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Profile Publications(36)
XB-PERS-760

Publications By Gerald H. Thomsen

Results 1 - 36 of 36 results

Page(s): 1


Gtpbp2 is a positive regulator of Wnt signaling and maintains low levels of the Wnt negative regulator Axin., Gillis WQ, Kirmizitas A, Iwasaki Y, Ki DH, Wyrick JM, Thomsen GH., Cell Commun Signal. August 2, 2016; 14 (1): 15.              


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y, Thomsen GH., Development. October 1, 2014; 141 (19): 3740-51.                                          


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A, Gillis WQ, Zhu H, Thomsen GH., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


Simple and efficient CRISPR/Cas9-mediated targeted mutagenesis in Xenopus tropicalis., Nakayama T, Fish MB, Fisher M, Oomen-Hajagos J, Thomsen GH, Grainger RM., Genesis. December 1, 2013; 51 (12): 835-43.            


Mustn1 is essential for craniofacial chondrogenesis during Xenopus development., Gersch RP, Kirmizitas A, Sobkow L, Sorrentino G, Thomsen GH, Hadjiargyrou M., Gene Expr Patterns. April 24, 2013; 145-53.                


Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM, Park CY, Xu X, Zhu H, Smith JC, Thomsen GH., Open Biol. April 1, 2012; 2 (4): 120060.                      


Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM, Gillis WQ, Oomen-Hajagos J, Thomsen GH., Evodevo. January 1, 2012; 3 (1): 22.              


A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus., Callery EM, Thomsen GH, Smith JC., Dev Biol. April 1, 2010; 340 (1): 75-87.                


Tumor necrosis factor-receptor-associated factor-4 is a positive regulator of transforming growth factor-beta signaling that affects neural crest formation., Kalkan T, Iwasaki Y, Park CY, Thomsen GH., Mol Biol Cell. July 1, 2009; 20 (14): 3436-50.                          


Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM, Thomsen GH., Dev Biol. November 15, 2006; 299 (2): 398-410.                      


Molecular evidence for deep evolutionary roots of bilaterality in animal development., Matus DQ, Pang K, Marlow H, Dunn CW, Thomsen GH, Martindale MQ., Proc Natl Acad Sci U S A. July 25, 2006; 103 (30): 11195-200.            


Dorso/ventral genes are asymmetrically expressed and involved in germ-layer demarcation during cnidarian gastrulation., Matus DQ, Thomsen GH, Martindale MQ., Curr Biol. March 7, 2006; 16 (5): 499-505.


A new century of amphibian developmental biology., Thomsen GH., Semin Cell Dev Biol. February 1, 2006; 17 (1): 78-9.


The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM, Smith JC, Thomsen GH., Dev Biol. February 15, 2005; 278 (2): 542-59.                              


Regulation of cell polarity and protrusion formation by targeting RhoA for degradation., Wang HR, Zhang Y, Ozdamar B, Ogunjimi AA, Alexandrova E, Thomsen GH, Wrana JL., Science. December 5, 2003; 302 (5651): 1775-9.


Smad7 binds to Smurf2 to form an E3 ubiquitin ligase that targets the TGF beta receptor for degradation., Kavsak P, Rasmussen RK, Causing CG, Bonni S, Zhu H, Thomsen GH, Wrana JL., Mol Cell. December 1, 2000; 6 (6): 1365-75.


A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation., Zhu H, Kavsak P, Abdollah S, Wrana JL, Thomsen GH., Nature. August 12, 1999; 400 (6745): 687-93.


Tbx5 is essential for heart development., Horb ME, Thomsen GH., Development. April 1, 1999; 126 (8): 1739-51.              


Dominant-negative Smad2 mutants inhibit activin/Vg1 signaling and disrupt axis formation in Xenopus., Hoodless PA, Tsukazaki T, Nishimatsu S, Attisano L, Wrana JL, Thomsen GH., Dev Biol. March 15, 1999; 207 (2): 364-79.


Ventral mesoderm induction and patterning by bone morphogenetic protein heterodimers in Xenopus embryos., Nishimatsu S, Thomsen GH., Mech Dev. June 1, 1998; 74 (1-2): 75-88.


A Xenopus homologue of aml-1 reveals unexpected patterning mechanisms leading to the formation of embryonic blood., Tracey WD, Pepling ME, Horb ME, Thomsen GH, Gergen JP., Development. April 1, 1998; 125 (8): 1371-80.                


Xenopus Cdc6 confers sperm binding competence to oocytes without inducing their maturation., Tian J, Thomsen GH, Gong H, Lennarz WJ., Proc Natl Acad Sci U S A. September 30, 1997; 94 (20): 10729-34.


Xenopus laevis sperm-egg adhesion is regulated by modifications in the sperm receptor and the egg vitelline envelope., Tian J, Gong H, Thomsen GH, Lennarz WJ., Dev Biol. July 15, 1997; 187 (2): 143-53.              


Antagonism within and around the organizer: BMP inhibitors in vertebrate body patterning., Thomsen GH., Trends Genet. June 1, 1997; 13 (6): 209-11.


A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME, Thomsen GH., Development. May 1, 1997; 124 (9): 1689-98.                    


Gamete interactions in Xenopus laevis: identification of sperm binding glycoproteins in the egg vitelline envelope., Tian J, Gong H, Thomsen GH, Lennarz WJ., J Cell Biol. March 10, 1997; 136 (5): 1099-108.              


Nomenclature: vertebrate mediators of TGFbeta family signals., Derynck R, Gelbart WM, Harland RM, Heldin CH, Kern SE, Massagué J, Melton DA, Mlodzik M, Padgett RW, Roberts AB, Smith J, Thomsen GH, Vogelstein B, Wang XF., Cell. October 18, 1996; 87 (2): 173.


MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma., Eppert K, Scherer SW, Ozcelik H, Pirone R, Hoodless P, Kim H, Tsui LC, Bapat B, Gallinger S, Andrulis IL, Thomsen GH, Wrana JL, Attisano L., Cell. August 23, 1996; 86 (4): 543-52.


Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor., Thomsen GH., Development. August 1, 1996; 122 (8): 2359-66.              


Ventral mesodermal patterning in Xenopus embryos: expression patterns and activities of BMP-2 and BMP-4., Hemmati-Brivanlou A, Thomsen GH., Dev Genet. January 1, 1995; 17 (1): 78-89.


Vg1 and regional specification in vertebrates: a new role for an old molecule., Vize PD, Thomsen GH., Trends Genet. October 1, 1994; 10 (10): 371-6.


Processed Vg1 protein is an axial mesoderm inducer in Xenopus., Thomsen GH, Melton DA., Cell. August 13, 1993; 74 (3): 433-41.


Expression of activin mRNA during early development in Xenopus laevis., Dohrmann CE, Hemmati-Brivanlou A, Thomsen GH, Fields A, Woolf TM, Melton DA., Dev Biol. June 1, 1993; 157 (2): 474-83.          


Activins are expressed early in Xenopus embryogenesis and can induce axial mesoderm and anterior structures., Thomsen G, Woolf T, Whitman M, Sokol S, Vaughan J, Vale W, Melton DA., Cell. November 2, 1990; 63 (3): 485-93.


Major transitions in histone gene expression do not occur during development in Xenopus laevis., Perry M, Thomsen GH, Roeder RG., Dev Biol. August 1, 1986; 116 (2): 532-8.


Genomic organization and nucleotide sequence of two distinct histone gene clusters from Xenopus laevis. Identification of novel conserved upstream sequence elements., Perry M, Thomsen GH, Roeder RG., J Mol Biol. October 5, 1985; 185 (3): 479-99.

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