Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP58819.RAvypWScC9WtHMjAbxflmB6REkSsnIJuGDMQBGvSWLuHw130_assertion description "[A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58819.RAvypWScC9WtHMjAbxflmB6REkSsnIJuGDMQBGvSWLuHw130_provenance.
- NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_assertion description "[ Mutations in genes encoding thin filament proteins are less prevalent in HCM than previously estimated. Patients with mutations in troponin T, troponin I, alpha-tropomyosin, and actin do not invariably present with any distinct clinical feature, thus limiting the utility of gene status for risk stratification or of clinical phenotype in guiding individual genetic screening at this time.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58820.RAnT7-c3poLQvux1t6Lch1EiAfWrnnLm03TN_q0q0GeyM130_provenance.
- NP58821.RAvUsl_wFLjsCdyTjg2GYO5cJTXvBAU6A_x6BAw3c6_OA130_assertion description "[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58821.RAvUsl_wFLjsCdyTjg2GYO5cJTXvBAU6A_x6BAw3c6_OA130_provenance.
- NP58822.RAhPlJmO_RtAzbA1d2IBX__mho85jeG2FL4l6O6LfecoQ130_assertion description "[Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58822.RAhPlJmO_RtAzbA1d2IBX__mho85jeG2FL4l6O6LfecoQ130_provenance.
- NP58827.RApqHzpk_VLXnCttqZs6cSPXSguSiQFOcex1IE4LqVqV0130_assertion description "[TPMT genotype is associated with tolerance in acute leukemia in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58827.RApqHzpk_VLXnCttqZs6cSPXSguSiQFOcex1IE4LqVqV0130_provenance.
- NP58831.RAnPv4m7uceQJMpQPqSZoFAZxUXpJvbciwU-28ozAhwx8130_assertion description "[To assess the association of TPMT genotype with minimal residual disease load before and after treatment with mercaptopurine in the early treatment course of childhood ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58831.RAnPv4m7uceQJMpQPqSZoFAZxUXpJvbciwU-28ozAhwx8130_provenance.
- NP58834.RAvvP18xyKrzs6ppizmAWDmvXoYkG6jtzAMqN7UYXVIFw130_assertion description "[This is the first comprehensive TPMT phenotype and genotype study in Asian populations, particularly in the Malays and Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58834.RAvvP18xyKrzs6ppizmAWDmvXoYkG6jtzAMqN7UYXVIFw130_provenance.
- NP58836.RAqJn4lLKk6KxXQEaZYGMw72e-4EKvtWr4LNSZegkt0tE130_assertion description "[ The PCR-SSCP assay established and adopted in this study was sensitive and reliable, which could be used to detect mutant TPMT alleles. Allele frequency of TPMT*3C is low among Jing Chinese (1.0%), and TPMT*3C appears to be the most prevalent deleterious allele in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58836.RAqJn4lLKk6KxXQEaZYGMw72e-4EKvtWr4LNSZegkt0tE130_provenance.
- NP58837.RAgNZ8FnzJe_BNSf0q6jQAiyJLOVURpgZODR20KmHK_zQ130_assertion description "[ The frequency of the known mutant TPMT alleles in Han Chinese population is low, and TPMT*3C appears to be the most prevalent among the known mutant TPMT allele in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58837.RAgNZ8FnzJe_BNSf0q6jQAiyJLOVURpgZODR20KmHK_zQ130_provenance.
- NP58840.RAuJKOj7vGxlS53rnBZbeK3Pyk7DMOdsRhHosvTqA9ujk130_assertion description "[Thiopurine methyltransferase gene polymorphisms in Chinese patients with inflammatory bowel disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58840.RAuJKOj7vGxlS53rnBZbeK3Pyk7DMOdsRhHosvTqA9ujk130_provenance.
- NP58841.RAkq_ucptxqcFFll0zuQIeB6OOyxEb75KD-aHK0G9GqGg130_assertion description "[Patients with inflammatory bowel disease (IBD) may have different thiopurine dose requirements in relation to thiopurine methyltransferase (TPMT) genotype and/or phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58841.RAkq_ucptxqcFFll0zuQIeB6OOyxEb75KD-aHK0G9GqGg130_provenance.
- NP58849.RAhNeGixgJV4Esq-_npZ12K1B3eFkmgxFLVI5cv3g4nyY130_assertion description "[ The study showed a TPMT genotype distribution amongst adult Danish patients with Crohn's disease which was similar to the distribution of TPMT variant alleles normally found in healthy Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58849.RAhNeGixgJV4Esq-_npZ12K1B3eFkmgxFLVI5cv3g4nyY130_provenance.
- NP58852.RAgOJ6HY2NtZOVGv_4T1xVd9TXlf6iBeLujmwvpT9FXlw130_assertion description "[We previously detected polymorphisms in the 52-kDa Ro/SSA gene (SSA1) with restriction enzymes, one of which is strongly associated with the presence of SLE (P < 0.0005) in African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58852.RAgOJ6HY2NtZOVGv_4T1xVd9TXlf6iBeLujmwvpT9FXlw130_provenance.
- NP58854.RAs1LIofdzpUFczvxNYgMPHYDSXxcO3XRBT9Jd3ix9mhw130_assertion description "[7216A/G polymorphism of SSA1 gene may be one of the genetic factors that determine the presence of anti-SS-A/Ro52 antibody in patients with primary SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58854.RAs1LIofdzpUFczvxNYgMPHYDSXxcO3XRBT9Jd3ix9mhw130_provenance.
- NP58863.RAp_pIDj1vklucUQXb9b7AQBcim8diFzY9ipxV4wlnBiE130_assertion description "[Clinical symptoms of tuberous sclerosis complex in patients with an identical TSC2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58863.RAp_pIDj1vklucUQXb9b7AQBcim8diFzY9ipxV4wlnBiE130_provenance.
- NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion description "[Together with recent identification of disease susceptibility markers in the region of the TSHr gene, these results are supportive of genetic factors existing in this region that may be in linkage disequilibrium with the inheritance of various TSHr polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance.
- NP58874.RAmsNMrbNyQwWE-Te6E7Vq7PatjKWtgIXEdSi5chP00Rg130_assertion description "[Although early studies investigating the TSHR and GD proved inconclusive, more recently we provided convincing evidence for association of the TSHR region with disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58874.RAmsNMrbNyQwWE-Te6E7Vq7PatjKWtgIXEdSi5chP00Rg130_provenance.
- NP58877.RAq0rcegLs5tmwFc1vWFuqmbFRH5e5ns_ZxTWMjfJ9qkI130_assertion description "[No significant association was seen with TSHR-P52T and TSHR-D727E genotypes and risk of NMTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58877.RAq0rcegLs5tmwFc1vWFuqmbFRH5e5ns_ZxTWMjfJ9qkI130_provenance.
- NP58878.RAtn7Uo8yKdKf3arIBjWtyFWmUV-pXhhn06DDobpA9gVE130_assertion description "[We have analyzed eight SNPs in five thyroid hormone pathway genes and found significant associations of three SNPs in two genes (D1, TSHR) with plasma TSH or iodothyronine levels in a normal population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58878.RAtn7Uo8yKdKf3arIBjWtyFWmUV-pXhhn06DDobpA9gVE130_provenance.
- NP58889.RAkQTvHcY6P8693U_AgLpZbjMTChGyPKrK5nIx3FS6puQ130_assertion description "[Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58889.RAkQTvHcY6P8693U_AgLpZbjMTChGyPKrK5nIx3FS6puQ130_provenance.
- NP58890.RAicPc-uUuSasSKNcDvs-NNHp6n66zJOL7RsNeLeiVhpk130_assertion description "[This is a family-based association study to investigate the genetic contribution of tyrosine kinase 2 (TYK2 ) to disease susceptibility in 380 UK systemic lupus erythematosus (SLE) families, consisting of parents and affected offspring.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58890.RAicPc-uUuSasSKNcDvs-NNHp6n66zJOL7RsNeLeiVhpk130_provenance.
- NP58891.RAuMbFjUkdiymXs-MeRiUrwGJv2ZCfJDeUDesedz_rCqs130_assertion description "[We analysed 12 unrelated patients with AROA, and found that two had abnormalities of the tyrosinase (TYR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58891.RAuMbFjUkdiymXs-MeRiUrwGJv2ZCfJDeUDesedz_rCqs130_provenance.
- NP58908.RAhu1ufKMLJVOj95U2RcAfwfvs3NSjQgegn8royO2auhs130_assertion description "[Association between the ubiquitin carboxyl-terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58908.RAhu1ufKMLJVOj95U2RcAfwfvs3NSjQgegn8royO2auhs130_provenance.
- NP58916.RAvI4YH42sP-kDfzZLjFf8vCZ9sf_l-cPeCmeP9CVVcrM130_assertion description "[Both the A-->C polymorphism and the Met229-->Leu polymorphism of UCP1 are in linkage disequilibrium and could be one of the diabetes associated single nucleotide polymorphisms (SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58916.RAvI4YH42sP-kDfzZLjFf8vCZ9sf_l-cPeCmeP9CVVcrM130_provenance.
- NP58921.RAtwUDLIAF8h2VlaaH1SBpsoaXyO7D4MFi2PxXEkq-vks130_assertion description "[Significant associations were found between carriers of the minor alleles of APOE-epsilon2, FABP2-A54T, UCP1-L229M, LPL-HindIII, LPL-S447X and LPL-T1973C, patients bearing a combination of LPL-D9N, LPL-N291S and LPL-P207L and obesity-related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58921.RAtwUDLIAF8h2VlaaH1SBpsoaXyO7D4MFi2PxXEkq-vks130_provenance.
- NP58925.RAjfAMpQnUsj0I1UqDbXSml_9By67lTvjz-YEOzwuMess130_assertion description "[Analysis of -3826A/G polymorphism in the promoter of the uncoupling protein-1 gene in Chinese non-obese and obese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58925.RAjfAMpQnUsj0I1UqDbXSml_9By67lTvjz-YEOzwuMess130_provenance.
- NP58926.RAtZhNiEgO1Cd3QuyBywGsbLp-uY6wkjocNLzREqZLhi8130_assertion description "[Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58926.RAtZhNiEgO1Cd3QuyBywGsbLp-uY6wkjocNLzREqZLhi8130_provenance.
- NP58931.RAnuaOKzdFhj_vkq9Yas7t_gu1GCNKovT5IfINXC0yTG4130_assertion description "[A common polymorphism in the promoter of UCP2 is associated with obesity and hyperinsulenemia in northern Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58931.RAnuaOKzdFhj_vkq9Yas7t_gu1GCNKovT5IfINXC0yTG4130_provenance.
- NP58934.RAn6b-tA3ziGZnyUBvYH0MKEjStsEgj__h4-nXNMxXPhM130_assertion description "[Influence of the -866G/A polymorphism of the UCP2 gene on an obese pediatric population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58934.RAn6b-tA3ziGZnyUBvYH0MKEjStsEgj__h4-nXNMxXPhM130_provenance.
- NP58937.RAnAX_davWUM3P5WnB4uFo70cxHya-lFEVAujkwQ_HfPM130_assertion description "[Common polymorphisms of the UCP2 gene have been implicated in diabetes, in obesity, and with changes in UCP2 mRNA levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58937.RAnAX_davWUM3P5WnB4uFo70cxHya-lFEVAujkwQ_HfPM130_provenance.
- NP58940.RAqRjIiWbXkVBGFsGi_Thg9NrsRyLOI2Olsif0HHtmxuE130_assertion description "[UCP2 and mitochondrial haplogroups as a multiple sclerosis risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58940.RAqRjIiWbXkVBGFsGi_Thg9NrsRyLOI2Olsif0HHtmxuE130_provenance.
- NP58941.RAgrsH7w5tXqFU7CWHs7xjPQW9l-_bK2woARfshmM-7E0130_assertion description "[ Our results suggest a role of UCP2 in atherogenesis as originally proposed from studies in animal and cell culture models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58941.RAgrsH7w5tXqFU7CWHs7xjPQW9l-_bK2woARfshmM-7E0130_provenance.
- NP58953.RApWSWBK5fjzkySJ5psjxynR5HngKq2y7CCOsry2FgFm0130_assertion description "[For most of the investigated genes (PPARA, PPARG2, UCP1, UCP2, UCP3, BAR-2, APM1, leptin, SORBS1, HSL, and TNFA) an indication for a minor effect on obesity risk was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58953.RApWSWBK5fjzkySJ5psjxynR5HngKq2y7CCOsry2FgFm0130_provenance.
- NP58954.RAhiyBDjiEn81S-U2iOD4qZ2WTZ89YCaXXRN9vCXlw0m0130_assertion description "[Therefore, UCP3 is a good candidate gene for obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58954.RAhiyBDjiEn81S-U2iOD4qZ2WTZ89YCaXXRN9vCXlw0m0130_provenance.
- NP58955.RAlCTLVYb2nIcjMA9MQZqiCYHalcYhRtjaQC8X5ZTKthY130_assertion description "[Obesity-related polymorphisms and their associations with the ability to regulate fat oxidation in obese Europeans: the NUGENOB study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58955.RAlCTLVYb2nIcjMA9MQZqiCYHalcYhRtjaQC8X5ZTKthY130_provenance.
- NP58958.RAngHhnjThk0DsPRnqpggDmQaYklXhO9DrGM5BIA0WNNk130_assertion description "[Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58958.RAngHhnjThk0DsPRnqpggDmQaYklXhO9DrGM5BIA0WNNk130_provenance.
- NP58960.RAlLfvQA7Oqmid7CKZNP5uywyuLPnrq4HLdRBOVBKsrTU130_assertion description "[ Polymorphism D85Y in gene UGT2B15 correlates with differentiation of PCa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58960.RAlLfvQA7Oqmid7CKZNP5uywyuLPnrq4HLdRBOVBKsrTU130_provenance.
- NP58962.RAiKwuHnuosv7abHK4OUGUHb_R4SljHJrdDz-d31vv94A130_assertion description "[For single polymorphisms, the presence of Y alleles showed a significantly lower risk of prostate cancer in comparison with the D/D genotype in UGT2B15 (odds ratio OR=0.41, 95% confidence interval CI=1.40-4.28, p=0.0015), and the presence of A2 alleles showed a weak tendency to decrease prostate cancer risk in comparison with the A1/A1 genotype in CYP17 (OR=0.69, 95% CI=0.39-1.23, p=0.21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58962.RAiKwuHnuosv7abHK4OUGUHb_R4SljHJrdDz-d31vv94A130_provenance.
- NP58964.RAvtKP_xPJ8gZFdDdMS9vQfpduN4EfmY5bvwBWNhDCgkw130_assertion description "[The allele frequency of this SNP was 79% in Japanese, suggesting this polymorphism to be a major genotype in Japanese people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58964.RAvtKP_xPJ8gZFdDdMS9vQfpduN4EfmY5bvwBWNhDCgkw130_provenance.
- NP58972.RAphINWUHrUitJt2xvrJCATS4PSxoMdaeSK8y85Jr2C7Y130_assertion description "[These results indicate that these alterations might be involved in male infertility or might increase the risk of male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58972.RAphINWUHrUitJt2xvrJCATS4PSxoMdaeSK8y85Jr2C7Y130_provenance.
- NP58974.RAkYdxKheEt8Kks4fP42utM9rpDJAZsvvPnM26SjYZwUs130_assertion description "[To study the incidence of single nucleotide polymorphisms in ubiquitin-specific protease 26 (USP26) gene and its involvement in idiopathic male infertility in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58974.RAkYdxKheEt8Kks4fP42utM9rpDJAZsvvPnM26SjYZwUs130_provenance.
- NP58975.RAp_5iWP-ytXVnrYCxQyr5bAkIi1deEH7noH1zjeaBZ6A130_assertion description "[Gene polymorphisms and male infertility--a meta-analysis and literature review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58975.RAp_5iWP-ytXVnrYCxQyr5bAkIi1deEH7noH1zjeaBZ6A130_provenance.
- NP58981.RAjMV7Tc2ePQRzr8CbIyqoA2Lg4IcNlaAWBhwatuGT1-c130_assertion description "[Of the 10 candidate SNPs analyzed in this pilot study, the variant allele of the non-synonymous SNP, VCAM1 G1238C, may be associated with protection from stroke (OR 0.35, 95% CI 0.15-0.83, P=0.04). Further study is required to confirm the importance of this variant in VCAM1 as a clinically useful modifier of outcome in SS disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58981.RAjMV7Tc2ePQRzr8CbIyqoA2Lg4IcNlaAWBhwatuGT1-c130_provenance.
- NP58982.RAiRtflS2IRUruXllGLhM1e_BpbC2d0nUVL-VADr8zd1M130_assertion description "[The distributions of VDR allelic frequencies were similar in patients and controls and therefore no influence of VDR polymorphisms on rheumatoid arthritis susceptibility could be demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58982.RAiRtflS2IRUruXllGLhM1e_BpbC2d0nUVL-VADr8zd1M130_provenance.
- NP58983.RAlu0KXP3tJXoft0-RsQR5DAhEAcoKrppUaXs1PrHtBx4130_assertion description "[ This study provides preliminary evidence for a genetic association between Crohn's disease susceptibility and a gene that lies within one of the candidate regions determined by linkage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58983.RAlu0KXP3tJXoft0-RsQR5DAhEAcoKrppUaXs1PrHtBx4130_provenance.
- NP58985.RAqXhdPdmqjAWnrTAAMxae5mc-QiyfWtXdOeredzY715E130_assertion description "[To update data on the role of vitamin D receptor (VDR) single nucleotide polymorphisms (SNPs) in susceptibility to prostate cancer, we performed a meta-analysis of 36 eligible publications on the association of Taql, Apal, Bsml, Fokl and CDX2 SNPs of the VDR gene with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58985.RAqXhdPdmqjAWnrTAAMxae5mc-QiyfWtXdOeredzY715E130_provenance.
- NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_assertion description "[The purpose of this study was to analyse the frequency and type of mutations in the coding region of androgen receptor (AR) and to determine the role of polymorphisms in the intron 1 of ERalpha, exon 5 of ERbeta, intron 7 of progesterone, exon 7 of the aromatase (CYP19) and exon 9 of VDR genes in the risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_provenance.
- NP58990.RAkUpuhCi6KBKEHSuCTZKRWtRiYMWzfGIknzvgUvyTK2I130_assertion description "[We studied the association of prostate cancer risk with five VDR single nucleotide polymorphisms (SNPs): G/A(1229) (SNP 1), A/G(3944) (SNP 2), T/C(30875) (SNP 3), C/T(48200) (SNP 4) and C/T(65013) (SNP 5), in 430 cancer and 310 benign prostatic hypertrophy (BPH) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58990.RAkUpuhCi6KBKEHSuCTZKRWtRiYMWzfGIknzvgUvyTK2I130_provenance.
- NP58994.RAjXqhGfxUdhtXhkaXhAIOOsikI4ViUaTwEGZfYm3W4Ak130_assertion description "[The VDR genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 80 patients with PCa and 96 normal male controls from the Han nationality in Hubei area, using endonuclease Fok I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58994.RAjXqhGfxUdhtXhkaXhAIOOsikI4ViUaTwEGZfYm3W4Ak130_provenance.
- NP59003.RAmJlMNE93lJX8KtqeOyanLYBkQLYnoskqFY6XyuN0A1c130_assertion description "[ The Achang and Han ethnic groups differ in the frequency distribution of VDR gene start codon polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59003.RAmJlMNE93lJX8KtqeOyanLYBkQLYnoskqFY6XyuN0A1c130_provenance.
- NP59005.RAvBO_ZGyYTDx0KwaEHvru477ViU-n4NBVImKfi_lSeVc130_assertion description "[These preliminary data suggest a role for these genes in MS pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59005.RAvBO_ZGyYTDx0KwaEHvru477ViU-n4NBVImKfi_lSeVc130_provenance.
- NP59008.RAtnrzFAARd4A83TF3utQqo2kot_IUw1sSW2zXXFsGzSo130_assertion description "[Past environmental sun exposure and risk of multiple sclerosis: a role for the Cdx-2 Vitamin D receptor variant in this interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59008.RAtnrzFAARd4A83TF3utQqo2kot_IUw1sSW2zXXFsGzSo130_provenance.
- NP59010.RAnuiST2UX2n7NAbgPf7MwGMVlyv4mfWJytOW5nD5f97Q130_assertion description "[The VDR gene polymorphism in patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59010.RAnuiST2UX2n7NAbgPf7MwGMVlyv4mfWJytOW5nD5f97Q130_provenance.
- NP59012.RAo9o8dPJ1yThWrhRQUSHDBSvnQoasGT4fFes9T0sXKZg130_assertion description "[Polymorphisms in vitamin D metabolism related genes and risk of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59012.RAo9o8dPJ1yThWrhRQUSHDBSvnQoasGT4fFes9T0sXKZg130_provenance.
- NP59018.RAn1PxYcImu6pzRhUqvnk-GuUqqb3DeZwt2yvL6V_y95g130_assertion description "[Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59018.RAn1PxYcImu6pzRhUqvnk-GuUqqb3DeZwt2yvL6V_y95g130_provenance.
- NP59025.RAqIqqj2kmyPpqMgZO1vmpZ0Nim7b93x4ysTEj_7qHLlg130_assertion description "[Its actions are mediated via the vitamin D receptor (VDR) and a number of polymorphisms in the VDR gene have been identified, some of which may alter susceptibility to breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59025.RAqIqqj2kmyPpqMgZO1vmpZ0Nim7b93x4ysTEj_7qHLlg130_provenance.
- NP59026.RAleVL-GnMC4jgrGZO9oA1E3hIe23osorvhyPaRCNrEdk130_assertion description "[Vitamin D receptor gene polymorphism(s) and breast cancer risk in north Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59026.RAleVL-GnMC4jgrGZO9oA1E3hIe23osorvhyPaRCNrEdk130_provenance.
- NP59027.RAn8mz8jnRVeNdh5YKH4SEyDGaGaxmbheERvAK6Sa2c4I130_assertion description "[this study has identified an association between the VDR gene and early onset breast cancer risk in the Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59027.RAn8mz8jnRVeNdh5YKH4SEyDGaGaxmbheERvAK6Sa2c4I130_provenance.
- NP59031.RAle9ORqbldaGuir8THWjpGR0ld0ADgI4wPI0ntMpDrpg130_assertion description "[ These data suggest that the VDR genotype is associated with Addison's disease. The mechanisms by which distinct receptor variants might confer disease susceptibility remain to be elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59031.RAle9ORqbldaGuir8THWjpGR0ld0ADgI4wPI0ntMpDrpg130_provenance.
- NP59035.RAhHKNNmXiF8xPw5t7ldtFto4anzqaOeJWEGAIrXw7JXc130_assertion description "[There was an interaction between the A-1012G and Fok 1 polymorphisms (P=0.025) and the Fok 1 variant enhanced the effect of the A allele of the A-1012G polymorphism on metastasis, the probability of metastasis for AAff at 5 years follow-up being 57%, CI 24-92%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59035.RAhHKNNmXiF8xPw5t7ldtFto4anzqaOeJWEGAIrXw7JXc130_provenance.
- NP59039.RAk05zwrKW58F8nvJmqfAOMC_JQFmvKUF_xD62BNjJZXc130_assertion description "[ These data indicate that carriage of the less frequent allele of the Taq I RFLP (t) in the VDR gene significantly increases the risk of developing L-EOP. However, VDR genotype may not affect the incidence of all cases of EOP. These findings contribute to our understanding of the genetic basis for periodontal disease and may help define sub-groups of this disease which share common pathogenic factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59039.RAk05zwrKW58F8nvJmqfAOMC_JQFmvKUF_xD62BNjJZXc130_provenance.
- NP59040.RAnqTI2T4Vd5FV9KblCi5lczSC1IgL9XcyxXmyyYP5-FI130_assertion description "[There was no significant difference in the genotype distribution or the allele frequencies of VDR BsmI and TaqI between the controls and CP patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59040.RAnqTI2T4Vd5FV9KblCi5lczSC1IgL9XcyxXmyyYP5-FI130_provenance.
- NP59043.RArYZShAvDYVAo6OUQhGlrNgUohkW6Y4DpcUZeVFP-q_g130_assertion description "[Vitamin D receptor polymorphism (-1056 Taq-I) interacts with smoking for the presence and progression of periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59043.RArYZShAvDYVAo6OUQhGlrNgUohkW6Y4DpcUZeVFP-q_g130_provenance.
- NP59045.RApBCXt7ppqhwPhoOpqBWFyJbnaiyqaACTF_3qgqYw8dg130_assertion description "[Restriction fragment length polymorphisms in the VDR gene detected by digestion with Taq I were found to be significantly associated with the occurrence of AP or EOP, suggesting that the VDR genotype a risk factor for periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59045.RApBCXt7ppqhwPhoOpqBWFyJbnaiyqaACTF_3qgqYw8dg130_provenance.
- NP59046.RApFSB9Vp1lg_oehLFGlxsI2uDCdxeUzbgy9PfkBHimvA130_assertion description "[The VDR haplotype constructed from the ApaI, BsmI, and FokI polymorphisms is related to the risk of severe chronic periodontitis in Japanese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59046.RApFSB9Vp1lg_oehLFGlxsI2uDCdxeUzbgy9PfkBHimvA130_provenance.
- NP59047.RAvQ8zLaiycmZt_t5W9DCiXoDjtOTfG3VIwZOKlAP0ZJU130_assertion description "[The study indicates that FokI polymorphism of vitamin D receptor gene might be associated with generalized aggressive periodontitis in Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59047.RAvQ8zLaiycmZt_t5W9DCiXoDjtOTfG3VIwZOKlAP0ZJU130_provenance.
- NP59052.RAtOE07DVwg9vBKHK7pNvSZDlnRsfmUOJQCyEFNt6cHHM130_assertion description "[Some studies showed predisposing and protective roles for VDR polymorphisms in pulmonary tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59052.RAtOE07DVwg9vBKHK7pNvSZDlnRsfmUOJQCyEFNt6cHHM130_provenance.
- NP59053.RApRZunR90hjJriNtoPG0LzXrVQKX8WAN2ArI9BmLTWs0130_assertion description "[The present study suggests that PTB patients may have increased 1,25(OH)(2) D(3) levels, and this might lead to downregulation of VDR expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59053.RApRZunR90hjJriNtoPG0LzXrVQKX8WAN2ArI9BmLTWs0130_provenance.
- NP59060.RAmeNj1IogVrDwodq_AO4FaI2pIX8RjQY1omN71iH4ZwA130_assertion description "[No association with tuberculosis was seen with 3 other SLC11A1 loci investigated, which previously have been associated with tuberculosis in other populations or with MBL2 and VDR polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59060.RAmeNj1IogVrDwodq_AO4FaI2pIX8RjQY1omN71iH4ZwA130_provenance.
- NP59061.RAqSYRvqNoS2nLICUFlxQOm9hcoc4rjAQSdZ7IU57t6SY130_assertion description "[Genomic DNA from 95 patients with pulmonary tuberculosis (PTB) and 117 ethnically matched, healthy controls were typed for HLA-DRB1, DRB3, DRB4, DRB5, DQB1, and VDR polymorphisms FokI, BsmI, ApaI, and TaqI using polymerase chain reaction-sequence specific primers (PCR-SSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59061.RAqSYRvqNoS2nLICUFlxQOm9hcoc4rjAQSdZ7IU57t6SY130_provenance.
- NP59063.RApzeIYnaFgswK-42wGTFYsu2syIC2_MdjMEKTBcPGyVw130_assertion description "[The VDR-ff genotype might be associated with the susceptibility to pulmonary tuberculosis in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59063.RApzeIYnaFgswK-42wGTFYsu2syIC2_MdjMEKTBcPGyVw130_provenance.
- NP59064.RAnnSJzj0ttP1jDhKoc9_3gAyLvoT-TONlalVptUGiwh0130_assertion description "[Polymorphisms at FokI loci (VDR-ff) showed statistically significant association between the VDR variants and susceptibility to tuberculosis, and variant in the TaqI locus failed to show statistically significant association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59064.RAnnSJzj0ttP1jDhKoc9_3gAyLvoT-TONlalVptUGiwh0130_provenance.
- NP59077.RAiuAb1r1HARSinFz4YKni6Qpx10EmWvRICdEgn8BV8sQ130_assertion description "[Studies on association between VDR polymorphisms and risk of type 2 diabetes (T2DM) in different ethnic populations are yet inconclusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59077.RAiuAb1r1HARSinFz4YKni6Qpx10EmWvRICdEgn8BV8sQ130_provenance.
- NP59088.RAoKfD1iZ_DLmN81ZdphWFJTmb_gYlvCYpFqYwPCybWDA130_assertion description "[There is the possibility that the VDRSC polymorphism might be important in determining the hereditary susceptibility of children to development of delayed rickets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59088.RAoKfD1iZ_DLmN81ZdphWFJTmb_gYlvCYpFqYwPCybWDA130_provenance.
- NP59093.RAnOHgH4O2KXOV3IjYdBcbedTJZVTUpkbU3KrYfvW8vUA130_assertion description "[The VDR polymorphism does not play a major role in the development of rickets in Mongolia and has no effect on TCSOS in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59093.RAnOHgH4O2KXOV3IjYdBcbedTJZVTUpkbU3KrYfvW8vUA130_provenance.
- NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_assertion description "[ Because folate-related and vitamin D-receptor genetic variants have been associated with bone and vasculature morbidity, these pharmacogenetic associations likely reflect the interaction of antileukemic medications with germline sensitivity to drug actions, and might identify ALL patients at highest risk to develop osteonecrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_provenance.
- NP59098.RAqCvTdf5b-Pnpj__NlUCdLEEDS00YY45H9sFPMQhR6s0130_assertion description "[Children with bone cancer are significantly taller than the reference population, which may be influenced by the genotype for the Fok I polymorphism of the VDR gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59098.RAqCvTdf5b-Pnpj__NlUCdLEEDS00YY45H9sFPMQhR6s0130_provenance.
- NP59101.RAhvzlGAwlBQUrTc7TsOazgreWAw2TWpkEo-zeQTxTodk130_assertion description "[ Certain GRF might have additive but small effects on the disposition for MI before the age of 65. In older patients the tested GRF had no effect, possibly indicating a mechanism of aging rather than a purely genetic determined entity. Given the small effect of the tested genetic polymorphisms the value of testing GRF remains uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59101.RAhvzlGAwlBQUrTc7TsOazgreWAw2TWpkEo-zeQTxTodk130_provenance.
- NP59103.RApVvNPR8OXBzjk8-kzogE2eAoL3WdwevIRDdNBxxfuNM130_assertion description "[Our data suggest that the LBP-1c/CP2/LSF polymorphism may have a moderate protective effect against the risk of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59103.RApVvNPR8OXBzjk8-kzogE2eAoL3WdwevIRDdNBxxfuNM130_provenance.
- NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_assertion description "[The UGT1A1 6/6 genotype predicted lower catechol AUC. Prednisone strongly induces etoposide clearance, genetic polymorphisms may predict the constitutive and induced clearance of etoposide, and the relationship between genotype and phenotype differs by race.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_provenance.
- NP59119.RAhzbzbUl9frzeSVWtAEq3vfTyAQ_KwuFXWLJ-eDjG4UM130_assertion description "[None of the SNPs examined seem likely to be importantly associated with risk of overall or advanced prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59119.RAhzbzbUl9frzeSVWtAEq3vfTyAQ_KwuFXWLJ-eDjG4UM130_provenance.
- NP59122.RAr0kTwbFFTiAzJs7ER0qBL0Z3A_nxL0h0-nk217AeGc0130_assertion description "[Synergistic effect and VEGF/HSP70-hom haplotype analysis: relationship to prostate cancer risk and clinical outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59122.RAr0kTwbFFTiAzJs7ER0qBL0Z3A_nxL0h0-nk217AeGc0130_provenance.
- NP59126.RAmgUXNNLiplDvAs8oH1OO4PA27Ulbd24eqADR2vg8oLQ130_assertion description "[A total of 144 female breast cancer patients and 263 cancer-free population controls were genotyped for the interleukin (IL)-1beta-511 (T/C), IL-6 -174 (G/C), tumour necrosis factor (TNF)-alpha-308 (A/G), IL-10 -1082 (A/G), IL-8 -251 (A/T) and vascular endothelial growth factor (VEGF) -1154 (A/G) SNPs, using amplification refractory mutation system polymerase chain reaction (ARMS-PCR) and TaqMan (Applied Biosystems, Foster City, CA, USA) 5' nuclease assays for allelic discrimination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59126.RAmgUXNNLiplDvAs8oH1OO4PA27Ulbd24eqADR2vg8oLQ130_provenance.
- NP59128.RAg4vXC1bA00p8sQRKpwHUKn9sz2j0Ddf2YL5Xnv6eijA130_assertion description "[The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59128.RAg4vXC1bA00p8sQRKpwHUKn9sz2j0Ddf2YL5Xnv6eijA130_provenance.
- NP59129.RAsY_-Fd55M4Lop2vZM8gQ4OoZz8lf21lDpd7S2rzvKiw130_assertion description "[Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59129.RAsY_-Fd55M4Lop2vZM8gQ4OoZz8lf21lDpd7S2rzvKiw130_provenance.
- NP59135.RAvvsg4Z81sICmJish9Av4iJWacX5eYX-f5mxOZPI6sao130_assertion description "[We have found no evidence that these three single nucleotide polymorphisms, shown previously to alter VEGF concentrations, are risk factors for type 2 diabetes in a large UK Caucasian case-control and family-based study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59135.RAvvsg4Z81sICmJish9Av4iJWacX5eYX-f5mxOZPI6sao130_provenance.
- NP59137.RAqERWdNmLZad8oaaB5oM6bED95CWLd-JmxwN1Hre7ipE130_assertion description "[Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59137.RAqERWdNmLZad8oaaB5oM6bED95CWLd-JmxwN1Hre7ipE130_provenance.
- NP59143.RArbMnzT_tToGXjkpqiI8DM-iHI6hLXcI2mquCgGiHQqA130_assertion description "[Metabolic markers, but not genotyping for 20 diabetogenic SNPs, improve discrimination of incident type 2 diabetes beyond lifestyle risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59143.RArbMnzT_tToGXjkpqiI8DM-iHI6hLXcI2mquCgGiHQqA130_provenance.
- NP59144.RAibL_fcdjKoShRJTTomVns0nKBQgkcPEXTmLVQOevTBQ130_assertion description "[These data suggest that the C(-634)G polymorphism in the 5'UTR of the VEGF gene is a novel genetic risk factor for diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59144.RAibL_fcdjKoShRJTTomVns0nKBQgkcPEXTmLVQOevTBQ130_provenance.
- NP59145.RAu2ifUd_RQsutpq2r2mOVyw6IfgeHlKVAby0tl3BQoyw130_assertion description "[Genes and diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59145.RAu2ifUd_RQsutpq2r2mOVyw6IfgeHlKVAby0tl3BQoyw130_provenance.
- NP59149.RApM59AZkRiBaGBAmUpbjhmriwUEyjVbl446Edz89_8q4130_assertion description "[These preliminary results indicate that VEGF genotype may influence tumour growth in CMM, possibly via the effects of differential VEGF expression on tumour angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59149.RApM59AZkRiBaGBAmUpbjhmriwUEyjVbl446Edz89_8q4130_provenance.
- NP59150.RAsdmKB3ati3stFJlBWs_gqsmjkNB_KKE5tc6R2txFUpc130_assertion description "[We suggest that in VEGF gene polymorphisms the T allele at + 813 may decrease susceptibility to sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59150.RAsdmKB3ati3stFJlBWs_gqsmjkNB_KKE5tc6R2txFUpc130_provenance.
- NP59154.RAoihrHILFmYGjHzw9iXUvnIkKhQL1wVEaYU8mdPXTloY130_assertion description "[We investigated the relationship between eight polymorphisms in the gene encoding for vascular endothelial growth factor (VEGF) (-1540C > A, -1512Ins18, -1451C > T, -460T > C, -160C > T, -152G > A, -116G > A and +405G > C) and plaque-type psoriasis stratified for age at onset, gender and family history of dermatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59154.RAoihrHILFmYGjHzw9iXUvnIkKhQL1wVEaYU8mdPXTloY130_provenance.
- NP65370.RAhj07NUqKuYE1nvlns4cFd0po1XDmf84C00-4gTmi7LY130_assertion description "[Variants in the interleukin 6 receptor gene are associated with obesity in Pima Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65370.RAhj07NUqKuYE1nvlns4cFd0po1XDmf84C00-4gTmi7LY130_provenance.
- NP65381.RAl2H4pH3-kPc7bujXoyWOqOKt6i42y-TW72QU1Y9sVko130_assertion description "[The aim of this study was to determine whether there are any associations between single nucleotide polymorphisms of the chemokine genes IL-8, MCP-1, their corresponding receptors CXCR1 and CCR2 and disease outcome in patients with acute idiopathic anterior uveitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65381.RAl2H4pH3-kPc7bujXoyWOqOKt6i42y-TW72QU1Y9sVko130_provenance.
- NP65389.RAheL8YOizpW8qAXQYtVxUIVYlIKdc98O5q7cCk0fun6U130_assertion description "[IL-8 (-251 A/T) and CXCR2 (+1208 C/T) gene polymorphisms and risk of multiple sclerosis in Iranian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65389.RAheL8YOizpW8qAXQYtVxUIVYlIKdc98O5q7cCk0fun6U130_provenance.
- NP65391.RAoMw5203QP9Xps7kkLNeAjfJNgR9XErwyWlcsb1YlFzE130_assertion description "[Association study of the INPP1, 5HTT, BDNF, AP-2beta and GSK-3beta GENE variants and restrospectively scored response to lithium prophylaxis in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65391.RAoMw5203QP9Xps7kkLNeAjfJNgR9XErwyWlcsb1YlFzE130_provenance.
- NP65398.RAmRWX8H7m13YOTDy6NzE31xn0dquu4qHVc1WrZm5YqpA130_assertion description "[The INSIG2 rs7566605 polymorphism was identified for obesity (BMI> or =30 kg/m(2)) in one of the first genome-wide association studies, but replications were inconsistent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65398.RAmRWX8H7m13YOTDy6NzE31xn0dquu4qHVc1WrZm5YqpA130_provenance.
- NP65400.RAsea3rqCJg1gh4ADU63nM17iULNsvirGa7RZdzlCocTg130_assertion description "[INSIG2 rs7566605 variant is not associated Chinese childhood obesity in two independent cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65400.RAsea3rqCJg1gh4ADU63nM17iULNsvirGa7RZdzlCocTg130_provenance.
- NP65403.RAvTXMBlBD3JWPQxR22zfR9N3YmztLZ47AaX6S-Sn-0Js130_assertion description "[We used a dense whole-genome scan of DNA samples from the Framingham Heart Study participants to identify a common genetic variant near the INSIG2 gene associated with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65403.RAvTXMBlBD3JWPQxR22zfR9N3YmztLZ47AaX6S-Sn-0Js130_provenance.