Papers associated with embryo (and pcna)

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	Human SLFN5 and its Xenopus Laevis ortholog regulate entry into mitosis and oocyte meiotic resumption., Vit G., Cell Death Discov. December 8, 2022; 8 (1): 484.
	Translesion DNA synthesis-driven mutagenesis in very early embryogenesis of fast cleaving embryos., Lo Furno E., Nucleic Acids Res. January 25, 2022; 50 (2): 885-898.
	Deep learning is widely applicable to phenotyping embryonic development and disease., Naert T., Development. November 1, 2021; 148 (21):
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
	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):
	RBL1 (p107) functions as tumor suppressor in glioblastoma and small-cell pancreatic neuroendocrine carcinoma in Xenopus tropicalis., Naert T., Oncogene. March 1, 2020; 39 (13): 2692-2706.
	SLC20A1 Is Involved in Urinary Tract and Urorectal Development., Rieke JM., Front Cell Dev Biol. January 1, 2020; 8 567.
	The Stemness Gene Mex3A Is a Key Regulator of Neuroblast Proliferation During Neurogenesis., Naef V., Front Cell Dev Biol. January 1, 2020; 8 549533.
	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.
	The age-regulated zinc finger factor ZNF367 is a new modulator of neuroblast proliferation during embryonic neurogenesis., Naef V., Sci Rep. August 7, 2018; 8 (1): 11836.
	NMDA Receptor Signaling Is Important for Neural Tube Formation and for Preventing Antiepileptic Drug-Induced Neural Tube Defects., Sequerra EB., J Neurosci. May 16, 2018; 38 (20): 4762-4773.
	A novel role for sox7 in Xenopus early primordial germ cell development: mining the PGC transcriptome., Butler AM., Development. January 8, 2018; 145 (1):
	Musashi and Plasticity of Xenopus and Axolotl Spinal Cord Ependymal Cells., Chernoff EAG., Front Cell Neurosci. January 1, 2018; 12 45.
	Cancer Models in Xenopus tropicalis by CRISPR/Cas9 Mediated Knockout of Tumor Suppressors., Naert T., Methods Mol Biol. January 1, 2018; 1865 147-161.
	Development of Xenopus laevis bipotential gonads into testis or ovary is driven by sex-specific cell-cell interactions, proliferation rate, cell migration and deposition of extracellular matrix., Piprek RP., Dev Biol. December 15, 2017; 432 (2): 298-310.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	Ptbp1 and Exosc9 knockdowns trigger skin stability defects through different pathways., Noiret M., Dev Biol. January 15, 2016; 409 (2): 489-501.
	Understanding How the Subcommissural Organ and Other Periventricular Secretory Structures Contribute via the Cerebrospinal Fluid to Neurogenesis., Guerra MM., Front Cell Neurosci. September 23, 2015; 9 480.
	YAP controls retinal stem cell DNA replication timing and genomic stability., Cabochette P., Elife. September 22, 2015; 4 e08488.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	RAD18 Is a Maternal Limiting Factor Silencing the UV-Dependent DNA Damage Checkpoint in Xenopus Embryos., Kermi C., Dev Cell. August 10, 2015; 34 (3): 364-72.
	TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis., Van Nieuwenhuysen T., Oncoscience. May 19, 2015; 2 (5): 555-66.
	A posttranscriptional mechanism that controls Ptbp1 abundance in the Xenopus epidermis., Méreau A., Mol Cell Biol. February 1, 2015; 35 (4): 758-68.
	Methylmercury exposure during early Xenopus laevis development affects cell proliferation and death but not neural progenitor specification., Huyck RW., Neurotoxicol Teratol. January 1, 2015; 47 102-13.
	Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.
	Transit amplification in the amniote cerebellum evolved via a heterochronic shift in NeuroD1 expression., Butts T., Development. July 1, 2014; 141 (14): 2791-5.
	Thyroid hormone-regulated Wnt5a/Ror2 signaling is essential for dedifferentiation of larval epithelial cells into adult stem cells in the Xenopus laevis intestine., Ishizuya-Oka A., PLoS One. January 1, 2014; 9 (9): e107611.
	Maturin is a novel protein required for differentiation during primary neurogenesis., Martinez-De Luna RI., Dev Biol. December 1, 2013; 384 (1): 26-40.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.
	Thyroid hormone signaling in the Xenopus laevis embryo is functional and susceptible to endocrine disruption., Fini JB., Endocrinology. October 1, 2012; 153 (10): 5068-81.
	Transgenic Xenopus laevis with the ef1-α promoter as an experimental tool for amphibian retinal regeneration study., Ueda Y., Genesis. August 1, 2012; 50 (8): 642-50.
	Dynamic interactions of high Cdt1 and geminin levels regulate S phase in early Xenopus embryos., Kisielewska J., Development. January 1, 2012; 139 (1): 63-74.
	Proliferation, migration and differentiation in juvenile and adult Xenopus laevis brains., D'Amico LA., Dev Biol. August 8, 2011; 1405 31-48.
	Sumoylation controls retinal progenitor proliferation by repressing cell cycle exit in Xenopus laevis., Terada K., Dev Biol. November 1, 2010; 347 (1): 180-94.
	RNA helicase Ddx39 is expressed in the developing central nervous system, limb, otic vesicle, branchial arches and facial mesenchyme of Xenopus laevis., Wilson JM., Gene Expr Patterns. January 1, 2010; 10 (1): 44-52.
	A directional Wnt/beta-catenin-Sox2-proneural pathway regulates the transition from proliferation to differentiation in the Xenopus retina., Agathocleous M., Development. October 1, 2009; 136 (19): 3289-99.
	ZFPIP/Zfp462 is maternally required for proper early Xenopus laevis development., Laurent A., Dev Biol. March 1, 2009; 327 (1): 169-76.
	hnRNP I inhibits Notch signaling and regulates intestinal epithelial homeostasis in the zebrafish., Yang J., PLoS Genet. February 1, 2009; 5 (2): e1000363.
	Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
	Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion., Schlosser G., Dev Biol. August 1, 2008; 320 (1): 199-214.
	Neural retinal regeneration in the anuran amphibian Xenopus laevis post-metamorphosis: transdifferentiation of retinal pigmented epithelium regenerates the neural retina., Yoshii C., Dev Biol. March 1, 2007; 303 (1): 45-56.
	Shh/BMP-4 signaling pathway is essential for intestinal epithelial development during Xenopus larval-to-adult remodeling., Ishizuya-Oka A., Dev Dyn. December 1, 2006; 235 (12): 3240-9.
	Ubiquitination of cyclin-dependent kinase inhibitor, Xic1, is mediated by the Xenopus F-box protein xSkp2., Lin HR., Cell Cycle. February 1, 2006; 5 (3): 304-14.
	Secondary neurogenesis in the brain of the African clawed frog, Xenopus laevis, as revealed by PCNA, Delta-1, Neurogenin-related-1, and NeuroD expression., Wullimann MF., J Comp Neurol. August 29, 2005; 489 (3): 387-402.
	Frzb modulates Wnt-9a-mediated beta-catenin signaling during avian atrioventricular cardiac cushion development., Person AD., Dev Biol. February 1, 2005; 278 (1): 35-48.
	Embryonic expression of pre-initiation DNA replication factors in Xenopus laevis., Walter BE., Gene Expr Patterns. November 1, 2004; 5 (1): 81-9.
	Hedgehog regulation of superficial slow muscle fibres in Xenopus and the evolution of tetrapod trunk myogenesis., Grimaldi A., Development. July 1, 2004; 131 (14): 3249-62.
	NO66, a highly conserved dual location protein in the nucleolus and in a special type of synchronously replicating chromatin., Eilbracht J., Mol Biol Cell. April 1, 2004; 15 (4): 1816-32.
	A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I., Mol Cell. August 1, 2003; 12 (2): 425-35.

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