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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates. , Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution. , Hossain N., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation. , Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
FGFR1 variants contributed to families with tooth agenesis. , Yao S., Hum Genomics. October 13, 2023; 17 (1): 93.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Gene expression in notochord and nuclei pulposi: a study of gene families across the chordate phylum. , Raghavan R., BMC Ecol Evol. October 27, 2023; 23 (1): 63.
FGF20. , Van Greenen JD., Differentiation. November 7, 2023; 100737.
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. , Bocquet B., JCI Insight. November 8, 2023; 8 (21):
The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
Developmental expression of peroxiredoxin gene family in early embryonic development of Xenopus tropicalis. , Zhong L., Gene Expr Patterns. December 1, 2023; 50 119345.