???pagination.result.count???
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. May 1, 2024; 342 (3): 212-240.
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.
The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A, Neilson KM , Majumdar HD, Yamauchi K, Klein SL, Moody SA ., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
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.
Appropriate Amounts and Activity of the Wilms' Tumor Suppressor Gene, wt1, Are Required for Normal Pronephros Development of Xenopus Embryos. , Shiraki T, Hayashi T, Ozue J, Watanabe M., J Dev Biol. October 29, 2022; 10 (4):
Normal Table of Xenopus development: a new graphical resource. , Zahn N , James-Zorn C , Ponferrada VG , Adams DS , Grzymkowski J, Buchholz DR , Nascone-Yoder NM , Horb M , Moody SA , Vize PD , Zorn AM ., Development. July 15, 2022; 149 (14):
Comparative anatomy on the development of sperm transporting pathway between the testis and mesonephros. , Omotehara T, Nakata H, Nagahori K, Itoh M., Histochem Cell Biol. March 1, 2022; 157 (3): 321-332.
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 , Tafforeau L, Sharma S, Marchand V, Wacheul L, Lattuca R, Desiderio S, Motorin Y, Bellefroid E , Lafontaine DLJ ., 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 , Tavares ALP, Shaidani NI , Wlizla M , Moody SA , Horb M ., Genesis. December 1, 2021; 59 (12): e23453.
Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism. , Vick P , Eberle B, Choukair D, Weiss B, Roeth R, Schneider I, Paramasivam N, Bettendorf M, Rappold GA., Genes (Basel). November 24, 2021; 12 (12):
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):
A temporally resolved transcriptome for developing "Keller" explants of the Xenopus laevis dorsal marginal zone. , Kakebeen AD, Huebner RJ, Shindo A, Kwon K, Kwon T , Wills AE , Wallingford JB ., Dev Dyn. May 1, 2021; 250 (5): 717-731.
Betel quid dependence mechanism and potential cessation therapy. , Ko AM, Lee CH , Ko AM, Ko YC., Prog Neuropsychopharmacol Biol Psychiatry. December 20, 2020; 103 109982.
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.
Regeneration enhancers: A clue to reactivation of developmental genes. , Suzuki N, Ochi H ., Dev Growth Differ. June 1, 2020; 62 (5): 343-354.
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.
A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation. , Hou K, Jiang H, Karim MR, Zhong C, Xu Z, Liu L, Guan M, Shao J, Huang X ., Cells. May 15, 2019; 8 (5):
Modeling congenital kidney diseases in Xenopus laevis. , Blackburn ATM, Miller RK ., Dis Model Mech. April 9, 2019; 12 (4):
Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS. , Kim E , Jeong I, Chung AY, Kim S, Kwon SH, Seong JY, Park HC., Sci Rep. March 22, 2019; 9 (1): 5025.
Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation. , Sullivan CH, Majumdar HD, Neilson KM , Moody SA ., Dev Biol. February 1, 2019; 446 (1): 68-79.
Arid3a regulates nephric tubule regeneration via evolutionarily conserved regeneration signal-response enhancers. , Suzuki N, Hirano K, Ogino H , Ochi H ., Elife. January 8, 2019; 8
Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development. , DeLay BD , Baldwin TA, Miller RK ., Front Physiol. January 1, 2019; 10 143.
Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus. , Watanabe T, Yamamoto T , Tsukano K, Hirano S, Horikawa A, Michiue 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, Sondalle SB, Robson A, Mis EK, Griffin G, Kulkarni SS , Deniz E , Baserga SJ, Khokha MK ., Development. October 18, 2018; 145 (20):
Phosphorylation states change Otx2 activity for cell proliferation and patterning in the Xenopus embryo. , Satou Y, Minami K, Hosono E, Okada H, Yasuoka Y , Shibano T, Tanaka T, Taira M ., Development. March 12, 2018; 145 (5):
EphA7 regulates claudin6 and pronephros development in Xenopus. , Sun J, Wang X , Shi Y , Shi Y , Li J, Li C, Shi Z, Chen Y , Chen Y , Mao B ., 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 , Gaul F, Hollemann T ., Int J Dev Biol. January 1, 2018; 62 (4-5): 319-324.
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.
Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels. , Chae S, Lee HK , Lee HK , Kim YK, Jung Sim H, Ji Y, Kim C, Ismail T, Park JW , Kwon OS, Kang BS, Lee DS, Bae JS, Kim SH, Min KJ, Kyu Kwon T, Park MJ, Han JK , Kwon T , Park TJ, Lee HS , Lee HS ., Sci Rep. August 21, 2017; 7 (1): 8874.
Pax2/Pax8-defined subdomains and the occurrence of apoptosis in the posterior placodal area of mice. , Washausen S, Knabe W., Brain Struct Funct. August 1, 2017; 222 (6): 2671-2695.
Bim gene dosage is critical in modulating nephron progenitor survival in the absence of microRNAs during kidney development. , Cerqueira DM, Bodnar AJ, Phua YL, Freer R, Hemker SL, Walensky LD, Hukriede NA, Ho J., FASEB J. August 1, 2017; 31 (8): 3540-3554.
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.
Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis. , Watanabe M, Yasuoka Y , Mawaribuchi S, Kuretani A, Ito M, Kondo M, Ochi H , Ogino H , Fukui A , Taira M , Kinoshita T., Dev Biol. June 15, 2017; 426 (2): 301-324.
Frizzled 3 acts upstream of Alcam during embryonic eye development. , Seigfried FA, Cizelsky W, Pfister AS, Dietmann P, Walther P, Kühl M , Kühl SJ., Dev Biol. June 1, 2017; 426 (1): 69-83.
Gabapentin Modulates HCN4 Channel Voltage-Dependence. , Tae HS, Smith KM, Phillips AM, Boyle KA, Li M, Forster IC, Hatch RJ, Richardson R, Hughes DI, Graham BA, Petrou S, Reid CA., Front Pharmacol. May 26, 2017; 8 554.
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.
Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors. , Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Müller AL, Pichler R, Grahammer F, Kretz O, Huber TB, Walz G , Arnold SJ, Lienkamp SS ., 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 , Jandt E, Ranft S, Lokapally A, Neuhaus H , Perron M , Hollemann 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 , Uzel SG, Akagi J, Wlodkowic D, Andreeva V, Yelick PC, Devitt-Lee A, Pare JF, Levin M ., J Physiol. June 15, 2016; 594 (12): 3245-70.
Proper Notch activity is necessary for the establishment of proximal cells and differentiation of intermediate, distal, and connecting tubule in Xenopus pronephros development. , Katada T, Sakurai H., Dev Dyn. April 1, 2016; 245 (4): 472-82.
Hmga2 is required for neural crest cell specification in Xenopus laevis. , Macrì S, Simula L, Pellarin I, Pegoraro S, Onorati M, Sgarra R, Manfioletti G, Vignali R ., Dev Biol. March 1, 2016; 411 (1): 25-37.
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.
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L, Lombard A, Moraldi T, Bibonne A, Leclerc C , Moreau M , Marlier A, Gilbert T ., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
Cooperative and independent functions of FGF and Wnt signaling during early inner ear development. , Wright KD, Mahoney Rogers AA, Zhang J, Shim K., BMC Dev Biol. October 6, 2015; 15 33.