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1

Sive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Einstecks." Cold Spring Harbor Protocols 2007, no. 12 (June 1, 2007): pdb.prot4750. http://dx.doi.org/10.1101/pdb.prot4750.

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2

Hadji-Azimi, I., V. Coosemans, and C. Canicatti. "Atlas of adult Xenopus laevis laevis hematology." Developmental & Comparative Immunology 11, no. 4 (September 1987): 807–74. http://dx.doi.org/10.1016/0145-305x(87)90068-1.

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3

Mohun, Tim, Robert Wilson, Elisa Gionti, and Malcolm Logan. "Myogenesis in Xenopus laevis." Trends in Cardiovascular Medicine 4, no. 3 (May 1994): 146–51. http://dx.doi.org/10.1016/1050-1738(94)90067-1.

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4

Kiefer, P., M. Mathieu, M. J. Close, G. Peters, and C. Dickson. "FGF3 from Xenopus laevis." EMBO Journal 12, no. 11 (November 1993): 4159–68. http://dx.doi.org/10.1002/j.1460-2075.1993.tb06100.x.

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5

Sive, H. L., R. M. Grainger, and R. M. Harland. "Dejellying Xenopus laevis Embryos." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.prot4731. http://dx.doi.org/10.1101/pdb.prot4731.

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6

Sive, H. L., R. M. Grainger, and R. M. Harland. "Handling Xenopus laevis Adults." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.prot4733. http://dx.doi.org/10.1101/pdb.prot4733.

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7

Sive, H. L., R. M. Grainger, and R. M. Harland. "Isolating Xenopus laevis Testes." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.prot4735. http://dx.doi.org/10.1101/pdb.prot4735.

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8

Sive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Egg Collection." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.prot4736. http://dx.doi.org/10.1101/pdb.prot4736.

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9

Sive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Keller Explants." Cold Spring Harbor Protocols 2007, no. 12 (June 1, 2007): pdb.prot4749. http://dx.doi.org/10.1101/pdb.prot4749.

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10

Shaidani, Nikko-Ideen, Sean McNamara, Marcin Wlizla, and Marko E. Horb. "Obtaining Xenopus laevis Embryos." Cold Spring Harbor Protocols 2021, no. 3 (December 3, 2020): pdb.prot106211. http://dx.doi.org/10.1101/pdb.prot106211.

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11

Shaidani, Nikko-Ideen, Sean McNamara, Marcin Wlizla, and Marko E. Horb. "Obtaining Xenopus laevis Eggs." Cold Spring Harbor Protocols 2021, no. 3 (December 3, 2020): pdb.prot106203. http://dx.doi.org/10.1101/pdb.prot106203.

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12

Serrano, Elba E., and Quincy A. Quick. "Auditory organs in Xenopus laevis and Xenopus tropicalis." Journal of the Acoustical Society of America 112, no. 5 (November 2002): 2229. http://dx.doi.org/10.1121/1.4808622.

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13

Jerome, Alexander S., Maria N. Vergara, and Katia Del Rio-Tsonis. "Transdifferentiation in Xenopus laevis eye." Developmental Biology 295, no. 1 (July 2006): 398. http://dx.doi.org/10.1016/j.ydbio.2006.04.220.

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14

Vignali, Robert, Simone Macrì, Marco Onorati, Emanuela Basaldella, Riccardo Sgarra, and Guidalberto Manfioletti. "HMGA proteins in Xenopus laevis." Developmental Biology 319, no. 2 (July 2008): 589–90. http://dx.doi.org/10.1016/j.ydbio.2008.05.487.

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15

Harland, Richard M., and Michael J. Gilchrist. "Editorial: The Xenopus laevis genome." Developmental Biology 426, no. 2 (June 2017): 139–42. http://dx.doi.org/10.1016/j.ydbio.2017.04.016.

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16

Bernardini, Giovanni, Rosalba Gornati, Silvana Rapelli, Federica Rossi, and Bruno Berra. "Lipids of Xenopus laevis Spermatozoa." Development, Growth and Differentiation 34, no. 3 (June 1992): 329–35. http://dx.doi.org/10.1111/j.1440-169x.1992.tb00022.x.

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17

Loidl, J., and D. Schweizer. "Synaptonemal Complexes of Xenopus laevis." Journal of Heredity 83, no. 4 (July 1, 1992): 307–9. http://dx.doi.org/10.1093/oxfordjournals.jhered.a111218.

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18

White-James, Jaime, Dustin McAndrew, James Badman, and Michael McGarry. "Alternative housing for Xenopus laevis." Lab Animal 37, no. 4 (April 2008): 161–63. http://dx.doi.org/10.1038/laban0408-161.

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19

Bassham, Susan, Aaron Beam, and Janis Shampay. "Telomere Variation in Xenopus laevis." Molecular and Cellular Biology 18, no. 1 (January 1, 1998): 269–75. http://dx.doi.org/10.1128/mcb.18.1.269.

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ABSTRACT Eukaryotic telomeres are variable at several levels, from the length of the simple sequence telomeric repeat tract in different cell types to the presence or number of telomere-adjacent DNA sequence elements in different strains or individuals. We have investigated the sequence organization of Xenopus laevis telomeres by use of the vertebrate telomeric repeat (TTAGGG) n and blot hybridization analysis. The (TTAGGG) n -hybridizing fragments, which ranged from less than 10 to over 50 kb with frequently cutting enzymes, defined a pattern that was polymorphic between individuals. BAL 31 exonuclease treatment confirmed that these fragments were telomeric. The polymorphic fragments analyzed did not hybridize to 5S RNA sequences, which are telomeric according to in situ hybridization. When telomeric fragments from offspring (whole embryos) were compared to those from the spleens of the parents, the inheritance pattern of some bands was found to be unusual. Furthermore, in one cross, the telomeres of the embryo were shorter than the telomeres of the parents’ spleen, and in another, the male’s testis telomeres were shorter than those of the male’s spleen. Our data are consistent with a model for chromosome behavior that involves a significant amount of DNA rearrangement at telomeres and suggest that length regulation ofXenopus telomeres is different from that observed forMus spretus and human telomeres.
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20

Mashoof, Sara, Breanna Breaux, and Michael F. Criscitiello. "Larval Thymectomy of Xenopus laevis." Cold Spring Harbor Protocols 2018, no. 7 (May 16, 2018): pdb.prot099192. http://dx.doi.org/10.1101/pdb.prot099192.

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21

Shaidani, Nikko-Ideen, Sean McNamara, Marcin Wlizla, and Marko E. Horb. "Animal Maintenance Systems: Xenopus laevis." Cold Spring Harbor Protocols 2020, no. 10 (May 13, 2020): pdb.prot106138. http://dx.doi.org/10.1101/pdb.prot106138.

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22

Sive, H. L., R. M. Grainger, and R. M. Harland. "Inducing Ovulation in Xenopus laevis." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.prot4734. http://dx.doi.org/10.1101/pdb.prot4734.

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23

Pope, Amanda Popielski, Chen Liu, Amy K. Sater, and Marc Servetnick. "FGFR3 expression in Xenopus laevis." Gene Expression Patterns 10, no. 2-3 (February 2010): 87–92. http://dx.doi.org/10.1016/j.gep.2009.12.002.

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24

Fischer, W. J., W. A. Koch, and A. Elepfandt. "Sympatry and hybridization between the clawed frogs Xenopus laevis laevis and Xenopus muelleri (Pipidae)." Journal of Zoology 252, no. 1 (September 2000): 99–107. http://dx.doi.org/10.1111/j.1469-7998.2000.tb00824.x.

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25

ZUASTI, A., C. JIMÉNEZ-CERVANTES, J. C. GARCÍA-BORRÓN, and C. FERRER. "The Melanogenic System of Xenopus laevis." Archives of Histology and Cytology 61, no. 4 (1998): 305–16. http://dx.doi.org/10.1679/aohc.61.305.

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26

Chen, Rey-Huei. "The spindle checkpoint in Xenopus Laevis." Frontiers in Bioscience 13, no. 13 (2008): 2231. http://dx.doi.org/10.2741/2837.

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27

Measey, G. John. "Terrestrial Prey Capture in Xenopus laevis." Copeia 1998, no. 3 (August 3, 1998): 787. http://dx.doi.org/10.2307/1447816.

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28

Gurdon, J. B. "Normal table of Xenopus laevis (Daudin)." Trends in Genetics 11, no. 10 (October 1995): 418. http://dx.doi.org/10.1016/s0168-9525(00)89129-5.

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29

Poulsen, Rikke, Xuan Luong, Martin Hansen, Bjarne Styrishave, and Tyrone Hayes. "Tebuconazole disrupts steroidogenesis in Xenopus laevis." Aquatic Toxicology 168 (November 2015): 28–37. http://dx.doi.org/10.1016/j.aquatox.2015.09.008.

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30

Rusciano, Giulia, Giuseppe Pesce, Marinella Salemme, Lara Selvaggi, Carmen Vaccaro, Antonio Sasso, and Rosa Carotenuto. "Raman spectroscopy of Xenopus laevis oocytes." Methods 51, no. 1 (May 2010): 27–36. http://dx.doi.org/10.1016/j.ymeth.2009.12.009.

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31

Kampf, N., C. Zohar, and A. Nussinovitch. "Hydrocolloid Coating of Xenopus laevis Embryos." Biotechnology Progress 16, no. 3 (June 2, 2000): 480–87. http://dx.doi.org/10.1021/bp0000252.

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32

Louza, Mariana P., Alice H. Reis, Karla L. Almeida, Marcelo Einicker-Lamas, Georgia C. Atella, Mirna S. Abreu, and José G. Abreu. "Lipidomic analysis during Xenopus laevis development." Developmental Biology 331, no. 2 (July 2009): 426–27. http://dx.doi.org/10.1016/j.ydbio.2009.05.143.

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33

Mitogawa, Kazumasa, Aki Makanae, and Akira Satoh. "Hyperinnervation improves Xenopus laevis limb regeneration." Developmental Biology 433, no. 2 (January 2018): 276–86. http://dx.doi.org/10.1016/j.ydbio.2017.10.007.

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34

Insdorf, N. F., and D. F. Bogenhagen. "DNA polymerase γ from Xenopus laevis." Journal of Biological Chemistry 264, no. 36 (December 1989): 21491–97. http://dx.doi.org/10.1016/s0021-9258(20)88211-8.

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35

Insdorf, N. F., and D. F. Bogenhagen. "DNA polymerase γ from Xenopus laevis." Journal of Biological Chemistry 264, no. 36 (December 1989): 21498–503. http://dx.doi.org/10.1016/s0021-9258(20)88212-x.

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36

Schoeman, Anneke L., Tracy-Lee Joubert, Louis H. du Preez, and Roman Svitin. "Xenopus laevis as UberXL for nematodes." African Zoology 55, no. 1 (January 2, 2020): 7–24. http://dx.doi.org/10.1080/15627020.2019.1681295.

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37

Fawcett, Shana R., and M. W. Klymkowsky. "Embryonic expression of Xenopus laevis SOX7." Gene Expression Patterns 4, no. 1 (January 2004): 29–33. http://dx.doi.org/10.1016/j.modgep.2003.08.003.

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38

Mukhi, Sandeep, Liquan Cai, and Donald D. Brown. "Gene switching at Xenopus laevis metamorphosis." Developmental Biology 338, no. 2 (February 2010): 117–26. http://dx.doi.org/10.1016/j.ydbio.2009.10.041.

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39

Rose, Matthew F., and Susan R. Rose. "Melatonin accelerates metamorphosis in Xenopus laevis." Journal of Pineal Research 24, no. 2 (March 1998): 90–95. http://dx.doi.org/10.1111/j.1600-079x.1998.tb00372.x.

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40

Kelley, Darcy, Taffeta Elliot, and Jakob Christiasen‐Dahlsgaard. "Auditory nerve recordings in Xenopus laevis." Journal of the Acoustical Society of America 112, no. 5 (November 2002): 2229. http://dx.doi.org/10.1121/1.4778823.

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41

Kampf, N., C. Zohar, and A. Nussinovitch. "Alginate Coating of Xenopus laevis Embryos." Biotechnology Progress 16, no. 3 (June 2, 2000): 497–505. http://dx.doi.org/10.1021/bp990153u.

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42

Ogawa, Motoyuki, Yoshiki Hiraoka, and Sadakazu Aiso. "Nuclear translocation of Xenopus laevis paxillin." Biochemical and Biophysical Research Communications 304, no. 4 (May 2003): 676–83. http://dx.doi.org/10.1016/s0006-291x(03)00640-5.

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43

Moudilou, E. N., N. Mouterfi, J. M. Exbrayat, and C. Brun. "Calpains expression during Xenopus laevis development." Tissue and Cell 42, no. 5 (October 2010): 275–81. http://dx.doi.org/10.1016/j.tice.2010.07.001.

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44

Sive, H. L., R. M. Grainger, and R. M. Harland. "Housing and Feeding of Xenopus laevis." Cold Spring Harbor Protocols 2007, no. 10 (May 1, 2007): pdb.top8. http://dx.doi.org/10.1101/pdb.top8.

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45

Roger, Benoit, André Moisand, François Amalric, and Philippe Bouvet. "rDNA Transcription during Xenopus laevis Oogenesis." Biochemical and Biophysical Research Communications 290, no. 4 (February 2002): 1151–60. http://dx.doi.org/10.1006/bbrc.2001.6304.

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46

Jornvall, H., K. H. Falchuk, G. Geraci, and B. L. Vallee. "1,10-Phenanthroline and Xenopus laevis Teratology." Biochemical and Biophysical Research Communications 200, no. 3 (May 1994): 1398–406. http://dx.doi.org/10.1006/bbrc.1994.1606.

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47

Cannatella, D. C., and R. O. de Sa. "Xenopus Laevis as a Model Organism." Systematic Biology 42, no. 4 (December 1, 1993): 476–507. http://dx.doi.org/10.1093/sysbio/42.4.476.

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48

Stiemke, Monica M., and Joe G. Hollyfield. "Cell birthdays in Xenopus laevis retina." Differentiation 58, no. 3 (March 1995): 189–93. http://dx.doi.org/10.1046/j.1432-0436.1995.5830189.x.

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49

Lake, Blue B., and Kenneth R. Kao. "Early Head Specification in Xenopus laevis." Scientific World JOURNAL 3 (2003): 655–76. http://dx.doi.org/10.1100/tsw.2003.54.

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The head represents the most dorsal and anterior extent of the body axis. InXenopus, the progressive determination of the head is an extremely complex process involving the activation and localized antagonism of a number of interdependent intracellular signaling pathways including the Wingless/Int-1 (Wnt), bone morphogenetic protein (BMP), and nodal-related pathways. The sequence of events that specify the head are: dorsal-ventral polarization and head organizer specification in the blastula; gastrulation; neural induction; and patterning of the anterior-posterior and dorsal-ventral neuraxes. Wnt signaling is required for the specification of the dorsal side initially but is then inhibited within the organizer once it has formed. Similarly, Wnt signaling is required along the length of the neural tube, but must be suppressed at its rostral end for normal brain development. Nodal signaling is also necessary for induction of the mesendoderm, but is subsequently suppressed in its dorsal-anterior extreme to specify head organizer. BMP signaling is required for ventral mesoderm and non-neural ectoderm, and must also be suppressed in the head organizer region and for the differentiation of the ventral midline of the neural tube. Thus, development of the head, and indeed the body plan in general, requires precisely timed and spatially restricted activation and repression of these signaling pathways.
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50

Suzuki, Makoto, Nayuta Yakushiji, Yasuaki Nakada, Akira Satoh, Hiroyuki Ide, and Koji Tamura. "Limb Regeneration in Xenopus laevis Froglet." TSW Development & Embryology 1 (May 12, 2006): 26–37. http://dx.doi.org/10.1100/tswde.2006.114.

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