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The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation. , Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates. , Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
Hnf1b renal expression directed by a distal enhancer responsive to Pax8. , Goea L., Sci Rep. November 19, 2022; 12 (1): 19921.
Appropriate Amounts and Activity of the Wilms' Tumor Suppressor Gene, wt1, Are Required for Normal Pronephros Development of Xenopus Embryos. , Shiraki T., J Dev Biol. October 29, 2022; 10 (4):
Normal Table of Xenopus development: a new graphical resource. , Zahn N ., Development. July 15, 2022; 149 (14):
Systematic mapping of rRNA 2'-O methylation during frog development and involvement of the methyltransferase Fibrillarin in eye and craniofacial development in Xenopus laevis. , Delhermite J ., PLoS Genet. January 18, 2022; 18 (1): e1010012.
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease. , Coppenrath K ., Genesis. December 1, 2021; 59 (12): e23453.
Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism. , Vick P ., Genes (Basel). November 24, 2021; 12 (12):
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):
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development. , Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
MiR-9 and the Midbrain- Hindbrain Boundary: A Showcase for the Limited Functional Conservation and Regulatory Complexity of MicroRNAs. , Alwin Prem Anand A., Front Cell Dev Biol. January 1, 2020; 8 586158.
BAP1 regulates epigenetic switch from pluripotency to differentiation in developmental lineages giving rise to BAP1-mutant cancers. , Kuznetsov JN ., Sci Adv. September 18, 2019; 5 (9): eaax1738.
A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation. , Hou K., Cells. May 15, 2019; 8 (5):
Modeling congenital kidney diseases in Xenopus laevis. , Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS. , Kim E ., Sci Rep. March 22, 2019; 9 (1): 5025.
Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation. , Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
Arid3a regulates nephric tubule regeneration via evolutionarily conserved regeneration signal-response enhancers. , Suzuki N., Elife. January 8, 2019; 8
Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development. , DeLay BD ., Front Physiol. January 1, 2019; 10 143.
Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus. , Watanabe T., Development. October 26, 2018; 145 (20):
RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus. , Griffin JN., Development. October 18, 2018; 145 (20):
Phosphorylation states change Otx2 activity for cell proliferation and patterning in the Xenopus embryo. , Satou Y., Development. March 12, 2018; 145 (5):
EphA7 regulates claudin6 and pronephros development in Xenopus. , Sun J., Biochem Biophys Res Commun. January 8, 2018; 495 (2): 1580-1587.
lrpap1 as a specific marker of proximal pronephric kidney tubuli in Xenopus laevis embryos. , Neuhaus H ., Int J Dev Biol. January 1, 2018; 62 (4-5): 319-324.
Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels. , Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.
no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development. , Nakayama T ., Dev Biol. June 15, 2017; 426 (2): 472-486.
Frizzled 3 acts upstream of Alcam during embryonic eye development. , Seigfried FA., Dev Biol. June 1, 2017; 426 (1): 69-83.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM ., Dev Biol. January 15, 2017; 421 (2): 171-182.
Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors. , Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
Hedgehog-dependent E3-ligase Midline1 regulates ubiquitin-mediated proteasomal degradation of Pax6 during visual system development. , Pfirrmann T ., Proc Natl Acad Sci U S A. September 6, 2016; 113 (36): 10103-8.
Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome. , Adams DS ., J Physiol. June 15, 2016; 594 (12): 3245-70.
Hmga2 is required for neural crest cell specification in Xenopus laevis. , Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.
CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus. , Bhattacharya D., Dev Biol. December 15, 2015; 408 (2): 196-204.
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus. , Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development. , Buisson I ., Dev Biol. January 15, 2015; 397 (2): 175-90.
Understanding early organogenesis using a simplified in situ hybridization protocol in Xenopus. , Deimling SJ., J Vis Exp. January 12, 2015; (95): e51526.
Heat shock 70-kDa protein 5 ( Hspa5) is essential for pronephros formation by mediating retinoic acid signaling. , Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
Custos controls β-catenin to regulate head development during vertebrate embryogenesis. , Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.
The Wnt/ JNK signaling target gene alcam is required for embryonic kidney development. , Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning. , Schlosser G ., Dev Biol. May 1, 2014; 389 (1): 98-119.
Sp8 regulates inner ear development. , Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus. , Young JJ ., Development. April 1, 2014; 141 (8): 1683-93.
The Prdm13 histone methyltransferase encoding gene is a Ptf1a- Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube. , Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
Stabilization of speckle-type POZ protein ( Spop) by Daz interacting protein 1 ( Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling. , Schwend T ., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.
Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein. , Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing. , del Viso F., BMC Genomics. November 21, 2012; 13 649.
Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning. , Steventon B ., Dev Biol. July 1, 2012; 367 (1): 55-65.