???pagination.result.count???
???pagination.result.page???
1
Xenopus as a model system for studying pigmentation and pigmentary disorders. , El Mir J., Pigment Cell Melanoma Res. June 7, 2024;
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. , Kaiyrzhanov R., Brain. April 4, 2024; 147 (4): 1436-1456.
Revealing mitf functions and visualizing allografted tumor metastasis in colorless and immunodeficient Xenopus tropicalis. , Ran R., Commun Biol. March 5, 2024; 7 (1): 275.
HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes. , Grand K., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.
Hnf1b renal expression directed by a distal enhancer responsive to Pax8. , Goea L., Sci Rep. November 19, 2022; 12 (1): 19921.
A convergent molecular network underlying autism and congenital heart disease. , Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease. , Getwan M ., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos. , Willsey HR ., Dev Biol. October 15, 2018; 442 (2): 276-287.
Tissue-Specific Gene Inactivation in Xenopus laevis: Knockout of lhx1 in the Kidney with CRISPR/Cas9. , DeLay BD ., Genetics. February 1, 2018; 208 (2): 673-686.