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Xenopus Interferon Complex: Inscribing the Amphibiotic Adaption and Species-Specific Pathogenic Pressure in Vertebrate Evolution?, Tian Y, Jennings J, Gong Y, Sang Y., Cells. December 26, 2019; 9 (1): 
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Xenopus as a model organism to study heterotrimeric G-protein pathway during collective cell migration of neural crest., Toro-Tapia G, Villaseca S, Leal JI, Beyer A, Fuentealba J, Torrejón M., Genesis. January 1, 2017; 55 (1-2):
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Xenopus laevis FGF16 activates the expression of genes coding for the transcription factors Sp5 and Sp5l., Elsy M, Rowbotham A, Lord H, Isaacs HV, Pownall ME., Int J Dev Biol. January 1, 2019; 63 (11-12): 631-639.
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Xenopus laevis macrophage-like cells produce XCL-1, an intelectin family serum lectin that recognizes bacteria., Nagata S., Immunol Cell Biol. September 1, 2018; 96 (8): 872-878.
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Xenopus: Driving the Discovery of Novel Genes in Patient Disease and Their Underlying Pathological Mechanisms Relevant for Organogenesis., Hwang WY, Marquez J, Khokha MK., Front Physiol. July 30, 2019; 10 953.
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Xenopus-FV3 host-pathogen interactions and immune evasion., Jacques R, Edholm ES, Jazz S, Odalys TL, Francisco JA., Virology. November 1, 2017; 511 309-319.
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Xenopus laevis Oocytes Preparation for in-Cell EPR Spectroscopy., John L, Drescher M., Bio Protoc. April 5, 2018; 8 (7): e2798.
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Xenopus laevis as a Model Organism for the Study of Spinal Cord Formation, Development, Function and Regeneration., Borodinsky LN., Front Neural Circuits. November 23, 2017; 11 90.
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Xenopus Models of Cancer: Expanding the Oncologist's Toolbox., Hardwick LJA, Philpott A., Front Physiol. January 1, 2018; 9 1660.
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Xenopus as a model for studies in mechanical stress and cell division., Stooke-Vaughan GA, Davidson LA, Woolner S., Genesis. January 1, 2017; 55 (1-2):
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XMAP215 promotes microtubule-F-actin interactions to regulate growth cone microtubules during axon guidance in Xenopuslaevis., Slater PG, Cammarata GM, Samuelson AG, Magee A, Hu Y, Lowery LA., J Cell Sci. April 30, 2019; 132 (9):
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Xenopus Vasa Homolog XVLG1 is Essential for Migration and Survival of Primordial Germ Cells., Shimaoka K, Mukumoto Y, Tanigawa Y, Komiya T., Zoolog Sci. April 1, 2017; 34 (2): 93-104.
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Xenopus egg extract: A powerful tool to study genome maintenance mechanisms., Hoogenboom WS, Klein Douwel D, Knipscheer P., Dev Biol. August 15, 2017; 428 (2): 300-309.
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Xenopus tropicalis: Joining the Armada in the Fight Against Blood Cancer., Dimitrakopoulou D, Tulkens D, Van Vlierberghe P, Vleminckx K., Front Physiol. January 1, 2019; 10 48.
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Xenopus Piwi proteins interact with a broad proportion of the oocyte transcriptome., Toombs JA, Sytnikova YA, Chirn GW, Ang I, Lau NC, Blower MD., RNA. April 1, 2017; 23 (4): 504-520.
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Xpo7 is a broad-spectrum exportin and a nuclear import receptor., Aksu M, Pleiner T, Karaca S, Kappert C, Dehne HJ, Seibel K, Urlaub H, Bohnsack MT, Görlich D., J Cell Biol. July 2, 2018; 217 (7): 2329-2340.
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Xenopus SOX5 enhances myogenic transcription indirectly through transrepression., Della Gaspera B, Chesneau A, Weill L, Charbonnier F, Chanoine C., Dev Biol. October 15, 2018; 442 (2): 262-275.
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Xenopus metamorphosis as a model to study thyroid hormone receptor function during vertebrate developmental transitions., Buchholz DR., Mol Cell Endocrinol. December 25, 2017; 459 64-70.
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Xenopus laevis M18BP1 Directly Binds Existing CENP-A Nucleosomes to Promote Centromeric Chromatin Assembly., French BT, Westhorpe FG, Limouse C, Straight AF., Dev Cell. July 24, 2017; 42 (2): 190-199.e10.
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Xenopus laevis oocyte as a model for the study of the cytoskeleton., Carotenuto R, Tussellino M., C R Biol. April 1, 2018; 341 (4): 219-227.
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Xenopus laevis Kif18A is a highly processive kinesin required for meiotic spindle integrity., Möckel MM, Heim A, Tischer T, Mayer TU., Biol Open. April 15, 2017; 6 (4): 463-470.
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Xenopus Hybrids Provide Insight Into Cell and Organism Size Control., Gibeaux R, Miller K, Acker R, Kwon T, Heald R., Front Physiol. January 1, 2018; 9 1758.
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XMAP215 is a microtubule nucleation factor that functions synergistically with the γ-tubulin ring complex., Thawani A, Kadzik RS, Petry S., Nat Cell Biol. May 1, 2018; 20 (5): 575-585.
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XenMine: A genomic interaction tool for the Xenopus community., Reid CD, Karra K, Chang J, Piskol R, Li Q, Li JB, Cherry JM, Baker JC., Dev Biol. June 15, 2017; 426 (2): 155-164.
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Xenopus genomic data and browser resources., Vize PD, Zorn AM., Dev Biol. June 15, 2017; 426 (2): 194-199.
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Xenopus Oocyte's Conductance for Bioactive Compounds Screening and Characterization., Cheikh A, Tabka H, Tlili Y, Santulli A, Bouzouaya N, Bouhaouala-Zahar B, Benkhalifa R., Int J Mol Sci. April 27, 2019; 20 (9):
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Xenopus embryos to study fetal alcohol syndrome, a model for environmental teratogenesis., Fainsod A, Kot-Leibovich H., Biochem Cell Biol. April 1, 2018; 96 (2): 77-87.
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Xenopus pitx3 target genes lhx1 and xnr5 are identified using a novel three-fluor flow cytometry-based analysis of promoter activation and repression., Hooker LN, Smoczer C, Abbott S, Fakhereddin M, Hudson JW, Crawford MJ., Dev Dyn. September 1, 2017; 246 (9): 657-669.
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Xenopus and the art of oxygen maintenance., Tattersall GJ, Burggren WW., J Exp Biol. November 15, 2017; 220 (Pt 22): 4084-4087.
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Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease., Blum M, Ott T., Cells Tissues Organs. January 1, 2018; 205 (5-6): 303-313.
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X-linked α-thalassemia with mental retardation is downstream of protein kinase A in the meiotic cell cycle signaling cascade in Xenopus oocytes and is dynamically regulated in response to DNA damage†., O'Shea LC, Fair T, Hensey C., Biol Reprod. May 1, 2019; 100 (5): 1238-1249.
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Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database., Fortriede JD, Pells TJ, Chu S, Chaturvedi P, Wang D, Fisher ME, James-Zorn C, Wang Y, Nenni MJ, Burns KA, Lotay VS, Ponferrada VG, Karimi K, Zorn AM, Vize PD., Nucleic Acids Res. January 8, 2020; 48 (D1): D776-D782.
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Xenopus: An alternative model system for identifying muco-active agents., Sim HJ, Kim SH, Myung KJ, Kwon T, Lee HS, Park TJ., PLoS One. February 14, 2018; 13 (2): e0193310.
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X-FaCT: Xenopus-Fast Clearing Technique., Affaticati P, Le Mével S, Jenett A, Rivière L, Machado E, Mughal BB, Fini JB., Methods Mol Biol. January 1, 2018; 1865 233-241.
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Xenopus fraseri: Mr. Fraser, where did your frog come from?, Evans BJ, Gansauge MT, Stanley EL, Furman BLS, Cauret CMS, Ofori-Boateng C, Gvoždík V, Streicher JW, Greenbaum E, Tinsley RC, Meyer M, Blackburn DC., PLoS One. September 3, 2019; 14 (9): e0220892.
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Xenopus, an ideal model organism to study laterality in conjoined twins., Tisler M, Schweickert A, Blum M., Genesis. January 1, 2017; 55 (1-2):
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Xenopus slc7a5 is essential for notochord function and eye development., Katada T, Sakurai H., Mech Dev. February 1, 2019; 155 48-59.
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Xenopus GLP-1-inspired discovery of novel GLP-1 receptor agonists as long-acting hypoglycemic and insulinotropic agents with significant therapeutic potential., Han J, Chen X, Wang Y, Fei Y, Zhou F, Zhang Y, Liu L, Si P, Fu J., Biochem Pharmacol. October 15, 2017; 142 155-167.
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Xenopus: leaping forward in kidney organogenesis., Krneta-Stankic V, DeLay BD, Miller RK., Pediatr Nephrol. April 1, 2017; 32 (4): 547-555.
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Xenopus laevis neuronal cell adhesion molecule (nrcam): plasticity of a CAM in the developing nervous system., Lokapally A, Metikala S, Hollemann T., Dev Genes Evol. January 1, 2017; 227 (1): 61-67.
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Xenbase: a genomic, epigenomic and transcriptomic model organism database., Karimi K, Fortriede JD, Lotay VS, Burns KA, Wang DZ, Fisher ME, Pells TJ, James-Zorn C, Wang Y, Ponferrada VG, Chu S, Chaturvedi P, Zorn AM, Vize PD., Nucleic Acids Res. January 4, 2018; 46 (D1): D861-D868.
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Xenopus-derived glucagon-like peptide-1 and polyethylene-glycosylated glucagon-like peptide-1 receptor agonists: long-acting hypoglycaemic and insulinotropic activities with potential therapeutic utilities., Han J, Fei Y, Zhou F, Chen X, Zhang Y, Liu L, Fu J., Br J Pharmacol. February 1, 2018; 175 (3): 544-557.
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Xenbase: Facilitating the Use of Xenopus to Model Human Disease., Nenni MJ, Fisher ME, James-Zorn C, Pells TJ, Ponferrada V, Chu S, Fortriede JD, Burns KA, Wang Y, Lotay VS, Wang DZ, Segerdell E, Chaturvedi P, Karimi K, Vize PD, Zorn AM., Front Physiol. January 1, 2019; 10 154.
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Xenopus laevis as a Bioindicator of Endocrine Disruptors in the Region of Central Chile., Rojas-Hucks S, Gutleb AC, González CM, Contal S, Mehennaoui K, Jacobs A, Witters HE, Pulgar J., Arch Environ Contam Toxicol. October 1, 2019; 77 (3): 390-408.
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Xbra and Smad-1 cooperate to activate the transcription of neural repressor ventx1.1 in Xenopus embryos., Kumar S, Umair Z, Yoon J, Lee U, Kim SC, Park JB, Lee JY, Kim J., Sci Rep. July 30, 2018; 8 (1): 11391.
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Xenopus oocytes as a heterologous expression system for analysis of tight junction proteins., Vitzthum C, Stein L, Brunner N, Knittel R, Fallier-Becker P, Amasheh S., FASEB J. April 1, 2019; 33 (4): 5312-5319.
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Xenopus ADAM19 regulates Wnt signaling and neural crest specification by stabilizing ADAM13., Li J, Perfetto M, Neuner R, Bahudhanapati H, Christian L, Mathavan K, Bridges LC, Alfandari D, Wei S., Development. April 4, 2018; 145 (7):
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Xenopus Resources: Transgenic, Inbred and Mutant Animals, Training Opportunities, and Web-Based Support., Horb M, Wlizla M, Abu-Daya A, McNamara S, Gajdasik D, Igawa T, Suzuki A, Ogino H, Noble A, Centre de Ressource Biologique Xenope team in France, Robert J, James-Zorn C, Guille M., Front Physiol. January 1, 2019; 10 387.
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Xenopus Tadpole Tissue Harvest., Patmann MD, Shewade LH, Schneider KA, Buchholz DR., Cold Spring Harb Protoc. November 1, 2017; 2017 (11): pdb.prot097675.
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Xenopus extract approaches to studying microtubule organization and signaling in cytokinesis., Field CM, Pelletier JF, Mitchison TJ., Methods Cell Biol. January 1, 2017; 137 395-435.
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