???pagination.result.count???
???pagination.result.page???
1
Human disease-causing NOG missense mutations: effects on noggin secretion, dimer formation, and bone morphogenetic protein binding. , Marcelino J, Sciortino CM, Romero MF , Ulatowski LM, Ballock RT, Economides AN, Eimon PM, Harland RM , Warman ML ., Proc Natl Acad Sci U S A. September 25, 2001; 98 (20): 11353-8.
Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX. , Blaschke RJ, Töpfer C, Marchini A, Steinbeisser H , Janssen JW, Rappold GA., J Biol Chem. November 28, 2003; 278 (48): 47820-6.
Bone density ligand, Sclerostin, directly interacts with LRP5 but not LRP5G171V to modulate Wnt activity. , Ellies DL, Viviano B, McCarthy J, Rey JP, Itasaki N, Saunders S, Krumlauf R ., J Bone Miner Res. November 1, 2006; 21 (11): 1738-49.
Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus. , Xu S, Cheng F, Liang J, Wu W, Zhang J., PLoS Biol. January 1, 2012; 10 (3): e1001286.
A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome. , Rienhoff HY, Yeo CY, Morissette R, Khrebtukova I, Melnick J, Luo S, Leng N, Kim YJ, Schroth G, Westwick J, Vogel H, McDonnell N, Hall JG, Whitman M ., Am J Med Genet A. August 1, 2013; 161A (8): 2040-6.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y , Thomsen GH ., Development. October 1, 2014; 141 (19): 3740-51.
The evolutionarily conserved transcription factor PRDM12 controls sensory neuron development and pain perception. , Nagy V, Cole T, Van Campenhout C, Khoung TM, Leung C, Vermeiren S, Novatchkova M, Wenzel D, Cikes D, Polyansky AA, Kozieradzki I, Meixner A, Bellefroid EJ , Neely GG, Penninger JM., Cell Cycle. January 1, 2015; 14 (12): 1799-808.
BMP signalling controls the construction of vertebrate mucociliary epithelia. , Cibois M, Luxardi G , Chevalier B, Thomé V, Mercey O, Zaragosi LE , Barbry P, Pasini A, Marcet B, Kodjabachian L ., Development. July 1, 2015; 142 (13): 2352-63.
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.
Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover. , Kirsch N, Chang LS, Koch S, Glinka A , Dolde C, Colozza G , Benitez MDJ, De Robertis EM , Niehrs C ., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus. , Bae CJ, Hong CS , Saint-Jeannet JP ., Biochem Biophys Res Commun. January 15, 2018; 495 (3): 2257-2263.
Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis. , Harata A, Hirakawa M, Sakuma T, Yamamoto T , Hashimoto C., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis. , Chen M, Amado N, Tan J, Reis A, Ge M, Abreu JG , He X ., Elife. September 14, 2020; 9
Modeling endoderm development and disease in Xenopus. , Edwards NA , Zorn AM ., Curr Top Dev Biol. January 1, 2021; 145 61-90.
Molecular mechanisms of hearing loss in Nager syndrome. , Maharana SK , Saint-Jeannet JP ., Dev Biol. August 1, 2021; 476 200-208.
Huntingtin CAG expansion impairs germ layer patterning in synthetic human 2D gastruloids through polarity defects. , Galgoczi S, Ruzo A, Markopoulos C, Yoney A, Phan-Everson T, Li S, Haremaki T , Metzger JJ, Etoc F, Brivanlou AH ., Development. October 1, 2021; 148 (19):