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“Association between adiponectin gene T45G polymorphism and nonalcoholic fatty liver disease risk: a meta-analysis”, vol. 15, p. -, 2016.
, “Association between adiponectin gene T45G polymorphism and nonalcoholic fatty liver disease risk: a meta-analysis”, vol. 15, p. -, 2016.
, “Association between adiponectin gene T45G polymorphism and nonalcoholic fatty liver disease risk: a meta-analysis”, vol. 15, p. -, 2016.
, “Characterization of RsMYB28 and RsMYB29 transcription factor genes in radish (Raphanus sativus L.)”, vol. 15, p. -, 2016.
, “Characterization of RsMYB28 and RsMYB29 transcription factor genes in radish (Raphanus sativus L.)”, vol. 15, p. -, 2016.
, “Clinical significance of CTHRC1 protein expression in human cancers: a meta-analysis”, vol. 15, p. -, 2016.
, “Clinical significance of CTHRC1 protein expression in human cancers: a meta-analysis”, vol. 15, p. -, 2016.
, “Detection of QTLs controlling fast kernel dehydration in maize (Zea mays L.)”, vol. 15, p. -, 2016.
, “Detection of QTLs controlling fast kernel dehydration in maize (Zea mays L.)”, vol. 15, p. -, 2016.
, , , “Association between polymorphism of β3-adrenoceptor gene and overactive bladder: a meta-analysis”, vol. 14, pp. 2495-2501, 2015.
, “Association between polymorphisms in insulin-like growth factor-1 and risk of osteoporosis”, vol. 14, pp. 7655-7660, 2015.
, “Association of a miR-34b binding site single nucleotide polymorphism in the 3'-untranslated region of the methylenetetrahydrofolate reductase gene with susceptibility to male infertility”, vol. 14, pp. 12196-12204, 2015.
, “Expression of aquaporin 1 and 4 in rats with acute hypoxic lung injury and its significance”, vol. 14, pp. 12756-12764, 2015.
, “Roles of the AIB1 protein in the proliferation and transformation of human esophageal squamous cell carcinoma”, vol. 14, pp. 10376-10383, 2015.
, “Association of MSX1 and TGF-β1 genetic polymorphisms with hypodontia: meta-analysis”, vol. 13, pp. 10007-10016, 2014.
, “Cell proliferation and apoptosis in the fetal and neonatal ovary of guinea pigs”, vol. 13, pp. 1570-1578, 2014.
, “Clinical application of carbon nanoparticle lymph node tracer in the VI region lymph node dissection of differentiated thyroid cancer”, vol. 13, pp. 3432-3437, 2014.
, “Clinical significance of fibroblast growth factor receptor-3 mutations in bladder cancer: a systematic review and meta-analysis”, vol. 13, pp. 1109-1120, 2014.
, “Complete mitochondrial genome sequence of Cheirotonus jansoni (Coleoptera: Scarabaeidae)”, vol. 13, pp. 1047-1058, 2014.
, “Dephosphorylation of NSSR1 regulates alternative splicing of the GluR-B minigene”, vol. 13, pp. 1753-1763, 2014.
, “Diagnostic value of cytological and microbiological methods in cryptococcal meningitis”, vol. 13, pp. 9253-9261, 2014.
, “Identification and characterization of RFRP gene in pigs and its association with reproductive traits”, vol. 13, pp. 1661-1671, 2014.
, “Molecular characteristic and expression analysis of collagenolytic serine protease from the Chinese mitten crab Eriocheir sinensis with defense response to Vibrio anguillarum challenge”, vol. 13, pp. 3885-3894, 2014.
, “PAX-9 polymorphism may be a risk factor for hypodontia: a meta-analysis”, vol. 13, pp. 9997-10006, 2014.
, “Molecular characterization and expression analysis of the Lrh-1 gene in Chinese Hu sheep”, vol. 12, pp. 1490-1500, 2013.
, “Molecular cytogenetic characterization of the Aegilops biuncialis karyotype”, vol. 12. pp. 683-692, 2013.
, Badaeva ED (2002). Evaluation of phylogenetic relationships between five polyploid Aegilops L. species of the U-genome cluster by means of chromosomal analysis. Genetika 38: 799-811.
PMid:12138779
Badaeva ED, Amosova AV, Samatadze TE, Zoshchuk SA, et al. (2004). Genome differentiation in Aegilops. 4. Evolution of the U-genome cluster. Plant Syst. Evol. 246: 45-76.
http://dx.doi.org/10.1007/s00606-003-0072-4
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http://dx.doi.org/10.1016/0092-8674(80)90529-2
Dhaliwal HS, Harjit-Singh and William M (2002). Transfer of rust resistance from Aegilops ovata into bread wheat (Triticum aestivum L.) and molecular characterisation of resistant derivatives. Euphytica 126: 153-159.
http://dx.doi.org/10.1023/A:1016312723040
Friebe B and Heun M (1989). C-banding pattern and powdery mildew resistance of Triticum ovatum and four T. aestivum - T. ovatum chromosome addition lines. Theor. Appl. Genet. 78: 417-424.
http://dx.doi.org/10.1007/BF00265306
Friebe B, Mukai Y and Gill BS (1992a). C-banding polymorphisms in several accessions of Triticum tauschii (Aegilops squarrosa). Genome 35: 192-199.
http://dx.doi.org/10.1139/g92-030
Friebe B, Schubert V, Blüthner W and Hammer K (1992b). C-banding pattern and polymorphism of Aegilops caudata and chromosomal constitutions of the amphiploid T. aestivum - Ae. caudata and six derived chromosome addition lines. Theor. Appl. Genet. 83: 589-596.
http://dx.doi.org/10.1007/BF00226902
Friebe B, Jiang J, Tuleen N and Gill BS (1995). Standard karyotype of Triticum umbellulatum and the characterization of derived chromosome addition and translocation lines in common wheat. Theor. Appl. Genet. 90: 150-156.
http://dx.doi.org/10.1007/BF00221010
Friebe B, Badaeva ED, Kammer K and Gill BS (1996). Standard karyotypes of Aegilops uniaristata, Ae. mutica, Ae. comosa subspecies comosa and heldreichii (Poaceae). Plant Syst. Evol. 202: 199-210.
http://dx.doi.org/10.1007/BF00983382
Friebe B, Qi LL, Nasuda S, Zhang P, et al. (2000). Development of a complete set of Triticum aestivum-Aegilops speltoides chromosome addition lines. Theor. Appl. Genet. 101: 51-58.
http://dx.doi.org/10.1007/s001220051448
Gerlach WL and Bedbrook JR (1979). Cloning and characterization of ribosomal RNA genes from wheat and barley. Nucleic Acids Res. 7: 1869-1885.
http://dx.doi.org/10.1093/nar/7.7.1869
PMid:537913 PMCid:342353
Gerlach WL and Dyer TA (1980). Sequence organization of the repeating units in the nucleus of wheat which contain 5S rRNA genes. Nucleic Acids Res. 8: 4851-4865.
http://dx.doi.org/10.1093/nar/8.21.4851
PMid:7443527 PMCid:324264
Gill BS and Kimber G (1974). Giemsa C-banding and the evolution of wheat. Proc. Natl. Acad. Sci. U. S. A. 71: 4086- 4090.
http://dx.doi.org/10.1073/pnas.71.10.4086
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Makkouk K, Ghulam W and Comeau A (1994). Resistance to barley yellow dwarf luteovirus in Aegilops species. Can. J. Plant Sci. 74: 631-634.
http://dx.doi.org/10.4141/cjps94-113
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http://dx.doi.org/10.1139/g90-094
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http://dx.doi.org/10.1071/FP03143
Mukai Y, Nakahara Y and Yamamoto M (1993). Simultaneous discrimination of the three genomes in hexaploid wheat by multicolor fluorescence in situ hybridization using total genomic and highly repeated DNA probes. Genome 36: 489-494.
http://dx.doi.org/10.1139/g93-067
PMid:18470003
Nagy ED, Molnar-Lang M, Linc G and Lang L (2002). Identification of wheat-barley translocations by sequential GISH and two-colour FISH in combination with the use of genetically mapped barley SSR markers. Genome 45: 1238- 1247.
http://dx.doi.org/10.1139/g02-068
PMid:12502270
Rayburn AL and Gill BS (1986). Isolation of a D-genome specific repeated DNA sequence from Aegilops squarrosa. Plant Mol. Biol. Rep. 4: 102-109.
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Riley R, Chapman V and Johnson R (1968). Introduction of yellow rust resistance of Aegilops comosa into wheat by genetically induced homoeologous recombination. Nature 217: 383-384.
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Schneider A, Linc G, Molnar I and Molnar-Lang M (2005). Molecular cytogenetic characterization of Aegilops biuncialis and its use for the identification of 5 derived wheat - Aegilops biuncialis disomic addition lines. Genome 48: 1070- 1082.
http://dx.doi.org/10.1139/g05-062
PMid:16391676
van Slageren MWSJ (1994). Wild Wheats: A Monograph of Aegilops L. and Amblyopyrum (Jaub. & Spach) Eig (Poaceae): A Revision of All Taxa Closely Related to Wheat, Excluding Wild Triticum Species, with Notes on Other Genera in the Tribe Triticcae, Especially Triticum: Wageningen Agricultural University, Wageningen.
Wang ZG, An TG, Li JM, Marta ML, et al. (2004). Fluorescent in situ hybridization analysis of rye chromatin in the background of "Xiaoyan No. 6". Acta Bot. Sin. 46: 436-442.
“Novel splice variants of the bovine PCK1 gene”, vol. 12, pp. 4028-4035, 2013.
, “Expression of the luteinizing hormone receptor (LHR) gene in ovine non-gonadal tissues during estrous cycle”, vol. 11, pp. 3766-3780, 2012.
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Ascoli M, Fanelli F and Segaloff DL (2002). The lutropin/choriogonadotropin receptor, a 2002 perspective. Endocr. Rev 23: 141-174.
http://dx.doi.org/10.1210/er.23.2.141
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Chen XY, Wen HS, He F, Chen CF, et al. (2010). Partial sequence cloning of LHR gene in Cynoglossus semilaevis and its tissue expression analysis. J. Ocean Univ. China 40: 71-77.
Gawronska B, Paukku T, Huhtaniemi I, Wasowicz G, et al. (1999). Oestrogen-dependent expression of LH/hCG receptors in pig Fallopian tube and their role in relaxation of the oviduct. J Reprod. Fertil. 115: 293-301.
http://dx.doi.org/10.1530/jrf.0.1150293
PMid:10434935
Gawronska B, Stepien A and Ziecik AJ (2000). Effect of estradiol and progesterone on oviductal LH-receptors and LH-dependent relaxation of the porcine oviduct. Theriogenology 53: 659-672.
http://dx.doi.org/10.1016/S0093-691X(99)00265-4
Jiang J, Cao SX, Mao DG and Hui FM (2011). Expression of uterine LHR mRNA during estrous cycle in Guinea pig. Sci. Agric. Sin. 44: 3420-3426.
Kwok HF, So WK, Wang Y and Ge W (2005). Zebrafish gonadotropins and their receptors: I. Cloning and characterization of zebrafish follicle-stimulating hormone and luteinizing hormone receptors--evidence for their distinct functions in follicle development. Biol. Reprod. 72: 1370-1381.
http://dx.doi.org/10.1095/biolreprod.104.038190
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Li GJ, Wang H, Wang SY, Hou YM, et al. (2009). Localization and differential expression of LHR and LHR mRNA in the oviduct of jining gray goat during estrous cycle. Sci. Agric. Sin. 44: 3235-3245.
Rao CV and Lei ZM (2007). The past, present and future of nongonadal LH/hCG actions in reproductive biology and medicine. Mol. Cell Endocrinol. 269: 2-8.
http://dx.doi.org/10.1016/j.mce.2006.07.007
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http://dx.doi.org/10.1210/en.138.11.4844
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Shemesh M, Mizrachi D, Gurevich M, Stram Y, et al. (2001). Functional importance of bovine myometrial and vascular LH receptors and cervical FSH receptors. Semin. Reprod. Med. 19: 87-96.
http://dx.doi.org/10.1055/s-2001-13915
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Shen Y, Wang H, Wang SY, Wang LQ, et al. (2009). Different expression of LHR mRNA in the uterus of four estrous cycle phases in jining gray goat. Chin. J. Anim. Vet. Sci. 40: 338-342.
Sun T, Lei ZM and Rao CV (1997). A novel regulation of the oviductal glycoprotein gene expression by luteinizing hormone in bovine tubal epithelial cells. Mol. Cell. Endocrinol. 131: 97-108.
http://dx.doi.org/10.1016/S0303-7207(97)00104-4
Vischer HF and Bogerd J (2003). Cloning and functional characterization of a gonadal luteinizing hormone receptor complementary DNA from the African catfish (Clarias gariepinus). Biol. Reprod. 68: 262-271.
http://dx.doi.org/10.1095/biolreprod.102.004515
PMid:12493722
Wang L, LI TY, Wang SY, Huang LB, et al. (2011). Studies on expression of GTH receptor genes in the oviduct of Yimeng Black goat during the estrous cycle. Chinese Veterinary Sci. 41: 832-838.
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“Protein transduction domain-hA20 fusion protein protects endothelial cells against high glucose-induced injury”, vol. 11, pp. 1899-1908, 2012.
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Hiroshi M, Takashi I, Reilo K, Shibagaki N, et al. (2006). Polyarginine-mediated protein delivery to dendritic cells presents antigen more efficiently onto MHC class I and class II and elicits superior antitumor immunity. J. Investig. Dermatol. 126: 1804-1812.
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Hou CL, Zhang W, Wei Y, Mi JH, et al. (2011). Zinc finger protein A20 overexpression inhibits monocyte homing and protects endothelial cells from injury induced by high glucose. Genet. Mol. Res. 10: 1050-1059.
http://dx.doi.org/10.4238/vol10-2gmr1102
PMid:21710455
Lutz J, Luong lA, Strobl M, Deng M, et al. (2008). The A20 gene protects kidneys from ischaemia/reperfusion injury by suppressing pro-inflammatory activation. J. Mol. Med. 86: 1329-1339.
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Papadopoulou LC and Tsiftsoglou AS (2011). Transduction of human recombinant proteins into mitochondria as a protein therapeutic approach for mitochondrial disorders. Pharm. Res. 28: 2639-2656.
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Patel VI, Daniel S, Longo CR, Shrikhande GV, et al. (2006). A20, a modulator of smooth muscle cell proliferation and apoptosis, prevents and induces regression of neointimal hyperplasia. FASEB J. 20: 1418-1430.
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Wang AB, Li HL, Zhang R, She ZG, et al. (2007). A20 attenuates vascular smooth muscle cell proliferation and migration through blocking PI3k/Akt singling in vitro and in vivo. J. Biomed. Sci. 14: 357-371.
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Zeng W, Li L, Yuan W, Wei Y, et al. (2009). A20 overexpression inhibits low shear flow-induced CD14-positive monocyte recruitment to endothelial cells. Biorheology 46: 21-30.
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“A novel single-nucleotide polymorphism in the 5' upstream region of the prolactin receptor gene is associated with fiber traits in Liaoning cashmere goats”, vol. 10. pp. 2511-2516, 2011.
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“Zinc finger protein A20 overexpression inhibits monocyte homing and protects endothelial cells from injury induced by high glucose”, vol. 10, pp. 1050-1059, 2011.
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Lutz J, Luong Le A, Strobl M, Deng M, et al. (2008). The A20 gene protects kidneys from ischaemia/reperfusion injury by suppressing pro-inflammatory activation. J. Mol. Med. 86: 1329-1339.
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McGinn S, Saad S, Poronnik P and Pollock CA (2003). High glucose-mediated effects on endothelial cell proliferation occur via p38 MAP kinase. Am. J. Physiol. Endocrinol. Metab. 285: E708-E717.
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Patel VI, Daniel S, Longo CR, Shrikhande GV, et al. (2006). A20, a modulator of smooth muscle cell proliferation and apoptosis, prevents and induces regression of neointimal hyperplasia. FASEB J. 20: 1418-1430.
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Romero MJ, Platt DH, Tawfik HE, Labazi M, et al. (2008). Diabetes-induced coronary vascular dysfunction involves increased arginase activity. Circ. Res. 102: 95-102.
doi:10.1161/CIRCRESAHA.107.155028
PMid:17967788 PMCid:2822539
Wang AB, Li HL, Zhang R, She ZG, et al. (2007). A20 attenuates vascular smooth muscle cell proliferation and migration through blocking PI3k/Akt singling in vitro and in vivo. J. Biomed. Sci. 14: 357-371.
doi:10.1007/s11373-007-9150-x
PMid:17260188
Yang WS, Seo JW, Han NJ, Choi J, et al. (2008). High glucose-induced NF-kappaB activation occurs via tyrosine phosphorylation of IkappaBalpha in human glomerular endothelial cells: involvement of Syk tyrosine kinase. Am. J. Physiol. Renal Physiol. 294: F1065-F1075.
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PMid:18353872
Zeng W, Li L, Yuan W, Wei Y, et al. (2009). A20 overexpression inhibits low shear flow-induced CD14-positive monocyte recruitment to endothelial cells. Biorheology 46: 21-30.
PMid:19252225
Zhu CH, Ying DJ, Mi JH, Zhang W, et al. (2004). The zinc finger protein A20 protects endothelial cells from burns serum injury. Burns 30: 127-133.
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PMid:15019119