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Summary Anatomy Item Literature (12667) Expression Attributions Wiki
XB-ANAT-175

Papers associated with nervous system (and myh6)

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Validation of TREK1 ion channel activators as an immunomodulatory and neuroprotective strategy in neuroinflammation., Schroeter CB., Biol Chem. March 28, 2023; 404 (4): 355-375.              

Inducible and tissue-specific cell labeling in Cre-ERT2 transgenic Xenopus lines., Lin TY., Dev Growth Differ. June 1, 2022; 64 (5): 243-253.        

Impact of glyphosate-based herbicide on early embryonic development of the amphibian Xenopus laevis., Flach H., Aquat Toxicol. March 1, 2022; 244 106081.

A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.                        

Anatomical and histological analyses reveal that tail repair is coupled with regrowth in wild-caught, juvenile American alligators (Alligator mississippiensis)., Xu C., Sci Rep. November 18, 2020; 10 (1): 20122.                

rad21 Is Involved in Corneal Stroma Development by Regulating Neural Crest Migration., Zhang BN., Int J Mol Sci. October 21, 2020; 21 (20):                             

Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.                  

CRISPR/Cas9-mediated efficient and precise targeted integration of donor DNA harboring double cleavage sites in Xenopus tropicalis., Mao CZ., FASEB J. June 13, 2018; fj201800093.              

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.                                            

Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. February 14, 2017; 7 42506.          

Genome evolution in the allotetraploid frog Xenopus laevis., Session AM., Nature. October 20, 2016; 538 (7625): 336-343.                              

A developmentally regulated switch from stem cells to dedifferentiation for limb muscle regeneration in newts., Tanaka HV., Nat Commun. January 12, 2016; 7 11069.        

MHC class I limits hippocampal synapse density by inhibiting neuronal insulin receptor signaling., Dixon-Salazar TJ., J Neurosci. August 27, 2014; 34 (35): 11844-56.

Ectopic blastema induction by nerve deviation and skin wounding: a new regeneration model in Xenopus laevis., Mitogawa K., Regeneration (Oxf). May 28, 2014; 1 (2): 26-36.            

Wiring the retinal circuits activated by light during early development., Bertolesi GE., Neural Dev. February 13, 2014; 9 3.              

The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            

Early development of the thymus in Xenopus laevis., Lee YH, Lee YH., Dev Dyn. February 1, 2013; 242 (2): 164-78.                            

Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms., Lobikin M., Proc Natl Acad Sci U S A. July 31, 2012; 109 (31): 12586-91.                    

Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.                            

Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.          

FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.                  

Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          

In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      

Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB., Rolo A., Dev Biol. March 15, 2009; 327 (2): 327-38.    

DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.            

Major histocompatibility complex based resistance to a common bacterial pathogen of amphibians., Barribeau SM., PLoS One. July 16, 2008; 3 (7): e2692.              

Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.                                

SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG., Development. November 1, 2007; 134 (22): 4119-30.    

xSyndecan-4 regulates gastrulation and neural tube closure in Xenopus embryos., Muñoz R., ScientificWorldJournal. October 9, 2006; 6 1298-301.  

Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.          

TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.                

Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.                        

p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.              

The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis., Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.                  

Wnt11-R, a protein closely related to mammalian Wnt11, is required for heart morphogenesis in Xenopus., Garriock RJ., Dev Biol. March 1, 2005; 279 (1): 179-92.          

Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.            

Myogenic regulatory factors: redundant or specific functions? Lessons from Xenopus., Chanoine C., Dev Dyn. December 1, 2004; 231 (4): 662-70.  

Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF., Development. April 1, 2004; 131 (8): 1703-15.              

Cutting edge: recruitment of the ancestral fyn gene during emergence of the adaptive immune system., Picard C., J Immunol. March 15, 2002; 168 (6): 2595-8.

Serrate and Notch specify cell fates in the heart field by suppressing cardiomyogenesis., Rones MS., Development. September 1, 2000; 127 (17): 3865-76.                  

Disruption of actin-myosin interactions results in the inhibition of focal adhesion assembly in Xenopus XR1 glial cells., Folsom TD., Glia. May 1, 1999; 26 (3): 245-59.

Isoform transition of contractile proteins related to muscle remodeling with an axial gradient during metamorphosis in Xenopus laevis., Nishikawa A., Dev Biol. September 1, 1994; 165 (1): 86-94.                      

Cloning of the cDNA encoding a myosin heavy chain B isoform of Xenopus nonmuscle myosin with an insert in the head region., Bhatia-Dey N., Proc Natl Acad Sci U S A. April 1, 1993; 90 (7): 2856-9.

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