Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP49224.RAml_KAC-KRICQU2rH7MN60kZhy4WyjGtB9cfY7ioCS7M130_assertion description "[The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49224.RAml_KAC-KRICQU2rH7MN60kZhy4WyjGtB9cfY7ioCS7M130_provenance.
- NP49225.RAjHLXTdadBVWfi9l-1L6lppWgJEJo1dSsrVYU9R2N744130_assertion description "[This study suggests that multivitamin supplement use may modify the association between folate pathway genes and colorectal cancer risk in a post-folic-acid-supplemented population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49225.RAjHLXTdadBVWfi9l-1L6lppWgJEJo1dSsrVYU9R2N744130_provenance.
- NP49229.RAh4553LEIe_D-oUr1cJNzuTx_qv-i1rdI6L4DUnIuEa4130_assertion description "[Alcohol metabolism, alcohol intake, and breast cancer risk: a sister-set analysis using the Breast Cancer Family Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49229.RAh4553LEIe_D-oUr1cJNzuTx_qv-i1rdI6L4DUnIuEa4130_provenance.
- NP49232.RAvu52HjwtXFQq3vCpzh7ZYzOBfm2ohjay96NUKaetvv0130_assertion description "[We analyzed the ADH1C genotype in 117 moderate alcohol consumers with breast cancer and in 111 age-matched women with alcohol associated diseases without cancer (74 cirrhotics, 22 patients with pancreatitis and 15 alcohol dependent patients).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49232.RAvu52HjwtXFQq3vCpzh7ZYzOBfm2ohjay96NUKaetvv0130_provenance.
- NP49233.RApw6iryZeb6dopcgw3RtRAYi7OHRl0gBXJVDqkeBh90E130_assertion description "[ ADH3 genotype is a possible risk factor for bladder cancer. Although moderate drinkers with the gamma1gamma1 genotype seem to have the highest risk, we did not get a clear indication that ADH3 genotype modifies the relationship between alcohol intake and bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49233.RApw6iryZeb6dopcgw3RtRAYi7OHRl0gBXJVDqkeBh90E130_provenance.
- NP49234.RAvr-LHCDDsFm_RCJn4685q_bBjepZLwnukINb5C5Xt_4130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49234.RAvr-LHCDDsFm_RCJn4685q_bBjepZLwnukINb5C5Xt_4130_provenance.
- NP49237.RAjzqsRtoyL-0rDU9GNPkEPOQXXCgU741POmmxGyWhDdw130_assertion description "[In the Polish men examined, ADH1C*1 and ADH1B*1 alleles and ADH1C*1/*1 and ADH1B*1/*1 genotypes favor alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49237.RAjzqsRtoyL-0rDU9GNPkEPOQXXCgU741POmmxGyWhDdw130_provenance.
- NP49247.RAvnh5XUkdVzCUbjVtm97wYQbqr5mUVfPXsS1oqfL_PsQ130_assertion description "[Candidate genes for alcohol dependence: a review of genetic evidence from human studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49247.RAvnh5XUkdVzCUbjVtm97wYQbqr5mUVfPXsS1oqfL_PsQ130_provenance.
- NP49255.RAmBFt9699T7ioGn2psCY0A8u8ylsc-ekujmVksp2-1Tc130_assertion description "[this study showed the strong effect of ADH2 His(47)Arg polymorphism on habitual drinking regardless of ALDH2 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49255.RAmBFt9699T7ioGn2psCY0A8u8ylsc-ekujmVksp2-1Tc130_provenance.
- NP49258.RAnfVP5DH6Ip7V0LRmP8C8Hhnp3RJxZEf42RpWYB1B1Ng130_assertion description "[The reason for the insignificant multivariate OR of ALDH2(1/1) may be due to the strong confounding of alcohol consumption on the association between ALDH2 genotype and ION. For females, the small sample size made it impossible to produce any meaningful univariate analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49258.RAnfVP5DH6Ip7V0LRmP8C8Hhnp3RJxZEf42RpWYB1B1Ng130_provenance.
- NP49262.RArV3AS4EYy_JQ5_ixZEKYpWwjTzmdH8PXlLbtTwDp4fA130_assertion description "[Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49262.RArV3AS4EYy_JQ5_ixZEKYpWwjTzmdH8PXlLbtTwDp4fA130_provenance.
- NP49264.RAt_EOexBucfak2rizO6BgIxwomAoJugnd6XJVgk-jlMA130_assertion description "[A novel polymorphism rs1329149 of CYP2E1 and a known polymorphism rs671 of ALDH2 of alcohol metabolizing enzymes are associated with colorectal cancer in a southwestern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49264.RAt_EOexBucfak2rizO6BgIxwomAoJugnd6XJVgk-jlMA130_provenance.
- NP49269.RAqIU0hTkfc318M6DPJGibsyTG8DXULMkcJ6ii2n9f9d8130_assertion description "[Compared with individuals carrying both ALDH2 G/G and ADH2 A/A alleles and with a cumulative amount of alcohol consumption <2.5 (kg * years), drinkers carrying both ALDH2 A and ADH2 G alleles and with a cumulative amount of alcohol consumption > or =2.5 (kg * years) showed a significantly elevated risk of esophageal cancer (OR=53.15, 95% CI: 4.24-666.84).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49269.RAqIU0hTkfc318M6DPJGibsyTG8DXULMkcJ6ii2n9f9d8130_provenance.
- NP49277.RAjl0AKTVNM2rnLECVInfUPKaLa-ren3M5uhNu2MgtOl0130_assertion description "[High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49277.RAjl0AKTVNM2rnLECVInfUPKaLa-ren3M5uhNu2MgtOl0130_provenance.
- NP49280.RAuXL9WRTvyvPaJtOzhy6DtiDOflps20AO5c3h9-vyzvU130_assertion description "[ADD1 460W allele associated with cardiovascular disease in hypertensive individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49280.RAuXL9WRTvyvPaJtOzhy6DtiDOflps20AO5c3h9-vyzvU130_provenance.
- NP49281.RArfhErKoBEwCO4WuqPoim75U-YhJtbixVXwmNAhG7bcg130_assertion description "[The influence of -adducin gene polymorphism on response of blood pressure to exercise in patients with hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49281.RArfhErKoBEwCO4WuqPoim75U-YhJtbixVXwmNAhG7bcg130_provenance.
- NP49288.RAriEGxQIhkqOPrk9puQ0EiawCHCrqz3XLQi9e0smSIg4130_assertion description "[The alpha-adducin gene is not an important modifier of antihypertensive treatment on cardiovascular risk, but women Trp allele carriers may have increased CHD risk if treated with C versus A or L. This must be confirmed to have implications for hypertension treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49288.RAriEGxQIhkqOPrk9puQ0EiawCHCrqz3XLQi9e0smSIg4130_provenance.
- NP49289.RAjeIRrlZrTj2JyiwJSd60k6XxjydQk1g-oSlaG3AOj9Q130_assertion description "[Further study will be needed to confirm the effect of the alpha adducin gene, the angiotensinogen gene and the renin gene on essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49289.RAjeIRrlZrTj2JyiwJSd60k6XxjydQk1g-oSlaG3AOj9Q130_provenance.
- NP49290.RAgrZblJnMt666F2RMwx-OGYJkmLUdXmfFjsJed08ss40130_assertion description "[Sodium-lithium countertransport and the Gly460-->Trp alpha-adducin polymorphism in essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49290.RAgrZblJnMt666F2RMwx-OGYJkmLUdXmfFjsJed08ss40130_provenance.
- NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_assertion description "[ The ADD genotype is predictive of the course of renal function loss in an unselected renal population and influences the effect of the ACE genotype to modulate the rate of progression to ESRD. Thus, the ADD genotype may play a role for the understanding of interindividual differences in the course of renal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_provenance.
- NP49296.RAgrgcSBC-L5ALtmMFWwne6vO8hFaQEweyclJ5jpswQOc130_assertion description "[ Alpha-adducin gene G/W 460 polymorphism is significantly associated with the risk of ICH. This association does not appear to be mediated by established ICH risk factors, specifically hypertension status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49296.RAgrgcSBC-L5ALtmMFWwne6vO8hFaQEweyclJ5jpswQOc130_provenance.
- NP49307.RAucyAKHSy7SFrbzoyUqO1o7m2-Hxu9zcMl8h9m7P921U130_assertion description "[Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49307.RAucyAKHSy7SFrbzoyUqO1o7m2-Hxu9zcMl8h9m7P921U130_provenance.
- NP49308.RAnoHoV1SDcuGslJMruRIq074oLuGIwUixx5N1C0eZKwA130_assertion description "[Association of IL-4 and ADAM33 gene polymorphisms with asthma in an Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49308.RAnoHoV1SDcuGslJMruRIq074oLuGIwUixx5N1C0eZKwA130_provenance.
- NP49311.RAowR_3HlxmZFzyqVElndVlOviSFvT16ejC42rz1fyjRE130_assertion description "[On the basis of the consistency of our findings with previous meta-analyses and large replication studies, IL13, TNF, ADAM33, IL4RA and TBXA2R might represent common major asthma and asthma-related trait genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49311.RAowR_3HlxmZFzyqVElndVlOviSFvT16ejC42rz1fyjRE130_provenance.
- NP49313.RAuRUJZ3pjvh_fVWGAHudQzxEtQudNIRTBJ2tSdr5dY8M130_assertion description "[To verify the association of transforming growth factor-beta1(TGF-beta1) (C-509T and T869C), CD14 (C-159T), IL-4 (C-590T), IL-4R (ILe50Val) and ADAM33 (S_2) gene polymorphisms with asthma severity in a sample of patients with mild, moderate and severe persistent atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49313.RAuRUJZ3pjvh_fVWGAHudQzxEtQudNIRTBJ2tSdr5dY8M130_provenance.
- NP49317.RAqsLolk4alZMOuRFo92LZSN2bfKwLwsMHDYBVlqskBUw130_assertion description "[The study population included 291 Roman children with bronchial asthma and 72 adult Romans with CD, and haptoglobin, adenosine deaminase (ADA), acid phosphatase locus 1 (ACP1) and MN phenotypes were determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49317.RAqsLolk4alZMOuRFo92LZSN2bfKwLwsMHDYBVlqskBUw130_provenance.
- NP49320.RAiyPSS38wHsP0vJndN7o3YddanLHGYba5j8Tc1HEJTL8130_assertion description "[At the ADA-TTTA locus, no significant differences were observed between Japanese and Chinese or between Japanese and Basques, but significant differences were found between our Japanese population and Italians and Mossi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49320.RAiyPSS38wHsP0vJndN7o3YddanLHGYba5j8Tc1HEJTL8130_provenance.
- NP49335.RAsql-GTT6I1Zp4gu6y61YratJI_xKD8129ZbyQUfnurI130_assertion description "[The allelic frequencies of the polymorphic systems]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49335.RAsql-GTT6I1Zp4gu6y61YratJI_xKD8129ZbyQUfnurI130_provenance.
- NP49339.RAkoyL3uPVL-d4sa6c4NXK-7yRxxBN_4657FVIsTXgOco130_assertion description "[ It is suggested that genotypes SS, 2F and FS have marked functional differences in fixation and transport of vitamin D active metabolites involved in metabolism of bone tissue in OP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49339.RAkoyL3uPVL-d4sa6c4NXK-7yRxxBN_4657FVIsTXgOco130_provenance.
- NP49345.RAn7SZG20YHs4DJt5UwZUVSJryD4GsKaOlXbU_fdnV3wE130_assertion description "[Here, we report previously nonperceived interrelationships between expression variations and nucleotide polymorphisms of the chromosome 7q21-22 acetylcholinesterase-paraoxonase 1 (ACHE-PON1) locus with the trait- and state-anxiety measures of 461 healthy subjects from the Health, Risk Factors, Exercise Training, and Genetics Family Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49345.RAn7SZG20YHs4DJt5UwZUVSJryD4GsKaOlXbU_fdnV3wE130_provenance.
- NP49352.RAkrrMaz6JQpBqO1j-yjdNc3DWSnM1rz3vIEMahzgyWBQ130_assertion description "[The REN-5312T allele had been shown previously to result in increased in vitro expression of the renin gene. We have now shown, in 2 independent populations, that carriage of a REN-5312T allele is associated with elevated diastolic blood pressure. These data provide evidence that renin is an important susceptibility gene for arterial hypertension in whites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49352.RAkrrMaz6JQpBqO1j-yjdNc3DWSnM1rz3vIEMahzgyWBQ130_provenance.
- NP49357.RAvFFcvALxh5PUw7hi-82S34SSR2JaJjs-sO74qNM7pDc130_assertion description "[The I/D polymorphism of angiotensin-converting enzyme (ACE) gene is associated with cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49357.RAvFFcvALxh5PUw7hi-82S34SSR2JaJjs-sO74qNM7pDc130_provenance.
- NP49364.RAshBkZ-h5U9byQG1xJZ7kpKMn-Iu-0QJXOgH3cuCFEco130_assertion description "[Cardiovascular diseases and molecular variants of the renin-angiotensin system components in Slovak population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49364.RAshBkZ-h5U9byQG1xJZ7kpKMn-Iu-0QJXOgH3cuCFEco130_provenance.
- NP49366.RAgR16kf8NLNj83SPtobFf2kTiWuz737JLaFGWDF3e_Vg130_assertion description "[Angiotensin-converting enzyme levels and activity in Alzheimer's disease: differences in brain and CSF ACE and association with ACE1 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49366.RAgR16kf8NLNj83SPtobFf2kTiWuz737JLaFGWDF3e_Vg130_provenance.
- NP49367.RAov2GfTO9KytdReRYQMkHkj1e_gY5KO5Uu993D4xtXQs130_assertion description "[In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49367.RAov2GfTO9KytdReRYQMkHkj1e_gY5KO5Uu993D4xtXQs130_provenance.
- NP49373.RAi0MauEzEzIOFUe2l7FCGsel_C0OGNTNj3ifRgRvgS5s130_assertion description "[A deletion polymorphism at intron 16 of the ACE gene has also been associated with AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49373.RAi0MauEzEzIOFUe2l7FCGsel_C0OGNTNj3ifRgRvgS5s130_provenance.
- NP49374.RAgbKwskSxUH0oR3XZNov_CtkXHAdy6ZGZrpXhnQUbm5w130_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." NP49374.RAgbKwskSxUH0oR3XZNov_CtkXHAdy6ZGZrpXhnQUbm5w130_provenance.
- NP49376.RAnPzMpl143wLMFL3MJXu7dj4FgsIhvyuAUKsvZQnZtgs130_assertion description "[Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49376.RAnPzMpl143wLMFL3MJXu7dj4FgsIhvyuAUKsvZQnZtgs130_provenance.
- NP49377.RAk1eGdrY35GJ_u5-0xpyFFmnu9YF7QFGwDghTZ20dpOY130_assertion description "[ The genetic variation at alpha2m is associated with the severity of RA. Carriers of the alpha2m deletion allele would have increased risk of developing an early active severe form of the disease. Our data suggest that alpha2m could be a valuable target in the treatment of RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49377.RAk1eGdrY35GJ_u5-0xpyFFmnu9YF7QFGwDghTZ20dpOY130_provenance.
- NP49379.RAqfqu0oxvbjBe8CHFmiPGcHSkI_N0LeXSSxusOPNESmg130_assertion description "[The purpose of this study was to determine if variants in the G-protein coupled receptor Kinase-4 (GRK4), nitric oxide synthase-3 (NOS3), or angiotensin converting enzyme (ACE) genes are associated singly or through complex interactions, with HBP in African Americans aged 18-49 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49379.RAqfqu0oxvbjBe8CHFmiPGcHSkI_N0LeXSSxusOPNESmg130_provenance.
- NP49380.RAos6JIfGSYNM82p0_sVdhGwhNsT4WFKMHu_V7tT8ToF0130_assertion description "[our results show that the ACE I/D polymorphism is common in Lebanon, and the combinations of ACE D allele and age is associated with an increased risk of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49380.RAos6JIfGSYNM82p0_sVdhGwhNsT4WFKMHu_V7tT8ToF0130_provenance.
- NP49381.RAqPFOym8l7BbmueCo5zzrXbB8q8O67dbf2hQeZquSdxk130_assertion description "[Although ACE has been reported to be one of the main polymorphisms associated with hypertension, we found no association with ACE's specific genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49381.RAqPFOym8l7BbmueCo5zzrXbB8q8O67dbf2hQeZquSdxk130_provenance.
- NP49383.RAh27vkifkQ5sxKSCU5UjF_bmTIO0oHAlD_BBNr6cMEjk130_assertion description "[Angiotensin-converting enzyme gene insertion/deletion polymorphism frequency in normotensive children with a positive family history of essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49383.RAh27vkifkQ5sxKSCU5UjF_bmTIO0oHAlD_BBNr6cMEjk130_provenance.
- NP49387.RAqQO3rBbMcTJYDt-BtfzWVni2LdYoXMEZPNabY-gBES8130_assertion description "[Moreover, individuals who are homozygous for the D allele of the ACE gene are more likely to have essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49387.RAqQO3rBbMcTJYDt-BtfzWVni2LdYoXMEZPNabY-gBES8130_provenance.
- NP49392.RApOGxAKON_70Lq4KpSmka0u9gmZLUMLOcjv_q3FtW82I130_assertion description "[Association between ACE gene polymorphism and therapeutic responsiveness of ACEI in diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49392.RApOGxAKON_70Lq4KpSmka0u9gmZLUMLOcjv_q3FtW82I130_provenance.
- NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_assertion description "[SNPs Met235Thr in angiotensinogen, T>C (-344) in aldosterone synthase, and G>A (-1903) in chymase genes are significantly associated with diabetic chronic renal insufficiency in Indian patients and warrant replication in larger sample sets. Use of such markers for prediction of susceptibility to diabetes specific renal disease in the ethnically Indian popula]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_provenance.
- NP49395.RAjlUXj9L9BzPYs_fsnWFN5e2Q2KsZNLoS_dSfGIqWEyw130_assertion description "[The ACE DD genotype is associated with the development of incipient diabetic nephropathy and established diabetic nephropathy in a Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49395.RAjlUXj9L9BzPYs_fsnWFN5e2Q2KsZNLoS_dSfGIqWEyw130_provenance.
- NP49404.RArnZl1fVQwwQqBOYiq-I5AqvLxka0mosqFT2PaQhnDAg130_assertion description "[In conclusion, our results suggest an association between LVH and the C825T allele of the G-protein beta3 subunit gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49404.RArnZl1fVQwwQqBOYiq-I5AqvLxka0mosqFT2PaQhnDAg130_provenance.
- NP49407.RArOSLutYG40rFTnq9xr1Id8AEF-CU1DFBzg-ATRmW3tU130_assertion description "[Antihypertensive treatment modulates the association between the D/I ACE gene polymorphism and left ventricular hypertrophy: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49407.RArOSLutYG40rFTnq9xr1Id8AEF-CU1DFBzg-ATRmW3tU130_provenance.
- NP49413.RAh2iz_cqG77qpTQZmmnMlon2zwjFSkSpza-shxRKzJyI130_assertion description "[The ACE and eNOS genotype polymorphisms were associated with risk of CAD and persons with DD and GT genotypes take higher risk of suffering from CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49413.RAh2iz_cqG77qpTQZmmnMlon2zwjFSkSpza-shxRKzJyI130_provenance.
- NP49418.RArJOxxXI4D9yYdCH6J5WeVOlQa0BOOHTMcS_9u4uZXio130_assertion description "[Our objective was to determine if DNA polymorphisms in the NOS3 and ACE genes were associated with early CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49418.RArJOxxXI4D9yYdCH6J5WeVOlQa0BOOHTMcS_9u4uZXio130_provenance.
- NP49419.RAgsZ1v1Kps23yCzOIg1N4k6Q3aIyFLk6lBGzh9e08kLY130_assertion description "[The frequencies of ACE D and ACE I allele among the patients with CAD were 62.26% and 37.73 % and in the control subjects were 49.3% and 50.76%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49419.RAgsZ1v1Kps23yCzOIg1N4k6Q3aIyFLk6lBGzh9e08kLY130_provenance.
- NP49424.RAmaTTAMRWjiALbHVXPhVOWBVId1zvp_A6ASylizc6BS8130_assertion description "[Predominantly linked ACE genotypes exhibited opposite effects on MI risks, e.g., the AA (rs12449782) genotype had a detrimental effect, whereas the predominantly linked AA (rs4363) genotype exhibited a protective effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49424.RAmaTTAMRWjiALbHVXPhVOWBVId1zvp_A6ASylizc6BS8130_provenance.
- NP49425.RAthV2T-Nbce7xEamvgtXUZC1QhIu1gHxPNPPn7dWSvRk130_assertion description "[We analyzed the implications of the insertion/deletion (I/D) polymorphism of the ACE gene on the presence of abnormal cardiovascular magnetic resonance (CMR)-derived microvascular perfusion after ST-segment elevation myocardial infarction (STEMI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49425.RAthV2T-Nbce7xEamvgtXUZC1QhIu1gHxPNPPn7dWSvRk130_provenance.
- NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_assertion description "[ It is suggested that ACE gene I/D polymorphism is a susceptible gene for stroke in DM2 patients in China. AT1R gene A1166C polymorphism contributes to the development of stroke in DM2 patients, but it is not an independent risk factor. There is synergistic effect of AT1R A1166C and ACE I/D gene polymorphisms on the occurrence and development of stroke in type 2 diabetics in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_provenance.
- NP49440.RAv0mE6wyX_zoGlRd2EUzcAc413b_D9lJ8UuLm68dwTyI130_assertion description "[Our findings suggest that genetic effects may differ between small and large vessel subtypes, although the evidence base is small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49440.RAv0mE6wyX_zoGlRd2EUzcAc413b_D9lJ8UuLm68dwTyI130_provenance.
- NP49441.RAviDDiX9XPqnf-B14JOFXOQiEXJHNHodgkXU-MTS3efw130_assertion description "[Associations between genetic variants in the ACE, AGT, AGTR1 and AGTR2 genes and renal function in the Multi-ethnic Study of Atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49441.RAviDDiX9XPqnf-B14JOFXOQiEXJHNHodgkXU-MTS3efw130_provenance.
- NP49442.RApCWsLCzkYMtMyRagFBligV64ALY6Nz-FfSjpYPYTTVE130_assertion description "[Pioglitazone may exert anti-atherosclerotic effects on type 2 diabetics carrying the ACE gene's D allele and/or MTHFR gene's 677T allele, who showed a progression of carotid atherosclerosis without the drug.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49442.RApCWsLCzkYMtMyRagFBligV64ALY6Nz-FfSjpYPYTTVE130_provenance.
- NP49443.RAsK_hKn02glRo6dIb9UiVgnY8eKUbmbjc1OcOyRcAYkQ130_assertion description "[The D allele of angiotensin I-converting enzyme gene insertion/deletion polymorphism is associated with the severity of atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49443.RAsK_hKn02glRo6dIb9UiVgnY8eKUbmbjc1OcOyRcAYkQ130_provenance.
- NP49454.RAs2lX720hKKVYaONeg63IhMXALnkSDPEmZhKWczjoEkw130_assertion description "[There is no association between ACE gene I/D polymorphism and the genesis and development of DR in Type 2 diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49454.RAs2lX720hKKVYaONeg63IhMXALnkSDPEmZhKWczjoEkw130_provenance.
- NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_assertion description "[Thus, knowledge of the haptoglobin phenotype may be useful in assessing and utilizing new therapies that attempt to reduce restenosis, and may have important implications for the risk stratification algorithm used in managing diabetic patients with coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_provenance.
- NP49466.RApPbVo7tIC7uRfIaYYlM51AHv0QkAflxEYWhLc9nZRDI130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49466.RApPbVo7tIC7uRfIaYYlM51AHv0QkAflxEYWhLc9nZRDI130_provenance.
- NP49469.RAug6CyYxNaz62zetsyHCbP6eTguiXaQfuc2m0dquWhP8130_assertion description "[ Our preliminary data suggest that mutation carriers might have an increased susceptibility to polydipsia through an undetermined mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49469.RAug6CyYxNaz62zetsyHCbP6eTguiXaQfuc2m0dquWhP8130_provenance.
- NP49477.RAmk5Y4X9CmTvxzcWrTNMVj3DvgASSqVTdmw3AnFtaFPo130_assertion description "[Patients (322; 162 males) with type 2 diabetes were categorised in this cross-sectional study into the following groups: normoalbuminuria (n=145), microalbuminuria (n=129) and macroalbuminuria (n=48).ACE gen I/D polymorphism genotypes were determined using the polymerase chain reaction method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49477.RAmk5Y4X9CmTvxzcWrTNMVj3DvgASSqVTdmw3AnFtaFPo130_provenance.
- NP49479.RAoLZ5i8UU_32GI0Cp1CnS6AA98qh34cLHIEZq0oKcWOo130_assertion description "[Impact of renin-angiotensin system polymorphisms on renal haemodynamic responsiveness to acute angiotensin-converting enzyme inhibition in type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49479.RAoLZ5i8UU_32GI0Cp1CnS6AA98qh34cLHIEZq0oKcWOo130_provenance.
- NP49487.RAvfsaQKT6FkLrejR64Dgtx5TkJbbWt_UIMxtpsE0dbFU130_assertion description "[We examined 118 CKD patients and 98 control subjects for the occurrence of common polymorphisms in angiotensin converting enzyme insertion/deletion (ACE; I/D), angiotensinogen (AGT; M235T), chymase (CMA; -1903G>A), angiotensin receptor type-1 (AGTR1-1166A>C), methylene tetrahydrofolate reductase (MTHFR; 677C>T), nephrin (NPHS1; R1160X) and podocin (NPHS2; R291W and R229Q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49487.RAvfsaQKT6FkLrejR64Dgtx5TkJbbWt_UIMxtpsE0dbFU130_provenance.
- NP49488.RAkBFnoenkClLIZnxdzc3xd0K37Ou3Tf1HJ5As5b22uaY130_assertion description "[ACE genotype and ACE inhibitor response in kidney disease: a perspective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49488.RAkBFnoenkClLIZnxdzc3xd0K37Ou3Tf1HJ5As5b22uaY130_provenance.
- NP49491.RAjRi7MxYPJea573_ZwCIXwVfRC0XO3fEiAzN0KxFApRk130_assertion description "[In an analysis of ED patients and their genotypes in the GNB3 C825T, the ACE I/D and the NOS3 G894T polymorphisms, there was no evidence for influence of the genotypes on the susceptibility to develop ED.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49491.RAjRi7MxYPJea573_ZwCIXwVfRC0XO3fEiAzN0KxFApRk130_provenance.
- NP49493.RAlI0RjdsKiUGaiKpX_6MH4Myj7ppxlTJYdmAJuXs6AQA130_assertion description "[ It appears that patients with elevated ACE serum concentrations, as associated with the D allele of the ACE I/D polymorphism, are less likely to respond to sildenafil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49493.RAlI0RjdsKiUGaiKpX_6MH4Myj7ppxlTJYdmAJuXs6AQA130_provenance.
- NP49503.RAsGy0nd08ku1oOKz1wWekniTkHdwOxdlDAUCCQpSE10w130_assertion description "[Our results suggest that in the Polish population the AT1R gene polymorphism might be associated with increased susceptibility to chronic renal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49503.RAsGy0nd08ku1oOKz1wWekniTkHdwOxdlDAUCCQpSE10w130_provenance.
- NP49505.RAh-oao1IuqyfCMKySDdkBQLaC4EGbFZiSpGm4EJP2b9E130_assertion description "[Variation at the Angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49505.RAh-oao1IuqyfCMKySDdkBQLaC4EGbFZiSpGm4EJP2b9E130_provenance.
- NP49508.RAkuijw33RWMkqmW41ieip3ZnA6FQgAIolNhuYh_ecvVQ130_assertion description "[The relationship between slow coronary flow and angiotensin converting enzyme and ATIIR1 gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49508.RAkuijw33RWMkqmW41ieip3ZnA6FQgAIolNhuYh_ecvVQ130_provenance.
- NP49510.RAoTZfwHpY1BhgSVMdANpvlixx4itWktH8uPwwcELgSsU130_assertion description "[The results of our study suggest that, in addition to prothrombotic mutations such as Factor V Leiden, single-nucleotide polymorphisms should be considered in all children with congenital cardiac malformations who develop thrombosis. Malformations of the]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49510.RAoTZfwHpY1BhgSVMdANpvlixx4itWktH8uPwwcELgSsU130_provenance.
- NP49518.RAn0fLfmlcof7Uj1yvJMBUZaakq-oV31GEetH4BsMqRdU130_assertion description "[It is suggested that I gene of ACE may play a role in perfomance of the pilots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49518.RAn0fLfmlcof7Uj1yvJMBUZaakq-oV31GEetH4BsMqRdU130_provenance.
- NP49522.RAuY1nAfZ_tnO_11h6U2SX5JlhAFT7yvhW8W5_v7OQbWE130_assertion description "[Angiotensin converting enzyme gene polymorphism and traditional Sasang classification in Koreans with cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49522.RAuY1nAfZ_tnO_11h6U2SX5JlhAFT7yvhW8W5_v7OQbWE130_provenance.
- NP49523.RAhenanvpzhgBUXq_YKtX37EtGG9LXG4tAO1UoU9iG1-Y130_assertion description "[The ACE/DD genotype was not associated with CI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49523.RAhenanvpzhgBUXq_YKtX37EtGG9LXG4tAO1UoU9iG1-Y130_provenance.
- NP49525.RAm7Ro4TYQRlL2iF1ZAFFdpXKk4VfMaYHtJ_oTVAE1lQA130_assertion description "[Also, in the case of combination of ACE and AT2 gene, the combination of ACE II genotype and AT2 A-1332G transition occurs infrequently in primary VUR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49525.RAm7Ro4TYQRlL2iF1ZAFFdpXKk4VfMaYHtJ_oTVAE1lQA130_provenance.
- NP49529.RAkgF4U4agN3V17JzbgPJeGbRU8wwUtS0MuxkN1byVgfA130_assertion description "[This study highlights the role of ACE gene in predisposing to both lone and secondary NVAF, further contributing to penetrate the genetic mechanisms responsible for this complex disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49529.RAkgF4U4agN3V17JzbgPJeGbRU8wwUtS0MuxkN1byVgfA130_provenance.
- NP49530.RAgbFuEeC1qb893kGzsbvgLAR9YJcAfJj0APvRKEqwP20130_assertion description "[These results provide further evidence for a role of RAAS activation in the pathophysiology of AF and point to a potential role for stratification of therapeutic approaches by ACE genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49530.RAgbFuEeC1qb893kGzsbvgLAR9YJcAfJj0APvRKEqwP20130_provenance.
- NP49534.RAnm-x8umEENXY6ZR_tVrRzplxq0xgJS9hDwujhvXdwH0130_assertion description "[Multiple regression analyses showed that the APOC1 polymorphism was the only variable which predicted NAA/Cr values in basal ganglia. NAA/Cr metabolites in the medial temporal lobe but not in the basal ganglia region were related with lower performance in verbal memory.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49534.RAnm-x8umEENXY6ZR_tVrRzplxq0xgJS9hDwujhvXdwH0130_provenance.
- NP49539.RAnhhuTNRExfYj715a2lEH-LbowqSGFfQpq12aPjEVT2c130_assertion description "[Interactions of lymphotoxin alpha (TNF-beta), angiotensin-converting enzyme (ACE), and endothelin-1 (ET-1) gene polymorphisms in adult periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49539.RAnhhuTNRExfYj715a2lEH-LbowqSGFfQpq12aPjEVT2c130_provenance.
- NP49541.RAkoHARJxgjrMcSFMINbdmYyPSOUOIsA2PQicPkHgbG8o130_assertion description "[We conclude that for the majority of adult patients with cystic fibrosis a new pulmonary exacerbation is not caused by the acquisition of a new strain of P. aeruginosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49541.RAkoHARJxgjrMcSFMINbdmYyPSOUOIsA2PQicPkHgbG8o130_provenance.
- NP49545.RAh7u53rBNTdlJfmXDF9EPj-MK2S3SrI8uGUxv8x8wk-8130_assertion description "[ACE gene polymorphism and cardiac structure in patients with insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49545.RAh7u53rBNTdlJfmXDF9EPj-MK2S3SrI8uGUxv8x8wk-8130_provenance.
- NP49548.RAs9Ekd6d0ICEzxAjP8bRttZ1Qu-3VpGSYZxW8EpROfGs130_assertion description "[Influence of the ACE gene insertion/deletion polymorphism on insulin sensitivity and impaired glucose tolerance in healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49548.RAs9Ekd6d0ICEzxAjP8bRttZ1Qu-3VpGSYZxW8EpROfGs130_provenance.
- NP49550.RAjzbzaiP_rUZVc68fs5a-QWhw4VrEmUZKKHNDA7z4u5E130_assertion description "[Lack of association between angiotensin converting enzyme gene polymorphism and Korean Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49550.RAjzbzaiP_rUZVc68fs5a-QWhw4VrEmUZKKHNDA7z4u5E130_provenance.
- NP49551.RAhHahYNKLoRhmOBxGfiwhPfxx81Z9u9sYw6CD5KltXEg130_assertion description "[Angiotensin-converting enzyme gene and endothelial nitric oxide synthase gene polymorphisms in Behet's disease with or without ocular involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49551.RAhHahYNKLoRhmOBxGfiwhPfxx81Z9u9sYw6CD5KltXEg130_provenance.
- NP49553.RAhQ-hkt5Z8sD56X1xs_8U2KgBOUlF-lH8wIl68uAUs1g130_assertion description "[An association between Behet's disease and ACE polymorphism may provide a useful basis for future molecular studies and therapeutic approaches in this complex disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49553.RAhQ-hkt5Z8sD56X1xs_8U2KgBOUlF-lH8wIl68uAUs1g130_provenance.
- NP49561.RAsfMMNxFhW3gtmoXktt7NI3GLq0-ROG1QUAJKEvh77QI130_assertion description "[These results suggest that the insertion polymorphism of the ACE gene may correlate with the activity of lupus nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49561.RAsfMMNxFhW3gtmoXktt7NI3GLq0-ROG1QUAJKEvh77QI130_provenance.
- NP49562.RAn5DJ3WnrGaKY9oMofxhxDxuK7gTwBb-zIY_PkDFxldg130_assertion description "[In this study, the correlation between ACE gene I/D polymorphism and the clinical features of lupus nephritis (LN) was determined in 144 LN patients and 150 normal controls by PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49562.RAn5DJ3WnrGaKY9oMofxhxDxuK7gTwBb-zIY_PkDFxldg130_provenance.
- NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_assertion description "[ The severity of colonic FAP may be modified by alleles at the NAT1 and/or NAT2 loci. The identity of any functional variation remains unknown as NAT1*10 appears to be non-functional and there is linkage disequilibrium between alleles at multiple sites within these loci which are adjacent on chromosome 8p22. While evidence from this study cannot be conclusive, our data suggest that NAT1 and NAT2 variants may explain an approximately twofold increase in polyp number in the FAP colon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_provenance.
- NP49570.RAnteExbiID6jPBe2sXHPf_eig8DyJM1EdviSVz2cuXm4130_assertion description "[ This study reports an association between the DD genotype of ACE and asthma, which is not related to the degree of airway obstruction. These results need to be confirmed by a larger case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49570.RAnteExbiID6jPBe2sXHPf_eig8DyJM1EdviSVz2cuXm4130_provenance.
- NP49572.RAjcb1_oP7SQWwVj0yyCu8JtuHpwziDjchNIWBs-YgkNo130_assertion description "[The angiotensin-converting enzyme (ACE) gene is a potential candidate gene for risk of asthma, COPD, and COPD co-morbidity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49572.RAjcb1_oP7SQWwVj0yyCu8JtuHpwziDjchNIWBs-YgkNo130_provenance.
- NP49573.RAqxxINB0r65garqcWI9NjwbUVGGaDlO1-Q5SMaDrDQP4130_assertion description "[An Angiotensin I converting enzyme polymorphism is associated with clinical phenotype when using differentiation-syndrome to categorize korean bronchial asthma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49573.RAqxxINB0r65garqcWI9NjwbUVGGaDlO1-Q5SMaDrDQP4130_provenance.
- NP49580.RAkeM4JUhba_Kn8wkyLsDe4wrC5hhcxmBGXpXBIj6plv8130_assertion description "[Association between polymorphisms of the angiotensin-converting enzyme and angiotensinogen genes and allergic rhinitis in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49580.RAkeM4JUhba_Kn8wkyLsDe4wrC5hhcxmBGXpXBIj6plv8130_provenance.
- NP49585.RAgi5L4assDMJgEEK3mEHGO5xDnehK3hTb-15RJbHYeLA130_assertion description "[These findings suggest that the ability of oxygen administration to improve tissue oxygenation during exercise is associated with the ACE genotypes in COPD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49585.RAgi5L4assDMJgEEK3mEHGO5xDnehK3hTb-15RJbHYeLA130_provenance.
- NP49588.RAnYH0Ng8UrSl8LbTpouU2GZEExX_WgmY80CPa_83z3vA130_assertion description "[Association of the G7831A polymorphism of the ACE gene with myocardial ischemia in the Moscow population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49588.RAnYH0Ng8UrSl8LbTpouU2GZEExX_WgmY80CPa_83z3vA130_provenance.
- NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_assertion description "[ This study supports the hypothesis that there may be different types of small vessel disease in patients with classic lacunar syndromes and that the influence of the ACE DD genotype may be relevant in mediating the diffuse form of vessel injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_provenance.
- NP49609.RApZCusvN1cDJeOtdw_cxqRRabkn9QHZhTsyEy_1lgOXo130_assertion description "[The ACE D allele in its homozygous form may confer susceptibility for autoimmune manifestations in sarcoidosis, possibly via the high levels of S-ACE it encodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49609.RApZCusvN1cDJeOtdw_cxqRRabkn9QHZhTsyEy_1lgOXo130_provenance.
- NP49613.RAuoHXnCPD0r4eeqRsodqCBsahPiLL2AITNa8Q2kZ__RE130_assertion description "[ACE is involved in the pathogenesis of sarcoidosis, but the ACE polymorphisms are not an inherited main cause of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49613.RAuoHXnCPD0r4eeqRsodqCBsahPiLL2AITNa8Q2kZ__RE130_provenance.
- NP49619.RAnEHeZh7oAibyTBqsO96fQ7yL82Kx1qumvtaItKSUxfI130_assertion description "[Previous studies have revealed changes in the central ACE levels for schizophrenic patients, possibly related to the polydipsia commonly demonstrated for chronic schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49619.RAnEHeZh7oAibyTBqsO96fQ7yL82Kx1qumvtaItKSUxfI130_provenance.