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Summary Anatomy Item Literature (14955) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and il1b)

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Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax., Wang S., Cell Biosci. February 23, 2023; 13 (1): 40.              


A Focal Impact Model of Traumatic Brain Injury in Xenopus Tadpoles Reveals Behavioral Alterations, Neuroinflammation, and an Astroglial Response., Spruiell Eldridge SL., Int J Mol Sci. July 8, 2022; 23 (14):                         


Acute multidrug delivery via a wearable bioreactor facilitates long-term limb regeneration and functional recovery in adult Xenopus laevis., Murugan NJ., Sci Adv. January 28, 2022; 8 (4): eabj2164.            


The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation., Aztekin C., Development. February 5, 2020; 147 (3):                                     


Targeting TMEM176B Enhances Antitumor Immunity and Augments the Efficacy of Immune Checkpoint Blockers by Unleashing Inflammasome Activation., Segovia M., Cancer Cell. May 13, 2019; 35 (5): 767-781.e6.                                          


Developmental expression profiles and thyroidal regulation of cytokines during metamorphosis in the amphibian Xenopus laevis., Gallant MJ., Gen Comp Endocrinol. July 1, 2018; 263 62-71.              


Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.                                            


Persistent fibrosis, hypertrophy and sarcomere disorganisation after endoscopy-guided heart resection in adult Xenopus., Marshall L., PLoS One. January 1, 2017; 12 (3): e0173418.                


GABAA currents are decreased by IL-1β in epileptogenic tissue of patients with temporal lobe epilepsy: implications for ictogenesis., Roseti C., Neurobiol Dis. October 1, 2015; 82 311-320.


Changes in the inflammatory response to injury and its resolution during the loss of regenerative capacity in developing Xenopus limbs., Mescher AL., PLoS One. January 1, 2013; 8 (11): e80477.          


The developing Xenopus limb as a model for studies on the balance between inflammation and regeneration., King MW, King MW., Anat Rec (Hoboken). October 1, 2012; 295 (10): 1552-61.


Cytokine components and mucosal immunity in the oviduct of Xenopus laevis (amphibia, pipidae)., Jantra S., Gen Comp Endocrinol. September 15, 2011; 173 (3): 454-60.      


Adenosine regulates the IL-1 beta-induced cellular functions of human gingival fibroblasts., Murakami S., Int Immunol. December 1, 2001; 13 (12): 1533-40.


Phylogeny of cytokines: molecular cloning and expression analysis of sea bass Dicentrarchus labrax interleukin-1beta., Scapigliati G., Fish Shellfish Immunol. November 1, 2001; 11 (8): 711-26.


The Toll/IL-1 receptor binding protein MyD88 is required for Xenopus axis formation., Prothmann C., Mech Dev. October 1, 2000; 97 (1-2): 85-92.            


Interleukin-1beta and its type 1 receptor are expressed in developing neural circuits in the frog, Xenopus laevis., Jelaso AM., J Comp Neurol. May 4, 1998; 394 (2): 242-51.              


Activation of stress-activated protein kinase-3 (SAPK3) by cytokines and cellular stresses is mediated via SAPKK3 (MKK6); comparison of the specificities of SAPK3 and SAPK2 (RK/p38)., Cuenda A., EMBO J. January 15, 1997; 16 (2): 295-305.


The ontogeny of interleukin production and responsivity in the frog, Xenopus., Watkins D., Thymus. January 1, 1988; 11 (2): 113-22.


A factor with interleukin-1-like activity is produced by peritoneal cells from the frog, Xenopus laevis., Watkins D., Immunology. December 1, 1987; 62 (4): 669-73.

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