Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP54051.RAmTddFZAc3xkOnN1aE3qAIoy7CxhV2SOyqb7uX_1tG44130_assertion description "[No significant correlation was found between the level of 8-OH-dG and the MnSOD, GSTM1, and hOGG1 polymorphisms. However, one novel polymorphism/mutation of the hOGG1 gene was found in a pancreatic tumor. Mutation at codon 12 of the K-ras gene was found in 25 (81%) of 31 pancreatic tumors, including three G-to-A transitions and 22 G-to-T transversions. Patients with the G-to-T mutation had a significantly higher level of aromatic DNA adducts than those with G-to-A or wild-type codon (P=0.02). On the other hand, the K-ras mutation profile was not related to the level of 8-OH-dG. Given the limitation of sample size, these preliminary data lend further support the hypothesis that carcinogen exposure and oxidative stress are involved in pancreatic carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54051.RAmTddFZAc3xkOnN1aE3qAIoy7CxhV2SOyqb7uX_1tG44130_provenance.
- NP54054.RAoZKow9kEHnzlj1wuJPEVVod4ef6BfpCq2tuyZaJw4uw130_assertion description "[Case-control study of genotypes in multiple chemical sensitivity: CYP2D6, NAT1, NAT2, PON1, PON2 and MTHFR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54054.RAoZKow9kEHnzlj1wuJPEVVod4ef6BfpCq2tuyZaJw4uw130_provenance.
- NP54057.RApuHfCUKCsg0OIeL34QJxFwk570Zf8reDiHVH_tb0Y60130_assertion description "[ Our results indicate a role of NAT2 polymorphisms in the carcinogenic pathway of prostate cancer, specifically in a population of Southern Europe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54057.RApuHfCUKCsg0OIeL34QJxFwk570Zf8reDiHVH_tb0Y60130_provenance.
- NP54059.RApi4Albb7K0NBjbi8RuhGsPn8F8uNqmIlbmGCCVEckBU130_assertion description "[Xenobiotic metabolizing gene variants, dietary heterocyclic amine intake, and risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54059.RApi4Albb7K0NBjbi8RuhGsPn8F8uNqmIlbmGCCVEckBU130_provenance.
- NP54060.RAp2cCWWZmb777TgZG1gWfc8w2Obx3MbNr0KLNQ6db47A130_assertion description "[The present study demonstrates the association of PCA and MnSOD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54060.RAp2cCWWZmb777TgZG1gWfc8w2Obx3MbNr0KLNQ6db47A130_provenance.
- NP54063.RAgnVphjjTYbbKGUkmb685rOBrX_zy4S3gqc2yGW3n3nw130_assertion description "[This study was conducted to examine; (1) whether the N-acetyltransferase 2 (NAT2) genotype is a risk factor for prostate cancer, (2) to study effect of NAT2 genotype on modifying prostate cancer risk from tobacco use.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54063.RAgnVphjjTYbbKGUkmb685rOBrX_zy4S3gqc2yGW3n3nw130_provenance.
- NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion description "[The results reported in this study suggest that NAT2 polymorphism is a genetic susceptibility factor involved in the carcinogenesis of cervical cancer, and also that the analysis of the allelic profile of populations in different geographic locations may help to understand the incidence of cervical cancer worldwide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance.
- NP54068.RAtnMlcjOueLNWhJD2Uj0rcZPrI5-Qm0vB5P9GE7J1b00130_assertion description "[In the current study, risk factors for developing cervical cancer were tobacco smoking and GSTM1 null; however, no association was observed between these two factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54068.RAtnMlcjOueLNWhJD2Uj0rcZPrI5-Qm0vB5P9GE7J1b00130_provenance.
- NP54071.RAswmTUSTufb1ldmKYyQBK8jOwPTB2M5aR9iiVM2E6YHI130_assertion description "[Polymorphisms of the xenobiotic-metabolizing enzymes CYP1A1 and NAT-2 in systemic sclerosis and lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54071.RAswmTUSTufb1ldmKYyQBK8jOwPTB2M5aR9iiVM2E6YHI130_provenance.
- NP54073.RAvj9N65UpMSNDphENvmSedNBXiYx7MTId0ETML12d_w4130_assertion description "[Cigarette smoking, N-acetyltransferase 2 polymorphisms and systemic lupus erythematosus in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54073.RAvj9N65UpMSNDphENvmSedNBXiYx7MTId0ETML12d_w4130_provenance.
- NP54076.RAue_gJlTm0c9UjWlDF6rxfVo-dMNZ-nQyTL-gJPyYfbE130_assertion description "[Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54076.RAue_gJlTm0c9UjWlDF6rxfVo-dMNZ-nQyTL-gJPyYfbE130_provenance.
- NP54077.RApZCSxWLvBua58Z5MCEi2s9XPNZjypcXpyTPSXzw2GTs130_assertion description "[Many small studies have reported associations between genetic polymorphisms and PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54077.RApZCSxWLvBua58Z5MCEi2s9XPNZjypcXpyTPSXzw2GTs130_provenance.
- NP54080.RAguM56gr0BNvEP2gXnJ0bLSK1nA8ReDwuhDtl8pbk2Nw130_assertion description "[N-acetyltransferase 2 polymorphism in sporadic Parkinson's disease in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54080.RAguM56gr0BNvEP2gXnJ0bLSK1nA8ReDwuhDtl8pbk2Nw130_provenance.
- NP54085.RAuRrcjXytY6haYgzqaCY4WkRjsW63-AViUhAZHK1Frec130_assertion description "[There were no statistically significant interactions between tobacco smoking and either NAT1 or NAT2 acetylator status in relation to CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54085.RAuRrcjXytY6haYgzqaCY4WkRjsW63-AViUhAZHK1Frec130_provenance.
- NP54086.RAm4kVA4_CiHouK3hgcHaLjTWN6GjHWaScLMhKtJdm1ZQ130_assertion description "[Meta analysis of these studies showed that GSTT1 deletion (pooled OR = 1.42), N-acetyltransferase 2 (NAT2)-rapid acetylator phenotype and genotye (pooled OR = 1.08) and NAT2-rapid acetylator phenotype (pooled OR = 1.15) had a significantly increased risk for colorectal cancer (P<0.05), other genotypes like GSTM1 deletion, GSTP1 1le105Val, NAT1*10, NAT2-rapid acetylator genotype CYP1A1 L1e462Val, CYP1A1 MspI*C, MTHFR C677T and MTR A2759G had no significant relationship with colorectal cancer (P>0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54086.RAm4kVA4_CiHouK3hgcHaLjTWN6GjHWaScLMhKtJdm1ZQ130_provenance.
- NP54089.RAuwarIwK9IAVBTSJzWYJ_n4Ww2RMk1qpdnUcvJGv6cPs130_assertion description "[The enhanced association between smoking and colorectal cancer risk in subjects with the NAT2 rapid genotype supports a role for NAT2 and tobacco smoke heterocyclic amines in the etiology of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54089.RAuwarIwK9IAVBTSJzWYJ_n4Ww2RMk1qpdnUcvJGv6cPs130_provenance.
- NP54093.RAl1PQ88_6es8vdWsSsddCzMk-lHM0JqAbvYL-5A2K6fw130_assertion description "[Effect of NAT1 and NAT2 genetic polymorphisms on colorectal cancer risk associated with exposure to tobacco smoke and meat consumption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54093.RAl1PQ88_6es8vdWsSsddCzMk-lHM0JqAbvYL-5A2K6fw130_provenance.
- NP54096.RAsBaKeUnKTuBmjCqvarNniDsqRnN49YBQVZnzKBuZxRQ130_assertion description "[Polymorphisms of cytochrome P4501A2 and N-acetyltransferase genes, smoking, and risk of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54096.RAsBaKeUnKTuBmjCqvarNniDsqRnN49YBQVZnzKBuZxRQ130_provenance.
- NP54100.RAqw4J0A7_ZAWb0IyDSJed2eUoxIAM2Og-CcuQG9S0o4c130_assertion description "[We assessed the association between common polymorphisms identified in the GSTM1, GSTT1, NAT1, and NAT2 genes and the risk of bladder cancer in two nested case-control studies within the Nurses' Health Study (n = 78 female cases, 234 female controls) and the Health Professionals' Follow-up Study (n = 139 male cases, 293 male controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54100.RAqw4J0A7_ZAWb0IyDSJed2eUoxIAM2Og-CcuQG9S0o4c130_provenance.
- NP54102.RAoWgnj_0o8e6pJfJUJx2vEoGrI9NNZOKbjMP3qU9A4gM130_assertion description "[The protective effect of carotenoids on bladder cancer seemed to be influenced by NAT1 genotype, NAT2 phenotype and CYP1A2 phenotype; the association was mainly confined to subjects possessing the putative NAT1-rapid, NAT2-rapid and CYP1A2-rapid genotype/phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54102.RAoWgnj_0o8e6pJfJUJx2vEoGrI9NNZOKbjMP3qU9A4gM130_provenance.
- NP54114.RArXTWaNV6iyjSnBMESNzmptT46LHtMKK12qBbKSffYIw130_assertion description "[GSTM1 null genotype increases breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54114.RArXTWaNV6iyjSnBMESNzmptT46LHtMKK12qBbKSffYIw130_provenance.
- NP54115.RApmxTHkDyBXssAAm5tg_yxKplnhj-a1F9K3nyYAU4tnA130_assertion description "[, our results provide support for the view that women who smoke and who have a genetically determined reduced inactivation of carcinogens (GSTM1 null genotype or slow NAT2 genotype (especially very slow NAT2 genotype)) are at increased risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54115.RApmxTHkDyBXssAAm5tg_yxKplnhj-a1F9K3nyYAU4tnA130_provenance.
- NP54120.RAg9VAQtyMQdocQ7EsaI7FBqQHemZFnHimi5q99J40DEc130_assertion description "[Genetic variations in xenobiotic metabolic pathway genes, personal hair dye use, and risk of non-Hodgkin lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54120.RAg9VAQtyMQdocQ7EsaI7FBqQHemZFnHimi5q99J40DEc130_provenance.
- NP54125.RApVZYry8Aq4ZURqKcSzZHIxpHSNY5uouVfuQgs_KLEDU130_assertion description "[ Our results indicate a role of NAT2 polymorphisms in the carcinogenic pathway of prostate cancer, specifically in a population of Southern Europe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54125.RApVZYry8Aq4ZURqKcSzZHIxpHSNY5uouVfuQgs_KLEDU130_provenance.
- NP54130.RAsfd8_buEXllnplRfFpNuduzOrSAMRiLZaVAaPDAlboU130_assertion description "[These results do not support the hypothesis that exposure to heterocyclic amines is associated with risk of PC. However, additional studies with more precise exposure measures are needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54130.RAsfd8_buEXllnplRfFpNuduzOrSAMRiLZaVAaPDAlboU130_provenance.
- NP54132.RAkajLL64Gs5zvXqXDCXpFjGjsjpxa2QJCMjiOeuPshRQ130_assertion description "[To clinically characterize 116 Chinese patients with primary congenital glaucoma and to determine the role of CYP1B1 and MYOC mutations in this cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54132.RAkajLL64Gs5zvXqXDCXpFjGjsjpxa2QJCMjiOeuPshRQ130_provenance.
- NP54136.RAo7fqTI90qYrnfbLFthtbCgBUbl4-XXJ8Bukkip2783E130_assertion description "[Family history, hypertension, smoking and the mutation of TIGR gene were also important risk factors of POAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54136.RAo7fqTI90qYrnfbLFthtbCgBUbl4-XXJ8Bukkip2783E130_provenance.
- NP54138.RAnJ1PM2CZeJCg48Y6FJkbbpHgyswr0no08McxcAEQvIY130_assertion description "[Allelic variants in the MYOC/TIGR gene in patients with primary open-angle, exfoliative glaucoma and unaffected controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54138.RAnJ1PM2CZeJCg48Y6FJkbbpHgyswr0no08McxcAEQvIY130_provenance.
- NP54159.RAo9oCQAslcH7_fCG5v_P1usC4zQ5Gcha3e_nrKHaAlHM130_assertion description "[ Multiple gene mutations occurring in HCM families may result in a more severe clinical phenotype because of a double dose effect. This highlights the importance of screening the entire panel of HCM genes even after a single mutation has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54159.RAo9oCQAslcH7_fCG5v_P1usC4zQ5Gcha3e_nrKHaAlHM130_provenance.
- NP54160.RAguSkRjMsH9Y6S6gU4-fenV8hgPPafOlYB9sJa4F7HE0130_assertion description "[ Abnormalities of diastolic function assessed by Doppler tissue imaging precede the development of LVH in individuals with HCM caused by beta -MHC mutations. Although Ea velocity alone was not sufficiently sensitive as a sole diagnostic criterion, the combination of Ea velocity and EF was highly predictive of affected genotype in individuals without overt manifestations of HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54160.RAguSkRjMsH9Y6S6gU4-fenV8hgPPafOlYB9sJa4F7HE0130_provenance.
- NP54164.RAhl8Hvhul--GOPqyNSAGV41UhwbW1PaeK6juZsrRrEYs130_assertion description "[Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54164.RAhl8Hvhul--GOPqyNSAGV41UhwbW1PaeK6juZsrRrEYs130_provenance.
- NP54165.RAuf0v8H8IQ9XBhq_P0mtIvfLeV9qqkELYfOKZon8CZTY130_assertion description "[Overall, 25 of 47 (53%) patients had myofilament-HCM, including 12 with MYBPC3-HCM and 9 with MYH7-HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54165.RAuf0v8H8IQ9XBhq_P0mtIvfLeV9qqkELYfOKZon8CZTY130_provenance.
- NP54168.RAnJbKCJpWP9hQDY94tEUtmyY47bIKAgD3eZG2ERAa-tQ130_assertion description "[Role of inherited defects of MYH in the development of sporadic colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54168.RAnJbKCJpWP9hQDY94tEUtmyY47bIKAgD3eZG2ERAa-tQ130_provenance.
- NP54169.RAmzeUslV9RQei1rSbhpETvPug5kHCf4KoZzNx_YBODes130_assertion description "[Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54169.RAmzeUslV9RQei1rSbhpETvPug5kHCf4KoZzNx_YBODes130_provenance.
- NP54172.RAkkizpVPOaJDCUG8xuq0OWoAhFom6NRtq6oIJ_lwHoQk130_assertion description "[The role of MYH gene in genetic predisposition to colorectal cancer: another piece of the puzzle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54172.RAkkizpVPOaJDCUG8xuq0OWoAhFom6NRtq6oIJ_lwHoQk130_provenance.
- NP54173.RAi3LAeGge1K7HcsZr7Z0tTV6T5toB4j9gZGYJ7jzHkyc130_assertion description "[Similar colorectal cancer risk in patients with monoallelic and biallelic mutations in the MYH gene identified in a population with adenomatous polyposis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54173.RAi3LAeGge1K7HcsZr7Z0tTV6T5toB4j9gZGYJ7jzHkyc130_provenance.
- NP54175.RAr2T2B3fNwX7gxqYyWZIqGCZsX22BOpNmEKY6ZecFKQ0130_assertion description "[Sequential bcl-2 and c-myc oncogene rearrangements associated with the clinical transformation of non-Hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54175.RAr2T2B3fNwX7gxqYyWZIqGCZsX22BOpNmEKY6ZecFKQ0130_provenance.
- NP54181.RAiL5t-4S_OHQrvCfkRM0ZocdwgOExU0Ac6MdGED7n-cU130_assertion description "[c-myc gene abnormalities in mucosa-associated lymphoid tissue (MALT) lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54181.RAiL5t-4S_OHQrvCfkRM0ZocdwgOExU0Ac6MdGED7n-cU130_provenance.
- NP54185.RAhWXzvg6xG9-BfaYqgzSEh4fo_1Ap_ahNO8-zYepOji8130_assertion description "[ The 2373insG mutation accounts for almost one-fourth of all HCM cases in the Netherlands (60/259), which is predominantly present in the northwestern part of the country (22/66) and is a founder mutation probably originating from the Netherlands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54185.RAhWXzvg6xG9-BfaYqgzSEh4fo_1Ap_ahNO8-zYepOji8130_provenance.
- NP54187.RAkiD15QdauNs4GoXzekrvpv0bBvXg507g7tXYUrblw-M130_assertion description "[Our results point out that GG genotype of MYBPC3 might be a genetic risk factor for the expression of cardiac hypertrophic phenotype in the patients with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54187.RAkiD15QdauNs4GoXzekrvpv0bBvXg507g7tXYUrblw-M130_provenance.
- NP54188.RAt-owquxA-VFeOpcl_LC9aoqQ3JIitB03ZRCuu2UrWcA130_assertion description "[Subset analysis of the two most common genetic subtypes of HCM, MYBPC3 (myosin binding protein C) and MYH7 (beta myosin heavy chain), demonstrated a significant pro-LVH effect of DD-ACE only in patients with MYBPC3-HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54188.RAt-owquxA-VFeOpcl_LC9aoqQ3JIitB03ZRCuu2UrWcA130_provenance.
- NP54189.RArfMIT_-Z7n6_8U34uHcHb5qZn2fKN9yK3lCvLfg50c0130_assertion description "[In a Portuguese population of 45 HCM patients, 5 (11.1%) had mutations in the MYBPC3 gene (3 missense mutations--theoretically less frequent in the MYBPC3 gene--and 2 deletions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54189.RArfMIT_-Z7n6_8U34uHcHb5qZn2fKN9yK3lCvLfg50c0130_provenance.
- NP54190.RAhHwgSBTs_j-ubsL0acoP92m5X5JOUZUMYpGaUloptZE130_assertion description "[A group of 99 unrelated adult patients with DCM (familial n=27, sporadic n=72) were screened for the following genes: cardiac beta-myosin heavy chain, cardiac myosin-binding protein C (MYBPC3), regulatory and essential myosin light chains, alpha cardiac actin, alpha tropomyosin, cardiac troponin T, cardiac troponin I, cardiac troponin C, dystrophin, and lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54190.RAhHwgSBTs_j-ubsL0acoP92m5X5JOUZUMYpGaUloptZE130_provenance.
- NP54191.RAjE17DDBxXTWPLVWAcZnjHyuxA2VJmR-j-QXydhYsELo130_assertion description "[Limited distribution of a cardiomyopathy-associated variant in India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54191.RAjE17DDBxXTWPLVWAcZnjHyuxA2VJmR-j-QXydhYsELo130_provenance.
- NP54192.RAk4I52qoo4w4q_E-FRbdWz6aCgAPcUFUeBQh_pv4ywpY130_assertion description "[Association of activated proto-oncogenes ras and myc in colorectal carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54192.RAk4I52qoo4w4q_E-FRbdWz6aCgAPcUFUeBQh_pv4ywpY130_provenance.
- NP54195.RAsaFZ5-hRTOs8D68KSSK9ckaipore4NOFC5XLXZ0J-UQ130_assertion description "[Influences of MxA gene -88 G/T and IFN-gamma +874 A/T on the natural history of hepatitis B virus infection in an endemic area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54195.RAsaFZ5-hRTOs8D68KSSK9ckaipore4NOFC5XLXZ0J-UQ130_provenance.
- NP54198.RAv9WsIJICdZCEX5GTuX3tH3l75GpCnh7sa_UQh5eumhI130_assertion description "[Our findings suggest the possibility that the -300AA IRF-1 genotype is associated with outcome in patients with HCV genotype 3 infection. In addition, in HCV genotype-1-infected patients, this genotype appears associated with response to therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54198.RAv9WsIJICdZCEX5GTuX3tH3l75GpCnh7sa_UQh5eumhI130_provenance.
- NP54200.RAkheOxCRnffg0OWtSWK0_0FWJgGk1vhdw4URcKRZK_F4130_assertion description "[SNPs in the OAS1 3-UTR and MxA promoter region appear associated with host susceptibility to SARS in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54200.RAkheOxCRnffg0OWtSWK0_0FWJgGk1vhdw4URcKRZK_F4130_provenance.
- NP54210.RAlwKeap-4vSDCapaq-JH0BLOkSmUmcMxY76peqpP_UJw130_assertion description "[In our cohort the prevalence of pathogenic MUTYH mutations was increased among fCRC patients compared to sporadic CRC and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54210.RAlwKeap-4vSDCapaq-JH0BLOkSmUmcMxY76peqpP_UJw130_provenance.
- NP54217.RAnv45_4DrlK5Rm6MiCKC3wJvVO9G5gRwi0F4AFU3mP9Q130_assertion description "[Variable number of tandem repeats polymorphism of MUC20 is associated with the progression of IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54217.RAnv45_4DrlK5Rm6MiCKC3wJvVO9G5gRwi0F4AFU3mP9Q130_provenance.
- NP54218.RAo3iUgbNY8n562jwRNiszuxyoJmMI4PciOCJ2zB9Lkgc130_assertion description "[The present study revealed that there is no association between the VNTR polymorphism of the MUC20 gene and the clinical manifestations in IgAN patients at the time of renal biopsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54218.RAo3iUgbNY8n562jwRNiszuxyoJmMI4PciOCJ2zB9Lkgc130_provenance.
- NP54219.RAqeLxqLEwTlG7c3dx0t15SFyqNhpEUraEbc72hj4NTK4130_assertion description "[Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54219.RAqeLxqLEwTlG7c3dx0t15SFyqNhpEUraEbc72hj4NTK4130_provenance.
- NP54222.RAjZh5oW_2WU1T9hmUH4sZ0_V0da9s96XT_t4yZ4fTFv8130_assertion description "[Inhibition of the O-glycan elongation limits MUC1 incorporation to cell membrane of human endometrial carcinoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54222.RAjZh5oW_2WU1T9hmUH4sZ0_V0da9s96XT_t4yZ4fTFv8130_provenance.
- NP54227.RAsQGwmjV6tnP2Rqxif6jcDAw2ZHG9Izzh6xp5T8b-rdQ130_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." NP54227.RAsQGwmjV6tnP2Rqxif6jcDAw2ZHG9Izzh6xp5T8b-rdQ130_provenance.
- NP54231.RAjuQdLbEAzIgjqusy6Ttlg1N1KaMmTE9l8y8gII7grUI130_assertion description "[MTHFR, MTR, DNMT3b, and EHMT2 polymorphisms are associated with colorectal cancer, and rare variants of MTR and MTRR may reduce promoter hypermethylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54231.RAjuQdLbEAzIgjqusy6Ttlg1N1KaMmTE9l8y8gII7grUI130_provenance.
- NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion description "[ Prothrombin and factor V polymorphisms increased the risk for VTE in women, independent from other established risk factors. Although hyperhomocysteinaemia also heightens this risk, common polymorphisms in two genes that are responsible for homocysteine remethylation do not. These findings are consistent with previous studies that included both men and women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance.
- NP54244.RAkiksNk9GIXikMibEGwI2n6S4jO4iIyNfECYxaZySeZo130_assertion description "[Maternal gene polymorphisms involved in folate metabolism and risk of Down syndrome offspring: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54244.RAkiksNk9GIXikMibEGwI2n6S4jO4iIyNfECYxaZySeZo130_provenance.
- NP54247.RAvO-k0iuXLsn1e6tcl6Avk-Xyh4GgW-G_AHxWPN4j5Jg130_assertion description "[ Genetic variation in the MTP promoter is likely to be highly involved in the production of dyslipidemia in type 2 diabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54247.RAvO-k0iuXLsn1e6tcl6Avk-Xyh4GgW-G_AHxWPN4j5Jg130_provenance.
- NP54251.RArHP9X7AoNOnHMC6TLjclUskosCc5ZdxRJVOa1vL30Mw130_assertion description "[Association between microsomal triglyceride transfer protein gene polymorphism and the biological features of liver steatosis in patients with type II diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54251.RArHP9X7AoNOnHMC6TLjclUskosCc5ZdxRJVOa1vL30Mw130_provenance.
- NP54255.RAn3NrrvI2nK5vi3kH0498lMjhN-FEwoiCcr-6tv1Tb7I130_assertion description "[The relationship between homocysteine and genes of folate-related enzymes in migraine patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54255.RAn3NrrvI2nK5vi3kH0498lMjhN-FEwoiCcr-6tv1Tb7I130_provenance.
- NP54259.RAkQ2NZcK3mJNKMvRkspvvEr9t1Ruz5sJeLit5vajDiiA130_assertion description "[These results indicated that the Delta 14 allele has nothing to do with MTAP deficiency in DHL-9. The Delta 14 allele is distributed among the general population irrespective of gender.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54259.RAkQ2NZcK3mJNKMvRkspvvEr9t1Ruz5sJeLit5vajDiiA130_provenance.
- NP54268.RAuu6s6TR7XxsEgE07pu-OAqAwEpEn6kgKw7rVG_Y0p2w130_assertion description "[A multigenic approach to evaluating prostate cancer risk in a systematic replication study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54268.RAuu6s6TR7XxsEgE07pu-OAqAwEpEn6kgKw7rVG_Y0p2w130_provenance.
- NP54270.RAt1GUmdYa--pGpljE9Tjrng9VfVFhzZsBlzy9Z4hEupw130_assertion description "[MSR1 variants and the risks of prostate cancer and benign prostatic hyperplasia: a population-based study in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54270.RAt1GUmdYa--pGpljE9Tjrng9VfVFhzZsBlzy9Z4hEupw130_provenance.
- NP54275.RArt4gTcXV5G1uZ6BXdrodw138R39sQmWHKbINQpnZgoo130_assertion description "[Patients (n = 112) from 285 families who were counseled between 1990 and 2005 at a clinic for patients at high risk for HNPCC were selected for screening to detect mutations in MMR genes MLH1, MSH2, MSH6, and PMS2 based on family history, microsatellite instability (MSI), and immunohistochemical analysis of MMR protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54275.RArt4gTcXV5G1uZ6BXdrodw138R39sQmWHKbINQpnZgoo130_provenance.
- NP54276.RAgFAYT6G8Ki6jeXEVVBam4c6Rz-rlPG-2DEuV9yTNoYs130_assertion description "[With surveillance intervals of 1-2 years, members of families with Lynch syndrome have a lower risk of developing CRC than with surveillance intervals of 2-3 years. Because of the low risk of CRC in non-Lynch syndrome families, a less intensive surveillance protocol can be recommended.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54276.RAgFAYT6G8Ki6jeXEVVBam4c6Rz-rlPG-2DEuV9yTNoYs130_provenance.
- NP54285.RApONYziUimI1gBoUUPBLg01RkxYoyuNucdgb791z23B8130_assertion description "[In 281 patients diagnosed with CRC before the age of 50 years or with CRC and at least one additional HNPCC-associated cancer, germline mutation analysis in MLH1, MSH2 and MSH6 was carried out with denaturing gradient gel electrophoresis and multiplex ligation-dependent probe amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54285.RApONYziUimI1gBoUUPBLg01RkxYoyuNucdgb791z23B8130_provenance.
- NP54288.RAqyU9g4Ff7JjeF0qmPs-gK3D54TSS8Y-MC13uYrpziK0130_assertion description "[Patients (n = 112) from 285 families who were counseled between 1990 and 2005 at a clinic for patients at high risk for HNPCC were selected for screening to detect mutations in MMR genes MLH1, MSH2, MSH6, and PMS2 based on family history, microsatellite instability (MSI), and immunohistochemical analysis of MMR protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54288.RAqyU9g4Ff7JjeF0qmPs-gK3D54TSS8Y-MC13uYrpziK0130_provenance.
- NP54289.RAgQtsjL3u0yVyqHVQUKlq15tbqQBbekYhBjDE7Yja_qs130_assertion description "[BRAF-V600E mutations were analysed by automatic sequencing in colorectal cancers from 206 sporadic cases with MSI-H and 111 HNPCC cases with known germline mutations in MLH1 and MSH2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54289.RAgQtsjL3u0yVyqHVQUKlq15tbqQBbekYhBjDE7Yja_qs130_provenance.
- NP54294.RAkNHYJatzlPV58nrfOiUVviWoMv9tKJAWD3spAaKlHOE130_assertion description "[ In 23% of the young endometrial cancer patients with at least one first-degree relative with an HNPCC-related cancer, an MMR gene mutation was detected. Therefore, presence of an HNPCC-related cancer in a first-degree relative seems to be an important selection criterion for mutation analysis. Subsequent immunostaining of MMR proteins will point to the gene(s) that should be analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54294.RAkNHYJatzlPV58nrfOiUVviWoMv9tKJAWD3spAaKlHOE130_provenance.
- NP54298.RAtYEC9zct_oxjeaKli_nIO9_gHfbYRNUZjOFIWFU7_I0130_assertion description "[Polymorphism in the hMSH2 gene (gIVS 12-6T-->C) and risk of non-Hodgkin lymphoma in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54298.RAtYEC9zct_oxjeaKli_nIO9_gHfbYRNUZjOFIWFU7_I0130_provenance.
- NP54301.RAugiMZQrDmYvdcEp_vyynkef09HQ7j1pNE-cQz-SJiws130_assertion description "[Replication of genetic association studies in asthma and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54301.RAugiMZQrDmYvdcEp_vyynkef09HQ7j1pNE-cQz-SJiws130_provenance.
- NP54303.RAuAKiQccUTcP1_GbzefkCCZAx2pFhMdsbVt8V-ODJUgg130_assertion description "[Involvement of Fc(epsilon)R1beta gene polymorphisms in susceptibility to atopy in Korean children with asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54303.RAuAKiQccUTcP1_GbzefkCCZAx2pFhMdsbVt8V-ODJUgg130_provenance.
- NP54306.RAnT1FtDC-Vns4MiGiwupUsxnMpRDDbkbTUIGZgiBfw2E130_assertion description "[This is the first study identifying a haplotype A_16_C that predisposes individuals to asthma in the Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54306.RAnT1FtDC-Vns4MiGiwupUsxnMpRDDbkbTUIGZgiBfw2E130_provenance.
- NP54312.RAr_RNEAfVFoCRpXtUrvkpNITOTwAeYSjh_8_3tdo1SJs130_assertion description "[Association between atopy and variants of the beta subunit of the high-affinity immunoglobulin E receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54312.RAr_RNEAfVFoCRpXtUrvkpNITOTwAeYSjh_8_3tdo1SJs130_provenance.
- NP54314.RAmcngHAiDVe5XO6uKz6NTYPmO2uehAlv40cn_uUQHfWU130_assertion description "[A new variant of the beta subunit of the high-affinity receptor for immunoglobulin E (Fc epsilon RI-beta E237G): associations with measures of atopy and bronchial hyper-responsiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54314.RAmcngHAiDVe5XO6uKz6NTYPmO2uehAlv40cn_uUQHfWU130_provenance.
- NP54315.RAh1sGR76eVeh5Y8JxcpS1sldOyEYSyDIc1iOl2ck-tv4130_assertion description "[Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54315.RAh1sGR76eVeh5Y8JxcpS1sldOyEYSyDIc1iOl2ck-tv4130_provenance.
- NP54318.RAn6MNRd4-ERX55U67F3fw9QGHe_foPiSOC5TtH16pGG0130_assertion description "[Our data suggest an equal maternal and paternal contribution to the inheritance of asthma and an association of the homozygous variant (Leu 181/Leu 183) of the IgE receptor FcepsilonRIbeta with disease severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54318.RAn6MNRd4-ERX55U67F3fw9QGHe_foPiSOC5TtH16pGG0130_provenance.
- NP54320.RAnSJAa8biyHSvr2tbFkcEq93USiogS7p0jodUxjMZtGE130_assertion description "[These results suggest that the Glu237Gly variant of the FcepsilonRIbeta gene is involved in the development of nasal allergy through the process for the production of both specific and nonspecific IgE antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54320.RAnSJAa8biyHSvr2tbFkcEq93USiogS7p0jodUxjMZtGE130_provenance.
- NP54322.RAhf1Kbb1MA49BdmGw8hXnN_DH2YFCuUPq91NsFCgWHko130_assertion description "[Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54322.RAhf1Kbb1MA49BdmGw8hXnN_DH2YFCuUPq91NsFCgWHko130_provenance.
- NP54330.RAheEW6aAKU2Re9ayE3Nw_zJKnUHuaPJVHD-iTgKb4dhw130_assertion description "[The aim of this study is to summarize the available molecular epidemiologic studies of lung cancer and metabolic genes, such as NAD(P)H quinone reductase 1 (NQO1) and myeloperoxidase (MPO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54330.RAheEW6aAKU2Re9ayE3Nw_zJKnUHuaPJVHD-iTgKb4dhw130_provenance.
- NP54332.RAh41r5-9sp-k4vON9LYcxDJy6dA_19ICHS3z-a8UBQs8130_assertion description "[There was weak risk reduction associated with GSTM1 null in heavy smokers (OR = 0.71; 95%CI 0.54-0.94; P = 0.02), but neither GSTM1 nor MPO genotypes affected the overall risk of NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54332.RAh41r5-9sp-k4vON9LYcxDJy6dA_19ICHS3z-a8UBQs8130_provenance.
- NP54335.RAjb54Km89S37yqP5Akp2fFPZUPApNUE7I7g88xKReoWE130_assertion description "[Together with data from the present study on DNA repair genes, we did not observe significant associations between any single variant genotype for several DNA-repair and chemical-metabolizing genes (XPD or ERCC2, XRCC1, XRCC3, GSTM1, GSTT1, MPO, and mEH or EPHX1) and lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54335.RAjb54Km89S37yqP5Akp2fFPZUPApNUE7I7g88xKReoWE130_provenance.
- NP54338.RAuCPmJd0jnJgr2D28khd43EdLs935aGztej4HYf1TtFY130_assertion description "[The results of this study indicated that the polymorphism of myeloperoxidase G-463A was not significantly associated with the lung cancer risk for Caucasian or East Asians. However, further studies for the East Asians is needed for the few subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54338.RAuCPmJd0jnJgr2D28khd43EdLs935aGztej4HYf1TtFY130_provenance.
- NP54343.RAivCA6nrAPB0Q4FZtiwzNIVc_l1bBZVm7gOmF8Eog4bk130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54343.RAivCA6nrAPB0Q4FZtiwzNIVc_l1bBZVm7gOmF8Eog4bk130_provenance.
- NP54344.RAgmfURlZL5_jYKTXbC5brp24PypnPhhyoXFWSaKEMVaA130_assertion description "[The association of myeloperoxidase promoter polymorphism with carotid atherosclerosis is abolished in patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54344.RAgmfURlZL5_jYKTXbC5brp24PypnPhhyoXFWSaKEMVaA130_provenance.
- NP54346.RAkasYuNT6teVHrSb0jvpMkR8KOgHbTQ7FV--a2NsuG7U130_assertion description "[MPO genotype GG is associated with cirrhosis in patients with hereditary hemochromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54346.RAkasYuNT6teVHrSb0jvpMkR8KOgHbTQ7FV--a2NsuG7U130_provenance.
- NP54348.RArb7kTrU4ifQZMVWSFV69NMpk2cuQ0IM0Hla160hGjW4130_assertion description "[Our results support the hypothesis of a possible linkage disequilibrium between the MPO G-463A gene polymorphism and another functional variant involved in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54348.RArb7kTrU4ifQZMVWSFV69NMpk2cuQ0IM0Hla160hGjW4130_provenance.
- NP54351.RAnok2JGDhD1oPCxNSsfz9PZ-weGB3pQvf-HM3RXrBjuY130_assertion description "[These findings suggest that the MPO polymorphism is a gender-specific risk factor for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54351.RAnok2JGDhD1oPCxNSsfz9PZ-weGB3pQvf-HM3RXrBjuY130_provenance.
- NP54355.RAgnMmdSrwXjGBbj4TPf-TDjyHoJN8ewfOBZLm6ZH4Dt0130_assertion description "[Bladder cancer risk and genetic variation in AKR1C3 and other metabolizing genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54355.RAgnMmdSrwXjGBbj4TPf-TDjyHoJN8ewfOBZLm6ZH4Dt0130_provenance.
- NP54359.RAlQh4c_ecByokUz1gclWsp4YzhiVuFOUmZZHhVwJveR0130_assertion description "[Susceptibility to arsenic-induced hyperkeratosis and oxidative stress genes myeloperoxidase and catalase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54359.RAlQh4c_ecByokUz1gclWsp4YzhiVuFOUmZZHhVwJveR0130_provenance.
- NP54364.RAv1ynrsT63qd2admEpJ0Tpdu6xypvOfa9CHMQ0KAdQE4130_assertion description "[The frequency of mutation in the exon 9 coding region was estimated to be one heterozygote in 129, thus the homozygote of such mutations would be revealed one in 16,000 in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54364.RAv1ynrsT63qd2admEpJ0Tpdu6xypvOfa9CHMQ0KAdQE4130_provenance.
- NP54368.RAlWc35G0XPfF8wAJR9xDkbdXKymTjiaZrxYrfsKTC70c130_assertion description "[Oxidative stress-related genotypes, fruit and vegetable consumption and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54368.RAlWc35G0XPfF8wAJR9xDkbdXKymTjiaZrxYrfsKTC70c130_provenance.
- NP54373.RAim69HGrangSqlWn54gxzn0ZUQKPa4_gRBQn61Un9bss130_assertion description "[An association study of two functional promotor polymorphisms in the myeloperoxidase (MPO) gene in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54373.RAim69HGrangSqlWn54gxzn0ZUQKPa4_gRBQn61Un9bss130_provenance.
- NP54376.RAsH3sSDeoGK6N4jq4z75Pr6s9cwZPTz9l-zuJR7-2EK4130_assertion description "[Our studies show that the TNF and MPO genes may play a role in chronic renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54376.RAsH3sSDeoGK6N4jq4z75Pr6s9cwZPTz9l-zuJR7-2EK4130_provenance.
- NP54377.RAgP-VXDRamHYVMR9imE_WjaIrGg2fBou-kcug-lPOlvQ130_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." NP54377.RAgP-VXDRamHYVMR9imE_WjaIrGg2fBou-kcug-lPOlvQ130_provenance.
- NP54378.RAlRxcEUSl2T224Q-x_tET4aYPFUHQJj7vENVGHFxEoSo130_assertion description "[This work verifies for the first time the association of myeloperoxidase (-468)G-->A polymorphism with antral H pylori density and DU disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54378.RAlRxcEUSl2T224Q-x_tET4aYPFUHQJj7vENVGHFxEoSo130_provenance.
- NP54381.RAmus48VcllACR0V-w0hCIaUhaUqDUcvm6ipglmC_YoH8130_assertion description "[Our findings suggest that the -463 G/A polymorphism of the MPO gene influences the risk of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54381.RAmus48VcllACR0V-w0hCIaUhaUqDUcvm6ipglmC_YoH8130_provenance.
- NP54394.RAsINa-XGzJmkL3D3xBEt-iD0Xt1VjxDiJgr6eLBTOR20130_assertion description "[Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54394.RAsINa-XGzJmkL3D3xBEt-iD0Xt1VjxDiJgr6eLBTOR20130_provenance.
- NP54400.RAttpgvo5owgrWU-0e0NR9oZuJyHbc02xk14fa9Z9BpmA130_assertion description "[ The MMP-3 5A allele is associated with the occurrence of CA. Our results suggest that an increased proteolysis in the arterial wall may act as a susceptibility factor for the development of CA in patients with coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54400.RAttpgvo5owgrWU-0e0NR9oZuJyHbc02xk14fa9Z9BpmA130_provenance.
- NP54409.RAkBchgoFren6alslJvqQ7KrhaEgRHbowqof6kl7qawdM130_assertion description "[ Because the T allele was associated with greater MMP-9 mRNA and protein levels, the greater large artery stiffness in T-allele carriers may be secondary to excessive degradation of the arterial elastic matrix. The consequent higher pulse pressure may increase susceptibility to myocardial ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54409.RAkBchgoFren6alslJvqQ7KrhaEgRHbowqof6kl7qawdM130_provenance.