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2012
Y. Hu, Wen, W., Yu, J. - G., Qu, S. - Q., Wang, S. - S., Liu, J., Li, B. - S., and Luo, Y., Genetic association of UBE2B variants with susceptibility to male infertility in a Northeast Chinese population, vol. 11, pp. 4226-4234, 2012.
Baarends WM, Wassenaar E, Hoogerbrugge JW, van Cappellen G, et al. (2003). Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase. Mol. Cell. Biol. 23: 1151-1162. http://dx.doi.org/10.1128/MCB.23.4.1151-1162.2003 PMid:12556476 PMCid:141135   Ciechanover A (1996). Ubiquitin-mediated proteolysis and male sterility. Nat. Med. 2: 1188-1190. http://dx.doi.org/10.1038/nm1196-1188 PMid:8898739   Escalier D and Serres C (1985). Aberrant distribution of the peri-axonemal structures in the human spermatozoon: possible role of the axoneme in the spatial organization of the flagellar components. Biol. Cell 53: 239-250. http://dx.doi.org/10.1111/j.1768-322X.1985.tb00372.x PMid:3160418   Escalier D, Bai XY, Silvius D, Xu PX, et al. (2003). Spermatid nuclear and sperm periaxonemal anomalies in the mouse Ube2b null mutant. Mol. Reprod. Dev. 65: 298-308. http://dx.doi.org/10.1002/mrd.10290 PMid:12784252   Grootegoed JA, Siep M and Baarends WM (2000). Molecular and cellular mechanisms in spermatogenesis. Baillieres Best Pract. Res. Clin. Endocrinol. Metab. 14: 331-343. http://dx.doi.org/10.1053/beem.2000.0083 PMid:11097779   Huang I, Emery BR, Christensen GL, Griffin J, et al. (2008). Novel UBE2B-associated polymorphisms in an azoospermic/ oligozoospermic population. Asian J. Androl. 10: 461-466. http://dx.doi.org/10.1111/j.1745-7262.2008.00386.x PMid:18385908   Li Z, Zhang Z, He Z, Tang W, et al. (2009). A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn). Cell Res. 19: 519-523. http://dx.doi.org/10.1038/cr.2009.33 PMid:19290020   Nishimune Y and Tanaka H (2006). Infertility caused by polymorphisms or mutations in spermatogenesis-specific genes. J. Androl. 27: 326-334. http://dx.doi.org/10.2164/jandrol.05162 PMid:16474012   Pengo M, Ferlin A, Arredi B, Ganz F, et al. (2006). FSH receptor gene polymorphisms in fertile and infertile Italian men. Reprod. Biomed. Online 13: 795-800. http://dx.doi.org/10.1016/S1472-6483(10)61026-7   Rajapurohitam V, Morales CR, El-Alfy M, Lefrancois S, et al. (1999). Activation of a UBC4-dependent pathway of ubiquitin conjugation during postnatal development of the rat testis. Dev. Biol. 212: 217-228. http://dx.doi.org/10.1006/dbio.1999.9342 PMid:10419697   Rajapurohitam V, Bedard N and Wing SS (2002). Control of ubiquitination of proteins in rat tissues by ubiquitin conjugating enzymes and isopeptidases. Am. J. Physiol. Endocrinol. Metab. 282: E739-E745. PMid:11882492   Roest HP, van Klaveren J, de Wit J, van Gurp CG, et al. (1996). Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification. Cell 86: 799-810. http://dx.doi.org/10.1016/S0092-8674(00)80154-3   Serres C, Feneux D and Jouannet P (1986). Abnormal distribution of the periaxonemal structures in a human sperm flagellar dyskinesia. Cell Motil. Cytoskeleton 6: 68-76. http://dx.doi.org/10.1002/cm.970060109 PMid:3698108   Shi YY and He L (2005). SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 15: 97-98. http://dx.doi.org/10.1038/sj.cr.7290272 PMid:15740637   Suryavathi V, Khattri A, Gopal K, Rani DS, et al. (2008). Novel variants in UBE2B gene and idiopathic male infertility. J. Androl. 29: 564-571. http://dx.doi.org/10.2164/jandrol.107.004580 PMid:18497339   World Health Organization (1999). WHO Laboratory Manual for the Examination of Human Semen and Sperm-Cervical Mucus Interaction. 4th edn. Cambridge University Press, Cambridge.
J. Liu, Li, X., Yu, N., Yang, Y. - Q., Li, X., Ye, Z. - Y., and Li, J. - C., Genetic instability and CpG methylation in the 5'-flanking region of the PAI-1 gene in Chinese patients with gastric cancer, vol. 11, pp. 2899-2908, 2012.
Andreasen PA, Egelund R and Petersen HH (2000). The plasminogen activation system in tumor growth, invasion, and metastasis. Cell Mol. Life Sci. 57: 25-40. http://dx.doi.org/10.1007/s000180050497 PMid:10949579   Baylin SB and Herman JG (2000). DNA hypermethylation in tumorigenesis: epigenetics joins genetics. Trends Genet. 16: 168-174. http://dx.doi.org/10.1016/S0168-9525(99)01971-X   Chakrabarti S, Sengupta S, Sengupta A, Basak SN, et al. (2006). Genomic instabilities in squamous cell carcinoma of head and neck from the Indian population. Mol. Carcinog. 45: 270-277. http://dx.doi.org/10.1002/mc.20178 PMid:16402388   Durand MK, Bodker JS, Christensen A, Dupont DM, et al. (2004). Plasminogen activator inhibitor-I and tumour growth, invasion, and metastasis. Thromb. Haemost. 91: 438-449. PMid:14983218   Esteller M (2003). Cancer epigenetics: DNA methylation and chromatin alterations in human cancer. Adv. Exp. Med. Biol. 532: 39-49. http://dx.doi.org/10.1007/978-1-4615-0081-0_5 PMid:12908548   Gao S, Skeldal S, Krogdahl A, Sorensen JA, et al. (2005). CpG methylation of the PAI-1 gene 5'-flanking region is inversely correlated with PAI-1 mRNA levels in human cell lines. Thromb. Haemost. 94: 651-660. PMid:16268485   Gonzalez-Zulueta M, Bender CM, Yang AS, Nguyen T, et al. (1995). Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing. Cancer Res. 55: 4531-4535. PMid:7553622   Gopalan V, Smith RA, Nassiri MR, Yasuda K, et al. (2010). GAEC1 and colorectal cancer: a study of the relationships between a novel oncogene and clinicopathologic features. Hum. Pathol. 41: 1009-1015. http://dx.doi.org/10.1016/j.humpath.2009.11.014 PMid:20236690   Jemal A, Siegel R, Ward E, Hao Y, et al. (2008). Cancer statistics, 2008. CA Cancer J. Clin. 58: 71-96. http://dx.doi.org/10.3322/CA.2007.0010 PMid:18287387   Juvan R, Hudler P, Gazvoda B, Repse S, et al. (2007). Significance of genetic abnormalities of p53 protein in Slovenian patients with gastric carcinoma. Croat. Med. J. 48: 207-217. PMid:17436385 PMCid:2080507   Nuovo GJ, Plaia TW, Belinsky SA, Baylin SB, et al. (1999). In situ detection of the hypermethylation-induced inactivation of the p16 gene as an early event in oncogenesis. Proc. Natl. Acad. Sci. U. S. A. 96: 12754-12759. http://dx.doi.org/10.1073/pnas.96.22.12754 PMid:10535995 PMCid:23084   Ozisik YY, Meloni AM, Surti U and Sandberg AA (1993). Deletion 7q22 in uterine leiomyoma. A cytogenetic review. Cancer Genet. Cytogenet. 71: 1-6. http://dx.doi.org/10.1016/0165-4608(93)90195-R   Sakakibara T, Hibi K, Koike M, Fujiwara M, et al. (2006). Plasminogen activator inhibitor-1 as a potential marker for the malignancy of gastric cancer. Cancer Sci. 97: 395-399. http://dx.doi.org/10.1111/j.1349-7006.2006.00185.x PMid:16630137   Sato N, Fukushima N, Maitra A, Matsubayashi H, et al. (2003). Discovery of novel targets for aberrant methylation in pancreatic carcinoma using high-throughput microarrays. Cancer Res. 63: 3735-3742. PMid:12839967   Sourla A, Polychronakos C, Zeng WR, Nepveu A, et al. (1996). Plasminogen activator inhibitor 1 messenger RNA expression and molecular evidence for del(7)(q22) in uterine leiomyomas. Cancer Res. 56: 3123-3128. PMid:8674071   Storchova Z and Pellman D (2004). From polyploidy to aneuploidy, genome instability and cancer. Nat. Rev. Mol. Cell Biol. 5: 45-54. http://dx.doi.org/10.1038/nrm1276 PMid:14708009   Strathdee G, Davies BR, Vass JK, Siddiqui N, et al. (2004). Cell type-specific methylation of an intronic CpG island controls expression of the MCJ gene. Carcinogenesis 25: 693-701. http://dx.doi.org/10.1093/carcin/bgh066 PMid:14729589   Wind T, Hansen M, Jensen JK and Andreasen PA (2002). The molecular basis for anti-proteolytic and non-proteolytic functions of plasminogen activator inhibitor type-1: roles of the reactive centre loop, the shutter region, the flexible joint region and the small serpin fragment. Biol. Chem. 383: 21-36. http://dx.doi.org/10.1515/BC.2002.003 PMid:11928815   Wu C and Morris JR (2001). Genes, genetics, and epigenetics: a correspondence. Science 293: 1103-1105. http://dx.doi.org/10.1126/science.293.5532.1103 PMid:11498582   Xiao YP, Wu DY, Xu L and Xin Y (2006). Loss of heterozygosity and microsatellite instabilities of fragile histidine triad gene in gastric carcinoma. World J. Gastroenterol. 12: 3766-3769. PMid:16773697   Yang YQ, Wu L, Chen JX, Sun JZ, et al. (2008). Relationship between nm23H1 genetic instability and clinical pathological characteristics in Chinese digestive system cancer patients. World J. Gastroenterol. 14: 5549-5556. http://dx.doi.org/10.3748/wjg.14.5549 PMid:18810774 PMCid:2746343
J. Liu, Sun, Z. - X., Chen, Y. - T., and Jiang, J. - M., Isolation and characterization of microsatellite loci from an endangered tree species, Toona ciliata var. pubescens, vol. 11, pp. 4411-4417, 2012.
Arif IA, Khan HA, Shobrak M, Al Homaidan AA, et al. (2010). Interpretation of electrophoretograms of seven microsatellite loci to determine the genetic diversity of the Arabian Oryx. Genet. Mol. Res. 9: 259-265. http://dx.doi.org/10.4238/vol9-1gmr714 PMid:20198581   Bellini E, Benelli C, Giordani E, Perria R, et al. (2003). Genetic and morphological relationships between possible Italian and Ancestral cultivars of persimmon. Acta Hortic. 601: 192-197.   Cardoso SR, Eloy NB, Provan J, Cardoso MA, et al. (2000). Genetic differentiation of Euterpe edulis Mart. populations 4417   Genetics and Molecular Research 11 (4): 4411-4417 (2012) ©FUNPEC-RP www.funpecrp.com.br   Isolation of microsatellite loci from T. ciliata var. pubescens estimated by AFLP analysis. Mol. Ecol. 9: 1753-1760. PMid:11091311   Vik U, Jorgensen MH, Kauserud H, Nordal I, et al. (2010). Microsatellite markers show decreasing diversity but unchanged level of clonality in Dryas octopetala (Rosaceae) with increasing latitude. Am. J. Bot. 97: 988-997. http://dx.doi.org/10.3732/ajb.0900215 PMid:21622468   White G and Powell W (1997). Isolation and characterization of microsatellite loci in Swietenia humilis (Meliaceae): an endangered tropical hardwood species. Mol. Ecol. 6: 851-860. http://dx.doi.org/10.1111/j.1365-294X.1997.tb00139.x   Zane L, Bargelloni L and Patarnello T (2002). Strategies for microsatellite isolation: a review. Mol. Ecol. 11: 1-16. http://dx.doi.org/10.1046/j.0962-1083.2001.01418.x PMid:11903900   Zang L, Zang L and Patarnello T (2002). Microsatellite in different eukaryotic genomes: survey and analysis. Genome Res. 10: 967-981.   Zhang GF (2000). Study on rare and threatened plants of Anhui and their conservation. J. Anhui Normal Univ. 23: 36-39.   Zhang L, Guo LH and Du TZ (2006). The effects of ehading and soil water content on photosynthesis of Toona ciliata var.
A. - X. Wang, Xu, B., Tong, N., Chen, S. - Q., Yang, Y., Zhang, X. - W., Jiang, H., Liu, N., Liu, J., Hu, X. - N., Sha, G. - Z., and Chen, M., 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
2010
X. C. Lin, Lou, Y. F., Liu, J., Peng, J. S., Liao, G. L., and Fang, W., Crossbreeding of Phyllostachys species (Poaceae) and identification of their hybrids using ISSR markers, vol. 9, pp. 1398-1404, 2010.
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