Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP49102.RATIyvlqb87YE8aHGnV4-CKdRMGX22M9PKE1UM7_jlxTs130_assertion description "[ Our findings suggest that the genotype of Arg389Gly polymorphism in the human ADRB1 gene is associated with AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49102.RATIyvlqb87YE8aHGnV4-CKdRMGX22M9PKE1UM7_jlxTs130_provenance.
- NP49104.RAcvuSJs7TIhVOl5m7BHKyt7Sbw82KlCoBmNbP3MrOhiE130_assertion description "[ This is the first study to investigate the relationship between the Gly389Arg ADRB1 variant and obesity. We found that the Arg allele is associated with greater body weight and BMI in Caucasian women due to a greater fat mass.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49104.RAcvuSJs7TIhVOl5m7BHKyt7Sbw82KlCoBmNbP3MrOhiE130_provenance.
- NP49108.RAcsu0x--DoowRYwh0PXVhTRuA7tEfiGhLANqx9v8iBDI130_assertion description "[We did not detect significant differences for allele and carrier frequencies of individual polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49108.RAcsu0x--DoowRYwh0PXVhTRuA7tEfiGhLANqx9v8iBDI130_provenance.
- NP49111.RAVR82y5pnyZ3FiQBDj4QvtA31uCkJaAqP-PIpkOT7jIY130_assertion description "[While Gly389 allele of the ADRB1 gene lowers obesity in black subjects, this allele in conjunction with Stop447 allele of the LPL gene lowers obesity in adults and attenuates the development of obesity from childhood to adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49111.RAVR82y5pnyZ3FiQBDj4QvtA31uCkJaAqP-PIpkOT7jIY130_provenance.
- NP49112.RATow73PDk9NAVGjgvUUaNnc2zOuICiWc41diMfcEu-Js130_assertion description "[Polymorphisms in ADRB1 and UCP3 may contribute to insulin resistance rather than obesity among Swedish women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49112.RATow73PDk9NAVGjgvUUaNnc2zOuICiWc41diMfcEu-Js130_provenance.
- NP49119.RAb9rbsUZi_tTb2FAEiTTvVJh8pJNPinvlA2WDw5y1KSM130_assertion description "[Polymorphisms of adrenoceptors are not associated with an increased risk of adverse event in heart failure: a MERIT-HF substudy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49119.RAb9rbsUZi_tTb2FAEiTTvVJh8pJNPinvlA2WDw5y1KSM130_provenance.
- NP49134.RAZB95-iaG-ql4x6JOIllvbNwudWZiaX9cSdtD9XH1ccE130_assertion description "[Resting sympathetic nerve activity is related to age, sex and arterial pressure but not to 2-adrenergic receptor subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49134.RAZB95-iaG-ql4x6JOIllvbNwudWZiaX9cSdtD9XH1ccE130_provenance.
- NP49144.RAX5jqQZQ1IlRiqelavZ3IW4QLf_Zg9E0k1hXVJQSdkR8130_assertion description "[Several EF measures showed association with ADRA2A, as well as moderation, but not mediation, of its association with ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49144.RAX5jqQZQ1IlRiqelavZ3IW4QLf_Zg9E0k1hXVJQSdkR8130_provenance.
- NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_assertion description "[These results showed that the ADRA2A gene was associated with symptoms of autonomic, sympathetic dysfunction from different diagnostic groups. The advantages of the `line item` approach include (a) the identification of the symptoms associated with each allele, (b) the identification of symptom clusters independent of DSM diagnoses, (c) the elucidation of heterosis and other mode of inheritance effects, (d) the distinction between an association with a primary disorder versus a comorbid disorder, (e) the identification of associations with sub-syndromal symptom clusters that do meet full DSM-IV criteria, and (f) the identification of symptom clusters across databases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_provenance.
- NP49153.RATDdLI6zJuje0fGDuJ2Fu--n6bp9Fh6484BbsALUbd8I130_assertion description "[To determine if common single nucleotide polymorphisms (SNPs) in beta(1)-adrenergic receptor (ADRB1), beta(2)-adrenergic receptor (ADRB2), beta(3)-adrenergic receptor (ADRB3), and alpha(2)-adrenergic receptor (ADRA2A) genes associate with obesity and metabolic alterations, we recruited 74 healthy African American and 161 white men and women (age, 18-49 years) to participate in this case-control genetic association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49153.RATDdLI6zJuje0fGDuJ2Fu--n6bp9Fh6484BbsALUbd8I130_provenance.
- NP49161.RASjN7W4m8_9E4WT_c0bQ98VigjwG6IgHUIpHFtWZC2Hk130_assertion description "[The thiazide-sensitive Na(+)-Cl(-) cotransporter gene, C1784T, and adrenergic receptor-beta3 gene, T727C, may be gene polymorphisms susceptible to the antihypertensive effect of thiazide diuretics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49161.RASjN7W4m8_9E4WT_c0bQ98VigjwG6IgHUIpHFtWZC2Hk130_provenance.
- NP49164.RAUcJmo7kXaF7EwiFKfC-wYZeSdxKrsmjsT8IHMTrSaaM130_assertion description "[Arg347Cys polymorphism of alpha1A-adrenoceptor gene is associated with blood pressure response to nifedipine GITS in Chinese hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49164.RAUcJmo7kXaF7EwiFKfC-wYZeSdxKrsmjsT8IHMTrSaaM130_provenance.
- NP49166.RAeqNUR4WCFGpzZuKpwr1ijEegfsKelNuOhFBuRGnTurQ130_assertion description "[Alpha 1a-adrenoceptor polymorphism: pharmacological characterization and association with benign prostatic hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49166.RAeqNUR4WCFGpzZuKpwr1ijEegfsKelNuOhFBuRGnTurQ130_provenance.
- NP49169.RAfJ-Yb44T_4l5aER78ff00PjcrWuJ0a_N0HLfRRn0F0k130_assertion description "[Individuals from 70 panic disorder pedigrees, and 83 child-parent 'trios', were genotyped at five single-nucleotide polymorphisms (SNPs) in and near the ADORA2A gene and were analyzed for genetic linkage and association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49169.RAfJ-Yb44T_4l5aER78ff00PjcrWuJ0a_N0HLfRRn0F0k130_provenance.
- NP49170.RAT4eAd1LUNg32ms-DB7CLgSXP-gx96DuFGPt-JL5Ou-c130_assertion description "[The adenosine A2a receptor (A2aAR) is thought to be implicated in the pathogenesis of panic disorder because caffeine, a potent antagonist for A2aAR, can precipitate panic attacks, and because disruption of the A2aAR gene increased anxiety-behaviors in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49170.RAT4eAd1LUNg32ms-DB7CLgSXP-gx96DuFGPt-JL5Ou-c130_provenance.
- NP49177.RAd-BSIuQ4LbfTBke3bIj27fDrXn299rCP8_b2t3DKAeM130_assertion description "[ The microsatellite DNA polymorphism of AM gene may be associated with the genetic predisposition to develop nephropathy in Japanese patients with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49177.RAd-BSIuQ4LbfTBke3bIj27fDrXn299rCP8_b2t3DKAeM130_provenance.
- NP49184.RAWTQ7VnTbhlLvMgUHZ_5hAkZOQH8NvEnnPy8ctsdintA130_assertion description "[Single-nucleotide polymorphisms (SNPs) of ADIPOQ, ADIPOR1, and ADIPOR2 have been associated with type 2 diabetes mellitus (T2DM), but there are many conflicting results especially in Chinese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49184.RAWTQ7VnTbhlLvMgUHZ_5hAkZOQH8NvEnnPy8ctsdintA130_provenance.
- NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion description "[an association between a certain ADH4 (formerly known as ADH7 in humans) allele and PD. This suggests a role for genetic variations of ADH4 as risk factors for the development of PD. Our data also show that the observed polymorphisms alone are not sufficient to cause symptoms. Further genetic and/or environmental factors have to be involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance.
- NP49199.RARt6lg3mpxLITNLl8HNTDVxbgzfycJJoL1Q5QJAgVaoE130_assertion description "[ Individuals heterozygous for ALDH2*2 exhibit strong alcohol hypersensitivity caused by persistent accumulation of large amounts of acetaldehyde, but homozygosity for ADH2*2 is not dependent upon this pathway against alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49199.RARt6lg3mpxLITNLl8HNTDVxbgzfycJJoL1Q5QJAgVaoE130_provenance.
- NP49200.RATNPTT147Q9IscNxwTHvnU2VuHaImYDwG64mAuwAWjaE130_assertion description "[Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49200.RATNPTT147Q9IscNxwTHvnU2VuHaImYDwG64mAuwAWjaE130_provenance.
- NP49201.RAbagoByPJ2ymc9eHbuIeydGIzNJAiI8V8-qjk-MIR0JE130_assertion description "[Therefore, no significant association between CYP2E1 RsaI, CYP2E1 DraI, ADH1C, NQO1 polymorphisms and alcohol consumption was observed in healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49201.RAbagoByPJ2ymc9eHbuIeydGIzNJAiI8V8-qjk-MIR0JE130_provenance.
- NP49203.RARB4P6bjSqWEJw3_jG3YbY99gRM2IYNSt_KbsIXqVvPQ130_assertion description "[We determined genotype and allele frequencies of ALDH2, CYP2E1, ADH2, and ADH3 in male Korean patients with alcoholic cirrhosis (n=56), alcoholics without evidence of liver disease (n=52), and nondrinkers (n=64) by using PCR or PCR-directed mutagenesis followed by restriction enzyme digestion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49203.RARB4P6bjSqWEJw3_jG3YbY99gRM2IYNSt_KbsIXqVvPQ130_provenance.
- NP49207.RAQfqlAUQH2yxz7ZZ_YZhEE4q41pcpyFlws2Q-HAsYTJg130_assertion description "[Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49207.RAQfqlAUQH2yxz7ZZ_YZhEE4q41pcpyFlws2Q-HAsYTJg130_provenance.
- NP49210.RAf2wSO_lcwvvgGmq4nb80hN4iRyB6qTpdZOgP8kTULJs130_assertion description "[ADH single nucleotide polymorphism associations with alcohol metabolism in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49210.RAf2wSO_lcwvvgGmq4nb80hN4iRyB6qTpdZOgP8kTULJs130_provenance.
- NP49217.RAUMtVW_dvd6OHclSd-pVltN83iwc6gEHfYl8UPAvDhc0130_assertion description "[We here investigated ADH1C Ile(350)Val, ADH1B Arg(48)His, ADH1B Arg(370)Cys and CYP2E1*5A PstI polymorphisms by PCR-RFLP Polymerase Chain Reaction - Restriction Fragment Length Polymorphism in 207 histopathologically confirmed HNC cases (184 males and 23 females) and 244 cancer-free controls (225 males and 19 females) admitted as in-patients in the same hospital.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49217.RAUMtVW_dvd6OHclSd-pVltN83iwc6gEHfYl8UPAvDhc0130_provenance.
- NP49219.RAQ_ANZ-7LXRpsLq-Ss8h3phhYzaht6Nyq1VlbDRW5VSI130_assertion description "[In conclusion, our findings are consistent with results of other studies, suggesting that alcohol consumption elevates the risk of adenomatous colorectal polyps. ADH3 polymorphism may modify the association between alcohol consumption and colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49219.RAQ_ANZ-7LXRpsLq-Ss8h3phhYzaht6Nyq1VlbDRW5VSI130_provenance.
- NP49227.RAemrSN3KDEjxHz03ncqn4q8eYwLhPzTjLYY5N9gxWSYw130_assertion description "[the ADH3 polymorphism modestly influences the response of some plasma hormones to alcohol consumption but is not independently associated with breast cancer risk and does not modify the association between alcohol and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49227.RAemrSN3KDEjxHz03ncqn4q8eYwLhPzTjLYY5N9gxWSYw130_provenance.
- NP49230.RATwnwQydxBxqPB_kcmzLiKJ-whkC-fIRRVoROc6_Q9JM130_assertion description "[Interaction between ADH1C Arg(272)Gln and alcohol intake in relation to breast cancer risk suggests that ethanol is the causal factor in alcohol related breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49230.RATwnwQydxBxqPB_kcmzLiKJ-whkC-fIRRVoROc6_Q9JM130_provenance.
- NP49235.RAQt2XI0G2ff6uq9LlmUjAgLopiJHHZLwn_SA-tzMbqIk130_assertion description "[Furthermore, in the international collaboration, the G78stop mutation in ADH1C was found in 22 (2.0%) of the PD patients but only in 6 controls (0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49235.RAQt2XI0G2ff6uq9LlmUjAgLopiJHHZLwn_SA-tzMbqIk130_provenance.
- NP49245.RAbozLNGiAigEUGI1QgwcInKGTfNzer5IlpIFgD3atb2A130_assertion description "[The frequencies of ADH2*1 and ADH3*2 alleles were significantly higher in men with type II alcoholism than in men with type I alcoholism and healthy men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49245.RAbozLNGiAigEUGI1QgwcInKGTfNzer5IlpIFgD3atb2A130_provenance.
- NP49246.RAXyFRwI2REY0f7RmH2GB-6hl5E0B5HfoNiZFGIKVTYMM130_assertion description "[We hypothesized that the ADH1B and ALDH2 genes might interact with the DRD2 gene and that the association between the DRD2 gene and alcohol dependence might be affected by different ADH1B and ALDH2 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49246.RAXyFRwI2REY0f7RmH2GB-6hl5E0B5HfoNiZFGIKVTYMM130_provenance.
- NP49249.RAS6nsyyQAmzkXyUh3uEYb4fxQABmP2KaDW150FhtMU2g130_assertion description "[ Individuals heterozygous for ALDH2*2 exhibit strong alcohol hypersensitivity caused by persistent accumulation of large amounts of acetaldehyde, but homozygosity for ADH2*2 is not dependent upon this pathway against alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49249.RAS6nsyyQAmzkXyUh3uEYb4fxQABmP2KaDW150FhtMU2g130_provenance.
- NP49254.RAdcK4fDQOObt02zo8BQgLZ7yGF55LyDzBlte3gjV4uIY130_assertion description "[ These results suggest that the absence of ALDH2 mutant genotype is strongly related to heavy drinking behavior. We can not prove, however, any evidence that the polymorphisms of other ethanol-metabolizing enzymes are associated with the determination of alcohol-drinking behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49254.RAdcK4fDQOObt02zo8BQgLZ7yGF55LyDzBlte3gjV4uIY130_provenance.
- NP49261.RAQDiSmtIZ7wg25MIvLdxuoyV59Hc9KZtUbHBKeePMDyw130_assertion description "[Alcohol dehydrogenase and aldehyde dehydrogenase polymorphisms and colorectal cancer: the Fukuoka Colorectal Cancer Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49261.RAQDiSmtIZ7wg25MIvLdxuoyV59Hc9KZtUbHBKeePMDyw130_provenance.
- NP49265.RAfDjSNCX0a8AWC7BXdS_7UwWKO8vrMPNZDv-qCRrYLfE130_assertion description "[We compared the frequencies of polymorphisms in ten genes that have been hypothesized to have a role in risk of EC (CYP1A1, CYP2A6, CYP2E1, GSTM1, GSTP1, GSTT1, ADH2, ADH3, ALDH2, and O6-MGMT) among three Iranian ethnic groups with highly varying rates of EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49265.RAfDjSNCX0a8AWC7BXdS_7UwWKO8vrMPNZDv-qCRrYLfE130_provenance.
- NP49266.RARFwg-l8Ne1Q4371YQ5pD3I_VayqWejuVCau3EVedzv0130_assertion description "[Both ADH2 G allele and ALDH2 A allele significantly increase the risk of esophageal cancer development in Southeast Chinese males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49266.RARFwg-l8Ne1Q4371YQ5pD3I_VayqWejuVCau3EVedzv0130_provenance.
- NP49268.RASXnNWbkgi6xJZSqIamiZEj-5VAsT5JjCzsVzzGALarU130_assertion description "[(4)Compared those non-drinkers with both ALDH2 G/G and ADH2 A/A, drinkers with ALDH2 G/A or A/A and ADH2 G/A or G/G genotypes showed a significantly elevated risk of developing esophageal cancer (OR = 8.36, 95% CI: 2.98-23.46).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49268.RASXnNWbkgi6xJZSqIamiZEj-5VAsT5JjCzsVzzGALarU130_provenance.
- NP49270.RAYbX4cT2sUOLfJdvm3isK70BQkIpYqlzzw58hGi6-XB0130_assertion description "[genetic polymorphism of the ALDH2 gene influences the risk of developing alcoholic pancreatitis in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49270.RAYbX4cT2sUOLfJdvm3isK70BQkIpYqlzzw58hGi6-XB0130_provenance.
- NP49271.RAXo4VLfy_6UpaiSx0mBqXfcDHaQibMT_jGUV7twY-m2M130_assertion description "[On analysis of ADH2 and ALDH2 gene polymorphisms an association was found between ADH2*2 allele and alcoholic CP, and the ADH2*2/2*2 genotype had a tendency to increase the risk of developing pancreatic pseudocyst.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49271.RAXo4VLfy_6UpaiSx0mBqXfcDHaQibMT_jGUV7twY-m2M130_provenance.
- NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion description "[Our findings suggest that hypertension candidate gene variation may influence BP responses to specific antihypertensive drug therapies and measurement of genetic variation may assist in identifying subgroups of hypertensive patients who will benefit most from particular antihypertensive drug therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance.
- NP49284.RARooGdLQhPgnwNZws_CytZubUb7G3hkMSiopDLXVhEhE130_assertion description "[To investigate the association between M235T and G-6A polymorphism of AGT gene, insertion/deletion (I/D) polymorphism of ACE gene, Gly460Trp polymorphism of ADD1 gene, C825T polymorphism of GNB3 gene and essential hypertension in Xinjiang Kazakhs group as well as to identify the interactions of gene-gene and gene-environment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49284.RARooGdLQhPgnwNZws_CytZubUb7G3hkMSiopDLXVhEhE130_provenance.
- NP49285.RAQbnfujHPucDSCtfrewgJpmTUoIzhiaEMg6ZjkmrZR7s130_assertion description "[The alpha-adducin gene may be a susceptible gene to EH in northern Chinese Han population, however, the GNB3 gene C825T polymorphism may not play a significant role in EH in the same population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49285.RAQbnfujHPucDSCtfrewgJpmTUoIzhiaEMg6ZjkmrZR7s130_provenance.
- NP49292.RAdEjws4vNltDaL17vnrS4HDuxV0w2YfM5xCve0r2UPS8130_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." NP49292.RAdEjws4vNltDaL17vnrS4HDuxV0w2YfM5xCve0r2UPS8130_provenance.
- NP49294.RAcRJSRBx-wYeQ2SkASAmQNn82xc5IJEr2k899Ay6n1-w130_assertion description "[We investigated the effect of ACE (I/D) polymorphism on the age at end-stage renal disease (ESRD) in a homogeneous population of 191 ADPKD patients, according to gender and genotype for the G460W polymorphism of ADD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49294.RAcRJSRBx-wYeQ2SkASAmQNn82xc5IJEr2k899Ay6n1-w130_provenance.
- NP49303.RAckBp0tuCnODo_RUOSso3mhLl601zLkKnvtvFsTgBlCw130_assertion description "[In conclusion, this pilot identified SNPs as potential markers that could predict hepatitis B patient response. These observations may help guide future large-scale studies in examining host SNPs for their clinical utility in predicting IFN response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49303.RAckBp0tuCnODo_RUOSso3mhLl601zLkKnvtvFsTgBlCw130_provenance.
- NP49304.RAckX5wzEDRfn5kK-IpMRQHquVP8xqUQDepDdgjVpbO3I130_assertion description "[Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49304.RAckX5wzEDRfn5kK-IpMRQHquVP8xqUQDepDdgjVpbO3I130_provenance.
- NP49305.RAQUfkcVHA7HHQvGdrsWGnl_V9SKP4opDZ8D6nuMUexTU130_assertion description "[ C1423T polymorphism is low frequency in both controls and patients of Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49305.RAQUfkcVHA7HHQvGdrsWGnl_V9SKP4opDZ8D6nuMUexTU130_provenance.
- NP49306.RATtDeZIdueuz5U1tc8-kU4epANidqHBcGWaMf8P0W8uc130_assertion description "[These findings suggest a potentially important role for the ADAMTS14 gene in predisposition to MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49306.RATtDeZIdueuz5U1tc8-kU4epANidqHBcGWaMf8P0W8uc130_provenance.
- NP49310.RAeQzV81fqh6e5LbBYD9tKIiNfyvdYZgvXUK4D7oiPQaQ130_assertion description "[The polymorphism of T(1) locus allele in ADAM33 gene is associated with the susceptibility to asthma in South China Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49310.RAeQzV81fqh6e5LbBYD9tKIiNfyvdYZgvXUK4D7oiPQaQ130_provenance.
- NP49316.RAYSSN3LuE0i2EgmRhP0JHRdV6neNy4hKqhtmXYj-TvI4130_assertion description "[These results indicate that polymorphisms in the ADAM33 gene are associated with susceptibility to allergic rhinitis due to Japanese cedar pollen, but the functional relationship still needs clarification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49316.RAYSSN3LuE0i2EgmRhP0JHRdV6neNy4hKqhtmXYj-TvI4130_provenance.
- NP49323.RAcEtmtS_iwEHSJHqzt2ENdkgT_ScEwnmeP0iBaRWd-30130_assertion description "[Adenosine deaminase (ADA) plays a relevant role in purine metabolism, immune responses, and peptidase activity, which may be altered in some autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49323.RAcEtmtS_iwEHSJHqzt2ENdkgT_ScEwnmeP0iBaRWd-30130_provenance.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion description "[Our questionnaire based study provides evidence that the HHT phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.
- NP49330.RATJvjvpNb2-_6lWdcn0qt49ZpG9AZvVdDjgYTv6rFCpI130_assertion description "[Mutation analysis of `Endoglin` and `Activin receptor-like kinase` genes in German patients with hereditary hemorrhagic telangiectasia and the value of rapid genotyping using an allele-specific PCR-technique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49330.RATJvjvpNb2-_6lWdcn0qt49ZpG9AZvVdDjgYTv6rFCpI130_provenance.
- NP49334.RAbInSPE8nX3WnZHfr33eHx_0Nw3o_KF3EzMMP8n3Ieoo130_assertion description "[Analysis of heterozygosity levels at P1,TF, PGM1, ACP1, HP, GC, GLO, C3, and ESD loci in pulmonary tuberculosis patients with different treatment outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49334.RAbInSPE8nX3WnZHfr33eHx_0Nw3o_KF3EzMMP8n3Ieoo130_provenance.
- NP49337.RAeyZMub-CYfAfE6ncqgiEWDFEfcD6h_OpwwNqV_--ICE130_assertion description "[Association between the low molecular weight cytosolic acid phosphatase gene ACP1*A and comorbid features of Tourette syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49337.RAeyZMub-CYfAfE6ncqgiEWDFEfcD6h_OpwwNqV_--ICE130_provenance.
- NP49343.RAV0etsjxSyKuT7aRfRrolxrARWJ7ogNq5Wlb7x3FdqkA130_assertion description "[Alzheimer's disease: case-control association study of polymorphisms in ACHE, CHAT, and BCHE genes in a Sardinian sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49343.RAV0etsjxSyKuT7aRfRrolxrARWJ7ogNq5Wlb7x3FdqkA130_provenance.
- NP49346.RAUCrkKmugBBi8DEYF19vVh94wp8_2n9x9L8UOZN0Qw-g130_assertion description "[Analysis of genetic polymorphisms in acetylcholinesterase as reflected in different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49346.RAUCrkKmugBBi8DEYF19vVh94wp8_2n9x9L8UOZN0Qw-g130_provenance.
- NP49350.RAbao-LrQaddDuJiuUNmqMUkQ7gtuWCHyPquYiVITJuyk130_assertion description "[Association of ACE, ACE2 and UTS2 polymorphisms with essential hypertension in Han and Dongxiang populations from north-western China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49350.RAbao-LrQaddDuJiuUNmqMUkQ7gtuWCHyPquYiVITJuyk130_provenance.
- NP49351.RAc4kPn717x7r9BUx82aMKP6PdUCud1YHx_fsT3jknvGo130_assertion description "[We performed a meta-analysis to assess the association of ACE2 G8790A polymorphism with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49351.RAc4kPn717x7r9BUx82aMKP6PdUCud1YHx_fsT3jknvGo130_provenance.
- NP49359.RATgSxyfLLLtJ4AXzSRHx9PinGYlcGjroLc0BSIyGw5jc130_assertion description "[The purpose of this study is to evaluate the association of the angiotensin converting enzyme (ACE) insertion/deletion (I/D) polymorphism with cardiovascular disease risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49359.RATgSxyfLLLtJ4AXzSRHx9PinGYlcGjroLc0BSIyGw5jc130_provenance.
- NP49360.RAePfUOk7ZlONDqYlYvyPMv8tMXjgguL4e8qODkHP7wqU130_assertion description "[The ACE gene is a candidate gene for cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49360.RAePfUOk7ZlONDqYlYvyPMv8tMXjgguL4e8qODkHP7wqU130_provenance.
- NP49361.RAfBcvAGQweUwMXoJ6vfFWknHkq2YP5lXFq0RAqCnBlok130_assertion description "[This study suggests possible interactions between genes from the RA, bradykinin, and fibrinolytic systems on the risk of cardiovascular disease, extending previous research that has demonstrated that interactions among genes from these systems influence plasma concentrations of both t-PA and PAI-1. Further explorations of these interactions are needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49361.RAfBcvAGQweUwMXoJ6vfFWknHkq2YP5lXFq0RAqCnBlok130_provenance.
- NP49378.RAaeOPV70Ldm0qIbXKTBwSRtqc0NF9i6D3gkwLapDjM1k130_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." NP49378.RAaeOPV70Ldm0qIbXKTBwSRtqc0NF9i6D3gkwLapDjM1k130_provenance.
- NP49389.RAeaFYiMGR2_EJTOlYxepjeFe0Joc7xT9HRAJKUPxnsTM130_assertion description "[The frequencies of ACE-DD genotype and ACE-D allele were much higher in DN(+) group than in DN (-) group (0.25 vs 0.05, 0.47 vs 0.29, respectively), so were the frequencies of TT genotype and T allele in AGT-M235T (0.73 vs 0.54, 0.85 vs 0.68, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49389.RAeaFYiMGR2_EJTOlYxepjeFe0Joc7xT9HRAJKUPxnsTM130_provenance.
- NP49396.RAUGHFXQ5o2AUoVTFq6q6qr8yYBTqKYPqCvnHk7T8UwnI130_assertion description "[Prevalence of genetic risk factors for coronary artery disease in Corsica island (France).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49396.RAUGHFXQ5o2AUoVTFq6q6qr8yYBTqKYPqCvnHk7T8UwnI130_provenance.
- NP49400.RAQK9cN8vFsVqCP4ZfhbPxiTwOYdsFp67pu4AMXvXe30o130_assertion description "[Interactive effects of the ACE DD polymorphism with the NOS III homozygous G849T (Glu298-->Asp) variant in determining endothelial function in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49400.RAQK9cN8vFsVqCP4ZfhbPxiTwOYdsFp67pu4AMXvXe30o130_provenance.
- NP49401.RAZxgTrQ3hXMvgjHx60ux7alJKnfVKDe1BKIJHwb-RWps130_assertion description "[Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49401.RAZxgTrQ3hXMvgjHx60ux7alJKnfVKDe1BKIJHwb-RWps130_provenance.
- NP49403.RARbTvYLXqywX31Csp6hNiimnIuquaZ3o4lEkeDPrED9w130_assertion description "[We examined the association of the angiotensin-converting enzyme and the plasminogen activator inhibitor type 1 genotypes, and their combinations, with early onset of coronary heart disease in a cohort of 907 patients with coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49403.RARbTvYLXqywX31Csp6hNiimnIuquaZ3o4lEkeDPrED9w130_provenance.
- NP49414.RAZGKupT8BZWCSQCQ-g-79URM0W7FwOwIvl1Kq45JS7rQ130_assertion description "[Angiotensin-converting enzyme insertion/deletion gene polymorphic variant as a marker of coronary artery disease: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49414.RAZGKupT8BZWCSQCQ-g-79URM0W7FwOwIvl1Kq45JS7rQ130_provenance.
- NP49415.RAYlmsT6LTGtu796IQ6YTf03b25ZW_VF3ZZ_edvo20SAI130_assertion description "[Angiotensin-I-converting enzyme (ACE) insertion/deletion (ID) polymorphism has been associated with the genetic susceptibility to coronary artery disease (CAD) and also with the lipid profile in several populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49415.RAYlmsT6LTGtu796IQ6YTf03b25ZW_VF3ZZ_edvo20SAI130_provenance.
- NP49420.RASRxCf6EEl77dSlwaD6zII4jxMD2jBJV_DjrOY49qU0g130_assertion description "[The insertion/deletion DNA polymorphism of the gene coding human angiotensin converting enzyme (ACE) was examined in 109 patients with coronary artery disease (CAD) and 93 non-coronary subjects (NCS) living in a northern part of Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49420.RASRxCf6EEl77dSlwaD6zII4jxMD2jBJV_DjrOY49qU0g130_provenance.
- NP49423.RAaivsuNdLkwfgJRqcfPHc1EfsBrYcwrgLYbfX0j_9PV4130_assertion description "[The role of the insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme gene (ACE) on acute myocardial infarction (AMI) is controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49423.RAaivsuNdLkwfgJRqcfPHc1EfsBrYcwrgLYbfX0j_9PV4130_provenance.
- NP49427.RAWhsZCxMIdwbYfO5bfujepAcuma2c2KH-FRqVw2UBm0Y130_assertion description "[Relation between angiotensin-converting enzyme I/D gene polymorphism and pulse pressure in patients with a first anterior acute myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49427.RAWhsZCxMIdwbYfO5bfujepAcuma2c2KH-FRqVw2UBm0Y130_provenance.
- NP49431.RAc3dLeXGlbyf4Fqak_quL4_0q9qDOdVfrIji9zH4yXHs130_assertion description "[Progression to severe, life-threatening PH occurs in the presence of additional genetic factors (non-N370S GBA mutation, positive family history, and ACE I gene polymorphism) and epigenetic modifiers (i.e., asplenia and female sex).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49431.RAc3dLeXGlbyf4Fqak_quL4_0q9qDOdVfrIji9zH4yXHs130_provenance.
- NP49432.RATrOoUs5Pen0sslwgrd1b2CU0bSIRikK7WPcM-NT3M9I130_assertion description "[Statistically significant associations with ischemic stroke were identified for factor V Leiden Arg506Gln (OR, 1.33; 95% CI, 1.12-1.58), methylenetetrahydrofolate reductase C677T (OR, 1.24; 95% CI, 1.08-1.42), prothrombin G20210A (OR, 1.44; 95% CI, 1.11-1.86), and angiotensin-converting enzyme insertion/deletion (OR, 1.21; 95% CI, 1.08-1.35).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49432.RATrOoUs5Pen0sslwgrd1b2CU0bSIRikK7WPcM-NT3M9I130_provenance.
- NP49435.RAdMBrbbL2icXjUw-jvKzzr7lfAgBnUWnpJ1Uy-nQEJYo130_assertion description "[253 patients with stroke were compared with 173 healthy blood donors on the basis of genetic polymorphisms of platelet GP IIb/IIIa receptor (33 LeuPro), prothrombin gene G20210A, Factor V Leiden mutation, ACE I/D, methylenetetrahydrofolate reductase (MTHFR) and beta fibrinogen gene G455A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49435.RAdMBrbbL2icXjUw-jvKzzr7lfAgBnUWnpJ1Uy-nQEJYo130_provenance.
- NP49437.RAe5t0jheiDUQ0pFd5Qk4KqAknuil3X2thu5RBtQv7U9E130_assertion description "[The insertion(I)/deletion(D) polymorphism of the angiotensin-converting-enzyme (ACE) gene has been associated with an increased risk of myocardial infarction, lacunar stroke, and with an increased intimal-medial thickness in several populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49437.RAe5t0jheiDUQ0pFd5Qk4KqAknuil3X2thu5RBtQv7U9E130_provenance.
- NP49438.RAadOChMfy34Ix_QjaXQ2UYj28XN6JSHQxkTWeKfpw2G8130_assertion description "[Association analysis of polymorphism in angiotensin-converting enzyme gene in ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49438.RAadOChMfy34Ix_QjaXQ2UYj28XN6JSHQxkTWeKfpw2G8130_provenance.
- NP49448.RAZO60P3mm6G3-M-OzjI6SFQ2B-AcNFtYl7U_irLe6Dg4130_assertion description "[We report on the results of a large autopsy study focusing upon the hypothesis that deletion of the Alu insert in the angiotensin converting enzyme (ACE) gene is associated with: (a) greater prevalence or extent of atherosclerosis in the aorta and coronary arteries; and (b) microscopic qualities of established atherosclerotic plaques in the coronary arteries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49448.RAZO60P3mm6G3-M-OzjI6SFQ2B-AcNFtYl7U_irLe6Dg4130_provenance.
- NP49452.RARO7SEAATe_qsm1lQuAYU6rMQ5aE3NnT-Yl5zzR34aS8130_assertion description "[Molecular genetics of microvascular disease in diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49452.RARO7SEAATe_qsm1lQuAYU6rMQ5aE3NnT-Yl5zzR34aS8130_provenance.
- NP49457.RAQ7-7bI8Mv4lgwmcUwTzyHy-Qa9Ese0tNPwTR3f4fVGw130_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." NP49457.RAQ7-7bI8Mv4lgwmcUwTzyHy-Qa9Ese0tNPwTR3f4fVGw130_provenance.
- NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_provenance.
- NP49462.RAaO8O9JRZ67A_AN2a1UIV9D3roMUlPZ5daVFjhMW24Vc130_assertion description "[Association analysis of angiotensin-converting enzyme gene polymorphism with end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49462.RAaO8O9JRZ67A_AN2a1UIV9D3roMUlPZ5daVFjhMW24Vc130_provenance.
- NP49468.RAYYXDGkPQijuVfSqoPfjjQp2OqP-CF-2Wni8UA6BAh8I130_assertion description "[Genetic risk factors for renal failure among north Indian ESRD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49468.RAYYXDGkPQijuVfSqoPfjjQp2OqP-CF-2Wni8UA6BAh8I130_provenance.
- NP49470.RASKVEu47nCBEARVm1aBCbdft32vFDgth6yfgJ7m9jwuA130_assertion description "[Association of variants in angiotensin-converting enzyme and endothelin-1 genes with phototherapy in cutaneous T-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49470.RASKVEu47nCBEARVm1aBCbdft32vFDgth6yfgJ7m9jwuA130_provenance.
- NP49475.RAfwDhN4FAdWt-QSUvz1kBRCtbUSdAq-KWBzhINT9ucUQ130_assertion description "[The ACE DD genotype is a risk factor for the development of renal disease in Mexican Mestizo females with type 2 diabetes, indicating a possible DD genotype-associated sex effect in renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49475.RAfwDhN4FAdWt-QSUvz1kBRCtbUSdAq-KWBzhINT9ucUQ130_provenance.
- NP49478.RAZdXQ6EShVAs4q0EQYcnxaHo6k-HwjZNwGRFRhtkGww0130_assertion description "[Angiotensin-converting enzyme gene and the brachial artery endothelial dysfunction in type 2 diabetes without angiopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49478.RAZdXQ6EShVAs4q0EQYcnxaHo6k-HwjZNwGRFRhtkGww0130_provenance.
- NP49484.RAexxmiPRSn8CMJUuURz_U5GQecqms8i_vd_CCNgYHLMs130_assertion description "[Interaction between ACE and ADD1 gene polymorphisms in the progression of IgA nephropathy in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49484.RAexxmiPRSn8CMJUuURz_U5GQecqms8i_vd_CCNgYHLMs130_provenance.
- NP49486.RAQ2IowKhZ2yIUDGyKrbUaHJ1RifdOgrfLIrqxVCu2xKs130_assertion description "[ Body fat measurements using ADP and DXA were correlated with those using BIA across a relatively wide range of body fat levels in adults with ESRD. However, BIA appeared to underestimate body fat and overestimate fat-free mass, possibly because of increased measurements of body water. Because ADP is convenient and does not use body water content in determination of body density and body composition, it has very good potential as a relatively new technique to estimate percent body fat in adults with ESRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49486.RAQ2IowKhZ2yIUDGyKrbUaHJ1RifdOgrfLIrqxVCu2xKs130_provenance.
- NP49490.RAaU19zm0vx7nf_PiS_3jKurRVbNjUOyYGA2cLOPj5thY130_assertion description "[This study suggests that genetic control of RAS activity correlates with production of anti-HLA antibodies, possibly explaining the relationship to chronic allograft outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49490.RAaU19zm0vx7nf_PiS_3jKurRVbNjUOyYGA2cLOPj5thY130_provenance.
- NP49494.RAZvwgNAgDSalZxcIx4pkqbax5Mp-KiuaST5u9J5W-FvQ130_assertion description "[Genetic association study of the GNB3 C825T, the ACE I/D and the eNOS G894T polymorphisms and the risk to develop erectile dysfunction in a German ED population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49494.RAZvwgNAgDSalZxcIx4pkqbax5Mp-KiuaST5u9J5W-FvQ130_provenance.
- NP49498.RASxH7YcKmsMPsN9gvesU7XWTu7vmkSVQ4XQNqohrZ08c130_assertion description "[Genetic and environmental factors associated with the development of hypertension in pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49498.RASxH7YcKmsMPsN9gvesU7XWTu7vmkSVQ4XQNqohrZ08c130_provenance.
- NP49502.RAfNukdgOWD9u6kgl9x5_0kzuNSlv7eftQJYyvHadCNHA130_assertion description "[The study was carried to determine the association of angiotensin converting enzyme (ACE) insertion/deletion (I/D) polymorphism with the risk of hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and restrictive cardiomyopathy (RCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49502.RAfNukdgOWD9u6kgl9x5_0kzuNSlv7eftQJYyvHadCNHA130_provenance.
- NP49507.RAa4GqdlBMBtDSgSWePHImWqIGgk0pFeleWSf2hWuZB48130_assertion description "[Insertion/deletion polymorphism in the angiotensin-I-converting enzyme gene is associated with coronary heart disease in IDDM patients with diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49507.RAa4GqdlBMBtDSgSWePHImWqIGgk0pFeleWSf2hWuZB48130_provenance.
- NP49512.RAcwFrRVmNknbOJzvnjZcq0AGotNYqRPrH7qrGxVDI9Sg130_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." NP49512.RAcwFrRVmNknbOJzvnjZcq0AGotNYqRPrH7qrGxVDI9Sg130_provenance.
- NP49514.RAXZrXPM7gf9O7OHQtb69SItRhM_PuJcHfaH3pWBAJWXE130_assertion description "[To date, there have been no complaints from the participants, indicating that the announcement of polymorphism genotypes may be accepted differently from that of hereditary disease genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49514.RAXZrXPM7gf9O7OHQtb69SItRhM_PuJcHfaH3pWBAJWXE130_provenance.
- NP49528.RAfgv2-RdbPNFGjftFRhHDSTAnM3cdzZlXCdVZHB3V42E130_assertion description "[The results suggested an association between ACE insertion/deletion and AF risk. More large-scale studies are warranted to document the conclusive evidence of the effects of the RAS genes on AF risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49528.RAfgv2-RdbPNFGjftFRhHDSTAnM3cdzZlXCdVZHB3V42E130_provenance.
- NP49532.RAXQrFJuvr7Cv8WHe28aly6J-c6B-mlhgeWyykxo6ppMI130_assertion description "[Thus, there is a relationship between insertion-deletion polymorphism of ACE gene and myocardial infarction. Deletion DD genotype raises the risk to develop MI and probability of life-threatening complications and repeated MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49532.RAXQrFJuvr7Cv8WHe28aly6J-c6B-mlhgeWyykxo6ppMI130_provenance.
- NP49536.RAayzDxXbdY4GlNiLGSVmklGSumadX9Lz_9FhhDzv96uI130_assertion description "[ AT1 receptor genotypes could influence arterial ageing in hypertensive subjects. These results also show that the association between genotypes and arterial stiffness may manifest itself later in life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49536.RAayzDxXbdY4GlNiLGSVmklGSumadX9Lz_9FhhDzv96uI130_provenance.
- NP49537.RAV56dPThSwvUJjOMy2yZYlCuFiw6v4xRYe3VYUTrqdlY130_assertion description "[To investigate the relationship of an insertion/deletion (I/D) polymorphism of the angiotension-converting enzyme (ACE) gene to obstructive sleep apnea syndrome (OSAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49537.RAV56dPThSwvUJjOMy2yZYlCuFiw6v4xRYe3VYUTrqdlY130_provenance.