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Dyrk1a is required for craniofacial development in Xenopus laevis. , Johnson HK, Wahl SE , Sesay F, Litovchick L, Dickinson AJ ., Dev Biol. April 13, 2024;
Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution. , Hossain N, Igawa T , Suzuki M , Tazawa I , Nakao Y, Hayashi T, Suzuki N, Ogino H ., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease. , Getwan M , Hoppmann A, Schlosser P, Grand K, Song W, Diehl R, Schroda S, Heeg F, Deutsch K, Hildebrandt F, Lausch E, Köttgen A, Lienkamp SS ., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development. , Forman TE, Dennison BJC, Fantauzzo KA., J Dev Biol. August 27, 2021; 9 (3):
Using Xenopus to analyze neurocristopathies like Kabuki syndrome. , Schwenty-Lara J, Pauli S, Borchers A ., Genesis. February 1, 2021; 59 (1-2): e23404.
The RNA helicase DDX3 induces neural crest by promoting AKT activity. , Perfetto M, Xu X, Lu C, Shi Y , Yousaf N, Li J, Yien YY, Wei S ., Development. January 19, 2021; 148 (2):
Mcrs1 interacts with Six1 to influence early craniofacial and otic development. , Neilson KM , Keer S, Bousquet N, Macrorie O, Majumdar HD, Kenyon KL , Alfandari D , Alfandari D , Moody SA ., Dev Biol. November 1, 2020; 467 (1-2): 39-50.
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome. , Greenberg RS, Long HK, Swigut T, Wysocka J., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM , Abbruzzesse G , Kenyon K , Bartolo V, Krohn P, Alfandari D , Alfandari D , Moody SA ., Dev Biol. January 15, 2017; 421 (2): 171-182.
WNT16 antagonises excessive canonical WNT activation and protects cartilage in osteoarthritis. , Nalesso G, Thomas BL, Sherwood JC, Yu J, Addimanda O, Eldridge SE, Thorup AS, Dale L , Schett G, Zwerina J, Eltawil N, Pitzalis C, Dell'Accio F., Ann Rheum Dis. January 1, 2017; 76 (1): 218-226.
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome. , Devotta A, Juraver-Geslin H , Gonzalez JA, Hong CS , Saint-Jeannet JP ., Dev Biol. July 15, 2016; 415 (2): 371-382.
Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin. , Gouignard N , Maccarana M, Strate I, von Stedingk K, Malmström A, Pera EM ., Dis Model Mech. June 1, 2016; 9 (6): 607-20.
Xenopus as a model system for studying pancreatic development and diabetes. , Kofent J, Spagnoli FM ., Semin Cell Dev Biol. March 1, 2016; 51 106-16.
Sox9 function in craniofacial development and disease. , Lee YH , Lee YH , Saint-Jeannet JP ., Genesis. April 1, 2011; 49 (4): 200-8.
Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis. , Tazumi S, Yabe S, Uchiyama H., Dev Biol. October 15, 2010; 346 (2): 170-80.
CHD7 cooperates with PBAF to control multipotent neural crest formation. , Bajpai R , Chen DA, Rada-Iglesias A, Zhang J, Xiong Y, Helms J, Chang CP , Zhao Y, Swigut T, Wysocka J., Nature. February 18, 2010; 463 (7283): 958-62.
A dominant-negative form of the E3 ubiquitin ligase Cullin-1 disrupts the correct allocation of cell fate in the neural crest lineage. , Voigt J, Papalopulu N ., Development. February 1, 2006; 133 (3): 559-68.