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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.
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;
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.
Paracrine regulation of neural crest EMT by placodal MMP28. , Gouignard N ., PLoS Biol. August 1, 2023; 21 (8): e3002261.
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation. , Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.
Deep learning is widely applicable to phenotyping embryonic development and disease. , Naert T., Development. November 1, 2021; 148 (21):
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
Dynamic expression of MMP28 during cranial morphogenesis. , Gouignard N ., Philos Trans R Soc Lond B Biol Sci. October 12, 2020; 375 (1809): 20190559.
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):
The neural border: Induction, specification and maturation of the territory that generates neural crest cells. , Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.
Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates. , Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.
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.
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development. , Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
The requirement of histone modification by PRDM12 and Kdm4a for the development of pre-placodal ectoderm and neural crest in Xenopus. , Matsukawa S ., Dev Biol. March 1, 2015; 399 (1): 164-176.
Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development. , Yan B ., Dev Dyn. February 1, 2015; 244 (2): 181-210.
Xenopus Nkx6.3 is a neural plate border specifier required for neural crest development. , Zhang Z ., PLoS One. December 15, 2014; 9 (12): e115165.
Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm. , Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling. , Watanabe T., Genesis. October 1, 2014; .
Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates. , Yajima H., BMC Biol. May 29, 2014; 12 40.
The evolutionary history of vertebrate cranial placodes--I: cell type evolution. , Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning. , Schlosser G ., Dev Biol. May 1, 2014; 389 (1): 98-119.
Setting appropriate boundaries: fate, patterning and competence at the neural plate border. , Groves AK., Dev Biol. May 1, 2014; 389 (1): 2-12.
Identification of Pax3 and Zic1 targets in the developing neural crest. , Bae CJ., Dev Biol. February 15, 2014; 386 (2): 473-83.
Early embryonic specification of vertebrate cranial placodes. , Schlosser G ., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm. , Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm. , Janesick A ., Development. March 1, 2012; 139 (6): 1213-24.
ΔNp63 is regulated by BMP4 signaling and is required for early epidermal development in Xenopus. , Tríbulo C ., Dev Dyn. February 1, 2012; 241 (2): 257-69.
The LIM adaptor protein LMO4 is an essential regulator of neural crest development. , Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
Origin and segregation of cranial placodes in Xenopus laevis. , Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
Yes-associated protein 65 ( YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. , Gee ST ., PLoS One. January 1, 2011; 6 (6): e20309.
Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors. , Neilson KM ., Dev Dyn. December 1, 2010; 239 (12): 3446-66.
The F-box protein Cdc4/ Fbxw7 is a novel regulator of neural crest development in Xenopus laevis. , Almeida AD., Neural Dev. January 4, 2010; 5 1.
The posteriorizing gene Gbx2 is a direct target of Wnt signalling and the earliest factor in neural crest induction. , Li B., Development. October 1, 2009; 136 (19): 3267-78.
Xhairy2 functions in Xenopus lens development by regulating p27( xic1) expression. , Murato Y., Dev Dyn. September 1, 2009; 238 (9): 2179-92.
Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.
Hairy2- Id3 interactions play an essential role in Xenopus neural crest progenitor specification. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm. , Carmona-Fontaine C., Dev Biol. September 15, 2007; 309 (2): 208-21.
The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border. , Hong CS ., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.
XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms. , van Grunsven LA., Dev Biol. June 1, 2007; 306 (1): 34-49.
Neural induction in Xenopus requires inhibition of Wnt-beta-catenin signaling. , Heeg-Truesdell E., Dev Biol. October 1, 2006; 298 (1): 71-86.
Induction and specification of cranial placodes. , Schlosser G ., Dev Biol. June 15, 2006; 294 (2): 303-51.
XNF-ATc3 affects neural convergent extension. , Borchers A ., Development. May 1, 2006; 133 (9): 1745-55.
An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation. , Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system. , Huang X ., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
Evolutionary origins of vertebrate placodes: insights from developmental studies and from comparisons with other deuterostomes. , Schlosser G ., J Exp Zool B Mol Dev Evol. July 15, 2005; 304 (4): 347-99.
Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. , Brugmann SA ., Development. December 1, 2004; 131 (23): 5871-81.
Role of BMP signaling and the homeoprotein Iroquois in the specification of the cranial placodal field. , Glavic A ., Dev Biol. August 1, 2004; 272 (1): 89-103.
Molecular anatomy of placode development in Xenopus laevis. , Schlosser G ., Dev Biol. July 15, 2004; 271 (2): 439-66.
Dlx proteins position the neural plate border and determine adjacent cell fates. , Woda JM., Development. January 1, 2003; 130 (2): 331-42.