Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP54872.RAjiCP9ij0UoqbOjxG6JvsqCAErYeGfdWo-Or3NpkCHGc130_assertion description "[MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54872.RAjiCP9ij0UoqbOjxG6JvsqCAErYeGfdWo-Or3NpkCHGc130_provenance.
- NP54874.RAilkuNBl-7va-PcqSqBA4YFeZ8BBlBua4Qfoa0MWkrBM130_assertion description "[The above findings provide evidence that IgAN patients with abundant immune deposits in glomeruli show a higher frequency of MBP gene variation which is associated with a high frequency of infection and a low serum MBP level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54874.RAilkuNBl-7va-PcqSqBA4YFeZ8BBlBua4Qfoa0MWkrBM130_provenance.
- NP54879.RAtakxXzS-84A6TDo-YwSiUsfMU1KNmaL1Jt5x2y9JGic130_assertion description "[Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54879.RAtakxXzS-84A6TDo-YwSiUsfMU1KNmaL1Jt5x2y9JGic130_provenance.
- NP54880.RApOAVSuoYJVU9en6N0gEGVLgxbeEFwgwqV1pm8KcDkY0130_assertion description "[Mannose-binding protein gene polymorphism in systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54880.RApOAVSuoYJVU9en6N0gEGVLgxbeEFwgwqV1pm8KcDkY0130_provenance.
- NP54886.RAvOhL0O_wVkikGXBRzeD0TTYQF-ZXDsYYAlZvqDuHD5Y130_assertion description "[An update on genetic studies of systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54886.RAvOhL0O_wVkikGXBRzeD0TTYQF-ZXDsYYAlZvqDuHD5Y130_provenance.
- NP54887.RAqcXOjqKKYtFQPNjkhCbwIeuWnHjoFZLk34PXTu1cjh8130_assertion description "[Only in SLE patients fulfilling > or =4 ACR criteria an increased frequency of MBL variant alleles was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54887.RAqcXOjqKKYtFQPNjkhCbwIeuWnHjoFZLk34PXTu1cjh8130_provenance.
- NP54888.RAnCQZkYDxKnm8ThItf4qvHQTdWTUTNB1z9xtXlsu71WE130_assertion description "[Using a combined approach of heteroduplex generator and polymerase chain reaction, a systematic search for mutations in exon 1 and the promoter region of the MBL gene was performed in a Chinese study population comprising 41 SLE patients and 111 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54888.RAnCQZkYDxKnm8ThItf4qvHQTdWTUTNB1z9xtXlsu71WE130_provenance.
- NP54890.RAhvsr-skMegqW40AxGp8PruhqzE9hZEK8cyKcwMz5QJQ130_assertion description "[Circulating surfactant protein D is decreased in systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54890.RAhvsr-skMegqW40AxGp8PruhqzE9hZEK8cyKcwMz5QJQ130_provenance.
- NP54893.RAkfSiIom52aqGc2S5azPuP9WpNTqyinkyP0czvMC80yE130_assertion description "[ MBL gene polymorphism influences susceptibility to SLE, but has no direct effect on disease characteristics. Serum MBL levels fluctuate during the course of SLE in individual patients. MBL genotyping may be useful in assessing the risk of infection during treatment of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54893.RAkfSiIom52aqGc2S5azPuP9WpNTqyinkyP0czvMC80yE130_provenance.
- NP54899.RAr14B85exg2rJWZJqcb3B0Zw_Uz40CmEzm6YYKklWFpQ130_assertion description "[Homozygosity at codons 54 (A/A) and -550 (H/H) appears to be associated with the severity, but not the outcome, of sepsis, whereas a low MBL level may be an independent risk factor for mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54899.RAr14B85exg2rJWZJqcb3B0Zw_Uz40CmEzm6YYKklWFpQ130_provenance.
- NP54903.RAteCy4JBq8hRS06II1fqG-vLmP1Kb8QeYCkK9mfICDh4130_assertion description "[Association of a new mannose-binding lectin variant with severe malaria in Gabonese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54903.RAteCy4JBq8hRS06II1fqG-vLmP1Kb8QeYCkK9mfICDh4130_provenance.
- NP54904.RArRRj45m7s9i5WbfyBi_We1HYDXY9QYVU-tYhcp-3FU8130_assertion description "[Novel MASP2 variants detected among North African and Sub-Saharan individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54904.RArRRj45m7s9i5WbfyBi_We1HYDXY9QYVU-tYhcp-3FU8130_provenance.
- NP54906.RAqnP-BLU2sfv9e8ujdutzZ9jL2mlYQvbmgI_8m7681Mw130_assertion description "[These results indicate that low levels of MBL and AB genotype may be involved in the protection against tuberculosis, especially extrapulmonary tuberculosis in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54906.RAqnP-BLU2sfv9e8ujdutzZ9jL2mlYQvbmgI_8m7681Mw130_provenance.
- NP54909.RAsiBDUCfRVuKU72OLAtKpQRMQqp9kYHae0Cz5kO_jZJ8130_assertion description "[Immunological status in the aetiology of recurrent otitis media with effusion: serum immunoglobulin levels, functional mannose-binding lectin and Fc receptor polymorphisms for IgG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54909.RAsiBDUCfRVuKU72OLAtKpQRMQqp9kYHae0Cz5kO_jZJ8130_provenance.
- NP54916.RAu5NHD-vJtSZ2DgpnrqWWsY7G5py5cZ0BHua_VWaVK_U130_assertion description "[It is possible that mutations of the MBL gene might be related to the trigger of the pathogenesis of Kawasaki disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54916.RAu5NHD-vJtSZ2DgpnrqWWsY7G5py5cZ0BHua_VWaVK_U130_provenance.
- NP54918.RAuNP5ViDqHIpAJDUnBj8ns-5wS_e11MqfFDbJmEXa61g130_assertion description "[ MBL*B carriage and reduced plasma MBL levels are more common in women with vulvar vestibulitis syndrome than in control patients, and may contribute to symptomatology in a subset of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54918.RAuNP5ViDqHIpAJDUnBj8ns-5wS_e11MqfFDbJmEXa61g130_provenance.
- NP54924.RAirobqD2yjjV56-zeO_w6Qe2L9WLsGO_sFlwzWsapEqw130_assertion description "[Only in SLE patients fulfilling > or =4 ACR criteria an increased frequency of MBL variant alleles was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54924.RAirobqD2yjjV56-zeO_w6Qe2L9WLsGO_sFlwzWsapEqw130_provenance.
- NP54927.RAqw4hVekcGsoyhfhdf939LC-X29OASXpVwZrXFYumVvA130_assertion description "[To test the hypothesis that a genetic predisposition to a proinflammatory state could favor the appearance of GDM during pregnancy, we studied R52C and G54D polymorphisms of MBL2 gene and plasma MBL levels from 105 consecutive GDM women and 173 healthy pregnant women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54927.RAqw4hVekcGsoyhfhdf939LC-X29OASXpVwZrXFYumVvA130_provenance.
- NP54930.RAlOCy13UMsOxTiPdx0KtU79mzyqnuejUjtsi2Ppnz86U130_assertion description "[The distribution of alleles in the Japanese population was significantly different from that reported among whites, blacks, and Hispanics (p < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54930.RAlOCy13UMsOxTiPdx0KtU79mzyqnuejUjtsi2Ppnz86U130_provenance.
- NP54932.RAms2LlNPHI1YKgkTqwvZh2BWvvlPETLam_GM_dVjLLiM130_assertion description "[Polymorphisms of the methyl-CpG binding domain 1 (MBD1) gene may influence MBD1 activity on gene expression profiles, thereby modulating individual susceptibility to lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54932.RAms2LlNPHI1YKgkTqwvZh2BWvvlPETLam_GM_dVjLLiM130_provenance.
- NP54944.RAvr0LDpVQ2-OmQP7aHC5j8x9eTrnBg5RLWZEW_xGz3R8130_assertion description "[We addressed this latter hypothesis by determining the DNA sequence of the entire MAO-B coding region comprising 15 exons and partial intronic sequences flanking each exon, in 33 cases with idiopathic PD and 38 unrelated controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54944.RAvr0LDpVQ2-OmQP7aHC5j8x9eTrnBg5RLWZEW_xGz3R8130_provenance.
- NP54952.RAsazMA6K17eDGvjfVrtpw_w9HW0NuunMnRv8nSy4BeF0130_assertion description "[HTR2A and TPH significantly predicted the depression group, independent of the effects of sex, environmental risk group and their interaction. In addition, there was a trend for an effect of 5HTTLPR, which was significant in female subjects. Furthermore, there was a significant genotype-environmental risk interaction for 5HTTLPR in female subjects only, with the effect being in the same direction as another recent study, reaffirming that an important source of genetic heterogeneity is exposure to environmental risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54952.RAsazMA6K17eDGvjfVrtpw_w9HW0NuunMnRv8nSy4BeF0130_provenance.
- NP54954.RArbnzo2X0_KuwCSiMT2K1oVOQR-AsG_I8lqM-w2XvkCA130_assertion description "[These results suggest that variations in genes encoding the components of serotonin metabolism may influence the basic mood level and that different genetic factors may apply in men and women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54954.RArbnzo2X0_KuwCSiMT2K1oVOQR-AsG_I8lqM-w2XvkCA130_provenance.
- NP54955.RAu1iYaS6PMeKIDjVlUlZhZplvI9fs1eANUX2-Olx4EEg130_assertion description "[It has been suggested that monoamine oxidase A (MAO-A) activity is involved in the pathogenesis of major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54955.RAu1iYaS6PMeKIDjVlUlZhZplvI9fs1eANUX2-Olx4EEg130_provenance.
- NP54958.RAu_rrHnwjbzwh1TReUJyM8JWBiUhctVxLkULQAabq_dw130_assertion description "[The association of the MAOA-uVNTR with both susceptibility to AD and dopamine metabolite (HVA) concentration lends further biological plausibility for high MAO-A enzyme activity as a mechanistic factor for genetic predisposition to AD through altered dopamine turnover.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54958.RAu_rrHnwjbzwh1TReUJyM8JWBiUhctVxLkULQAabq_dw130_provenance.
- NP54959.RAiALJO7GaApePp-_7B_lK-OXZgQGBR9RLedahu9blblA130_assertion description "[MAOA gene polymorphisms and response to mirtazapine in major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54959.RAiALJO7GaApePp-_7B_lK-OXZgQGBR9RLedahu9blblA130_provenance.
- NP54967.RAmgB2vgPBynCQC89oqi3dejdp11Q_m-DAYP30dGgAV4Y130_assertion description "[Many small studies have reported associations between genetic polymorphisms and PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54967.RAmgB2vgPBynCQC89oqi3dejdp11Q_m-DAYP30dGgAV4Y130_provenance.
- NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion description "[We found weak evidence for association with COMT genotype, when the females and males were considered separately, and for MAOA genotype in males only. There was no significant interaction between COMT and MAOA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance.
- NP54979.RAiie0DUkfnEr6k9GtOrXc3ngLai1b0dPx9ZIW4xDhaXc130_assertion description "[Monoamine oxidase a polymorphism in Brazilian patients: risk factor for late-onset Alzheimer's disease?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54979.RAiie0DUkfnEr6k9GtOrXc3ngLai1b0dPx9ZIW4xDhaXc130_provenance.
- NP54980.RAp28VxZje03eHLrHXsACrvKEtNXUqRb88_WP_Fkbr5Ok130_assertion description "[These results suggest that polymorphisms within the MAOA gene may have implication in AD pathology shared by pure AD and LBV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54980.RAp28VxZje03eHLrHXsACrvKEtNXUqRb88_WP_Fkbr5Ok130_provenance.
- NP54987.RAnycu1CvALLjYK1q-EH-Ahf7BsUjREYLAevRtAJTtdtY130_assertion description "[The present results support the involvement of the MAOA gene in men with schizophrenia in the investigated Swedish population but should be interpreted with caution until replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54987.RAnycu1CvALLjYK1q-EH-Ahf7BsUjREYLAevRtAJTtdtY130_provenance.
- NP54990.RAuq5GeGY2NN7Q1qi7apPTkRq9ucWAhxCHH48ZyhTne6s130_assertion description "[Association of functional genes polymorphisms of key enzymes in the metabolism of biogenic amines with paranoid schizophrenia susceptibility and the influence of these polymorphisms on PANSS results in antipsychotic treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54990.RAuq5GeGY2NN7Q1qi7apPTkRq9ucWAhxCHH48ZyhTne6s130_provenance.
- NP54992.RAgjeX3-cZ8UCminMNeJqoDPTx5nu0doB7_HY99GNzOLc130_assertion description "[These findings suggest that genetic variants in MAOA may play a role in susceptibility to schizophrenia in Chinese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54992.RAgjeX3-cZ8UCminMNeJqoDPTx5nu0doB7_HY99GNzOLc130_provenance.
- NP54995.RAipzzU_0Q6FNdPuL7pWXiZf6QP5vxIs--md-yb5e7z8M130_assertion description "[To investigate the relationship between monoamine oxidase A (MAOA) gene polymorphisms and schizophrenia in a Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54995.RAipzzU_0Q6FNdPuL7pWXiZf6QP5vxIs--md-yb5e7z8M130_provenance.
- NP55003.RAjqkEEu9DMDvRT7A2zoi41nqKOABzU2E0xd6_tKO1k0Q130_assertion description "[A case group of males with type 2 alcoholism (N=59) and a control group of healthy males (N=282), both of Croatian origin, were analyzed for the frequency distribution of polymorphisms in 5HT transporter (5HTT-VNTR2, 5HTT-LPR), monoamine oxidase A (MAOA-uVNTR) and B (MAOB-A/G) and tryptophan hydroxylase 1 (TPH1 A218C) and 2 (TPH2 G-703T) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55003.RAjqkEEu9DMDvRT7A2zoi41nqKOABzU2E0xd6_tKO1k0Q130_provenance.
- NP55004.RApq1m74COCJVQUPNIk4EragF0fM7LHKC_ikl7Izjr0vs130_assertion description "[Serotonin transporter (5-HTTLPR) and monoamine oxidase (MAOA) promoter polymorphisms in women with severe alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55004.RApq1m74COCJVQUPNIk4EragF0fM7LHKC_ikl7Izjr0vs130_provenance.
- NP55006.RAlij1TmYFx9QGJ6FgNDhlILo5lzLnpPRJ_F8s4T4UWgM130_assertion description "[The high activity allele of the MAOA gene may represent a modifying factor involved in the severity of RLS manifestations in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55006.RAlij1TmYFx9QGJ6FgNDhlILo5lzLnpPRJ_F8s4T4UWgM130_provenance.
- NP55012.RAn7e1TQbdgnXzSy3r_AwDnwHmmyZRCb59OIFrKCb_ONM130_assertion description "[Monoamine oxidase a and catechol-o-methyltransferase functional polymorphisms and the placebo response in major depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55012.RAn7e1TQbdgnXzSy3r_AwDnwHmmyZRCb59OIFrKCb_ONM130_provenance.
- NP55013.RAqBdZIcbrBpH_sf3Eat0q41LJRWLjO4NtR2isPgCrocg130_assertion description "[Sex-specific interaction between MAOA promoter polymorphism and Apo epsilon 2 allele in major depressive disorder in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55013.RAqBdZIcbrBpH_sf3Eat0q41LJRWLjO4NtR2isPgCrocg130_provenance.
- NP55016.RApeB-eat0QkLQWA75UmycEXt3DuY7Vh1dQpGN544fIoc130_assertion description "[Gene-lifecourse interaction for alcohol consumption in adolescence and young adulthood: five monoamine genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55016.RApeB-eat0QkLQWA75UmycEXt3DuY7Vh1dQpGN544fIoc130_provenance.
- NP55020.RAkYEX_NcfQtWiE3WbyhIKtVVaT7SlSbZAAQGItL7wU_I130_assertion description "[The promoter of the monoamine oxidase A (MAO-A) gene was analysed to test whether length variation of the repeat polymorphism contributes to variation in individual vulnerability to aggressive-criminal behaviour, and liability to heroin dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55020.RAkYEX_NcfQtWiE3WbyhIKtVVaT7SlSbZAAQGItL7wU_I130_provenance.
- NP55029.RAolkmjSexQ7Ijs4N0h8dyvO5tRuqbwh18m3Lu9IuZWEs130_assertion description "[As we tested for epistasis between MAOA VNTR and COMT Val/Met, we found no significant interaction in conferring risk for suicide attempts (P = 0.545).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55029.RAolkmjSexQ7Ijs4N0h8dyvO5tRuqbwh18m3Lu9IuZWEs130_provenance.
- NP55030.RAj4_mbIXSuJ8ceZYI706w7ioYKm1MMvJ_At0SMZwXmT8130_assertion description "[Family-based association study between the monoamine oxidase A gene and obesity: implications for psychopharmacogenetic studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55030.RAj4_mbIXSuJ8ceZYI706w7ioYKm1MMvJ_At0SMZwXmT8130_provenance.
- NP55034.RAhZYH1BS2MJoKkcTwTrwKRuy8Pi91_Fbx4ysWJm-Z3ro130_assertion description "[The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55034.RAhZYH1BS2MJoKkcTwTrwKRuy8Pi91_Fbx4ysWJm-Z3ro130_provenance.
- NP55040.RAs8QIQRcnbONHTsMPhWDjU6zGjM477cIz2K65sJJeqlQ130_assertion description "[Furthermore, we performed a particular gene-gene interaction for the X-linked serotonergic genes (HTR2C and MAOA), and found no association among this intergenic haplotype combination and suicidal behaviour in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55040.RAs8QIQRcnbONHTsMPhWDjU6zGjM477cIz2K65sJJeqlQ130_provenance.
- NP55042.RAj6-__S55Sqmk9Ejw2XrQXucIQBw9zK4SPg3cJi4ap6g130_assertion description "[Given the link between abnormalities in serotonergic neurotransmission and bipolar disorder, a candidate gene association approach was applied to study the involvement of the monoamine oxidase A (MAOA) gene, which codes for a catabolic enzyme of serotonin, in the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55042.RAj6-__S55Sqmk9Ejw2XrQXucIQBw9zK4SPg3cJi4ap6g130_provenance.
- NP55044.RAjjJLuL1JHMfnjfzL5KSZ5VuiY1Rpj8PK7Wdiv2VjYqA130_assertion description "[A linkage and family-based association analysis of a potential neurocognitive endophenotype of bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55044.RAjjJLuL1JHMfnjfzL5KSZ5VuiY1Rpj8PK7Wdiv2VjYqA130_provenance.
- NP55055.RAjjL6fhEzN8Nnxpa5RZ5bx6iIJcgFneEAwt562lMtzqw130_assertion description "[Polymorphisms of myelin-associated glycoprotein gene are associated with schizophrenia in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55055.RAjjL6fhEzN8Nnxpa5RZ5bx6iIJcgFneEAwt562lMtzqw130_provenance.
- NP55057.RAtUmyotXFQI5VfK7Bd34JtXIQbm1JFLo-yi6ligGxF18130_assertion description "[Analysis of 927T > C CYSLTR1 and -444A > C LTC4S polymorphisms in children with asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55057.RAtUmyotXFQI5VfK7Bd34JtXIQbm1JFLo-yi6ligGxF18130_provenance.
- NP55059.RAsmLKAvNW879TJzp8EX7ifammpa8ExMNlNcuWRkkBC1U130_assertion description "[This study evaluated associations between the clinical requirement for LTRA and genetic polymorphisms of the ALOX5, LTC4S, COX-2, CysLTR1 and TBXA2R genes in the arachidonic acid cascade in the long-term management of 89 AIA patients from a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55059.RAsmLKAvNW879TJzp8EX7ifammpa8ExMNlNcuWRkkBC1U130_provenance.
- NP55061.RAsm2LTD8LN9gwgnwjOUWe8ilbXiptOuWqJ3sYvyVw0MU130_assertion description "[We examined the interaction between the clinical response to a cysLT(1) antagonist, pranlukast, and DNA sequence variant A(-444)C in leukotriene C(4) synthase (LTC(4) S) gene in Japanese patients with moderate asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55061.RAsm2LTD8LN9gwgnwjOUWe8ilbXiptOuWqJ3sYvyVw0MU130_provenance.
- NP55062.RAgECYU52OibytEFuoABJYfdY9fSr6ecQCKV1qGhltIMw130_assertion description "[Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55062.RAgECYU52OibytEFuoABJYfdY9fSr6ecQCKV1qGhltIMw130_provenance.
- NP55074.RAs8i4CS0NVLAgyCX_tZMpI4s-JRD9734tffpxDzFFisA130_assertion description "[Our results support the role of LTA4H and ALOX5AP variants as risk factors for asthma in Latino populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55074.RAs8i4CS0NVLAgyCX_tZMpI4s-JRD9734tffpxDzFFisA130_provenance.
- NP55079.RArGNkXBVIrcOBSLyccl5BZi1DtWRIxQgkllzeSum7UBs130_assertion description "[ Our results suggest that common genetic variants in proinflammatory cytokine genes could influence the risk for spontaneous preterm birth. Selected TNF/LTA haplotypes were associated with spontaneous preterm birth in both African-American and white subjects. Our data do not support an inflammatory etiology for SGA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55079.RArGNkXBVIrcOBSLyccl5BZi1DtWRIxQgkllzeSum7UBs130_provenance.
- NP55081.RAskoCtHHkD5tUfqlur6LpqkgDxKY1j-Q1P2oC9fgjQ7U130_assertion description "[A haplotype comprising SNPs in two proinflammatory cytokines, tumor necrosis factor-alpha and lymphotoxin-alpha (rs1800629, rs361525, rs1799724, rs909253, and rs2239704), increased non-Hodgkin lymphoma risk overall (OR, 1.31; 95% CI, 1.06-1.63; P = 0.01) and notably for diffuse large B cell (OR, 1.64; 95% CI, 1.23-2.19; P = 0.0007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55081.RAskoCtHHkD5tUfqlur6LpqkgDxKY1j-Q1P2oC9fgjQ7U130_provenance.
- NP55083.RAou63SIO5YjfE5-aXyep9A_uOGifhF4QhlppZXk9MReg130_assertion description "[Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55083.RAou63SIO5YjfE5-aXyep9A_uOGifhF4QhlppZXk9MReg130_provenance.
- NP55085.RAlh8JwTv23cAdTPiIo8gU8HQzUDbGYZxXDBFB3ihq3FA130_assertion description "[Genetic polymorphisms in tumor necrosis factor (TNF)-alpha and TNF-beta in a population-based study of systemic lupus erythematosus: associations and interaction with the interleukin-1alpha-889 C/T polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55085.RAlh8JwTv23cAdTPiIo8gU8HQzUDbGYZxXDBFB3ihq3FA130_provenance.
- NP55091.RAkynLV9Ds4jBdTZOPEXGi2DKJnSALsfzhTa10AYJa40U130_assertion description "[These data indicate an association between TNFbeta polymorphism and postoperative complications and they suggest the B2/B2 genotype as a high risk factor for the development of sepsis after elective operative trauma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55091.RAkynLV9Ds4jBdTZOPEXGi2DKJnSALsfzhTa10AYJa40U130_provenance.
- NP55093.RApw1vHb-xzXXhi5n1HK2_LJJq56eG5BhmFikvVwvPvn0130_assertion description "[Results found by TDT-STDT have confirmed the involvement of the TNF -308 gene polymorphism in AITD pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55093.RApw1vHb-xzXXhi5n1HK2_LJJq56eG5BhmFikvVwvPvn0130_provenance.
- NP55099.RAiVTRl-uLbrXRiAL1owmIVxnsodm9vy0gg8eD4PEegb0130_assertion description "[Both biochemical and genetic evidence have implicated the genes for TNF-alpha (TNFA) and lymphotoxin-alpha (LTA) in atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55099.RAiVTRl-uLbrXRiAL1owmIVxnsodm9vy0gg8eD4PEegb0130_provenance.
- NP55101.RAl6gzk-_tYvHDsWdorCgMObv913AaJQhC5ObSWR2Enjc130_assertion description "[We genotyped the TNF -308 and LTA NcoI polymorphisms, and two other haplotype-tagging polymorphisms in the TNF and LTA genes, in 708 children with mild to moderate asthma enrolled in the Childhood Asthma Management Program and in their parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55101.RAl6gzk-_tYvHDsWdorCgMObv913AaJQhC5ObSWR2Enjc130_provenance.
- NP55108.RArmv9FOMkeySos5ZhVzWTcqsmEqU4BnXyEYM1y9K_3Cc130_assertion description "[ Genetic variation in the HLA-DRB1 and the LTA-TNF regions is significantly associated with response to treatment of early RA. These findings may have clinical application through the identification of patients who are most likely to benefit from treatment with methotrexate or etanercept.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55108.RArmv9FOMkeySos5ZhVzWTcqsmEqU4BnXyEYM1y9K_3Cc130_provenance.
- NP55115.RApBvhEgaVfNuI77M97rwXwDucjlZlq9a2G7G1BwaDEEs130_assertion description "[We conclude that further study of genetic factors that may influence susceptibility to CP in very preterm infants is warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55115.RApBvhEgaVfNuI77M97rwXwDucjlZlq9a2G7G1BwaDEEs130_provenance.
- NP55126.RAk1NdNFjL9fgRrUhwUH-osjEdPrWpAp-a-BVXozKEOTA130_assertion description "[To determine the association between 17 single nucleotide polymorphisms (SNPs) of tumor necrosis factor-alpha, lymphotoxin-alpha, and the TNF-receptors genes (TNF, LTA, and TNFRSF1A and -B) and idiopathic acute anterior uveitis (IAU) and to investigate their association with HLA-B27 and/or the development of visually significant complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55126.RAk1NdNFjL9fgRrUhwUH-osjEdPrWpAp-a-BVXozKEOTA130_provenance.
- NP55128.RAsGKt5bu7wseTFXpVJNW0x7vtzt5-w3HsuDrqfSNU1ag130_assertion description "[Thirty Caucasians with cirrhosis due to chronic HCV infection and 114 HCV-infected patients histopathologically free of cirrhosis were genotyped for genetic variants in TNF, lymphotoxin alpha and TNF-receptor type I using PCR-based techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55128.RAsGKt5bu7wseTFXpVJNW0x7vtzt5-w3HsuDrqfSNU1ag130_provenance.
- NP55130.RAs0myVGAiuFNOYc4Yc45skrUdWbQuxm9DnfuLm2pp-Dw130_assertion description "[A PCR restriction fragment length polymorphism assay was used to analyse single-nucleotide polymorphisms in the tumour necrosis factor (TNF)-alpha and TNF-beta genes of 56 patients with chronic severe hepatitis B virus (HBV) infection, 71 patients who either had chronic mild HBV infection or who were asymptomatic carriers, and 90 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55130.RAs0myVGAiuFNOYc4Yc45skrUdWbQuxm9DnfuLm2pp-Dw130_provenance.
- NP55135.RAjmRqgrK82oVhBAgKfBelt9anGnHY76yEd_zIFANdlPo130_assertion description "[Polymorphism in the tumor necrosis factor B gene is associated with Palmoplantar pustulosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55135.RAjmRqgrK82oVhBAgKfBelt9anGnHY76yEd_zIFANdlPo130_provenance.
- NP55136.RAhwo4yAJyu1DtdOMlvRARQhtKXSnhvVLHCeU3UwUfj5I130_assertion description "[The finding may imply a multifunctional etiological factor of TNF-alpha in OSF pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55136.RAhwo4yAJyu1DtdOMlvRARQhtKXSnhvVLHCeU3UwUfj5I130_provenance.
- NP55142.RAnrSnRyAZijBvSXzWRX9atPO5E_Dv_kt7hmPqUuswOoA130_assertion description "[Systemic lupus erythematosus with nephritis is strongly associated with the TNFB*2 homozygote in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55142.RAnrSnRyAZijBvSXzWRX9atPO5E_Dv_kt7hmPqUuswOoA130_provenance.
- NP55147.RArFH2WUjmPPFukurBsGBfjQEaq3yN9xZGyq64rIp0ENU130_assertion description "[Association analysis between polymorphisms of the lymphotoxin-alpha gene and myocardial infarction in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55147.RArFH2WUjmPPFukurBsGBfjQEaq3yN9xZGyq64rIp0ENU130_provenance.
- NP55153.RAueFiedUyQ5V4TD2GcDa6jtw44DbCmukN9vw3i3BLOZg130_assertion description "[This observation indicates that low C4B copy number is a strong risk factor for short-term mortality after AMI in smoking Icelandic patients, whereas LTA 252 G allele is not a risk factor in Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55153.RAueFiedUyQ5V4TD2GcDa6jtw44DbCmukN9vw3i3BLOZg130_provenance.
- NP55155.RAp8i-xPsnZZ6W8-HdvOhJcoFQKIHKBSTNQyDAxDhc3mY130_assertion description "[A tumor necrosis factor-beta polymorphism associated with hypertriglyceridemia in non-insulin-dependent diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55155.RAp8i-xPsnZZ6W8-HdvOhJcoFQKIHKBSTNQyDAxDhc3mY130_provenance.
- NP55158.RAh0qM4DlUtGWUU_0VLki94NMXX3FNMOSBHmA9adHDwhw130_assertion description "[Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55158.RAh0qM4DlUtGWUU_0VLki94NMXX3FNMOSBHmA9adHDwhw130_provenance.
- NP55170.RAjL54W7kvA4NIEsL_UOTeIpPWuTXrHThRWvU2UpkTsjs130_assertion description "[PARK8 patients did not have a relevant family history of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55170.RAjL54W7kvA4NIEsL_UOTeIpPWuTXrHThRWvU2UpkTsjs130_provenance.
- NP55176.RAq5EKzkqrX1bdbav42lHAP3NNBvFIqHh5XTh_Hp0lv6M130_assertion description "[LRRK2 mutations do not appear to be a common cause of Parkinson's disease in Extremadura, Spain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55176.RAq5EKzkqrX1bdbav42lHAP3NNBvFIqHh5XTh_Hp0lv6M130_provenance.
- NP55182.RAvirDYsQIkS_dgy5390EmhI66O1L-k8-NFwTTl3d6rkQ130_assertion description "[Case control analysis of LRRK2 Gly2385Arg in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55182.RAvirDYsQIkS_dgy5390EmhI66O1L-k8-NFwTTl3d6rkQ130_provenance.
- NP55185.RAnCYcTImrbM8k66Xc63yW79n4EyWS_B9QRCTZlQD3N-Y130_assertion description "[According to our data, the variation at the LRPAP1 gene could contribute to the risk of developing an early episode of MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55185.RAnCYcTImrbM8k66Xc63yW79n4EyWS_B9QRCTZlQD3N-Y130_provenance.
- NP55187.RAmfZCj04SGgGIDiVIEyDptCuXE2lLAUdOd05-5gW3QcY130_assertion description "[Alpha2-macroglobulin, lipoprotein receptor-related protein and lipoprotein receptor-associated protein and the genetic risk for developing Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55187.RAmfZCj04SGgGIDiVIEyDptCuXE2lLAUdOd05-5gW3QcY130_provenance.
- NP55189.RAswqlvz3klYyNCrwrpyfAVaeqmtgsP84RQ1iIp52k-EM130_assertion description "[Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55189.RAswqlvz3klYyNCrwrpyfAVaeqmtgsP84RQ1iIp52k-EM130_provenance.
- NP55191.RAnYRxps3u98V3J54Jy_1U7gkPdJcqAwNcKICoOOldCeE130_assertion description "[Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55191.RAnYRxps3u98V3J54Jy_1U7gkPdJcqAwNcKICoOOldCeE130_provenance.
- NP55192.RAozqOmuQJJHetsd4WrhZkpuyLtRi1OJu04h-ZmXprF1g130_assertion description "[Our results revealed an association between AD cases without capillary CAA (i.e., AD cases with CAA but lacking capillary CAA and AD cases without CAA) and the T-allele of the alpha(2)macroglobulin receptor/low-density lipoprotein receptor-related protein-1 (LRP-1) C766T polymorphism as opposed to AD cases with capillary CAA and non-AD controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55192.RAozqOmuQJJHetsd4WrhZkpuyLtRi1OJu04h-ZmXprF1g130_provenance.
- NP55196.RAq3HY1aI7vvUcwhfTFBbRe_6lPYSg3xGnxiHavghiqqA130_assertion description "[These data suggest that LRP polymorphism influences the risk as well as the age at onset of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55196.RAq3HY1aI7vvUcwhfTFBbRe_6lPYSg3xGnxiHavghiqqA130_provenance.
- NP55197.RAimtoghsxuoRxa8CrNugWA7UV2FjJTPStRTUeijYJrJ8130_assertion description "[The multifactorial genetic dysfunction in AD includes mutational loci (APP, PS1, PS2) and diverse susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS3) distributed across the human genome, probably converging in common pathogenic mechanisms that lead to premature neuronal death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55197.RAimtoghsxuoRxa8CrNugWA7UV2FjJTPStRTUeijYJrJ8130_provenance.
- NP55201.RAqRQkY0oV5TTgSh4-ppYRix405q1hP5le-FsFWIDKCaU130_assertion description "[We examined the influence of LRP polymorphisms on CAA in 125 post-mortem cases genotyped for APOE and classified according to the neurofibrillary Braak and Braak staging of AD (indicating neurodegeneration grade).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55201.RAqRQkY0oV5TTgSh4-ppYRix405q1hP5le-FsFWIDKCaU130_provenance.
- NP55205.RAilxjx-ycNiHWbaTFtvmw6B3VE7jhcpqxX0lysOkpAw4130_assertion description "[In conclusion, LRP gene polymorphisms, particularly the relatively common exon 22 C200T polymorphism, are a significant risk factor for premature CAD in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55205.RAilxjx-ycNiHWbaTFtvmw6B3VE7jhcpqxX0lysOkpAw4130_provenance.
- NP55209.RAkJkHM5Wc1JQBF2zIEZ1wWlpndVQZeMbSuZKIXD2yOs0130_assertion description "[Our results highlight the potential of microarray-based technology for SNP genotyping in pharmacogenetics.(1)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55209.RAkJkHM5Wc1JQBF2zIEZ1wWlpndVQZeMbSuZKIXD2yOs0130_provenance.
- NP55210.RAmF7nJxK6AbsyETt0jOHFWXyTjSRRWSPZfqHyqcJdIpQ130_assertion description "[The polymorphisms of intron 8 in lipoprotein lipase influence the blood-lipid metabolism, induce blood vessel rebuilding and play an important role in the invasion and development of Essential Hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55210.RAmF7nJxK6AbsyETt0jOHFWXyTjSRRWSPZfqHyqcJdIpQ130_provenance.
- NP55218.RAgamyIFK325JPIwSsq4G0CL-vxFxhNtj6KxMLkO1iQBk130_assertion description "[Three of the genetic variants analysed, PPAR-alpha-L162V, LPL-HindIII, and TNF-alpha-G-308A, were associated with non-classical risk factors, specifically lipid profile, inflammation, and oxidative status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55218.RAgamyIFK325JPIwSsq4G0CL-vxFxhNtj6KxMLkO1iQBk130_provenance.
- NP55227.RAnuEjP08qWd6E_BItHI5JCrXbgQIlxdxD-tcNS4rmdx4130_assertion description "[Among Mexican-Americans, homozygosity for LPL haplotype 1 was protective against coronary artery disease (OR = 0.50, 95% CI 0.27-0.91).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55227.RAnuEjP08qWd6E_BItHI5JCrXbgQIlxdxD-tcNS4rmdx4130_provenance.
- NP55230.RAmdwXu8BaoGK-OBE8F1sg8H7ZtnLxjv6AZBUl-Dbpo80130_assertion description "[Two mutations in the lipoprotein lipase (LPL) gene, a T to G transition at position -93 of the proximal promoter region and an Asp9Asn substitution in exon 2, were examined in 762 Dutch males with angiographically-diagnosed coronary artery disease (CAD) and 296 healthy normolipidemic Dutch males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55230.RAmdwXu8BaoGK-OBE8F1sg8H7ZtnLxjv6AZBUl-Dbpo80130_provenance.
- NP55231.RAtg8WBzYCKxdAno1HY7pUOiHXvAyFeac1w3dUMBIcxBg130_assertion description "[To determine whether lipoprotein lipase gene variants are relevant to ongoing atherogenesis, we explored relationships between two common lipoprotein lipase gene polymorphic markers, Pvu II at intron 6 and HindIII at intron 8; the severity of coronary artery disease (CAD); and lipid variables in 475 white patients 65 years of age or younger.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55231.RAtg8WBzYCKxdAno1HY7pUOiHXvAyFeac1w3dUMBIcxBg130_provenance.
- NP55232.RAigJbbtDj0rNSdqZmQ8SpI6Opr2mpl87V83aHoXwctVY130_assertion description "[Polymorphisms within the genes encoding apolipoprotein E (ApoE), apolipoprotein CI (ApoCI), alpha1-antichymotrypsin (ACT), the low-density lipoprotein (LDL) receptor and lipoprotein lipase were investigated in patients suffering from Alzheimer's dementia and non-demented psychiatric patients as control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55232.RAigJbbtDj0rNSdqZmQ8SpI6Opr2mpl87V83aHoXwctVY130_provenance.
- NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_assertion description "[These results indicate that a common polymorphism in the lipoprotein lipase gene modulates the risk level for sporadic AD in the eastern Canadian population but more importantly, indirectly modulates the pathophysiology of the brain in autopsy-confirmed cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_provenance.
- NP55240.RAgvWRPjKIfH9P48LlKAWQXykHjtU7FX82fPh_kr_hSaE130_assertion description "[Thus genetic factors play a role not only in formation of coronary atherosclerosis but determine the course of ischemic heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55240.RAgvWRPjKIfH9P48LlKAWQXykHjtU7FX82fPh_kr_hSaE130_provenance.
- NP55241.RAnfGaKqYN2_qXIXHT0kEbetBqxQW_GjBlGaGqMDyC378130_assertion description "[An application of the patient rule-induction method for evaluating the contribution of the Apolipoprotein E and Lipoprotein Lipase genes to predicting ischemic heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55241.RAnfGaKqYN2_qXIXHT0kEbetBqxQW_GjBlGaGqMDyC378130_provenance.
- NP55247.RAhPsozb2O1YmaKh5hJNEWmhHZXs5-Q1m1Jmho9Go1JJo130_assertion description "[Variants of exon 4 and its flanking region of LPL Gene in patients with hyperlipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55247.RAhPsozb2O1YmaKh5hJNEWmhHZXs5-Q1m1Jmho9Go1JJo130_provenance.
- NP55252.RAlrL_gxlP4Pi8A0gtoHNSOieaugTGRLtIpaFBJlZ_3VI130_assertion description "[The 495TT genotype of LPL gene HindIII polymorphism was associated with changes of HDL subclasses distribution in Chinese population with hyperlipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55252.RAlrL_gxlP4Pi8A0gtoHNSOieaugTGRLtIpaFBJlZ_3VI130_provenance.
- NP55253.RAi4xdzcUAl2dmF-YeBPLK1xXjgM0u4_xakEATCQCD7xA130_assertion description "[We examined the association of a Hind RFLP (restriction fragment length polymorphism) in the lipoprotein lipase (LPL) gene with type 2 diabetes (T2DM) in Chinese Han population in Hubei Province.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55253.RAi4xdzcUAl2dmF-YeBPLK1xXjgM0u4_xakEATCQCD7xA130_provenance.
- NP55261.RAsjtbxKSGINdQd0fBgpWOIUTXPYWOCs33AT13gd3CRzA130_assertion description "[Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55261.RAsjtbxKSGINdQd0fBgpWOIUTXPYWOCs33AT13gd3CRzA130_provenance.
- NP55269.RAjcgudEtx57rQ3qGCu9XoO7fV1noSNS2692lDvaOko6k130_assertion description "[Genetic variants of the lipoprotein lipase gene and myocardial infarction in the Central Valley of Costa Rica.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55269.RAjcgudEtx57rQ3qGCu9XoO7fV1noSNS2692lDvaOko6k130_provenance.