???pagination.result.count???
???pagination.result.page???
1
The histone H4K20 methyltransferase SUV4-20H1/KMT5B is required for multiciliated cell differentiation in Xenopus. , Angerilli A., Life Sci Alliance. July 1, 2023; 6 (7):
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
Ptbp1 and Exosc9 knockdowns trigger skin stability defects through different pathways. , Noiret M ., Dev Biol. January 15, 2016; 409 (2): 489-501.
BMP signalling controls the construction of vertebrate mucociliary epithelia. , Cibois M., Development. July 1, 2015; 142 (13): 2352-63.
A novel RIPK4- IRF6 connection is required to prevent epithelial fusions characteristic for popliteal pterygium syndromes. , De Groote P., Cell Death Differ. June 1, 2015; 22 (6): 1012-24.
Mutations in PYCR1 cause cutis laxa with progeroid features. , Reversade B ., Nat Genet. September 1, 2009; 41 (9): 1016-21.
The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos. , Stubbs JL., Nat Genet. December 1, 2008; 40 (12): 1454-60.
Hedgehog family member is expressed throughout regenerating and developing limbs. , Stark DR., Dev Dyn. July 1, 1998; 212 (3): 352-63.
A set of novel tadpole specific genes expressed only in the epidermis are down-regulated by thyroid hormone during Xenopus laevis metamorphosis. , Furlow JD ., Dev Biol. February 15, 1997; 182 (2): 284-98.
Spatial, temporal, and hormonal regulation of epidermal keratin expression during development of the frog, Xenopus laevis. , Nishikawa A., Dev Biol. May 1, 1992; 151 (1): 145-53.