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2.     Isolation of high quality RNA and molecular manipulations with various tissues of Populus. Russian Journal of Plant Physiology, 2009, 56(5):716-719.

3.     EST-SSRs development and paternity analysis for Liriodendron spp. New Forests, 2010, 40: 361-382.

4.     Reference gene selection for quantitative real-time polymerase chain reaction in Populus. Analytical Biochemistry, 2011, 408:337-339.

5.     Overexpression of PeRHD3 alters the root architecture in Populus. Biochemical and Biophysical Research Communications, 2012, 424:239-244.

6.     Development of novel chloroplast microsatellite markers for Ginkgo biloba. Genetics and Molecular Research, 2015, 14(2):7715-7720.

7.     Two WUSCHEL-related HOMEOBOX genes, PeWOX11a and PeWOX11b, are involved in adventitious root formation of poplar. Physiologia Plantarum, 2015, 155(4):446-456.

8.     A computational framework for mapping the timing of vegetative phase change. New Phytologist, 2016, 211(2): 750-760.

9.     Isolation and characterization of a poplar D-type cyclin gene associated with the SHORT-ROOT/SCARECROW network. Trees, 2016, 30:255-263.

10.   Transcriptome sequencing and development of novel genic SSR markers for Dendrobium officinale. Molecular Breeding, 2017, 37:18.

11.   Overexpression of PeHKT1;1 improves salt tolerance in Populus. Genes, 2018, 9:475.

12.   RNA sequencing and SSR marker development for genetic diversity research in Woonyoungia septentrionalis (Magnoliaceae). Conservation Genet Resour, 2018, 10:867-872.

13.   鹅掌楸EST-SSR引物开发及通用性分析. 分子植物育种, 2008, 6(3):615-618.

14.   林木遗传改良中的分子生物学研究进展. 林业科学, 2019, 45(1):136-143.

15.   杨树AGRONATUTE基因的克隆及序列分析. 林学科学, 2011, 47(3):46-51.

16.   胡杨耐盐基因PeuHKT1的克隆与表达分析. 分子植物育种, 2016, 14(9):2312-2318.

17.   杨树ProWOX11启动子克隆及组织特异表达分析. 分子植物育种, 2017, 15(11):4405-4410.

18.   Transient expression for functional gene analysis using Populus protoplasts. Plant Cell, Tissue and Culture, 2013, 114:11-18.

19.   Identification and expression analysis of twenty ARF genes in Populus. Gene, 2014, 544:134-144.

20.   Identification and characterization of three PeSHRs and one PeSCR involved in adventitious root development of Populus. Plant Cell, Tissue and Culture, 2014, 117:253-264.

21.   Molecular cloning, expression analysis and subcellular localization of four DELLA genes from hybrid poplar. SpringerPlus, 2016, 5:1129.

22.   Identification and characterization of nine PAT1 branch genes in poplar. Plant Growth Regul, 2017, 81:355-364.

23.   De Novo transcriptome sequencing in Passiflora edulis Sims to identify genes and signaling pathways involved in cold tolerance. Forests, 2017, 8:435.

24.   The complete chloroplast genome of Cinnamomum camphora and its comparison with related Lauraceae species. Peer J, 2017, 5:e3820.

25.   Identification and characterization of long non-coding RNAs involved in the formation and development of poplar adventitious roots. Industrial Crops & Products, 2018, 118:334-346.

26.   Identification and expression analysis of PeWOX5 and PeWOX13 genes in hyrid poplar. Russian Journal of Plant Physiology, 2018, 65(1):30-37.

27.   Novel SSR marker development and genetic diversity analysis of Cinnamomum camphora based on transcriptome sequencing. Plant Genetic Resources, 2018, 16(6):568-571.

28.   Transcriptome analysis and identification of genes related to terpenoid biosynthesis in Cinnamoumum camphora. BMC Genomics, 2018, 19:550.

29.   LncRNA/circRNA-miRNA-mRNA networks regulate the development of root and shoot meristems of Populus. Industrial Crops & Products,2019,133:333-347.

30.   杨树PeNHLd基因的克隆与表达模式分析.分子植物育种,2019,17:780-788.

31.   Characterization of masson pine (Pinus massoniana Lamb.) microsatellite DNA by 454 genome shotgun sequencing. Tree Genetics & Genomes, 2014, 10:429-437.

32.   De novo sequencing, assembly, and analysis of the Taxodium ‘Zhongshansa’ roots and shoots transcriptome in response to short-term waterlogging. BMC Plant Biology, 2014, 14:201.

33.   De novo transcriptome analysis of Liriodendron chinense petals and leaves by illumina sequencing. Gene, 534:155-162.

34.   High genetic diversity but limited gene flow among remnant and fragmented natural populations of Liriodendron chinense Sarg. Biochemical Systematics and Ecology, 2014, 54:230-236.

35.   杨树MAGPIE和JACKDAW基因克隆、表达及蛋白互作研究. 南京林业大学学报(自然科学版), 2014, 38(3): 29-34.

36.   植物中miR160/miR167/miR390家族及其靶基因研究进展. 南京林业大学学报(自然科学版), 2014, 38(3): 155-159.

37.     北美鹅掌楸LtCHS基因的克隆及生物信息学与组织表达特征分析. 林业科学, 2015, 51(5):37-45.