Publications
Found 28 results
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“Association of APOA1 gene polymorphisms (rs670, rs5069, and rs2070665) with dyslipidemia in the Kazakhs of Xinjiang”, vol. 15, p. -, 2016.
, “Association of APOA1 gene polymorphisms (rs670, rs5069, and rs2070665) with dyslipidemia in the Kazakhs of Xinjiang”, vol. 15, p. -, 2016.
, “Association of APOA1 gene polymorphisms (rs670, rs5069, and rs2070665) with dyslipidemia in the Kazakhs of Xinjiang”, vol. 15, p. -, 2016.
, “Changes in methylation of genomic DNA from chicken immune organs in response to H5N1 influenza virus infection”, vol. 15, p. -, 2016.
, “Changes in methylation of genomic DNA from chicken immune organs in response to H5N1 influenza virus infection”, vol. 15, p. -, 2016.
, “Detection of Piwi-interacting RNAs based on sequence features”, vol. 15, p. -, 2016.
, “Detection of Piwi-interacting RNAs based on sequence features”, vol. 15, p. -, 2016.
, “Prognostic significance of long non-coding RNA MALAT-1 in various human carcinomas: a meta-analysis”, vol. 15, p. -, 2016.
, “Prognostic significance of long non-coding RNA MALAT-1 in various human carcinomas: a meta-analysis”, vol. 15, p. -, 2016.
, “Prognostic significance of long non-coding RNA MALAT-1 in various human carcinomas: a meta-analysis”, vol. 15, p. -, 2016.
, “Time-series microarray data simulation modeled with a case-control label”, vol. 15, p. -, 2016.
, “Time-series microarray data simulation modeled with a case-control label”, vol. 15, p. -, 2016.
, “Association between polymorphisms of fat mass and obesity-associated gene and metabolic syndrome in Kazakh adults of Xinjiang, China”, vol. 14, pp. 14597-14606, 2015.
, “Expression of B7-H3 in cancer tissue during osteosarcoma progression in nude mice”, vol. 14, pp. 14253-14261, 2015.
, “Genetic expression and functional characterization of the RUNX2 gene in human adult bone marrow mesenchymal stem cells”, vol. 14, pp. 18210-18217, 2015.
, “Glutathione S-transferase polymorphisms in varicocele patients: a meta-analysis”, vol. 14, pp. 18851-18858, 2015.
, “Isolation and characterization of cancer stem cells from medulloblastoma”, vol. 14, pp. 3355-3361, 2015.
, “Isolation and characterization of novel microsatellite markers from the sika deer (Cervus nippon) genome”, vol. 14, pp. 11524-11534, 2015.
, “Polymorphisms in the PPARγ gene and their association with metabolic syndrome in Uyghurs and Kazakhs from Xinjiang, China”, vol. 14, pp. 6279-6288, 2015.
, , “Analysis of the haplotype and linkage disequilibrium of PPARγ gene polymorphisms rs3856806, rs12490265, rs1797912, and rs1175543 among patients with metabolic syndrome in Kazakh of Xinjiang Province”, vol. 13, pp. 8686-8694, 2014.
, “Epidemiological analysis of dyslipidemia in adults of three ethnicities in Xinjiang, China”, vol. 13, pp. 2385-2393, 2014.
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“Absence of SH2B3 mutation in nonobese diabetic mice”, vol. 11, pp. 1266-1271, 2012.
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Cui J, Zhu N, Wang Q, Yu M, et al. (2009). p38 MAPK contributes to CD54 expression and the enhancement of phagocytic activity during macrophage development. Cell Immunol. 256: 6-11.
http://dx.doi.org/10.1016/j.cellimm.2008.12.003
PMid:19185295
D'Alise AM, Auyeung V, Feuerer M, Nishio J, et al. (2008). The defect in T-cell regulation in NOD mice is an effect on the T-cell effectors. Proc. Natl. Acad. Sci. U. S. A. 105: 19857-19862.
http://dx.doi.org/10.1073/pnas.0810713105
PMid:19073938 PMCid:2604930
Delovitch TL and Singh B (1997). The nonobese diabetic mouse as a model of autoimmune diabetes: immune dysregulation gets the NOD. Immunity 7: 727-738.
http://dx.doi.org/10.1016/S1074-7613(00)80392-1
Hung JT, Liao JH, Lin YC, Chang HY, et al. (2005). Immunopathogenic role of TH1 cells in autoimmune diabetes: evidence from a T1 and T2 doubly transgenic non-obese diabetic mouse model. J. Autoimmun. 25: 181-192.
http://dx.doi.org/10.1016/j.jaut.2005.08.010
PMid:16263243
Hunt KA, Zhernakova A, Turner G, Heap GA, et al. (2008). Newly identified genetic risk variants for celiac disease related to the immune response. Nat. Genet. 40: 395-402.
http://dx.doi.org/10.1038/ng.102
PMid:18311140 PMCid:2673512
Li Y, He X, Schembri-King J, Jakes S, et al. (2000). Cloning and characterization of human Lnk, an adaptor protein with pleckstrin homology and Src homology 2 domains that can inhibit T cell activation. J. Immunol. 164: 5199-5206.
PMid:10799879
Marleau AM, Summers KL and Singh B (2008). Differential contributions of APC subsets to T cell activation in nonobese diabetic mice. J. Immunol. 180: 5235-5249.
PMid:18390704
Todd JA, Walker NM, Cooper JD, Smyth DJ, et al. (2007). Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat. Genet. 39: 857-864.
http://dx.doi.org/10.1038/ng2068
PMid:17554260 PMCid:2492393
Velazquez L, Cheng AM, Fleming HE, Furlonger C, et al. (2002). Cytokine signaling and hematopoietic homeostasis are disrupted in Lnk-deficient mice. J. Exp. Med. 195: 1599-1611.
http://dx.doi.org/10.1084/jem.20011883
PMid:12070287 PMCid:2193556
Zhang J, Zhu N, Wang Q, Wang J, et al. (2010). MEKK3 overexpression contributes to the hyperresponsiveness of IL-12- overproducing cells and CD4+ T conventional cells in nonobese diabetic mice. J. Immunol. 185: 3554-3563.
http://dx.doi.org/10.4049/jimmunol.1000431
PMid:20720201
“Expression patterns of the STAG gene in intact and regenerating planarians (Dugesia japonica)”, vol. 10, pp. 410-418, 2011.
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Adell T, Marsal M and Salo E (2008). Planarian GSK3s are involved in neural regeneration. Dev. Genes Evol. 218: 89-103.
http://dx.doi.org/10.1007/s00427-007-0199-3
PMid:18202849
Anderson DE, Losada A, Erickson HP and Hirano T (2002). Condensin and cohesin display different arm conformations with characteristic hinge angles. J. Cell Biol. 156: 419-424.
http://dx.doi.org/10.1083/jcb.200111002
PMid:11815634 PMCid:2173330
Baguñà J, Saló E and Auladell C (1989). Regeneration and pattern formation in planarians III. Evidence that neoblasts are totipotent stem cells and the source of blastema cells. Development 107: 77-86.
Baguñà J, Saló E, Romero RR, Garcia-Fernandez J, et al. (1994). Regeneration and pattern formation in planarians: cell, molecules and genes. Zool. Sci. 11: 781-795.
Chen F, Kamradt M, Mulcahy M, Byun Y, et al. (2002). Caspase proteolysis of the cohesin component RAD21 promotes apoptosis. J. Biol. Chem. 277: 16775-16781.
http://dx.doi.org/10.1074/jbc.M201322200
PMid:11875078
Coward SJ (1968). Effects of actinomycin D on regeneration give evidence of sequential gene activation. Nature 219: 1257-1258.
http://dx.doi.org/10.1038/2191257a0
PMid:4971121
Gruber S, Haering CH and Nasmyth K (2003). Chromosomal cohesin forms a ring. Cell 112: 765-777.
http://dx.doi.org/10.1016/S0092-8674(03)00162-4
Haering CH and Nasmyth K (2003). Building and breaking bridges between sister chromatids. Bioessays 25: 1178-1191.
http://dx.doi.org/10.1002/bies.10361
PMid:14635253
Handberg-Thorsager M, Fernandez E and Salo E (2008). Stem cells and regeneration in planarians. Front. Biosci. 13: 6374-6394.
http://dx.doi.org/10.2741/3160
PMid:18508666
Jiang Y, Loker ES and Zhang SM (2006). In vivo and in vitro knockdown of FREP2 gene expression in the snail Biomphalaria glabrata using RNA interference. Dev. Comp. Immunol. 30: 855-866.
http://dx.doi.org/10.1016/j.dci.2005.12.004
PMid:16442620
Krasikova A, Barbero JL and Gaginskaya E (2005). Cohesion proteins are present in centromere protein bodies associated with avian lampbrush chromosomes. Chromosome Res. 13: 675-685.
http://dx.doi.org/10.1007/s10577-005-1005-6
PMid:16235117
Lara-Pezzi E, Pezzi N, Prieto I, Barthelemy I, et al. (2004). Evidence of a transcriptional co-activator function of cohesin STAG/SA/Scc3. J. Biol. Chem. 279: 6553-6559.
http://dx.doi.org/10.1074/jbc.M307663200
PMid:14660624
Losada A, Hirano M and Hirano T (1998). Identification of Xenopus SMC protein complexes required for sister chromatid cohesion. Genes Dev. 12: 1986-1997.
http://dx.doi.org/10.1101/gad.12.13.1986
PMid:9649503 PMCid:316973
Losada A, Yokochi T, Kobayashi R and Hirano T (2000). Identification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexes. J. Cell Biol. 150: 405-416.
http://dx.doi.org/10.1083/jcb.150.3.405
PMid:10931856 PMCid:2175199
Michaelis C, Ciosk R and Nasmyth K (1997). Cohesins: chromosomal proteins that prevent premature separation of sister chromatids. Cell 91: 35-45.
http://dx.doi.org/10.1016/S0092-8674(01)80007-6
Molina MD, Salo E and Cebria F (2009). Expression pattern of the expanded noggin gene family in the planarian Schmidtea mediterranea. Gene Expr. Patterns 9: 246-253.
http://dx.doi.org/10.1016/j.gep.2008.12.008
PMid:19174194
Newmark PA and Sanchez AA (2002). Not your father's planarian: a classic model enters the era of functional genomics. Nat. Rev. Genet 3: 210-219.
http://dx.doi.org/10.1038/nrg759
PMid:11972158
Palakodeti D, Smielewska M, Lu YC, Yeo GW, et al. (2008). The PIWI proteins SMEDWI-2 and SMEDWI-3 are required for stem cell function and piRNA expression in planarians. RNA 14: 1174-1186.
http://dx.doi.org/10.1261/rna.1085008
PMid:18456843 PMCid:2390803
Pati D, Zhang N and Plon SE (2002). Linking sister chromatid cohesion and apoptosis: role of Rad21. Mol. Cell Biol. 22: 8267-8277.
http://dx.doi.org/10.1128/MCB.22.23.8267-8277.2002
PMid:12417729 PMCid:134054
Pezzi N, Prieto I, Kremer L, Perez Jurado LA, et al. (2000). STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion. FASEB J. 14: 581-592.
PMid:10698974
Prieto I, Suja JA, Pezzi N, Kremer L, et al. (2001). Mammalian STAG3 is a cohesin specific to sister chromatid arms in meiosis I. Nat. Cell Biol. 3: 761-766.
http://dx.doi.org/10.1038/35087082
PMid:11483963
Reddien PW and Sanchez AA (2004). Fundamentals of planarian regeneration. Annu. Rev. Cell Dev. Biol. 20: 725-757.
http://dx.doi.org/10.1146/annurev.cellbio.20.010403.095114
PMid:15473858
Reddien PW, Bermange AL, Kicza AM and Sanchez AA (2007). BMP signaling regulates the dorsal planarian midline and is needed for asymmetric regeneration. Development 134: 4043-4051.
http://dx.doi.org/10.1242/dev.007138
PMid:17942485
Rossi L, Salvetti A, Lena A, Batistoni R, et al. (2006). DjPiwi-1, a member of the PAZ-Piwi gene family, defines a subpopulation of planarian stem cells. Dev. Genes Evol. 216: 335-346.
http://dx.doi.org/10.1007/s00427-006-0060-0
PMid:16532341
Salo E (2006). The power of regeneration and the stem-cell kingdom: freshwater planarians (Platyhelminthes). Bioessays 28: 546-559.
http://dx.doi.org/10.1002/bies.20416
PMid:16615086
Salo E and Baguna J (1984). Regeneration and pattern formation in planarians. I. The pattern of mitosis in anterior and posterior regeneration in Dugesia (G) tigrina, and a new proposal for blastema formation. J. Embryol. Exp. Morphol. 83: 63-80.
PMid:6502076
Salvetti A, Batistoni R, Deri P, Rossi L, et al. (1998). Expression of DjY1, a protein containing a cold shock domain and RG repeat motifs, is targeted to sites of regeneration in planarians. Dev. Biol. 201: 217-229.
http://dx.doi.org/10.1006/dbio.1998.8996
PMid:9740660
Sanchez AA and Kang H (2005). Multicellularity, stem cells, and the neoblasts of the planarian Schmidtea mediterranea. Exp. Cell Res. 306: 299-308.
http://dx.doi.org/10.1016/j.yexcr.2005.03.020
PMid:15925584
Sjogren C and Nasmyth K (2001). Sister chromatid cohesion is required for postreplicative double-strand break repair in Saccharomyces cerevisiae. Curr. Biol. 11: 991-995.
http://dx.doi.org/10.1016/S0960-9822(01)00271-8
Sumara I, Vorlaufer E, Gieffers C, Peters BH, et al. (2000). Characterization of vertebrate cohesin complexes and their regulation in prophase. J. Cell Biol. 151: 749-762.
http://dx.doi.org/10.1083/jcb.151.4.749
PMid:11076961 PMCid:2169443
Wang Y, Zayas RM, Guo T and Newmark PA (2007). Nanos function is essential for development and regeneration of planarian germ cells. Proc. Natl. Acad. Sci. U. S. A. 104: 5901-5906.
http://dx.doi.org/10.1073/pnas.0609708104
PMid:17376870 PMCid:1851589
“Rapid determination of transgene copy number in tobacco by competitive PCR using a pair of SSR primers”, vol. 9, pp. 935-940, 2010.
, Bindler G, van der Hoeven R, Gunduz I, Plieske J, et al. (2007). A microsatellite marker based linkage map of tobacco. Theor. Appl. Genet. 114: 341-349.
http://dx.doi.org/10.1007/s00122-006-0437-5
PMid:17115128
Hofgen R and Willmitzer L (1988). Storage of competent cells for Agrobacterium transformation. Nucleic Acids Res. 16: 9877.
http://dx.doi.org/10.1093/nar/16.20.9877
PMid:3186459 PMCid:338805
Horsch RB, Fry JE, Hoffmann NL, Eichholtz D, et al. (1985). A Simple and General Method for Transferring Genes into Plants. Sci. 227: 1229-1231.
http://dx.doi.org/10.1126/science.227.4691.1229
PMid:17757866
Kumpatla SP, Teng W, Buchholz WG and Hall TC (1997). Epigenetic transcriptional silencing and 5-azacytidine-mediated reactivation of a complex transgene in rice. Plant Physiol. 115: 361-373.
http://dx.doi.org/10.1104/pp.115.2.361
PMid:9342860 PMCid:158494
Mason G, Provero P, Vaira AM and Accotto GP (2002). Estimating the number of integrations in transformed plants by quantitative real-time PCR. BMC Biotechnol. 2: 20.
http://dx.doi.org/10.1186/1472-6750-2-20
PMid:12398792 PMCid:137580
Murray MG and Thompson WF (1980). Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res. 8: 4321- 4325.
http://dx.doi.org/10.1093/nar/8.19.4321
PMid:7433111 PMCid:324241
Yamamoto T, Kimura T, Sawamura Y, Kotobuki K, et al. (2001). SSRs isolated from apple can identify polymorphism and genetic diversity in pear. Theor. Appl. Genet. 102: 865-870.
http://dx.doi.org/10.1007/s001220000524
Yang L, Ding J, Zhang C, Jia J, et al. (2005). Estimating the copy number of transgenes in transformed rice by real-time quantitative PCR. Plant Cell Rep. 23: 759-763.
http://dx.doi.org/10.1007/s00299-004-0881-0
PMid:15459795
Yi CX, Zhang J, Chan KM, Liu XK, et al. (2008). Quantitative real-time PCR assay to detect transgene copy number in cotton (Gossypium hirsutum). Anal. Biochem. 375: 150-152.
http://dx.doi.org/10.1016/j.ab.2007.11.022
PMid:18078801