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Journal articles on the topic 'Xenopuslaeyis'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Hadji-Azimi, I., V. Coosemans, and C. Canicatti. "Hematopoiesis in adult Xenopuslaevis." Developmental & Comparative Immunology 11, no. 2 (1987): 449. http://dx.doi.org/10.1016/0145-305x(87)90107-8.

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2

Coosemans, V., and I. Hadji-Azimi. "Xenopuslaevis splenocyte receptors for immunoglobulins." Developmental & Comparative Immunology 11, no. 2 (1987): 447. http://dx.doi.org/10.1016/0145-305x(87)90104-2.

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3

Bacchetta, Renato, Anna Winkler, Nadia Santo, and Paolo Tremolada. "The Toxicity of Polyester Fibers in Xenopuslaevis." Water 13, no. 23 (2021): 3446. http://dx.doi.org/10.3390/w13233446.

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Microplastics are practically ubiquitous and pose a serious survival challenge for many species. Most of the exposure experiments for determining the toxicological effects of microplastics were performed with a microplastic varying little in shape and size (often purchased microplastic beads), but few studies deal with non-homogeneous samples. We analyzed the effect on Xenopuslaevis larva on the early development of polyester fibers, PEFs, taken from a dryer machine in which 100% polyester fabrics were dried after washing. Three concentrations were tested. The results showed that the gastroint

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4

Guirguis, S. M. E., J. C. Yee, and D. F. Stiffler. "Active calcium ion transport in Xenopuslaevis skin." Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology 167, no. 5 (1997): 328–34. http://dx.doi.org/10.1007/s003600050081.

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5

Jackson, Cynthia L., and David J. Shapiro. "Dexamethasone and estrogen regulate Xenopuslaevis albumin mRNA levels." Biochemical and Biophysical Research Communications 136, no. 1 (1986): 8–15. http://dx.doi.org/10.1016/0006-291x(86)90869-7.

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6

Seetharam, S., N. Dahms, N. Li, and B. Seetharam. "Functional expression of transcoabalamin II cDNA In Xenopuslaevis oocytes." Biochemical and Biophysical Research Communications 181, no. 3 (1991): 1151–55. http://dx.doi.org/10.1016/0006-291x(91)92059-s.

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7

Young, George Pei Herng, Samuel S. Koide, and John Ding-E. Young. "Phosphorylation activity associated with plasma membrane-cortical granule complex of xenopuslaevis oocytes." Biochemical and Biophysical Research Communications 153, no. 3 (1988): 1025–31. http://dx.doi.org/10.1016/s0006-291x(88)81331-7.

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8

Mizuno, Kensaku, Junichiro Sakata, Masayasu Kojima, Kenji Kangawa та Hisayuki Matsuo. "Peptide C-terminal α-amidating enzyme purified to homogeneity from Xenopuslaevis skin". Biochemical and Biophysical Research Communications 137, № 3 (1986): 984–91. http://dx.doi.org/10.1016/0006-291x(86)90322-0.

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9

Shioda, Masaki, Tomoji Higaki, Kunizo Mori, and Susumu Ikegami. "DNA replication of single-stranded DNA of phage fd microinjected into Xenopuslaevis eggs." Biochemical and Biophysical Research Communications 132, no. 3 (1985): 871–77. http://dx.doi.org/10.1016/0006-291x(85)91888-1.

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10

Lorenz, Claudia, Valeska Contardo-Jara, Stephan Pflugmacher, et al. "The Synthetic Gestagen Levonorgestrel Impairs Metamorphosis in Xenopuslaevis by Disruption of the Thyroid System." Toxicological Sciences 123, no. 1 (2011): 94–102. http://dx.doi.org/10.1093/toxsci/kfr159.

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11

Fort, Douglas J., and Sascha Pawlowski. "Triclosan Enhances Larval Amphibian Growth, but Does Not Alter Thyroid-Driven Metamorphosis in Xenopuslaevis." Toxicological Sciences 123, no. 2 (2011): 603–5. http://dx.doi.org/10.1093/toxsci/kfr186.

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12

Farley-Ewens, E. K., and M. J. Manning. "Some aspects of high zone tolerance to human-gamma-globulin induced in larval Xenopuslaevis." Developmental & Comparative Immunology 11, no. 2 (1987): 448. http://dx.doi.org/10.1016/0145-305x(87)90105-4.

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13

Ronzier, Elsa, Claire Corratgé-Faillie, Frédéric Sanchez, Christian Brière, and Tou Cheu Xiong. "Ca2+-Dependent Protein Kinase 6 Enhances KAT2 Shaker Channel Activity in Arabidopsis thaliana." International Journal of Molecular Sciences 22, no. 4 (2021): 1596. http://dx.doi.org/10.3390/ijms22041596.

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Post-translational regulations of Shaker-like voltage-gated K+ channels were reported to be essential for rapid responses to environmental stresses in plants. In particular, it has been shown that calcium-dependent protein kinases (CPKs) regulate Shaker channels in plants. Here, the focus was on KAT2, a Shaker channel cloned in the model plant Arabidopsis thaliana, where is it expressed namely in the vascular tissues of leaves. After co-expression of KAT2 with AtCPK6 in Xenopuslaevis oocytes, voltage-clamp recordings demonstrated that AtCPK6 stimulates the activity of KAT2 in a calcium-depende

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14

MARCHENKO, George N., Natalia D. MARCHENKO, and Alex Y. STRONGIN. "The structure and regulation of the human and mouse matrix metalloproteinase-21 gene and protein." Biochemical Journal 372, no. 2 (2003): 503–15. http://dx.doi.org/10.1042/bj20030174.

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Matrix metalloproteinases (MMPs) play key roles in tissue remodelling under normal development and, especially, in diseases ranging from malignancies to stroke. We cloned and thoroughly characterized the novel human and mouse MMP gene encoding MMP-21. MMP-21 is the last uncharacterized MMP coded by the human genome. Human and mouse MMP-21 is the orthologue of Xenopuslaevis X-MMP. The latent proenzyme of MMP-21 (569 amino acid residues) consists of the prodomain, the catalytic domain and the haemopexin-like domain, and is potentially capable of being activated in its secretory pathway to the ex

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15

FUJIMOTO, Wakako, Masako SUZUKI, Kazuhiro KIMURA, and Toshihiko IWANAGA. "Cellular Expression of the Gut Chitinase in the Stomach of Frogs Xenopuslaevis and Rana catesbeiana." Biomedical Research 23, no. 2 (2002): 91–99. http://dx.doi.org/10.2220/biomedres.23.91.

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16

Mizuno, Kensaku, Kazuhiro Ohsuye, Yayoi Wada, Kayoko Fuchimura, Shoji Tanaka та Hisayuki Matsuo. "Cloning and sequence of cDNA encoding a peptide C-terminal α-amidating enzyme from Xenopuslaevis". Biochemical and Biophysical Research Communications 148, № 2 (1987): 546–52. http://dx.doi.org/10.1016/0006-291x(87)90911-9.

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17

Martens, Gerard J. M., Koen A. P. Weterings, Ingrid D. van Zoest, and Bruce G. Jenks. "Physiologically-induced changes in proopiomelanocortin mRNA levels in the pituitary gland of the amphibian Xenopuslaevis." Biochemical and Biophysical Research Communications 143, no. 2 (1987): 678–84. http://dx.doi.org/10.1016/0006-291x(87)91407-0.

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18

Fernhout, Bart Jan H., Fred A. Dijcks, Wouter H. Moolenaar, and GéS F. Ruigt. "Lysophosphatidic acid induces inward currents in Xenopuslaevis oocytes; evidence for an extracellular site of action." European Journal of Pharmacology 213, no. 2 (1992): 313–15. http://dx.doi.org/10.1016/0014-2999(92)90698-4.

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19

Slater, Paula G., Garrett M. Cammarata, Annika G. Samuelson, Alexandra Magee, Yuhan Hu, and Laura Anne Lowery. "XMAP215 promotes microtubule-F–actin interactions to regulate growth cone microtubules during axon guidance in Xenopuslaevis." Journal of Cell Science 132, no. 9 (2019): jcs224311. http://dx.doi.org/10.1242/jcs.224311.

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20

Fukumoto, Gary H., and Craig V. Byus. "Putrescine export in Xenopuslaevis oocytes occurs against a concentration gradient: evidence for a non-diffusional export process." Biochimica et Biophysica Acta (BBA) - Biomembranes 1324, no. 2 (1997): 215–22. http://dx.doi.org/10.1016/s0005-2736(96)00227-1.

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21

Kimura, Koji. "Expression of vasopressin V2 receptor in Xenopuslaevis oocytes by porcine kidney cell line (LLC-PK1) messenger RNA." Biochemical and Biophysical Research Communications 174, no. 1 (1991): 149–55. http://dx.doi.org/10.1016/0006-291x(91)90498-v.

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22

Roopa, Y. Mohana, B. Bhasker Reddy, K. Sree Latha, and M. Ramesh Babu. "Prediction Evaluation of Gene Ontology Using Support Vector Machine." International Journal on Recent and Innovation Trends in Computing and Communication 11, no. 5s (2023): 522–26. http://dx.doi.org/10.17762/ijritcc.v11i5s.7113.

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The present state of sequenced programs requires the assignment of gene product functions in a timely, accurate and trustworthy manner. Many approaches to large-scale label designs have been developed. On the other hand, these approaches can only be used on a limited number of sub-sets. Their conclusions are not formalized. On the other hand, such approaches can only be used on a limited number of subsets, as their conclusions are not standardized. Annotation was supplied using Gene Ontology (GO) or categorization of valid or incorrect prediction using Support Vector Machines (SVM). A large da

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23

Liou, Horng-Huei, Wen Lin, Houng-Chi Liou, Tur-Fu Huang, and Wen-Mei Fu. "Modulation of Protein Kinase A Activation by Fibronectin Matrix Proteins at Developing Neuromuscular Synapses in Xenopuslaevis Cell Cultures." Molecular Pharmacology 60, no. 2 (2001): 348–54. http://dx.doi.org/10.1124/mol.60.2.348.

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24

Ossipova, Olga, Xi He, and Jeremy Green. "RETRACTED: Molecular cloning and developmental expression of Par-1/MARK homologues XPar-1A and XPar-1B from Xenopuslaevis." Gene Expression Patterns 2, no. 1-2 (2002): 145–50. http://dx.doi.org/10.1016/s0925-4773(02)00306-4.

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25

Vallet, Véronique, Corinne Pfister, Johannes Loffing, and Bernard C. Rossier. "Cell-Surface Expression of the Channel Activating Protease xCAP-1 Is Required for Activation of ENaC in the Xenopus Oocyte." Journal of the American Society of Nephrology 13, no. 3 (2002): 588–94. http://dx.doi.org/10.1681/asn.v133588.

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ABSTRACT. Sodium balance, extracellular fluid volume, and ultimately BP are maintained by precise regulation of the activity of the epithelial sodium channel (ENaC). Using a functional complementation assay in the Xenopuslaevis oocyte expression system, a channel-activating protease (CAP-1) that increases ENaC activity two to threefold in the Xenopus oocyte expression system is here identified. External application of trypsin mimics the effect of Xenopus CAP-1 (xCAP-1) on ENaC activity, which can be blocked by aprotinin, a serine protease inhibitor, suggesting the existence of a novel extracel

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26

AOUFOUCHI, Sad, and Sidney SHALL. "Regulation by phosphorylation of Xenopus laevis poly(ADP-ribose) polymerase enzyme activity during oocyte maturation." Biochemical Journal 325, no. 2 (1997): 543–51. http://dx.doi.org/10.1042/bj3250543.

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Poly(ADP-ribose) polymerase (PARP) is an abundant nuclear enzyme that is dependent on DNA breaks and nicks for its enzyme activity. These DNA nicks and breaks function as allosteric effectors of the enzyme activity. This reaction is important for efficient DNA base excision repair, although it is not a component of the elementary repair pathway itself. The physiological relevance of this reaction might be to ensure correct and efficient DNA repair. We have examined the enzyme activity of PARP in oocytes and eggs of Xenopuslaevis. Although both oocytes and eggs contain approximately the same am

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27

Werdehausen, Robert, David Kremer, Timo Brandenburger, et al. "Lidocaine Metabolites Inhibit Glycine Transporter 1." Anesthesiology 116, no. 1 (2012): 147–58. http://dx.doi.org/10.1097/aln.0b013e31823cf233.

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Background Lidocaine exerts antinociceptive effects when applied systemically. The mechanisms are not fully understood but glycinergic mechanisms might be involved. The synaptic glycine concentration is controlled by glycine transporters. Whereas neurons express two types of glycine transporters, astrocytes specifically express glycine transporter 1 (GlyT1). This study focuses on effects of lidocaine and its major metabolites on GlyT1 function. Methods The effects of lidocaine and its metabolites monoethylglycinexylidide (MEGX), glycinexylidide, and N-ethylglycine on GlyT1 function were invest

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28

Ohsuye, Kazuhiro, Katsuhiko Kitano, Yayoi Wada та ін. "Cloning of cDNA encoding a new peptide C-terminal α-amidating enzyme having a putative membrane-spanning domain from Xenopuslaevis skin". Biochemical and Biophysical Research Communications 150, № 3 (1988): 1275–81. http://dx.doi.org/10.1016/0006-291x(88)90767-x.

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29

Coosemans, Véronique, and Irandokht Hadji-Azimi. "Partial characterization of different cell types found in the Xenopuslaevis lymphoreticular tumor based on the presence or absence of surface immunoglobulins and Fc receptor molecules." Developmental & Comparative Immunology 10, no. 4 (1986): 547–59. http://dx.doi.org/10.1016/0145-305x(86)90176-x.

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30

LAN, Ling, Helen BRERETON, and J. Greg BARRITT. "The role of calmodulin-binding sites in the regulation of the Drosophila TRPL cation channel expressed in Xenopus laevis oocytes by Ca2+, inositol 1,4,5-trisphosphate and GTP-binding proteins." Biochemical Journal 330, no. 3 (1998): 1149–58. http://dx.doi.org/10.1042/bj3301149.

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The roles of calmodulin-binding sites in the regulation by Ca2+, inositol 1,4,5-trisphosphate (InsP3) and GTP-binding regulatory proteins (G-proteins) of the Drosophila melanogaster TRPL (transient-receptor-potential-like) non-specific Ca2+ channel were investigated. Wild-type TRPL protein and two mutant forms, TRPL (W713G) and TRPL (W814G), in which a key tryptophan residue in each of the two putative calmodulin-binding sites (Sites 1 and 2, respectively) was replaced by glycine, were expressed heterologously in Xenopuslaevis oocytes. Immunofluorescence studies indicated that the expressed TR

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31

Joshi-Mukherjee, R. "Heart-on-a-Chip Model for Cardiomyopathies." March 3, 2017. https://doi.org/10.19070/2328-3548-1700011e.

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Cardiovascular disease is the number one cause of death in the US. According to US Center for Disease Control and Prevention (CDC), about 800,000 American deaths is attributed to cardiovascular disease and each year about hundreds of thousands of people die well before the current life expectancy of 78 years in the US. By 2030, approximately 20% of the population will be aged 65 or older and cardiovascular diseases will be the leading cause of death. Over the past 4 decades, there have been remarkable advances in our understanding and treatment of ischemic heart disease, while our understandin

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32

Chilije, Maxwell, Elesha Hoffarth, Gabriel Bertolesi, Sarah McFarlane, and Vanina Zaremberg. "Dihydroxyacetone Phosphate Acyltransferase is a Peripheral Membrane Protein." FASEB Journal 30, S1 (2016). http://dx.doi.org/10.1096/fasebj.30.1_supplement.875.4.

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Dihydroxyacetone phosphate acyltransferase(DHAPAT) catalyzes the initial acylation step in the synthesis of ether basedphospholipids in peroxisomes. DHAPAT adds an acyl group to dihydroxyacetonephosphate, a metabolic intermediate from glycolysis, to yield 1‐acyl‐dihydroxyacetonephosphate (1‐acyl‐DHAP). Ether lipids are abundant in the central nervoussystem and DHAPAT deficiency has been associated with many human disordersincluding cataracts and blindness. We will present results from studies using the tractable model organism Xenopuslaevis that also point to a role of DHAPAT in eye developmen

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33

Battistoni, Maria, Francesca Metruccio, Francesca Di Renzo, Renato Bacchetta, and Elena Menegola. "Predictive assays for craniofacial malformations: evaluation in Xenopus laevis embryos exposed to triadimefon." Archives of Toxicology, June 24, 2022. http://dx.doi.org/10.1007/s00204-022-03327-w.

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AbstractCraniofacial defects are one of the most frequent abnormalities at birth, but their experimental evaluation in animal models requires complex procedures. The aim of the present work is the comparison of different methodologies to identify dose- and stage-related craniofacial malformations in Xenopuslaevis assay (R-FETAX, where the full cartilage evaluation, including flat mount technique, is the gold standard for skeletal defect detection). Different methods (external morphological evaluation of fresh samples, deglutition test, whole mount cartilage evaluation and Meckel–palatoquadrate

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34

Shen, Bowen, Leena R. Pade, Sam B. Choi, Pablo Muñoz-LLancao, M. Chiara Manzini, and Peter Nemes. "Capillary Electrophoresis Mass Spectrometry for Scalable Single-Cell Proteomics." Frontiers in Chemistry 10 (April 8, 2022). http://dx.doi.org/10.3389/fchem.2022.863979.

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Understanding the biochemistry of the cell requires measurement of all the molecules it produces. Single-cell proteomics recently became possible through advances in microanalytical sample preparation, separation by nano-flow liquid chromatography (nanoLC) and capillary electrophoresis (CE), and detection using electrospray ionization (ESI) high-resolution mass spectrometry (HRMS). Here, we demonstrate capillary microsampling CE-ESI-HRMS to be scalable to proteomics across broad cellular dimensions. This study established proof-of-principle using giant, ∼250-µm-diameter cells from embryos of t

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