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The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation. , Acosta H, Iliev D, Grahn TH, Gouignard N , Maccarana M, Griesbach J, Herzmann S, Sagha M, Climent M , Pera EM ., Development. March 15, 2015; 142 (6): 1146-58.
The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation. , Acosta H, Iliev D, Grahn TH, Gouignard N , Maccarana M, Griesbach J, Herzmann S, Sagha M, Climent M , Pera EM ., Development. March 15, 2015; 142 (6): 1146-58.
The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus. , Griffin JN, Sondalle SB, Del Viso F, Baserga SJ, Khokha MK ., PLoS Genet. March 10, 2015; 11 (3): e1005018.
E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation. , Wills AE , Baker JC ., Dev Cell. February 9, 2015; 32 (3): 345-57.
Nkx2.5 is involved in myeloid cell differentiation at anterior ventral blood islands in the Xenopus embryo. , Sakata H, Maéno M., Dev Growth Differ. October 1, 2014; 56 (8): 544-54.
Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis. , Rozario T, Mead PE , DeSimone DW ., Mech Dev. August 1, 2014; 133 203-17.
Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis. , Rozario T, Mead PE , DeSimone DW ., Mech Dev. August 1, 2014; 133 203-17.
Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis. , Guo Y, Kühl SJ , Pfister AS, Cizelsky W, Denk S, Beer-Molz L, Kühl M ., PLoS One. January 17, 2014; 9 (1): e87294.
Jun N-terminal kinase maintains tissue integrity during cell rearrangement in the gut. , Dush MK, Nascone-Yoder NM ., Development. April 1, 2013; 140 (7): 1457-66.
sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling. , Gibb N , Lavery DL, Hoppler S ., Development. April 1, 2013; 140 (7): 1537-49.
Functional analysis of Rfx6 and mutant variants associated with neonatal diabetes. , Pearl EJ , Jarikji Z , Horb ME ., Dev Biol. March 1, 2011; 351 (1): 135-45.
Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus. , Smith SJ , Mohun TJ ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
Claudin5 genes encoding tight junction proteins are required for Xenopus heart formation. , Yamagishi M , Ito Y , Ariizumi T, Komazaki S, Danno H, Michiue T , Asashima M ., Dev Growth Differ. September 1, 2010; 52 (7): 665-75.
Focal adhesion kinase is essential for cardiac looping and multichamber heart formation. , Doherty JT, Conlon FL , Mack CP, Taylor JM., Genesis. August 1, 2010; 48 (8): 492-504.
FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis. , Schuff M, Siegel D , Bardine N, Oswald F, Donow C, Knöchel W ., Dev Biol. January 15, 2010; 337 (2): 259-73.
FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis. , Schuff M, Siegel D , Bardine N, Oswald F, Donow C, Knöchel W ., Dev Biol. January 15, 2010; 337 (2): 259-73.
Wnt6 signaling regulates heart muscle development during organogenesis. , Lavery DL, Martin J, Turnbull YD, Hoppler S ., Dev Biol. November 15, 2008; 323 (2): 177-88.
Fli1 acts at the top of the transcriptional network driving blood and endothelial development. , Liu F, Walmsley M, Rodaway A, Patient R ., Curr Biol. August 26, 2008; 18 (16): 1234-40.
Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1. , Movassagh M, Philpott A ., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1. , Movassagh M, Philpott A ., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage. , Ito Y , Seno S, Nakamura H, Fukui A , Asashima M ., Dev Biol. July 1, 2008; 319 (1): 34-45.
XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage. , Ito Y , Seno S, Nakamura H, Fukui A , Asashima M ., Dev Biol. July 1, 2008; 319 (1): 34-45.
A crucial role of a high mobility group protein HMGA2 in cardiogenesis. , Monzen K, Ito Y , Naito AT, Kasai H, Hiroi Y, Hayashi D, Shiojima I, Yamazaki T, Miyazono K, Asashima M , Nagai R, Komuro I., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
A crucial role of a high mobility group protein HMGA2 in cardiogenesis. , Monzen K, Ito Y , Naito AT, Kasai H, Hiroi Y, Hayashi D, Shiojima I, Yamazaki T, Miyazono K, Asashima M , Nagai R, Komuro I., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus. , Nagao K, Taniyama Y, Kietzmann T, Doi T, Komuro I, Morishita R., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus. , Nagao K, Taniyama Y, Kietzmann T, Doi T, Komuro I, Morishita R., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline. , Christine KS , Conlon FL ., Dev Cell. April 1, 2008; 14 (4): 616-23.
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm. , Spagnoli FM , Brivanlou AH ., Development. February 1, 2008; 135 (3): 451-61.
Redundancy and evolution of GATA factor requirements in development of the myocardium. , Peterkin T, Gibson A, Patient R ., Dev Biol. November 15, 2007; 311 (2): 623-35.
Redundancy and evolution of GATA factor requirements in development of the myocardium. , Peterkin T, Gibson A, Patient R ., Dev Biol. November 15, 2007; 311 (2): 623-35.
The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development. , Brade T, Gessert S, Kühl M , Pandur P ., Dev Biol. November 15, 2007; 311 (2): 297-310.
The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo. , Hou S, Maccarana M, Min TH, Strate I, Pera EM ., Dev Cell. August 1, 2007; 13 (2): 226-41.
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination. , Hilton EN , Manson FD, Urquhart JE, Johnston JJ , Slavotinek AM, Hedera P, Stattin EL, Nordgren A, Biesecker LG, Black GC ., Hum Mol Genet. July 15, 2007; 16 (14): 1773-82.
Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus. , Zhao H , Rebbert ML, Dawid IB ., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.
ADMP2 is essential for primitive blood and heart development in Xenopus. , Kumano G , Ezal C, Smith WC ., Dev Biol. November 15, 2006; 299 (2): 411-23.
Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis. , Inui M, Fukui A , Ito Y , Asashima M ., Dev Biol. October 1, 2006; 298 (1): 188-200.
Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart. , Allen BG , Allen-Brady K, Weeks DL ., Mech Dev. October 1, 2006; 123 (10): 719-29.
TBX5 is required for embryonic cardiac cell cycle progression. , Goetz SC, Brown DD , Conlon FL ., Development. July 1, 2006; 133 (13): 2575-84.
SOX7 and SOX18 are essential for cardiogenesis in Xenopus. , Zhang C, Basta T, Klymkowsky MW ., Dev Dyn. December 1, 2005; 234 (4): 878-91.
Myocardin is sufficient and necessary for cardiac gene expression in Xenopus. , Small EM , Warkman AS , Wang DZ, Sutherland LB, Olson EN, Krieg PA ., Development. March 1, 2005; 132 (5): 987-97.
Myocardin is sufficient and necessary for cardiac gene expression in Xenopus. , Small EM , Warkman AS , Wang DZ, Sutherland LB, Olson EN, Krieg PA ., Development. March 1, 2005; 132 (5): 987-97.
Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis. , Brown DD , Martz SN, Binder O , Goetz SC, Price BM, Smith JC , Conlon FL ., Development. February 1, 2005; 132 (3): 553-63.