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Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax. , Wang S., Cell Biosci. February 23, 2023; 13 (1): 40.
Differential nuclear import sets the timing of protein access to the embryonic genome. , Nguyen T., Nat Commun. October 6, 2022; 13 (1): 5887.
Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism. , Vick P ., Genes (Basel). November 24, 2021; 12 (12):
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes. , Mehdizadeh T., J Dev Biol. June 30, 2021; 9 (3):
Mcrs1 interacts with Six1 to influence early craniofacial and otic development. , Neilson KM ., Dev Biol. November 1, 2020; 467 (1-2): 39-50.
The Borealin dimerization domain interacts with Sgo1 to drive Aurora B-mediated spindle assembly. , Bonner MK., Mol Biol Cell. September 15, 2020; 31 (20): 2207-2218.
Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development. , Yan B ., Dev Dyn. February 1, 2015; 244 (2): 181-210.
Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors. , Neilson KM ., Dev Dyn. December 1, 2010; 239 (12): 3446-66.
EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis. , Li Y., Biol Cell. February 17, 2010; 102 (5): 277-92.