Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP44349.RAsO7h9RbU7kqfHajmQ52wfX7P0dR61IwSfvPmMYrSoH0130_assertion description "[Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44349.RAsO7h9RbU7kqfHajmQ52wfX7P0dR61IwSfvPmMYrSoH0130_provenance.
- NP44351.RAvacZ3TuD9yYNxsjyZXbelfJSe4ZZKoBV2xzvADeco0k130_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." NP44351.RAvacZ3TuD9yYNxsjyZXbelfJSe4ZZKoBV2xzvADeco0k130_provenance.
- NP44355.RAszjJIMUEGXLsyGVIt9ER3vtvMhh3KCwwrFEgCpThhlw130_assertion description "[Factor VII, blood lipids and fat intake: gene-nutrient interaction and risk of coronary heart disease with the factor VII R353Q polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44355.RAszjJIMUEGXLsyGVIt9ER3vtvMhh3KCwwrFEgCpThhlw130_provenance.
- NP44360.RAuVJa0BlBAk-YM62RNnEmyNEgnMXgIs4HQ7jcFQW1fBg130_assertion description "[Factor VII gene polymorphisms, factor VII:C levels and features of insulin resistance in non-insulin-dependent diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44360.RAuVJa0BlBAk-YM62RNnEmyNEgnMXgIs4HQ7jcFQW1fBg130_provenance.
- NP44363.RAj9bKXPA2_uHb6bFa4cZCadq6vJSTDK5MbJGzdLWGQww130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44363.RAj9bKXPA2_uHb6bFa4cZCadq6vJSTDK5MbJGzdLWGQww130_provenance.
- NP44368.RAuOHUPrBe5CvhLhCazbRRZG636DI-2DHOH7NdnwehMp8130_assertion description "[Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44368.RAuOHUPrBe5CvhLhCazbRRZG636DI-2DHOH7NdnwehMp8130_provenance.
- NP44372.RApIq0HjGZuwXgWnrEb0QeBoX8MEsZFQQpqCHbHEWwRU8130_assertion description "[ Our data fail to document an independent significant influence of the investigated polymorphisms on the risk of severe preeclampsia. In an attempt to build a multigenetic model of severe preeclampsia, the combination of F5 Leiden, NOS 3 T768C, NOS 3 Glu298Asp, and ER alpha Pvu II was the most effective combination to predict the presence of severe preeclampsia in this small series of white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44372.RApIq0HjGZuwXgWnrEb0QeBoX8MEsZFQQpqCHbHEWwRU8130_provenance.
- NP44373.RAnPaCCR_o2LGQV7YCAiBM76YviY5NhFaHpR8QL0gEVFc130_assertion description "[Our results underline the need for a clear distinction of ethnicity in association studies of functional gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44373.RAnPaCCR_o2LGQV7YCAiBM76YviY5NhFaHpR8QL0gEVFc130_provenance.
- NP44374.RAmKSmDV3grosUJjeJb5M-osksOKa6hSPI_zrAyBGIE_M130_assertion description "[Susceptibility to pre-eclampsia in Finnish women is associated with R485K polymorphism in the factor V gene, not with Leiden mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44374.RAmKSmDV3grosUJjeJb5M-osksOKa6hSPI_zrAyBGIE_M130_provenance.
- NP44375.RAvM_EUSwU7fa7l3MfFY_J4e-qh_ZzK5eyTMX5cXy7djE130_assertion description "[ We didn't find any difference in the prevalence of genetic mutations in patients with preeclampsia compared to the control group. The prevalence of APC resistance was statistically higher in preeclamptic patients compared to the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44375.RAvM_EUSwU7fa7l3MfFY_J4e-qh_ZzK5eyTMX5cXy7djE130_provenance.
- NP44376.RAtj6alW7O0_jzRkI8to1YPq6MDhTIj0hc6h5ZwiBs_d0130_assertion description "[In this population, we found no difference in the prevalence of genetic risk factors for thrombosis in women with preeclampsia compared with control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44376.RAtj6alW7O0_jzRkI8to1YPq6MDhTIj0hc6h5ZwiBs_d0130_provenance.
- NP44383.RAjBTlJoZMnwfV_DIiv4NbZjyboKf9GD3o8fAydkB84OQ130_assertion description "[The results demonstrated that Sao Miguel islanders have increased genetic predisposition to thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44383.RAjBTlJoZMnwfV_DIiv4NbZjyboKf9GD3o8fAydkB84OQ130_provenance.
- NP44384.RAloGX4lyLybIXHOilyNYsmlNmC0jC84YMxXMzCAZZOg0130_assertion description "[Anti-prothrombin antibodies are associated with thrombosis in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44384.RAloGX4lyLybIXHOilyNYsmlNmC0jC84YMxXMzCAZZOg0130_provenance.
- NP44396.RAhQM8eQY9sHiqYThk9KaUuM8t9zatWHk7GbjMGMpPMLQ130_assertion description "[This study therefore aimed to establish the prevalence of the GpIa/IIa polymorphisms and the three commonest hereditary thrombophilic disorders (prothrombin gene G20210A (PT) mutation, Factor V Leiden (FVL), and the thermolabile methylene tetrahydrofolate reductase C677T (MTHFR) mutation) in patients with RVO and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44396.RAhQM8eQY9sHiqYThk9KaUuM8t9zatWHk7GbjMGMpPMLQ130_provenance.
- NP44398.RAmghbCfcI0m87kvtD_uranQx0VjBGfFoPocq2DVxhXAg130_assertion description "[Based on our data, we determined that (1) the FII 20210A allele is a risk factor for MI, possibly important for early onset; (2) FVL may predispose for early-onset MI; (3) the FXIII-A Leu34 allele predisposes for MI in males only; however, (4) interaction between the FII 20210A and FXIII-A Leu34 alleles forms a synergistic coeffect that strongly predisposes for MI, placing combined carriers at high risk for MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44398.RAmghbCfcI0m87kvtD_uranQx0VjBGfFoPocq2DVxhXAg130_provenance.
- NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_assertion description "[In a large cohort of young AMI patients the gain-of-function variant F5 G1691A was associated with an increased risk of AMI. The findings on the variant F2 G20210A confirmed the previously reported results, but the association was statistically not significant. These data suggest that a number of young patients with AMI carry gene variants associated with a procoagulant phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44399.RApz3a6X80OO6cfQ7fNBvDcHFhSchcKHjq1X0ztwLuP-Q130_provenance.
- NP44404.RAgUti05WHO1AX0oTqCm-3ffdYB0rLEvZRoI1WX6bWh8U130_assertion description "[Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44404.RAgUti05WHO1AX0oTqCm-3ffdYB0rLEvZRoI1WX6bWh8U130_provenance.
- NP44408.RAm0A9BfWOPJYJNMkizpqb_Nt3aEHIholXj8F55YeH0VE130_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." NP44408.RAm0A9BfWOPJYJNMkizpqb_Nt3aEHIholXj8F55YeH0VE130_provenance.
- NP44411.RAmLxLKf6atU-R2q707PpdeKSR53AM1LJ3QFwHfRuRMqg130_assertion description "[The coagulation factor V Leiden, MTHFRC677T variant and eNOS 4ab polymorphism in young Chinese population with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44411.RAmLxLKf6atU-R2q707PpdeKSR53AM1LJ3QFwHfRuRMqg130_provenance.
- NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_assertion description "[Since identification of genetic risk factors for CAD in different ethnic groups is important for the development of new intervention and prevention programs, we investigated the association between the R353Q and -323ins10 polymorphisms in Factor VII gene, C677T mutation in MTHFR, Factor V Leiden and PT G20210A mutations and CAD in Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44414.RAhqOtmyZ_KOzw5NhgIoiytiYD1Qz5YllZkozWunc2y4w130_provenance.
- NP44415.RAj5aOdil0RJCQ0fDFeRtuUsIy9ONNG0uvfLB_lJESFFU130_assertion description "[Our study supports the association between MTHFR C677T and patients with early RPL among north Indian Rajputs and strengthens the notion that thrombophilia plays a role in this clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44415.RAj5aOdil0RJCQ0fDFeRtuUsIy9ONNG0uvfLB_lJESFFU130_provenance.
- NP44416.RArHwbYCRbYoY6LXykhbaj8YY0unp4vi0tSLxq7eEdfIY130_assertion description "[Inherited thrombophilia is associated with pregnancy losses that occur after 12th gestational week in Serbian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44416.RArHwbYCRbYoY6LXykhbaj8YY0unp4vi0tSLxq7eEdfIY130_provenance.
- NP44418.RAsGC0ZcnpabaS48i_kFy0ev9Mo_rjCHHPaLO_f5MAmxw130_assertion description "[Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44418.RAsGC0ZcnpabaS48i_kFy0ev9Mo_rjCHHPaLO_f5MAmxw130_provenance.
- NP44421.RAv2sMVf2pGNGRgORkppnv2x4id9Uwwq3OeOrEd8vNzh8130_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." NP44421.RAv2sMVf2pGNGRgORkppnv2x4id9Uwwq3OeOrEd8vNzh8130_provenance.
- NP44430.RAvMueqnf821FwhkL6cFgSLJMk-ULwC_M8q0sN5f4BfXw130_assertion description "[Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44430.RAvMueqnf821FwhkL6cFgSLJMk-ULwC_M8q0sN5f4BfXw130_provenance.
- NP44433.RAgKmN8d7vOnZA-s853FciY0oFArXvNclp6R6kFEd_VcY130_assertion description "[Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44433.RAgKmN8d7vOnZA-s853FciY0oFArXvNclp6R6kFEd_VcY130_provenance.
- NP44444.RApVKSEGHXGY76No5JYv3wUpR4kb-6N5V_W1b6T7U5y0M130_assertion description "[ It is important to evaluate the hemocoagulation patterns in women with a history of complicated pregnancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44444.RApVKSEGHXGY76No5JYv3wUpR4kb-6N5V_W1b6T7U5y0M130_provenance.
- NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_assertion description "[Although both the heterozygote Factor VLeiden and Prothrombin gene mutations were more frequent in patients with CAD than in control subjects, there was no statistical relationship found to exist between coronary artery disease and the Factor VLeiden and]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_provenance.
- NP44457.RArisp71d1IVNy7Nxreu7jSo6F9oWwudDuTmhDA_eEOEQ130_assertion description "[Present data suggest that carriership of the His79 allele modulate plasma levels of FV coagulant activity and, in subjects carrying the FV Leiden mutation, affects APC sensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44457.RArisp71d1IVNy7Nxreu7jSo6F9oWwudDuTmhDA_eEOEQ130_provenance.
- NP44460.RAqY1AVY1AXe3dxwK-APkSrufFUtXyZxCPZrCJu2dkIlI130_assertion description "[The mutation in factor V (FV) G1691A, known as factor V Leiden, and prothrombin (FII) gene G20210A are the two most prevalent causes of inherited thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44460.RAqY1AVY1AXe3dxwK-APkSrufFUtXyZxCPZrCJu2dkIlI130_provenance.
- NP44465.RArlh2xEY0ZbERv1v0RPvceql9xfZV4t2615jHHhAKBAc130_assertion description "[Thrombophilic polymorphisms in Israel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44465.RArlh2xEY0ZbERv1v0RPvceql9xfZV4t2615jHHhAKBAc130_provenance.
- NP44480.RApbZc3T5k7vO-4CzZjxvCQ5kT6grmP26o4U3UrRyBPuA130_assertion description "[Distributions of polymorphisms of genes of some components of hemostasis in patients with ischemic heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44480.RApbZc3T5k7vO-4CzZjxvCQ5kT6grmP26o4U3UrRyBPuA130_provenance.
- NP44483.RAgWUBxmUXCBgEURgNVlzNh_GNYJNipWjf5lRN6kOMil0130_assertion description "[Early recurrent miscarriage before 10 weeks of pregnancy is significantly associated with Factor V or G20210A prothrombin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44483.RAgWUBxmUXCBgEURgNVlzNh_GNYJNipWjf5lRN6kOMil0130_provenance.
- NP44484.RAm3gAFVfI2XlqbSSMfSYEso0d_ClXkh0SNXBJmXyvipE130_assertion description "[Attention should be directed at screening women with recurrent miscarriage associated with placental thrombosis for Factor V Leiden and a policy of targeted thromboprophylaxis during future pregnancies should be assessed in the form of a randomized controlled trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44484.RAm3gAFVfI2XlqbSSMfSYEso0d_ClXkh0SNXBJmXyvipE130_provenance.
- NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_assertion description "[Our study did not demonstrate that women who are carriers of the factor V, prothrombin, or MTHFR mutations are at higher risk of recurrent fetal loss than women without these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_provenance.
- NP44486.RAu-Si0Xb19JO75g4IuOh7l4sm0HnLmsK2g8wsJFqnsS8130_assertion description "[Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44486.RAu-Si0Xb19JO75g4IuOh7l4sm0HnLmsK2g8wsJFqnsS8130_provenance.
- NP44487.RAmteOhHcGGb8C3C7c0lFBn3qXNe-ZMEeQ5LZOV6mAFTg130_assertion description "[MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44487.RAmteOhHcGGb8C3C7c0lFBn3qXNe-ZMEeQ5LZOV6mAFTg130_provenance.
- NP44493.RAorOtdbFAEjUv9ZbWry2Mp_3TiOqgct6zlv_bk6sBPZc130_assertion description "[Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44493.RAorOtdbFAEjUv9ZbWry2Mp_3TiOqgct6zlv_bk6sBPZc130_provenance.
- NP44500.RAsDUOUwanclFLCVyRZzZ9AlDctZ8ojNmQ-wYpw_hzhSY130_assertion description "[In this population, we found no difference in the prevalence of genetic risk factors for thrombosis in women with preeclampsia compared with control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44500.RAsDUOUwanclFLCVyRZzZ9AlDctZ8ojNmQ-wYpw_hzhSY130_provenance.
- NP44503.RAj9Ai7fcfOAgWlWw_gbmV2wJ4pCzzZ0Lxq3XGpKLRnIM130_assertion description "[A role of TNF-alpha gene variant on juvenile ischemic stroke: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44503.RAj9Ai7fcfOAgWlWw_gbmV2wJ4pCzzZ0Lxq3XGpKLRnIM130_provenance.
- NP44505.RAm-TrrEjIV6vGib3R7QlCTxw482_HKjQn3gSnVkDkReA130_assertion description "[This study suggests that the analysis of prothrombin 20210G-->A and factor XIII Val34Leu is not a useful diagnostic procedure in the work-up of ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44505.RAm-TrrEjIV6vGib3R7QlCTxw482_HKjQn3gSnVkDkReA130_provenance.
- NP44512.RAiLKAEFY1F2bI1CI8u8tPz_-pXefJFVS3nO-X0FkqL8s130_assertion description "[A pilot study of genetic polymorphisms and hemodialysis vascular access thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44512.RAiLKAEFY1F2bI1CI8u8tPz_-pXefJFVS3nO-X0FkqL8s130_provenance.
- NP44515.RAiMZogGdv9aXNgVjyosxObvBCETdUOjen5Iwgw-0qnDE130_assertion description "[Incidence of five prothrombotic gene polymorphisms in healthy Saudi Arabians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44515.RAiMZogGdv9aXNgVjyosxObvBCETdUOjen5Iwgw-0qnDE130_provenance.
- NP44516.RAsgD-soELd3cfttnv3EXkNsmBz6ATkHkkA88q4OC0VZg130_assertion description "[Parent-of-origin transmission of thrombophilic alleles to intrauterine growth-restricted newborns and transmission-ratio distortion in unaffected newborns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44516.RAsgD-soELd3cfttnv3EXkNsmBz6ATkHkkA88q4OC0VZg130_provenance.
- NP44517.RAjYnIsE1ekEyCEIOGp8OCHB5AwFkigdWyq1x0TZGb0uE130_assertion description "[We conclude that FXIII antigen levels and FXIII V34L polymorphism may play a crucial role in the complex cascade of CVU pathophysiology, being significantly related to the CVU progression and extension because of the direct effects they have on the FXIII molecular activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44517.RAjYnIsE1ekEyCEIOGp8OCHB5AwFkigdWyq1x0TZGb0uE130_provenance.
- NP44519.RAjmTAOVRnsl8SsaRO6XjYBZaTHCZZX3JIDW6rg2jHUD4130_assertion description "[This study therefore aimed to establish the prevalence of the GpIa/IIa polymorphisms and the three commonest hereditary thrombophilic disorders (prothrombin gene G20210A (PT) mutation, Factor V Leiden (FVL), and the thermolabile methylene tetrahydrofolate reductase C677T (MTHFR) mutation) in patients with RVO and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44519.RAjmTAOVRnsl8SsaRO6XjYBZaTHCZZX3JIDW6rg2jHUD4130_provenance.
- NP44520.RAio44nTjMI1hXUTde7e7RlXIpLpuzW7GkHua6mTuYcO8130_assertion description "[Based on our data, 1) the FII 20210A allele is a risk factor for MI, possibly important for early onset; 2) FVL may predispose for early onset MI; 3) the FXIII-A L34 allele predisposes for MI in males only; however, 4) interaction between the FII 20210A and FXIII-A L34 alleles form a synergistic co-effect which strongly predisposes for MI, placing combined carriers at high risk for MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44520.RAio44nTjMI1hXUTde7e7RlXIpLpuzW7GkHua6mTuYcO8130_provenance.
- NP44529.RAhawcOSUwlYj1B1wHwyQh7xh1EhT38adDgRJb8G1XGWM130_assertion description "[Common genetic variation in the prothrombin gene, hormone therapy, and incident nonfatal myocardial infarction in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44529.RAhawcOSUwlYj1B1wHwyQh7xh1EhT38adDgRJb8G1XGWM130_provenance.
- NP44532.RAtKubwyIgwGrlqmnCWYZoSKawrIN8xRtw_mppurQqqVI130_assertion description "[This study suggests that prothrombin 20210A polymorphism may play a role in stroke under 60 years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44532.RAtKubwyIgwGrlqmnCWYZoSKawrIN8xRtw_mppurQqqVI130_provenance.
- NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_assertion description "[ Factor II gene 3'-UT G20210A mutant allele is absent in the 99 Chinese Zhuang ethnic patients with ischemic stroke and myocardial infarction and is absent in 106 normal healthy Zhuang people. FII G20210A mutation may not be a major risk factor for thrombogenesis in ethnic Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_provenance.
- NP44537.RAgPY3yebtKi3g82lwxfvO2KoDPFuMB34iFOpupiuSlzo130_assertion description "[were similar in a multivariable analysis controlling for age, race, prior pregnancy loss, prior SGA neonates, and family history of thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44537.RAgPY3yebtKi3g82lwxfvO2KoDPFuMB34iFOpupiuSlzo130_provenance.
- NP44540.RAs1252YG0tDFIR7DrXcQ8px2mzHKJiViVv_OHeX3jr3w130_assertion description "[Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44540.RAs1252YG0tDFIR7DrXcQ8px2mzHKJiViVv_OHeX3jr3w130_provenance.
- NP44544.RAsZcYc9DnAL4qrF9lYjEDGXZavoccG1zsavwujhCrxq0130_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." NP44544.RAsZcYc9DnAL4qrF9lYjEDGXZavoccG1zsavwujhCrxq0130_provenance.
- NP44546.RAmHxj2HtrHDthjKRdv9Rvg2-IbUfrG-eB-e8UAY3aeDU130_assertion description "[Inherited thrombophilia screening is not indicated as an initial approach in Greek women with RFL and negative personal thromboembolic history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44546.RAmHxj2HtrHDthjKRdv9Rvg2-IbUfrG-eB-e8UAY3aeDU130_provenance.
- NP44547.RAh9fT544eQnUZEp-OolYYcwpkEU4gRMRhiiZQ5KIgwYM130_assertion description "[ Only Factor II:C activity levels, uterine arterial Doppler and a history of familial hypertension are useful in predicting poor pregnancy outcome in gestational hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44547.RAh9fT544eQnUZEp-OolYYcwpkEU4gRMRhiiZQ5KIgwYM130_provenance.
- NP44548.RAuZFauCifqZZ71kLlN6F02VYM7r2LZwCLhJUvY5gZPu0130_assertion description "[Association of common genetic variations and idiopathic venous thromboembolism. Results from EDITh, a hospital-based case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44548.RAuZFauCifqZZ71kLlN6F02VYM7r2LZwCLhJUvY5gZPu0130_provenance.
- NP44550.RAp8k8UQZk2pniyYUelwIChXfV1vu4RrFQhEy6ctwmO4E130_assertion description "[Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44550.RAp8k8UQZk2pniyYUelwIChXfV1vu4RrFQhEy6ctwmO4E130_provenance.
- NP44551.RAunAQ3fl9iqZQl5wihRQZ4AUNEKScIQ_nK2RvCLInFSk130_assertion description "[Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44551.RAunAQ3fl9iqZQl5wihRQZ4AUNEKScIQ_nK2RvCLInFSk130_provenance.
- NP44553.RAtanUK5Nmto-G2HCbzl5BiiQtnlF428lHw8q0MQEmS9c130_assertion description "[Carriership of FV Leiden or FII A20210 mutations identifies an at-risk condition for venous thrombosis in the lower extremities, SVT or CVT. In patients with SVT, screening for the JAK2 V617F mutation may be useful in recognising patients who should be carefully observed for the subsequent development of overt MPD. Thus, genetic tests may play a different ro]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44553.RAtanUK5Nmto-G2HCbzl5BiiQtnlF428lHw8q0MQEmS9c130_provenance.
- NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_assertion description "[As gene variants predisposing to thrombophilia and influencing the increased risk of vein thrombosis might influence response to local thrombolysis, the aim of the work was to characterize the pharmacogenetic conditions for local streptokinase treatment in patients with a deep vein thrombosis (DVT) of lower extremities based on the following polymorphism analyses: G1691A polymorphism of factor V (FV), G20210A polymorphism of prothrombin (PT), A4250G (Thr312Ala) polymorphism of fibrinogen-alpha (FGA), G(-455)A polymorphism of fibrinogen-beta (FGB), 4G/5G polymorphism of plasminogen activator inhibitor type 1(PAI-1) and insertion/deletion (I/D) polymorphism of tissue plasminogen activator (t-PA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_provenance.
- NP44570.RAr3SedCaNgrN0aXLb0BTwIEpbUNljSCSs4q62g3Vsscs130_assertion description "[A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44570.RAr3SedCaNgrN0aXLb0BTwIEpbUNljSCSs4q62g3Vsscs130_provenance.
- NP44576.RArDedN7CiNgQLH9vKkVnxzJEYPgWVIBFCU4xDlbVgLKA130_assertion description "[Polymorphisms in the genes for coagulation factor II, V, VII in patients undergoing coronary angiography.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44576.RArDedN7CiNgQLH9vKkVnxzJEYPgWVIBFCU4xDlbVgLKA130_provenance.
- NP44577.RAkpQpLVksOewhQBQJk14e5_oz9Iq_cGksN1SZCPEgm88130_assertion description "[In agreement with the results of recent meta-analyses, our data from northeast Anatolia show a 5-fold higher prevalence of the G20210A prothrombin variant among the patients with angiographically-documented CAD when compared with those without angiographic signs of significant CAD and its variant cannot be considered as a risk factor for CAD in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44577.RAkpQpLVksOewhQBQJk14e5_oz9Iq_cGksN1SZCPEgm88130_provenance.
- NP44580.RAqCtRh-F4bq2m4qvZRC67QNyTuA6WX3F1n2t3emc9s4w130_assertion description "[To evaluate the frequency and type of vascular lesions and to study the association of factor V gene G1691A (Leiden) and prothrombin gene G20210A polymorphisms with venous thrombosis in Italian patients with Behet's disease (BD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44580.RAqCtRh-F4bq2m4qvZRC67QNyTuA6WX3F1n2t3emc9s4w130_provenance.
- NP44586.RAl4g7xkVJtuQNnlItHrmBa7XRUgG_71VVz-a3pYMEBSE130_assertion description "[Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44586.RAl4g7xkVJtuQNnlItHrmBa7XRUgG_71VVz-a3pYMEBSE130_provenance.
- NP44589.RAiQDlEOVIUI3ZOSPpSKkM4fwl6kgdXPfJdjH-phiteis130_assertion description "[The association of protein S Tokushima-K196E with a risk of deep vein thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44589.RAiQDlEOVIUI3ZOSPpSKkM4fwl6kgdXPfJdjH-phiteis130_provenance.
- NP44591.RAh7Fg43SaEh7nbwJ-Mo4z7G7IzFiL6W80JenHlyOa44E130_assertion description "[The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44591.RAh7Fg43SaEh7nbwJ-Mo4z7G7IzFiL6W80JenHlyOa44E130_provenance.
- NP44595.RApcuMJbUn7fetTM6My_MUPz04IRieUB9h1lz81Fsifms130_assertion description "[Mutation of prothrombin gene G20210A in Chinese patients is rare, and there is no correlation between the genetic mutation and deep vein thrombosis after total joint replacement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44595.RApcuMJbUn7fetTM6My_MUPz04IRieUB9h1lz81Fsifms130_provenance.
- NP44598.RAuvZndKayu6glVH19L8OwyPdnFEqFr0z5iCq3XB7gfB0130_assertion description "[Vitamin K epoxide reductase genetic polymorphism is associated with venous thromboembolism: results from the EDITH Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44598.RAuvZndKayu6glVH19L8OwyPdnFEqFr0z5iCq3XB7gfB0130_provenance.
- NP44603.RAi44VI-ejCBlckIwu44xPfwY31BiEvTM2IzR6C_kagy8130_assertion description "[If confirmed, these findings may permit a better assessment of the cardiovascular risks and benefits associated with postmenopausal estrogen therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44603.RAi44VI-ejCBlckIwu44xPfwY31BiEvTM2IzR6C_kagy8130_provenance.
- NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion description "[There is a genetic component to common stroke. No single gene with major effect was identified; rather, common variants in several genes, each exerting a modest effect, contribute to the risk of stroke. These findings have important implications for the design of future genetic studies and for predictive genetic testing for stroke and other multifactorial diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance.
- NP44620.RAhoxUdbXokqXFnjCvk3xVXM_QFjm60e_Ccx7pMw2mVNU130_assertion description "[Factor XIII Val34Leu polymorphism and gamma-chain cross-linking at the site of microvascular injury in healthy and coumadin-treated subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44620.RAhoxUdbXokqXFnjCvk3xVXM_QFjm60e_Ccx7pMw2mVNU130_provenance.
- NP44624.RAlQBQaObKQgvDp2QbQuUzHTBEhuOrPXjco0HmaRI09bM130_assertion description "[ FXIII Val34Leu polymorphism was independently associated with IL6 levels in AF. The Leu34 allele may potentially influence the prothrombotic state in these patients by modulating the inflammatory state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44624.RAlQBQaObKQgvDp2QbQuUzHTBEhuOrPXjco0HmaRI09bM130_provenance.
- NP44628.RAuADipzG2xq30OiahLzIa8KsLZQqMlDFOIO-89hQ6yeY130_assertion description "[There was no difference in genotype frequency at the FXIII Val34Leu polymorphism between relatives and controls. FXIII B-subunit levels are elevated in the relatives of CAD patients and this is independent of other cardiovascular risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44628.RAuADipzG2xq30OiahLzIa8KsLZQqMlDFOIO-89hQ6yeY130_provenance.
- NP44633.RAg9ebzXPll0V-FOef5hmGPXX6oWZyUlIjUWIHnCt7Hz4130_assertion description "[In conclusion, the technique presented allows for easy, reliable, and rapid detection of this polymorphism, and is suitable for typing both small and large numbers of DNA samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44633.RAg9ebzXPll0V-FOef5hmGPXX6oWZyUlIjUWIHnCt7Hz4130_provenance.
- NP44635.RAvkCPQOUfibISpihTuiLWY9UStvLbK9sU6n1SrsptIYE130_assertion description "[Homozygosity for the C-->T polymorphism at nucleotide 46 in the 5' untranslated region of the factor XII gene protects from development of acute coronary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44635.RAvkCPQOUfibISpihTuiLWY9UStvLbK9sU6n1SrsptIYE130_provenance.
- NP44637.RAoid9_xPQtEyxDTKjdYyewk1MdOZTzZ3MceiUc8lSI4M130_assertion description "[the prevalence of the mutant allele was 0.005]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44637.RAoid9_xPQtEyxDTKjdYyewk1MdOZTzZ3MceiUc8lSI4M130_provenance.
- NP44638.RAmzjDEcI5zZiNml7Tpadc9eU0r78_ZdYKgqlVqiHWh8M130_assertion description "[An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44638.RAmzjDEcI5zZiNml7Tpadc9eU0r78_ZdYKgqlVqiHWh8M130_provenance.
- NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion description "[ We have possibly identified haplotypes which mark alleles that have a beneficial effect on the development of prostate cancer. Moreover, our results suggest that genetic variations of the EZH2 gene are not responsible for the linkage of 7q to aggressive prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance.
- NP44642.RAlgOUctQv1j0ux4PUss6Kk0-kHTgYyALOIihsFqMYUoI130_assertion description "[A factor XI deficiency associated with a nonsense mutation (Trp501stop) in the catalytic domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44642.RAlgOUctQv1j0ux4PUss6Kk0-kHTgYyALOIihsFqMYUoI130_provenance.
- NP44646.RAmUvqLcMMNOpF62XOUn1TDvuJlA2UjoXXpK4pVcD51EM130_assertion description "[Association of EXT1 and EXT2, hereditary multiple exostoses gene products, in Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44646.RAmUvqLcMMNOpF62XOUn1TDvuJlA2UjoXXpK4pVcD51EM130_provenance.
- NP44652.RArvrALoZB2okooegcYxiUWrs3ZMJp2TRjFIMgtXp1r98130_assertion description "[Genetic variation in the DNA repair genes is predictive of outcome in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44652.RArvrALoZB2okooegcYxiUWrs3ZMJp2TRjFIMgtXp1r98130_provenance.
- NP44658.RAp-cI79090znuG8a7iZn4PmhxOYQvex6OelvQ00Rt-fg130_assertion description "[Association between single-nucleotide polymorphisms in estrogen receptor beta gene and risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44658.RAp-cI79090znuG8a7iZn4PmhxOYQvex6OelvQ00Rt-fg130_provenance.
- NP44661.RAiBrk9UUwSwQOf9pBURuSClq16VDauWFYbwVlMC2jpz4130_assertion description "[Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44661.RAiBrk9UUwSwQOf9pBURuSClq16VDauWFYbwVlMC2jpz4130_provenance.
- NP44665.RAhoD1Mf7wCs4LYGWNkiV2lDKDbzdoREII6pt2zwSL2hE130_assertion description "[In our analysis focused on genetic variation common in Whites, we observed little evidence for any substantial association of inherited variation in ESR2 with risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44665.RAhoD1Mf7wCs4LYGWNkiV2lDKDbzdoREII6pt2zwSL2hE130_provenance.
- NP44673.RAhsK0WGLYybnKIga7i1OGn6v7sjY17WS5jAztD_Uawqk130_assertion description "[We examined reported associations between radiographic hand osteoarthritis (OA) and single-nucleotide polymorphisms (SNP) in 2 candidate genes associated with OA in other joints: estrogen receptor alpha (ESR1) and beta (ESR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44673.RAhsK0WGLYybnKIga7i1OGn6v7sjY17WS5jAztD_Uawqk130_provenance.
- NP44676.RAivCCE8KEDYfcdD-3Gp4VkC49pkmDXYmxKHL7FRD2WCA130_assertion description "[Estrogen receptor-beta gene polymorphism in women with breast cancer at the Imam Khomeini Hospital Complex, Iran.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44676.RAivCCE8KEDYfcdD-3Gp4VkC49pkmDXYmxKHL7FRD2WCA130_provenance.
- NP44681.RAkggfT3HNZEGbmEm3_39UvoAmd6GJywnGufUULz3s0no130_assertion description "[Isoflavone, polymorphisms in estrogen receptor genes and breast cancer risk in case-control studies in Japanese, Japanese Brazilians and non-Japanese Brazilians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44681.RAkggfT3HNZEGbmEm3_39UvoAmd6GJywnGufUULz3s0no130_provenance.
- NP44683.RAg4crkI1Va1IdmszOfl-z6Bkn2Uy5rfAmd3U_qjvhelo130_assertion description "[ We conclude that ERalpha genotypes play no role in the incidence of CAD disease, however, ERalpha codon 10 may be a genetic factor controlling some vessels' angiographic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44683.RAg4crkI1Va1IdmszOfl-z6Bkn2Uy5rfAmd3U_qjvhelo130_provenance.
- NP44689.RArzMzUsgVVmNUjr7tTdML63XnPmE3jZq0wUuzOjkOGjo130_assertion description "[Consistent with these results, also the frequency of the haplotype containing the two above ESR2 gene risk alleles was elevated in AD women (P=0.027, OR=1.3, 95% CI=1.02-1.65).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44689.RArzMzUsgVVmNUjr7tTdML63XnPmE3jZq0wUuzOjkOGjo130_provenance.
- NP44692.RApgGol3YjxyVDKjk8JeY_g9dyU59Ob6QdKJKnVZZ0TPc130_assertion description "[Our results indicate that the G-174C SNP in the IL-6 promoter may influence the risk for developing PD, particularly regarding early age of onset PD, and that the effect is modified by interaction of the G-1730A SNP in the ERbeta gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44692.RApgGol3YjxyVDKjk8JeY_g9dyU59Ob6QdKJKnVZZ0TPc130_provenance.
- NP44698.RAp7f8PCjlIUJfy88jMhU3whgwLQXIS0SONmHNmD21cSI130_assertion description "[Polymorphism of the ER alpha gene may be a genetic risk factor for sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44698.RAp7f8PCjlIUJfy88jMhU3whgwLQXIS0SONmHNmD21cSI130_provenance.
- NP44704.RAhUyn81bsChzGFV7zI6fOMDlpf_DuLU26Y3KT_0u0Jys130_assertion description "[The present data suggest that the involvement of ESR1 polymorphisms in AD onset is mediated by the regulation of apoE expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44704.RAhUyn81bsChzGFV7zI6fOMDlpf_DuLU26Y3KT_0u0Jys130_provenance.
- NP44709.RAosQlYQB-SxiO8LkfEbVQo3pQpfqReyrpoa1UF3VyUTQ130_assertion description "[Ten polymorphisms of estrogen-metabolizing genes and a family history of colon cancer--an association study of multiple gene-gene interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44709.RAosQlYQB-SxiO8LkfEbVQo3pQpfqReyrpoa1UF3VyUTQ130_provenance.
- NP44712.RAiIGRTNbmAmtTzrkxXZ1NIAoEIASeEby2rKXA9LK4X9U130_assertion description "[Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44712.RAiIGRTNbmAmtTzrkxXZ1NIAoEIASeEby2rKXA9LK4X9U130_provenance.
- NP44716.RAr8tztd62fWGdKkokO_LK6QDWO6-pgy6kWia7QEjfSpU130_assertion description "[The AluI polymorphism in the ERbeta gene is associated with an increased risk of stage IV endometriosis in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44716.RAr8tztd62fWGdKkokO_LK6QDWO6-pgy6kWia7QEjfSpU130_provenance.
- NP44717.RAp4jscxg8UB3y0HOlzmTII2-j_I-xAbS1rImuT1KkDhw130_assertion description "[women affected by endometriosis with the ERalpha polymorphic allele, even if heterozygous, have a worse prognosis, and these results suggest that the ERalpha gene polymorphisms may be included among the genetic risk factors for endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44717.RAp4jscxg8UB3y0HOlzmTII2-j_I-xAbS1rImuT1KkDhw130_provenance.
- NP44725.RAsAJtrmcbNbdHqQT1qoBZIm1bPW4QRMq9etRnMB98Ke4130_assertion description "[To determine the possible contribution of genetic variation in the ESR1 (ER-alpha), ESR2 (ER-beta) and AR genes in breast cancer risk the -1174(TA)(7-27), c. 1092+3607(CA)(10-26) and c. 172(CAG)(6-40) repeat variants were studied in a case-control study of 79 women with sporadic breast cancer and 155 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44725.RAsAJtrmcbNbdHqQT1qoBZIm1bPW4QRMq9etRnMB98Ke4130_provenance.
- NP44726.RArvlOsc1bDB6znmMkla_rRAkMIfQq-pECIGMcYNhq9g0130_assertion description "[These epidemiological findings highlight the role of newly identified novel ER-related pathways in breast cancer development and provide a more comprehensive picture of the tumorigenic effect of estrogen in breast cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44726.RArvlOsc1bDB6znmMkla_rRAkMIfQq-pECIGMcYNhq9g0130_provenance.
- NP44734.RArJn824npazjAhjkZFd-Fr4MC6HLMnxG3TC3Sv7aY8eE130_assertion description "[Role of genetic polymorphism of estrogen receptor-alpha gene and risk of prostate cancer in north Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44734.RArJn824npazjAhjkZFd-Fr4MC6HLMnxG3TC3Sv7aY8eE130_provenance.