Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP51585.RAoTzEbLcyLvJ9t9k_LLV1QMJHzWfqSBUIcWjWI2mMnig130_assertion description "[Neurotransmission and bipolar disorder: a systematic family-based association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51585.RAoTzEbLcyLvJ9t9k_LLV1QMJHzWfqSBUIcWjWI2mMnig130_provenance.
- NP51588.RAiM4gJnxihap3HjHoxlyIerSLUo4NBpEp10iYkyr5lAk130_assertion description "[These results suggest that variants of the dopamine transporter gene may be related to obesity in African-American smokers. Possible mechanisms responsible for the association between dopamine transport and obesity in African-American smokers are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51588.RAiM4gJnxihap3HjHoxlyIerSLUo4NBpEp10iYkyr5lAk130_provenance.
- NP51590.RAjgxdA2fRC_PsR3Ew1Tfr2YztYxE7DfnIIVEo7pSX9sM130_assertion description "[Association between the dopamine transporter gene and posttraumatic stress disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51590.RAjgxdA2fRC_PsR3Ew1Tfr2YztYxE7DfnIIVEo7pSX9sM130_provenance.
- NP51591.RArpC1i2RvRC91cU-9PczOG35tozxcO2tTsuQwhM1eJdk130_assertion description "[The response rates at the 3rd and 7th days after medication did not differ with either the drug group or the dopamine transporter polymorphism. Relatively low doses of risperidone and haloperidol exhibited similar efficacies, and dopamine transporter polymorphisms do not appear to play a major role in the action of antipsychotics on delirium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51591.RArpC1i2RvRC91cU-9PczOG35tozxcO2tTsuQwhM1eJdk130_provenance.
- NP51592.RAvNmxxoy2N3hLY8lfXkJW1y5BuOYJj_X2xxxNsIv1TCk130_assertion description "[The A9 allele of the dopamine transporter gene increases the risk of visual hallucinations during alcohol withdrawal in alcohol-dependent women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51592.RAvNmxxoy2N3hLY8lfXkJW1y5BuOYJj_X2xxxNsIv1TCk130_provenance.
- NP51596.RAj6jp0953SN0vnEfdk4wsSyk8o0H4H-tutZW2se1GrNI130_assertion description "[Although replication studies are warranted, these results in schizophrenia further support the hypothesis that 5HTTLPR polymorphism is a risk factor for violent suicidal behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51596.RAj6jp0953SN0vnEfdk4wsSyk8o0H4H-tutZW2se1GrNI130_provenance.
- NP51597.RAoyygWelKbJGwki38j5lQ0LmBkuYCaZfOkbY_hbRT87Q130_assertion description "[The combination of hSERT genotype 10/10 with DAT1 genotype 10/10 was shown to be a risk factor of opiate abuse under 16 years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51597.RAoyygWelKbJGwki38j5lQ0LmBkuYCaZfOkbY_hbRT87Q130_provenance.
- NP51598.RAtckN8rYqf85ybikBhGxaIshtYnXhjDiM-0ylFxJpquw130_assertion description "[It seems plausible that the association between the DAT1 VNTR and binge-eating behaviour indicates that dysregulation of dopamine reuptake may act as a common pathophysiologic mechanism in eating disorders with binge-eating behaviour and in disorders related to substance use.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51598.RAtckN8rYqf85ybikBhGxaIshtYnXhjDiM-0ylFxJpquw130_provenance.
- NP51601.RAgyh_FxMJ-N02tWcXh-Bt5mYY2lo8KPsb9r9Qh5tgfic130_assertion description "[A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51601.RAgyh_FxMJ-N02tWcXh-Bt5mYY2lo8KPsb9r9Qh5tgfic130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion description "[The SLC6A2 haplotype map and 25-marker panel (excluding the monomorphic one) is a comprehensive tool for genetic linkage studies on phenotypes related to NET function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51607.RAk2clcBKaqUCZ5xQjE_RQ5w9fvpDeF0S1CYGWoq8-Ceo130_assertion description "[Although the transcriptional activity related to the NET gene expression is little known, it may be a good candidate gene for major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51607.RAk2clcBKaqUCZ5xQjE_RQ5w9fvpDeF0S1CYGWoq8-Ceo130_provenance.
- NP51627.RAvBmkDmTHejZWXaKPdPWBVm3NpL42gSpYDlzth2TFWlM130_assertion description "[Analysis of polymorphism of the GLUT2 promoter in NIDDM patients and its functional consequence to the promoter activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51627.RAvBmkDmTHejZWXaKPdPWBVm3NpL42gSpYDlzth2TFWlM130_provenance.
- NP51629.RAmaD8zZS0zvCr1bBNeMcl-tXPCB1qNZufvAA_y-q6uvs130_assertion description "[Genetic polymorphisms at the human liver/islet glucose transporter (GLUT2) gene locus in Caucasian and West Indian subjects with type 2 (non-insulin-dependent) diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51629.RAmaD8zZS0zvCr1bBNeMcl-tXPCB1qNZufvAA_y-q6uvs130_provenance.
- NP51631.RAobAZX8MV-T-2DLuxsfbMoJ9R2GWzOwlxafB1TK0SbUc130_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." NP51631.RAobAZX8MV-T-2DLuxsfbMoJ9R2GWzOwlxafB1TK0SbUc130_provenance.
- NP51635.RApc4EdEakxXRFqz0ItT6yfUd4qm5DxboB5fSjKPcM9Go130_assertion description "[Role of GLUT1 gene in susceptibility to diabetic nephropathy in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51635.RApc4EdEakxXRFqz0ItT6yfUd4qm5DxboB5fSjKPcM9Go130_provenance.
- NP51639.RAmRI3GZcQ07lP782CUF9642H8v7RVzK17cIysym4RiC4130_assertion description "[Our results suggest that the T8356C and GLUT1 gene mutations may have an important role in developing late-onset T2D in Coimbatore population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51639.RAmRI3GZcQ07lP782CUF9642H8v7RVzK17cIysym4RiC4130_provenance.
- NP51645.RAmj6fOqEL7oERYpWgY-R3haHBZp7xKT98W_wqe0kUULc130_assertion description "[Polymorphisms at the GLUT1 (HepG2) and GLUT4 (muscle/adipocyte) glucose transporter genes and non-insulin-dependent diabetes mellitus (NIDDM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51645.RAmj6fOqEL7oERYpWgY-R3haHBZp7xKT98W_wqe0kUULc130_provenance.
- NP51650.RAsRIJlL1yj6kJsQ6r0A-vkmQ1ch-xQiZNxjWI-3T7xf4130_assertion description "[Linkage and association were observed between autistic disorder and the two SNPs, rs2056202 and rs2292813, found in SLC25A12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51650.RAsRIJlL1yj6kJsQ6r0A-vkmQ1ch-xQiZNxjWI-3T7xf4130_provenance.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_assertion description "[We report here that two variants in the organic cation transporter cluster at 5q31 (a missense substitution in SLC22A4 and a G-->C transversion in the SLC22A5 promoter) form a haplotype associated with susceptibility to Crohn disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51664.RAkdGnkorgXV-NEuFGv-Br_2RydQLyeWjMEK1yRAIGno0130_provenance.
- NP51667.RAhd7Ze86urkJygnfvsBy0xPcZtb1SdcEZkkASV9eTLPo130_assertion description "[Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were associated with specific phenotypes in this pediatric-onset CD cohort.(Inflamm Bowel Dis 2007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51667.RAhd7Ze86urkJygnfvsBy0xPcZtb1SdcEZkkASV9eTLPo130_provenance.
- NP51671.RAmPpgyuU5DxI4fski7vcnRRK0okmryZqB0Jlv-frbEis130_assertion description "[Collectively, our results suggest that the 1672T variant of the OCTN1 gene and the -207C variant of the OCTN2 gene represent risk factors for CD in the Greek population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51671.RAmPpgyuU5DxI4fski7vcnRRK0okmryZqB0Jlv-frbEis130_provenance.
- NP51672.RAj5RMEYvkOw5VyUeXWl2EaFsqVdVhiSPTaIy6dPdH8iU130_assertion description "[Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51672.RAj5RMEYvkOw5VyUeXWl2EaFsqVdVhiSPTaIy6dPdH8iU130_provenance.
- NP51678.RAk7nSYZjLqbaO95ILQ9Zs1_RA5CVNSHbnfzukvfzEgxU130_assertion description "[ These results suggest that the SLC22A4, RUNX1, and SUMO4 polymorphisms analysed do not play a role in the susceptibility to or severity of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51678.RAk7nSYZjLqbaO95ILQ9Zs1_RA5CVNSHbnfzukvfzEgxU130_provenance.
- NP51680.RAvsC_aA_Nk0LxjQ5AJwSGk1SNdVg59A6S6ABGkRT8sxk130_assertion description "[An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51680.RAvsC_aA_Nk0LxjQ5AJwSGk1SNdVg59A6S6ABGkRT8sxk130_provenance.
- NP51682.RAjN5fCHmZvkEjdBJ4McMt4xmDBMSP5kJvS0jIIlEO0wA130_assertion description "[Data of the current study do not confirm the universal and population independent susceptibility role of the SLC22A4 C6607T and RUNX1 G24658C variants for rheumatoid arthritis; furthermore, the data presented here show, that there are no significant carnitine-metabolism associated functional consequences of the different genotypes evidenced by the lack of detectable differences in the carnitine ester profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51682.RAjN5fCHmZvkEjdBJ4McMt4xmDBMSP5kJvS0jIIlEO0wA130_provenance.
- NP51685.RAh0ia3Xkz2458PWYbJBwp2bNGisSSuL7rjRLIKwH8OGc130_assertion description "[ SLC22A12 is a major gene for hypouricemia but not hyperuricemia in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51685.RAh0ia3Xkz2458PWYbJBwp2bNGisSSuL7rjRLIKwH8OGc130_provenance.
- NP51687.RAj2m9SQEkrGDcCzmSZJK3r_neIk8oTO6_GsQLRzs75Hg130_assertion description "[The present association study tested the candidate gene hypothesis that variation of the gene encoding the astroglial glutamate transporter EAAT2 confers vulnerability to alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51687.RAj2m9SQEkrGDcCzmSZJK3r_neIk8oTO6_GsQLRzs75Hg130_provenance.
- NP51689.RAjGqVvunnA4bFPdmFIhIHLh3gUi90wj_fpdbdAUiUmnU130_assertion description "[Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51689.RAjGqVvunnA4bFPdmFIhIHLh3gUi90wj_fpdbdAUiUmnU130_provenance.
- NP51699.RAmyHVX9jpdIONAfplaF5TJyR3wUYeNrS6rSdLoNJDFNo130_assertion description "[Genetic factors are relevant and independent determinants of antihypertensive drug effects in a multiracial population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51699.RAmyHVX9jpdIONAfplaF5TJyR3wUYeNrS6rSdLoNJDFNo130_provenance.
- NP51702.RArYJsoRv2DC7y_M6_KrNfGRmLuqMbOy9xGQgolfKiP74130_assertion description "[Moreover, our study suggests that the distribution of mutations in the NCCT gene in Japanese GS patients potentially differs from that in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51702.RArYJsoRv2DC7y_M6_KrNfGRmLuqMbOy9xGQgolfKiP74130_provenance.
- NP51706.RApPziLcIhfQF_TPtsGilRQKN1zDAHXnAYhEwHEmBLjuU130_assertion description "[The data are compelling that ATP1A1 and NKCC2 genes are candidate interacting hypertension-susceptibility loci in human essential hypertension and affirm gene interaction as an important genetic mechanism underlying hypertension susceptibility. Although corroboration in other cohorts and identification of functionally significant mutations are imperative next steps, the data provide a genotype-stratification scheme, with 4-fold predictive value (odds ratio, 4.28; 95% confidence interval, 2.29 to 8.0), which could help decipher the complex genetics of essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51706.RApPziLcIhfQF_TPtsGilRQKN1zDAHXnAYhEwHEmBLjuU130_provenance.
- NP51707.RAl-6YbaLfZBhSyDkN5lWLh69BHtmksHVq9MAiYizfvZ0130_assertion description "[These data exclude a primary role of the TSC gene in hypertension pathogenesis in the hypertension cohorts studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51707.RAl-6YbaLfZBhSyDkN5lWLh69BHtmksHVq9MAiYizfvZ0130_provenance.
- NP51708.RAmlpcGwWHBU3n7MLnhYK7SEeqxETZkp-P6hL4gjH0WKA130_assertion description "[Rare independent mutations in renal salt handling genes contribute to blood pressure variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51708.RAmlpcGwWHBU3n7MLnhYK7SEeqxETZkp-P6hL4gjH0WKA130_provenance.
- NP51709.RAoj2jiYH_iQulHSHMnRzvYOslYOYJE0yJvOxT8jWSgLk130_assertion description "[These results indicate a possible genetic role in the expression of overt chronic Q fever. Further studies will be undertaken to increase sample sizes, to survey other forms of crhonic Q fever and to examine Q fever patietns who have recovered without sequelae]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51709.RAoj2jiYH_iQulHSHMnRzvYOslYOYJE0yJvOxT8jWSgLk130_provenance.
- NP51711.RAnPuDJG4OhzbWZI548t1u6SOLSqBq9LXFTvdXC2TuMGs130_assertion description "[SLC11A1 (NRAMP1) but not SLC11A2 (NRAMP2) polymorphisms are associated with susceptibility to tuberculosis in a high-incidence community in South Africa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51711.RAnPuDJG4OhzbWZI548t1u6SOLSqBq9LXFTvdXC2TuMGs130_provenance.
- NP51713.RAi40AYeXt6KrhTeZOqx9SFwwb76ORMoDBIunMR5UdYXQ130_assertion description "[Genetic epidemiology of juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51713.RAi40AYeXt6KrhTeZOqx9SFwwb76ORMoDBIunMR5UdYXQ130_provenance.
- NP51715.RAoJyYwOGlC5yv0k07uxMqeOD83WNP1hBOs1w8QvGJpsU130_assertion description "[Genetic epidemiology of juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51715.RAoJyYwOGlC5yv0k07uxMqeOD83WNP1hBOs1w8QvGJpsU130_provenance.
- NP51718.RAqvLZURJvh5JxPaGPL19w85dMjRkvNILL8JXXj8TJU6s130_assertion description "[Association of NRAMP1 polymorphism with leprosy type but not susceptibility to leprosy per se in west Africans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51718.RAqvLZURJvh5JxPaGPL19w85dMjRkvNILL8JXXj8TJU6s130_provenance.
- NP51719.RAok9rO4nYqpnVcVB_qw4gMRcOyYbXMUsuG_wEWSJZ288130_assertion description "[Susceptibility to leprosy may be conditioned by an interaction between the NRAMP1 promoter polymorphisms and the lepromin response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51719.RAok9rO4nYqpnVcVB_qw4gMRcOyYbXMUsuG_wEWSJZ288130_provenance.
- NP51721.RAuIA1x_sXz-N6hW9GOPfsbbluLT158DSKXtWktz7uyLI130_assertion description "[To provide a quantitative summary in estimating the association between polymorphisms of 3 loci in NRAMP1 gene and susceptibility to tuberculosis in East-Asia population by means of meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51721.RAuIA1x_sXz-N6hW9GOPfsbbluLT158DSKXtWktz7uyLI130_provenance.
- NP51723.RAgizQlE0xuvnLsKrBZGOkwhyQpqtFKVAYHwkNGpEGBKs130_assertion description "[Multilocus analyses between polymorphisms in SLC11A1 and 11 TB candidate genes detected interactions between SLC11A1 and inducible nitric oxide synthase (NOS2A) in Caucasians (rs3731863 SLC11A1 x rs8073782 NOS2A, P = 0.009; rs3731863 SLC11A1 x rs17722851 NOS2A, P = 0.007) and toll-like receptor 2 (TLR2) in African-Americans (rs3731865 SLC11A1 x rs1816702, P = 0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51723.RAgizQlE0xuvnLsKrBZGOkwhyQpqtFKVAYHwkNGpEGBKs130_provenance.
- NP51725.RAh_rLnm9_TZdJmjKz8vYAX5b4QeRSvtCUVOjC5P2GMVM130_assertion description "[SLC11A1 (Formerly NRAMP1) gene polymorphisms associated with pediatric tuberculosis in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51725.RAh_rLnm9_TZdJmjKz8vYAX5b4QeRSvtCUVOjC5P2GMVM130_provenance.
- NP51727.RAn5nYBFH3xMqBbaWjgfKVvehSXv5YxiFZucbmVtMuLC8130_assertion description "[Reduced in vitro functional activity of human NRAMP1 (SLC11A1) allele that predisposes to increased risk of pediatric tuberculosis disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51727.RAn5nYBFH3xMqBbaWjgfKVvehSXv5YxiFZucbmVtMuLC8130_provenance.
- NP51731.RAvW0jAR8QJOB0qdNcpOJV6K5VfoDXTPJcX6l5Ee2ugVM130_assertion description "[Analysis of the NRAMP1 gene implicated in iron transport: association with multiple sclerosis and age effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51731.RAvW0jAR8QJOB0qdNcpOJV6K5VfoDXTPJcX6l5Ee2ugVM130_provenance.
- NP51732.RAmgnAQGnPC7nLIY10k6VzjmcsvDpUktgVXu55PohHUU0130_assertion description "[NRAMP1 polymorphism and viral factors in Sardinian multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51732.RAmgnAQGnPC7nLIY10k6VzjmcsvDpUktgVXu55PohHUU0130_provenance.
- NP51734.RAvPJXs6IfVNTemXcTdKph0FM-BzPxMTZC78v3AL9-RaE130_assertion description "[Association between SLC11A1 (formerly NRAMP1) and the risk of sarcoidosis in Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51734.RAvPJXs6IfVNTemXcTdKph0FM-BzPxMTZC78v3AL9-RaE130_provenance.
- NP51736.RAu9A6frUPeFGzCE7rNDbbXHpkdgftdTqEnBzFbtUIUGI130_assertion description "[We demonstrate association of genetic variation in both the promoter region and intron 1 of the SLC11A1 gene with EC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51736.RAu9A6frUPeFGzCE7rNDbbXHpkdgftdTqEnBzFbtUIUGI130_provenance.
- NP51738.RAotcb6IQesTDp6Q90lFLLVomUXlTpuspJvPRCGd9r2YE130_assertion description "[Stratification by BCG vaccination unmasked a potential genetic risk factor for atopy in the region of the SLC11A1 locus, and point to the importance of genotype by environment interactions in determining disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51738.RAotcb6IQesTDp6Q90lFLLVomUXlTpuspJvPRCGd9r2YE130_provenance.
- NP51744.RAvvGE3sMgpJfWMId-L21SmHEwzow9UZn-GE3m2X7_wu0130_assertion description "[ In a subset of sib-pairs that shared one or zero HLA haplotypes, LOD scores suggestive of linkage were observed. This suggests a role for NRAMP1 polymorphism in a subset of patients who do not possess HLA susceptibility alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51744.RAvvGE3sMgpJfWMId-L21SmHEwzow9UZn-GE3m2X7_wu0130_provenance.
- NP51747.RAsZXEkOBESFzP9S9OXVkq4NYKjTSDhOMreB8IwA7ZKlA130_assertion description "[In a case-control study, we investigated the association between two sequence variations in SLC10A2, the gene encoding ISBT, and colorectal adenomas, a precursor lesion of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51747.RAsZXEkOBESFzP9S9OXVkq4NYKjTSDhOMreB8IwA7ZKlA130_provenance.
- NP51749.RAmFTzRu78Ox1aZS3QJS0GvIOi_3RMAUYPQNznZty-ZM4130_assertion description "[We report a potential association of variants in the CCND1 and CDH1 genes with fCRC using a unique study design with phenotypic extremes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51749.RAmFTzRu78Ox1aZS3QJS0GvIOi_3RMAUYPQNznZty-ZM4130_provenance.
- NP51752.RApTbPAwP-hUie5psjXZmLaR0cAak8ENYM_UPDllITIFk130_assertion description "[Positive association between SIAT8B and schizophrenia in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51752.RApTbPAwP-hUie5psjXZmLaR0cAak8ENYM_UPDllITIFk130_provenance.
- NP51756.RAhJPGI6_IuIJmfLAVi6z4DUdrsde81bHTfmclVpjQO_A130_assertion description "[In conclusion, the study on vegetarians and seniors documents interesting lifestyle-genotype interactions. Although the TC and COMT mutations influence cellular vitamin B12 metabolism, this effect did not result in overt homocysteine elevation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51756.RAhJPGI6_IuIJmfLAVi6z4DUdrsde81bHTfmclVpjQO_A130_provenance.
- NP51758.RAhrFSibeu6i11N9uVTQKpz1MCoYzpgVc5pi_9HlmdqAY130_assertion description "[Risk of non-Hodgkin lymphoma associated with polymorphisms in folate-metabolizing genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51758.RAhrFSibeu6i11N9uVTQKpz1MCoYzpgVc5pi_9HlmdqAY130_provenance.
- NP51765.RAnQlRh_DvwAH5Xw9JiqeFG2Er3lYD1GtPjpHXV9rYYyk130_assertion description "[This study suggests that the Asn allele in the SHBG gene may be related to a reduced risk of breast cancer among postmenopausal women by increasing their blood SHBG levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51765.RAnQlRh_DvwAH5Xw9JiqeFG2Er3lYD1GtPjpHXV9rYYyk130_provenance.
- NP51766.RAlhmlcQjI04_wLciI0TgH_BQrwbCRQpfFA74dYdesO68130_assertion description "[Molecular mechanisms of the D327N SHBG protective role on breast cancer development after estrogen exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51766.RAlhmlcQjI04_wLciI0TgH_BQrwbCRQpfFA74dYdesO68130_provenance.
- NP51769.RApYV07djJgcOuJOALGtkPZKxX5ke4y0m5bjRIVB2ocFk130_assertion description "[We tested the hypothesis that polymorphisms in cytochrome P450c17alpha (CYP17), aromatase (CYP19), 17beta-hydroxysteroid dehydrogenase type I (17beta-HSD1) and sex hormone-binding globulin (SHBG) genes may modify the association between isoflavone intake and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51769.RApYV07djJgcOuJOALGtkPZKxX5ke4y0m5bjRIVB2ocFk130_provenance.
- NP51770.RAgTbzy1Nr9hUbMGQYiMfMCI1vkR8tZ3H1FzmYoiKreW0130_assertion description "[We therefore evaluated whether a polymorphic GA repeat (GA(13)-GA(33)) within the promoter region of the SH2D2A gene shows association to multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51770.RAgTbzy1Nr9hUbMGQYiMfMCI1vkR8tZ3H1FzmYoiKreW0130_provenance.
- NP51774.RAs071kx6zSqzA5tejkz2d40MzwTD5JQaCUjHb-fDLfv4130_assertion description "[These results demonstrate that SAP defects are rarely observed in CVID patients. We suggest that routine screening of SAP may only be necessary in patients with other suggestive clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51774.RAs071kx6zSqzA5tejkz2d40MzwTD5JQaCUjHb-fDLfv4130_provenance.
- NP51776.RAtEwVOVcXQjzpbMC6Dira42CY3HVGTMDcdqdta1onf40130_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." NP51776.RAtEwVOVcXQjzpbMC6Dira42CY3HVGTMDcdqdta1onf40130_provenance.
- NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_assertion description "[X-linked lymphoproliferative disease (XLP), a genetic disorder characterized by immunodeficiency to Epstein-Barr virus (EBV) infection, has been linked to mutations in the SH2D1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51777.RAnGzTltj5263TROoUJTw_0Z1OI6f_iEkFOgIUDtF0sAo130_provenance.
- NP51783.RAk6UuDSxQMMqXtrwUKDoqoiIrgLFfQ83KezZsW5IBmDM130_assertion description "[We propose that two separate SP-B gene polymorphisms have a phenotypic significance via]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51783.RAk6UuDSxQMMqXtrwUKDoqoiIrgLFfQ83KezZsW5IBmDM130_provenance.
- NP51787.RAi8hnP9ueBHsOkXRCqTMnjYy3nnwc9tcwthNWjwT7E8s130_assertion description "[We examined associations between IPF and genetic polymorphic variants of surfactant proteins, SP-A1, SP-A2, SP-B, SP-C, and SP-D. One SP-A1 (6A(4)) allele and single nucleotide polymorphisms (SNPs) that characterize the 6A(4) allele, and one SP-B (B1580_C) were found with higher frequency ( P</=0.01) in nonsmoker and smoker IPF ( n=84) subgroups, respectively, compared with healthy controls ( n=194).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51787.RAi8hnP9ueBHsOkXRCqTMnjYy3nnwc9tcwthNWjwT7E8s130_provenance.
- NP51795.RAhU_uNb_I_0VENAfH4bZHMWAcY4g9POccd0jCA9QT-jY130_assertion description "[Mutations in the surfactant protein C gene associated with interstitial lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51795.RAhU_uNb_I_0VENAfH4bZHMWAcY4g9POccd0jCA9QT-jY130_provenance.
- NP51796.RAkQrtbrfUbEiEcAx8Eiew8bv9O7FsjNzoS-6ppVZZQe8130_assertion description "[We propose that the SP-B Ile131Thr polymorphism is a determinant for certain SP-A alleles as factors causing genetic susceptibility to RDS (6A(2), 1A(0)) or protection against it (6A(3), 1A(2)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51796.RAkQrtbrfUbEiEcAx8Eiew8bv9O7FsjNzoS-6ppVZZQe8130_provenance.
- NP51800.RAgmJx63bGB_67O9CE1Ejjck4GHDNRwOO0CJhPNj1prJw130_assertion description "[Family-based association tests suggest linkage between surfactant protein B (SP-B) (and flanking region) and respiratory distress syndrome (RDS): SP-B haplotypes and alleles from SP-B-linked loci are risk factors for RDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51800.RAgmJx63bGB_67O9CE1Ejjck4GHDNRwOO0CJhPNj1prJw130_provenance.
- NP51805.RAmus1knkRFO49Gb4M0iafl3pYx_i1gqnNiGsU0bOYuCs130_assertion description "[These results indicate an association of the surfactant protein B intron 4 variants and/or its flanking loci with mechanisms that may enhance lung cancer susceptibility, especially to squamous cell carcinoma of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51805.RAmus1knkRFO49Gb4M0iafl3pYx_i1gqnNiGsU0bOYuCs130_provenance.
- NP51806.RApSm_rY7Hq3UovP4WbtcqvA9xugnx61wLQa9wdK53J28130_assertion description "[These findings indicate a very strong association of the SP-B intron-4 variants with mechanisms that may enhance lung cancer susceptibility, especially in workers who are employed in chromate industry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51806.RApSm_rY7Hq3UovP4WbtcqvA9xugnx61wLQa9wdK53J28130_provenance.
- NP51821.RAs_IhU8FjuRg6ZNiM5eeb6tAbMWLsLpU3HM3vhJeKdXc130_assertion description "[A novel missense mutation in the human plasmin inhibitor (alpha2-antiplasmin) gene associated with a bleeding tendency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51821.RAs_IhU8FjuRg6ZNiM5eeb6tAbMWLsLpU3HM3vhJeKdXc130_provenance.
- NP51824.RAmeL8NhEvwIGJPefXc0icrWKDThnYuhQqKbt6ZNG9_Og130_assertion description "[The subjects with the 4G/4G genotype had a higher prevalence of CHD, compared to those with the 5G/5G PAI-1 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51824.RAmeL8NhEvwIGJPefXc0icrWKDThnYuhQqKbt6ZNG9_Og130_provenance.
- NP51827.RAkqyFb1xQXvFPvQRZNEEOFHO_sB_Ilk2jdyaEKSKGO30130_assertion description "[ An increasing number of risk alleles are associated with an elevated risk for CAD. An analysis of multiple polymorphisms, some several hundred, each with a small impact, may allow improved assessment of the individual genetic burden for CAD. Larger studies are needed to prove this hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51827.RAkqyFb1xQXvFPvQRZNEEOFHO_sB_Ilk2jdyaEKSKGO30130_provenance.
- NP51832.RAuaOo1hiRtJAZH3FG_n1ho37nt4sDw4ET-6Yf7jN6Y-Q130_assertion description "[To explore the effect of plasminogen activator inhibitor-1 (PAI-1) gene variations on the risk of coronary heart disease (CHD) in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51832.RAuaOo1hiRtJAZH3FG_n1ho37nt4sDw4ET-6Yf7jN6Y-Q130_provenance.
- NP51833.RAjlD8UzbFaVqVzYt2nIaUZgHxQtDNk4VCATZ-bVUXmEs130_assertion description "[Genotype combinations of plasminogen activator inhibitor-1 and angiotensin-converting enzyme genes and risk for early onset of coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51833.RAjlD8UzbFaVqVzYt2nIaUZgHxQtDNk4VCATZ-bVUXmEs130_provenance.
- NP51838.RAhbIxgdMHWoSQm03_TGzMF2OOXsNHZtVIfv3hJSH9AHo130_assertion description "[Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51838.RAhbIxgdMHWoSQm03_TGzMF2OOXsNHZtVIfv3hJSH9AHo130_provenance.
- NP51839.RAvo55mlL4oYm0Gvamvz-3Z5lXyNxh-Bb4FVeSCmoCNk4130_assertion description "[The -844 G/A PAI-1 polymorphism is associated with mRNA expression in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51839.RAvo55mlL4oYm0Gvamvz-3Z5lXyNxh-Bb4FVeSCmoCNk4130_provenance.
- NP51846.RAqRbRSMdeL2JGLwA_2MSOjWZd1Oi9KgIy6FQm-BgZz0Y130_assertion description "[The SERPINE1 and CD14 polymorphisms studied here are associated with different aspects of bronchial reactivity and IgE response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51846.RAqRbRSMdeL2JGLwA_2MSOjWZd1Oi9KgIy6FQm-BgZz0Y130_provenance.
- NP51847.RAtY1BqkOB_9jwZSjRrjjTBtHphj7ttHvedrsukqQprOA130_assertion description "[We adapted template-directed dye-terminator incorporation with fluorescence polarization detection (TDI-FP) to the analysis of eight SNPs implicated in mediating the sepsis syndrome: TNF-alpha (-308), TNF-alpha (-238), TNF-beta (+250), IL-1beta (+3953), IL-6 (-174), IL-10 (-592), plasminogen activator inhibitor-1 (PAI-1 (-675)), and TLR4 299 (+1032).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51847.RAtY1BqkOB_9jwZSjRrjjTBtHphj7ttHvedrsukqQprOA130_provenance.
- NP51849.RAgBY4uSTi4GNGt7zMUv6HqfoHbi6XGIVFG4sjYurRUdM130_assertion description "[In this study, the relationship between the TNF-alpha 308G/A, the IL-6-174 G/C, the PAI-1, the FVL, the EPCR, and the Cathepsin G (Ars 125 Ser) polymorphisms and the development and outcome of sepsis in pediatric patients was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51849.RAgBY4uSTi4GNGt7zMUv6HqfoHbi6XGIVFG4sjYurRUdM130_provenance.
- NP51855.RArtFcO24r2PFKRagGOt9nrTesrh4k8sDMskzo7M0_w5g130_assertion description "[Comparison of the plasminogen activator inhibitor-1 4G/5G gene polymorphism in females with venous thromboembolism during pregnancy or spontaneous abortion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51855.RArtFcO24r2PFKRagGOt9nrTesrh4k8sDMskzo7M0_w5g130_provenance.
- NP51856.RAtogrDtVMONEATwexIrzqLl2XfqwPhdDff_BR88jDsgc130_assertion description "[Screening for risk factors for inherited thrombophilia with only polymorphisms for factor V von Leiden, factor II prothrombin and MTHFR may be missing the more prevalent identifiers of jeopardy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51856.RAtogrDtVMONEATwexIrzqLl2XfqwPhdDff_BR88jDsgc130_provenance.
- NP51858.RAnZXcWPvniGrMC0Br8FBDHiD42X3vIYjFaJTZZzVY9CE130_assertion description "[Thrombophilia is an important factor in both early and late pregnancy losses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51858.RAnZXcWPvniGrMC0Br8FBDHiD42X3vIYjFaJTZZzVY9CE130_provenance.
- NP51860.RAgFaui0a96izaPc-Q-acSJ_lVGpPWPjvmsXiEMIk6S88130_assertion description "[The compiled results demonstrate that the Invader biplex assay provides results more than 99.9% concordant with standard PCR-based techniques and is a rapid and highly accurate alternative to target amplification-based methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51860.RAgFaui0a96izaPc-Q-acSJ_lVGpPWPjvmsXiEMIk6S88130_provenance.
- NP51863.RAgJtHQwZSUhS7wXeiceDJh4EDbdNRUwJ5XlMoCAxqWwg130_assertion description "[The distribution of PAI-1 promoter 4G/5G polymorphism in Chinese is obviously different from that in Caucasians with the 4G allele more frequently found in Chinese. PAI-1 promoter 4G/5G polymorphism does not alter basic transcription activity and 4G promoter has increased response to IL-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51863.RAgJtHQwZSUhS7wXeiceDJh4EDbdNRUwJ5XlMoCAxqWwg130_provenance.
- NP51867.RAkSJXxjnJWRt-PsuFEBgUheI7nSeYjlG0OatJe64kLYs130_assertion description "[To reveal the association of 4G/5G polymorphism in the promoter region of the plasminogen activator inhibitor 1 gene (PAI1) with plasma PAI1 level in deep vein thrombosis (DVT) in Chinese Han ethnic group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51867.RAkSJXxjnJWRt-PsuFEBgUheI7nSeYjlG0OatJe64kLYs130_provenance.
- NP51869.RAq5NvnBIeGkjaje8o2gE2p2kuhX22GPsgBv-O9hkfrl4130_assertion description "[ Present data indicate that testing for heritable thrombophilia would be important to identify aPL subjects with an increased risk of developing APS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51869.RAq5NvnBIeGkjaje8o2gE2p2kuhX22GPsgBv-O9hkfrl4130_provenance.
- NP51876.RAjxzHzWbKS8Dq8t06FRzcpoguJ2uyVE9UzyZtn1m-7rI130_assertion description "[To investigate the role of the 4G/5G polymorphism in the plasminogen activator inhibitor-1 (PAI-1) gene in patients with ST-elevation myocardial infarction (STEMI) aged < or =45 years and its influence on regulation of the plasma PAI-1 concentration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51876.RAjxzHzWbKS8Dq8t06FRzcpoguJ2uyVE9UzyZtn1m-7rI130_provenance.
- NP51880.RAhZgATd1WoBWJ83AJ4g64f-wfwekkRAlUU1os2y-4wk4130_assertion description "[To examine interactions among the angiotensin converting enzyme (ACE) insertion/deletion, plasminogen activator inhibitor-1 (PAI-1) 4G/5G, and tissue plasminogen activator (t-PA) insertion/deletion gene polymorphisms on risk of myocardial infarction using data from 343 matched case-control pairs from the Physicians Health Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51880.RAhZgATd1WoBWJ83AJ4g64f-wfwekkRAlUU1os2y-4wk4130_provenance.
- NP51882.RAngGx5Q6eTnDMfIeEkmIylnPF-z2SXHI_XMRtyP08JRQ130_assertion description "[The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Etude CasTemoins de I'nfarctus du Mycocarde.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51882.RAngGx5Q6eTnDMfIeEkmIylnPF-z2SXHI_XMRtyP08JRQ130_provenance.
- NP51883.RAjNeaLwnGURDvhrCp9EuKsXjOrFFTzOZXVhdUYERuvik130_assertion description "[among all the investigated polymorphisms only the 5709G and eNOS4a alleles seem to confer protection against MI in the young age of Sardinian people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51883.RAjNeaLwnGURDvhrCp9EuKsXjOrFFTzOZXVhdUYERuvik130_provenance.
- NP51884.RAr8W5SIbrG8CQYUvXETsx36-lySf-Vl-YUiwyDUL9nbI130_assertion description "[The 4G/4G-PAI-1 genotype might be a protective factor against ACI, whereas the factor V point mutation (1691G-A) and the factor VII Arg/Gln353 gene polymorphism have not proved to be risk factors for ACI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51884.RAr8W5SIbrG8CQYUvXETsx36-lySf-Vl-YUiwyDUL9nbI130_provenance.
- NP51890.RAumcFG6XMySt7AYFpGx44pMdvPC2LjQFIAUWHVdZ5Fgo130_assertion description "[ The present study showed that the 4G/4G genotype was associated with elevated plasma PAI-1 activity in Chinese patients with and without hypertension. The contribution of the PAI-1 genotype seemed larger in women. In hypertensives carrying the 4G/4G genotype, higher TG was correlated with higher PAI-1, suggesting a possible contribution of gene-environmental interaction to their high risk for atherothrombotic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51890.RAumcFG6XMySt7AYFpGx44pMdvPC2LjQFIAUWHVdZ5Fgo130_provenance.
- NP51891.RAt6DjyZrThSxcB6iA3gkiklIREE9AdW-4-1mexTNbI1Y130_assertion description "[Our results show that the 4G/4G PAI-1 genotype appears to be associated with an elevated relative risk of developing arterial hypertension, regardless of PAI-1 levels and other hypertension-related factors, in a representative sample of the Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51891.RAt6DjyZrThSxcB6iA3gkiklIREE9AdW-4-1mexTNbI1Y130_provenance.
- NP51895.RAh_ruXG3RWpphA0Vz4HJCQquOJkAPU3em08h_quULayQ130_assertion description "[Impaired fibrinolysis in retinal vein occlusion: a role for genetic determinants of PAI-1 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51895.RAh_ruXG3RWpphA0Vz4HJCQquOJkAPU3em08h_quULayQ130_provenance.
- NP51903.RAtCDHUrw1IPMx5qrCFVXkt5_sGv1XDKkTGRFXTVxXLVg130_assertion description "[The risk of dialysis access thrombosis is related to the transforming growth factor-beta1 production haplotype and is modified by polymorphisms in the plasminogen activator inhibitor-type 1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51903.RAtCDHUrw1IPMx5qrCFVXkt5_sGv1XDKkTGRFXTVxXLVg130_provenance.
- NP51911.RAhUnFpH0fTaJr5gn4dsprjzYXM2tp4R1gyesFRR1IMJ0130_assertion description "[Plasminogen activator inhibitor 1 (PAI-1) increases in several insulin-resistant conditions such as obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51911.RAhUnFpH0fTaJr5gn4dsprjzYXM2tp4R1gyesFRR1IMJ0130_provenance.
- NP51916.RAl4grLJh3Nx4e5W9v8_EWWj8HCetWz7fuVhYbSbhV4JI130_assertion description "[The prevalence of 4G5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in polycystic ovarian syndrome and its association with plasma PAI-1 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51916.RAl4grLJh3Nx4e5W9v8_EWWj8HCetWz7fuVhYbSbhV4JI130_provenance.
- NP51919.RAg5FqykraGpbtky9svwRjkoY2kh6LHR-6U34OAdqk3Ro130_assertion description "[DNA samples from forty-four adolescent girls with PCOS and 50 healthy controls were analyzed by PCR-RFLP and direct DNA sequencing to determine the genotypic frequency of 17 different polymorphic loci on the FSHR (A307T, N680S), CYP17 (-34 T/C), CYP1A1 (T6235C), CAPN10 (44, 43, 19, 63), INSR (exon 17 C/T), SERPINE1 (4G/5G) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51919.RAg5FqykraGpbtky9svwRjkoY2kh6LHR-6U34OAdqk3Ro130_provenance.
- NP51931.RAsD58OY0wTGLzdwXTGNnQjytEMOvkqqn6oi-vJFdW03s130_assertion description "[This study confirms that Caucasian pediatric patients carrying the functional PAI-1 4G/4G genotype are at an increased risk of developing vascular complications and dying from meningococcal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51931.RAsD58OY0wTGLzdwXTGNnQjytEMOvkqqn6oi-vJFdW03s130_provenance.
- NP51937.RAiaeZ65hBBESgXSYeAn4SosCwmcYvfcJv0Q1DHV1Ubyg130_assertion description "[To investigate the interaction of metabolic and genetic factors in relation to PAI-1, genotype was determined at a 4G/5G polymorphism in the PAI-1 gene promoter and a Hind III RFLP of the PAI-1 gene in 189 Caucasian NIDDM patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51937.RAiaeZ65hBBESgXSYeAn4SosCwmcYvfcJv0Q1DHV1Ubyg130_provenance.