Publications
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“Aldehyde dehydrogenase 2 protects human umbilical vein endothelial cells against oxidative damage and increases endothelial nitric oxide production to reverse nitroglycerin tolerance”, vol. 15, p. -, 2016.
, “Aldehyde dehydrogenase 2 protects human umbilical vein endothelial cells against oxidative damage and increases endothelial nitric oxide production to reverse nitroglycerin tolerance”, vol. 15, p. -, 2016.
, “Association between C677T and A1298C polymorphisms of the MTHFR gene and risk of male infertility: a meta-analysis”, vol. 15, p. -, 2016.
, “Association between C677T and A1298C polymorphisms of the MTHFR gene and risk of male infertility: a meta-analysis”, vol. 15, p. -, 2016.
, “Association between C677T and A1298C polymorphisms of the MTHFR gene and risk of male infertility: a meta-analysis”, vol. 15, p. -, 2016.
, “Effect of uric acid on mitochondrial function and oxidative stress in hepatocytes”, vol. 15, p. -, 2016.
, “Effect of uric acid on mitochondrial function and oxidative stress in hepatocytes”, vol. 15, p. -, 2016.
, “Enhancement of pectinase production by ultraviolet irradiation and diethyl sulfate mutagenesis of a Fusarium oxysporum isolate”, vol. 15, p. -, 2016.
, “Enhancement of pectinase production by ultraviolet irradiation and diethyl sulfate mutagenesis of a Fusarium oxysporum isolate”, vol. 15, p. -, 2016.
, “A functional insertion/deletion polymorphism in the IL1A gene is associated with decreased risk of breast cancer”, vol. 15, p. -, 2016.
, “A functional insertion/deletion polymorphism in the IL1A gene is associated with decreased risk of breast cancer”, vol. 15, p. -, 2016.
, “JNK pathway and relative transcriptional factor were involved in ginsenoside Rh2-mediated G1 growth arrest and apoptosis in human lung adenocarcinoma A549 cells”, vol. 15, p. -, 2016.
, “JNK pathway and relative transcriptional factor were involved in ginsenoside Rh2-mediated G1 growth arrest and apoptosis in human lung adenocarcinoma A549 cells”, vol. 15, p. -, 2016.
, “MTHFR C677T and A1298C polymorphisms and risk of lung cancer: a comprehensive evaluation”, vol. 15, p. -, 2016.
, “MTHFR C677T and A1298C polymorphisms and risk of lung cancer: a comprehensive evaluation”, vol. 15, p. -, 2016.
, “MTHFR C677T and A1298C polymorphisms and risk of lung cancer: a comprehensive evaluation”, vol. 15, p. -, 2016.
, “Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome”, vol. 15, p. -, 2016.
, “Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome”, vol. 15, p. -, 2016.
, “Overexpression of NaKR3 enhances salt tolerance in Arabidopsis”, vol. 15, p. -, 2016.
, “Overexpression of NaKR3 enhances salt tolerance in Arabidopsis”, vol. 15, p. -, 2016.
, “Association of a let-7 KRAS rs712 polymorphism with the risk of breast cancer”, vol. 14, pp. 16913-16920, 2015.
, “Association of TCF7L2 gene polymorphisms with susceptibility to type 2 diabetes mellitus in a Chinese Hui population”, vol. 14, pp. 10064-10071, 2015.
, “Characterization and significance of MUC1 and c-myc expression in elderly patients with papillary thyroid carcinoma”, vol. 14, pp. 15325-15330, 2015.
, “A cytological study of anther and pollen development in Camellia oleifera”, vol. 14, pp. 8755-8765, 2015.
, “Development of simple sequence repeat markers in persimmon (Diospyros L.) and their potential use in related species”, vol. 14, pp. 609-618, 2015.
, “Forkhead box protein O1 mediates apoptosis in a cancer cervical cell line treated with the antitumor agent tumor necrosis factor-α”, vol. 14, pp. 7446-7454, 2015.
, “Functional characterization and analysis of the Arabidopsis UGT71C5 promoter region”, vol. 14, pp. 19173-19183, 2015.
, “Gene annotation and functional analysis of a newly sequenced Synechococcus strain”, vol. 14, pp. 12416-12426, 2015.
, “Identification of genes and pathways related to lipopolysaccharide signaling in duckling spleens”, vol. 14, pp. 17312-17321, 2015.
, “Microbial diversity in Paris polyphylla var. yunnanensis rhizomes of varying ages”, vol. 14, pp. 17612-17621, 2015.
, “Partial least squares-based gene expression analysis in preeclampsia”, vol. 14, pp. 6598-6604, 2015.
, “Potassium contributes to zinc stress tolerance in peach (Prunus persica) seedlings by enhancing photosynthesis and the antioxidant defense system”, vol. 14, pp. 8338-8351, 2015.
, “VDAC2 involvement in the stress response pathway in Arabidopsis thaliana”, vol. 14, pp. 15511-15519, 2015.
, “Association of VDR polymorphisms with type 2 diabetes mellitus in Chinese Han and Hui populations”, vol. 13, pp. 9588-9598, 2014.
, “Effect of CYP2C9*3 mutant variants on meloxicam pharmacokinetics in a healthy Chinese population”, vol. 13, pp. 831-837, 2014.
, “Effect of miR-146a polymorphism on biochemical recurrence risk after radical prostatectomy in southern Chinese population”, vol. 13, pp. 10615-10621, 2014.
, “An elevated plasma level of visfatin increases the risk of myocardial infarction”, vol. 13, pp. 8586-8595, 2014.
, “Polymorphisms of +2836 G>A in the apoE gene are strongly associated with the susceptibility to essential hypertension in the Chinese Hui population”, vol. 13, pp. 1212-1219, 2014.
, “Proteomics comparison of the sera from multiple sclerosis patients and neuromyelitis optica patients”, vol. 13, pp. 9292-9299, 2014.
, “Separation, purification, and identification of flagellin, and preparation of its antisera”, vol. 13, pp. 9161-9170, 2014.
, “Association of insulin growth factor-1 receptor gene polymorphisms with genetic susceptibility to idiopathic short stature”, vol. 12, pp. 4768-4779, 2013.
, “Characterization and molecular mapping of a dwarf mutant in wheat”, vol. 12, pp. 3555-3565, 2013.
, “Clinical value of surfactant protein-A in serum and sputum for pulmonary tuberculosis diagnosis”, vol. 12, pp. 4918-4924, 2013.
, “Identification of a novel human testicular interstitial gene, RNF148, and its expression regulated by histone deacetylases”, vol. 12, pp. 4060-4069, 2013.
, “MicroRNA expression profiling studies on bronchopulmonary dysplasia: a systematic review and meta-analysis”, vol. 12, pp. 5195-5206, 2013.
, , “A common genetic variant of 5p15.33 is associated with risk for prostate cancer in the Chinese population”, vol. 11, pp. 1349-1356, 2012.
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Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, et al. (2009). Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat. Genet. 41: 986-990.
http://dx.doi.org/10.1038/ng.429
PMid:19648918 PMCid:2839871
Crawford ED (2003). Epidemiology of prostate cancer. Urology 62: 3-12.
http://dx.doi.org/10.1016/j.urology.2003.10.013
PMid:14706503
Dennis LK, Lynch CF and Torner JC (2002). Epidemiologic association between prostatitis and prostate cancer. Urology 60: 78-83.
http://dx.doi.org/10.1016/S0090-4295(02)01637-0
Gleason DF and Mellinger GT (1974). Prediction of prognosis for prostatic adenocarcinoma by combined histological grading and clinical staging. J. Urol. 111: 58-64.
PMid:4813554
Gudmundsson J, Sulem P, Manolescu A, Amundadottir LT, et al. (2007). Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat. Genet. 39: 631-637.
http://dx.doi.org/10.1038/ng1999
PMid:17401366
Jemal A, Siegel R, Ward E, Hao Y, et al. (2009). Cancer statistics, 2009. CA Cancer J. Clin. 59: 225-249.
http://dx.doi.org/10.3322/caac.20006
PMid:19474385
Jemal A, Bray F, Center MM, Ferlay J, et al. (2011). Global cancer statistics. CA Cancer J. Clin. 61: 69-90.
http://dx.doi.org/10.3322/caac.20107
PMid:21296855
Kiemeney LA, Thorlacius S, Sulem P, Geller F, et al. (2008). Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nat. Genet. 40: 1307-1312.
http://dx.doi.org/10.1038/ng.229
PMid:18794855
Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, et al. (2000). Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland. N. Engl. J. Med. 343: 78-85.
http://dx.doi.org/10.1056/NEJM200007133430201
PMid:10891514
Mandal RK, Kapoor R and Mittal RD (2010). Polymorphic variants of DNA repair gene XRCC3 and XRCC7 and risk of prostate cancer: a study from North Indian population. DNA Cell Biol. 29: 669-674.
http://dx.doi.org/10.1089/dna.2010.1047
PMid:20590474
McCracken M, Olsen M, Chen MS Jr, Jemal A, et al. (2007). Cancer incidence, mortality, and associated risk factors among Asian Americans of Chinese, Filipino, Vietnamese, Korean, and Japanese ethnicities. CA Cancer J. Clin. 57: 190-205.
http://dx.doi.org/10.3322/canjclin.57.4.190
PMid:17626117
McKay JD, Hung RJ, Gaborieau V, Boffetta P, et al. (2008). Lung cancer susceptibility locus at 5p15.33. Nat. Genet. 40: 1404-1406.
http://dx.doi.org/10.1038/ng.254
PMid:18978790 PMCid:2748187
Rafnar T, Sulem P, Stacey SN, Geller F, et al. (2009). Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nat. Genet. 41: 221-227.
http://dx.doi.org/10.1038/ng.296
PMid:19151717
Rodriguez C, Calle EE, Miracle-McMahill HL, Tatham LM, et al. (1997). Family history and risk of fatal prostate cancer. Epidemiology 8: 653-657.
PMid:9345665
Schaid DJ (2004). The complex genetic epidemiology of prostate cancer. Hum. Mol. Genet. 13 (Spec No. 1): R103-R121.
Truong T, Hung RJ, Amos CI, Wu X, et al. (2010). Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. J. Natl. Cancer Inst. 102: 959-971.
http://dx.doi.org/10.1093/jnci/djq178
PMid:20548021 PMCid:2897877
Yang P, Li Y, Jiang R, Cunningham JM, et al. (2010). A rigorous and comprehensive validation: common genetic variations and lung cancer. Cancer Epidemiol. Biomark. Prev. 19: 240-244.
http://dx.doi.org/10.1158/1055-9965.EPI-09-0710
PMid:20056643 PMCid:2805461
Yeager M, Orr N, Hayes RB, Jacobs KB, et al. (2007). Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat. Genet. 39: 645-649.
http://dx.doi.org/10.1038/ng2022
PMid:17401363
“Increased expression of a novel splice variant of the complement component 4 (C4A) gene in mastitis-infected dairy cattle”, vol. 11, pp. 2909-2916, 2012.
,
Andersson L, Lunden A, Sigurdardottir S, Davies CJ, et al. (1988). Linkage relationships in the bovine MHC region. High recombination frequency between class II subregions. Immunogenetics 27: 273-280.
http://dx.doi.org/10.1007/BF00376122
PMid:2894354
Ast G (2004). How did alternative splicing evolve? Nat. Rev. Genet. 5: 773-782.
http://dx.doi.org/10.1038/nrg1451
PMid:15510168
Awdeh ZL and Alper CA (1980). Inherited structural polymorphism of the fourth component of human complement. Proc. Natl. Acad. Sci. U. S. A. 77: 3576-3580.
http://dx.doi.org/10.1073/pnas.77.6.3576
PMid:6932037 PMCid:349660
Belt KT, Yu CY, Carroll MC and Porter RR (1985). Polymorphism of human complement component C4. Immunogenetics 21: 173-180.
http://dx.doi.org/10.1007/BF00364869
PMid:3838531
Bradley A (2002). Bovine mastitis: an evolving disease. Vet. J. 164: 116-128.
http://dx.doi.org/10.1053/tvjl.2002.0724
PMid:12359466
Chacko E and Ranganathan S (2009). Genome-wide analysis of alternative splicing in cow: implications in bovine as a model for human diseases. BMC Genomics 10 (Suppl 3): S11.
http://dx.doi.org/10.1186/1471-2164-10-S3-S11
PMid:19958474 PMCid:2788363
Cox BJ and Robins DM (1988). Tissue-specific variation in C4 and Slp gene regulation. Nucleic Acids Res. 16: 6857-6870.
http://dx.doi.org/10.1093/nar/16.14.6857
PMid:3405752 PMCid:338338
Dahl MR, Thiel S, Matsushita M, Fujita T, et al. (2001). MASP-3 and its association with distinct complexes of the mannan-binding lectin complement activation pathway. Immunity 15: 127-135.
http://dx.doi.org/10.1016/S1074-7613(01)00161-3
Dodds AW and Law SK (1990). The complement component C4 of mammals. Biochem. J. 265: 495-502.
PMid:2302180 PMCid:1136911
Galante PA, Sakabe NJ, Kirschbaum-Slager N and de Souza SJ (2004). Detection and evaluation of intron retention events in the human transcriptome. RNA 10: 757-765.
http://dx.doi.org/10.1261/rna.5123504
PMid:15100430 PMCid:1370565
Garcia-Blanco MA, Baraniak AP and Lasda EL (2004). Alternative splicing in disease and therapy. Nat. Biotechnol. 22: 535-546.
http://dx.doi.org/10.1038/nbt964
PMid:15122293
Giles CM (1984). A new genetic variant for Chido. Vox Sang. 46: 149-156.
http://dx.doi.org/10.1111/j.1423-0410.1984.tb00067.x
PMid:6710967
Guerra-Junior G, Grumach AS, de Lemos-Marini SH, Kirschfink M, et al. (2008). Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency. Clin. Exp. Immunol. 155: 182-188.
http://dx.doi.org/10.1111/j.1365-2249.2008.03838.x
PMid:19137635 PMCid:2675248
Günther J, Koczan D, Yang W, Nurnberg G, et al. (2009). Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge with Escherichia coli. Vet. Res. 40: 31.
http://dx.doi.org/10.1051/vetres/2009014
PMid:19321125 PMCid:2695127
Hull J, Campino S, Rowlands K, Chan MS, et al. (2007). Identification of common genetic variation that modulates alternative splicing. PLoS Genet. 3: e99.
http://dx.doi.org/10.1371/journal.pgen.0030099
PMid:17571926 PMCid:1904363
Ju Z, Wang C, Li Q, Hou M, et al. (2011). Alternative splicing and mRNA expression analysis of bovine SLAMF7 gene in healthy and mastitis mammary tissues. Mol. Biol. Rep. DOI: 10.1007/s11033-011-1198-z.
http://dx.doi.org/10.1007/s11033-011-1198-z
Keren H, Lev-Maor G and Ast G (2010). Alternative splicing and evolution: diversification, exon definition and function. Nat. Rev. Genet. 11: 345-355.
http://dx.doi.org/10.1038/nrg2776
PMid:20376054
Kim E, Magen A and Ast G (2007). Different levels of alternative splicing among eukaryotes. Nucleic Acids Res. 35: 125-131.
http://dx.doi.org/10.1093/nar/gkl924
PMid:17158149 PMCid:1802581
Larionov A, Krause A and Miller W (2005). A standard curve based method for relative real time PCR data processing. BMC Bioinformatics 6: 62.
http://dx.doi.org/10.1186/1471-2105-6-62
PMid:15780134 PMCid:1274258
Le Hir H, Charlet-Berguerand N, de Franciscis V and Thermes C (2002). 5'-End RET splicing: absence of variants in normal tissues and intron retention in pheochromocytomas. Oncology 63: 84-91.
http://dx.doi.org/10.1159/000065725
PMid:12187076
Liu HX, Cartegni L, Zhang MQ and Krainer AR (2001). A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes. Nat. Genet. 27: 55-58.
http://dx.doi.org/10.1038/83762
PMid:11137998
Morera AL, Henry M, Garcia-Hernandez A and Fernandez-Lopez L (2007). Acute phase proteins as biological markers of negative psychopathology in paranoid schizophrenia. Actas Esp. Psiquiatr. 35: 249-252.
PMid:17592787
Pattanakitsakul S, Zheng JH, Natsuume-Sakai S, Takahashi M, et al. (1992). Aberrant splicing caused by the insertion of the B2 sequence into an intron of the complement C4 gene is the basis for low C4 production in H-2k mice. J. Biol. Chem. 267: 7814-7820.
PMid:1373139
Petri M, Watson R, Winkelstein JA and McLean RH (1993). Clinical expression of systemic lupus erythematosus in patients with C4A deficiency. Medicine 72: 236-244.
http://dx.doi.org/10.1097/00005792-199307000-00003
PMid:8341140
Rainard P and Poutrel B (1995). Deposition of complement components on Streptococcus agalactiae in bovine milk in the absence of inflammation. Infect. Immun. 63: 3422-3427.
PMid:7642272 PMCid:173471
Rio DC (1991). Regulation of Drosophila P element transposition. Trends Genet. 7: 282-287.
PMid:1662417
Rupp R and Boichard D (2003). Genetics of resistance to mastitis in dairy cattle. Vet. Res. 34: 671-688.
http://dx.doi.org/10.1051/vetres:2003020
PMid:14556700
Vergani D, Johnston C, Abdullah N and Barnett AH (1983). Low serum C4 concentrations: an inherited predisposition to insulin dependent diabetes? Br. Med. J. 286: 926-928.
http://dx.doi.org/10.1136/bmj.286.6369.926
Wang Z, Zhang S and Wang G (2008). Response of complement expression to challenge with lipopolysaccharide in embryos/larvae of zebrafish Danio rerio: acquisition of immunocompetent complement. Fish Shellfish Immunol. 25: 264-270.
http://dx.doi.org/10.1016/j.fsi.2008.05.010
PMid:18657447
Witte DP, Welch TR and Beischel LS (1991). Detection and cellular localization of human C4 gene expression in the renal tubular epithelial cells and other extrahepatic epithelial sources. Am. J. Pathol. 139: 717-724.
PMid:1928296 PMCid:1886325
Yang Y, Chung EK, Zhou B, Blanchong CA, et al. (2003). Diversity in intrinsic strengths of the human complement system: serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index. J. Immunol. 171: 2734-2745.
PMid:12928427
Yu CY, Belt KT, Giles CM, Campbell RD, et al. (1986). Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity. EMBO J. 5: 2873-2881.
PMid:2431902 PMCid:1167237
“Lack of an association between TSC gene Arg904Gln polymorphisms and essential hypertension risk based on a meta-analysis”, vol. 11, pp. 3511-3517, 2012.
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Capewell S, Ford ES, Croft JB, Critchley JA, et al. (2010). Cardiovascular risk factor trends and potential for reducing coronary heart disease mortality in the United States of America. Bull. World Health Organ. 88: 120-130.
http://dx.doi.org/10.2471/BLT.08.057885
PMid:20428369 PMCid:2814476
Chang PY, Zhao LG and Su XL (2011). Association of TSC gene variants and hypertension in Mongolian and Han populations. Genet. Mol. Res. 10: 902-909.
http://dx.doi.org/10.4238/vol10-2gmr1227
PMid:21644207
Fu L, Zhao Y, Wu X, Liu H, et al. (2011). CYP7A1 genotypes and haplotypes associated with hypertension in an obese Han Chinese population. Hypertens. Res. 34: 722-727.
http://dx.doi.org/10.1038/hr.2011.18
PMid:21346769
Glorioso N, Filigheddu F, Troffa C, Soro A, et al. (2001). Interaction of a(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension. Hypertension 38: 204-209.
http://dx.doi.org/10.1161/01.HYP.38.2.204
PMid:11509477
Hasi T, Hao L, Yang L and Su XL (2011). Acetaldehyde dehydrogenase 2 SNP rs671 and susceptibility to essential hypertension in Mongolians: a case control study. Genet. Mol. Res. 10: 537-543.
http://dx.doi.org/10.4238/vol10-1gmr1056
PMid:21476199
Johnson AD, Newton-Cheh C, Chasman DI, Ehret GB, et al. (2011). Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. Hypertension 57: 903-910.
http://dx.doi.org/10.1161/HYPERTENSIONAHA.110.158667
PMid:21444836 PMCid:3099407
Little J, Bradley L, Bray MS, Clyne M, et al. (2002). Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations. Am. J. Epidemiol. 156: 300-310.
http://dx.doi.org/10.1093/oxfordjournals.aje.a000179
PMid:12181099
Luo F, Wang Y, Wang X, Sun K, et al. (2009). A functional variant of NEDD4L is associated with hypertension, antihypertensive response, and orthostatic hypotension. Hypertension 54: 796-801.
http://dx.doi.org/10.1161/HYPERTENSIONAHA.109.135103
PMid:19635985
Matsuo A, Katsuya T, Ishikawa K, Sugimoto K, et al. (2004). G2736A polymorphism of thiazide-sensitive Na-Cl cotransporter gene predisposes to hypertension in young women. J. Hypertens. 22: 2123-2127.
http://dx.doi.org/10.1097/00004872-200411000-00014
PMid:15480096
Melander O, Orho-Melander M, Bengtsson K, Lindblad U, et al. (2000). Genetic variants of thiazide-sensitive NaClcotransporter in gitelman's syndrome and primary hypertension. Hypertension 36: 389-394.
http://dx.doi.org/10.1161/01.HYP.36.3.389
PMid:10988270
Niu W, Wu S, Zhang Y, Li W, et al. (2010). Validation of genetic association in apelin-AGTRL1 system with hypertension in a larger Han Chinese population. J. Hypertens. 28: 1854-1861.
http://dx.doi.org/10.1097/HJH.0b013e32833b1fad
PMid:20485192
Plotkin MD, Kaplan MR, Verlander JW, Lee WS, et al. (1996). Localization of the thiazide sensitive Na-Cl cotransporter, rTSC1 in the rat kidney. Kidney Int. 50: 174-183.
http://dx.doi.org/10.1038/ki.1996.300
PMid:8807586
Shimodaira M, Nakayama T, Sato N, Naganuma T, et al. (2010). Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension. Am. J. Hypertens. 23: 547-555.
http://dx.doi.org/10.1038/ajh.2010.16
PMid:20186130
Song Y, Herrera VL, Filigheddu F, Troffa C, et al. (2001). Non-association of the thiazide-sensitive Na,Cl-cotransporter gene with polygenic hypertension in both rats and humans. J. Hypertens. 19: 1547-1551.
http://dx.doi.org/10.1097/00004872-200109000-00005
PMid:11564973
Stanton JL, Braitman LE, Riley AM Jr, Khoo CS, et al. (1982). Demographic, dietary, life style, and anthropometric correlates of blood pressure. Hypertension 4: III135-III142.
PMid:7106943
Tabara Y, Kohara K, Kita Y, Hirawa N, et al. (2010). Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project. Hypertension 56: 973-980.
http://dx.doi.org/10.1161/HYPERTENSIONAHA.110.153429
PMid:20921432
Wang XF, Lin RY, Wang SZ, Zhang LP, et al. (2008). Association study of variants in two ion-channel genes (TSC and CLCNKB) and hypertension in two ethnic groups in Northwest China. Clin. Chim. Acta 388: 95-98.
http://dx.doi.org/10.1016/j.cca.2007.10.017
PMid:17997379
Ward NC, Tsai IJ, Barden A, van Bockxmeer FM, et al. (2008). A single nucleotide polymorphism in the CYP4F2 but not CYP4A11 gene is associated with increased 20-HETE excretion and blood pressure. Hypertension 51: 1393-1398.
http://dx.doi.org/10.1161/HYPERTENSIONAHA.107.104463
PMid:18391101
Zhan YY, Jiang X, Lin G, Li J, et al. (2007). Association of thiazide-sensitive Na+-Cl* cotransporter gene polymorphisms with the risk of essential hypertension. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 24: 703-705.
PMid:18067089
“Meta-analysis confirms that a common G/C variant in the pre-miR-146a gene contributes to cancer susceptibility and that ethnicity, gender and smoking status are risk factors”, vol. 11, pp. 3051-3062, 2012.
,
Akkiz H, Bayram S, Bekar A, Akgollu E, et al. (2011). No association of pre-microRNA-146a rs2910164 polymorphism and risk of hepatocellular carcinoma development in Turkish population: a case-control study. Gene 486: 104-109.
http://dx.doi.org/10.1016/j.gene.2011.07.006
PMid:21807077
Ambros V (2004). The functions of animal microRNAs. Nature 431: 350-355.
http://dx.doi.org/10.1038/nature02871
PMid:15372042
Bartel DP (2004). MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116: 281-297.
http://dx.doi.org/10.1016/S0092-8674(04)00045-5
Bentwich I, Avniel A, Karov Y, Aharonov R, et al. (2005). Identification of hundreds of conserved and nonconserved human microRNAs. Nat. Genet. 37: 766-770.
http://dx.doi.org/10.1038/ng1590
PMid:15965474
Bhaumik D, Scott GK, Schokrpur S, Patil CK, et al. (2008). Expression of microRNA-146 suppresses NF-kappaB activity with reduction of metastatic potential in breast cancer cells. Oncogene 27: 5643-5647.
http://dx.doi.org/10.1038/onc.2008.171
PMid:18504431 PMCid:2811234
Bond GL and Levine AJ (2007). A single nucleotide polymorphism in the p53 pathway interacts with gender, environmental stresses and tumor genetics to influence cancer in humans. Oncogene 26: 1317-1323.
http://dx.doi.org/10.1038/sj.onc.1210199
PMid:17322917
Catucci I, Yang R, Verderio P, Pizzamiglio S, et al. (2010). Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases. Hum. Mutat. 31: E1052-E1057.
http://dx.doi.org/10.1002/humu.21141
PMid:19847796
Gao LB, Bai P, Pan XM, Jia J, et al. (2011). The association between two polymorphisms in pre-miRNAs and breast cancer risk: a meta-analysis. Breast Cancer Res. Treat. 125: 571-574.
http://dx.doi.org/10.1007/s10549-010-0993-x
PMid:20640596
Garcia AI, Cox DG, Barjhoux L, Verny-Pierre C, et al. (2011). The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Hum Mutat. DOI 10.1002/humu.21539.
http://dx.doi.org/10.1002/humu.21539
George GP, Gangwar R, Mandal RK, Sankhwar SN, et al. (2011). Genetic variation in microRNA genes and prostate cancer risk in North Indian population. Mol. Biol. Rep. 38: 1609-1615.
http://dx.doi.org/10.1007/s11033-010-0270-4
PMid:20842445
Guo H, Wang K, Xiong G, Hu H, et al. (2010). A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han. Fam. Cancer 9: 599-603.
http://dx.doi.org/10.1007/s10689-010-9370-5
PMid:20680470
Hecht SS (2002). Cigarette smoking and lung cancer: chemical mechanisms and approaches to prevention. Lancet Oncol. 3: 461-469.
http://dx.doi.org/10.1016/S1470-2045(02)00815-X
Hirschhorn JN, Lohmueller K, Byrne E and Hirschhorn K (2002). A comprehensive review of genetic association studies. Genet. Med. 4: 45-61.
http://dx.doi.org/10.1097/00125817-200203000-00002
PMid:11882781
Hishida A, Matsuo K, Goto Y, Naito M, et al. (2011). Combined effect of miR-146a rs2910164 G/C polymorphism and Toll-like receptor 4 +3725 G/C polymorphism on the risk of severe gastric atrophy in Japanese. Dig. Dis. Sci. 56: 1131-1137.
http://dx.doi.org/10.1007/s10620-010-1376-1
PMid:20721625
Hoffman AE, Zheng T, Yi C, Leaderer D, et al. (2009). microRNA miR-196a-2 and breast cancer: a genetic and epigenetic association study and functional analysis. Cancer Res. 69: 5970-5977.
http://dx.doi.org/10.1158/0008-5472.CAN-09-0236
PMid:19567675 PMCid:2716085
Hu Z, Liang J, Wang Z, Tian T, et al. (2009). Common genetic variants in pre-microRNAs were associated with increased risk of breast cancer in Chinese women. Hum. Mutat. 30: 79-84.
http://dx.doi.org/10.1002/humu.20837
PMid:18634034
Jazdzewski K, Murray EL, Franssila K, Jarzab B, et al. (2008). Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinoma. Proc. Natl. Acad. Sci. U. S. A. 105: 7269-7274.
http://dx.doi.org/10.1073/pnas.0802682105
PMid:18474871 PMCid:2438239
Ji X, Zhang W, Xie C, Wang B, et al. (2011). Nasopharyngeal carcinoma risk by histologic type in central China: impact of smoking, alcohol and family history. Int. J. Cancer 129: 724-732.
http://dx.doi.org/10.1002/ijc.25696
PMid:20878958
Liang PS, Chen TY and Giovannucci E (2009). Cigarette smoking and colorectal cancer incidence and mortality: systematic review and meta-analysis. Int. J. Cancer 124: 2406-2415.
http://dx.doi.org/10.1002/ijc.24191
PMid:19142968
Liu Z, Li G, Wei S, Niu J, et al. (2010). Genetic variants in selected pre-microRNA genes and the risk of squamous cell carcinoma of the head and neck. Cancer 116: 4753-4760.
http://dx.doi.org/10.1002/cncr.25323
PMid:20549817 PMCid:3030480
Mittal RD, Gangwar R, George GP, Mittal T, et al. (2011). Investigative role of pre-microRNAs in bladder cancer patients: a case-control study in North India. DNA Cell Biol. 30: 401-406.
http://dx.doi.org/10.1089/dna.2010.1159
PMid:21345130
Okubo M, Tahara T, Shibata T, Yamashita H, et al. (2010). Association between common genetic variants in pre-microRNAs and gastric cancer risk in Japanese population. Helicobacter 15: 524-531.
http://dx.doi.org/10.1111/j.1523-5378.2010.00806.x
PMid:21073609
Pallante P, Visone R, Ferracin M, Ferraro A, et al. (2006). MicroRNA deregulation in human thyroid papillary carcinomas. Endocr. Relat. Cancer 13: 497-508.
http://dx.doi.org/10.1677/erc.1.01209
PMid:16728577
Pastrello C, Polesel J, Della Puppa L, Viel A, et al. (2010). Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patients. Carcinogenesis 31: 2124-2126.
http://dx.doi.org/10.1093/carcin/bgq184
PMid:20810544
Permuth-Wey J, Thompson RC, Burton NL, Olson JJ, et al. (2011). A functional polymorphism in the pre-miR-146a gene is associated with risk and prognosis in adult glioma. J. Neurooncol. 105: 639-646.
http://dx.doi.org/10.1007/s11060-011-0634-1
PMid:21744077
Perry MM, Moschos SA, Williams AE, Shepherd NJ, et al. (2008). Rapid changes in microRNA-146a expression negatively regulate the IL-1beta-induced inflammatory response in human lung alveolar epithelial cells. J. Immunol. 180: 5689-5698.
PMid:18390754 PMCid:2639646
Qiu LX, He J, Wang MY, Zhang RX, et al. (2011). The association between common genetic variant of microRNA-146a and cancer susceptibility. Cytokine 56: 695-698.
http://dx.doi.org/10.1016/j.cyto.2011.09.001
PMid:21978540
Reis LO, Pereira TC, Lopes-Cendes I and Ferreira U (2010). MicroRNAs: a new paradigm on molecular urological oncology. Urology 76: 521-527.
http://dx.doi.org/10.1016/j.urology.2010.03.012
PMid:20472270
Srivastava K, Srivastava A and Mittal B (2010). Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population. J. Hum. Genet. 55: 495-499.
http://dx.doi.org/10.1038/jhg.2010.54
PMid:20520619
Taganov KD, Boldin MP, Chang KJ and Baltimore D (2006). NF-kappaB-dependent induction of microRNA miR-146, an inhibitor targeted to signaling proteins of innate immune responses. Proc. Natl. Acad. Sci. U. S. A. 103: 12481-12486.
http://dx.doi.org/10.1073/pnas.0605298103
PMid:16885212 PMCid:1567904
Tian T, Shu Y, Chen J, Hu Z, et al. (2009). A functional genetic variant in microRNA-196a2 is associated with increased susceptibility of lung cancer in Chinese. Cancer Epidemiol. Biomarkers Prev. 18: 1183-1187.
http://dx.doi.org/10.1158/1055-9965.EPI-08-0814
PMid:19293314
Volinia S, Calin GA, Liu CG, Ambs S, et al. (2006). A microRNA expression signature of human solid tumors defines cancer gene targets. Proc. Natl. Acad. Sci. U. S. A. 103: 2257-2261.
http://dx.doi.org/10.1073/pnas.0510565103
PMid:16461460 PMCid:1413718
Wang J, Bi J, Liu X, Li K, et al. (2012). Has-miR-146a polymorphism (rs2910164) and cancer risk: a meta-analysis of 19 case-control studies. Mol. Biol. Rep. 39: 4571-4579.
http://dx.doi.org/10.1007/s11033-011-1247-7
PMid:21947843
Wang X, Tang S, Le SY, Lu R, et al. (2008). Aberrant expression of oncogenic and tumor-suppressive microRNAs in cervical cancer is required for cancer cell growth. PLoS One 3: e2557.
http://dx.doi.org/10.1371/journal.pone.0002557
PMid:18596939 PMCid:2438475
Xu B, Feng NH, Li PC, Tao J, et al. (2010). A functional polymorphism in Pre-miR-146a gene is associated with prostate cancer risk and mature miR-146a expression in vivo. Prostate 70: 467-472.
http://dx.doi.org/10.1002/pros.21149
Xu T, Zhu Y, Wei QK, Yuan Y, et al. (2008). A functional polymorphism in the miR-146a gene is associated with the risk for hepatocellular carcinoma. Carcinogenesis 29: 2126-2131.
http://dx.doi.org/10.1093/carcin/bgn195
PMid:18711148
Xu W, Xu J, Liu S, Chen B, et al. (2011). Effects of common polymorphisms rs11614913 in miR-196a2 and rs2910164 in miR-146a on cancer susceptibility: a meta-analysis. PLoS One 6: e20471.
http://dx.doi.org/10.1371/journal.pone.0020471
PMid:21637771 PMCid:3102728
Yue C, Wang M, Ding B, Wang W, et al. (2011). Polymorphism of the pre-miR-146a is associated with risk of cervical cancer in a Chinese population. Gynecol. Oncol. 122: 33-37.
http://dx.doi.org/10.1016/j.ygyno.2011.03.032
PMid:21529907
Zeng Y, Sun QM, Liu NN, Dong GH, et al. (2010). Correlation between pre-miR-146a C/G polymorphism and gastric cancer risk in Chinese population. World J. Gastroenterol. 16: 3578-3583.
http://dx.doi.org/10.3748/wjg.v16.i28.3578
PMid:20653068 PMCid:2909559
Zhou B, Wang K, Wang Y, Xi M, et al. (2011). Common genetic polymorphisms in pre-microRNAs and risk of cervical squamous cell carcinoma. Mol. Carcinog. 50: 499-505.
http://dx.doi.org/10.1002/mc.20740
PMid:21319225
Zhou J, Lv R, Song X, Li D, et al. (2012). Association between two genetic variants in miRNA and primary liver cancer risk in the Chinese population. DNA Cell Biol. 31: 524-530.
http://dx.doi.org/10.1089/dna.2011.1340
PMid:21861697