Papers associated with sensory system (and pam)

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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.
	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.
	Purine Biosynthesis Pathways Are Required for Myogenesis in Xenopus laevis., Duperray M., Cells. September 28, 2023; 12 (19):
	Tissue-specific expression of carbohydrate sulfotransferases drives keratan sulfate biosynthesis in the notochord and otic vesicles of Xenopus embryos., Yasuoka Y., Front Cell Dev Biol. January 1, 2023; 11 957805.
	CRISPR/Cas9-based simple transgenesis in Xenopus laevis., Shibata Y., Dev Biol. September 1, 2022; 489 76-83.
	Functions of block of proliferation 1 during anterior development in Xenopus laevis., Gärtner C., PLoS One. August 2, 2022; 17 (8): e0273507.
	inka1b expression in the head mesoderm is dispensable for facial cartilage development., Jeon H., Gene Expr Patterns. January 1, 2022; 45 119262.
	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):
	Wnt-inducible Lrp6-APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway., Colozza G., Sci Rep. December 9, 2020; 10 (1): 21555.
	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):
	Modeling ocular lens disease in Xenopus., Viet J., Dev Dyn. May 1, 2020; 249 (5): 610-621.
	CRISPR/Cas9-mediated efficient and precise targeted integration of donor DNA harboring double cleavage sites in Xenopus tropicalis., Mao CZ., FASEB J. June 13, 2018; fj201800093.
	The atypical mitogen-activated protein kinase ERK3 is essential for establishment of epithelial architecture., Takahashi C., J Biol Chem. June 1, 2018; 293 (22): 8342-8361.
	CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing., Moreno-Mateos MA., Nat Commun. December 8, 2017; 8 (1): 2024.
	Targeted Base Editing via RNA-Guided Cytidine Deaminases in Xenopus laevis Embryos., Park DS., Mol Cells. November 30, 2017; 40 (11): 823-827.
	Co-accumulation of cis-regulatory and coding mutations during the pseudogenization of the Xenopus laevis homoeologs six6.L and six6.S., Ochi H., Dev Biol. July 1, 2017; 427 (1): 84-92.
	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.
	The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
	Simple and efficient CRISPR/Cas9-mediated targeted mutagenesis in Xenopus tropicalis., Nakayama T., Genesis. December 1, 2013; 51 (12): 835-43.
	Temporal and spatial expression patterns of FoxD2 during the early development of Xenopus laevis., Pohl BS., Mech Dev. February 1, 2002; 111 (1-2): 181-4.

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