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1-20 of 67
Keywords: activin
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Journal Articles
Journal:
Development
Development (2021) 148 (1): dev190868.
Published: 10 January 2021
...Myung-Jun Kim; Michael B. O'Connor ABSTRACT The Myostatin/Activin branch of the TGF-β superfamily acts as a negative regulator of vertebrate skeletal muscle size, in part, through downregulation of insulin/insulin-like growth factor 1 (IGF-1) signaling. Surprisingly, recent studies in Drosophila...
Includes: Supplementary data
Journal Articles
Reduced expression of the Nodal co-receptor Oep causes loss of mesendodermal competence in zebrafish
Journal:
Development
Development (2018) 145 (5): dev158832.
Published: 6 March 2018
... between shield stage (6 hpf) and 75% epiboly (8 hpf). Next, we asked whether the loss of Nodal responsiveness at 75% epiboly is caused by extracellular or intracellular changes. We used photoswitchable Activin receptors I and II, which activate the Nodal signaling pathway upon blue light...
Includes: Supplementary data
Journal Articles
In collection:
Stem cells & regeneration
Charles Arber, Sophie V. Precious, Serafí Cambray, Jessica R. Risner-Janiczek, Claire Kelly, Zoe Noakes, Marija Fjodorova, Andreas Heuer, Mark A. Ungless, Tristan A. Rodríguez, Anne E. Rosser, Stephen B. Dunnett, Meng Li
Journal:
Development
Development (2015) 142 (7): 1375–1386.
Published: 1 April 2015
... degenerate in the early phase of Huntington's disease. Here we report that activin A induces lateral ganglionic eminence (LGE) characteristics in nascent neural progenitors derived from hESCs and hiPSCs in a sonic hedgehog-independent manner. Correct specification of striatal phenotype was further...
Includes: Supplementary data
Journal Articles
In collection:
Stem cells & regeneration
Journal:
Development
Development (2015) 142 (5): 883–892.
Published: 1 March 2015
... precursors and two steps of cell shape change to form the mature TF cells. The Activin receptor Baboon (Babo) is required for somatic precursor cell proliferation and therefore determines the pool of TF precursors available for TF differentiation. During the final differentiation stage, Babo facilitates TF...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2015) 142 (4): 607–619.
Published: 15 February 2015
...Siim Pauklin; Ludovic Vallier Activin/Nodal growth factors control a broad range of biological processes, including early cell fate decisions, organogenesis and adult tissue homeostasis. Here, we provide an overview of the mechanisms by which the Activin/Nodal signalling pathway governs stem cell...
Journal Articles
Dipankar J. Dutta, Andleeb Zameer, John N. Mariani, Jingya Zhang, Linnea Asp, Jimmy Huynh, Sean Mahase, Benjamin M. Laitman, Azeb Tadesse Argaw, Nesanet Mitiku, Mateusz Urbanski, Carmen V. Melendez-Vasquez, Patrizia Casaccia, Fernand Hayot, Erwin P. Bottinger, Chester W. Brown, Gareth R. John
Journal:
Development
Development (2014) 141 (12): 2414–2428.
Published: 15 June 2014
... In the embryonic CNS, development of myelin-forming oligodendrocytes is limited by bone morphogenetic proteins, which constitute one arm of the transforming growth factor-β (Tgfβ) family and signal canonically via Smads 1/5/8. Tgfβ ligands and Activins comprise the other arm and signal via Smads 2/3...
Includes: Supplementary data
Journal Articles
Laura Faas, Fiona C. Warrander, Richard Maguire, Simon A. Ramsbottom, Diana Quinn, Paul Genever, Harry V. Isaacs
Journal:
Development
Development (2013) 140 (5): 976–986.
Published: 1 March 2013
... signals. The development of axial and paraxial mesoderm is severely abnormal in lin28 knockdown (morphant) embryos. In culture, the ability of pluripotent cells from the embryo to respond to the FGF and activin/nodal-like mesoderm-inducing pathways is compromised following inhibition of lin28 function...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2013) 140 (3): 675–686.
Published: 1 February 2013
... and liver, and animal studies have revealed an essential role for Nodal in development of the definitive endoderm. Activin A is a related TGFβ member that acts through many of the same downstream signaling effectors as Nodal and is thought to mimic Nodal activity. Detailed characterization of ES cell...
Includes: Multimedia, Supplementary data
Journal Articles
Andrey V. Bayramov, Fedor M. Eroshkin, Natalia Y. Martynova, Galina V. Ermakova, Elena A. Solovieva, Andrey G. Zaraisky
Journal:
Development
Development (2011) 138 (24): 5345–5356.
Published: 15 December 2011
... of Noggin proteins, our findings demonstrate that specification of the forebrain requires isolation of its cells from BMP, Activin/Nodal and Wnt signaling not only during gastrulation but also at post-gastrulation stages. When tALK4- or Dkk1-expressing plasmids were co-injected (4 ng/μl) with Noggin2 MO...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2011) 138 (13): 2693–2703.
Published: 1 July 2011
... TGFβ/Activin signaling, specifically in the Drosophila prothoracic gland, results in developmental arrest prior to metamorphosis. The terminal, giant third instar larval phenotype results from a failure to induce the large rise in ecdysteroid titer that triggers metamorphosis. We further demonstrate...
Includes: Supplementary data
Journal Articles
Véronique Duboc, François Lapraz, Alexandra Saudemont, Nathalie Bessodes, Flavien Mekpoh, Emmanuel Haillot, Magali Quirin, Thierry Lepage
Journal:
Development
Development (2010) 137 (2): 223–235.
Published: 15 January 2010
... the cell-autonomous expression of gcm and the cell-autonomous repression of gata1/2/3 . Taken with our previous finding that preventing translation of Nodal, but not of Activin or of TGFβ sensu stricto (data not shown), disrupts D/V patterning of the SMCs, these results strongly suggest that Nodal...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2009) 136 (16): 2803–2813.
Published: 15 August 2009
..., is still poorly understood. In Xenopus , members of the TGF-β family such as the nodal-related proteins and activin act as morphogens to induce mesoderm and endoderm. In an effort to understand the mechanisms and dynamics of morphogen gradient formation, we have used fluorescently labelled activin to study...
Includes: Multimedia, Supplementary data
Journal Articles
Journal:
Development
Development (2009) 136 (12): 1995–2004.
Published: 15 June 2009
... cells and the formation of the anterior border of the kidney morphogenetic field. We identified the dorsal neural tube as the potential kidney-inductive tissue and showed that activin, a secreted morphogen, is necessary but insufficient for Lim1 induction and establishment of the kidney field. Activin...
Journal Articles
Ludovic Vallier, Sasha Mendjan, Stephanie Brown, Zhenzhi Chng, Adrian Teo, Lucy E. Smithers, Matthew W. B. Trotter, Candy H.-H. Cho, Amelie Martinez, Peter Rugg-Gunn, Gabrielle Brons, Roger A. Pedersen
Journal:
Development
Development (2009) 136 (8): 1339–1349.
Published: 15 April 2009
... applications. The Activin/Nodal signalling pathway is necessary to maintain pluripotency in human ESCs and in mouse epiblast stem cells (EpiSCs), but the molecular mechanisms by which it achieves this effect remain obscure. Here, we demonstrate that Activin/Nodal signalling controls expression of the key...
Includes: Supplementary data
Journal Articles
Changqi C. Zhu, Jason Q. Boone, Philip A. Jensen, Scott Hanna, Lynn Podemski, John Locke, Chris Q. Doe, Michael B. O'Connor
Journal:
Development
Development (2008) 135 (3): 513–521.
Published: 1 February 2008
...Changqi C. Zhu; Jason Q. Boone; Philip A. Jensen; Scott Hanna; Lynn Podemski; John Locke; Chris Q. Doe; Michael B. O'Connor The Drosophila Activin-like ligands Activin-β and Dawdle control several aspects of neuronal morphogenesis, including mushroom body remodeling, dorsal neuron morphogenesis...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2007) 134 (23): 4209–4218.
Published: 1 December 2007
...Yasushi Saka; Anja I. Hagemann; Olaf Piepenburg; James C. Smith Activin and the Nodal-related proteins induce mesendodermal tissues during Xenopus development. These signals act through specific receptors to cause the phosphorylation, at their carboxyl termini, of Smad2 and Smad3...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2006) 133 (24): 4981–4991.
Published: 15 December 2006
... pathfinding in Drosophila . In daw mutants, ISNb and SNa axons fail to extend completely and are unable to innervate their targets. We find that Daw initiates an activin signaling pathway via the receptors Punt and Baboon (Babo) and the signal-transducer Smad2. Furthermore, mutations in these signaling...
Journal Articles
Journal:
Development
Development (2006) 133 (24): 4969–4979.
Published: 15 December 2006
.... We show that Tlr is a circulating enzyme that processes the pro-domains of three Drosophila TGF-β-type ligands, and, in the case of the Activin-like protein Dawdle (Daw), this processing enhances the signaling activity of the ligand in vitro and in vivo. Null mutants of daw, as well as mutations...
Journal Articles
Positive and negative regulations by FGF8 contribute to midbrain roof plate developmental plasticity
Journal:
Development
Development (2006) 133 (15): 2905–2913.
Published: 1 August 2006
... by members of the TGFβ superfamily belonging to the BMP, GDF and activin subgroups. We show in particular that FGF8 tightly modulates follistatin expression, thus progressively restraining the inhibitory influence of activin B on RP differentiation. These regulations, together with FGF8 triggered apoptosis...
Journal Articles
Journal:
Development
Development (2005) 132 (4): 763–774.
Published: 15 February 2005
..., suggesting that GATA4 induces these genes via GATA6 in this assay. All three GATA factors were induced by activin, although GATA4 and 6 required lower concentrations. GATA MOs inhibited Sox17α and HNF1β induction by activin at low and high concentrations in the order:GATA6>GATA4>GATA5. Together...
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