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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.
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):
Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders. , Wyatt BH., Genesis. February 1, 2021; 59 (1-2): e23394.
A simple and practical workflow for genotyping of CRISPR-Cas9-based knockout phenotypes using multiplexed amplicon sequencing. , Iida M., Genes Cells. July 1, 2020; 25 (7): 498-509.
The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos. , Willsey HR ., Development. June 22, 2020; 147 (21):
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.
CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing. , Moreno-Mateos MA., Nat Commun. December 8, 2017; 8 (1): 2024.
Rapid and efficient analysis of gene function using CRISPR-Cas9 in Xenopus tropicalis founders. , Shigeta M., Genes Cells. July 1, 2016; 21 (7): 755-71.