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Summary Anatomy Item Literature (2201) Expression Attributions Wiki
XB-ANAT-1506

Papers associated with skeletal element

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4-Octylphenol induces developmental abnormalities and interferes the differentiation of neural crest cells in Xenopus laevis embryos., Xu Y., Environ Pollut. April 1, 2021; 274 116560.  


Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders., Wyatt BH., Genesis. January 1, 2021; 59 (1-2): e23394.                        


Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J., Genesis. January 1, 2021; 59 (1-2): e23404.      


Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis., Lee H., Antioxidants (Basel). December 12, 2020; 9 (12):               


De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome., Ufartes R., Hum Genet. November 1, 2020; 139 (11): 1363-1379.                                        


Endoparasites infecting exotic captive amphibian pet and zoo animals (Anura, Caudata) in Germany., Hallinger MJ., Parasitol Res. November 1, 2020; 119 (11): 3659-3673.            


De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy., Park J., J Med Genet. January 1, 2020; 57 (4): 283-288.


Odontomas in Frogs., LaDouceur EEB., Vet Pathol. January 1, 2020; 57 (1): 147-150.


The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration., Schwenty-Lara J., Hum Mol Genet. January 1, 2020; 29 (2): 305-319.                


Heparan sulfate proteoglycans regulate BMP signalling during neural crest induction., Pegge J., Dev Biol. January 1, 2020; 460 (2): 108-114.        


Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects., Marquez J., J Clin Invest. January 1, 2020; 130 (2): 813-826.                                


Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. January 1, 2020; 13 (3):                                               


Evolutionary repression of chondrogenic genes in the vertebrate osteoblast., Nguyen JKB., FEBS J. January 1, 2020; 287 (20): 4354-4361.


Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.                    


Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. January 1, 2020; 29 (11): 1900-1921.                  


Enrichment of Mammalian Tissues and Xenopus Oocytes with Cholesterol., Slayden A., J Vis Exp. January 1, 2020; (157):


Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin., Vonica A., Dev Biol. January 1, 2020; 464 (1): 71-87.


Effect of nano-encapsulation of β-carotene on Xenopus laevis embryos development (FETAX)., Battistoni M., Toxicol Rep. January 1, 2020; 7 510-519.                  


The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled., Kratzer MC., Development. January 1, 2020; 147 (10):                                   


M-Channel Activation Contributes to the Anticonvulsant Action of the Ketone Body β-Hydroxybutyrate., Manville RW., J Pharmacol Exp Ther. January 1, 2020; 372 (2): 148-156.


Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development., Farley-Barnes KI., PLoS Genet. January 1, 2020; 16 (8): e1008967.                                    


SLC20A1 Is Involved in Urinary Tract and Urorectal Development., Rieke JM., Front Cell Dev Biol. January 1, 2020; 8 567.          


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


Axial Skeletal Malformations in Genetically Modified Xenopus laevis and Xenopus tropicalis., Zlatow AL., Comp Med. January 1, 2020; 70 (6): 532-541.


Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting., Schönauer R., Urolithiasis. December 1, 2019; 47 (6): 511-519.        


Larger Genomes Linked to Slower Development and Loss of Late-Developing Traits., Womack MC., Am Nat. December 1, 2019; 194 (6): 854-864.


Effects of antidepressants with different modes of action on early life stages of fish and amphibians., Sehonova P., Environ Pollut. November 1, 2019; 254 (Pt A): 112999.


Cdc2-like kinase 2 (Clk2) promotes early neural development in Xenopus embryos., Virgirinia RP., Dev Growth Differ. August 1, 2019; 61 (6): 365-377.                              


Gene Regulatory Networks Governing the Generation and Regeneration of Blood., Ciau-Uitz A., J Comput Biol. July 1, 2019; 26 (7): 719-725.


The comet assay in animal models: From bugs to whales - (Part 2 Vertebrates)., Gajski G., Mutat Res. July 1, 2019; 781 130-164.


Proteolytic Activation of Bmps: Analysis of Cleavage in Xenopus Oocytes and Embryos., Kim HS., Methods Mol Biol. January 1, 2019; 1891 115-133.


How thyroid hormones and their inhibitors affect cartilage growth and shape in the frog Xenopus laevis., Rose CS., J Anat. January 1, 2019; 234 (1): 89-105.


The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals., Kwong-Brown U., Elife. January 1, 2019; 8               


Class A Scavenger Receptors Are Used by Frog Virus 3 During Its Cellular Entry., Vo NTK., Viruses. January 1, 2019; 11 (2):       


The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1., Ott T., Front Physiol. January 1, 2019; 10 134.                


Latrophilin2 is involved in neural crest cell migration and placode patterning in Xenopus laevis., Yokote N., Int J Dev Biol. January 1, 2019; 63 (1-2): 29-35.                    


Activation of the calcium sensing receptor attenuates TRPV6-dependent intestinal calcium absorption., Lee JJ., JCI Insight. January 1, 2019; 5


Human mutations highlight an intersubunit cation-π bond that stabilizes the closed but not open or inactivated states of TRPV channels., Teng J., Proc Natl Acad Sci U S A. January 1, 2019; 116 (19): 9410-9416.


Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis., Mills A., Front Physiol. January 1, 2019; 10 431.                                          


PDGF-B: The missing piece in the mosaic of PDGF family role in craniofacial development., Corsinovi D., Dev Dyn. January 1, 2019; 248 (7): 603-612.            


Epithelial-Mesenchymal Transition Promotes the Differentiation Potential of Xenopus tropicalis Immature Sertoli Cells., Nguyen TMX., Stem Cells Int. January 1, 2019; 2019 8387478.                                            


Environmental Oxygen Exposure Allows for the Evolution of Interdigital Cell Death in Limb Patterning., Cordeiro IR., Dev Cell. January 1, 2019; 50 (2): 155-166.e4.            


Adaptive correction of craniofacial defects in pre-metamorphic Xenopus laevis tadpoles involves thyroid hormone-independent tissue remodeling., Pinet K., Development. January 1, 2019; 146 (14):                               


Comparative analysis of p4ha1 and p4ha2 expression during Xenopus laevis development., Martini D., Int J Dev Biol. January 1, 2019; 63 (6-7): 311-316.          


Skeletal Mineralization in Association with Type X Collagen Expression Is an Ancestral Feature for Jawed Vertebrates., Debiais-Thibaud M., Mol Biol Evol. January 1, 2019; 36 (10): 2265-2276.          


The Many Faces of Xenopus: Xenopus laevis as a Model System to Study Wolf-Hirschhorn Syndrome., Lasser M., Front Physiol. January 1, 2019; 10 817.                    


A new transgenic reporter line reveals Wnt-dependent Snai2 re-expression and cranial neural crest differentiation in Xenopus., Li J., Sci Rep. January 1, 2019; 9 (1): 11191.              


HIF-1α metabolically controls collagen synthesis and modification in chondrocytes., Stegen S., Nature. January 1, 2019; 565 (7740): 511-515.


Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. January 1, 2019; 178 (6): 1421-1436.e24.                                


Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD., PLoS Biol. January 1, 2019; 17 (9): e3000437.                                                    

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