assertion description "[This study suggests that polymorphisms in some alleles of B and C in HLA class I genes are associated with Kawasaki disease in Korean children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87347.RAtOsvu_ojqHT4R8x1WM7e3XX3LNR7uOH48NW_sOPdYHI130_provenance.
- NP87352.RAgWUGeAmpndNKgdtPITVUzQ3w6JcYKdG4cV4GL2QFeeQ130_assertion description "[HLA-C(*)03 is a risk factor for cardiomyopathy in Chagas disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87352.RAgWUGeAmpndNKgdtPITVUzQ3w6JcYKdG4cV4GL2QFeeQ130_provenance.
- NP87361.RAnyQ94kEu4TcH9K1MVylUElWr9keuGyRtwn6rv_Bjro0130_assertion description "[Associations of Moyamoya patients with HLA class I and class II alleles in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87361.RAnyQ94kEu4TcH9K1MVylUElWr9keuGyRtwn6rv_Bjro0130_provenance.
- NP87362.RAvXhRmNA4fm09NYhgMprk7wa9ZWZidH0KwRbhRbkEiwo130_assertion description "[The frequency of the HLA-B*2705 allele among the B27 positive uSpA patients of this series was closely similar to that reported for patients with ankylosing spondylitis (AS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87362.RAvXhRmNA4fm09NYhgMprk7wa9ZWZidH0KwRbhRbkEiwo130_provenance.
- NP87367.RAvzzYplH9Tcf2L0UmcLkNINgo5Zet-WQ32kVl8Bzouzk130_assertion description "[B-cell numbers in the blood of patients with non-HLA*B8 or non-HLA*B44 common variable immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87367.RAvzzYplH9Tcf2L0UmcLkNINgo5Zet-WQ32kVl8Bzouzk130_provenance.
- NP87368.RAu-MW8IAE2Apm30kYmu4v9e6tvPiXn3ttT7UQ9q3twMU130_assertion description "[Human leukocyte antigens in undifferentiated spondyloarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87368.RAu-MW8IAE2Apm30kYmu4v9e6tvPiXn3ttT7UQ9q3twMU130_provenance.
- NP87373.RArdyZ0fEUPOmpS_wPJXYzJmcv0fY-gbCsHgjBaBUy4lk130_assertion description "[Haplotype-specific pattern of association of human major histocompatibility complex with non-Hodgkin's lymphoma outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87373.RArdyZ0fEUPOmpS_wPJXYzJmcv0fY-gbCsHgjBaBUy4lk130_provenance.
- NP87374.RAmQvmdaOwsodoTqyYU4-xYgmi1a_AR-6_cytscpzyjsI130_assertion description "[These results suggest that some genes in HLA-B*51-DRB1*09-DQB1*03 haplotype may contribute to NHL susceptibility in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87374.RAmQvmdaOwsodoTqyYU4-xYgmi1a_AR-6_cytscpzyjsI130_provenance.
- NP87376.RAr3M51V0RhkBH9EP2-mdOAkJ3XiJbp9TOm_u9rP5E9wI130_assertion description "[This study suggests that polymorphisms in some alleles of B and C in HLA class I genes are associated with Kawasaki disease in Korean children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87376.RAr3M51V0RhkBH9EP2-mdOAkJ3XiJbp9TOm_u9rP5E9wI130_provenance.
- NP87379.RAmBrhIbbuVpK54_tVEexVydIeR_mKWl2IalW6KtY3j5c130_assertion description "[HLA class I in three West African ethnic groups: genetic distances from sub-Saharan and Caucasoid populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87379.RAmBrhIbbuVpK54_tVEexVydIeR_mKWl2IalW6KtY3j5c130_provenance.
- NP87388.RAgpAzaKIvMVJlw1Qxi0GUR-B1S8SR2N-eL8-OZrWbHAw130_assertion description "[The purpose of this study was to identify the alleles of the HLA-A, -B, -C, -DR, and -DQ, which are present at higher frequencies in USpA patients compared with an ethnically matched control population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87388.RAgpAzaKIvMVJlw1Qxi0GUR-B1S8SR2N-eL8-OZrWbHAw130_provenance.
- NP87390.RAo70CLoYfDizfOVFT4QYslGRGdEj_LY2-AfKeizPMokA130_assertion description "[Study on correlation between HLA-A, B, DR alleles and Duchenne muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87390.RAo70CLoYfDizfOVFT4QYslGRGdEj_LY2-AfKeizPMokA130_provenance.
- NP87392.RAvguaMUtMWVFa6a-nIs19-emoRf8Jhfvm5NiW5txHQvk130_assertion description "[Haplotype-specific pattern of association of human major histocompatibility complex with non-Hodgkin's lymphoma outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87392.RAvguaMUtMWVFa6a-nIs19-emoRf8Jhfvm5NiW5txHQvk130_provenance.
- NP87399.RAmlsBUzNIsGuJsXP0ciX_PI9IONi5ZH2XUf6lNYBQpoM130_assertion description "[Thus, our study, performed in two samples of genetically homogeneous patients and controls, does not support the suggestion that HFE mutations may be associated with acute myocardial infarction in susceptible individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87399.RAmlsBUzNIsGuJsXP0ciX_PI9IONi5ZH2XUf6lNYBQpoM130_provenance.
- NP87406.RAujSusq769Q4bQ4Q9KGutZU3k_qSOz4uUGUETXvCwd8I130_assertion description "[HFE genotype influences erythropoiesis support requirement in hemodialysis patients: a prospective study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87406.RAujSusq769Q4bQ4Q9KGutZU3k_qSOz4uUGUETXvCwd8I130_provenance.
- NP87407.RApaxvDKH8iZZWVDXS1DlpaeGcvQ901yuWOxOSX3LGMT0130_assertion description "[The aim of the present study was to determine the allelic and genotypic frequencies of the HFE gene polymorphisms in malaria patients and blood donors from the Brazilian Amazon region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87407.RApaxvDKH8iZZWVDXS1DlpaeGcvQ901yuWOxOSX3LGMT0130_provenance.
- NP87419.RAtw-KRWao1BnpxehV_sRwGloXIsip5qHeuablbMVlSvc130_assertion description "[For the current study, we hypothesized that 3 of the genes in this region could be involved in the development of autism: 1) paired-like homeodomain transcription factor 1 (PITX1), which is a key regulator of hormones within the pituitary-hypothalamic axis, 2) neurogenin 1, a transcription factor involved in neurogenesis, and 3) histone family member Y (H2AFY), which is involved in X-chromosome inactivation in females and could explain the 4:1 male:female gender distortion present in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87419.RAtw-KRWao1BnpxehV_sRwGloXIsip5qHeuablbMVlSvc130_provenance.
- NP87433.RAqk35_Mf4DGshGS8MruDotu9633AusglLJX2YZ6wEx1s130_assertion description "[The present study confirms a role for genetic alterations of GSTM1 detoxifying enzyme as a risk factor for the development of HNSCC in patients from the Italian Lazio Region, independently of age, sex and other confounding variables.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87433.RAqk35_Mf4DGshGS8MruDotu9633AusglLJX2YZ6wEx1s130_provenance.
- NP87434.RAm01-AL3TrLG8oUE75hjE1lNqMSszZ6EotHJ8m4vn0gw130_assertion description "[No relationship was observed between the null combination of the GSTM1 and GSTT1 genotype polymorphisms and drug eruption risk (OR 2.65, 95% CI 0.62-11.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87434.RAm01-AL3TrLG8oUE75hjE1lNqMSszZ6EotHJ8m4vn0gw130_provenance.
- NP87437.RAibYj2zvZKEb9_OWURsnF9VPMZoV2x4sQegh5m88xgUs130_assertion description "[In this study, to investigate the association of CYP1A1 (MspI), GSTM1 and GSTT1 polymorphisms with hypospadias, a case-control study of 31 case mothers who had boys with hypospadias and 64 control mothers was performed in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87437.RAibYj2zvZKEb9_OWURsnF9VPMZoV2x4sQegh5m88xgUs130_provenance.
- NP87440.RApTUC0SZmGdqaPaxhcZSavkMG3qobe5dgZRQKG0SxRkQ130_assertion description "[The V allele may be a risk factor for AD, mainly in the presence of the apoE 4 allele, while the presence of GSTT1 may indicate protection against the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87440.RApTUC0SZmGdqaPaxhcZSavkMG3qobe5dgZRQKG0SxRkQ130_provenance.
- NP87441.RAtq1ZfDlkMjina93NgL2u7-8rCeK8Yxiqcz7Tt9Jb4mk130_assertion description "[The present study suggests that the GSTM1 null genotype may be a genetic risk factor for development of primary open angle glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87441.RAtq1ZfDlkMjina93NgL2u7-8rCeK8Yxiqcz7Tt9Jb4mk130_provenance.
- NP87451.RAm1ILCSd0UEUlGoXTJpP7SkPrz4Z3m75dmnb3euFXgs8130_assertion description "[Alternative genotyping method of GSTT1 null/present polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87451.RAm1ILCSd0UEUlGoXTJpP7SkPrz4Z3m75dmnb3euFXgs8130_provenance.
- NP87456.RAgohbkHpYHsMn-WBvdFeFbHd2cIDeEztO1AiF-KqIHvQ130_assertion description "[Glutathione-S-transferase (GST) M1 null genotype and combined GSTM1 and GSTT1 null genotypes as a risk factor for alcoholic mild liver dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87456.RAgohbkHpYHsMn-WBvdFeFbHd2cIDeEztO1AiF-KqIHvQ130_provenance.
- NP87457.RAspiISyGgc8GFYApUqeszCXnu9TNS7vcutATH6IPz-Iw130_assertion description "[Antibodies against glutathione S-transferase T1 (GSTT1) in patients with GSTT1 null genotype as prognostic marker: long-term follow-up after liver transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87457.RAspiISyGgc8GFYApUqeszCXnu9TNS7vcutATH6IPz-Iw130_provenance.
- NP87466.RAmmbOzQ9cJfh8i33AeaCyAAfewsZpkNYyRggAldk9ttY130_assertion description "[Polymorphisms of drug-metabolizing enzymes CYP1A1, GSTT and GSTP contribute to the development of diffuse large B-cell lymphoma risk in the Saudi Arabian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87466.RAmmbOzQ9cJfh8i33AeaCyAAfewsZpkNYyRggAldk9ttY130_provenance.
- NP87477.RAmzaFSiI4av4Nz3Thxlk-1wpyOf1LfZPozm0r4QddKOg130_assertion description "[The present study suggests that the GSTM1 null genotype may be a genetic risk factor for development of primary open angle glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87477.RAmzaFSiI4av4Nz3Thxlk-1wpyOf1LfZPozm0r4QddKOg130_provenance.
- NP87481.RAoHFgaJ-wZkUGl39ERQuztNx1JOi3d9Ags8ATH-sXQ1w130_assertion description "[In the present study, we investigated the GSTM1, GSTT1 and GSTP1 gene polymorphisms in diabetic patients and healthy individuals and searched whether polymorphisms in GST genes are associated with diabetes mellitus (DM) in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87481.RAoHFgaJ-wZkUGl39ERQuztNx1JOi3d9Ags8ATH-sXQ1w130_provenance.
- NP87483.RAig4RDqAlJES-J6KQ4c4R1R0TDKIsDjhpE2ldTABPi84130_assertion description "[Polymorphism at the glutathione S-transferase P1 locus in Korean patients with perennial allergic rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87483.RAig4RDqAlJES-J6KQ4c4R1R0TDKIsDjhpE2ldTABPi84130_provenance.
- NP87487.RAiJ9XaVLbcJw_PNOqobp4qA6hcYExEkpYqIvbWjrVS3s130_assertion description "[Re-assessment of the influence of polymorphisms of phase-II metabolic enzymes on renal cell cancer risk of trichloroethylene-exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87487.RAiJ9XaVLbcJw_PNOqobp4qA6hcYExEkpYqIvbWjrVS3s130_provenance.
- NP87488.RAhSpexm5fAf9SCFAgMxA_4Scnrm9fP_ZlZF8Er1ZoqSk130_assertion description "[We investigated the role of the I105V polymorphism in GSTP1, parental periconception smoking, and their interaction with nonsyndromic cleft lip with or without cleft palate (CL/P) risk in the offspring.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87488.RAhSpexm5fAf9SCFAgMxA_4Scnrm9fP_ZlZF8Er1ZoqSk130_provenance.
- NP87499.RAjmgwykZ5DWrFDqQi1x_tdc5sKYzwRMRfwVkFh5wAs-o130_assertion description "[GSTM1 and GSTT1 polymorphisms, cigarette smoking, and risk of colon cancer: a population-based case-control study in North Carolina (United States).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87499.RAjmgwykZ5DWrFDqQi1x_tdc5sKYzwRMRfwVkFh5wAs-o130_provenance.
- NP87501.RAprwmKDsTHWbIk5TdenE54qn4SGffpn33TCxqiK6Es2k130_assertion description "[The association between the GSTM1 and GSTT1 genotypes, and the levels of aminotransferases and total bilirubin was retrospectively investigated in 149 Japanese epileptic patients treated with VPA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87501.RAprwmKDsTHWbIk5TdenE54qn4SGffpn33TCxqiK6Es2k130_provenance.
- NP87505.RAsN_22_tuN9MLGh4zU7QrOaFElFhIHwm16jEAH3dur4I130_assertion description "[The present study suggests that the GSTM1 null genotype may be a genetic risk factor for development of primary open angle glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87505.RAsN_22_tuN9MLGh4zU7QrOaFElFhIHwm16jEAH3dur4I130_provenance.
- NP87507.RAheP-AVRE66eUbqqihGMo2J5mkrox95PIlZXex6m95TI130_assertion description "[Multiple sclerosis and exposure to organic solvents, investigated by genetic polymorphisms of the GSTM1 and CYP2D6 enzyme systems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87507.RAheP-AVRE66eUbqqihGMo2J5mkrox95PIlZXex6m95TI130_provenance.
- NP87509.RAgG6ok556W_4mZiuwM0EyXpXFkkXkg4-NL0kOqalk8I0130_assertion description "[No relationship was observed between the null combination of the GSTM1 and GSTT1 genotype polymorphisms and drug eruption risk (OR 2.65, 95% CI 0.62-11.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87509.RAgG6ok556W_4mZiuwM0EyXpXFkkXkg4-NL0kOqalk8I0130_provenance.
- NP87519.RAp55FZlHMs2XHb47zCKfuvX0gkW31l75Gs5RlasyCuHI130_assertion description "[Evaluation of the association between null genotypes of glutathione-S-transferases and Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87519.RAp55FZlHMs2XHb47zCKfuvX0gkW31l75Gs5RlasyCuHI130_provenance.
- NP87523.RAvTcY5ENXDAyFovzUl5UGWWiU-FR7b8a_DywHLwOBSeM130_assertion description "[Arsenic methylation, GSTT1, GSTM1, GSTP1 polymorphisms, and skin lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87523.RAvTcY5ENXDAyFovzUl5UGWWiU-FR7b8a_DywHLwOBSeM130_provenance.
- NP87526.RAoqLKyK9AuXcHjj2-qQTUzvDnQnC3ZsdKr1GMC_8oXB8130_assertion description "[Glutathione S-transferase M1 and GST T1 genetic polymorphisms and Raynaud's phenomenon in French vinyl chloride monomer-exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87526.RAoqLKyK9AuXcHjj2-qQTUzvDnQnC3ZsdKr1GMC_8oXB8130_provenance.
- NP87527.RArbUlMJFDjavng92YVzfS5MSRK07tSIH_uC0gJzzRDKE130_assertion description "[GSTM1 and GSTP1 are important cytoprotective factors that reduce SHS and DEP exacerbation of allergic responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87527.RArbUlMJFDjavng92YVzfS5MSRK07tSIH_uC0gJzzRDKE130_provenance.
- NP87533.RAt_sr0nY67I0R1BaV6cm8Gc3GZ22pqIY7G7cceab-KC4130_assertion description "[Re-assessment of the influence of polymorphisms of phase-II metabolic enzymes on renal cell cancer risk of trichloroethylene-exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87533.RAt_sr0nY67I0R1BaV6cm8Gc3GZ22pqIY7G7cceab-KC4130_provenance.
- NP87534.RAseSUaZ7PANU2IdXqm8FAIbr2mDsBndWcvRFN7EW9DJ0130_assertion description "[Glutathione S-transferases GSTM1 and GSTT1 polymorphisms and asbestosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87534.RAseSUaZ7PANU2IdXqm8FAIbr2mDsBndWcvRFN7EW9DJ0130_provenance.
- NP87537.RAsdeOlZ48uZe-ypFlIo9BT7-B5DSpk9sAWnHpjJsn67U130_assertion description "[Association of GSTM1, GSTT1, and GSTM3 gene polymorphisms and susceptibility to cervical cancer in a North Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87537.RAsdeOlZ48uZe-ypFlIo9BT7-B5DSpk9sAWnHpjJsn67U130_provenance.
- NP87540.RArx3RwgmLShjWeK-2lA-6qbYSsz3e0mm1m--vtejjmXQ130_assertion description "[In order to investigate the association between effects of genetic polymorphisms of GSTT1 and GSTM1 and depression score of individuals chronically exposed to natural sour gas containing sulfur compounds, the present cross-sectional study was done.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87540.RArx3RwgmLShjWeK-2lA-6qbYSsz3e0mm1m--vtejjmXQ130_provenance.
- NP87547.RAmZQ8o0Piv_5oRn-_UnIzbfk3phVmYlCtAyhhsVdBa3c130_assertion description "[Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87547.RAmZQ8o0Piv_5oRn-_UnIzbfk3phVmYlCtAyhhsVdBa3c130_provenance.
- NP87549.RAg06wAruz5HF7FWqabb-fUtWrWPEr907EydsEUeMoVNY130_assertion description "[Application of machine learning algorithms to predict coronary artery calcification with a sibship-based design.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87549.RAg06wAruz5HF7FWqabb-fUtWrWPEr907EydsEUeMoVNY130_provenance.
- NP87553.RAtm00ShQHYaQDJme_AjNySrNmIBtRG-35QYBsrmBASeQ130_assertion description "[Role of Kozak sequence polymorphism of platelet glycoprotein Ibalpha as a risk factor for coronary artery disease and catheter interventions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87553.RAtm00ShQHYaQDJme_AjNySrNmIBtRG-35QYBsrmBASeQ130_provenance.
- NP87555.RAjYmZyH4vI4w5Lj7St0K_MohKo3WRrSIetDSGXxKk1qk130_assertion description "[the LHR insLQ and GnRH 16Ser alleles are independently associated with shorter DFS in premenopausal patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87555.RAjYmZyH4vI4w5Lj7St0K_MohKo3WRrSIetDSGXxKk1qk130_provenance.
- NP87558.RAhN9wkHJVCorfchA75xuS8-QRbffmxgDolfk7-ANt2t0130_assertion description "[Frequencies of the G-protein beta3 subunit C825T polymorphism and the delta 32 mutation of the chemokine receptor-5 in patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87558.RAhN9wkHJVCorfchA75xuS8-QRbffmxgDolfk7-ANt2t0130_provenance.
- NP87559.RAg6bi0aN26QZzbh8r2xNwKxq3dO45ziYLGHJkwznKOiY130_assertion description "[Polymorphism in genes involved in adrenergic signaling associated with Alzheimer's.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87559.RAg6bi0aN26QZzbh8r2xNwKxq3dO45ziYLGHJkwznKOiY130_provenance.
- NP87561.RAt_vF5zklD7t2M_tg5U2boAXdWEfietsoUDNDsqxhJVg130_assertion description "[Association study of the G-protein beta3 subunit C825T polymorphism with disease progression in patients with bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87561.RAt_vF5zklD7t2M_tg5U2boAXdWEfietsoUDNDsqxhJVg130_provenance.
- NP87564.RArnAxf_P2Er25_O0-kQ9PHam01KOOtxzQPb72YV9HPTk130_assertion description "[The present study examined the relationship between genetic combinations of the C1429T polymorphism in the G-protein beta-3 subunit (GNB3) gene and the A1330V polymorphism in the low-density lipoprotein receptor-related protein 5 (LRP5) gene and the risk of hypercholesterolaemia in Japanese workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87564.RArnAxf_P2Er25_O0-kQ9PHam01KOOtxzQPb72YV9HPTk130_provenance.
- NP87567.RAhYFwvseuciMZvc8VqDdqqCYkPVewVmcL_jG9gQ8790Y130_assertion description "[Significance of transporter associated with antigen processing 2 (TAP2) gene polymorphisms in susceptibility to dengue viral infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87567.RAhYFwvseuciMZvc8VqDdqqCYkPVewVmcL_jG9gQ8790Y130_provenance.
- NP87571.RAqVKjQyYVEjAfS7qsQzJqK5a3IL4aY9CfsD-DscyxtNE130_assertion description "[ALOX5 variants associated with susceptibility to human pulmonary tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87571.RAqVKjQyYVEjAfS7qsQzJqK5a3IL4aY9CfsD-DscyxtNE130_provenance.
- NP87574.RAq9wXbV0dzyWn8JT6g6XJlSBePlqCpgfD1xr3cMeUYBM130_assertion description "[By multiple logistic regression analysis, male sex (P = .027), hypertension (P = .001), and GCLC C/T genotype (P = .009) were the only variables associated with events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87574.RAq9wXbV0dzyWn8JT6g6XJlSBePlqCpgfD1xr3cMeUYBM130_provenance.