Articles de revues sur le sujet « Xenopus laevi »
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Munck, B. G., and L. K. Munck. "Na+-independent transport of bipolar and cationic amino acids across the luminal membrane of the small intestine." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 272, no. 4 (1997): R1060—R1068. http://dx.doi.org/10.1152/ajpregu.1997.272.4.r1060.
Texte intégralLiu, Xia, Xue-mei Ji, Xi-ning Du, et al. "Molecular Cloning, Expression, Bioinformatics Analysis, and Bioactivity of TNFSF13 (APRIL) in the South African Clawed Frog (Xenopus laevi): A New Model to Study Immunological Diseases." OMICS: A Journal of Integrative Biology 17, no. 7 (2013): 384–92. http://dx.doi.org/10.1089/omi.2013.0004.
Texte intégralde Koning, Harry P., Bruce G. Jenks, Wim J. J. M. Scheenen, Eveline P. C. T. de Rijk, Raymond T. J. M. Caris та Eric W. Roubos. "Indirect Action of Elevated Potassium and Neuropeptide Y on αMSH Secretion from the Pars Intermedia of Xenopus laevis: A Biochemical and Morphological Study". Neuroendocrinology 54, № 1 (1991): 68–76. http://dx.doi.org/10.1159/000125853.
Texte intégralDores, Robert M., Tami C. Steveson, and Kristin Lopez. "Differential Mechanisms for the N-Acetylation of Alpha-Melanocyte-Stimulating Hormone and Beta-Endorphin in the Intermediate Pituitary of the Frog, Xenopus laevis." Neuroendocrinology 53, no. 1 (1991): 54–62. http://dx.doi.org/10.1159/000125697.
Texte intégralRahman Khan, Tanwirur, and Ian R Duce. "Expression of Tick Receptor Protein in Xenopus laevis Oocyte." International Journal of Science and Research (IJSR) 10, no. 8 (2021): 424–26. https://doi.org/10.21275/mr21725205900.
Texte intégralVredenburg, Vance T., Stephen A. Felt, Erica C. Morgan, et al. "Prevalence of Batrachochytrium dendrobatidis in Xenopus Collected in Africa (1871–2000) and in California (2001–2010)." PLoS ONE 8, no. 5 (2013): e63791. https://doi.org/10.5281/zenodo.13508598.
Texte intégralVredenburg, Vance T., Stephen A. Felt, Erica C. Morgan, et al. "Prevalence of Batrachochytrium dendrobatidis in Xenopus Collected in Africa (1871–2000) and in California (2001–2010)." PLoS ONE 8, no. 5 (2013): e63791. https://doi.org/10.5281/zenodo.13508598.
Texte intégralVredenburg, Vance T., Stephen A. Felt, Erica C. Morgan, et al. "Prevalence of Batrachochytrium dendrobatidis in Xenopus Collected in Africa (1871–2000) and in California (2001–2010)." PLoS ONE 8, no. 5 (2013): e63791. https://doi.org/10.5281/zenodo.13508598.
Texte intégralVredenburg, Vance T., Stephen A. Felt, Erica C. Morgan, et al. "Prevalence of Batrachochytrium dendrobatidis in Xenopus Collected in Africa (1871–2000) and in California (2001–2010)." PLoS ONE 8, no. 5 (2013): e63791. https://doi.org/10.5281/zenodo.13508598.
Texte intégralSaveliev, S. V., N. V. Besova, E. S. Savelieva, and V. I. Gulimova. "NEUROBLASTS MIGRATION AND PATTERN FORMATION DURING DEVELOPMENT OF THE XENOPUS LAEVIS." CLINICAL AND EXPERIMENTAL MORPHOLOGY 29, no. 1 (2019): 63–70. http://dx.doi.org/10.31088/2226-5988-2019-29-1-63-70.
Texte intégralParain, Karine, Sophie Lourdel, Alicia Donval, et al. "CRISPR/Cas9-Mediated Models of Retinitis Pigmentosa Reveal Differential Proliferative Response of Müller Cells between Xenopus laevis and Xenopus tropicalis." Cells 11, no. 5 (2022): 807. http://dx.doi.org/10.3390/cells11050807.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Einstecks." Cold Spring Harbor Protocols 2007, no. 12 (2007): pdb.prot4750. http://dx.doi.org/10.1101/pdb.prot4750.
Texte intégralShrestha, Bindesh, Prabhakar Sripadi, Brent R. Reschke, et al. "Subcellular Metabolite and Lipid Analysis of Xenopus laevis Eggs by LAESI Mass Spectrometry." PLoS ONE 9, no. 12 (2014): e115173. http://dx.doi.org/10.1371/journal.pone.0115173.
Texte intégralAsada-Kubota, M. "A monoclonal antibody specific for an epidermal cell antigen of Xenopus laevis: electron microscopic observations using a gold-labeling method." Journal of Histochemistry & Cytochemistry 36, no. 5 (1988): 515–21. http://dx.doi.org/10.1177/36.5.3356895.
Texte intégralArystarhova, E. "Toxicological biotesting of waters of surface sources of water service and drinking water using larvas of Хenopus laevis". Visnyk agrarnoi nauky 96, № 2 (2018): 60–63. http://dx.doi.org/10.31073/agrovisnyk201802-10.
Texte intégralShaidani, Nikko-Ideen, Sean McNamara, Marcin Wlizla, and Marko E. Horb. "Obtaining Xenopus laevis Embryos." Cold Spring Harbor Protocols 2021, no. 3 (2020): pdb.prot106211. http://dx.doi.org/10.1101/pdb.prot106211.
Texte intégralShaidani, Nikko-Ideen, Sean McNamara, Marcin Wlizla, and Marko E. Horb. "Obtaining Xenopus laevis Eggs." Cold Spring Harbor Protocols 2021, no. 3 (2020): pdb.prot106203. http://dx.doi.org/10.1101/pdb.prot106203.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Dejellying Xenopus laevis Embryos." Cold Spring Harbor Protocols 2007, no. 10 (2007): pdb.prot4731. http://dx.doi.org/10.1101/pdb.prot4731.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Handling Xenopus laevis Adults." Cold Spring Harbor Protocols 2007, no. 10 (2007): pdb.prot4733. http://dx.doi.org/10.1101/pdb.prot4733.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Isolating Xenopus laevis Testes." Cold Spring Harbor Protocols 2007, no. 10 (2007): pdb.prot4735. http://dx.doi.org/10.1101/pdb.prot4735.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Egg Collection." Cold Spring Harbor Protocols 2007, no. 10 (2007): pdb.prot4736. http://dx.doi.org/10.1101/pdb.prot4736.
Texte intégralSive, H. L., R. M. Grainger, and R. M. Harland. "Xenopus laevis Keller Explants." Cold Spring Harbor Protocols 2007, no. 12 (2007): pdb.prot4749. http://dx.doi.org/10.1101/pdb.prot4749.
Texte intégralMohun, Tim, Robert Wilson, Elisa Gionti, and Malcolm Logan. "Myogenesis in Xenopus laevis." Trends in Cardiovascular Medicine 4, no. 3 (1994): 146–51. http://dx.doi.org/10.1016/1050-1738(94)90067-1.
Texte intégralKiefer, P., M. Mathieu, M. J. Close, G. Peters, and C. Dickson. "FGF3 from Xenopus laevis." EMBO Journal 12, no. 11 (1993): 4159–68. http://dx.doi.org/10.1002/j.1460-2075.1993.tb06100.x.
Texte intégralClaußen, Maike, Thomas Lingner, Claudia Pommerenke, Lennart Opitz, Gabriela Salinas, and Tomas Pieler. "Global analysis of asymmetric RNA enrichment in oocytes reveals low conservation between closely related Xenopus species." Molecular Biology of the Cell 26, no. 21 (2015): 3777–87. http://dx.doi.org/10.1091/mbc.e15-02-0115.
Texte intégralHadji-Azimi, I., V. Coosemans, and C. Canicatti. "Atlas of adult Xenopus laevis laevis hematology." Developmental & Comparative Immunology 11, no. 4 (1987): 807–74. http://dx.doi.org/10.1016/0145-305x(87)90068-1.
Texte intégralTix, Leonie, Lisa Ernst, Britta Bungardt, Steven R. Talbot, Gero Hilken, and René H. Tolba. "Establishment of the body condition score for adult female Xenopus laevis." PLOS ONE 18, no. 4 (2023): e0280000. http://dx.doi.org/10.1371/journal.pone.0280000.
Texte intégralFoulkrod, Ashley M., Gretchen M. Geibel, Yuthana Kongprachaya, and Pierette M. Appasamy. "Expression of T cell genes in adult Xenopus laevis and TCR gene expression in the Xenopus tadpole tail." Journal of Immunology 196, no. 1_Supplement (2016): 216.3. http://dx.doi.org/10.4049/jimmunol.196.supp.216.3.
Texte intégralRoco, Álvaro S., Thomas Liehr, Adrián Ruiz-García, Kateryna Guzmán, and Mónica Bullejos. "Comparative Distribution of Repetitive Sequences in the Karyotypes of Xenopus tropicalis and Xenopus laevis (Anura, Pipidae)." Genes 12, no. 5 (2021): 617. http://dx.doi.org/10.3390/genes12050617.
Texte intégralChang, W. Y., F. KhosrowShahian, M. Wolanski, et al. "Conservation of Pitx1 expression during amphibian limb morphogenesis." Biochemistry and Cell Biology 84, no. 2 (2006): 257–62. http://dx.doi.org/10.1139/o06-036.
Texte intégralMorrow, S., J. Gosálvez, C. López-Fernández, F. Arroyo, W. V. Holt, and M. J. Guille. "Effects of freezing and activation on membrane quality and DNA damage in Xenopus tropicalis and Xenopus laevis spermatozoa." Reproduction, Fertility and Development 29, no. 8 (2017): 1556. http://dx.doi.org/10.1071/rd16190.
Texte intégralKelley, Darcy B., Martha L. Tobias, and Mark Ellisman. "Androgen-induced plasticity at a “vocal” neuromuscular synapse." Proceedings, annual meeting, Electron Microscopy Society of America 52 (1994): 32–33. http://dx.doi.org/10.1017/s0424820100167895.
Texte intégralScherer, Warren J., and Susan B. Udin. "Differential intertectal delay between Rana pipiens and Xenopus laevis: Implications for species-specific visual plasticity." Visual Neuroscience 12, no. 5 (1995): 1007–11. http://dx.doi.org/10.1017/s0952523800009548.
Texte intégralSerrano, Elba E., and Quincy A. Quick. "Auditory organs in Xenopus laevis and Xenopus tropicalis." Journal of the Acoustical Society of America 112, no. 5 (2002): 2229. http://dx.doi.org/10.1121/1.4808622.
Texte intégralMatsuda, Yoichi, Yoshinobu Uno, Mariko Kondo, et al. "A New Nomenclature of Xenopus laevis Chromosomes Based on the Phylogenetic Relationship to Silurana/Xenopus tropicalis." Cytogenetic and Genome Research 145, no. 3-4 (2015): 187–91. http://dx.doi.org/10.1159/000381292.
Texte intégralGhaseminejad, Farhad, Beatrice M. Tam, Colette N. Chiu, Joanna M. Feehan, and Orson L. Moritz. "Gene editing treatment strategies for retinitis pigmentosa assessed in Xenopus laevis carrying a mutant Rhodopsin allele." Journal of Translational Genetics and Genomics 6 (2022): 111–25. http://dx.doi.org/10.20517/jtgg.2021.49.
Texte intégralMcCallum, F. S., and B. E. H Maden. "Human 18 S ribosomal RNA sequence inferred from DNA sequence. Variations in 18 S sequences and secondary modification patterns between vertebrates." Biochemical Journal 232, no. 3 (1985): 725–33. http://dx.doi.org/10.1042/bj2320725.
Texte intégralShum, B. P., D. Avila, L. Du Pasquier, M. Kasahara, and M. F. Flajnik. "Isolation of a classical MHC class I cDNA from an amphibian. Evidence for only one class I locus in the Xenopus MHC." Journal of Immunology 151, no. 10 (1993): 5376–86. http://dx.doi.org/10.4049/jimmunol.151.10.5376.
Texte intégralGinal, Philipp, Francisco D. Moreira, Raquel Marques, Rui Rebelo, and Dennis Rödder. "Predicting terrestrial dispersal corridors of the invasive African clawed frog Xenopus laevis in Portugal." NeoBiota 64 (January 28, 2021): 103–18. https://doi.org/10.3897/neobiota.64.60004.
Texte intégralCharalambous, Anna, Maria Koyioni, Ioanna Antoniades, et al. "1,2,3-Dithiazoles – new reversible melanin synthesis inhibitors: a chemical genomics study." MedChemComm 6, no. 5 (2015): 935–46. http://dx.doi.org/10.1039/c5md00052a.
Texte intégralHammoud, Lamis, Logan A. Walsh, and Sashko Damjanovski. "Cloning and developmental characterization of Xenopus laevis membrane type-3 matrix metalloproteinase (MT3-MMP)." Biochemistry and Cell Biology 84, no. 2 (2006): 167–77. http://dx.doi.org/10.1139/o05-175.
Texte intégralBaronsky, Thilo, Aliaksandr Dzementsei, Marieelen Oelkers, Juliane Melchert, Tomas Pieler, and Andreas Janshoff. "Reduction in E-cadherin expression fosters migration of Xenopus laevis primordial germ cells." Integrative Biology 8, no. 3 (2016): 349–58. http://dx.doi.org/10.1039/c5ib00291e.
Texte intégralNonaka, M., C. Namikawa-Yamada, M. Sasaki, L. Salter-Cid, and M. F. Flajnik. "Evolution of proteasome subunits delta and LMP2: complementary DNA cloning and linkage analysis with MHC in lower vertebrates." Journal of Immunology 159, no. 2 (1997): 734–40. http://dx.doi.org/10.4049/jimmunol.159.2.734.
Texte intégralPauwels, Olivier S. G., Jonathan Brecko, Dimitri Baeghe, Jeroen Venderickx, Ann Vanderheyden, and Thierry Backeljau. "Morphological, acoustic and genetic identification of a reproducing population of the invasive African clawed frog Xenopus laevis (Anura, Pipidae) recently discovered in Belgium." ZooKeys 1184 (November 14, 2023): 41–64. http://dx.doi.org/10.3897/zookeys.1184.103702.
Texte intégralBOĞA, Ayper, Seçil BİNOKAY, Ayşe KENDİRCİ, and Tuncay ÖZGÜNEN. "Experimental Embryology in Xenopus Laevis." Turkish Journal of Biology 21, no. 2 (1997): 141–48. http://dx.doi.org/10.55730/1300-0152.2515.
Texte intégralLoidl, J., and D. Schweizer. "Synaptonemal Complexes of Xenopus laevis." Journal of Heredity 83, no. 4 (1992): 307–9. http://dx.doi.org/10.1093/oxfordjournals.jhered.a111218.
Texte intégralBernardini, Giovanni, Rosalba Gornati, Silvana Rapelli, Federica Rossi, and Bruno Berra. "Lipids of Xenopus laevis Spermatozoa." Development, Growth and Differentiation 34, no. 3 (1992): 329–35. http://dx.doi.org/10.1111/j.1440-169x.1992.tb00022.x.
Texte intégralBassham, Susan, Aaron Beam, and Janis Shampay. "Telomere Variation in Xenopus laevis." Molecular and Cellular Biology 18, no. 1 (1998): 269–75. http://dx.doi.org/10.1128/mcb.18.1.269.
Texte intégralWhite-James, Jaime, Dustin McAndrew, James Badman, and Michael McGarry. "Alternative housing for Xenopus laevis." Lab Animal 37, no. 4 (2008): 161–63. http://dx.doi.org/10.1038/laban0408-161.
Texte intégralVignali, Robert, Simone Macrì, Marco Onorati, Emanuela Basaldella, Riccardo Sgarra, and Guidalberto Manfioletti. "HMGA proteins in Xenopus laevis." Developmental Biology 319, no. 2 (2008): 589–90. http://dx.doi.org/10.1016/j.ydbio.2008.05.487.
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