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Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis. , Saumweber E, Mzoughi S, Khadra A, Werberger A, Schumann S, Guccione E, Schmeisser MJ, Kühl SJ ., Front Cell Dev Biol. January 1, 2024; 12 1316048.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ, Rajasekaran A, Jusić N, Taylor L , Read M, Alfandari D , Alfandari D , Pignoni F, Moody SA ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation. , Cervino AS, Collodel MG, Lopez IA, Roa C, Hochbaum D, Hukriede NA, Cirio MC ., 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, Nemes P , Moody SA ., iScience. September 15, 2023; 26 (9): 107665.
Hnf1b renal expression directed by a distal enhancer responsive to Pax8. , Goea L, Buisson I , Bello V, Eschstruth A, Paces-Fessy M, Le Bouffant R , Chesneau A, Cereghini S, Riou JF , Umbhauer M ., Sci Rep. November 19, 2022; 12 (1): 19921.
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease. , Coppenrath K , Tavares ALP, Shaidani NI , Wlizla M , Moody SA , Horb M ., Genesis. December 1, 2021; 59 (12): e23453.
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease. , Getwan M , Hoppmann A, Schlosser P, Grand K, Song W, Diehl R, Schroda S, Heeg F, Deutsch K, Hildebrandt F, Lausch E, Köttgen A, Lienkamp SS ., 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, Jourdeuil K, Neilson KM , Majumdar HD, Moody SA ., Development. September 1, 2021; 148 (17):
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA , Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M , Marciano DK, Lakhani SA, Liu KJ , Liu KJ ., 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, Krohn P, Baxi AB, Tavares ALP, Sullivan CH, Chillakuru YR, Majumdar HD, Neilson KM , Moody SA ., 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, Alvarez-Bolado G, Wizenmann 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 , Aguero TH , Owens DA , Kurtenbach S, Field MG, Durante MA, Rodriguez DA, King ML , Harbour JW., Sci Adv. September 18, 2019; 5 (9): eaax1738.
Modeling congenital kidney diseases in Xenopus laevis. , Blackburn ATM, Miller RK ., Dis Model Mech. April 9, 2019; 12 (4):
A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates. , Plouhinec JL, Medina-Ruiz S, Borday C, Bernard E, Vert JP, Eisen MB, Harland RM , Monsoro-Burq AH ., PLoS Biol. October 19, 2017; 15 (10): e2004045.
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 , Nakajima K , Cox A, Fisher M , Fisher M , Howell M, Fish MB, Yaoita Y , Grainger RM ., Dev Biol. June 15, 2017; 426 (2): 472-486.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM , Abbruzzesse G , Kenyon K , Bartolo V, Krohn P, Alfandari D , Alfandari D , Moody SA ., Dev Biol. January 15, 2017; 421 (2): 171-182.
Using Xenopus to study genetic kidney diseases. , Lienkamp SS ., Semin Cell Dev Biol. March 1, 2016; 51 117-24.
CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus. , Bhattacharya D, Marfo CA, Li D, Lane M, Khokha MK ., Dev Biol. December 15, 2015; 408 (2): 196-204.
Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing. , del Viso F, Bhattacharya D, Kong Y, Gilchrist MJ , Khokha MK ., BMC Genomics. November 21, 2012; 13 649.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C, Yazgan O, Kuo HC, Malakar S, Thomas T, Fitzgerald A, Harbour W, Henry JJ , Krebs JE., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
Xenopus as a model system for the study of GOLPH2/ GP73 function: Xenopus GOLPH2 is required for pronephros development. , Li L, Wen L, Gong Y, Mei G, Liu J , Chen Y , Peng T., PLoS One. January 1, 2012; 7 (6): e38939.
The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim1/ Lhx1. , Agrawal R , Tran U , Wessely O ., Development. December 1, 2009; 136 (23): 3927-36.
Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase. , Koide T, Hayata T, Cho KW ., Development. June 1, 2006; 133 (12): 2395-405.