Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP50454.RAsbPSEcdRudbjqu3pq7vHWMx76AULfkbPrws-DEjF6g4130_assertion description "[Genes involved in the development and function of regulatory T cells, specifically IL2RA, TLR2, TGFBR2, and FOXP3, associate with atopy and asthma by gene-gene interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50454.RAsbPSEcdRudbjqu3pq7vHWMx76AULfkbPrws-DEjF6g4130_provenance.
- NP50455.RAv9lEdLDQNw3bk1LfbwUHOcoOMM6cEBE3ZclWt-210aY130_assertion description "[Variant alleles of TLR2 and TLR4 genes influence the susceptibility to adverse effects of traffic-related air pollution on childhood asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50455.RAv9lEdLDQNw3bk1LfbwUHOcoOMM6cEBE3ZclWt-210aY130_provenance.
- NP50456.RAsTbqB2wPACNVAqQKsxtIB_dbB9D17Baet5REcmMmbe0130_assertion description "[Our results indicate that a genetic variant in the TLR2 subfamily may play a role in susceptibility to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50456.RAsTbqB2wPACNVAqQKsxtIB_dbB9D17Baet5REcmMmbe0130_provenance.
- NP50457.RAq4nKRdvIubn1W4x5N3JTK2DGgU2W-uE2oIssBnP3e3M130_assertion description "[Atopy and new-onset asthma in young Danish farmers and CD14, TLR2, and TLR4 genetic polymorphisms: a nested case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50457.RAq4nKRdvIubn1W4x5N3JTK2DGgU2W-uE2oIssBnP3e3M130_provenance.
- NP50458.RAlU7jeqwWJWPaunX2kuC-RX3vqilrGsfs0iuMMc196Uw130_assertion description "[Toll-like receptors and CD14 genes polymorphisms and susceptibility to asthma in Tunisian children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50458.RAlU7jeqwWJWPaunX2kuC-RX3vqilrGsfs0iuMMc196Uw130_provenance.
- NP50468.RAsUi195a_61g7O37q3D1nQlY7m35ptlm8puha_1gnT5M130_assertion description "[Our results indicate that a genetic variant in the TLR2 subfamily may play a role in susceptibility to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50468.RAsUi195a_61g7O37q3D1nQlY7m35ptlm8puha_1gnT5M130_provenance.
- NP50470.RAmxVX6AoTRjIDMTzuznaF7MwGzMzpLpNXxxmRhmAsgRM130_assertion description "[The interaction of four genes in the inflammation pathway significantly predicts prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50470.RAmxVX6AoTRjIDMTzuznaF7MwGzMzpLpNXxxmRhmAsgRM130_provenance.
- NP50471.RAutoEfVspW7CVLzaTYf_4NnCjk2T6dQI9bXQM21L2Kpc130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50471.RAutoEfVspW7CVLzaTYf_4NnCjk2T6dQI9bXQM21L2Kpc130_provenance.
- NP50472.RAqIkqGvWfpfc4ZUBnYPi556-dO-Ioy4DbOhOGFYAYcDs130_assertion description "[ These results document the importance of screening the TK2 gene in patients with myopathic mitochondrial DNA depletion syndrome and confirm that exon 5 is a hot spot for TK2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50472.RAqIkqGvWfpfc4ZUBnYPi556-dO-Ioy4DbOhOGFYAYcDs130_provenance.
- NP50479.RAozHJbR_Ie0tEuI7cVnyCxER4Q1WOFvR7GW1Mvd-RvCg130_assertion description "[For TIMP-2, women with the rs7501477 TT genotype were 3 times more likely to be breast cancer cases than women with the CC genotype (OR: 2.9, 95% CI: 1.2-7.0).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50479.RAozHJbR_Ie0tEuI7cVnyCxER4Q1WOFvR7GW1Mvd-RvCg130_provenance.
- NP50483.RAkfsgBn-HCwt9ssOJwIqzxCNFw3sg56QqhjMke1hUX2E130_assertion description "[Three of these polymorphisms were associated with a significant risk of AAA, ACE RR 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50483.RAkfsgBn-HCwt9ssOJwIqzxCNFw3sg56QqhjMke1hUX2E130_provenance.
- NP50485.RAsCJ3i3j3fcHfa_Xm-WZ3dlXo3tCodkvCWcga7xmmSSs130_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." NP50485.RAsCJ3i3j3fcHfa_Xm-WZ3dlXo3tCodkvCWcga7xmmSSs130_provenance.
- NP50486.RAv7X7BbcjgJYh7c-fDidNY2f30qCJTA1QVj5tj5POUbc130_assertion description "[MMP-9 -1562C>T and 836G>A (Arg279Gln) were not associated with asthma (p> or =0.15) or asthma severity (p> or =0.13), and TIMP-1 434T>C (Phe124Phe) was not associated with asthma in women (p = 0.094) or men (p = 0.207).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50486.RAv7X7BbcjgJYh7c-fDidNY2f30qCJTA1QVj5tj5POUbc130_provenance.
- NP50487.RAhVr3I1wSFUHw7mJiVhKR8mNXYnGmlP8JD79hBoCxJ-E130_assertion description "[Our results strongly suggest that the variations of Tim-1 exon 4 might be associated with the susceptibility to RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50487.RAhVr3I1wSFUHw7mJiVhKR8mNXYnGmlP8JD79hBoCxJ-E130_provenance.
- NP50489.RAmTJ2gr9vLAGAA--ru76-oB-XMr6bZ8fjyLA6KtxIUjE130_assertion description "[This study showed a highly significant and independent association between preoperative plasma TIMP-1 levels and survival in rectal cancer patients, thus confirming our previous findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50489.RAmTJ2gr9vLAGAA--ru76-oB-XMr6bZ8fjyLA6KtxIUjE130_provenance.
- NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_assertion description "[ Our findings suggest that the A387P variant of the THBS4 gene may be an important determinant in the development of MI at any age. Careful assessment of clinical covariates helped to unmask a significant association and therefore may be an important reason for why studies do not replicate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_provenance.
- NP50493.RAgCBiLFpGIcgN5Eh7ce_5NCIrAWaNdCXT_X0bhKcrZHY130_assertion description "[Based on a study examining 500 myocardial infarction (MI) patients and 500 controls from the genetically isolated Newfoundland population, we previously reported that thrombospondin-4 (THBS-4) 1186G>C variant associates with MI in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50493.RAgCBiLFpGIcgN5Eh7ce_5NCIrAWaNdCXT_X0bhKcrZHY130_provenance.
- NP50495.RAvqnvJImdOn8gSx4p_brfpHRfQQHzcf9ajy6qbttznS0130_assertion description "[ despite known caveats of genetic association studies, they can be an effective means of hypothesis generation and complement classic linkage studies for understanding the genetic basis of coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50495.RAvqnvJImdOn8gSx4p_brfpHRfQQHzcf9ajy6qbttznS0130_provenance.
- NP50499.RAqfAL-J4Qjbe3GTr8WyV8_ouJmqwzpBoFkFzwizJkEPA130_assertion description "[ despite known caveats of genetic association studies, they can be an effective means of hypothesis generation and complement classic linkage studies for understanding the genetic basis of coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50499.RAqfAL-J4Qjbe3GTr8WyV8_ouJmqwzpBoFkFzwizJkEPA130_provenance.
- NP50501.RAnwC26iRLkaGxm0UOO2NMNNAGnShHtg-0xAg6doNoYXo130_assertion description "[Despite the fact that TM promoter G-33A and C1418T polymorphisms are common in the Chinese population, the association between G-33A mutation and premature AMI indicates that we must focus on promoter G-33A polymorphism rather than C1418T polymorphism in terms of the role of TM gene mutation on premature AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50501.RAnwC26iRLkaGxm0UOO2NMNNAGnShHtg-0xAg6doNoYXo130_provenance.
- NP50513.RAqQuSUZ1QnM16pNXqXR3JgC7mVhkFBvEMUQdyKmgudpw130_assertion description "[The polymorphism of INS may play a role in the aetiology of prostate cancer. Given the high prevalence of the CC genotype and its association with late age of onset of low-grade tumours, this polymorphism may contribute to the unique characteristics of prostate cancer, namely a high prevalence of indolent cancers and the dramatic increase in incidence with age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50513.RAqQuSUZ1QnM16pNXqXR3JgC7mVhkFBvEMUQdyKmgudpw130_provenance.
- NP50517.RAsf2hkIfdYDSfH-7jWRhSTOSh-pbqhx_0CcslfKxtDjk130_assertion description "[The present study examined the association of the Tyrosine hydroxylase Val-81-Met polymorphism with alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50517.RAsf2hkIfdYDSfH-7jWRhSTOSh-pbqhx_0CcslfKxtDjk130_provenance.
- NP50519.RAr3J96EZXpRdU0uQu4SB15-zmMp9TiHQ8dmrlpR2xhyY130_assertion description "[Association of polymorphic VNTR region in the first intron of the human TH gene with disturbances of the catecholamine pathway in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50519.RAr3J96EZXpRdU0uQu4SB15-zmMp9TiHQ8dmrlpR2xhyY130_provenance.
- NP50522.RAlGbhVq_3LLuAnBEaQLul-cikd2oOn9tNhlyMlqp-n3A130_assertion description "[Will genetic polymorphism of tetranucleotide sequences help in the diagnostics of major psychiatric disorders?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50522.RAlGbhVq_3LLuAnBEaQLul-cikd2oOn9tNhlyMlqp-n3A130_provenance.
- NP50525.RAhURpO1egyFr1rzlXSy65wUbOLfjri7lMX0yXC3xi58g130_assertion description "[Association of the tyrosine hydroxylase gene polymorphism with schizophrenia in the population of central Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50525.RAhURpO1egyFr1rzlXSy65wUbOLfjri7lMX0yXC3xi58g130_provenance.
- NP50527.RAhxPny9scbjlXHBUeMMkoM7NOAtFUT3xDCHtE1qrR8RA130_assertion description "[These preliminary results replicate a previous association between tobacco use and the K4 allele of the TH gene (Lerman et al., 1997). The potential significance of including time to first cigarette in definitions of tobacco dependence and the possible role that these TH variants might play in tobacco dependence are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50527.RAhxPny9scbjlXHBUeMMkoM7NOAtFUT3xDCHtE1qrR8RA130_provenance.
- NP50528.RAlz99MW_wEnOSnze5s0xlSCNv-Y_dTNrAoOkvCBM8fsA130_assertion description "[This study examined a possible association of two polymorphisms, both of which result in an amino acid change of the TH protein, with schizophrenia and Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50528.RAlz99MW_wEnOSnze5s0xlSCNv-Y_dTNrAoOkvCBM8fsA130_provenance.
- NP50533.RAny_fq_ztr20Guyap6g6v6Dm7ITvWUtO24ose5MbX24U130_assertion description "[Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50533.RAny_fq_ztr20Guyap6g6v6Dm7ITvWUtO24ose5MbX24U130_provenance.
- NP50536.RAuVMyS1MKOXPVFS6daCzrFjmceZm0vogx26QnGd7KKNw130_assertion description "[Positive association of tyrosine hydroxylase microsatellite marker to essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50536.RAuVMyS1MKOXPVFS6daCzrFjmceZm0vogx26QnGd7KKNw130_provenance.
- NP50542.RAkmX87vRknRCmmGF7k38upBinmBTGPWJ7fGuNI7nYycU130_assertion description "[However, there were no significant difference in genotype or allele frequency distributions between cases and controls for the TGFbetaRII and TGFbetaRIII SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50542.RAkmX87vRknRCmmGF7k38upBinmBTGPWJ7fGuNI7nYycU130_provenance.
- NP50543.RAuJwsjtGzOgC64GUFZe6dAaouvONqDDcl0PVs-F_Upms130_assertion description "[Our findings suggest that Ki-ras and ERCC2 SNPs are possible markers for meningioma formation, whereas cyclin D1 and p16 SNPs may be markers of genes that have an inverse effect on the risk to develop meningioma in irradiated and nonirradiated populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50543.RAuJwsjtGzOgC64GUFZe6dAaouvONqDDcl0PVs-F_Upms130_provenance.
- NP50545.RAoutlF5a6y9xqejQsUu9UZh5oV_Q_R3t3KQSyVmLMynI130_assertion description "[However, there were no significant difference in genotype or allele frequency distributions between cases and controls for the TGFbetaRII and TGFbetaRIII SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50545.RAoutlF5a6y9xqejQsUu9UZh5oV_Q_R3t3KQSyVmLMynI130_provenance.
- NP50546.RAkISMMcA70iUGMP8Ufr0g0ssTUs8TgeSwwyowz5AdM0c130_assertion description "[Association between CagA+ Helicobacter pylori infection and p53, bax and transforming growth factor-beta-RII gene mutations in gastric cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50546.RAkISMMcA70iUGMP8Ufr0g0ssTUs8TgeSwwyowz5AdM0c130_provenance.
- NP50551.RAtVg3i4LbIRU2PXsd4_DOhlGiG0IFywzzvJuO8njW5vc130_assertion description "[there remains an unidentified susceptibility locus in the region 9q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50551.RAtVg3i4LbIRU2PXsd4_DOhlGiG0IFywzzvJuO8njW5vc130_provenance.
- NP50553.RAnJPyeR1fL9pMHNm4FIBPQ_X8uoNoUtc3uOLH8y5oHfQ130_assertion description "[Colorectal cancers in patients with the (9A/6A) polymorphism of TGFBR1 exhibit lesser inter-(simple sequence repeat) PCR genomic instability and present clinically at greater age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50553.RAnJPyeR1fL9pMHNm4FIBPQ_X8uoNoUtc3uOLH8y5oHfQ130_provenance.
- NP50561.RAkDhLqwAolK_fcOVfb91kppZ0cFvgXwBPTzi6vdyAmWc130_assertion description "[These data suggest that the germline Int7G24A variant may represent a risk factor for invasive breast cancer and a marker for breast cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50561.RAkDhLqwAolK_fcOVfb91kppZ0cFvgXwBPTzi6vdyAmWc130_provenance.
- NP50569.RAuW-gZ7j63eqhK_ieKQDvdKvo-uQYDnkvIBszcSqMtgQ130_assertion description "[Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 --> Cys mutation in the kerato-epithelin gene. sgupta@ogh.on.ca.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50569.RAuW-gZ7j63eqhK_ieKQDvdKvo-uQYDnkvIBszcSqMtgQ130_provenance.
- NP50577.RAqPnMBhpxRxyiqQ_w7B12wNAxxW6N8ohe7P0nuASL4q8130_assertion description "[TGFB1 T29C polymorphism and breast cancer risk: a meta-analysis based on 10,417 cases and 11,455 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50577.RAqPnMBhpxRxyiqQ_w7B12wNAxxW6N8ohe7P0nuASL4q8130_provenance.
- NP50582.RAinzIE2XJO3IKNfZSeAU6hAOe0E4D8o37PUVAxahznao130_assertion description "[Transforming growth factor-beta1 polymorphisms and breast cancer risk: a meta-analysis based on 27 case-control studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50582.RAinzIE2XJO3IKNfZSeAU6hAOe0E4D8o37PUVAxahznao130_provenance.
- NP50584.RArhkwN6MfaBee37CXDDuPE-dLg1MV7OiFKYTwS0uv3go130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50584.RArhkwN6MfaBee37CXDDuPE-dLg1MV7OiFKYTwS0uv3go130_provenance.
- NP50598.RAmHNRZ_WXiZu8q_eQ0LPPIoV_LJ733F9X2-3lFmWPsWo130_assertion description "[TNF, LTA and TGFB1 genotype distributions among acute graft-vs-host disease subsets after HLA-matched unrelated hematopoietic stem cell transplantation: a pilot study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50598.RAmHNRZ_WXiZu8q_eQ0LPPIoV_LJ733F9X2-3lFmWPsWo130_provenance.
- NP50601.RArd2CRUF6zm9DNN46Vk4ZQrxzfTbGYyweFJ3MVnSU7kQ130_assertion description "[The purpose of the present investigation was to find out the possible association between transforming growth factor beta-1 (TGF-beta1) codon 25 polymorphism (rs:1800471) and acute graft versus host disease (aGVHD) after bone marrow transplantation from the sibling with the similar HLA among the Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50601.RArd2CRUF6zm9DNN46Vk4ZQrxzfTbGYyweFJ3MVnSU7kQ130_provenance.
- NP50603.RAv-j10ILYvMdTMmV7mEX1ZtPxvhRGjdLqz9KIdc41WlQ130_assertion description "[These findings suggest that - with the possible exception of IL-1beta- genetic variation associated with differential expression of the selected pro- and anti-inflammatory cytokines is unlikely to play a major role in susceptibility to and prognosis in CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50603.RAv-j10ILYvMdTMmV7mEX1ZtPxvhRGjdLqz9KIdc41WlQ130_provenance.
- NP50615.RArxSGC7HDy0YZ0VA6yQ8wCST3HlVYT6aK-ZX_bH11GfE130_assertion description "[Genetic predisposition to multiple sclerosis as a polygenic autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50615.RArxSGC7HDy0YZ0VA6yQ8wCST3HlVYT6aK-ZX_bH11GfE130_provenance.
- NP50618.RAhl67PQsUo-T6FSvYS9Ur64IPCr5LT1VfPznioutpPCU130_assertion description "[Our objective was to investigate whether polymorphisms and haplotypes in the TGFB1 gene are associated with susceptibility or disease characteristics of multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50618.RAhl67PQsUo-T6FSvYS9Ur64IPCr5LT1VfPznioutpPCU130_provenance.
- NP50625.RAudeWUE_M4CADqFt7UPhk1FJPn1GjkRFaRIUyQ9JBoHw130_assertion description "[These results suggest that inheritance of the interleukin-10 -1082 G/G and the transforming growth factor-beta 1 +29 C/C genotypes, which appear to affect the cytokine production, may be associated with susceptibility to chronic hepatitis C infection and resistance to combined antiviral therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50625.RAudeWUE_M4CADqFt7UPhk1FJPn1GjkRFaRIUyQ9JBoHw130_provenance.
- NP50626.RAiQbPJC4zwS8B6ern49o9epbN7Nclnm83JZaxD2Rb-wo130_assertion description "[Ethnic differences in polymorphisms of tumor necrosis factor-alpha, interleukin-10, and transforming growth factor-beta1 genes in patients with chronic hepatitis C virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50626.RAiQbPJC4zwS8B6ern49o9epbN7Nclnm83JZaxD2Rb-wo130_provenance.
- NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_assertion description "[Our results suggest that variant alleles of the five markers are absent or too rare to be useful genetic makers in Chinese, despite the fact that they have been commonly used as polymorphic markers in osteoporosis genetic research in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_provenance.
- NP50631.RAoWqGnnfpxb2k6_L8YaZKSHzyC_IGpni3mhH5gMj9lpc130_assertion description "[The results suggest that production of TGF-beta in CML patients is higher and production of IL-4 and IL-10 is lower than in normal subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50631.RAoWqGnnfpxb2k6_L8YaZKSHzyC_IGpni3mhH5gMj9lpc130_provenance.
- NP50635.RAl0cDqxjrciDKi3ySV9gwgWptfyX-1aVaU7tJCOyPdNo130_assertion description "[However, although they do not reach statistical significance (which may be due to the relatively restricted number of subjects included in this study), the distribution differences (in normotensives and hypertensives) observed in the cases of EGF and TNF-alpha reflect trends that could be expected from a mechanistic explanation of the pathways that underlie the patho-physiology of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50635.RAl0cDqxjrciDKi3ySV9gwgWptfyX-1aVaU7tJCOyPdNo130_provenance.
- NP50639.RAn_0MlE24uJ8pTfxW0_vk-VXK6prMKylxQdjkY7Od8ps130_assertion description "[Arg25Pro polymorphism of transforming growth factor-beta1 and its role in the pathogenesis of essential hypertension in Russian population of the Central Chernozem Region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50639.RAn_0MlE24uJ8pTfxW0_vk-VXK6prMKylxQdjkY7Od8ps130_provenance.
- NP50641.RAlPYX6pRuSgViYCOWl_cIsnbuREcd3sEVvJmeLENGTok130_assertion description "[Transforming growth factor-beta-1 variants are not associated with chronic nonalcoholic pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50641.RAlPYX6pRuSgViYCOWl_cIsnbuREcd3sEVvJmeLENGTok130_provenance.
- NP50644.RAtjdCcn9Vq5FZ6DY8sxqrIf3voMuvZMMgyod9WDR0P_s130_assertion description "[Statistical comparisons of the allele and genotype frequencies between the clinical defined sarcoidosis groups and the healthy blood donors revealed no significant differences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50644.RAtjdCcn9Vq5FZ6DY8sxqrIf3voMuvZMMgyod9WDR0P_s130_provenance.
- NP50655.RAqwMdd1JIG0iPnat3gzDBoD0xveunKOnE3E5juIyhc9I130_assertion description "[ No relationship is found between -509C > T polymorphism of TGFbeta1 and liver cirrhosis in Chinese populations, but the presence of C allele at position -509 may play an important role in the progression of liver cirrhosis and may influence plasma concentration of TGFbeta1 in liver cirrhosis patients. Codon10T > C polymorphism may play a significant role in development of liver cirrhosis, but has no correlation with plasma concentration of TGFbeta1 and progression of liver cirrhosis. The -509C > T and codon10T > C polymorphisms are in tight linkage disequilibrium, and the major haplotypes are C-T and T-C. The haplotype C-T influences plasma concentration of TGFbeta1 and is closely related to liver cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50655.RAqwMdd1JIG0iPnat3gzDBoD0xveunKOnE3E5juIyhc9I130_provenance.
- NP50669.RAlLLKiCd23stvlqvAUeyUud5s6DbDW1RD7EsdGT8P77U130_assertion description "[We studied EGF+61G>A and TGFB1+869T>C functional polymorphisms in 234 patients with PC and 243 healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50669.RAlLLKiCd23stvlqvAUeyUud5s6DbDW1RD7EsdGT8P77U130_provenance.
- NP50672.RAiY7Zdi7SgMOHt45j8Iq4PSkeWw-33WKC79aeGP4IKOU130_assertion description "[Transforming growth factor-beta 1 gene polymorphisms and expression in the blood of prostate cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50672.RAiY7Zdi7SgMOHt45j8Iq4PSkeWw-33WKC79aeGP4IKOU130_provenance.
- NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_assertion description "[ These results suggest that patients with SSc are genetically predisposed to high TGFbeta1 production. These polymorphisms do not, however, explain the difference in the clinical phenotypes of limited and diffuse SSc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_provenance.
- NP50679.RAlLagQfcwr5UIXd2ZU-k69KWC7_3-clRl05to9mLLqo4130_assertion description "[The -174IL-6 and TGF-beta1 (codon 25) single-nucleotide polymorphisms are associated with susceptibility to chronic periodontitis in the population studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50679.RAlLagQfcwr5UIXd2ZU-k69KWC7_3-clRl05to9mLLqo4130_provenance.
- NP50685.RAtZiGkESSHxSXTvwe-ckrzoXutzt9MQ0J0cbV2v3vhRk130_assertion description "[The use of DNA pooling technology increased the throughput and decreased the cost of our association analysis of nephropathy in our type 2 diabetes sample, which demonstrated sufficient sensitivity to support previous positive findings of association with]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50685.RAtZiGkESSHxSXTvwe-ckrzoXutzt9MQ0J0cbV2v3vhRk130_provenance.
- NP50691.RAqggcxE-H2fhx-wdL8km7EKi1C0jJPppestIGWnsnEl8130_assertion description "[The aim of our study was to investigate the role of molecular variants of the TGF-beta1 (transforming growth factor beta 1) and the TSC-22 (transforming growth factor beta stimulated clone 22) genes in diabetic nephropathy and diabetic retinopathy in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50691.RAqggcxE-H2fhx-wdL8km7EKi1C0jJPppestIGWnsnEl8130_provenance.
- NP50693.RAg_z9BKpoLx2Pr9zANz4lVSJFxFf3lpYUokCvMRNLkV0130_assertion description "[ The proline allele at codon 10 of the TGF-beta1 gene occurs more commonly in control subjects than in individuals with COPD. This allele is associated with increased production of TGF-beta1 which raises the possibility that TGF-beta1 has a protective role in COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50693.RAg_z9BKpoLx2Pr9zANz4lVSJFxFf3lpYUokCvMRNLkV0130_provenance.
- NP50694.RArXX8XxBVRe4KqlKPvaBZj9ZqXS4XyF5wewJzCf8EU40130_assertion description "[genetic variation in surfactant protein B is associated with chronic obstructive pulmonary disease susceptibility and exacerbation frequency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50694.RArXX8XxBVRe4KqlKPvaBZj9ZqXS4XyF5wewJzCf8EU40130_provenance.
- NP50700.RAlMcU65Q0YpetJh7BvRXL0IMxjUbLkZILWHsMXzCfI3A130_assertion description "[Decorin and TGF-beta1 polymorphisms and development of COPD in a general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50700.RAlMcU65Q0YpetJh7BvRXL0IMxjUbLkZILWHsMXzCfI3A130_provenance.
- NP50705.RAtEdVmWy9XIpBDzVEU9bkTBUQEJ1LRFD8ua3bq_pDHvM130_assertion description "[our data suggest that several gene polymorphisms may be cooperatively involved in the development of osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50705.RAtEdVmWy9XIpBDzVEU9bkTBUQEJ1LRFD8ua3bq_pDHvM130_provenance.
- NP50706.RArt3mnTRAwRAjtq0KobE46t3KWT7QHbW-YaqCVgDcqAI130_assertion description "[The implementation of personalized treatment for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50706.RArt3mnTRAwRAjtq0KobE46t3KWT7QHbW-YaqCVgDcqAI130_provenance.
- NP50710.RAvihTodpNA4D-IRVYc-zbkzzKLXt8zQ0WIATZt0Q9qmE130_assertion description "[Genomic approaches to bone and joint diseases. An order made medical system for management of osteoporosis: an attempt using genetic information.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50710.RAvihTodpNA4D-IRVYc-zbkzzKLXt8zQ0WIATZt0Q9qmE130_provenance.
- NP50712.RAmk4fQ48FWs5b9JfIx9srbp-gFpqSCnHHOeqWVt66tBo130_assertion description "[Positive association findings in this study suggest that TGFB1 is a susceptibility locus for myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50712.RAmk4fQ48FWs5b9JfIx9srbp-gFpqSCnHHOeqWVt66tBo130_provenance.
- NP50713.RAk3qYGZk33vXs_IQOhURNGitMgaUTSh4DxelCKtqwplo130_assertion description "[Transforming growth factor beta 1 (TGF-beta1) gene play an important role in the acute myocardial infarction (AMI), however no investigation has been conducted so far in young AMI patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50713.RAk3qYGZk33vXs_IQOhURNGitMgaUTSh4DxelCKtqwplo130_provenance.
- NP50723.RAmJHKGng6zNz0Y4ceyHkrWOCgbeZz7GpJCLXtOJvv6ww130_assertion description "[Our data suggest that variants of the hemochromatosis-transferrin receptor system have no direct effect on the incidence of breast cancer in Germany. Possible effects on tumor progression and prognosis remain elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50723.RAmJHKGng6zNz0Y4ceyHkrWOCgbeZz7GpJCLXtOJvv6ww130_provenance.
- NP50726.RAigMT77g_uWBpaO9pABVHjCYcklecdrv3cBf3l_QAgMg130_assertion description "[ The conclusion is drawn that this mutation may be correlated to various rheumatic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50726.RAigMT77g_uWBpaO9pABVHjCYcklecdrv3cBf3l_QAgMg130_provenance.
- NP50727.RAu9DD1o_Sd_bll02HlmBarHWaW9GtoEJUuaHBkBmgoqs130_assertion description "[Our data suggest that variants of the hemochromatosis-transferrin receptor system have no direct effect on the incidence of breast cancer in Germany. Possible effects on tumor progression and prognosis remain elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50727.RAu9DD1o_Sd_bll02HlmBarHWaW9GtoEJUuaHBkBmgoqs130_provenance.
- NP50737.RAjaXYNLwtlfrsq2jaqhvcJiEaHa11-H9LQ2XwNNdLlTo130_assertion description "[In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50737.RAjaXYNLwtlfrsq2jaqhvcJiEaHa11-H9LQ2XwNNdLlTo130_provenance.
- NP50749.RAi_ZEQTw1zglyYltXwMazOlfixbEHSEEL_mxT9r7TL38130_assertion description "[Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50749.RAi_ZEQTw1zglyYltXwMazOlfixbEHSEEL_mxT9r7TL38130_provenance.
- NP50750.RAh51jSwxWdDuDX4iHJcyIEpw6MoyYVLV4WoJtE16_C4Q130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50750.RAh51jSwxWdDuDX4iHJcyIEpw6MoyYVLV4WoJtE16_C4Q130_provenance.
- NP50755.RAjmF5-Gc-asfbh_FgfCscOAkOUEPM-Urnd6phuAEV16Y130_assertion description "[Genes related to iron metabolism and susceptibility to Alzheimer's disease in Basque population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50755.RAjmF5-Gc-asfbh_FgfCscOAkOUEPM-Urnd6phuAEV16Y130_provenance.
- NP50761.RAmBQoNi5sMmaH193dh5bQSdC_NbPecFXVJFmb2_FgZHY130_assertion description "[ The 259-Pro allele seems to have beneficial influences during embryogenesis, conceivably through its positive effect on vitamin B(12) intracellular bioavailability. Our results warrant additional investigations addressing the question if vitamin B(12) supplementation in addition to folic acid supplementation may prevent spontaneous abortion in women planning a pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50761.RAmBQoNi5sMmaH193dh5bQSdC_NbPecFXVJFmb2_FgZHY130_provenance.
- NP50762.RAqXbqdQAkA7JOeUK7NKpqIZ0gGgfk3zcnpWjJUB4-G5g130_assertion description "[In conclusion, the study on vegetarians and seniors documents interesting lifestyle-genotype interactions. Although the TC and COMT mutations influence cellular vitamin B12 metabolism, this effect did not result in overt homocysteine elevation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50762.RAqXbqdQAkA7JOeUK7NKpqIZ0gGgfk3zcnpWjJUB4-G5g130_provenance.
- NP50764.RAqpviqjnSHRtqWwQzOID4nPDsVhtzQ6Pw1t5GkaTbf6k130_assertion description "[ Distinct determinants of the IL-1 gene cluster are related to the generation and progression of Alzheimer's disease. MTR only influences progression of the disease, which may be enhanced by carriage of allele epsilon4 of APO-E.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50764.RAqpviqjnSHRtqWwQzOID4nPDsVhtzQ6Pw1t5GkaTbf6k130_provenance.
- NP50771.RAprnFTOGAMpPmBVAjPjljloFxhQGatzm7SlJs0EMBS40130_assertion description "[The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50771.RAprnFTOGAMpPmBVAjPjljloFxhQGatzm7SlJs0EMBS40130_provenance.
- NP50779.RAuvalr6ua8beVYlrpTu-2_GfjX42KRtBmMrejzahQn8Q130_assertion description "[Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50779.RAuvalr6ua8beVYlrpTu-2_GfjX42KRtBmMrejzahQn8Q130_provenance.
- NP50783.RAiKEnwvNlk4yuVduQJ0KyGfVnXifv8vTXjN4J90dfEOM130_assertion description "[Fifteen robustly associated type 2 diabetes variants were successfully genotyped in 410 individuals from 203 HNF1A-MODY families, from two study centers in the U.K. and Norway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50783.RAiKEnwvNlk4yuVduQJ0KyGfVnXifv8vTXjN4J90dfEOM130_provenance.
- NP50787.RAiudqvc_LOxyVpZuGTl0aQ7lsWBFavg3961UvwHBlZlc130_assertion description "[Mutations and intronic variants in the HNF-1 beta gene in a group of German and Czech Caucasians with type 2 diabetes mellitus and progressive diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50787.RAiudqvc_LOxyVpZuGTl0aQ7lsWBFavg3961UvwHBlZlc130_provenance.
- NP50788.RArKOYF1Nkcj9qSGTBzI6u0VCdw4Tylwxh1Ktmy8nSf9M130_assertion description "[The probable etiologic heterogeneity of type 2 diabetes in the Oji-Cree created a situation in which association analysis was much more sensitive to detect a relationship between HNF1A S319 and diabetes than was linkage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50788.RArKOYF1Nkcj9qSGTBzI6u0VCdw4Tylwxh1Ktmy8nSf9M130_provenance.
- NP50791.RAsbuYRBqnhsXDsVlNSQ-g-GdBKP0joom7h_tHdtFHUcI130_assertion description "[ MODY mutations but not autoimmunity contribute to GDM in Swedish women with a family history of diabetes and increase the risk of subsequent diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50791.RAsbuYRBqnhsXDsVlNSQ-g-GdBKP0joom7h_tHdtFHUcI130_provenance.
- NP50793.RAjbTmPBqvynYaUzoeuzcLgU8NERyFdxt4MJSnOwl_4x4130_assertion description "[ The -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50793.RAjbTmPBqvynYaUzoeuzcLgU8NERyFdxt4MJSnOwl_4x4130_provenance.
- NP50796.RAsLKkKxDdL4l4al_RQCvSYFoTiLBIC0QmGMmExJyRYik130_assertion description "[The aim of this study was to determine the prevalence of mutations in the hepatocyte nuclear factor (HNF)-1alpha gene (TCF1) in a large group of Japanese patients with early-onset non-Type I (insulin-dependent) diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50796.RAsLKkKxDdL4l4al_RQCvSYFoTiLBIC0QmGMmExJyRYik130_provenance.
- NP50798.RAuKedC8XoESnNu4JiufGFsHUIb8dIQZd7Ux2d83MT7ns130_assertion description "[A considerable number of non-obese Japanese patients with non-Type 1 diabetes of youth have HNF-1alpha-deficient diabetes. Lack of obesity could well be a characteristic feature of this form of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50798.RAuKedC8XoESnNu4JiufGFsHUIb8dIQZd7Ux2d83MT7ns130_provenance.
- NP50800.RAr4WvobGM0fLUUezboWb4Vr121VGpIj6xyYrtmQKcBAk130_assertion description "[Scanning for MODY5 gene mutations in Chinese early onset or multiple affected diabetes pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50800.RAr4WvobGM0fLUUezboWb4Vr121VGpIj6xyYrtmQKcBAk130_provenance.
- NP50801.RAkGDlh8SDBPrWdXG0Gg3kcR-nP2FOrpKj9ROx7JI_3cE130_assertion description "[TCF1 gene is not a common cause of early-onset and/or multiplex diabetes among Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50801.RAkGDlh8SDBPrWdXG0Gg3kcR-nP2FOrpKj9ROx7JI_3cE130_provenance.
- NP50803.RApbDYCtIHZ3VyfM1yPGFi3dQviE2E6yI850lbtYZ23rA130_assertion description "[We conclude that the I27L polymorphism is associated with insulin resistance, but not beta-cell function. The mechanism of this association is unclear, but HNF-1alpha may play a role in regulating hepatic glucose metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50803.RApbDYCtIHZ3VyfM1yPGFi3dQviE2E6yI850lbtYZ23rA130_provenance.
- NP50821.RAr4FZXVvd-ObOqTbmkXxVL5_-uzRj46sClAvAFpYzwHk130_assertion description "[These results indicate that both heterozygosity (odds ratio, 0.592; 95% confidence interval, 0.23??1.54) and homozygosity (odds ratio, 0.08; 95% confidence interval, 0.01??1.97) for T???xR-I(6A) allele are not predisposition factors for the development of colorectal cancer in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50821.RAr4FZXVvd-ObOqTbmkXxVL5_-uzRj46sClAvAFpYzwHk130_provenance.
- NP50823.RAjSbhSSHC2aaeGblE9zmuHrjbktlKADch7RJOBmy3etY130_assertion description "[Patients with expansions in the TBP or JPH3 genes had HDL phenotypes indistinguishable from Huntington's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50823.RAjSbhSSHC2aaeGblE9zmuHrjbktlKADch7RJOBmy3etY130_provenance.
- NP50826.RAnFd4MIWN7go89uJkoj4qXgCIR0ngx9v83z0RhJ1BVRc130_assertion description "[We found one intermediate (CAG)(43) allele for SCA17 in a 44-year-old female with RLS starting at the age of 43.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50826.RAnFd4MIWN7go89uJkoj4qXgCIR0ngx9v83z0RhJ1BVRc130_provenance.
- NP50848.RAt5T0LhFpwiGo7NwvKgSPiiQygjfW7f-DPqPkH2dck-s130_assertion description "[Thus, in European Caucasoids with chronic hepatitis C, we could not demonstrate a strong association between HLA class II, TNF, and TAP gene polymorphisms and response to interferon treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50848.RAt5T0LhFpwiGo7NwvKgSPiiQygjfW7f-DPqPkH2dck-s130_provenance.
- NP50852.RAvWGDqfk3Q10BzBHhPV3ScTam_UlnxDI8990f9zAjZIA130_assertion description "[As TAP2*Bky2 had a strong linkage disequilibrium with DRB1*08032, TAP2*Bky2 or its haplotype with DRB1*08032 may be involved in SS-A/Ro antibody production not only in SS but also SLE patients, indicating that TAP2*Bky2 may be a susceptible gene not only to the disease of SS but also to the SS-A/Ro autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50852.RAvWGDqfk3Q10BzBHhPV3ScTam_UlnxDI8990f9zAjZIA130_provenance.
- NP50861.RApXrmE6cn0sKu5CbmFJdjRE83dfY2QaZ9wz0Gir0xXck130_assertion description "[These results suggest the possibility that TAP molecule play some part in formation of skin lesion, such as erythema nodosum in BD in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50861.RApXrmE6cn0sKu5CbmFJdjRE83dfY2QaZ9wz0Gir0xXck130_provenance.
- NP50867.RAvahOv6TgqH4z1yiX1DRy-0u9xSRxavQohYF3FVY8SdI130_assertion description "[TAP1 and TAP2 gene polymorphisms in childhood cystic echinococcosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50867.RAvahOv6TgqH4z1yiX1DRy-0u9xSRxavQohYF3FVY8SdI130_provenance.
- NP50868.RAtkEqvLsD3dHWCeBoxVxgvUk3trgKfqZ3YTLx_chxPcA130_assertion description "[Although TAP gene associations were generally weak, some associations (TAP2*A1/C, TAP2*C, and TAP2*B/E) with different subsets of SSc were independent of HLA-DR associations, revealing even stronger associations (TAP2*A1/C and TAP2*C) among individuals not possessing the risk HLA-DR alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50868.RAtkEqvLsD3dHWCeBoxVxgvUk3trgKfqZ3YTLx_chxPcA130_provenance.
- NP50873.RAv8cKuMuKpaGlgdOH5XzCu83Vfn60oT2oASvwz3sqHbM130_assertion description "[LMP7/TAP2 haplotype C may act as the risk factor in esophageal carcinoma development and it may influence the tumorigenesis in HPV infected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50873.RAv8cKuMuKpaGlgdOH5XzCu83Vfn60oT2oASvwz3sqHbM130_provenance.
- NP50878.RAt5EPHObPrKzRMUOpspUnKXEhbwgjkZmv5ggF2CEtQog130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50878.RAt5EPHObPrKzRMUOpspUnKXEhbwgjkZmv5ggF2CEtQog130_provenance.