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Summary Anatomy Item Literature (3673) Expression Attributions Wiki
XB-ANAT-490

Papers associated with tail (and pam)

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Purine Biosynthesis Pathways Are Required for Myogenesis in Xenopus laevis., Duperray M., Cells. September 28, 2023; 12 (19):               

Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.                                            

CRISPR/Cas9-based simple transgenesis in Xenopus laevis., Shibata Y., Dev Biol. September 1, 2022; 489 76-83.                                                        

Functions of block of proliferation 1 during anterior development in Xenopus laevis., Gärtner C., PLoS One. August 2, 2022; 17 (8): e0273507.                        

Xenopus laevis il11ra.L is an experimentally proven interleukin-11 receptor component that is required for tadpole tail regeneration., Suzuki S., Sci Rep. February 3, 2022; 12 (1): 1903.                      

The molecular basis of coupling between poly(A)-tail length and translational efficiency., Xiang K., Elife. July 2, 2021; 10                       

Simple embryo injection of long single-stranded donor templates with the CRISPR/Cas9 system leads to homology-directed repair in Xenopus tropicalis and Xenopus laevis., Nakayama T., Genesis. June 1, 2020; 58 (6): e23366.                

The AP-1 transcription factor JunB functions in Xenopus tail regeneration by positively regulating cell proliferation., Nakamura M., Biochem Biophys Res Commun. February 19, 2020; 522 (4): 990-995.              

KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targeting., Wrobel E., Nat Commun. October 12, 2016; 7 12795.                  

Poly(A)-tail profiling reveals an embryonic switch in translational control., Subtelny AO., Nature. April 3, 2014; 508 (7494): 66-71.        

K-aggravated myotonia mutations at residue G1306 differentially alter deactivation gating of human skeletal muscle sodium channels., Groome JR., Cell Mol Neurobiol. November 1, 2005; 25 (7): 1075-92.

Pharmacological evaluation of 1-(carboxymethyl)-3,5-diphenyl-2-methylbenzene, a novel arylacetic acid with potential anti-inflammatory properties., Cutler SJ., Inflamm Res. July 1, 1998; 47 (7): 316-24.

Molecular cloning of the large subunit of glutathione synthetase from Xenopus laevis embryos., Habenicht A., Biochim Biophys Acta. September 23, 1993; 1174 (3): 295-8.      

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