Publications
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, “Expression analysis of Gli1 and Gli2 in different tissues and muscle-derived cells of Qinchuan cattle”, vol. 13, pp. 8767-8775, 2014.
, “Increased serum ADAMTS-4 in knee osteoarthritis: a potential indicator for the diagnosis of osteoarthritis in early stages”, vol. 13, pp. 9642-9649, 2014.
, “Isolation and characterization of polymorphic microsatellite loci of the Chinese muntjac (Muntiacus reevesi)”, vol. 13, pp. 1905-1908, 2014.
, “Mutation screening of TSC1 and TSC2 genes in Chinese Han children with tuberous sclerosis complex”, vol. 13. pp. 2102-2106, 2014.
, “Polymorphisms in the delta-like 2 homolog gene and their association with growth and meat-quality traits in Qinchuan cattle”, vol. 13, pp. 2130-2139, 2014.
, “Acquisition of pig intramuscular preadipocytes through dedifferentiation of mature adipocytes and establishment of optimal induction conditions”, vol. 12, pp. 5926-5936, 2013.
, “Association between IL-1RN gene polymorphisms and susceptibility to ankylosing spondylitis: a large Human Genome Epidemiology review and meta-analysis”, vol. 12, pp. 1720-1730, 2013.
, “Effect of inhibition of MEK pathway on 5-aza-deoxycytidine-suppressed pancreatic cancer cell proliferation”, vol. 12, pp. 5560-5573, 2013.
, “Expression of a GDP-L-galactose phosphorylase-like gene in a Chinese wild Vitis species induces responses to Erysiphe necator and defense signaling molecules”, vol. 12, pp. 3830-3844, 2013.
, “The genetic variant rs401681C/T is associated with the risk of non-small cell lung cancer in a Chinese mainland population”, vol. 12. pp. 67-73, 2013.
Bae EY, Lee SY, Kang BK, Lee EJ, et al. (2012). Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population. Respirology 17: 699-706.
http://dx.doi.org/10.1111/j.1440-1843.2012.02165.x
PMid:22404340
Ginsberg MS (2005). Epidemiology of lung cancer. Semin. Roentgenol. 40: 83-89.
http://dx.doi.org/10.1053/j.ro.2005.01.007
PMid:15898406
Girard N, Lou E, Azzoli CG, Reddy R, et al. (2010). Analysis of genetic variants in never-smokers with lung cancer facilitated by an Internet-based blood collection protocol: a preliminary report. Clin. Cancer Res. 16: 755-763.
http://dx.doi.org/10.1158/1078-0432.CCR-09-2437
PMid:20068085 PMCid:2808124
Haiman CA, Chen GK, Vachon CM, Canzian F, et al. (2011). A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat. Genet. 43: 1210-1214.
http://dx.doi.org/10.1038/ng.985
PMid:22037553 PMCid:3279120
Hardin M, Zielinski J, Wan ES, Hersh CP, et al. (2012). CHRNA3/5, IREB2, and ADCY2 are associated with Severe COPD in Poland. Am. J. Respir. Cell Mol. Biol. [Epub ahead of print].
http://dx.doi.org/10.1165/rcmb.2012-0011OC
PMid:22461431
Haugen A, Ryberg D, Mollerup S, Zienolddiny S, et al. (2000). Gene-environment interactions in human lung cancer. Toxicol. Lett. 112-113: 233-237.
http://dx.doi.org/10.1016/S0378-4274(99)00275-1
Hung RJ, McKay JD, Gaborieau V, Boffetta P, et al. (2008). A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature 452: 633-637.
http://dx.doi.org/10.1038/nature06885
PMid:18385738
Kiyohara C, Yoshimasu K, Takayama K and Nakanishi Y (2007). Lung cancer susceptibility: are we on our way to identifying a high-risk group? Future Oncol. 3: 617-627.
http://dx.doi.org/10.2217/14796694.3.6.617
PMid:18041914
Kollarova H, Janout V and Cizek L (2002). Epidemiology of lung cancer. Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech. Repub. 146: 103-114.
http://dx.doi.org/10.5507/bp.2002.022
PMid:12572908
Lam WK (2005). Lung cancer in Asian women-the environment and genes. Respirology 10: 408-417.
http://dx.doi.org/10.1111/j.1440-1843.2005.00723.x
PMid:16135162
Law MH, Montgomery GW, Brown KM, Martin NG, et al. (2012). Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. J. Invest. Dermatol. 132: 485-487.
http://dx.doi.org/10.1038/jid.2011.322
PMid:21993562 PMCid:3258346
Liu Z, Li G, Wei S, Niu J, et al. (2010). Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck. Carcinogenesis 31: 1977-1981.
http://dx.doi.org/10.1093/carcin/bgq179
PMid:20802237 PMCid:2966556
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
Sanchez-Cespedes M (2009). Lung cancer biology: a genetic and genomic perspective. Clin. Transl. Oncol. 11: 263-269.
http://dx.doi.org/10.1007/s12094-009-0353-7
PMid:19451058
Sugimura H, Tao H, Suzuki M, Mori H, et al. (2011). Genetic susceptibility to lung cancer. Front Biosci. 3: 1463-1477.
http://dx.doi.org/10.2741/237
Thill PG, Goswami P, Berchem G and Domon B (2011). Lung cancer statistics in Luxembourg from 1981 to 2008. Bull. Soc. Sci. Med. Grand Duche Luxemb. 43-55.
PMid:22272445
Vossen RH, Aten E, Roos A and den Dunnen JT (2009). High-resolution melting analysis (HRMA): more than just sequence variant screening. Hum. Mutat. 30: 860-866.
http://dx.doi.org/10.1002/humu.21019
PMid:19418555
Weinrich SL, Pruzan R, Ma L, Ouellette M, et al. (1997). Reconstitution of human telomerase with the template RNA component hTR and the catalytic protein subunit hTRT. Nat. Genet. 17: 498-502.
http://dx.doi.org/10.1038/ng1297-498
PMid:9398860
Wu C, Hu Z, Yu D, Huang L, et al. (2009). Genetic variants on chromosome 15q25 associated with lung cancer risk in Chinese populations. Cancer Res. 69: 5065-5072.
http://dx.doi.org/10.1158/0008-5472.CAN-09-0081
PMid:19491260
, “Inhibitory effect of microRNA-24 on fatty acid-binding protein expression on 3T3-L1 adipocyte differentiation”, vol. 12, pp. 5267-5277, 2013.
, “Meta-analysis demonstrates association of the TGF-β1 gene -C509T polymorphism with susceptibility to IgA nephropathy in European but not in Asian populations”, vol. 12, pp. 434-442, 2013.
Awad MR, El-Gamel A, Hasleton P, Turner DM, et al. (1998). Genotypic variation in the transforming growth factor-beta1 gene: association with transforming growth factor-beta1 production, fibrotic lung disease, and graft fibrosis after lung transplantation. Transplantation 66: 1014-1020.
http://dx.doi.org/10.1097/00007890-199810270-00009
PMid:9808485
Baan CC, Balk AH, Holweg CT, van Riemsdijk IC, et al. (2000). Renal failure after clinical heart transplantation is associated with the TGF-beta 1 codon 10 gene polymorphism. J. Heart Lung Transplant. 19: 866-872.
http://dx.doi.org/10.1016/S1053-2498(00)00155-8
Bantis C, Heering PJ, Aker S, Klein-Vehne N, et al. (2004). Association of interleukin-10 gene G-1082A polymorphism with the progression of primary glomerulonephritis. Kidney Int. 66: 288-294.
http://dx.doi.org/10.1111/j.1523-1755.2004.00730.x
PMid:15200436
Bhowmik D, Sinha S, Gupt A, Tiwari SC, et al. (2011). Clinical approach to rapidly progressive renal failure. J. Assoc. Physicians India 59: 38-41.
PMid:21751663
Brezzi B, Del Prete D, Lupo A, Magistroni R, et al. (2009). Primary IgA nephropathy is more severe in TGF-beta1 high secretor patients. J. Nephrol. 22: 747-759.
PMid:19967654
Carturan S, Roccatello D, Menegatti E, Di Simone D, et al. (2004). Association between transforming growth factor beta1 gene polymorphisms and IgA nephropathy. J. Nephrol. 17: 786-793.
PMid:15593052
Chen BP, Wei YS, Xie JS and Huang HL (2005). Transforming growth factor beta1 gene polymorphisms in ZHUANG and HAN nationality in Guangxi Province. Chin. J. Anat. 28: 379-380.
Cotton SA, Gbadegesin RA, Williams S, Brenchley PE, et al. (2002). Role of TGF-beta1 in renal parenchymal scarring following childhood urinary tract infection. Kidney Int. 61: 61-67.
http://dx.doi.org/10.1046/j.1523-1755.2002.00110.x
PMid:11786085
Egger M, Davey SG, Schneider M and Minder C (1997). Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629-634.
http://dx.doi.org/10.1136/bmj.315.7109.629
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Grainger DJ, Heathcote K, Chiano M, Snieder H, et al. (1999). Genetic control of the circulating concentration of transforming growth factor type beta1. Hum. Mol. Genet. 8: 93-97.
http://dx.doi.org/10.1093/hmg/8.1.93
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Higgins JP and Thompson SG (2002). Quantifying heterogeneity in a meta-analysis. Stat. Med. 21: 1539-1558.
http://dx.doi.org/10.1002/sim.1186
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Hohenstein B, Daniel C, Wittmann S and Hugo C (2008). PDE-5 inhibition impedes TSP-1 expression, TGF-beta activation and matrix accumulation in experimental glomerulonephritis. Nephrol. Dial. Transplant. 23: 3427-3436.
http://dx.doi.org/10.1093/ndt/gfn319
PMid:18596129
Holla LI, Fassmann A, Benes P, Halabala T, et al. (2002). 5 polymorphisms in the transforming growth factor-β 1 gene (TGF-beta1) in adult periodontitis. J. Clin. Periodontol. 29: 336-341.
http://dx.doi.org/10.1034/j.1600-051X.2002.290409.x
PMid:11966931
Iwano M (2010). EMT and TGF-beta in renal fibrosis. Front Biosci. 2: 229-238.
http://dx.doi.org/10.2741/s60
Julian BA, Wyatt RJ, Matousovic K, Moldoveanu Z, et al. (2007). IgA nephropathy: a clinical overview. Contrib. Nephrol. 157: 19-26.
PMid:17495433
Kovacs TJ, Harris S, Vas TK, Seres I, et al. (2006). Paraoxonase gene polymorphism and serum activity in progressive IgA nephropathy. J. Nephrol. 19: 732-738.
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Lacha J, Hubacek JA, Potmesil P, Viklicky O, et al. (2001). TGF-beta I gene polymorphism in heart transplant recipients - effect on renal function. Ann. Transplant. 6: 39-43.
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Li SL, Lin X, Wang J, Yang F, et al. (2011). Relationship of transforming growth factorß1 gene -509C/T polymorphism with IgA nephropathy in Western Guangxi. China J. Modern Med. 21: 1607-1610.
Lim CS, Kim YS, Chae DW, Ahn C, et al. (2005). Association of C-509T and T869C polymorphisms of transforming growth factor-beta1 gene with susceptibility to and progression of IgA nephropathy. Clin. Nephrol. 63: 61-67.
PMid:15730046
Narita I, Saito N, Goto S, Jin S, et al. (2002). Role of uteroglobin G38A polymorphism in the progression of IgA nephropathy in Japanese patients. Kidney Int. 61: 1853-1858.
http://dx.doi.org/10.1046/j.1523-1755.2002.00336.x
PMid:11967037
Narita I, Goto S, Saito N, Song J, et al. (2003). Genetic polymorphism of NPHS1 modifies the clinical manifestations of Ig A nephropathy. Lab. Invest. 83: 1193-1200.
http://dx.doi.org/10.1097/01.LAB.0000080600.49276.31
PMid:12920248
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Qin W, Zhang YJ, Tan CY, Liu XR, et al. (2008). Association of TGF-β1 gene polymorphism with IgA nephropathy. West China Med. J. 23: 61-63.
Sato F, Narita I, Goto S, Kondo D, et al. (2004). Transforming growth factor-beta1 gene polymorphism modifies the histological and clinical manifestations in Japanese patients with IgA nephropathy. Tissue Antigens 64: 35-42.
http://dx.doi.org/10.1111/j.1399-0039.2004.00256.x
PMid:15191521
Song JH, Lee SW, Suh JH, Kim ES, et al. (2003). The effects of dual blockade of the renin-angiotensin system on urinary protein and transforming growth factor-beta excretion in 2 groups of patients with IgA and diabetic nephropathy. Clin. Nephrol. 60: 318-326.
PMid:14640237
Syrjanen J, Hurme M, Lehtimaki T, Mustonen J, et al. (2002). Polymorphism of the cytokine genes and IgA nephropathy. Kidney Int. 61: 1079-1085.
http://dx.doi.org/10.1046/j.1523-1755.2002.00193.x
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Vuong MT, Lundberg S, Gunnarsson I, Wramner L, et al. (2009). Genetic variation in the transforming growth factor-β1 gene is associated with susceptibility to IgA nephropathy. Nephrol. Dial. Transplant. 24: 3061-3067.
http://dx.doi.org/10.1093/ndt/gfp079
PMid:19258388 PMCid:2747497
Wiwanitkit V (2006). Angiotensin-converting enzyme gene polymorphism is correlated to the progression of disease in patients with IgA nephropathy: a meta-analysis. Ren. Fail. 28: 697-699.
http://dx.doi.org/10.1080/08860220600925636
PMid:17162429
Xue C, Li YJ, Li CX, Du Y, et al. (2005). Relationship of TGF-β1 -509C/T polymorphism with IgA nephropathy in HAN Nationality of Chinese Population. J. Sun Yat-Sen Univ. 26: 260-263.
Yamada Y, Miyauchi A, Goto J, Takagi Y, et al. (1998). Association of a polymorphism of the transforming growth factor-beta1 gene with genetic susceptibility to osteoporosis in postmenopausal Japanese women. J. Bone Miner. Res. 13: 1569-1576.
http://dx.doi.org/10.1359/jbmr.1998.13.10.1569
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Yamada Y, Miyauchi A, Takagi Y, Tanaka M, et al. (2001). Association of the C-509→T polymorphism, alone of in combination with the T869→C polymorphism, of the transforming growth factor-beta1 gene with bone mineral density and genetic susceptibility to osteoporosis in Japanese women. J. Mol. Med. 79: 149-156.
http://dx.doi.org/10.1007/s001090100190
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Yamamoto R, Nagasawa Y, Shoji T, Katakami N, et al. (2012). A candidate gene approach to genetic contributors to the development of IgA nephropathy. Nephrol. Dial. Transplant. 27: 1020-1030.
http://dx.doi.org/10.1093/ndt/gfr369
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, “SNPs at 3'-UTR of the bovine CDIPT gene associated with Qinchuan cattle meat quality traits”, vol. 12, pp. 775-782, 2013.
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, “Cloning, expression analysis and sequence prediction of the CCAAT/enhancer-binding protein alpha gene of Qinchuan cattle”, vol. 11, pp. 1651-1661, 2012.
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