Publications
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“Changes in T-lymphocytes in lung cancer patients after hyperthermic intraperitoneal chemotherapy or radiotherapy”, vol. 15, p. -, 2016.
, “Changes in T-lymphocytes in lung cancer patients after hyperthermic intraperitoneal chemotherapy or radiotherapy”, vol. 15, p. -, 2016.
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“MTHFR C677T polymorphism and osteoporotic fracture in postmenopausal women: a meta-analysis”, vol. 13, pp. 7356-7364, 2014.
, “CTLA-4 and CD86 genetic variants and haplotypes in patients with rheumatoid arthritis in southeastern China”, vol. 12, pp. 1373-1382, 2013.
, Abdallah AM, Renzoni EA, Anevlavis S, Lagan AL, et al. (2006). A polymorphism in the promoter region of the CD86 (B7.2) gene is associated with systemic sclerosis. Int. J. Immunogenet. 33: 155-161.
http://dx.doi.org/10.1111/j.1744-313X.2006.00580.x
PMid:16712644
Almasi S, Erfani N, Mojtahedi Z, Rajaee A, et al. (2006). Association of CTLA-4 gene promoter polymorphisms with systemic sclerosis in Iranian population. Genes Immun. 7: 401-406.
http://dx.doi.org/10.1038/sj.gene.6364313
PMid:16775619
Arnett FC, Edworthy SM, Bloch DA, McShane DJ, et al. (1988). The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 31: 315-324.
http://dx.doi.org/10.1002/art.1780310302
PMid:3358796
Catalan D, Aravena O, Sabugo F, Wurmann P, et al. (2010). B cells from rheumatoid arthritis patients show important alterations in the expression of CD86 and FcgammaRIIb, which are modulated by anti-tumor necrosis factor therapy. Arthritis Res. Ther. 12: R68.
http://dx.doi.org/10.1186/ar2985
PMid:20398308 PMCid:2888223
Chang JC, Liu CA, Chuang H, Ou CY, et al. (2004). Gender-limited association of cytotoxic T-lymphocyte antigen-4 (CTLA-4) polymorphism with cord blood IgE levels. Pediatr. Allergy Immunol. 15: 506-512.
http://dx.doi.org/10.1111/j.1399-3038.2004.00161.x
PMid:15610363
Fox D (2005). Etiology and Pathogenesis of Rheumatoid Arthritis. In: Arthritis and Allied Conditions (Koopman W, ed.). Lippincott Williams & Wilkins, Philadephia, 1089-1115.
Haimila K, Einarsdottir E, de Kauwe A, Koskinen LL, et al. (2009). The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency. Genes Immun. 10: 151-161.
http://dx.doi.org/10.1038/gene.2008.89
PMid:19020530
Howson JM, Walker NM, Smyth DJ and Todd JA (2009). Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families. Genes Immun. 10 (Suppl 1): S74-S84.
http://dx.doi.org/10.1038/gene.2009.96
PMid:19956106 PMCid:2810493
Jones AL, Holliday EG, Mowry BJ, McLean DE, et al. (2009). CTLA-4 single-nucleotide polymorphisms in a Caucasian population with schizophrenia. Brain Behav. Immun. 23: 347-350.
http://dx.doi.org/10.1016/j.bbi.2008.09.008
PMid:18848621
Kouki T, Gardine CA, Yanagawa T and Degroot LJ (2002). Relation of three polymorphisms of the CTLA-4 gene in patients with Graves' disease. J. Endocrinol. Invest. 25: 208-213.
PMid:11936461
Kusztal M, Kościelska-Kasprzak K, Drulis-Fajdasz D, Magott-Procelewska M, et al. (2010). The influence of CTLA-4 gene polymorphism on long-term kidney allograft function in Caucasian recipients. Transpl. Immunol. 23: 121-124.
http://dx.doi.org/10.1016/j.trim.2010.05.002
PMid:20470888
Landi D, Moreno V, Guino E, Vodicka P, et al. (2011). Polymorphisms affecting micro-RNA regulation and associated with the risk of dietary-related cancers: a review from the literature and new evidence for a functional role of rs17281995 (CD86) and rs1051690 (INSR), previously associated with colorectal cancer. Mutat. Res. 717: 109-115.
http://dx.doi.org/10.1016/j.mrfmmm.2010.10.002
PMid:20971123
Liang YL, Wu H, Li PQ, Xie XD, et al. (2011). Signal transducer and activator of transcription 4 gene polymorphisms associated with rheumatoid arthritis in Northwestern Chinese Han population. Life Sci. 89: 171-175.
http://dx.doi.org/10.1016/j.lfs.2011.05.012
PMid:21683716
Ligers A, Teleshova N, Masterman T, Huang WX, et al. (2001). CTLA-4 gene expression is influenced by promoter and exon 1 polymorphisms. Genes Immun. 2: 145-152.
http://dx.doi.org/10.1038/sj.gene.6363752
PMid:11426323
Liu MF, Kohsaka H, Sakurai H, Azuma M, et al. (1996). The presence of costimulatory molecules CD86 and CD28 in rheumatoid arthritis synovium. Arthritis Rheum. 39: 110-114.
http://dx.doi.org/10.1002/art.1780390115
PMid:8546719
Liu Y, Liang WB, Gao LB, Pan XM, et al. (2010). CTLA4 and CD86 gene polymorphisms and susceptibility to chronic obstructive pulmonary disease. Hum. Immunol. 71: 1141-1146.
http://dx.doi.org/10.1016/j.humimm.2010.08.007
PMid:20732370
Magistrelli G, Jeannin P, Herbault N, Benoit De CA, et al. (1999). A soluble form of CTLA-4 generated by alternative splicing is expressed by nonstimulated human T cells. Eur. J. Immunol. 29: 3596-3602.
http://dx.doi.org/10.1002/(SICI)1521-4141(199911)29:11<3596::AID-IMMU3596>3.0.CO;2-Y
Marin LA, Moya-Quiles MR, Miras M, Muro M, et al. (2005). Evaluation of CD86 gene polymorphism at +1057 position in liver transplant recipients. Transpl. Immunol. 15: 69-74.
http://dx.doi.org/10.1016/j.trim.2005.04.003
PMid:16223675
Matsushita M, Tsuchiya N, Oka T, Yamane A, et al. (2000). New polymorphisms of human CD80 and CD86: lack of association with rheumatoid arthritis and systemic lupus erythematosus. Genes Immun. 1: 428-434.
http://dx.doi.org/10.1038/sj.gene.6363704
PMid:11196673
Maurer M, Loserth S, Kolb-Maurer A, Ponath A, et al. (2002). A polymorphism in the human cytotoxic T-lymphocyte antigen 4 (CTLA4) gene (exon 1 +49) alters T-cell activation. Immunogenetics 54: 1-8.
http://dx.doi.org/10.1007/s00251-002-0429-9
PMid:11976786
Orozco G, Rueda B and Martin J (2006). Genetic basis of rheumatoid arthritis. Biomed. Pharmacother. 60: 656-662.
http://dx.doi.org/10.1016/j.biopha.2006.09.003
PMid:17055211
Pawlak E, Karabon L, Wlodarska-Polinska I, Jedynak A, et al. (2010). Influence of CTLA-4/CD28/ICOS gene polymorphisms on the susceptibility to cervical squamous cell carcinoma and stage of differentiation in the Polish population. Hum. Immunol. 71: 195-200.
http://dx.doi.org/10.1016/j.humimm.2009.11.006
PMid:19913589
Plant D, Flynn E, Mbarek H, Dieude P, et al. (2010). Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers. Ann. Rheum. Dis. 69: 1548-1553.
http://dx.doi.org/10.1136/ard.2009.121020
PMid:20498205 PMCid:2938898
Rai E and Wakeland EK (2011). Genetic predisposition to autoimmunity - what have we learned? Semin. Immunol. 23: 67-83.
http://dx.doi.org/10.1016/j.smim.2011.01.015
PMid:21288738
Scalapino KJ and Daikh DI (2008). CTLA-4: a key regulatory point in the control of autoimmune disease. Immunol. Rev. 223: 143-155.
http://dx.doi.org/10.1111/j.1600-065X.2008.00639.x
PMid:18613834
Sharpe AH and Freeman GJ (2002). The B7-CD28 superfamily. Nat. Rev. Immunol. 2: 116-126.
http://dx.doi.org/10.1038/nri727
PMid:11910893
Sole X, Guino E, Valls J, Iniesta R, et al. (2006). SNPStats: a web tool for the analysis of association studies. Bioinformatics 22: 1928-1929.
http://dx.doi.org/10.1093/bioinformatics/btl268
PMid:16720584
Su TH, Chang TY, Lee YJ, Chen CK, et al. (2007). CTLA-4 gene and susceptibility to human papillomavirus-16- associated cervical squamous cell carcinoma in Taiwanese women. Carcinogenesis 28: 1237-1240.
http://dx.doi.org/10.1093/carcin/bgm043
PMid:17341658
Tivol EA, Borriello F, Schweitzer AN, Lynch WP, et al. (1995). Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity 3: 541-547.
http://dx.doi.org/10.1016/1074-7613(95)90125-6
Wang XB, Zhao X, Giscombe R and Lefvert AK (2002). A CTLA-4 gene polymorphism at position -318 in the promoter region affects the expression of protein. Genes Immun. 3: 233-234.
http://dx.doi.org/10.1038/sj.gene.6363869
PMid:12058260
Yadav D and Sarvetnick N (2007). B7-2 regulates survival, phenotype, and function of APCs. J. Immunol. 178: 6236- 6241.
PMid:17475851
Zaletel K, Krhin B, Gaberscek S and Hojker S (2006). Thyroid autoantibody production is influenced by exon 1 and promoter CTLA-4 polymorphisms in patients with Hashimoto's thyroiditis. Int. J. Immunogenet. 33: 87-91.
http://dx.doi.org/10.1111/j.1744-313X.2006.00574.x
PMid:16611252
“Novel single nucleotide polymorphisms of the bovine methyltransferase 3b gene and their association with meat quality traits in beef cattle”, vol. 11, pp. 2569-2577, 2012.
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Amara K, Ziadi S, Hachana M, Soltani N, et al. (2010). DNA methyltransferase DNMT3b protein overexpression as a prognostic factor in patients with diffuse large B-cell lymphomas. Cancer Sci. 101: 1722-1730.
http://dx.doi.org/10.1111/j.1349-7006.2010.01569.x
PMid:20398054
Barres R and Zierath JR (2011). DNA methylation in metabolic disorders. Am. J. Clin. Nutr. 93: 897S-900.
http://dx.doi.org/10.3945/ajcn.110.001933
PMid:21289222
de Vogel S, Wouters KA, Gottschalk RW, van Schooten FJ, et al. (2011). Dietary methyl donors, methyl metabolizing enzymes, and epigenetic regulators: diet-gene interactions and promoter CpG island hypermethylation in colorectal cancer. Cancer Causes Control 22: 1-12.
http://dx.doi.org/10.1007/s10552-010-9659-6
PMid:20960050 PMCid:3002163
Fan YY, Zan LS, Wang HB and Yang YJ (2010). Study on the relationship between polymorphism of PLIN gene and carcass and meat quality traits in Qinchuan cattle. Chin. J. Anim. Vet. Sci. 41: 268-273.
Fraga MF, Ballestar E, Paz MF, Ropero S, et al. (2005). Epigenetic differences arise during the lifetime of monozygotic twins. Proc. Natl. Acad. Sci. U. S. A. 102: 10604-10609.
http://dx.doi.org/10.1073/pnas.0500398102
PMid:16009939 PMCid:1174919
Guo X, Liu X, Xu X, Wu M, et al. (2012). The expression levels of DNMT3a/3b and their relationship with meat quality in beef cattle. Mol. Biol. Rep. 39: 5473-5479.
http://dx.doi.org/10.1007/s11033-011-1349-2
PMid:22193622
Haggarty P, Hoad G, Harris SE, Starr JM, et al. (2010). Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking. PLoS One 5: e11329.
http://dx.doi.org/10.1371/journal.pone.0011329
PMid:20593030 PMCid:2892514
Halaschek-Wiener J, Amirabbasi-Beik M, Monfared N, Pieczyk M, et al. (2009). Genetic variation in healthy oldest-old. PLoS One 4: e6641.
http://dx.doi.org/10.1371/journal.pone.0006641
PMid:19680556 PMCid:2722017
Hoey AJ, Reich MM, Davis G, Shorthose R, et al. (1995). Beta 2-adrenoceptor densities do not correlate with growth, carcass quality, or meat quality in cattle. J. Anim. Sci. 73: 3281-3286.
PMid:8586585
Ji AG, Zhou ZK, Zhang LP, Yang RJ, et al. (2009). PON1 gene SNPs and association with growth and carcass traits in beef cattle. Acta Vet. Zootechnica Sin. 40: 122-128.
Kamei Y, Suganami T, Ehara T, Kanai S, et al. (2010). Increased expression of DNA methyltransferase 3a in obese adipose tissue: studies with transgenic mice. Obesity 18: 314-321.
http://dx.doi.org/10.1038/oby.2009.246
PMid:19680236
Kurita S, Higuchi H, Saito Y, Nakamoto N, et al. (2010). DNMT1 and DNMT3b silencing sensitizes human hepatoma cells to TRAIL-mediated apoptosis via up-regulation of TRAIL-R2/DR5 and caspase-8. Cancer Sci. 101: 1431-1439.
http://dx.doi.org/10.1111/j.1349-7006.2010.01565.x
PMid:20398055
Li WF, Yang RJ, Gan QF, Zhang LP, et al. (2009). Polymorphism of PRKAG3 gene and Its association with carcass and meat quality traits in beef cattle. Acta Vet. Zootechnica Sin. 40: 1106-1111.
Liu Y, Li K, Liu WJ, Wang JF, et al. (2009). Study on the effect of down-regulation of DNMT1 on cell proliferation, metastasis ability of esophageal squamous cell carcinoma cell line EC9706 cells and its related mechanisms. China Oncol. 19: 826-830.
Maier S and Olek A (2002). Diabetes: a candidate disease for efficient DNA methylation profiling. J. Nutr. 132: 2440S-2443S.
PMid:12163708
Okano M, Bell DW, Haber DA and Li E (1999). DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 99: 247-257.
http://dx.doi.org/10.1016/S0092-8674(00)81656-6
Page BT, Casas E, Heaton MP, Cullen NG, et al. (2002). Evaluation of single-nucleotide polymorphisms in CAPN1 for association with meat tenderness in cattle. J. Anim. Sci. 80: 3077-3085.
PMid:12542147
Tidball JG and Spencer MJ (2002). Expression of a calpastatin transgene slows muscle wasting and obviates changes in myosin isoform expression during murine muscle disuse. J. Physiol. 545: 819-828.
http://dx.doi.org/10.1113/jphysiol.2002.024935
PMid:12482888 PMCid:2290726
Turek-Plewa J and Jagodzinski PP (2005). The role of mammalian DNA methyltransferases in the regulation of gene expression. Cell Mol. Biol. Lett. 10: 631-647.
PMid:16341272
Wang X, Zhu H, Snieder H, Su S, et al. (2010). Obesity related methylation changes in DNA of peripheral blood leukocytes. BMC Med. 8: 87.
http://dx.doi.org/10.1186/1741-7015-8-87
PMid:21176133 PMCid:3016263
Yu Y, Zhang H, Tian F, Zhang W, et al. (2008). An integrated epigenetic and genetic analysis of DNA methyltransferase genes (DNMTs) in tumor resistant and susceptible chicken lines. PLoS One 3: e2672.
http://dx.doi.org/10.1371/journal.pone.0002672
PMid:18648519 PMCid:2481300