Publications

Found 21 results
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2016
X. F. Li, Pan, D., Zhang, W. L., Zhou, J., Liang, J. J., Li, X. F., Pan, D., Zhang, W. L., Zhou, J., and Liang, J. J., “Association of NT-proBNP and interleukin-17 levels with heart failure in elderly patients”, vol. 15, p. -, 2016.
X. F. Li, Pan, D., Zhang, W. L., Zhou, J., Liang, J. J., Li, X. F., Pan, D., Zhang, W. L., Zhou, J., and Liang, J. J., “Association of NT-proBNP and interleukin-17 levels with heart failure in elderly patients”, vol. 15, p. -, 2016.
X. F. Li, Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., and Jia, Y. J., “Association of the programmed cell death-1 PD1.5 C>T polymorphism with cervical cancer risk in a Chinese population”, vol. 15, p. -, 2016.
X. F. Li, Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., and Jia, Y. J., “Association of the programmed cell death-1 PD1.5 C>T polymorphism with cervical cancer risk in a Chinese population”, vol. 15, p. -, 2016.
X. F. Li, Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., Jia, Y. J., Li, X. F., Jiang, X. Q., Zhang, J. W., and Jia, Y. J., “Association of the programmed cell death-1 PD1.5 C>T polymorphism with cervical cancer risk in a Chinese population”, vol. 15, p. -, 2016.
M. F. Gan, Yang, H. L., Qian, J. L., Wu, C. S., Yuan, C. X., Li, X. F., Zou, J., Gan, M. F., Yang, H. L., Qian, J. L., Wu, C. S., Yuan, C. X., Li, X. F., and Zou, J., “Comparison of two methods for RNA extraction from the nucleus pulposus of intervertebral discs”, vol. 15, p. -, 2016.
M. F. Gan, Yang, H. L., Qian, J. L., Wu, C. S., Yuan, C. X., Li, X. F., Zou, J., Gan, M. F., Yang, H. L., Qian, J. L., Wu, C. S., Yuan, C. X., Li, X. F., and Zou, J., “Comparison of two methods for RNA extraction from the nucleus pulposus of intervertebral discs”, vol. 15, p. -, 2016.
P. Y. Xing, Liu, T., Song, Z. Q., Li, X. F., Xing, P. Y., Liu, T., Song, Z. Q., and Li, X. F., “Genetic diversity of Toona sinensis Roem in China revealed by ISSR and SRAP markers”, vol. 15, p. -, 2016.
P. Y. Xing, Liu, T., Song, Z. Q., Li, X. F., Xing, P. Y., Liu, T., Song, Z. Q., and Li, X. F., “Genetic diversity of Toona sinensis Roem in China revealed by ISSR and SRAP markers”, vol. 15, p. -, 2016.
2015
H. W. Fan, Liu, G. Y., Zhao, C. F., Li, X. F., and Yang, X. Y., “Differential expression of COX-2 in osteoarthritis and rheumatoid arthritis”, vol. 14, pp. 12872-12879, 2015.
Z. Liu, Luo, Q. H., Wang, J. M., Li, X. F., and Yang, Y., “Functional characterization and analysis of the Arabidopsis UGT71C5 promoter region”, vol. 14, pp. 19173-19183, 2015.
N. Zhao, Sui, Y., Li, X. F., Liu, W., Lu, Y. P., Feng, W. H., Ma, C., Wang, Y. W., Bao, H. X., Huang, F., Wang, H., Yi, D. X., Han, W. T., and Jiang, M., “Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutation”, vol. 14, pp. 14690-14697, 2015.
M. Li, Gao, W. J., Ma, J. J., Zhu, Y., and Li, X. F., “Relationship between urinary protein changes in lupus nephritis and renal pathology”, vol. 14, pp. 8352-8358, 2015.
Z. Liu, Luo, Q. H., Wen, G. Q., Wang, J. M., Li, X. F., and Yang, Y., “VDAC2 involvement in the stress response pathway in Arabidopsis thaliana”, vol. 14, pp. 15511-15519, 2015.
2014
X. F. Li, Chen, Y. X., Ye, W. W., Tao, X. F., Zhu, J. H., Wu, S., and Lou, L. Q., “Association between a single nucleotide polymorphism of the XRCC1 gene and hepatocellular carcinoma susceptibility in the Chinese Han population”, vol. 13, pp. 160-166, 2014.
Z. Q. Wang, Cao, Y. L., Huang, Y. F., Liu, D. Q., and Li, X. F., “Cross-leg repair of large soft-tissue defects in distal sites of the feet by distally based neuro-fasciocutaneous flaps with perforating vessels”, vol. 13, pp. 5484-5491, 2014.
2013
L. Zhang, Zhang, H. G., and Li, X. F., “Analysis of genetic diversity in Larix gmelinii (Pinaceae) with RAPD and ISSR markers”, vol. 12. pp. 196-207, 2013.
Bucci G, Vendramin GG, Lelli L and Vicario F (1997). Assessing the genetic divergence of Pinus leucodermis Ant. endangered populations: use of molecular markers for conservation purposes. Theor. Appl. Genet. 95: 1138-1146. http://dx.doi.org/10.1007/s001220050674   Changtragoon S (1995). Inheritance of isozyme phenotypes of Pinus merkusii. J. Trop. For. Sci. 8: 167-177.   Goto S, Thakur RC and Ishii K (1998). Determination of genetic stability in long-term micropropagated shoots of Pinus thunbergii Parl. using RAPD markers. Plant Cell Rep. 18: 193-197. http://dx.doi.org/10.1007/s002990050555   Labra M, Grassi F, Sgorbati S and Ferrari C (2006). Distribution of genetic variability in southern populations of Scots pine (Pinus sylvestris L.) from the Alps to the Pennines. Flora Morph. Distrib. Func. Ecol. Plants 201: 468-476. http://dx.doi.org/10.1016/j.flora.2005.10.004   Larionova AI, Iakhneva NV and Abaimov AP (2004). Genetic diversity and differentiation of Gmelin larch Larix gmelinii populations from Evenkia (Central Siberia). Genetika 40: 1370-1377. PMid:15575504   Lee SW, Ledig FT and Johnson DR (2002). Genetic variation at allozyme and RAPD markers in Pinus longaeva (Pinaceae) of the White Mountains, California. Am. J. Bot. 89: 566-577. http://dx.doi.org/10.3732/ajb.89.4.566 PMid:21665657   Li W (2004). Study on genetic diversity of Pinus sibirica du tour with ISSR-PCR. Northeast For. Univ.   Liu GF, Dong JX, Jiang Y, Lu YF, et al. (2005). Analysis of genetic relationship in 12 species of Section Strobus with ISSR markers. J. For. Res. 16: 213-215. http://dx.doi.org/10.1007/BF02856817   Majourhat K, Jabbar A, Hafidi A and Martínez-Gomez P (2008). Molecular characterization and genetic relationships among most common identified morphotypes of critically endangered rare Moroccan species Argania spinosa (Sapotaceae) using RAPD and SSR markers. Ann. For. Sci. 65: 805. http://dx.doi.org/10.1051/forest:2008069   Messaoud C, Afif M, Boulila A, Rejeb MN, et al. (2007). Genetic variation of Tunisian Myrtus communis L. (Myrtaceae) populations assessed by isozymes and RAPDs. Ann. For. Sci. 64: 845-853. http://dx.doi.org/10.1051/forest:2007061   Na D, Yang C and Jiang J (2006). Analysis on the genetic diversity of Larix gmelinii provenance by using ISSR markers. For. Sci. Tech. 31: 1-4.   Nei M and Li WH (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. U. S. A. 76: 5269-5273. http://dx.doi.org/10.1073/pnas.76.10.5269 PMid:291943 PMCid:413122   Oreshkova NV, Larionova AY, Milyutin LI and Abaimov AP (2006). Genetic diversity structure and differentiation of Gmelin Larch (Larix gmelinii (Rupr.) Rupr.) populations from Central Evenkia and Eastern Zabaikalje. Eurasian J. For. Res. 9-1: 1-8.   Porebski S, Bailey LG and Baum BR (1997). Modification of a CTAB DNA extraction protocol for plants containing high polysaccharide and polyphenol components. Plant Mol. Biol. Rep. 15: 8-15. http://dx.doi.org/10.1007/BF02772108   Raymond PG and Ledig FT (1982). Genetic diversity and population structure in pitch pine (Pinus rigida mill.). Evolution 36: 387-402. http://dx.doi.org/10.2307/2408058   Shahraji TR, Kazempour MN and Adbesh Z (2009). Genetic (RAPD) diversity in loblolly pine unknown provenance plantation in Iran. Indian J. Hortic. 66: 35-38.   Wang MB and Gao FQ (2009). Genetic variation in Chinese pine (Pinus tabulaeformis), a woody species endemic to China. Biochem. Genet. 47: 154-164. http://dx.doi.org/10.1007/s10528-009-9225-7 PMid:19169805   Xue X, Wang Y, Korpelainen H and Li C (2007). Genetic diversity of Picea asperata populations based on RAPDs. Plant Biol. 9: 101-108. http://dx.doi.org/10.1055/s-2006-924455 PMid:17006797   Yang CP, Jiang J, Tang SS, Li JY, et al. (2002). The provenance test of 21-year Old Larix gmelinii at Maoershan area. J. Northeast For. Univ. 30: 6.   Yeh FC, Yang R and Boyle T (1999). POPGENE, Version 1.31, Microsoft Window-Based Freeware for Population Genetic Analysis. Centre for International Forestry Research, University of Alberta and Tim Boyle. Available at [http://www.ualberta.ca/~fyeh/popgene.pdf]. Accessed August 30, 1999.   Zemanová E, Jirku M, Mauricio IL, Miles MA, et al. (2004). Genetic polymorphism within the Leishmania donovani complex: correlation with geographic origin. Am. J. Trop. Med. Hyg. 70: 613-617. PMid:15211001   Zhang HG, Wang H, Xiao Y and Zhang CF (2002). Population genetic diversity of Picea koraiensis with allozyme techniques. J. Northeast For. Univ. 30: 21-25.
2012
Y. W. Wang, Han, W. T., Jiang, M., Lu, C. X., Li, X. F., Zhang, X., and Li, J. X., “A novel mutation of the MFN2 gene in a Chinese family with Charcot-Marie-Tooth disease”, vol. 11. pp. 1454-1459, 2012.
Banchs I, Casasnovas C, Montero J, Martinez-Matos JA, et al. (2008). Two Spanish families with Charcot-Marie-Tooth type 2A: clinical, electrophysiological and molecular findings. Neuromuscul. Disord. 18: 974-978.http://dx.doi.org/10.1016/j.nmd.2008.09.006PMid:18996695Barisic N, Claeys KG, Sirotkovic-Skerlev M, Lofgren A, et al. (2008). Charcot-Marie-Tooth disease: a clinico-genetic confrontation. Ann. Hum. Genet. 72: 416-441.http://dx.doi.org/10.1111/j.1469-1809.2007.00412.xPMid:18215208Cartoni R and Martinou JC (2009). Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A. Exp. Neurol. 218: 268-273.http://dx.doi.org/10.1016/j.expneurol.2009.05.003PMid:19427854Chung KW, Kim SB, Park KD, Choi KG, et al. (2006). Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations. Brain 129: 2103-2118.http://dx.doi.org/10.1093/brain/awl174PMid:16835246Engelfried K, Vorgerd M, Hagedorn M, Haas G, et al. (2006). Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2). BMC Med. Genet. 7: 53.http://dx.doi.org/10.1186/1471-2350-7-53PMid:16762064 PMCid:1524942Honda S, Aihara T, Hontani M, Okubo K, et al. (2005). Mutational analysis of action of mitochondrial fusion factor mitofusin-2. J. Cell Sci. 118: 3153-3161.http://dx.doi.org/10.1242/jcs.02449PMid:15985463Kijima K, Numakura C, Izumino H, Umetsu K, et al. (2005). Mitochondrial GTPase mitofusin 2 mutation in Charcot- Marie-Tooth neuropathy type 2A. Hum. Genet. 116: 23-27.http://dx.doi.org/10.1007/s00439-004-1199-2PMid:15549395Koshiba T, Detmer SA, Kaiser JT, Chen H, et al. (2004). Structural basis of mitochondrial tethering by mitofusin complexes. Science 305: 858-862.http://dx.doi.org/10.1126/science.1099793PMid:15297672Nicolaou P, Zamba-Papanicolaou E, Koutsou P, Kleopa KA, et al. (2010). Charcot-Marie-Tooth disease in Cyprus: epidemiological, clinical and genetic characteristics. Neuroepidemiology 35: 171-177.http://dx.doi.org/10.1159/000314351PMid:20571287Rojo M, Legros F, Chateau D and Lombes A (2002). Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo. J. Cell Sci. 115: 1663-1674.PMid:11950885Santel A and Fuller MT (2001). Control of mitochondrial morphology by a human mitofusin. J. Cell Sci. 114: 867-874.PMid:11181170Verhoeven K, Claeys KG, Zuchner S, Schroder JM, et al. (2006). MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain 129: 2093-2102.http://dx.doi.org/10.1093/brain/awl126PMid:16714318Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, et al. (2004). Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nat. Genet. 36: 449-451.http://dx.doi.org/10.1038/ng1341PMid:15064763
2010
X. Z. Kan, Li, X. F., Zhang, L. Q., Chen, L., Qian, C. J., Zhang, X. W., and Wang, L., “Characterization of the complete mitochondrial genome of the Rock pigeon, Columba livia (Columbiformes: Columbidae)”, vol. 9, pp. 1234-1249, 2010.
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Complete mitochondrial DNA genome sequences of extinct birds: ratite phylogenetics and the vicariance biogeography hypothesis. Proc. Biol. Sci. 268: 939-945. http://dx.doi.org/10.1098/rspb.2001.1587 PMid:11370967 PMCid:1088691   Hall AT (1999). BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/ NT. Nucleic Acids Symp. Ser. 41: 95-98.   Harlid A, Janke A and Arnason U (1998). The complete mitochondrial genome of Rhea americana and early avian divergences. J. Mol. Evol. 46: 669-679. http://dx.doi.org/10.1007/PL00006347 PMid:9608049   Harrison GL, McLenachan PA, Phillips MJ, Slack KE, et al. (2004). Four new avian mitochondrial genomes help get to basic evolutionary questions in the late cretaceous. Mol. Biol. Evol. 21: 974-983. http://dx.doi.org/10.1093/molbev/msh065 PMid:14739240   Hazkani-Covo E, Zeller RM and Martin W (2010). Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes. 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X. Z. Kan, Li, X. F., Lei, Z. P., Wang, M., Chen, L., Gao, H., and Yang, Z. Y., “Complete mitochondrial genome of Cabot’s tragopan, Tragopan caboti (Galliformes: Phasianidae)”, vol. 9, pp. 1204-1216, 2010.
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