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Modulation of potassium channel function confers a hyperproliferative invasive phenotype on embryonic stem cells. , Morokuma J., Proc Natl Acad Sci U S A. October 28, 2008; 105 (43): 16608-13.
A new role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification. , Bonano M., Dev Biol. November 1, 2008; 323 (1): 114-29.
Segmentation of the vertebrate skull: neural-crest derivation of adult cartilages in the clawed frog, Xenopus laevis. , Gross JB ., Integr Comp Biol. November 1, 2008; 48 (5): 681-96.
Raldh expression in embryos of the direct developing frog Eleutherodactylus coqui and the conserved retinoic acid requirement for forelimb initiation. , Elinson RP ., J Exp Zool B Mol Dev Evol. November 15, 2008; 310 (7): 588-95.
Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus. , Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
PTK7 recruits dsh to regulate neural crest migration. , Shnitsar I., Development. December 1, 2008; 135 (24): 4015-24.
Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis. , Koestner U., Dev Dyn. December 1, 2008; 237 (12): 3853-63.
RNA isolation from Xenopus inner ear sensory endorgans for transcriptional profiling and molecular cloning. , Trujillo-Provencio C., Methods Mol Biol. January 1, 2009; 493 3-20.
Samba, a Xenopus hnRNP expressed in neural and neural crest tissues. , Yan CY., Dev Dyn. January 1, 2009; 238 (1): 204-9.
Expression patterns of Src-family tyrosine kinases during Xenopus laevis development. , Ferjentsik Z., Int J Dev Biol. January 1, 2009; 53 (1): 163-8.
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.
Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1. , Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
Evolution of non-coding regulatory sequences involved in the developmental process: reflection of differential employment of paralogous genes as highlighted by Sox2 and group B1 Sox genes. , Kamachi Y., Proc Jpn Acad Ser B Phys Biol Sci. January 1, 2009; 85 (2): 55-68.
Developmental expression and regulation of the chemokine CXCL14 in Xenopus. , Park BY., Int J Dev Biol. January 1, 2009; 53 (4): 535-40.
Dynamic expression pattern of distinct genes in the presomitic and somitic mesoderm during Xenopus development. , Bourdelas A., Int J Dev Biol. January 1, 2009; 53 (7): 1075-9.
Expression of CAP2 during early Xenopus embryogenesis. , Wolanski M., Int J Dev Biol. January 1, 2009; 53 (7): 1063-7.
STRUCTURE AND FUNCTION OF THE MIDDLE EAR APPARATUS OF THE AQUATIC FROG, XENOPUS LAEVIS. , Mason M., Proc Inst Acoust. January 1, 2009; 31 13-21.
Xenopus NM23-X4 regulates retinal gliogenesis through interaction with p27Xic1. , Mochizuki T., Neural Dev. January 5, 2009; 4 1.
Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system. , Strate I., Development. February 1, 2009; 136 (3): 461-72.
Comparative expression analysis of the neurogenins in Xenopus tropicalis and Xenopus laevis. , Nieber F., Dev Dyn. February 1, 2009; 238 (2): 451-8.
Complementary expression of HSPG 6-O-endosulfatases and 6-O-sulfotransferase in the hindbrain of Xenopus laevis. , Winterbottom EF., Gene Expr Patterns. March 1, 2009; 9 (3): 166-72.
Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis. , Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms? , Choi BY., Hum Mutat. April 1, 2009; 30 (4): 599-608.
FGF signalling during embryo development regulates cilia length in diverse epithelia. , Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.
Zebrafish gbx1 refines the midbrain- hindbrain boundary border and mediates the Wnt8 posteriorization signal. , Rhinn M., Neural Dev. April 2, 2009; 4 12.
Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome. , Yang T., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations. , Bockenhauer D., N Engl J Med. May 7, 2009; 360 (19): 1960-70.
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.
Beyond early development: Xenopus as an emerging model for the study of regenerative mechanisms. , Beck CW ., Dev Dyn. June 1, 2009; 238 (6): 1226-48.
Temporal and spatial expression of FGF ligands and receptors during Xenopus development. , Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.
The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets. , Lee C , Lee C , Lee C ., Dev Dyn. June 1, 2009; 238 (6): 1480-91.
LIMK1 acts downstream of BMP signaling in developing retinal ganglion cell axons but not dendrites. , Hocking JC ., Dev Biol. June 15, 2009; 330 (2): 273-85.
Tumor necrosis factor-receptor-associated factor-4 is a positive regulator of transforming growth factor-beta signaling that affects neural crest formation. , Kalkan T., Mol Biol Cell. July 1, 2009; 20 (14): 3436-50.
Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians. , Choi BY., Genet Test Mol Biomarkers. October 1, 2009; 13 (5): 679-87.
Myosin-X is required for cranial neural crest cell migration in Xenopus laevis. , Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.
Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases. , Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.
Characterization of the expression pattern of the PRC2 core subunit Suz12 during embryonic development of Xenopus laevis. , Aldiri I ., Dev Dyn. December 1, 2009; 238 (12): 3185-92.
Regulatory elements of Xenopus col2a1 drive cartilaginous gene expression in transgenic frogs. , Kerney R., Int J Dev Biol. January 1, 2010; 54 (1): 141-50.
RNA helicase Ddx39 is expressed in the developing central nervous system, limb, otic vesicle, branchial arches and facial mesenchyme of Xenopus laevis. , Wilson JM., Gene Expr Patterns. January 1, 2010; 10 (1): 44-52.
Distinct roles for Robo2 in the regulation of axon and dendrite growth by retinal ganglion cells. , Hocking JC ., Mech Dev. January 1, 2010; 127 (1-2): 36-48.
Zebrafish fetal alcohol syndrome model: effects of ethanol are rescued by retinoic acid supplement. , Marrs JA., Alcohol. January 1, 2010; 44 (7-8): 707-15.
Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo. , Kurauchi T., Differentiation. January 1, 2010; 79 (4-5): 251-9.
Identification and gastrointestinal expression of Xenopus laevis FoxF2. , McLin VA ., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
The lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) receptor gene families: cloning and comparative expression analysis in Xenopus laevis. , Massé K ., Int J Dev Biol. January 1, 2010; 54 (8-9): 1361-74.
Transplantation of Xenopus laevis ears reveals the ability to form afferent and efferent connections with the spinal cord. , Elliott KL., Int J Dev Biol. January 1, 2010; 54 (10): 1443-51.
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.
EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis. , Li Y., Biol Cell. February 17, 2010; 102 (5): 277-92.
CHD7 cooperates with PBAF to control multipotent neural crest formation. , Bajpai R ., Nature. February 18, 2010; 463 (7283): 958-62.
Genomic code for Sox10 activation reveals a key regulatory enhancer for cranial neural crest. , Betancur P., Proc Natl Acad Sci U S A. February 23, 2010; 107 (8): 3570-5.
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf. , Tekin M., Ann Hum Genet. March 1, 2010; 74 (2): 155-64.