???pagination.result.count???
???pagination.result.page???
1
The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
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.
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
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):
A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation. , Hou K., Cells. May 15, 2019; 8 (5):
Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation. , Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
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.
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.
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.
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.
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., 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., BMC Dev Biol. October 6, 2015; 15 33.
Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular context. , Jahan I., Front Cell Neurosci. February 5, 2015; 9 26.
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.
Identification of distal enhancers for Six2 expression in pronephros. , Suzuki N., Int J Dev Biol. January 1, 2015; 59 (4-6): 241-6.
Sp8 regulates inner ear development. , Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
HNF1B controls proximal-intermediate nephron segment identity in vertebrates by regulating Notch signalling components and Irx1/2. , Heliot C., Development. February 1, 2013; 140 (4): 873-85.
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.
Evolution of a tissue-specific silencer underlies divergence in the expression of pax2 and pax8 paralogues. , Ochi H ., Nat Commun. May 22, 2012; 3 848.
Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney. , Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C., 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., PLoS One. January 1, 2012; 7 (6): e38939.
Origin and segregation of cranial placodes in Xenopus laevis. , Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
PAPC and the Wnt5a/ Ror2 pathway control the invagination of the otic placode in Xenopus. , Jung B., BMC Dev Biol. June 10, 2011; 11 36.
Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns. , Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.
Long-term consequences of Sox9 depletion on inner ear development. , Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx. , Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
Zebrafish gbx1 refines the midbrain- hindbrain boundary border and mediates the Wnt8 posteriorization signal. , Rhinn M., Neural Dev. April 2, 2009; 4 12.
Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis. , Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.
Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development. , Fujimi TJ ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.
Sox9 is required for invagination of the otic placode in mice. , Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase. , Koide T., Development. June 1, 2006; 133 (12): 2395-405.
Regulation of melanoblast and retinal pigment epithelium development by Xenopus laevis Mitf. , Kumasaka M., Dev Dyn. November 1, 2005; 234 (3): 523-34.
Identification of mutants in inbred Xenopus tropicalis. , Grammer TC ., Mech Dev. March 1, 2005; 122 (3): 263-72.
Xenopus aristaless-related homeobox ( xARX) gene product functions as both a transcriptional activator and repressor in forebrain development. , Seufert DW ., Dev Dyn. February 1, 2005; 232 (2): 313-24.
Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development. , Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.
The role of XTRAP-gamma in Xenopus pronephros development. , Li DH., Int J Dev Biol. January 1, 2005; 49 (4): 401-8.
The role of Pax2 in mouse inner ear development. , Burton Q., Dev Biol. August 1, 2004; 272 (1): 161-75.
Molecular anatomy of placode development in Xenopus laevis. , Schlosser G ., Dev Biol. July 15, 2004; 271 (2): 439-66.
The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway. , Merlo GR., Dev Biol. August 1, 2002; 248 (1): 157-69.
Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo. , Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
Expression of the Xvax2 gene demarcates presumptive ventral telencephalon and specific visual structures in Xenopus laevis. , Liu Y ., Mech Dev. January 1, 2001; 100 (1): 115-8.
Competence, specification and commitment in otic placode induction. , Groves AK., Development. August 1, 2000; 127 (16): 3489-99.
Synergism between Pax-8 and lim-1 in embryonic kidney development. , Carroll TJ ., Dev Biol. October 1, 1999; 214 (1): 46-59.
Role of Xrx1 in Xenopus eye and anterior brain development. , Andreazzoli M ., Development. June 1, 1999; 126 (11): 2451-60.
Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development. , Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.