Publications

Found 109 results
Filters: Author is J. Li  [Clear All Filters]
2015
X. S. Shi, Li, J., Yang, R. H., Zhao, G. R., Zhou, H. P., Zeng, W. X., and Zhou, M., Correlation of increased MALAT1 expression with pathological features and prognosis in cancer patients: a meta-analysis, vol. 14, pp. 18808-18819, 2015.
J. Li, Wang, J. S., Xie, Z. X., Wang, W. Z., Wang, L., Ma, G. Y., Li, Y. Q., and Wang, P., Correlations among copeptin, ischemia-modified albumin, and the extent of myocardial injury in patients with acute carbon monoxide poisoning, vol. 14, pp. 10384-10389, 2015.
W. Yan, Sun, T. - Y., Yang, C. - M., Jia, M., Li, J., Tang, H. - L., and Zhou, Y. - F., CpG ODN 1826 enhances radiosensitivity of the human lung cancer cell line A549 in a rat model, vol. 14, pp. 9804-9812, 2015.
N. Ding, Han, Q., Zhao, X. Z., Li, Q., Li, J., Zhang, H. F., Gao, G. L., Luo, Y., Xie, Y. H., Su, J., and Wang, Q. G., Differential gene expression in pre-laying and laying period ovaries of Sichuan White geese (Anser cygnoides), vol. 14, pp. 6773-6785, 2015.
B. Sun, Li, J., Dong, M., Yang, L., Wu, C., Zhu, L., and Cong, Y. L., Diversity of platelet function and genetic polymorphism in clopidogrel-treated Chinese patients, vol. 14, pp. 1434-1442, 2015.
W. Zhou, Yuan, Y., Li, J., Yuan, W. M., Huang, L. G., and Zheng, S. W., Effect of Bifidobacterium on the mRNA expression levels of TRAF6, GSK-3β, and microRNA-146a in LPS-stimulated rat intestinal epithelial cells, vol. 14, pp. 10050-10056, 2015.
Y. - F. Jia, Gao, H. - L., Ma, L. - J., and Li, J., Effect of nimodipine on rat spinal cord injury, vol. 14, pp. 1269-1276, 2015.
X. L. Qu, Wang, H. T., Zou, J. L., Cheng, L., Wang, F., Ma, L. L., and Li, J., Effect of transvaginal ultrasound on human chorionic villus cell apoptosis during pregnancy, vol. 14, pp. 18771-18777, 2015.
G. Y. Shi, Zhao, L. L., Zhang, K., Zhou, H. X., Liu, A. H., Li, J., Li, G., and Zhu, L. H., Effects of BCL2 transfection on the cell cycle and proliferation of human GES-1 cells, vol. 14, pp. 12022-12029, 2015.
J. Z. Gao, Wang, Y. L., Li, J., and Wei, L. X., Effects of VEGF/VEGFR/K-ras signaling pathways on miRNA21 levels in hepatocellular carcinoma tissues in rats, vol. 14, pp. 671-679, 2015.
Y. F. Ma, Yang, B., Li, J., Zhang, T., Guo, J. T., Chen, L., Li, M., Chu, J., Liang, C. Y., and Liu, Y., Expression of Ras-related protein 25 predicts chemotherapy resistance and prognosis in advanced non-small cell lung cancer, vol. 14, pp. 13998-14008, 2015.
Q. Y. Liu, Gao, F. Y., Liu, X. R., Li, J., Ji, M., Dong, J., and Wang, X. T., Investigations into the association between polymorphisms in the interleukin-10 gene and risk of early-onset preeclampsia, vol. 14, pp. 19323-19328, 2015.
J. Li, Tang, H. L., Chen, Y., Fan, Q., Shao, Y. T., Jia, M., Wang, J. C., and Yang, C. M., Malondialdehyde and SOD-induced changes of gastric tissues in acute gastric mucosal injury under positive acceleration, vol. 14, pp. 4361-4368, 2015.
M. W. Li, Yu, H. J., Yi, X. L., Li, J., Dai, F. Y., and Hou, C. X., Marker-assisted selection in breeding silkworm strains with high tolerance to fluoride, scaleless wings, and high silk production, vol. 14, pp. 11162-11170, 2015.
L. F. Sun, Li, J., Liang, X. F., Yi, T. L., Fang, L., Sun, J., He, Y. H., Luo, X. N., Dou, Y. Q., and Yang, M., Microsatellite DNA markers and their correlation with growth traits in mandarin fish (Siniperca chuatsi), vol. 14, pp. 19128-19135, 2015.
J. Li, Wang, L., Qian, C., Zhang, C. F., Dai, L. S., Liu, Q. N., Wei, G. Q., Sun, Y., Liu, D. R., Zhu, B. J., and Liu, C. L., Molecular characterization, tissue distribution, and immune reaction expression of karyopherins in the domestic silkworm (Bombyx mori), vol. 14, pp. 13049-13065, 2015.
S. Y. Yang, Aisimutula, D., Li, H. F., Hu, Y., Du, X., Li, J., and Luan, M. X., Mutational analysis of BRCA1/2 gene and pathologic characteristics from Kazakh population with sporadic breast cancer in northwestern China, vol. 14, pp. 13151-13161, 2015.
F. Jiang, Yang, Y., Li, J., Li, W., Luo, Y., Li, Y., Zhao, H., Wang, X., Yin, G., and Wu, G., Partial least squares-based gene expression analysis in preeclampsia, vol. 14, pp. 6598-6604, 2015.
P. Sun, Su, N., Lin, F. Z., Ma, L., Wang, H. J., Rong, X., Dai, Y. D., Li, J., Jian, Z. W., Tang, L. H., Xiao, W., and Li, C. Q., Prevalence of hepatitis A viral RNA and antibodies among Chinese blood donors, vol. 14, pp. 16431-16437, 2015.
J. Li, Liu, C. Y., Jiang, Y. F., Wei, X. Z., and Li, J. U., Proliferation and differentiation of human osteoblasts from a type 2 diabetic patient in vitro, vol. 14, pp. 11292-11299, 2015.
S. - T. Yan, Li, C. - X., Li, C. - L., Li, J., Shao, Y. - H., Liu, Y., Zhong, W. - W., Fang, F. - S., Sun, B. - R., and Tian, H., Promotive effect of comprehensive management on achieving blood glucose control in senile type 2 diabetics, vol. 14, pp. 3062-3070, 2015.
W. Zhou, Lv, H., Li, M. X., Su, H., Huang, L. G., Li, J., and Yuan, W. M., Protective effects of bifidobacteria on intestines in newborn rats with necrotizing enterocolitis and its regulation on TLR2 and TLR4, vol. 14, pp. 11505-11514, 2015.
J. Zhang, Yu, H. - W., Li, J., Zhu, Y. - K., Wang, K. - F., Jia, L., and Meng, Q. - H., Reduced cortisol in the absence of bacterial infection in patients with hepatitis B virus cirrhosis, vol. 14, pp. 7957-7963, 2015.
J. Li, Jia, X. F., Liu, J., Liu, J. J., and Zhao, H. B., Relationship of EGFR DNA methylation with the severity of non-small cell lung cancer, vol. 14, pp. 11915-11923, 2015.
L. Zhang, Liu, R. X., Wang, J., Zhang, T., Li, J., Shi, J. H., Kang, B. Y., and Chen, S. Q., A SCAR marker for the analysis of chloroplast DNA from different cultivars of Cornus officinalis, vol. 14, pp. 17170-17181, 2015.
J. K. Feng, Lu, Y. F., Li, J., Qi, Y. H., Yi, M. L., and Ma, D. Y., Upregulation of salivary α2 macroglobulin in patients with type 2 diabetes mellitus, vol. 14, pp. 2268-2274, 2015.
C. Y. Zhang, Qu, B., Ye, P., Li, J., and Bao, C. D., Vulnerability of atherosclerotic plaques is as­sociated with type I interferon in a murine model of lupus and atherosclerosis, vol. 14, pp. 14871-14881, 2015.
2014
Z. Xie, Zhang, M., Zhao, B., Wang, Q., Li, J., Liu, Y. Y., and Chen, Y. H., Advanced oxidation protein products as a biomarker of cutaneous lupus erythematosus complicated by nephritis: a case-control study, vol. 13, pp. 9213-9219, 2014.
S. S. Wen, He, D. W., Liao, C. M., Li, J., Wen, G. Q., and Liu, X. H., Cloning and sequence analysis of an actin gene in aloe, vol. 13, pp. 4949-4955, 2014.
Q. J. Chao, Li, Y. D., Geng, X. X., Zhang, L., Dai, X., Zhang, X., Li, J., and Zhang, H. J., Complete mitochondrial genome sequence of Marmota himalayana (Rodentia: Sciuridae) and phylogenetic analysis within Rodentia, vol. 13, pp. 2739-2751, 2014.
L. - H. Yang, Wang, M. - S., Zheng, F. - X., Li, J., Chen, Y., Jin, Y. - H., Xie, H. - X., Yang, X. - L., and Chen, B. - C., Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis, vol. 13, pp. 2969-2977, 2014.
H. F. Wang, Yang, H., Hu, L. B., Lei, Y. H., Qin, Y., Li, J., Bi, C. W., Wang, J. S., and Huo, Q.,  Effect of siRNA targeting EZH2 on cell viability and apoptosis of bladder cancer T24 cells, vol. 13, pp. 9939-9950, 2014.
C. M. Liao, Li, J., Liu, X. H., and Zhang, Y. S., An effective method for extracting total RNA from Dioscorea opposita Thunb., vol. 13, pp. 462-468, 2014.
H. Zhang, Li, J., Zhang, Y., Sun, M., Zhao, P., Zhang, G., Jin, C., Sun, L., He, M., Wang, B., and Zhang, X., ERCC1 mRNA expression is associated with the clinical outcome of non-small cell lung cancer treated with platinum-based chemotherapy, vol. 13, pp. 10215-10222, 2014.
G. Q. Wen, Li, J., Liu, X. H., Zhang, Y. S., and Wen, S. S., Extraction of total DNA and optimization of the RAPD reaction system in Dioscorea opposita Thunb., vol. 13, pp. 1339-1347, 2014.
B. Q. Gao, Liu, P., Li, J., Wang, Q. Y., and Li, X. P., Genetic diversity of different populations and improved growth in the F1 hybrids in the swimming crab (Portunus trituberculatus), vol. 13, pp. 10454-10463, 2014.
H. Ma, Li, H., Li, J., Wang, X. F., Wei, P. C., Li, L., and Yang, J. B., High-throughput, low-cost, and event-specific polymerase chain reaction detection of herbicide tolerance in genetically modified soybean A2704-12, vol. 13, pp. 696-703, 2014.
J. Li, Chen, H. - X., Yang, J. - G., Li, W., Du, R., and Tian, L., MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population, vol. 13, pp. 8396-8402, 2014.
J. Li, Zhang, Y. S., Liao, C. M., and Liu, X. H., Optimization of the procedure for extracting nucleic acids from aloe, vol. 13, pp. 276-282, 2014.
S. - S. Li, Li, J., Xiao, Z., Ren, A. - G., and Jin, L., Prospective study of MTHFR genetic polymorphisms as a possible etiology of male infertility, vol. 13, pp. 6367-6374, 2014.
J. Li, Zhang, L., Xie, N. Z., Deng, B., Lv, L. X., and Zheng, L. Q., Relationship between the cholesterol ester transfer protein TaqIB polymorphism and the lipid-lowering effect of atorvastatin in patients with coronary atherosclerotic heart disease, vol. 13, pp. 2140-2148, 2014.
M. Bakeyi, Wulasihan, M., Lu, W. H., Yang, Y. C., Li, J., Liu, Z. Q., and He, P. Y., Relationship between the TaqI B polymorphism of the cholesterol ester transfer protein gene and atrial fibrillation in Han and Kazak populations, vol. 13, pp. 9300-9307, 2014.
2013
H. Li, Li, J., Cong, X. H., Duan, Y. B., Li, L., Wei, P. C., Lu, X. Z., and Yang, J. B., A high-throughput, high-quality plant genomic DNA extraction protocol, vol. 12, pp. 4526-4539, 2013.
S. W. Jia, Liu, P., Li, J., Li, J. T., and Pan, L. Q., Isolation and characterization of polymorphic microsatellite loci in the ridgetail white prawn Exopalaemon carinicauda, vol. 12, pp. 2816-2820, 2013.
W. Peng, Chen, Z. - Y., Wang, L., Wang, Z., and Li, J., MicroRNA-199a-3p is downregulated in gastric carcinomas and modulates cell proliferation, vol. 12, pp. 3038-3047, 2013.
L. X. Wang, Hu, Z. D., Hu, Y. M., Tian, B., Li, J., Wang, F. X., Yang, H., Xu, H. R., Li, Y. C., and Li, J., Molecular analysis and frequency of Staphylococcus aureus virulence genes isolated from bloodstream infections in a teaching hospital in Tianjin, China, vol. 12, pp. 646-654, 2013.
Arvidson S and Tegmark K (2001). Regulation of virulence determinants in Staphylococcus aureus. Int. J. Med. Microbiol. 291: 159-170. http://dx.doi.org/10.1078/1438-4221-00112 PMid:11437338   Cao H, Wang M, Li XP and Cao W (2010). Detection of enterotoxin gene in clinical S. aureus. Guangdong Med. J. 31: 2749-2752.   Charles PG, Ward PB, Johnson PD, Howden BP, et al. (2004). Clinical features associated with bacteremia due to heterogeneous vancomycin-intermediate Staphylococcus aureus. Clin. Infect. Dis. 38: 448-451. http://dx.doi.org/10.1086/381093 PMid:14727222   Chen R, Shen DX, Yan ZQ and Wang H (2010). Genotyping on 47 Staphylococcus aureus strains associated with bloodstream infection. Zhonghua Liu Xing Bing Xue Za Zhi 31: 312-315. PMid:20510061   Garbacz K, Piechowicz L, Baranska-Rybak W and Dabrowska-Szponar M (2011). Staphylococcus aureus isolated from patients with recurrent furunculosis carrying Panton-Valentine leukocidin genes represent agr specificity group IV. Eur. J. Dermatol. 21: 43-46. PMid:21233065   Gasch O, Ayats J, Angeles DM, Tubau F, et al. (2011). Epidemiology of methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infection: secular trends over 19 years at a university hospital. Medicine 90: 319-327. PMid:21862935   Goering RV and Winters MA (1992). Rapid method for epidemiological evaluation of gram-positive cocci by field inversion gel electrophoresis. J. Clin. Microbiol. 30: 577-580. PMid:1313045 PMCid:265112   Gomes AR, Westh H and de LH (2006). Origins and evolution of methicillin-resistant Staphylococcus aureus clonal lineages. Antimicrob. Agents Chemother. 50: 3237-3244. http://dx.doi.org/10.1128/AAC.00521-06 PMid:17005800 PMCid:1610072   Hesje CK, Sanfilippo CM, Haas W and Morris TW (2011). Molecular epidemiology of methicillin-resistant and methicillin-susceptible Staphylococcus aureus isolated from the eye. Curr. Eye Res. 36: 94-102. http://dx.doi.org/10.3109/02713683.2010.534229 PMid:21158584 PMCid:3021952   Ho CM, Ho MW, Lee CY, Tien N, et al. (2012). Clonal spreading of methicillin-resistant SCCmec Staphylococcus aureus with specific spa and dru types in central Taiwan. Eur. J. Clin. Microbiol. Infect. Dis. 31: 499-504. http://dx.doi.org/10.1007/s10096-011-1338-3 PMid:21789606   Holtfreter S, Grumann D, Schmudde M, Nguyen HT, et al. (2007). Clonal distribution of superantigen genes in clinical Staphylococcus aureus isolates. J. Clin. Microbiol. 45: 2669-2680. http://dx.doi.org/10.1128/JCM.00204-07 PMid:17537946 PMCid:1951235   Johnson WM, Tyler SD, Ewan EP, Ashton FE, et al. (1991). Detection of genes for enterotoxins, exfoliative toxins, and toxic shock syndrome toxin 1 in Staphylococcus aureus by the polymerase chain reaction. J. Clin. Microbiol. 29: 426-430. PMid:2037659 PMCid:269793   Kim T, Yi J, Hong KH, Park JS, et al. (2011). Distribution of virulence genes in spa types of methicillin-resistant Staphylococcus aureus isolated from patients in intensive care units. Korean J. Lab. Med. 31: 30-36. http://dx.doi.org/10.3343/kjlm.2011.31.1.30 PMid:21239868 PMCid:3111032   Li DZ, Chen YS, Yang JP, Zhang W, et al. (2011). Preliminary molecular epidemiology of the Staphylococcus aureus in lower respiratory tract infections: a multicenter study in China. Chin. Med. J. 124: 687-692. http://dx.doi.org/10.1142/S0192415X11009123 PMid:21721149   Lina G, Piemont Y, Godail-Gamot F, Bes M, et al. (1999a). Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin. Infect. Dis. 29: 1128-1132. http://dx.doi.org/10.1086/313461 PMid:10524952   Lina G, Quaglia A, Reverdy ME, Leclercq R, et al. (1999b). Distribution of genes encoding resistance to macrolides, lincosamides, and streptogramins among staphylococci. Antimicrob. Agents Chemother. 43: 1062-1066. PMid:10223914 PMCid:89111   Lo WT, Lin WJ, Tseng MH, Wang SR, et al. (2008). Risk factors and molecular analysis of panton-valentine leukocidin-positive methicillin-resistant Staphylococcus aureus colonization in healthy children. Pediatr. Infect. Dis. J 27: 713-718. http://dx.doi.org/10.1097/INF.0b013e31816f63b5 PMid:18600194   Lubin AS, Snydman DR, Ruthazer R, Bide P, et al. (2011). Predicting high vancomycin minimum inhibitory concentration in methicillin-resistant Staphylococcus aureus bloodstream infections. Clin. Infect. Dis. 52: 997-1002. http://dx.doi.org/10.1093/cid/cir118 PMid:21460313 PMCid:3070034   Luzzaro F, Ortisi G, Larosa M, Drago M, et al. (2011). Prevalence and epidemiology of microbial pathogens causing bloodstream infections: results of the OASIS multicenter study. Diagn. Microbiol. Infect. Dis. 69: 363-369. http://dx.doi.org/10.1016/j.diagmicrobio.2010.10.016 PMid:21396530   Malachowa N, Whitney AR, Kobayashi SD, Sturdevant DE, et al. (2011). Global changes in Staphylococcus aureus gene expression in human blood. PLoS One 6: e18617. http://dx.doi.org/10.1371/journal.pone.0018617 PMid:21525981 PMCid:3078114   Marra AR, Camargo LF, Pignatari AC, Sukiennik T, et al. (2011). Nosocomial bloodstream infections in Brazilian hospitals: analysis of 2,563 cases from a prospective nationwide surveillance study. J. Clin. Microbiol. 49: 1866-1871. http://dx.doi.org/10.1128/JCM.00376-11 PMid:21411591 PMCid:3122653   Moore CL, Lu M, Cheema F, Osaki-Kiyan P, et al. (2011). Prediction of failure in vancomycin-treated methicillin-resistant Staphylococcus aureus bloodstream infection: a clinically useful risk stratification tool. Antimicrob. Agents Chemother. 55: 4581-4588. http://dx.doi.org/10.1128/AAC.00115-11 PMid:21825294 PMCid:3186992   Moore CL, Osaki-Kiyan P, Haque NZ, Perri MB, et al. (2012). Daptomycin versus vancomycin for bloodstream infections due to methicillin-resistant Staphylococcus aureus with a high vancomycin minimum inhibitory concentration: a case-control study. Clin. Infect. Dis. 54: 51-58. http://dx.doi.org/10.1093/cid/cir764 PMid:22109947   Năstase E, Dorneanu O, Vremera T, Logigan C, et al. (2010). MecA and pvl genes detection in Staphylococcus aureus strains isolated from lower respiratory tract infections. Rev. Med. Chir. Soc. Med. Nat. Iasi 114: 1162-1168. PMid:21500473   National Committee for Clinical Laboratory Standards (2010). Performance Standards for Antimicrobial Susceptibility Testing. Twentieth Informational Supplement, M100-S20. National Committee for Clinical Laboratory Standards, Wayne.   Oliveira DC and de Lencastre H (2002). Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus. Antimicrob. Agents Chemother. 46: 2155-2161. http://dx.doi.org/10.1128/AAC.46.7.2155-2161.2002 PMid:12069968 PMCid:127318   Scazzocchio F, Aquilanti L, Tabacchini C, Iebba V, et al. (2011). Microbiological and molecular characterization of nosocomial and community Staphylococcus aureus isolates. Epidemiol. Infect. 139: 613-622. http://dx.doi.org/10.1017/S095026881000138X PMid:20561388   Shallcross LJ, Williams K, Hopkins S, Aldridge RW, et al. (2010). Panton-Valentine leukocidin associated staphylococcal disease: a cross-sectional study at a London hospital, England. Clin. Microbiol. Infect. 16: 1644-1648. http://dx.doi.org/10.1111/j.1469-0691.2010.03153.x PMid:20969671   Taj Y, Abdullah FE and Kazmi SU (2010). Current pattern of antibiotic resistance in Staphylococcus aureus clinical isolates and the emergence of vancomycin resistance. J. Coll. Physicians Surg. Pak. 20: 728-732. PMid:21078245   Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, et al. (1995). Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J. Clin. Microbiol. 33: 2233-2239. PMid:7494007 PMCid:228385   Vandenesch F, Naimi T, Enright MC, Lina G, et al. (2003). Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence. Emerg. Infect. Dis. 9: 978-984. http://dx.doi.org/10.3201/eid0908.030089 PMid:12967497 PMCid:3020611   Wang J, Liang J and Xiao YH (2010). Mohnarin of 2008: Bacterial Composing and Resistance in Bloodstream Infections. Chin. J. Nosocomiol. 20: 2399-2404.   Wu D, Li X, Yang Y, Zheng Y, et al. (2011). Superantigen gene profiles and presence of exfoliative toxin genes in community-acquired meticillin-resistant Staphylococcus aureus isolated from Chinese children. J. Med. Microbiol. 60: 35-45. http://dx.doi.org/10.1099/jmm.0.023465-0 PMid:20829395   Zhang K, McClure JA, Elsayed S, Louie T, et al. (2005). Novel multiplex PCR assay for characterization and concomitant subtyping of staphylococcal cassette chromosome mec types I to V in methicillin-resistant Staphylococcus aureus. J. Clin. Microbiol. 43: 5026-5033. http://dx.doi.org/10.1128/JCM.43.10.5026-5033.2005 PMid:16207957 PMCid:1248471
M. L. Li, Chen, J. H., Zhao, Z. Y., Zhang, K. J., Li, Z., Li, J., Mai, J. Y., Zhu, X. M., and Cai, M. S., Molecular cloning and characterization of the pseudorabies virus US1 gene, vol. 12, pp. 85-98, 2013.
Advani SJ, Weichselbaum RR and Roizman B (2003). Herpes simplex virus 1 activates cdc2 to recruit topoisomerase II alpha for post-DNA synthesis expression of late genes. Proc. Natl. Acad. Sci. U. S. A. 100: 4825-4830. http://dx.doi.org/10.1073/pnas.0730735100 PMid:12665617 PMCid:153640   Ambagala AP and Cohen JI (2007). Varicella-Zoster virus IE63, a major viral latency protein, is required to inhibit the alpha interferon-induced antiviral response. J. Virol. 81: 7844-7851. http://dx.doi.org/10.1128/JVI.00325-07 PMid:17507475 PMCid:1951283   Antunes RS, Gomes VN, Prioli SM, Prioli RA, et al. (2010). Molecular characterization and phylogenetic relationships among species of the genus Brycon (Characiformes: Characidae) from four hydrographic basins in Brazil. Genet. Mol. Res. 9: 674-684. http://dx.doi.org/10.4238/vol9-2gmr759 PMid:20449799   Barbara KE, Willis KA, Haley TM, Deminoff SJ, et al. (2007). Coiled coil structures and transcription: an analysis of the S. cerevisiae coilome. Mol. Genet. Genomics 278: 135-147. http://dx.doi.org/10.1007/s00438-007-0237-x PMid:17476531   Bastian TW, Livingston CM, Weller SK and Rice SA (2010). Herpes simplex virus type 1 immediate-early protein ICP22 is required for VICE domain formation during productive viral infection. J. Virol. 84: 2384-2394. http://dx.doi.org/10.1128/JVI.01686-09 PMid:20032172 PMCid:2820935   Bowman JJ, Orlando JS, Davido DJ, Kushnir AS, et al. (2009). Transient expression of herpes simplex virus type 1 ICP22 represses viral promoter activity and complements the replication of an ICP22 null virus. J. Virol. 83: 8733-8743. http://dx.doi.org/10.1128/JVI.00810-09 PMid:19535441 PMCid:2738139   Brandt CR and Kolb AW (2003). Tyrosine 116 of the herpes simplex virus type 1 IEalpha22 protein is an ocular virulence determinant and potential phosphorylation site. Invest. Ophthalmol. Vis. Sci. 44: 4601-4607. http://dx.doi.org/10.1167/iovs.03-0582 PMid:14578374   Brukman A and Enquist LW (2006). Pseudorabies virus EP0 protein counteracts an interferon-induced antiviral state in a species-specific manner. J. Virol. 80: 10871-10873. http://dx.doi.org/10.1128/JVI.01308-06 PMid:16928746 PMCid:1641768   Coller KE, Lee JI, Ueda A and Smith GA (2007). The capsid and tegument of the alphaherpesviruses are linked by an interaction between the UL25 and VP1/2 proteins. J. Virol. 81: 11790-11797. http://dx.doi.org/10.1128/JVI.01113-07 PMid:17715218 PMCid:2168758   Feng ZP (2002). An overview on predicting the subcellular location of a protein. In Silico Biol. 2: 291-303. PMid:12542414   Ferrari M, Gualandi GL, Corradi A, Monaci C, et al. (2000). The response of pigs inoculated with a thymidine kinase-negative (TK-) pseudorabies virus to challenge infection with virulent virus. Comp. Immunol. Microbiol. Infect. Dis. 23: 15-26. http://dx.doi.org/10.1016/S0147-9571(99)00019-3   Geiss BJ, Tavis JE, Metzger LM, Leib DA, et al. (2001). Temporal regulation of herpes simplex virus type 2 VP22 expression and phosphorylation. J. Virol. 75: 10721-10729. http://dx.doi.org/10.1128/JVI.75.22.10721-10729.2001 PMid:11602713 PMCid:114653   Habran L, Bontems S, Di VE, Sadzot-Delvaux C, et al. (2005). Varicella-zoster virus IE63 protein phosphorylation by roscovitine-sensitive cyclin-dependent kinases modulates its cellular localization and activity. J. Biol. Chem. 280: 29135-29143. http://dx.doi.org/10.1074/jbc.M503312200 PMid:15955820   Hopp TP and Woods KR (1981). Prediction of protein antigenic determinants from amino acid sequences. Proc. Natl. Acad. Sci. U. S. A. 78: 3824-3828. http://dx.doi.org/10.1073/pnas.78.6.3824 PMid:6167991 PMCid:319665   Jahedi S, Markovitz NS, Filatov F and Roizman B (1999). Colocalization of the herpes simplex virus 1 UL4 protein with infected cell protein 22 in small, dense nuclear structures formed prior to onset of DNA synthesis. J. Virol. 73: 5132- 5138. PMid:10233976 PMCid:112558   Jones JO and Arvin AM (2005). Viral and cellular gene transcription in fibroblasts infected with small plaque mutants of varicella-zoster virus. Antiviral Res. 68: 56-65. http://dx.doi.org/10.1016/j.antiviral.2005.06.011 PMid:16118026   Kalamvoki M and Roizman B (2011). The histone acetyltransferase CLOCK is an essential component of the herpes simplex virus 1 transcriptome that includes TFIID, ICP4, ICP27, and ICP22. J. Virol. 85: 9472-9477. http://dx.doi.org/10.1128/JVI.00876-11 PMid:21734043 PMCid:3165755   Kost RG, Kupinsky H and Straus SE (1995). Varicella-zoster virus gene 63: transcript mapping and regulatory activity. Virology 209: 218-224. http://dx.doi.org/10.1006/viro.1995.1246 PMid:7747473   Kramer T, Greco TM, Enquist LW and Cristea IM (2011). Proteomic characterization of pseudorabies virus extracellular virions. J. Virol. 85: 6427-6441. http://dx.doi.org/10.1128/JVI.02253-10 PMid:21525350 PMCid:3126529   Krautwald M, Maresch C, Klupp BG, Fuchs W, et al. (2008). Deletion or green fluorescent protein tagging of the pUL35 capsid component of pseudorabies virus impairs virus replication in cell culture and neuroinvasion in mice. J. Gen. Virol. 89: 1346-1351. http://dx.doi.org/10.1099/vir.0.83652-0 PMid:18474549   Kyte J and Doolittle RF (1982). A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157: 105-132. http://dx.doi.org/10.1016/0022-2836(82)90515-0   Li M, Wang S, Cai M, Guo H, et al. (2011a). Characterization of molecular determinants for nucleocytoplasmic shuttling of PRV UL54. Virology 417: 385-393. http://dx.doi.org/10.1016/j.virol.2011.06.004 PMid:21777931   Li M, Wang S, Cai M and Zheng C (2011b). Identification of nuclear and nucleolar localization signals of pseudorabies virus (PRV) early protein UL54 reveals that its nuclear targeting is required for efficient production of PRV. J. Virol. 85: 10239-10251. http://dx.doi.org/10.1128/JVI.05223-11 PMid:21795331 PMCid:3196411   Lin HW, Hsu WL, Chang YY, Jan MS, et al. (2010). Role of the UL41 protein of pseudorabies virus in host shutoff, pathogenesis and induction of TNF-alpha expression. J. Vet. Med. Sci. 72: 1179-1187. http://dx.doi.org/10.1292/jvms.10-0059 PMid:20448414   Luxton GW, Lee JI, Haverlock-Moyns S, Schober JM, et al. (2006). The pseudorabies virus VP1/2 tegument protein is required for intracellular capsid transport. J. Virol. 80: 201-209. http://dx.doi.org/10.1128/JVI.80.1.201-209.2006 PMid:16352544 PMCid:1317523   Mason JM and Arndt KM (2004). Coiled coil domains: stability, specificity, and biological implications. Chembiochem 5: 170-176. http://dx.doi.org/10.1002/cbic.200300781 PMid:14760737   McGeoch DJ, Dolan A and Ralph AC (2000). Toward a comprehensive phylogeny for mammalian and avian herpesviruses. J. Virol. 74: 10401-10406. http://dx.doi.org/10.1128/JVI.74.22.10401-10406.2000 PMid:11044084 PMCid:110914   Mueller NH, Walters MS, Marcus RA, Graf LL, et al. (2010). Identification of phosphorylated residues on varicella-zoster virus immediate-early protein ORF63. J. Gen. Virol. 91: 1133-1137. http://dx.doi.org/10.1099/vir.0.019067-0 PMid:20089801 PMCid:2888152   Nixdorf R, Klupp BG and Mettenleiter TC (2001a). Restoration of function of carboxy-terminally truncated pseudorabies virus glycoprotein B by point mutations in the ectodomain. J. Virol. 75: 11526-11533. http://dx.doi.org/10.1128/JVI.75.23.11526-11533.2001 PMid:11689634 PMCid:114739   Nixdorf R, Klupp BG and Mettenleiter TC (2001b). Role of the cytoplasmic tails of pseudorabies virus glycoproteins B, E and M in intracellular localization and virion incorporation. J. Gen. Virol. 82: 215-226. PMid:11125174   Orlando JS, Balliet JW, Kushnir AS, Astor TL, et al. (2006). ICP22 is required for wild-type composition and infectivity of herpes simplex virus type 1 virions. J. Virol. 80: 9381-9390. http://dx.doi.org/10.1128/JVI.01061-06 PMid:16973544 PMCid:1617265   Pelletier A, Do F, Brisebois JJ, Lagace L, et al. (1997). Self-association of herpes simplex virus type 1 ICP35 is via coiled-coil interactions and promotes stable interaction with the major capsid protein. J. Virol. 71: 5197-5208. PMid:9188587 PMCid:191755   Pomeranz LE and Blaho JA (1999). Modified VP22 localizes to the cell nucleus during synchronized herpes simplex virus type 1 infection. J. Virol. 73: 6769-6781. PMid:10400775 PMCid:112762   Ren X, Harms JS and Splitter GA (2001). Tyrosine phosphorylation of bovine herpesvirus 1 tegument protein VP22 correlates with the incorporation of VP22 into virions. J. Virol. 75: 9010-9017. http://dx.doi.org/10.1128/JVI.75.19.9010-9017.2001 PMid:11533164 PMCid:114469   Smith GA and Enquist LW (2000). A self-recombining bacterial artificial chromosome and its application for analysis of herpesvirus pathogenesis. Proc. Natl. Acad. Sci. U. S. A. 97: 4873-4878. http://dx.doi.org/10.1073/pnas.080502497 PMid:10781094 PMCid:18325   Szpara ML, Tafuri YR, Parsons L, Shamim SR, et al. (2011). A wide extent of inter-strain diversity in virulent and vaccine strains of alphaherpesviruses. PLoS Pathog. 7: e1002282. http://dx.doi.org/10.1371/journal.ppat.1002282 PMid:22022263 PMCid:3192842   Tomioka Y, Miyazaki T, Taharaguchi S, Yoshino S, et al. (2008). Cerebellar pathology in transgenic mice expressing the pseudorabies virus immediate-early protein IE180. Eur. J. Neurosci. 27: 2115-2132. http://dx.doi.org/10.1111/j.1460-9568.2008.06174.x PMid:18412631   Walters MS, Kyratsous CA, Wan S and Silverstein S (2008). Nuclear import of the varicella-zoster virus latency-associated protein ORF63 in primary neurons requires expression of the lytic protein ORF61 and occurs in a proteasome-dependent manner. J. Virol. 82: 8673-8686. http://dx.doi.org/10.1128/JVI.00685-08 PMid:18562514 PMCid:2519623   Welling GW, Weijer WJ, van der Zee R and Welling-Wester S (1985). Prediction of sequential antigenic regions in proteins. FEBS Lett. 188: 215-218. http://dx.doi.org/10.1016/0014-5793(85)80374-4   Xing J, Wang S, Lin F, Pan W, et al. (2011). Comprehensive characterization of interaction complexes of herpes simplex virus type 1 ICP22, UL3, UL4, and UL20.5. J. Virol. 85: 1881-1886. http://dx.doi.org/10.1128/JVI.01730-10 PMid:21147926 PMCid:3028915   Zhang G and Leader DP (1990). The structure of the pseudorabies virus genome at the end of the inverted repeat sequences proximal to the junction with the short unique region. J. Gen. Virol. 71: 2433-2441. http://dx.doi.org/10.1099/0022-1317-71-10-2433 PMid:2172457
Y. L. Hou, Ding, X., Hou, W., Song, B., Wang, T., Wang, F., Li, J., Zhong, J., Xu, T., Ma, B. X., Zhu, H. Q., Li, J. H., and Zhong, J. C., Overexpression, purification, and pharmacologic evaluation of anticancer activity of ribosomal protein L24 from the giant panda (Ailuropoda melanoleuca), vol. 12, pp. 4735-4750, 2013.
H. Li, Ni, D. H., Duan, Y. B., Chen, Y., Li, J., Song, F. S., Li, L., Wei, P. C., and Yang, J. B., Quantitative detection of the rice false smut pathogen Ustilaginoidea virens by real-time PCR, vol. 12, pp. 6433-6441, 2013.
J. Li, Wang, L., Li, H., Zhang, R., Li, X., and Guo, M., Relationship of common expression quantitative trait loci genes to the immune system, vol. 12, pp. 6546-6553, 2013.

Pages